From a78689f64122c6fb1907f3e60865d5f63cba8907 Mon Sep 17 00:00:00 2001
From: Maria Marin <maria.marin.tercero@alumnos.upm.es>
Date: Wed, 7 Feb 2024 11:53:43 +0000
Subject: [PATCH] Upload New File

---
 Network Science/Data/Nodes/dis.tsv | 30732 +++++++++++++++++++++++++++
 1 file changed, 30732 insertions(+)
 create mode 100644 Network Science/Data/Nodes/dis.tsv

diff --git a/Network Science/Data/Nodes/dis.tsv b/Network Science/Data/Nodes/dis.tsv
new file mode 100644
index 0000000..49a66bd
--- /dev/null
+++ b/Network Science/Data/Nodes/dis.tsv	
@@ -0,0 +1,30732 @@
+id	name
+C0000727	Abdomen, Acute
+C0000729	Abdominal cramps
+C0000731	Abdomen distended
+C0000734	Abdominal mass
+C0000735	Abdominal neoplasm
+C0000737	Abdominal Pain
+C0000744	Abetalipoproteinemia
+C0000766	X-ray abnormal
+C0000768	Congenital Abnormality
+C0000771	Abnormalities, Drug-Induced
+C0000772	Multiple congenital abnormalities
+C0000786	Abortion, Spontaneous
+C0000809	Abortion, Habitual
+C0000810	Abortion, Incomplete
+C0000814	Abortion missed
+C0000817	Abortion infected
+C0000821	Abortion threatened
+C0000822	Abortion, Tubal
+C0000823	Abortion, Veterinary
+C0000832	Abruptio Placentae
+C0000833	Abscess
+C0000846	Agenesis
+C0000880	Acanthamoeba Keratitis
+C0000887	Acantholysis
+C0000889	Acanthosis Nigricans
+C0000924	Accident
+C0001075	Achlorhydria
+C0001079	Achondrogenesis
+C0001080	Achondroplasia
+C0001118	Acid-Base Imbalance
+C0001122	Acidosis
+C0001125	Acidosis, Lactic
+C0001126	Renal tubular acidosis
+C0001127	Acidosis, Respiratory
+C0001139	Acinetobacter infection
+C0001144	Acne Vulgaris
+C0001145	Acne Keloid
+C0001163	Vestibulocochlear Nerve Diseases
+C0001175	Acquired Immunodeficiency Syndrome
+C0001193	Apert syndrome
+C0001197	Acrodermatitis
+C0001198	Acrodynia
+C0001202	Acrokeratosis
+C0001206	Acromegaly
+C0001231	ACTH Syndrome, Ectopic
+C0001255	Actinomycetales Infections
+C0001261	Actinomycosis
+C0001306	Acute alcoholic liver disease
+C0001308	Acute and subacute liver necrosis (disorder)
+C0001311	Acute bronchiolitis
+C0001314	Acute Disease
+C0001338	Herpetic Acute Necrotizing Encephalitis
+C0001339	Acute pancreatitis
+C0001342	Acute periodontitis
+C0001349	Acute phase reaction
+C0001361	Acute tonsillitis
+C0001364	Acute yellow liver atrophy
+C0001396	Adams-Stokes syndrome
+C0001403	Addison Disease
+C0001416	Adenitis
+C0001418	Adenocarcinoma
+C0001420	Papillary adenocarcinoma
+C0001422	Adenofibroma
+C0001425	Adenoidectomy
+C0001429	Adenolymphoma
+C0001430	Adenoma
+C0001432	Adenoma, Chromophobe
+C0001433	Adenoma, Acidophil
+C0001442	Adenosarcoma
+C0001486	Adenoviridae Infections
+C0001487	Adenovirus Infections, Human
+C0001510	Adhesions NOS postoperative
+C0001511	Adhesion
+C0001519	Adie's syndrome
+C0001529	Adiposis Dolorosa
+C0001539	Adjustment disorder with depressed mood
+C0001546	Adjustment disorder
+C0001576	Adnexal Diseases
+C0001577	Adnexitis
+C0001614	Adrenal Cortex Diseases
+C0001618	Adrenal Cortex Neoplasms
+C0001621	Adrenal Gland Diseases
+C0001622	Adrenal Gland Hyperfunction
+C0001623	Adrenal gland hypofunction
+C0001624	Adrenal Gland Neoplasms
+C0001627	Adrenal Hyperplasia, Congenital
+C0001630	Adrenal Rest Tumor
+C0001676	Adult Antisocial Behavior
+C0001707	Aerophagy
+C0001723	Affective Disorders, Psychotic
+C0001726	Affective Symptoms
+C0001733	Afibrinogenemia
+C0001752	African swine fever
+C0001768	Agammaglobulinemia
+C0001787	Osteoporosis, Age-Related
+C0001807	Aggression
+C0001811	Aging
+C0001815	Primary Myelofibrosis
+C0001816	Agnosia
+C0001818	Agoraphobia
+C0001824	Agranulocytosis
+C0001825	Agraphia
+C0001828	Agricultural Workers' Diseases
+C0001849	AIDS Dementia Complex
+C0001857	AIDS related complex
+C0001882	Airsickness
+C0001883	Airway Obstruction
+C0001889	Akinetic Mutism
+C0001890	Akinetic Petit Mal
+C0001916	Albinism
+C0001925	Albuminuria
+C0001948	Alcohol consumption
+C0001956	Alcohol Use Disorder
+C0001957	Alcohol Withdrawal Delirium
+C0001969	Alcoholic Intoxication
+C0001973	Alcohol dependence
+C0002016	Aleutian Mink Disease
+C0002018	Alexia
+C0002020	Alexithymia
+C0002063	Alkalosis
+C0002064	Alkalosis, Respiratory
+C0002066	Alkaptonuria
+C0002103	Atopic rhinitis
+C0002152	Alloxan Diabetes
+C0002170	Alopecia
+C0002171	Alopecia Areata
+C0002173	Follicular mucinosis
+C0002312	alpha-Thalassemia
+C0002351	Altitude Sickness
+C0002382	Alveolar Bone Loss
+C0002390	Alveolitis, Extrinsic Allergic
+C0002393	Alveoloplasty
+C0002395	Alzheimer Disease
+C0002418	Amblyopia
+C0002438	Amebiasis
+C0002445	Ameboma
+C0002447	Amelia
+C0002448	Ameloblastoma
+C0002452	Amelogenesis Imperfecta
+C0002453	Amenorrhea
+C0002514	Amino Acid Metabolism, Inborn Errors
+C0002534	Renal Aminoacidurias
+C0002622	Amnesia
+C0002624	Retrograde amnesia
+C0002625	Amnestic Disorder
+C0002631	Amniotic cavity infection
+C0002688	Amputation
+C0002690	Amputation Stumps
+C0002726	Amyloidosis
+C0002735	Oppenheim's Disease
+C0002736	Amyotrophic Lateral Sclerosis
+C0002766	Pain management
+C0002768	Congenital Pain Insensitivity
+C0002792	Anaphylactic shock
+C0002793	Anaplasia
+C0002797	Bovine Anaplasmosis
+C0002871	Anemia
+C0002873	Anaemia of chronic disease
+C0002874	Anemia, Aplastic
+C0002875	Cooley's anemia
+C0002876	Congenital dyserythropoietic anemia
+C0002878	Anemia, Hemolytic
+C0002879	Anemia, Hemolytic, Acquired
+C0002880	Anemia, Hemolytic, Autoimmune
+C0002881	Anemia, Hemolytic, Congenital
+C0002882	Anemia, Hemolytic, Congenital Nonspherocytic
+C0002883	Anemia, Hemolytic, Idiopathic Acquired
+C0002884	Hypochromic anaemia
+C0002886	Anaemia macrocytic
+C0002888	Anaemia megaloblastic
+C0002889	Anemia, Microangiopathic
+C0002890	Leukoerythroblastic Anemia
+C0002891	Anaemia neonatal
+C0002892	Anemia, Pernicious
+C0002893	Anemia, Refractory
+C0002894	Anemia, Refractory, with Excess of Blasts
+C0002895	Anemia, Sickle Cell
+C0002896	Sideroblastic anemia
+C0002897	Anemia, Splenic
+C0002902	Anencephaly
+C0002903	Anesthesia
+C0002915	GA
+C0002928	Spinal anaesthesia
+C0002938	Aneuploidy
+C0002940	Aneurysm
+C0002949	Aneurysm, Dissecting
+C0002957	Anger
+C0002962	Angina Pectoris
+C0002963	Angina Pectoris, Variant
+C0002965	Angina, Unstable
+C0002978	Angiogram
+C0002982	Angioid Streaks
+C0002985	Angiokeratoma
+C0002986	Fabry Disease
+C0002989	Epithelioid hemangioma of skin
+C0002991	Cutaneous Fibrous Histiocytoma
+C0002992	Angiomatosis
+C0002994	Angioedema
+C0003028	Anhidrosis
+C0003044	Animal bite
+C0003076	Aniridia
+C0003079	Anisocoria
+C0003081	Anisometropia
+C0003089	Ankylosing spondylitis and other inflammatory spondylopathies
+C0003090	Ankylosis
+C0003099	Anniversary Reaction
+C0003113	Anomia
+C0003119	Anophthalmos
+C0003123	Anorexia
+C0003125	Anorexia Nervosa
+C0003126	Anosmia
+C0003128	Anovulation
+C0003129	Anoxemia
+C0003130	Anoxia
+C0003132	Anoxic Encephalopathy
+C0003152	Anterior Compartment Syndrome
+C0003165	Anthracosis
+C0003175	Anthrax
+C0003177	Cutaneous anthrax
+C0003257	Antibody Deficiency Syndrome
+C0003431	Antisocial Personality Disorder
+C0003460	Anuria
+C0003463	Anus Neoplasms
+C0003466	Anal atresia
+C0003467	Anxiety
+C0003469	Anxiety Disorders
+C0003477	Anxiety, Separation
+C0003486	Aortic Aneurysm
+C0003492	Aortic coarctation
+C0003493	Aortic Diseases
+C0003496	Aortic Rupture
+C0003499	Supravalvular aortic stenosis
+C0003504	Aortic valve incompetence
+C0003506	Aortic valve replacement
+C0003507	Aortic Valve Stenosis
+C0003509	Aortitis
+C0003510	Aortitis Syndrome
+C0003516	Aortopulmonary Septal Defect
+C0003534	Aphakia
+C0003537	Aphasia
+C0003546	Aphasia, Acquired
+C0003550	Broca Aphasia
+C0003564	Aphonia
+C0003578	Apnea
+C0003611	Appendicectomy
+C0003614	Appendiceal Neoplasms
+C0003615	Appendicitis
+C0003621	Appetite disorder
+C0003635	Apraxia
+C0003650	Apudoma
+C0003706	Arachnodactyly
+C0003708	Arachnoiditis
+C0003723	Arbovirus Infections
+C0003742	Arcus Senilis
+C0003756	Arenaviridae Infections
+C0003782	Argyria
+C0003803	Arnold Chiari Malformation
+C0003810	Sertoli-Leydig cell tumor of ovary
+C0003811	Arrhythmias, Cardiac
+C0003813	Sinus arrhythmia
+C0003824	Arson
+C0003834	Arterial insufficiency
+C0003838	Arterial Occlusive Diseases
+C0003850	Arteriosclerosis
+C0003851	Arteriosclerosis Obliterans
+C0003855	Arteriovenous fistula
+C0003857	Arteriovenous malformation
+C0003860	Arteritis
+C0003862	Arthralgia
+C0003864	Arthritis
+C0003865	Arthritis, Adjuvant-Induced
+C0003868	Arthritis, Gouty
+C0003869	Arthritis, Infectious
+C0003872	Arthritis, Psoriatic
+C0003873	Arthritis, Rheumatoid
+C0003875	Arthritis, Viral
+C0003881	Arthrodesis NOS
+C0003886	Arthrogryposis
+C0003892	Arthropathy, Neurogenic
+C0003893	Joint arthroplasty
+C0003904	Arthroscopy
+C0003907	Arthus Reaction
+C0003910	Articulation Disorders
+C0003944	As If Personality
+C0003949	Asbestosis
+C0003950	Ascariasis
+C0003962	Ascites
+C0003964	Peritoneal effusion
+C0003969	Ascorbic Acid Deficiency
+C0004030	Aspergillosis
+C0004031	Allergic bronchopulmonary aspergillosis
+C0004044	Asphyxia
+C0004045	Asphyxia Neonatorum
+C0004046	Aspiculariasis
+C0004059	aspirin intolerance
+C0004076	Glucose urine
+C0004090	Astasia-abasia
+C0004093	Asthenia
+C0004095	Asthenopia
+C0004096	Asthma
+C0004099	Asthma, Exercise-Induced
+C0004106	Astigmatism
+C0004114	Astrocytoma
+C0004134	Ataxia
+C0004135	Ataxia Telangiectasia
+C0004138	Ataxias, Hereditary
+C0004144	Atelectasis
+C0004153	Atherosclerosis
+C0004158	Athetosis
+C0004161	Athletic Injuries
+C0004238	Atrial Fibrillation
+C0004239	Atrial Flutter
+C0004245	Atrioventricular Block
+C0004277	Tooth Attrition
+C0004310	Auditory Perceptual Disorders
+C0004331	Atrioventricular dissociation
+C0004352	Autistic Disorder
+C0004364	Autoimmune disease NOS
+C0004368	Autoimmune state
+C0004377	Automatism
+C0004403	Autosome Abnormalities
+C0004444	Avoidant Personality Disorder
+C0004509	Azoospermia
+C0004565	Melanoma, B16
+C0004576	Babesiosis
+C0004601	Back injury
+C0004604	Back Pain
+C0004606	Nonproliferative diabetic retinopathy
+C0004608	Retinopathy background
+C0004610	Bacteremia
+C0004623	Bacterial Infections
+C0004626	Pneumonia, Bacterial
+C0004659	Bacteriuria
+C0004669	Bacteroides infection
+C0004681	Bagassosis
+C0004690	Balanitis
+C0004691	Balanoposthitis
+C0004698	Balkan Nephropathy
+C0004712	Balo's Concentric Sclerosis
+C0004763	Barrett Esophagus
+C0004767	Bartholin's cyst
+C0004771	Bartonella Infections
+C0004775	Bartter Disease
+C0004779	Basal Cell Nevus Syndrome
+C0004782	Basal Ganglia Diseases
+C0004812	Basilar Artery Insufficiency
+C0004903	Beckwith-Wiedemann Syndrome
+C0004910	Bed rest
+C0004930	Behavior Disorders
+C0004936	Mental disorders
+C0004941	Behavioral Symptoms
+C0004943	Behcet Syndrome
+C0004968	Bence Jones proteinuria
+C0004991	Benign neoplasm of colon
+C0004997	Benign Ovarian Neoplasm
+C0004998	Benign neoplasm of skin
+C0005001	Benign prostatic hypertrophy
+C0005119	Bereavement reaction
+C0005122	Beriberi
+C0005129	Bernard-Soulier Syndrome
+C0005136	Berry Aneurysm
+C0005137	Bertielliasis
+C0005138	Berylliosis
+C0005146	Besnoitiasis
+C0005283	beta Thalassemia
+C0005395	Bile Duct Diseases
+C0005396	Bile Duct Neoplasms
+C0005398	Cholestasis, Extrahepatic
+C0005403	Bile Reflux
+C0005411	Biliary Atresia
+C0005416	Biliary Dyskinesia
+C0005417	Biliary fistula
+C0005424	Biliary Tract Diseases
+C0005426	Biliary Tract Neoplasm
+C0005558	Biopsy
+C0005586	Bipolar Disorder
+C0005587	Depression, Bipolar
+C0005612	Birth Weight
+C0005658	Bite
+C0005659	Bites and Stings
+C0005683	Calculus bladder
+C0005684	Bladder cancer
+C0005686	Bladder disorder
+C0005687	Bladder distension
+C0005689	Bladder Exstrophy
+C0005690	Urinary Bladder Fistula
+C0005694	Bladder neck obstruction
+C0005695	Bladder Neoplasm
+C0005697	Neurogenic bladder
+C0005699	Blast cell crisis
+C0005716	Blastomycosis
+C0005717	Gilchrist Disease
+C0005741	Blepharitis
+C0005742	Blepharochalasis
+C0005744	Blepharophimosis
+C0005745	Blepharoptosis
+C0005747	Blepharospasm
+C0005754	Congenital blindness
+C0005758	Blister
+C0005779	Blood coagulation disorder
+C0005806	Blood Group Incompatibility
+C0005818	Blood Platelet Disorders
+C0005823	Blood Pressure
+C0005826	Blood pressure abnormal
+C0005833	Blood Sedimentation
+C0005841	Transfusion
+C0005845	Blood urea
+C0005858	Bloodshot eye
+C0005859	Bloom Syndrome
+C0005866	Bluetongue infection
+C0005874	Blushing
+C0005887	Body dysmorphic disorder
+C0005890	Body Height
+C0005899	Body Rocking
+C0005904	Body Temperature Changes
+C0005910	Body Weight
+C0005911	Body Weight Changes
+C0005933	Biopsy bone
+C0005937	Bone cyst NOS
+C0005938	Bone Density
+C0005940	Bone Diseases
+C0005941	Bone Diseases, Developmental
+C0005942	Bone Diseases, Endocrine
+C0005943	Bone Diseases, Infectious
+C0005944	Bone Diseases, Metabolic
+C0005954	Biopsy bone marrow
+C0005956	Bone Marrow Diseases
+C0005959	Marrow hyperplasia
+C0005961	Bone marrow transplant NOS
+C0005967	Bone neoplasms
+C0005974	Bone Resorption
+C0005976	Bone graft
+C0006009	Borderline mental retardation (I.Q. 70-85)
+C0006012	Borderline Personality Disorder
+C0006015	Bordetella Infections
+C0006019	Boredom
+C0006023	Borna Disease
+C0006035	Borrelia Infections
+C0006057	Botulism
+C0006060	Boutonneuse Fever
+C0006079	Bowen's disease
+C0006091	Brachial plexus lesion
+C0006105	Brain Abscess
+C0006107	Concussion
+C0006109	Brain Damage, Chronic
+C0006110	Brain death
+C0006111	Brain Diseases
+C0006112	Brain Diseases, Metabolic
+C0006114	Cerebral Edema
+C0006118	Brain Neoplasms
+C0006123	Branch Retinal Artery Occlusion
+C0006131	Branchioma
+C0006142	Breast cancer
+C0006144	Breast Cyst
+C0006145	Breast Diseases
+C0006147	Breast feeding
+C0006152	Breast swelling
+C0006157	Breech Presentation
+C0006160	Brenner Tumor
+C0006261	Bronchial Diseases
+C0006262	Bronchial fistula
+C0006264	Bronchial Neoplasms
+C0006266	Bronchial Spasm
+C0006267	Bronchiectasis
+C0006271	Bronchiolitis
+C0006272	Bronchiolitis Obliterans
+C0006274	Bronchiolitis, Viral
+C0006277	Bronchitis
+C0006281	Congenital bronchogenic cyst
+C0006285	Bronchopneumonia
+C0006287	Bronchopulmonary Dysplasia
+C0006288	Bronchopulmonary Sequestration
+C0006290	Bronchoscopy
+C0006309	Brucellosis
+C0006318	Bruit
+C0006325	Bruxism
+C0006370	Bulimia
+C0006384	Bundle branch block
+C0006386	Bunion
+C0006389	Bunostomiasis
+C0006413	Burkitt Lymphoma
+C0006430	Burning Mouth Syndrome
+C0006434	Burn injury
+C0006435	Chemical Burns
+C0006444	Bursitis
+C000656484	SARS-CoV-2
+C000657245	Coronavirus Disease 2019
+C0006625	Cachexia
+C0006635	Cadmium poisoning
+C0006663	Calcinosis
+C0006664	Calcinosis cutis
+C0006666	Calciphylaxis
+C0006705	Calcium metabolism disorder
+C0006736	Calculi
+C0006818	Campylobacter infection
+C0006826	Malignant Neoplasms
+C0006840	Candidiasis
+C0006845	Candidiasis, Chronic Mucocutaneous
+C0006846	Cutaneous Candidiasis
+C0006848	Mucocutaneous candidiasis
+C0006849	Candidiasis, Oral
+C0006852	Candidiasis of vagina
+C0006868	Cannabis Abuse
+C0006870	Cannabis Dependence
+C0006895	Capgras syndrome
+C0006897	Capillariasis
+C0006902	Capillaritis
+C0006905	Capillary fragility
+C0007001	Carbohydrate Metabolism, Inborn Errors
+C0007020	Carbon monoxide poisoning
+C0007078	Carbuncle
+C0007093	Carcinoid Heart Disease
+C0007095	Carcinoid Tumor
+C0007097	Carcinoma
+C0007098	Carcinoma 256, Walker
+C0007099	Carcinoma in Situ
+C0007102	Colon cancer
+C0007103	Malignant neoplasm of endometrium
+C0007104	Female Breast Carcinoma
+C0007107	Laryngeal cancer
+C0007112	Adenocarcinoma of prostate
+C0007113	Rectal cancer
+C0007114	Malignant neoplasm of skin
+C0007115	Malignant neoplasm of thyroid
+C0007117	Basal cell carcinoma
+C0007118	Basosquamous carcinoma of skin
+C0007120	Adenocarcinoma, Bronchiolo-Alveolar
+C0007121	Bronchogenic Carcinoma
+C0007124	Carcinoma, Intraductal, Noninfiltrating
+C0007125	Carcinoma, Ehrlich Tumor
+C0007129	Carcinoma, Merkel Cell
+C0007130	Adenocarcinoma, Mucinous
+C0007131	Carcinoma, Non-Small-Cell Lung
+C0007133	Carcinoma, Papillary
+C0007134	Carcinoma, Renal Cell
+C0007135	Adenocarcinoma, Scirrhous
+C0007137	Carcinoma, Squamous Cell
+C0007138	Carcinoma, Transitional Cell
+C0007140	Carcinosarcoma
+C0007166	Cardiac output decreased
+C0007172	Heart Rupture, Traumatic
+C0007177	Cardiac Tamponade
+C0007192	Cardiomyopathy alcoholic
+C0007193	Cardiomyopathy, Dilated
+C0007194	Cardiomyopathy, Hypertrophic
+C0007196	Restrictive cardiomyopathy
+C0007222	Cardiovascular Diseases
+C0007273	Carotid Artery Diseases
+C0007274	Carotid Artery Thrombosis
+C0007279	Carotid Body Paraganglioma
+C0007280	Carotid bruit
+C0007282	Carotid Stenosis
+C0007286	Carpal Tunnel Syndrome
+C0007297	Carsickness
+C0007302	Cartilage Diseases
+C0007350	Cat Diseases
+C0007361	Cat-Scratch Disease
+C0007370	Catalepsy
+C0007384	Cataplexy
+C0007398	Catatonia
+C0007435	Central venous catheterisation
+C0007453	Cattle Diseases
+C0007462	Causalgia
+C0007527	Cecal Diseases
+C0007528	Cecal Neoplasms
+C0007570	Celiac Disease
+C0007587	Cell death
+C0007621	Neoplastic Cell Transformation
+C0007622	Cell Transformation, Viral
+C0007642	Cellulitis
+C0007682	CNS disorder
+C0007684	Central Nervous System Infection
+C0007688	Central Retinal Artery Occlusion
+C0007711	Cenuriasis
+C0007722	Cephalhaematoma
+C0007758	Cerebellar Ataxia
+C0007760	Cerebellar Diseases
+C0007761	Myoclonic Cerebellar Dyssynergia
+C0007762	Cerebellar Neoplasms
+C0007766	Intracranial Aneurysm
+C0007771	Intracranial Arteriosclerosis
+C0007772	Intracranial Arteriovenous Malformation
+C0007773	Cerebral arteritis
+C0007774	Cerebral Arterial Diseases
+C0007775	Cerebral Atherosclerosis
+C0007780	Cerebral artery embolism
+C0007781	Intracranial Embolism and Thrombosis
+C0007785	Cerebral Infarction
+C0007786	Brain Ischemia
+C0007787	Ischemic Attack, Transient
+C0007789	Cerebral Palsy
+C0007795	Diffuse Cerebral Sclerosis of Schilder
+C0007814	Cerebrospinal fluid otorrhea
+C0007815	Cerebrospinal fluid rhinorrhea
+C0007820	Cerebrovascular disease NOS
+C0007847	Malignant tumor of cervix
+C0007852	Cervical Migraine Syndrome
+C0007855	Cervical polyp
+C0007859	Neck Pain
+C0007860	Cervicitis
+C0007862	Cervico-Brachial Neuralgia
+C0007863	Occipital neuralgia
+C0007867	Cervix Diseases
+C0007868	Cervical dysplasia
+C0007871	Cervical incompetence
+C0007873	Neoplasm of uterine cervix
+C0007876	Caesarean section
+C0007894	Cestode Infections
+C0007930	Chagas Cardiomyopathy
+C0007932	Chagas\' disease without mention of organ involvement
+C0007933	Chalazion
+C0007947	Chancroid
+C0007959	Charcot-Marie-Tooth Disease
+C0007965	Chediak-Higashi Syndrome
+C0007971	Cheilitis
+C0008029	Cherubism
+C0008031	Chest Pain
+C0008033	Pleuritic pain
+C0008035	Chest wall pain
+C0008039	Cheyne Stokes respiration
+C0008043	Chiari-Frommel Syndrome
+C0008049	Chickenpox
+C0008055	Chikungunya Fever
+C0008058	Chilblains
+C0008060	Child abuse
+C0008066	Child Behavior Disorders
+C0008073	Developmental Disabilities
+C0008074	Child Development Disorders, Pervasive
+C0008087	Child Nutrition Disorders
+C0008149	Chlamydia Infections
+C0008272	Asiderotic anemia
+C0008297	Choanal Atresia
+C0008298	Polyp in nasopharynx
+C0008301	Choking
+C0008309	Bile duct adenoma
+C0008311	Cholangitis
+C0008312	Primary biliary cholangitis
+C0008313	Cholangitis, Sclerosing
+C0008320	Cholecystectomy
+C0008325	Cholecystitis
+C0008340	Choledochal Cyst
+C0008350	Cholelithiasis
+C0008352	Cholemia
+C0008354	Cholera
+C0008370	Cholestasis
+C0008372	Intrahepatic Cholestasis
+C0008373	Cholesteatoma
+C0008384	Cholesterol Ester Storage Disease
+C0008412	Choline Deficiency
+C0008439	Chondritis
+C0008441	Chondroblastoma
+C0008445	Chondrodysplasia Punctata
+C0008449	Chondrodystrophy
+C0008476	Chondromatosis, Synovial
+C0008479	Chondrosarcoma
+C0008487	Chordoma
+C0008489	Chorea
+C0008493	Hydatidiform Mole, Invasive
+C0008495	Chorioamnionitis
+C0008497	Choriocarcinoma
+C0008513	Chorioretinitis
+C0008519	Ectopic Tissue
+C0008521	Choroid Diseases
+C0008522	Choroid Hemorrhage
+C0008525	Choroideremia
+C0008526	Choroiditis
+C0008533	Hemophilia B
+C0008582	Chromoblastomycosis
+C0008625	Chromosome Aberrations
+C0008626	Congenital chromosomal disease
+C0008628	Chromosomal deletion NOS
+C0008629	Chromosome Fragility
+C0008677	Bronchitis, Chronic
+C0008679	Chronic disease
+C0008680	Cryptogenic pulmonary eosinophilia
+C0008684	Chronic gingivitis
+C0008690	Chronic anterior uveitis
+C0008701	Chronic Motor or Vocal Tic Disorder
+C0008707	Chronic osteomyelitis
+C0008711	Chronic rhinitis
+C0008715	Chronically Ill
+C0008728	Churg-Strauss Syndrome
+C0008732	Chylous Ascites
+C0008733	Chylothorax
+C0008767	Cicatrization
+C0008775	Ciguatera Poisoning
+C0008780	Ciliary Motility Disorders
+C0008909	Claustrophobia
+C0008924	Cleft Lip
+C0008925	Cleft Palate
+C0008928	Cleidocranial Dysplasia
+C0009021	Clonorchiasis
+C0009024	Clonus
+C0009062	Clostridium Infections
+C0009075	Melanoma, Cloudman S91
+C0009080	Clubbed Fingers
+C0009081	Congenital clubfoot
+C0009084	Cluster A personality disorder
+C0009086	Cluster B personality disorder
+C0009087	Cluster C personality disorder
+C0009088	Cluster Headache
+C0009090	Cluttering
+C0009144	Tongue coated
+C0009171	Cocaine Abuse
+C0009176	Cocaine intoxication
+C0009178	Cocaine withdrawal
+C0009186	Coccidioidomycosis
+C0009187	Coccidiosis
+C0009193	Coccydynia
+C0009197	Cochlear Diseases
+C0009207	Cockayne Syndrome
+C0009225	Coenuriasis
+C0009240	Cognition
+C0009241	Cognition Disorders
+C0009269	Cold intolerance
+C0009270	Cold Panniculitis
+C0009274	Colectomy
+C0009319	Colitis
+C0009324	Colitis, Ulcerative
+C0009326	Collagen Diseases
+C0009348	Collateral circulation
+C0009363	Coloboma
+C0009373	Colonic Diseases
+C0009374	Colonic Diseases, Functional
+C0009375	Colonic Neoplasms
+C0009376	Colonic polyp
+C0009377	Colonic pseudo-obstruction
+C0009378	Colonoscopy
+C0009398	Color vision defect
+C0009402	Colorectal Carcinoma
+C0009404	Colorectal Neoplasms
+C0009405	Colorectal Neoplasms, Hereditary Nonpolyposis
+C0009410	Colostomy
+C0009421	Coma
+C0009426	Combat Disorders
+C0009438	Common Bile Duct Calculi
+C0009439	Choledochal Cyst, Type I
+C0009440	Common Bile Duct Diseases
+C0009443	Common Cold
+C0009447	Common Variable Immunodeficiency
+C0009450	Communicable Diseases
+C0009451	Communicating Hydrocephalus
+C0009460	Communication impairment
+C0009492	Compartment syndrome
+C0009592	Brain compression
+C0009595	Obsessive-Compulsive Personality
+C0009663	Condylomata Acuminata
+C0009676	Confusion
+C0009677	Congenital macroglossia
+C0009681	Anomalous pulmonary artery
+C0009691	Congenital cataract
+C0009714	Hepatic Fibrosis, Congenital
+C0009730	Spinal meningocele
+C0009759	Conjunctival Diseases
+C0009760	Conjunctival haemorrhage
+C0009761	Conjunctival Neoplasms
+C0009763	Conjunctivitis
+C0009765	Acute haemorrhagic conjunctivitis
+C0009766	Allergic Conjunctivitis
+C0009768	Conjunctivitis, Bacterial
+C0009769	Conjunctivitis, Giant Papillary
+C0009773	Conjunctivitis, Vernal
+C0009774	Conjunctivitis, Viral
+C0009777	Conn Adenoma
+C0009782	Connective Tissue Diseases
+C0009792	Consciousness Disorders
+C0009806	Constipation
+C0009812	Constitutional Symptom
+C0009917	Contracture
+C0009918	Contracture of joint
+C0009938	Contusion
+C0009946	Conversion disorder
+C0009952	Febrile Convulsions
+C0010032	Corneal abrasion
+C0010034	Corneal Diseases
+C0010035	Hereditary corneal dystrophy
+C0010036	Corneal dystrophy
+C0010037	Corneal edema
+C0010038	Corneal Opacity
+C0010042	Corneal transplant
+C0010043	Corneal Ulcer
+C0010046	Corn of toe
+C0010051	Coronary Aneurysm
+C0010054	Coronary Arteriosclerosis
+C0010055	Coronary artery bypass
+C0010068	Coronary Disease
+C0010072	Coronary artery thrombosis
+C0010073	Coronary Artery Vasospasm
+C0010074	Coronary Vessel Anomalies
+C0010093	Corpus Luteum Cyst
+C0010153	Corynebacteria infections
+C0010200	Cough
+C0010201	Chronic cough
+C0010232	Cowpox
+C0010246	Coxsackievirus Infections
+C0010263	Limb Cramp
+C0010266	Cranial nerve diseases
+C0010273	Craniofacial Dysostosis
+C0010276	Craniopharyngioma
+C0010278	Craniosynostoses
+C0010308	Congenital Hypothyroidism
+C0010314	Cri-du-Chat Syndrome
+C0010324	Crigler Najjar syndrome, type 1
+C0010334	Crisscross Heart
+C0010340	Critical Illness
+C0010346	Crohn Disease
+C0010356	Cross Infection
+C0010380	Croup
+C0010392	Crush syndrome
+C0010398	Cruveilhier-Baumgarten Syndrome
+C0010399	Crying
+C0010403	Cryoglobulinemia
+C0010414	Cryptococcosis
+C0010417	Cryptorchidism
+C0010418	Cryptosporidiosis
+C0010474	Curling Ulcer
+C0010481	Cushing Syndrome
+C0010495	Cutis Laxa
+C0010520	Cyanosis
+C0010598	Cyclothymic Disorder
+C0010606	Adenoid Cystic Carcinoma
+C0010626	Congenital cyst
+C0010631	Cystadenocarcinoma
+C0010633	Cystadenoma
+C0010635	Cystadenoma, Mucinous
+C0010651	Urinary cystectomy
+C0010666	Acne cystic
+C0010668	Cystic Adenomatoid Malformation of Lung, Congenital
+C0010674	Cystic Fibrosis
+C0010678	Cysticercosis
+C0010691	Cystinuria
+C0010692	Cystitis
+C0010695	Cystocele
+C0010701	Phyllodes Tumor
+C0010705	Cystostomy
+C0010709	Cyst
+C0010823	Cytomegalovirus Infections
+C0010828	Cytopenia
+C0010930	Dacryocystitis
+C0010964	Dandy-Walker Syndrome
+C0011018	Daydreaming
+C0011052	Prelingual Deafness
+C0011053	Deafness
+C0011057	Hearing Loss, Sudden
+C0011065	Cessation of life
+C0011071	Sudden death
+C0011079	Debridement
+C0011103	Decerebrate rigidity
+C0011119	Decompression Sickness
+C0011124	Decreased Libido
+C0011127	Pressure Ulcer
+C0011156	Deficiency Diseases
+C0011168	Deglutition Disorders
+C0011175	Dehydration
+C0011194	Deja vu
+C0011195	Dejerine-Sottas Disease (disorder)
+C0011206	Delirium
+C0011209	Delivery
+C0011226	Hepatitis D
+C0011251	Delusional disorder
+C0011253	Delusion
+C0011263	Multi-infarct dementia
+C0011265	Presenile dementia
+C0011268	Senile dementia
+C0011269	Dementia, Vascular
+C0011302	Demyelinating disease of central nervous system
+C0011303	Demyelinating Diseases
+C0011304	Demyelination
+C0011311	Dengue
+C0011317	Denial (Psychology)
+C0011330	Dental Calculus
+C0011331	Dental care
+C0011334	Dental caries
+C0011346	Tooth deposit
+C0011351	Dental Enamel Hypoplasia
+C0011361	Dental fistula
+C0011370	Dental implantation
+C0011389	Dental Plaque
+C0011400	Dental Pulp Autolysis
+C0011405	Dental Pulp Diseases
+C0011406	Dental Pulp Exposure
+C0011407	Dental necrosis
+C0011428	Dentigerous Cyst
+C0011430	Dentin Dysplasia
+C0011432	Sensitivity of teeth
+C0011434	Dentin, Secondary
+C0011436	Dentinogenesis Imperfecta
+C0011548	Dependent Personality Disorder
+C0011551	Depersonalisation
+C0011570	Depression
+C0011573	Endogenous depression
+C0011574	Involutional Depression
+C0011579	Reactive depression
+C0011580	Depression, Reactive, Psychotic
+C0011581	Depressive disorder
+C0011593	Dermabrasion
+C0011599	Dermal Sinus
+C0011603	Dermatitis
+C0011606	Dermatitis, Exfoliative
+C0011608	Dermatitis Herpetiformis
+C0011609	Drug eruption
+C0011615	Dermatitis, Atopic
+C0011616	Contact Dermatitis
+C0011620	Stasis dermatitis
+C0011630	Dermatomycoses
+C0011633	Dermatomyositis
+C0011636	Dermatophytosis
+C0011644	Scleroderma
+C0011645	Dermatosis Papulosa Nigra
+C0011649	Dermoid Cyst
+C0011757	Developmental Coordination Disorder
+C0011813	Dextrocardia
+C0011818	Dextraposition of aorta
+C0011847	Diabetes
+C0011848	Diabetes Insipidus
+C0011849	Diabetes Mellitus
+C0011853	Diabetes Mellitus, Experimental
+C0011854	Diabetes Mellitus, Insulin-Dependent
+C0011859	Lipoatrophic Diabetes Mellitus
+C0011860	Diabetes Mellitus, Non-Insulin-Dependent
+C0011875	Diabetic Angiopathies
+C0011876	Diabetic cataract
+C0011880	Diabetic Ketoacidosis
+C0011881	Diabetic Nephropathies
+C0011882	Diabetic Neuropathies
+C0011884	Diabetic Retinopathy
+C0011974	Dermatitis diaper
+C0011981	Diaphragmatic Eventration
+C0011989	Camurati-Engelmann Syndrome
+C0011991	Diarrhea
+C0011992	Diarrhea, Infantile
+C0011993	Vipoma
+C0011998	Diastema of Teeth
+C0011999	Diastematomyelia
+C0012236	DiGeorge Syndrome
+C0012241	Anomaly congenital gastrointestinal (NOS)
+C0012242	Digestive System Diseases
+C0012243	Digestive System Neoplasms
+C0012358	Dilatation & curettage (uterus)
+C0012359	Pathological Dilatation
+C0012546	Diphtheria
+C0012561	Diphyllobothriasis
+C0012569	Diplopia
+C0012602	Dirofilariasis
+C0012619	disc disorder
+C0012624	Discitis
+C0012634	Disease
+C0012644	Animal Disease Models
+C0012655	Disease susceptibility
+C0012684	Blastocyst Disintegration
+C0012691	Dislocations
+C0012714	Disorder of copper metabolism
+C0012715	Iron Metabolism Disorders
+C0012716	Disorder of magnesium metabolism
+C0012734	Disruptive Behavior Disorder
+C0012736	Dissecting aortic aneurysm
+C0012739	Disseminated Intravascular Coagulation
+C0012746	Dissociative disorder
+C0012754	Distemper
+C0012811	Colon diverticulum anatomic structure
+C0012813	Diverticulitis
+C0012814	Colonic Diverticulitis
+C0012817	Diverticula
+C0012819	Diverticular disease of colon
+C0012826	Adhesiolysis
+C0012833	Dizziness
+C0012922	DNA Virus Infections
+C0012979	Dog Diseases
+C0013069	Double Outlet Right Ventricle
+C0013080	Down Syndrome
+C0013124	Drinking behavior processes
+C0013132	Drooling
+C0013142	Drowning
+C0013144	Drowsiness
+C0013146	Drug abuse
+C0013170	Drug habituation
+C0013182	Drug Allergy
+C0013203	Drug resistance
+C0013216	Drug therapy
+C0013220	Drug tolerance
+C0013221	Drug toxicity
+C0013222	Drug Use Disorders
+C0013238	Dry eye syndrome
+C0013240	Alveolar osteitis
+C0013261	Duane Retraction Syndrome
+C0013264	Muscular Dystrophy, Duchenne
+C0013274	Ductus Arteriosus, Patent
+C0013288	Dumping Syndrome
+C0013289	Duodenal Diseases
+C0013291	Duodenal Neoplasms
+C0013292	Duodenal obstruction
+C0013295	Duodenal Ulcer
+C0013298	Duodenitis
+C0013299	Duodenogastric Reflux
+C0013312	Dupuytren Contracture
+C0013336	Dwarfism
+C0013338	Dwarfism, Pituitary
+C0013362	Dysarthria
+C0013363	Dysautonomia
+C0013364	Dysautonomia, Familial
+C0013366	Dyschondroplasias
+C0013369	Dysentery
+C0013370	Amebic colitis
+C0013371	Shigella Infections
+C0013374	Dysgammaglobulinemia
+C0013377	Dysgerminoma
+C0013378	Dysgeusia
+C0013384	Dyskinesia
+C0013386	Dyskinesia, Drug-Induced
+C0013390	Dysmenorrhea
+C0013393	Dysostoses
+C0013394	Dyspareunia
+C0013395	Dyspepsia
+C0013403	Dysplastic Nevus Syndrome
+C0013404	Dyspnea
+C0013405	Dyspnea, Paroxysmal
+C0013409	Dyssocial Behavior
+C0013415	Dysthymic Disorder
+C0013418	Dystocia
+C0013420	Uterine contractions abnormal
+C0013421	Dystonia
+C0013423	Dystonia Musculorum Deformans
+C0013426	Dystrophy of vulva
+C0013428	Dysuria
+C0013447	Ear Diseases
+C0013449	Ear Neoplasms
+C0013456	Ear pain
+C0013473	Eating disorder
+C0013481	Ebstein Anomaly
+C0013491	Ecchymosis
+C0013502	Echinococciasis
+C0013504	Echinococcosis, Hepatic
+C0013528	Echolalia
+C0013537	Eclampsia
+C0013568	Ecthyma
+C0013570	Ecthyma, Contagious
+C0013575	Ectodermal Dysplasia
+C0013578	Ectoparasitic Infestations
+C0013580	Ectopia cordis
+C0013581	Ectopia Lentis
+C0013589	Ectromelia
+C0013591	Ectromelia, Infectious
+C0013592	Ectropion
+C0013595	Eczema
+C0013604	Edema
+C0013608	Cardiac edema
+C0013609	Localised oedema
+C0013687	Effusion
+C0013720	Ehlers-Danlos Syndrome
+C0013743	Eisenmenger Complex
+C0013755	Elaeophoriasis
+C0013778	Cardioversion
+C0013781	Electric shock
+C0013798	Electrocardiogram
+C0013806	Electroconvulsive therapy
+C0013832	Electrolytes
+C0013882	Elephantiasis
+C0013884	Elephantiasis, Filarial
+C0013902	Elliptocytosis, Hereditary
+C0013903	Ellis-Van Creveld Syndrome
+C0013911	Emaciation
+C0013921	Tumor Cells, Embolic
+C0013922	Embolism
+C0013926	Air embolism
+C0013927	Embolism, Amniotic Fluid
+C0013928	Fat embolism
+C0013930	Embolism, Tumor
+C0013931	Therapeutic embolisation
+C0013937	Embryo Resorption
+C0013949	Embryopathies
+C0013985	Emotional Disturbances
+C0013990	Emphysema
+C0014008	Empty Sella Syndrome
+C0014009	Empyema
+C0014012	Empyema, Gallbladder
+C0014013	Empyema, Pleural
+C0014034	Enanthema
+C0014038	Encephalitis
+C0014040	Encephalitis Lethargica
+C0014057	Encephalitis, Japanese
+C0014059	Acute disseminated encephalomyelitis
+C0014060	Encephalitis, St. Louis
+C0014061	Tick-Borne Encephalitis
+C0014065	Congenital cerebral hernia
+C0014067	Occipital Encephalocele
+C0014068	Encephalomalacia
+C0014070	Encephalomyelitis
+C0014072	Experimental Autoimmune Encephalomyelitis
+C0014077	Leukoencephalitis, Acute Hemorrhagic
+C0014078	Venezuelan equine encephalomyelitis
+C0014084	Enchondromatosis
+C0014089	Functional encopresis
+C0014098	Endarterectomy
+C0014099	Carotid endarterectomy
+C0014100	Endarteritis
+C0014116	Endocardial Cushion Defects
+C0014117	Endocardial Fibroelastosis
+C0014118	Endocarditis
+C0014121	Bacterial Endocarditis
+C0014122	Subacute Bacterial Endocarditis
+C0014127	Endocervicitis
+C0014130	Endocrine system disease, NOS
+C0014132	Endocrine Gland Neoplasms
+C0014145	Yolk Sac Tumor
+C0014170	Endometrial Neoplasms
+C0014173	Endometrial Hyperplasia
+C0014175	Endometriosis
+C0014179	Endometritis
+C0014236	Endophthalmitis
+C0014245	Endoscopy
+C0014306	Enophthalmos
+C0014324	Entamoebiasis
+C0014326	Entamoebiasis, Intestinal
+C0014327	Enteral nutrition
+C0014335	Enteritis
+C0014347	Enterobacteriaceae Infections
+C0014356	Enterocolitis
+C0014358	Enterocolitis, Pseudomembranous
+C0014370	Enterostomy
+C0014378	Enterovirus infection
+C0014390	Entropion
+C0014394	Enuresis
+C0014412	Environmental exposure
+C0014431	Enzyme induction
+C0014457	Eosinophilia
+C0014458	Eosinophilia, Tropical
+C0014461	Eosinophilic Granuloma
+C0014474	Ependymoma
+C0014476	Eperythrozoonosis
+C0014488	Epicondylitis
+C0014493	Epidemic keratoconjunctivitis
+C0014511	Epithelial cyst
+C0014518	Toxic Epidermal Necrolysis
+C0014522	Epidermodysplasia Verruciformis
+C0014527	Epidermolysis Bullosa
+C0014531	Epidermophytosis
+C0014534	Epididymitis
+C0014536	Extradural neoplasm
+C0014541	Epiglottitis
+C0014544	Epilepsy
+C0014547	Epilepsies, Partial
+C0014548	Epilepsy, Generalized
+C0014549	Epilepsy, Tonic-Clonic
+C0014550	Epilepsies, Myoclonic
+C0014553	Absence Epilepsy
+C0014556	Epilepsy, Temporal Lobe
+C0014558	Uncinate Epilepsy
+C0014571	Epiphyses, Slipped
+C0014583	Episcleritis
+C0014591	Epistaxis
+C0014599	Epithelial hyperplasia
+C0014714	Ergot poisoning
+C0014724	Eructation
+C0014733	Erysipelas
+C0014736	Erysipelothrix infection
+C0014740	Erythema Chronicum Migrans
+C0014741	Erythema induratum
+C0014742	Erythema Multiforme
+C0014743	Erythema Nodosum
+C0014745	Palmar erythema
+C0014752	Erythrasma
+C0014761	Erythroblastosis, Fetal
+C0014772	Red Blood Cell Count measurement
+C0014799	Erythroderma, Maculopapular
+C0014800	Erythroid hyperplasia
+C0014804	Erythromelalgia
+C0014805	Primary Erythermalgia
+C0014818	Erythroplasia
+C0014836	Escherichia coli Infections
+C0014848	Esophageal Achalasia
+C0014849	Esophageal and Gastric Varices
+C0014850	Esophageal Atresia
+C0014852	Esophageal Diseases
+C0014854	Diverticulum oesophageal
+C0014856	Oesophageal fistula
+C0014857	Hernia hiatus repair
+C0014858	Dyskinesia oesophageal
+C0014859	Esophageal Neoplasms
+C0014860	Oesophageal perforation
+C0014863	Esophageal spasm
+C0014866	Esophageal Stenosis
+C0014867	Esophageal Varices
+C0014868	Esophagitis
+C0014869	Esophagitis, Peptic
+C0014877	Esotropia
+C0015187	Euthanasia
+C0015190	Euthyroid Sick Syndromes
+C0015230	Exanthema
+C0015256	Excoriation
+C0015263	Bronchospasm, Exercise-Induced
+C0015269	Exhibitionism
+C0015300	Exophthalmos
+C0015302	External exotoses
+C0015306	Hereditary Multiple Exostoses
+C0015310	Exotropia
+C0015357	Extracorporeal membrane oxygenation
+C0015371	Extrapyramidal disorder
+C0015376	Extravasation
+C0015378	Extravasation of Contrast Media
+C0015379	Extravasation of Diagnostic and Therapeutic Materials
+C0015382	Extraversion (Psychology)
+C0015393	Congenital eye disorder
+C0015395	Eye Burns
+C0015396	Eye Color
+C0015397	Disorder of eye
+C0015398	Eye Diseases, Hereditary
+C0015401	Foreign body retained in eye
+C0015402	Eye haemorrhage
+C0015403	Eye infection
+C0015404	Bacterial eye infection
+C0015405	Eye infection fungal NOS
+C0015408	Eye Injuries
+C0015411	Eye Manifestations
+C0015414	Eye Neoplasms
+C0015423	Eyelid Diseases
+C0015424	Eyelid Neoplasms
+C0015456	Facial Dermatoses
+C0015457	Facial expression
+C0015458	Facial Hemiatrophy
+C0015459	Face injury
+C0015461	Facial Neoplasms
+C0015464	Facial Nerve Diseases
+C0015467	Facial Neuralgia
+C0015468	Facial Pain
+C0015469	Facial nerve palsy
+C0015480	Factitious disorders
+C0015499	Factor V deficiency
+C0015503	Factor VII Deficiency
+C0015519	Factor X Deficiency
+C0015523	Factor XI deficiency
+C0015526	Factor XII Deficiency
+C0015530	Hereditary Factor XIII Deficiency
+C0015544	Failure to Thrive
+C0015556	Fallopian tube disorder
+C0015558	Fallopian Tube Neoplasms
+C0015624	Fanconi Syndrome
+C0015625	Fanconi Anemia
+C0015634	Farmer's Lung
+C0015643	Fascicular Block
+C0015644	Muscular fasciculation
+C0015645	Fasciitis
+C0015652	Fascioliasis
+C0015656	Fasciolopsiasis
+C0015663	Fasting
+C0015668	Fat necrosis NOS
+C0015672	Fatigue
+C0015674	Chronic Fatigue Syndrome
+C0015695	Fatty Liver
+C0015696	Fatty Liver, Alcoholic
+C0015697	Arterial Fatty Streak
+C0015702	Favism
+C0015704	Favre-Racouchot Syndrome
+C0015708	Fazio-Londe Syndrome
+C0015726	Fear
+C0015732	Fecal Incontinence
+C0015734	Faecalith
+C0015745	Feeding behaviors
+C0015773	Felty Syndrome
+C0015786	Female sexual arousal disorder
+C0015787	Female sterilisation
+C0015799	Feminization
+C0015802	Femoral Fractures
+C0015806	Femoral Neck Fractures
+C0015814	Femur Head Necrosis
+C0015826	Fenestration (morphologic abnormality)
+C0015923	FAS
+C0015924	Fetal Anoxia
+C0015927	Fetal Death
+C0015929	Fetal Diseases
+C0015930	Fetal Distress
+C0015934	Fetal Growth Retardation
+C0015938	Fetal Macrosomia
+C0015944	Fetal Membranes, Premature Rupture
+C0015951	Fetal Resorption
+C0015957	Fetishism, Psychiatric
+C0015967	Fever
+C0015970	Fever of unknown origin
+C0015974	Periodic fever
+C0016024	Fibroadenosis
+C0016033	Nonproliferative fibrocystic disease
+C0016034	Breast Fibrocystic Disease
+C0016037	Fibrodysplasia Ossificans Progressiva
+C0016045	fibroma
+C0016048	Fibromatosis
+C0016049	Fibromatosis, Gingival
+C0016052	Fibromuscular Dysplasia
+C0016053	Fibromyalgia
+C0016057	Fibrosarcoma
+C0016059	Fibrosis
+C0016063	Osteitis Fibrosa Disseminata
+C0016064	Fibrous Dysplasia, Monostotic
+C0016065	Fibrous Dysplasia, Polyostotic
+C0016085	Filariasis
+C0016124	Finger Injuries
+C0016142	Firesetting Behavior
+C0016154	Fish Diseases
+C0016167	Anal fissure
+C0016169	Fistula
+C0016199	Flank Pain
+C0016202	Flatfoot
+C0016204	Flatulence
+C0016242	Vitreous floaters
+C0016325	Fluoride Poisoning
+C0016382	Flushing
+C0016385	Cardiac flutter
+C0016395	Focal Dermal Hypoplasia
+C0016397	Focal Infection
+C0016399	Epilepsy, Partial, Motor
+C0016412	Folate deficiency
+C0016427	Follicular cyst
+C0016436	Folliculitis
+C0016470	Food Allergy
+C0016479	Food Poisoning
+C0016506	Foot Deformities
+C0016508	Congenital Foot Deformity
+C0016509	Foot Dermatoses
+C0016510	Foot Diseases
+C0016512	Foot pain
+C0016514	Foot and mouth disease
+C0016522	Foramen Ovale, Patent
+C0016529	Forced expiratory volume function
+C0016542	Foreign body
+C0016549	Foreign body reaction
+C0016579	Formication
+C0016627	Influenza in Birds
+C0016629	Fowlpox
+C0016642	Internal fixation of fracture
+C0016655	Fractures, Multiple
+C0016658	Fracture
+C0016659	Fractures, Closed
+C0016662	Fracture of unspecified bone, open
+C0016663	Pathological fracture
+C0016664	Stress fracture
+C0016665	Fracture nonunion
+C0016667	Fragile X Syndrome
+C0016689	Ephelides
+C0016719	Friedreich Ataxia
+C0016722	Frigidity
+C0016724	Froehlich's Syndrome
+C0016736	Frostbite
+C0016751	Hereditary fructose intolerance syndrome
+C0016756	Fructose-1,6-Diphosphatase Deficiency
+C0016770	Frustration
+C0016781	Fuchs Endothelial Dystrophy
+C0016782	Fuchs\' heterochromic cyclitis
+C0016788	Fucosidase Deficiency Disease
+C0016807	Unspecified functional disorder of intestine
+C0016842	Congenital pectus excavatum
+C0016867	Furunculosis
+C0016873	Fused Teeth
+C0016927	Gagging
+C0016952	Galactosemias
+C0016977	Gall Bladder Diseases
+C0016978	gallbladder neoplasm
+C0016995	Gambling
+C0017075	Ganglioneuroma
+C0017083	Gangliosidoses
+C0017086	Gangrene
+C0017097	Gardner Syndrome
+C0017105	Gas gangrene
+C0017107	Gas Poisoning
+C0017118	Gastrectomy NOS
+C0017125	Gastric bypass NOS
+C0017128	Gastric Fistula
+C0017145	Gastric varices
+C0017150	Gastrinoma
+C0017152	Gastritis
+C0017154	Gastritis, Atrophic
+C0017155	Gastric mucosal hypertrophy
+C0017160	Gastroenteritis
+C0017162	Gastroenteritis, Transmissible, of Swine
+C0017168	Gastroesophageal Reflux
+C0017178	Gastrointestinal Diseases
+C0017181	Gastrointestinal Hemorrhage
+C0017185	Gastrointestinal neoplasm
+C0017196	Gastrostomy
+C0017205	Gaucher Disease
+C0017250	Psychosexual identity disorder
+C0017332	Generalized Nonconvulsive Seizure Disorder
+C0017407	Geniculate Ganglionitis
+C0017409	Herpes Zoster Oticus
+C0017411	Female Genital Diseases
+C0017412	Genital Diseases, Male
+C0017416	Genital Neoplasms, Female
+C0017417	Genital Neoplasms, Male
+C0017455	Geotrichum infection
+C0017494	Gerstmann Syndrome
+C0017495	Gerstmann-Straussler-Scheinker Disease
+C0017525	Giant Cell Tumors
+C0017531	Angiolymphoid hyperplasia
+C0017536	Giardiasis
+C0017547	Gigantism
+C0017551	Gilbert Disease (disorder)
+C0017563	Gingival Diseases
+C0017565	Gingival bleeding
+C0017566	Gingival Hyperplasia
+C0017567	Gingival Hypertrophy
+C0017570	Gingival Neoplasms
+C0017572	Gingival Recession
+C0017574	Gingivitis
+C0017575	Necrotizing Ulcerative Gingivitis
+C0017577	Chronic desquamative gingivitis
+C0017601	Glaucoma
+C0017605	Angle Closure Glaucoma
+C0017606	Primary angle-closure glaucoma
+C0017609	Glaucoma, Neovascular
+C0017612	Glaucoma, Open-Angle
+C0017614	Glaucoma, Suspect
+C0017636	Glioblastoma
+C0017638	Glioma
+C0017639	Gliosis
+C0017650	Globus hystericus
+C0017653	Glomus Tumor
+C0017658	Glomerulonephritis
+C0017661	Glomerulonephritis, IGA
+C0017662	Glomerulonephritis, Membranoproliferative
+C0017665	Glomerulonephritis, Membranous
+C0017667	Nodular glomerulosclerosis
+C0017668	Focal glomerulosclerosis
+C0017671	Glomus Jugulare Tumor
+C0017672	Glossalgia
+C0017675	Glossitis
+C0017677	Benign migratory glossitis
+C0017689	Glucagonoma
+C0017741	Glucose tolerance test
+C0017919	Glycogen Storage Disease
+C0017920	Glycogen Storage Disease Type I
+C0017921	Glycogen storage disease type II
+C0017922	Glycogen Storage Disease Type III
+C0017923	Glycogen Storage Disease Type IV
+C0017924	Glycogen Storage Disease Type V
+C0017925	Glycogen Storage Disease Type VI
+C0017926	Glycogen Storage Disease Type VII
+C0017927	Glycogen Storage Disease Type VIII
+C0017979	Glycosuria
+C0017980	Glycosuria, Renal
+C0018021	Goiter
+C0018022	Endemic goiter
+C0018023	Goiter, Nodular
+C0018036	Hypertension, Goldblatt
+C0018050	Gonadal Disorders
+C0018051	Gonadal Dysgenesis
+C0018054	Gonadal Dysgenesis, 46,XY
+C0018055	Gonadal Dysgenesis, Mixed
+C0018078	Gonococcal urethritis
+C0018081	Gonorrhea
+C0018099	Gout
+C0018128	Graft Occlusion, Vascular
+C0018129	Transplant rejection
+C0018133	Graft vs Host Disease
+C0018179	Granular Dystrophy, Corneal
+C0018188	Granuloma
+C0018190	Granuloma Inguinale
+C0018193	Granuloma, Foreign-Body
+C0018194	Giant Cell Granuloma
+C0018196	Granuloma, Laryngeal
+C0018197	Granuloma, Lethal Midline
+C0018199	Granuloma, Plasma Cell
+C0018200	Granuloma, Respiratory Tract
+C0018202	Granulomatous Angiitis
+C0018203	Chronic granulomatous disease
+C0018204	Granulomatous prostatitis
+C0018206	granulosa cell tumor
+C0018213	Graves Disease
+C0018235	Grief reaction
+C0018245	Groenouw's Dystrophies
+C0018273	Growth Disorders
+C0018378	Guillain-Barre Syndrome
+C0018379	Feeling guilty
+C0018413	Gynandroblastoma
+C0018418	Gynaecomastia
+C0018425	Gyrate Atrophy
+C0018482	Haemophilus Infections
+C0018498	Hair Color
+C0018500	Hair Diseases
+C0018520	Breath odour
+C0018522	Hallermann\'s Syndrome
+C0018523	Hallervorden-Spatz Syndrome
+C0018524	Hallucination
+C0018536	Hallux Valgus
+C0018552	Hamartoma
+C0018553	Hamartoma Syndrome, Multiple
+C0018564	Hand deformities
+C0018566	Congenital Hand Deformities
+C0018567	Hand Dermatoses
+C0018571	Hand Injuries
+C0018572	Hand, Foot and Mouth Disease
+C0018598	Melanoma, Harding-Passey
+C0018609	Hartnup Disease
+C0018614	Hashish Abuse
+C0018621	Hay fever
+C0018671	Head and Neck Neoplasms
+C0018672	Head Banging
+C0018674	Craniocerebral Trauma
+C0018675	Head Neoplasms
+C0018681	Headache
+C0018772	Hearing Loss, Partial
+C0018775	Bilateral hearing loss
+C0018776	Central hearing loss
+C0018777	Conductive deafness
+C0018780	Hearing Loss, High-Frequency
+C0018781	Hearing Loss, Noise-Induced
+C0018784	Hearing Loss, Sensorineural
+C0018789	Cardiac aneurysm
+C0018790	Cardiac Arrest
+C0018794	Block - heart
+C0018795	Catheterisation cardiac
+C0018798	Congenital heart defect
+C0018799	Heart Diseases
+C0018800	Cardiomegaly
+C0018801	Heart failure
+C0018802	Cardiac failure congestive
+C0018805	Heart Injuries
+C0018808	Cardiac murmur
+C0018809	Heart Neoplasm
+C0018810	heart rate
+C0018811	Foetal heart rate
+C0018813	Myocardial rupture
+C0018814	Heart Rupture, Post-Infarction
+C0018816	Cardiac septal defect
+C0018817	Atrial Septal Defects
+C0018818	Heart Septal Defects, Ventricular
+C0018821	Cardiac operation NOS
+C0018823	Heart transplant
+C0018824	Cardiac valve disease
+C0018833	Heart and lung transplant
+C0018834	Heartburn
+C0018835	Heartwater Disease
+C0018839	Heat exhaustion
+C0018843	Heat Stroke
+C0018852	Heavy Chain Disease
+C0018854	gamma-Chain Disease
+C0018862	Heberden's node
+C0018889	Helminthiasis
+C0018891	Helminthiasis, Animal
+C0018915	Hemangioendothelioma
+C0018916	Hemangioma
+C0018920	Hemangioma, Cavernous
+C0018922	hemangiopericytoma
+C0018923	Hemangiosarcoma
+C0018924	Haemarthrosis
+C0018926	Haematemesis
+C0018932	Haematochezia
+C0018935	Hematocrit procedure
+C0018939	Hematologic Diseases
+C0018944	Haematoma
+C0018946	Hematoma, Subdural
+C0018949	Hematomyelia
+C0018965	Haematuria
+C0018975	Hemeralopia
+C0018979	Hemianopia
+C0018984	Hemicrania migraine
+C0018987	Hemimelia
+C0018989	Hemiparesis
+C0018991	Hemiplegia
+C0018994	Biliary Tract Hemorrhage
+C0018995	Hemochromatosis
+C0019004	Haemodialysis
+C0019021	Hemoglobin C Disease
+C0019025	Hemoglobin F Disease
+C0019034	Hemoglobin SC Disease
+C0019045	Hemoglobinopathies
+C0019048	Haemoglobinuria
+C0019050	Hemoglobinuria, Paroxysmal
+C0019054	Hemolysis
+C0019061	Haemolytic uraemic syndrome
+C0019064	Hemopericardium
+C0019065	Hemoperitoneum
+C0019068	Reactive Hemophagocytic Syndrome
+C0019069	Hemophilia A
+C0019079	Haemoptysis
+C0019080	Hemorrhage
+C0019086	Haemorrhagic ascites
+C0019087	Haemorrhagic disorder
+C0019096	Hemorrhagic Fever, American
+C0019097	Hemorrhagic Fever, Argentinian
+C0019099	Hemorrhagic Fever, Crimean
+C0019100	Severe Dengue
+C0019101	Hemorrhagic Fever with Renal Syndrome
+C0019104	Hemorrhagic Fevers, Viral
+C0019112	Hemorrhoids
+C0019114	Haemosiderosis
+C0019123	Haemothorax
+C0019125	Hematotympanum
+C0019144	Hepatectomy NOS
+C0019147	Coma hepatic
+C0019151	Hepatic Encephalopathy
+C0019154	Hepatic Vein Thrombosis
+C0019156	Hepatic Veno-Occlusive Disease
+C0019158	Hepatitis
+C0019159	Hepatitis A
+C0019163	Hepatitis B
+C0019169	HBV
+C0019187	Hepatitis, Alcoholic
+C0019188	Hepatitis, Animal
+C0019189	Chronic hepatitis
+C0019191	Infectious Canine Hepatitis
+C0019193	Hepatitis toxic
+C0019195	Hepatitis, Viral, Human
+C0019196	Hepatitis C
+C0019202	Hepatolenticular Degeneration
+C0019207	Hepatoma, Morris
+C0019208	Hepatoma, Novikoff
+C0019209	Hepatomegaly
+C0019212	Hepatorenal Syndrome
+C0019214	Hepatosplenomegaly
+C0019243	Angioedemas, Hereditary
+C0019247	Hereditary Diseases
+C0019269	Hermaphroditism
+C0019270	Hernia
+C0019284	Diaphragmatic Hernia
+C0019288	Femoral hernias
+C0019294	Hernia, Inguinal
+C0019295	Inguinal Hernia, Direct
+C0019296	Inguinal Hernia, Indirect
+C0019322	Umbilical hernia
+C0019326	Hernia, Ventral
+C0019328	Hernia repairs
+C0019329	Abdominal hernia repair
+C0019333	Umbilical hernia repair
+C0019337	Heroin Dependence
+C0019340	Herpes NOS
+C0019342	Genital Herpes
+C0019343	Pemphigoid Gestationis
+C0019345	Herpes Labialis
+C0019348	Herpes Simplex
+C0019357	Keratitis, Herpetic
+C0019360	Herpes Zoster
+C0019364	Herpes Zoster Ophthalmicus
+C0019372	Herpes virus infection
+C0019385	Herpetic meningoencephalitis
+C0019489	Deficiency, Hexosediphosphatase
+C0019521	Hiccough
+C0019522	Adenoma, Sweat Gland
+C0019539	High T4 Syndrome
+C0019553	Hip Contracture
+C0019554	Hip Dislocation
+C0019555	Developmental hip dysplasia
+C0019557	Hip Fractures
+C0019559	Hip pain
+C0019562	von Hippel-Lindau Disease
+C0019569	Hirschsprung Disease
+C0019572	Hirsutism
+C0019613	Histiocytic Disorders, Malignant
+C0019618	Histiocytosis
+C0019621	Histiocytosis, Langerhans-Cell
+C0019623	Malignant histiocytosis
+C0019624	Histiocytosis, Non-Langerhans-Cell
+C0019625	Sinus histiocytosis
+C0019640	Histomoniasis
+C0019655	Histoplasmosis
+C0019681	Histrionic personality disorder
+C0019682	HIV
+C0019693	HIV Infections
+C0019699	HIV Seropositivity
+C0019816	Hereditary, Type VII, Motor and Sensory Neuropathy
+C0019825	Hoarse voice
+C0019829	Hodgkin Disease
+C0019872	Homicide
+C0019880	Homocystinuria
+C0019911	Hookworm Infections
+C0019917	Hordeolum
+C0019937	Horner Syndrome
+C0019940	Horse Diseases
+C0019993	Hospitalisation
+C0020039	Hostility
+C0020071	Hereditary Sensory Autonomic Neuropathy, Type 1
+C0020072	Hereditary Sensory Autonomic Neuropathy, Type 2
+C0020074	HSAN Type IV
+C0020075	Hereditary Sensory Autonomic Neuropathy, Type 5
+C0020097	HTLV-I Infections
+C0020102	HTLV-II Infections
+C0020162	Humerus fracture
+C0020175	Hunger
+C0020179	Huntington Disease
+C0020186	Hutchinson teeth
+C0020192	Hyaline Membrane Disease
+C0020217	Hydatidiform Mole
+C0020224	Polyhydramnios
+C0020225	Hydranencephaly
+C0020241	Hydroa Vacciniforme
+C0020255	Hydrocephalus
+C0020256	Congenital Hydrocephalus
+C0020258	Hydrocephalus, Normal Pressure
+C0020295	Hydronephrosis
+C0020302	Developmental glaucoma
+C0020303	Hydropneumothorax
+C0020305	Hydrops Fetalis
+C0020312	Hydrothorax
+C0020413	Hymenolepiasis
+C0020428	Hyperaldosteronism
+C0020429	Hyperalgesia
+C0020431	Hyperbaric oxygen therapy
+C0020433	Hyperbilirubinaemia
+C0020435	Hyperbilirubinemia, Hereditary
+C0020437	Hypercalcemia
+C0020438	Hypercalciuria
+C0020440	Hypercapnia
+C0020443	Hypercholesterolemia
+C0020445	Hypercholesterolemia, Familial
+C0020449	Hyperdistention
+C0020450	Hyperemesis Gravidarum
+C0020452	Hyperemia
+C0020453	Hyperaesthesia
+C0020455	Hypergammaglobulinaemia
+C0020456	Hyperglycemia
+C0020457	Diabetic hyperosmolar coma
+C0020458	Hyperhidrosis
+C0020459	Hyperinsulinaemia
+C0020461	Hyperkalemia
+C0020473	Hyperlipidemia
+C0020474	Hyperlipidemia, Familial Combined
+C0020476	Hyperlipoproteinemias
+C0020479	Hyperlipoproteinemia Type III
+C0020480	Hyperlipoproteinemia Type IV
+C0020481	Hyperlipoproteinemia Type V
+C0020488	Hypernatraemia
+C0020490	Hyperopia
+C0020492	Hyperostosis
+C0020494	Hyperostosis Frontalis Interna
+C0020496	Hyperostosis of skull
+C0020497	Cortical Congenital Hyperostosis
+C0020498	Senile ankylosing vertebral hyperostosis
+C0020500	Hyperoxaluria
+C0020501	Hyperoxaluria, Primary
+C0020502	Hyperparathyroidism
+C0020503	Hyperparathyroidism, Secondary
+C0020505	Hyperphagia
+C0020507	Hyperplasia
+C0020510	Nodular regenerative hyperplasia
+C0020514	Hyperprolactinemia
+C0020517	Hypersensitivity
+C0020522	Delayed Hypersensitivity
+C0020523	Immediate hypersensitivity
+C0020524	Disorders of Excessive Somnolence
+C0020529	Hypersomnia with Periodic Respiration
+C0020532	Hypersplenism
+C0020534	Hypertelorism of orbit
+C0020538	Hypertension
+C0020540	Malignant Hypertension
+C0020541	Hypertension, Portal
+C0020542	Hypertension, Pulmonary
+C0020544	Renal hypertension
+C0020545	Hypertension, Renovascular
+C0020546	Hypertensive crisis
+C0020550	Hyperthyroidism
+C0020551	Hyperthyroxinemia
+C0020555	Hypertrichosis
+C0020557	Hypertriglyceridemia
+C0020564	Hypertrophy
+C0020565	Hypertrophy of breast NOS
+C0020569	Salivary gland enlargement
+C0020575	Hypertropia
+C0020578	Hyperventilation
+C0020579	Hypervitaminosis A
+C0020580	Hypesthesia
+C0020581	Hyphaema
+C0020594	Hypoactive Sexual Desire Disorder
+C0020595	Hypoaldosteronism
+C0020597	Hypobetalipoproteinemias
+C0020598	Hypocalcemia
+C0020599	Hypocalciuria
+C0020604	Hypochondriasis
+C0020607	Hypodermyiasis
+C0020608	Hypodontia
+C0020610	Hypogalactia
+C0020615	Hypoglycemia
+C0020617	Hypoglycaemic coma
+C0020619	Hypogonadism
+C0020620	Hypohidrosis
+C0020621	Hypokalaemia
+C0020623	Hypolipoproteinemias
+C0020624	Hypomenorrhea
+C0020625	Hyponatremia
+C0020626	Hypoparathyroidism
+C0020627	Hypopharyngeal Neoplasms
+C0020630	Hypophosphatasia
+C0020631	Familial hypophosphatemia
+C0020635	Hypopituitarism
+C0020636	Congenital hypoplasia
+C0020639	Hypoproteinaemia
+C0020640	Factor II deficiency
+C0020641	Hypopyon
+C0020649	Hypotension
+C0020651	Hypotension, Orthostatic
+C0020655	Hypothalamic Diseases
+C0020672	Decreased body temperature
+C0020676	Hypothyroidism
+C0020678	Hypotrichosis
+C0020681	Sleep-related respiratory failure
+C0020683	Hypovolaemic shock
+C0020699	Hysterectomy
+C0020701	Hysteria
+C0020703	Dissociative Hysteria
+C0020725	Type II Mucolipidosis
+C0020732	Iatrogenic Disease
+C0020757	Ichthyoses
+C0020758	Congenital ichthyosis
+C0020796	Profound Mental Retardation
+C0020800	Idiopathic Hypercatabolic Hypoproteinemia
+C0020875	Ileal Diseases
+C0020877	Ileitis
+C0020883	Ileostomy
+C0020899	Illiteracy
+C0020901	Poisoning, Illuminating Gas
+C0020903	Illusion
+C0020951	Immune Complex Diseases
+C0020981	Angioimmunoblastic Lymphadenopathy
+C0021051	Immunodeficiency
+C0021053	Immune System Diseases
+C0021071	Immunoproliferative Small Intestinal Disease
+C0021092	Cerumen impaction
+C0021099	Impetigo
+C0021100	Bullous impetigo
+C0021122	Disruptive, Impulse Control, and Conduct Disorders
+C0021124	Impulse-Ridden Personality
+C0021125	Impulsive Behavior
+C0021139	Inadequate Personality
+C0021141	Inappropriate ADH Syndrome
+C0021151	Incipient Schizophrenia
+C0021167	Incontinence
+C0021171	Bloch Sulzberger syndrome
+C0021177	Increased libido
+C0021280	Infant Nutrition Disorders
+C0021290	Neonatal disorder
+C0021294	Infant, Premature
+C0021295	Infant, Premature, Diseases
+C0021296	Infant, Small for Gestational Age
+C0021308	Infarction
+C0021313	Infection of kidney
+C0021342	Enteritis infectious
+C0021345	Infectious Mononucleosis
+C0021359	Infertility
+C0021361	Female infertility
+C0021364	Infertility, Male
+C0021367	Mammary Ductal Carcinoma
+C0021368	Inflammation
+C0021390	Inflammatory bowel disease, NOS
+C0021400	Influenza
+C0021432	Infratentorial Neoplasms
+C0021446	Inguinal hernia repair
+C0021459	Inhalation therapy
+C0021479	INJECTED EYE
+C0021488	Joint injection
+C0021508	Disorders of Environmental Origin
+C0021564	Insect Bites
+C0021568	Insect Bites and Stings
+C0021603	Sleep Initiation and Maintenance Disorders
+C0021655	Insulin Resistance
+C0021670	insulinoma
+C0021704	Intelligence
+C0021712	Intention myoclonus
+C0021775	Intermittent Claudication
+C0021776	Intermittent Explosive Disorder
+C0021807	Intertrigo
+C0021818	Intervertebral Disc Displacement
+C0021828	Intestinal Atresia
+C0021831	Intestinal Diseases
+C0021832	Intestinal Diseases, Parasitic
+C0021833	Intestinal fistula
+C0021841	Intestinal Neoplasms
+C0021843	Intestinal Obstruction
+C0021845	Intestinal Perforation
+C0021846	Intestinal Polyps
+C0021847	Intestinal Pseudo-Obstruction
+C0021888	Intraocular Pressure
+C0021890	Intraoperative Complications
+C0021897	Intrathoracic Goiters
+C0021899	Intra-uterine contraceptive device expelled
+C0021925	Intubation NOS
+C0021931	Gastrointestinal tube insertion
+C0021932	Endotracheal intubation
+C0021933	Intussusception
+C0021963	Iodamoebiasis
+C0022073	Iridocyclitis
+C0022078	Iridopathy
+C0022079	Iris neoplasm
+C0022081	Iritis
+C0022104	Irritable Bowel Syndrome
+C0022107	Irritability
+C0022116	Ischemia
+C0022118	Transient ischemia
+C0022134	Adenoma, Islet Cell
+C0022281	Eye pruritus
+C0022283	Incontinentia Pigmenti Achromians
+C0022333	Jacksonian Seizure
+C0022336	Creutzfeldt-Jakob disease
+C0022340	Late-Infantile Neuronal Ceroid Lipfuscinosis
+C0022346	Icterus
+C0022350	Jaundice, Chronic Idiopathic
+C0022353	Jaundice, Neonatal
+C0022354	Jaundice, Obstructive
+C0022360	Jaw Abnormalities
+C0022361	Jaw cyst
+C0022362	Diseases of the jaws
+C0022363	Jaw fracture
+C0022373	Jejunal Diseases
+C0022387	Jervell-Lange Nielsen Syndrome
+C0022408	Arthropathy
+C0022410	Joint Instability
+C0022411	Loose body in joint
+C0022415	Joint Tuberculosis
+C0022492	Kandinsky Syndrome
+C0022504	Kaposi\'s varicelliform eruption
+C0022521	Kartagener Syndrome
+C0022541	Kearns-Sayre syndrome
+C0022548	Keloid
+C0022568	Keratitis
+C0022572	keratoacanthoma
+C0022573	Keratoconjunctivitis
+C0022575	Keratoconjunctivitis Sicca
+C0022577	Keratoconjunctivitis, Vernal
+C0022578	Keratoconus
+C0022579	Keratoderma
+C0022582	Keratoderma, diffuse
+C0022584	Keratoderma, Palmoplantar, Diffuse
+C0022593	Keratosis
+C0022594	Keratosis Blennorrhagica
+C0022595	Keratosis Follicularis
+C0022596	Palmoplantar Keratosis
+C0022602	Actinic keratosis
+C0022603	Keratosis, Seborrheic
+C0022610	Kernicterus
+C0022638	Ketosis
+C0022650	Calculus of kidney
+C0022656	Kidney Cortex Necrosis
+C0022658	Kidney Diseases
+C0022660	Acute renal failure NOS
+C0022661	Kidney Failure, Chronic
+C0022665	Kidney Neoplasm
+C0022667	Kidney Papillary Necrosis
+C0022671	Renal transplant
+C0022672	Acute Kidney Tubular Necrosis
+C0022679	Cystic kidney
+C0022680	Polycystic Kidney Diseases
+C0022681	Medullary sponge kidney
+C0022682	Kienbock Disease
+C0022716	Menkes Kinky Hair Syndrome
+C0022729	Klebsiella Infections
+C0022734	Kleptomania
+C0022735	Klinefelter Syndrome
+C0022738	Klippel-Feil Syndrome
+C0022739	Klippel-Trenaunay-Weber Syndrome
+C0022744	Knee Injuries
+C0022783	Vulvar Lichen Sclerosus
+C0022790	Krukenberg Tumor
+C0022797	Adult Neuronal Ceroid Lipofuscinosis
+C0022802	Kuru
+C0022806	Kwashiorkor
+C0022821	Kyphosis
+C0022865	Obstetric Labor Complications
+C0022875	Induced labour
+C0022876	Premature labour
+C0022890	Labyrinth Diseases
+C0022893	Labyrinthitis
+C0022904	Lacrimal Apparatus Diseases
+C0022906	Lacrimal Duct Obstruction
+C0022927	Lactation Disorder
+C0022951	Lactose Intolerance
+C0022958	Lacunar Dementias
+C0022972	Lambert-Eaton Myasthenic Syndrome
+C0022976	Lameness, Animal
+C0022983	Spinal laminectomy
+C0023003	Langer-Giedion Syndrome
+C0023009	Speech and language disorder
+C0023012	Language Delay
+C0023014	Language development disorder
+C0023015	Language Disorders
+C0023038	Laparotomy
+C0023048	Larva Migrans
+C0023051	Laryngeal Diseases
+C0023052	Laryngeal Edema
+C0023055	Laryngeal neoplasm
+C0023059	Laryngeal Perichondritis
+C0023066	Laryngismus
+C0023067	Laryngitis
+C0023075	Laryngeal stenosis
+C0023092	Lassa Fever
+C0023105	Schizophrenia, Latent
+C0023114	Handedness
+C0023138	Laurence-Moon Syndrome
+C0023176	Lead Poisoning
+C0023182	Cerebrospinal fluid leak
+C0023186	Learning disorder
+C0023195	Lecithin Acyltransferase Deficiency
+C0023211	Bundle branch block left
+C0023212	Left ventricular failure
+C0023213	Ventricular Outflow Obstruction, Left
+C0023218	Leg cramps
+C0023221	Leg Length Inequality
+C0023222	Pain in lower limb
+C0023223	Leg Ulcer
+C0023234	Legg-Calve-Perthes Disease
+C0023240	Legionella infections
+C0023241	Legionnaires' Disease
+C0023264	Leigh Disease
+C0023267	Fibroid Tumor
+C0023269	leiomyosarcoma
+C0023281	Leishmaniasis
+C0023283	Leishmaniasis, Cutaneous
+C0023288	Infection by Leishmania braziliensis
+C0023290	Leishmaniasis, Visceral
+C0023308	Lens Diseases
+C0023309	Lens dislocation
+C0023310	Lens Dislocation and Subluxation
+C0023311	Intraocular lens implant
+C0023316	Lens Subluxation
+C0023321	Lentigo
+C0023343	Leprosy
+C0023346	Borderline leprosy
+C0023348	Lepromatous leprosy
+C0023351	Tuberculoid leprosy
+C0023364	Leptospirosis
+C0023370	Leriche Syndrome
+C0023374	Lesch-Nyhan Syndrome
+C0023380	Lethargy
+C0023381	Letterer-Siwe Disease
+C0023418	leukemia
+C0023420	Leukemia L1210
+C0023434	Chronic Lymphocytic Leukemia
+C0023437	Acute Basophilic Leukemia
+C0023439	Leukemia, Eosinophilic, Acute
+C0023440	Acute Erythroblastic Leukemia
+C0023441	Leukemia, Experimental
+C0023443	Hairy Cell Leukemia
+C0023448	Leukemia, Lymphoid
+C0023449	Acute lymphocytic leukaemia
+C0023452	Childhood Acute Lymphoblastic Leukemia
+C0023453	L2 Acute Lymphoblastic Leukemia
+C0023461	Leukemia, Mast-Cell
+C0023462	Acute Megakaryocytic Leukemias
+C0023464	Acute biphenotypic leukemia
+C0023465	Acute monocytic leukemia
+C0023466	Leukemia, Monocytic, Chronic
+C0023467	Leukemia, Myelocytic, Acute
+C0023470	Myeloid leukaemia
+C0023472	Leukemia, Myeloid, Accelerated Phase
+C0023473	Leukemia, Myelogenous, Chronic, BCR-ABL Positive
+C0023474	Leukemia, Myeloid, Chronic-Phase
+C0023479	Acute myelomonocytic leukemia
+C0023480	Leukemia, Myelomonocytic, Chronic
+C0023481	Chronic Neutrophilic Leukemia
+C0023484	Leukemia, Plasma Cell
+C0023485	Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
+C0023486	Prolymphocytic Leukemia
+C0023487	Acute Promyelocytic Leukemia
+C0023488	Leukemia, Radiation-Induced
+C0023492	Leukemia, T-Cell
+C0023493	Adult T-Cell Lymphoma/Leukemia
+C0023494	Leukemia, T-Cell, Chronic
+C0023501	Leukaemoid reaction
+C0023508	White blood cell count
+C0023510	Leukocyte Disorders
+C0023518	Leukocytosis
+C0023520	Leukodystrophy
+C0023521	Globoid cell leukodystrophy
+C0023522	Leukodystrophy, Metachromatic
+C0023524	Leukoencephalopathy, Progressive Multifocal
+C0023529	Leukomalacia, Periventricular
+C0023530	Leukopenia
+C0023531	Leukoplakia
+C0023532	Leukoplakia, Oral
+C0023533	Leukorrhea
+C0023600	Leydig cell hyperplasia
+C0023601	Leydig Cell Tumor
+C0023643	Lichen disease
+C0023645	Lichen planus follicularis
+C0023646	Lichen Planus
+C0023652	Lichen Sclerosus et Atrophicus
+C0023653	Lichenification
+C0023743	Linitis Plastica
+C0023760	Diseases of lips
+C0023772	Lipid Metabolism, Inborn Errors
+C0023786	Mucopolysaccharidosis I
+C0023787	Lipodystrophy
+C0023788	Whipple Disease
+C0023794	Lipidosis
+C0023795	Lipoid Proteinosis of Urbach and Wiethe
+C0023798	Lipoma
+C0023801	Lipomatosis
+C0023804	Lipomatosis, Multiple Symmetrical
+C0023806	Lipomucopolysaccharidosis
+C0023817	Hyperlipoproteinemia Type I
+C0023827	liposarcoma
+C0023860	Listeriosis
+C0023869	Lithiasis
+C0023878	Lithotripsy NOS
+C0023882	Little's Disease
+C0023885	Liver Abscess
+C0023886	Amebic liver abscess
+C0023890	Cirrhosis of liver NOS
+C0023891	Liver Cirrhosis, Alcoholic
+C0023892	Biliary cirrhosis
+C0023893	Liver Cirrhosis, Experimental
+C0023895	Liver diseases
+C0023896	Alcoholic Liver Diseases
+C0023897	Liver Diseases, Parasitic
+C0023903	Hepatic neoplasm
+C0023904	Liver Neoplasms, Experimental
+C0023911	Liver transplant
+C0023931	Lobstein Disease
+C0023944	Locked in syndrome
+C0023968	Loiasis
+C0023974	Loneliness
+C0023976	Long QT Syndrome
+C0023980	Longevity
+C0024003	Lordosis
+C0024025	Louping Ill
+C0024031	Low Back Pain
+C0024032	Low birth weight
+C0024042	Low T3-High T4 Syndrome
+C0024043	Low T3 Syndrome
+C0024050	Lower gastrointestinal haemorrhage
+C0024054	Lown-Ganong-Levine Syndrome
+C0024103	Breast mass
+C0024110	Lung Abscess
+C0024115	Lung diseases
+C0024116	Lung Diseases, Fungal
+C0024117	Chronic Obstructive Airway Disease
+C0024121	Lung Neoplasms
+C0024128	Lung transplant
+C0024131	Lupus Vulgaris
+C0024137	Lupus Erythematosus, Cutaneous
+C0024138	DLE
+C0024140	Lupus Erythematosus, Subacute Cutaneous
+C0024141	Lupus Erythematosus, Systemic
+C0024143	Lupus Nephritis
+C0024145	Chilblain lupus 1
+C0024167	Luteoma
+C0024198	Lyme Disease
+C0024203	Lymphadenectomy
+C0024205	Lymphadenitis
+C0024214	Lymphangiectasis
+C0024215	Lymphangiectasis, Intestinal
+C0024217	Lymphangioendothelioma
+C0024221	Lymphangioma
+C0024224	lymphangiosarcoma
+C0024225	Lymphangitis
+C0024228	Lymphatic Diseases
+C0024232	Lymphatic Metastasis
+C0024236	Lymphedema
+C0024248	Lymphocele
+C0024266	Lymphocytic Choriomeningitis
+C0024282	Lymphocytosis
+C0024286	Lymphogranuloma Venereum
+C0024291	Lymphohistiocytosis, Hemophagocytic
+C0024299	Lymphoma
+C0024301	Lymphoma, Follicular
+C0024302	Reticulosarcoma
+C0024303	Small Cell Lymphoma
+C0024304	Lymphoma, Mixed-Cell
+C0024305	Lymphoma, Non-Hodgkin
+C0024306	Lymphoma, Undifferentiated
+C0024307	Lymphomatoid Granulomatosis
+C0024312	Lymphopenia
+C0024314	Lymphoproliferative Disorders
+C0024408	Machado-Joseph Disease
+C0024419	Waldenstrom Macroglobulinemia
+C0024421	Macroglossia
+C0024433	Macrostomia
+C0024437	Macular degeneration
+C0024439	Macular corneal dystrophy
+C0024440	Cystoid macular oedema
+C0024441	Macular hole
+C0024445	Lipomatosis, Familial Benign Cervical
+C0024449	Mycetoma
+C0024454	Maffucci Syndrome
+C0024473	Magnesium Deficiency
+C0024485	NMR
+C0024507	Majewski Syndrome
+C0024517	Major depression, single episode
+C0024523	Malabsorption
+C0024528	Malaise and fatigue
+C0024530	Malaria
+C0024534	Malaria, Cerebral
+C0024535	Malaria, Falciparum
+C0024537	Malaria, Vivax
+C0024586	Malignant Carcinoid Syndrome
+C0024588	Malignant essential hypertension
+C0024591	Malignant hyperpyrexia due to anesthesia
+C0024620	Primary Malignant Liver Neoplasm
+C0024622	Malignant neoplasm of retina
+C0024623	Malignant neoplasm of stomach
+C0024624	Malignant neoplasm of upper lobe, bronchus or lung
+C0024633	Mallory-Weiss syndrome
+C0024636	Malocclusion
+C0024667	Animal Mammary Neoplasms
+C0024668	Mammary Neoplasms, Experimental
+C0024689	Mandibular Diseases
+C0024694	Mandibular Neoplasms
+C0024709	Mange
+C0024710	Mange, Sarcoptic
+C0024713	Manic Disorder
+C0024748	alpha-Mannosidosis
+C0024759	Mansonelliasis
+C0024776	Maple Syrup Urine Disease
+C0024788	Marburg Virus Disease
+C0024790	Paroxysmal nocturnal haemoglobinuria
+C0024793	Marek Disease
+C0024796	Marfan Syndrome
+C0024799	Marginal ulcer
+C0024809	Marijuana Abuse
+C0024814	Marinesco-Sjogren syndrome
+C0024881	Mastectomies
+C0024883	Modified radical mastectomy
+C0024894	Mastitis
+C0024897	Mastocytoma
+C0024899	Mastocytosis
+C0024900	Mastocytosis, Bullous
+C0024901	Mastocytosis, Diffuse Cutaneous
+C0024902	Mastodynia
+C0024904	Mastoiditis
+C0024950	Maxillary Diseases
+C0024954	Maxillary Neoplasms
+C0024958	Maxillary Sinus Neoplasms
+C0024959	Maxillary Sinusitis
+C0024967	Maximal Voluntary Ventilation
+C0025007	Measles
+C0025037	Meckel Diverticulum
+C0025048	Meconium Aspiration Syndrome
+C0025061	Mediastinal disorder
+C0025062	Mediastinal Emphysema
+C0025063	Mediastinal Neoplasms
+C0025064	Mediastinitis
+C0025115	Medication error
+C0025149	Medulloblastoma
+C0025160	Megacolon
+C0025162	Megacolon toxic
+C0025164	Megaesophagus
+C0025167	Megakaryocytic hyperplasia
+C0025183	Meige Syndrome
+C0025184	Meigs Syndrome
+C0025193	Melancholia
+C0025202	melanoma
+C0025205	Melanoma, Experimental
+C0025209	Melanosis
+C0025218	Chloasma
+C0025221	Meleda Disease
+C0025222	Melaena
+C0025229	Melioidosis
+C0025237	Melnick-Needles Syndrome
+C0025239	Melorheostosis
+C0025261	Memory Disorders
+C0025265	Memory, Short-Term
+C0025267	Multiple Endocrine Neoplasia Type 1
+C0025268	Multiple Endocrine Neoplasia Type 2a
+C0025269	Multiple Endocrine Neoplasia Type 2b
+C0025281	Meniere Disease
+C0025284	Meningeal Neoplasms
+C0025286	Meningioma
+C0025287	Meningism
+C0025289	Meningitis
+C0025290	Aseptic Meningitis
+C0025292	Meningitis, Haemophilus
+C0025293	Meningitis listeria
+C0025294	Meningitis, Meningococcal
+C0025295	Meningitis, Pneumococcal
+C0025297	Meningitis viral
+C0025299	Meningocele
+C0025303	Meningococcal Infections
+C0025306	Meningococcemia
+C0025309	Meningoencephalitis
+C0025312	Meningomyelocele
+C0025319	Menopausal disorder
+C0025320	Menopause
+C0025322	Premature Menopause
+C0025323	Menorrhagia
+C0025345	Menstrual disorder
+C0025349	Menstruation, Retrograde
+C0025361	Mental Processes
+C0025362	Mental Retardation
+C0025363	Mental Retardation, Psychosocial
+C0025427	Mercury Poisoning
+C0025464	Mesenchymoma
+C0025470	Mesenteric Panniculitis
+C0025472	Mesenteric Vascular Occlusion
+C0025500	Mesothelioma
+C0025517	Metabolic Diseases
+C0025521	Inborn Errors of Metabolism
+C0025530	Metagonimiasis
+C0025534	Metal Metabolism, Inborn Errors
+C0025568	Metaplasia
+C0025585	Deformity of metatarsal
+C0025587	Metatarsalgia
+C0025637	Methaemoglobinaemia
+C0025874	Metrorrhagia
+C0025945	Diabetic microangiopathy
+C0025958	Microcephaly
+C0025988	Microglossia
+C0025990	Micrognathia
+C0025995	Micromelia
+C0026010	Microphthalmos
+C0026034	Microstomia
+C0026069	Middle Lobe Syndrome
+C0026103	Mikulicz Disease
+C0026106	Mild Mental Retardation
+C0026113	Miliaria
+C0026141	Milk-Alkali Syndrome
+C0026205	Miosis
+C0026229	Mite Infestations
+C0026265	Diseases of mitral valve
+C0026266	Mitral valve incompetence
+C0026267	Mitral valve prolapse
+C0026268	Mitral valve replacement
+C0026269	Mitral Valve Stenosis
+C0026272	Mixed Connective Tissue Disease
+C0026277	Mixed Salivary Gland Tumor
+C0026351	Moderate mental retardation (I.Q. 35-49)
+C0026363	Mohr Syndrome
+C0026393	Molluscum Contagiosum
+C0026431	Monkey Diseases
+C0026470	Hypergammaglobulinaemia benign monoclonal
+C0026471	Monoclonal paraproteinemia
+C0026499	Monosomy
+C0026552	Morphine Dependence
+C0026603	Motion Sickness
+C0026613	Motor skill disorder
+C0026618	Dental Fluorosis, Acquired
+C0026633	Congenital oral malformation
+C0026635	Mouth breathing
+C0026636	Mouth Diseases
+C0026640	Mouth Neoplasms
+C0026644	Edentulous
+C0026650	Movement disorder
+C0026654	Moyamoya Disease
+C0026683	Mucocele
+C0026684	Mucocele of appendix
+C0026691	Mucocutaneous Lymph Node Syndrome
+C0026697	Mucolipidoses
+C0026703	Mucopolysaccharidoses
+C0026705	Mucopolysaccharidosis II
+C0026706	Mucopolysaccharidosis III
+C0026707	Mucopolysaccharidosis IV
+C0026708	Mucopolysaccharidosis V
+C0026709	Mucopolysaccharidosis VI
+C0026718	Mucormycosis
+C0026755	Multiple Carboxylase Deficiency
+C0026760	Multiple Epiphyseal Dysplasia
+C0026764	Multiple Myeloma
+C0026766	Multiple Organ Failure
+C0026769	Multiple Sclerosis
+C0026771	Multiple injuries
+C0026773	Dissociative identity disorder
+C0026780	Mumps
+C0026820	Muscle Contraction
+C0026821	Muscle Cramp
+C0026825	Flaccid Muscle Tone
+C0026826	Hypertonia
+C0026827	Hypotonia
+C0026836	Muscle Relaxation
+C0026837	Muscle Rigidity
+C0026838	Muscle Spasticity
+C0026846	Muscle atrophy
+C0026847	Muscular Atrophy, Spinal
+C0026848	Muscular Diseases
+C0026850	Muscular Dystrophies
+C0026851	Muscular Dystrophy, Animal
+C0026857	Musculoskeletal Diseases
+C0026858	Musculoskeletal Pain
+C0026865	Mushroom Poisoning
+C0026884	Mutism
+C0026896	Myasthenia Gravis
+C0026916	Mycobacterium avium-intracellulare Infection
+C0026918	Mycobacterial infection
+C0026919	Atypical mycobacterial infection
+C0026936	Mycoplasma Infections
+C0026946	Mycoses
+C0026948	Mycosis Fungoides
+C0026961	Mydriasis
+C0026975	Myelitis
+C0026976	Myelitis transverse
+C0026985	Myelodysplasia
+C0026986	Myelodysplastic syndrome
+C0026987	Myelofibrosis
+C0026996	Myeloid hyperplasia
+C0026998	Acute Myeloid Leukemia, M1
+C0027013	Myeloid Metaplasia
+C0027019	Myelomonocytic leukemia
+C0027022	Myeloproliferative disease
+C0027051	Myocardial Infarction
+C0027055	Myocardial Reperfusion Injury
+C0027059	Myocarditis
+C0027066	Myoclonus
+C0027070	Myoepithelioma
+C0027073	Myofascial Pain Syndromes
+C0027080	Myoglobinuria
+C0027086	Myoma
+C0027092	Myopia
+C0027095	Myosarcoma
+C0027121	Myositis
+C0027122	Myositis Ossificans
+C0027125	Myotonia
+C0027126	Myotonic Dystrophy
+C0027127	Myotonia Congenita
+C0027145	Myxedema
+C0027149	Myxoma
+C0027333	Nagana
+C0027339	Nail Diseases
+C0027341	Nail-Patella Syndrome
+C0027343	Ingrowing nail
+C0027344	Nails, Malformed
+C0027401	Narcissism
+C0027402	Narcissistic Personality Disorder
+C0027404	Narcolepsy
+C0027412	Opioid-Related Disorders
+C0027424	Nasal congestion
+C0027429	Nasal obstruction
+C0027430	Nasal polyp NOS
+C0027438	Nasopharyngeal disorder
+C0027439	Nasopharyngeal Neoplasms
+C0027441	Nasopharyngitis
+C0027443	Natal Teeth
+C0027497	Nausea
+C0027498	Nausea and vomiting
+C0027528	Necatoriasis
+C0027531	Neck injury
+C0027533	Neck Neoplasms
+C0027538	Necrobiosis Lipoidica
+C0027540	Necrosis
+C0027543	Avascular necrosis of bone
+C0027547	Necrotising scleritis
+C0027562	Negativism
+C0027577	Nelson Syndrome
+C0027583	Nematode infections
+C0027585	Infections, Nematomorpha
+C0027609	Neonatal Abstinence Syndrome
+C0027612	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
+C0027613	Neonatal hepatitis
+C0027625	Circulating Neoplastic Cells
+C0027626	Neoplasm Invasiveness
+C0027627	Neoplasm Metastasis
+C0027643	Neoplasm Recurrence, Local
+C0027644	Neoplasm Regression, Spontaneous
+C0027645	Neoplasm Seeding
+C0027651	Neoplasms
+C0027654	Embryonal Neoplasm
+C0027656	Neoplasms, Connective Tissue
+C0027658	Neoplasms, Germ Cell and Embryonal
+C0027659	Neoplasms, Experimental
+C0027660	Neoplasms, Glandular and Epithelial
+C0027661	Neoplasms, Hormone-Dependent
+C0027662	Multiple Endocrine Neoplasia
+C0027663	Neoplasms, Multiple Primary
+C0027666	Neoplasms, Radiation-Induced
+C0027667	Neoplasms, Unknown Primary
+C0027668	Neoplasms, Vascular Tissue
+C0027671	Neoplastic Processes
+C0027672	Neoplastic Syndromes, Hereditary
+C0027686	Neovascularisation
+C0027695	Nephrectomy
+C0027697	Nephritis
+C0027706	Hereditary nephritis
+C0027707	Nephritis interstitial
+C0027708	Nephroblastoma
+C0027709	Nephrocalcinosis
+C0027719	Nephrosclerosis
+C0027720	Nephrosis
+C0027721	Glomerulonephritis minimal lesion
+C0027726	Nephrotic Syndrome
+C0027741	Nerve block
+C0027743	Nerve compression syndrome
+C0027746	Nerve Degeneration
+C0027765	Nervous System Diseases
+C0027766	Nervous System Neoplasms
+C0027769	Nervousness
+C0027773	Nesidioblastosis
+C0027794	Neural Tube Defects
+C0027796	Neuralgia
+C0027804	Neurasthenia
+C0027806	Neurenteric Cyst
+C0027809	Neurilemmoma
+C0027813	Neuritis
+C0027814	Neuritis, Autoimmune, Experimental
+C0027819	Neuroblastoma
+C0027821	Neurocirculatory Asthenia
+C0027822	Neurodermatitis
+C0027830	neurofibroma
+C0027831	Neurofibromatosis 1
+C0027832	Neurofibromatosis 2
+C0027849	Neuroleptic Malignant Syndrome
+C0027854	Neurologic Manifestations
+C0027858	Neuroma
+C0027859	Acoustic Neuroma
+C0027868	Neuromuscular Diseases
+C0027873	Neuromyelitis Optica
+C0027877	Neuronal Ceroid-Lipofuscinoses
+C0027888	Hereditary Motor and Sensory Neuropathies
+C0027889	Hereditary Sensory and Autonomic Neuropathies
+C0027927	Neurosyphilis
+C0027932	Neurotic Disorders
+C0027947	Neutropenia
+C0027960	Nevus
+C0027961	Nevus of Ota
+C0027962	Melanocytic naevus
+C0027983	Newcastle Disease
+C0028043	Nicotine addiction
+C0028047	Nicotine withdrawal
+C0028064	Niemann-Pick Diseases
+C0028077	Night Blindness
+C0028081	Night sweats
+C0028084	Nightmare
+C0028242	Nocardia Infections
+C0028250	Nocturnal Leg Cramps
+C0028259	Nodule
+C0028313	Organic Brain Syndrome, Nonpsychotic
+C0028326	Noonan Syndrome
+C0028431	Nose Deformities, Acquired
+C0028432	Nasal disorder
+C0028433	Nose Neoplasms
+C0028643	Numbness
+C0028705	Nutcracker Esophagus
+C0028715	Nutritional and Metabolic Diseases
+C0028734	Nocturia
+C0028738	Nystagmus
+C0028754	Obesity
+C0028756	Morbid obesity
+C0028768	Obsessive-Compulsive Disorder
+C0028778	Obstruction
+C0028790	Cerebral artery occlusion
+C0028792	Occult blood
+C0028796	Dermatitis, Occupational
+C0028797	Occupational Diseases
+C0028817	Ochronosis
+C0028838	Ocular Headache
+C0028840	Ocular Hypertension
+C0028841	Hypotony of eye
+C0028848	Ocular Larva Migrans
+C0028850	Eye movement disorder
+C0028856	Ocular torticollis
+C0028860	Oculocerebrorenal Syndrome
+C0028866	IIIrd nerve paralysis
+C0028877	Odontogenesis
+C0028878	Odontogenesis Imperfecta
+C0028879	Odontogenic Cysts
+C0028880	Odontogenic Tumors
+C0028882	Odontoma
+C0028945	oligodendroglioma
+C0028949	Oligomenorrhea
+C0028960	Oligospermia
+C0028961	Oliguria
+C0028962	Oliguria and anuria
+C0028968	Olivopontocerebellar Atrophies
+C0028975	Omental Panniculitis
+C0029001	Onchocerciasis
+C0029002	Onchocerciasis, Ocular
+C0029076	Ophthalmia neonatorum (gonococcal)
+C0029077	Ophthalmia, Sympathetic
+C0029089	Ophthalmoplegia
+C0029095	Opioid abuse
+C0029104	Opioid withdrawal
+C0029106	Opisthorchiasis
+C0029118	Opportunistic infection
+C0029121	Oppositional Defiant Disorder
+C0029124	Optic Atrophy
+C0029125	Hereditary optic atrophy
+C0029128	Optic Disk Drusen
+C0029131	Abnormality of the optic nerve
+C0029132	Disorder of the optic nerve
+C0029134	ON - Optic neuritis
+C0029163	Mouth haemorrhage
+C0029166	Oral Manifestations
+C0029172	Oral Submucous Fibrosis
+C0029182	orbit (eye disorders)
+C0029191	Orchitis
+C0029226	Hallucinations, Organic
+C0029227	Delirium, Dementia, Amnestic, Cognitive Disorders
+C0029230	Organic Mental Disorders, Psychotic
+C0029231	Organic Mental Disorders, Substance-Induced
+C0029261	Orgasm abnormal
+C0029293	Oroantral fistula
+C0029294	Orofaciodigital Syndromes
+C0029295	Oropharyngeal Neoplasms
+C0029307	Oroya Fever
+C0029342	Orthomyxoviridae Infections
+C0029396	Heterotopic Ossification
+C0029400	Osteitis
+C0029401	Osteitis Deformans
+C0029405	Osteitis Fibrosa Cystica
+C0029408	Degenerative polyarthritis
+C0029410	Osteoarthritis of hip
+C0029411	Osteoarthropathy, Primary Hypertrophic
+C0029412	Osteoarthropathy, Secondary Hypertrophic
+C0029417	Osteoblastoma
+C0029420	Osteochondritis
+C0029421	Osteochondritis Dissecans
+C0029422	Osteochondrodysplasias
+C0029423	Cartilaginous exostosis
+C0029427	Synovial osteochondromatosis
+C0029429	Osteochondrosis
+C0029434	Osteogenesis Imperfecta
+C0029437	Idiopathic Multicentric Osteolyses
+C0029438	Massive Osteolyses
+C0029440	Osteoma
+C0029441	Osteoid osteoma
+C0029442	Osteomalacia
+C0029443	Osteomyelitis
+C0029445	Bone necrosis
+C0029453	Osteopenia
+C0029454	Osteopetrosis
+C0029455	Osteopoikilosis (disorder)
+C0029456	Osteoporosis
+C0029458	Osteoporosis, Postmenopausal
+C0029459	Osteoporosis, Senile
+C0029461	Osteoradionecrosis
+C0029463	Osteosarcoma
+C0029464	Osteosclerosis
+C0029468	Osteotomy
+C0029488	Other acute reactions to stress
+C0029531	Other cataract
+C0029574	Other dermatoses
+C0029591	Other disorders of lipoid metabolism
+C0029607	Other emphysema
+C0029630	Other heart block
+C0029771	Other specified diseases of pancreas
+C0029799	Other specified forms of pleural effusion, except tuberculous
+C0029804	Other specified hemorrhagic conditions
+C0029806	Other specified infantile cerebral palsy
+C0029810	Other specified iron deficiency anemias
+C0029823	Other specified peritonitis
+C0029827	Other specified schistosomiasis
+C0029838	Other specified types of schizophrenia, unspecified
+C0029866	Other ureteric obstruction
+C0029877	Ear Inflammation
+C0029878	Otitis Externa
+C0029882	Otitis Media
+C0029883	Otitis Media with Effusion
+C0029888	Otitis Media, Suppurative
+C0029895	Otomycosis
+C0029899	Otosclerosis
+C0029925	Ovarian Carcinoma
+C0029927	Ovarian Cysts
+C0029928	Ovarian Diseases
+C0029936	Ovariectomy
+C0029942	Overanxious disorder
+C0029944	Drug Overdose
+C0029947	Overinclusion
+C0030044	Acrocephaly
+C0030100	Oxyuriasis
+C0030167	Pachymeningitis
+C0030185	Paget\'s Disease, Mammary
+C0030186	Paget Disease Extramammary
+C0030193	Pain
+C0030196	Pain in extremity
+C0030200	Pain, Intractable
+C0030201	Pain, Postoperative
+C0030214	Myoclonus, Palatal
+C0030231	Palliative care
+C0030232	Pallor
+C0030246	Pustulosis of Palms and Soles
+C0030252	Palpitations
+C0030275	Pancreas transplant
+C0030279	Pancreatectomy
+C0030283	Pancreatic Cyst
+C0030286	Pancreatic Diseases
+C0030290	Pancreatic fistula
+C0030293	Pancreatic Insufficiency
+C0030297	Pancreatic Neoplasm
+C0030299	Pancreatic Pseudocyst
+C0030305	Pancreatitis
+C0030312	Pancytopenia
+C0030318	Panic
+C0030319	Panic Disorder
+C0030326	Panniculitides
+C0030327	Panniculitis, Lupus Erythematosus
+C0030328	Panniculitis, Nodular Nonsuppurative
+C0030330	Panniculitis, Peritoneal
+C0030331	Panniculitis, Subacute Nodular Migratory
+C0030332	Panophthalmitis
+C0030343	Panuveitis
+C0030353	Papilledema
+C0030354	Papilloma
+C0030360	Papillon-Lefevre Disease
+C0030372	Phlebotomus Fever
+C0030389	Parainfluenza
+C0030409	Paracoccidioides infections
+C0030421	Paraganglioma
+C0030422	Extra-Adrenal Paraganglioma
+C0030424	Paragonimiasis
+C0030436	Parakeratosis
+C0030437	Parakeratosis Variegata
+C0030442	Progressive bulbar palsy
+C0030443	Familial Periodic Paralysis
+C0030445	Paralysis, Obstetric
+C0030446	Ileus paralytic
+C0030455	Parametritis
+C0030469	Paranasal Sinus Diseases
+C0030470	Paranasal Sinus Neoplasms
+C0030472	Paraneoplastic syndrome
+C0030477	Paranoid personality disorder
+C0030481	Paraparesis, Tropical Spastic
+C0030482	Paraphilia
+C0030486	Paraplegia
+C0030489	Paraproteinemias
+C0030491	Parapsoriasis
+C0030499	Parasitic Diseases
+C0030500	Parasitic Diseases, Animal
+C0030508	Parasomnia
+C0030517	Parathyroid Diseases
+C0030521	Parathyroid Neoplasms
+C0030524	Paratuberculosis
+C0030528	Paratyphoid Fever
+C0030547	Parenteral nutrition
+C0030552	Paresis
+C0030554	Paraesthesia
+C0030567	Parkinson Disease
+C0030568	Parkinson Disease, Postencephalitic
+C0030569	Parkinson Disease, Secondary
+C0030578	Paronychia
+C0030581	Parotid Neoplasms
+C0030583	Parotitis
+C0030584	Parovarian Cyst
+C0030590	Paroxysmal supraventricular tachycardia
+C0030591	Paroxysmal ventricular tachycardia
+C0030593	Pars Planitis
+C0030605	Activated Partial Thromboplastin Time measurement
+C0030623	Passive Addiction, Neonatal
+C0030636	Pasteurella Infections
+C0030662	Gambling, Pathological
+C0030756	Lice Infestations
+C0030757	Pediculus capitis infestation
+C0030764	Pedophilia
+C0030779	Pelger-Huet Anomaly
+C0030781	Peliosis Hepatis
+C0030783	Pellagra
+C0030785	Pelvic abscess
+C0030790	Pelvic infection
+C0030793	Pelvic neoplasm NOS
+C0030794	Pelvic Pain
+C0030804	Pemphigoid, Benign Mucous Membrane
+C0030805	Bullous pemphigoid
+C0030807	Pemphigus
+C0030809	Pemphigus Vulgaris
+C0030824	Allergy to penicillin
+C0030846	Penile Diseases
+C0030848	Penile Induration
+C0030849	Penile Neoplasms
+C0030920	Peptic Ulcer
+C0030922	Peptic ulcer haemorrhage
+C0030925	Peptic ulcer perforation
+C0030975	Perceptual Disorders
+C0031019	Perianal abscess
+C0031022	Chronic periaortitis
+C0031024	Suppurative Periapical Periodontitis
+C0031028	Periapical Diseases
+C0031029	Apical granuloma
+C0031030	Periapical Periodontitis
+C0031036	Polyarteritis Nodosa
+C0031037	Periarthritis
+C0031039	Pericardial effusion
+C0031042	Pericardial excision
+C0031046	Pericarditis
+C0031048	Pericarditis constrictive
+C0031051	Pericementitis
+C0031053	Perichondritis
+C0031055	Pericoronitis
+C0031069	Familial Mediterranean Fever
+C0031090	Periodontal Diseases
+C0031094	Periodontal Pocket
+C0031099	Periodontitis
+C0031106	Aggressive Periodontitis
+C0031111	Periostitis
+C0031115	Peripheral angiopathy in diseases classified elsewhere
+C0031117	Neuropathy peripheral
+C0031118	Peripheral Nervous System Neoplasms
+C0031129	Periphlebitis
+C0031139	Peritoneal dialysis
+C0031142	Unspecified disorder of peritoneum
+C0031144	Chronic peritoneal effusion (disorder)
+C0031149	Peritoneal Neoplasms
+C0031150	Laparoscopy
+C0031154	Peritonitis
+C0031157	Peritonsillar Abscess
+C0031189	Persistent Common Atrioventricular Canal
+C0031190	Persistent Fetal Circulation Syndrome
+C0031192	Persistent Ostium Primum
+C0031212	Personality disorder
+C0031256	Petechiae
+C0031269	Peutz-Jeghers Syndrome
+C0031306	Phagocyte Bactericidal Dysfunction
+C0031315	Phantom Limb Syndrome
+C0031345	Pharyngeal Diseases
+C0031347	Pharyngeal Neoplasms
+C0031350	Pharyngitis
+C0031391	Phencyclidine Abuse
+C0031485	Phenylketonurias
+C0031511	Pheochromocytoma
+C0031538	Phimosis
+C0031542	Phlebitis
+C0031547	Phlebolith
+C0031556	Phlegmasia Alba Dolens
+C0031557	Phlegmon
+C0031570	Phobia, School
+C0031572	Phobia, Social
+C0031575	Phocomelia
+C0031707	Disorders of phosphorus metabolism
+C0031736	Polymorphous light eruption
+C0031762	Photodermatitis, NOS
+C0031873	Abnormal craving
+C0031876	Pick Disease of Heart
+C0031880	Pickwickian syndrome
+C0031887	Picornaviridae Infections
+C0031898	Piedra
+C0031900	Pierre Robin Syndrome
+C0031903	Pigeon Breeder\'s Lung
+C0031924	Piloerection
+C0031925	Pilonidal Cyst
+C0031941	Pineal Gland Neoplasm
+C0032000	Pituitary Adenoma
+C0032001	Pituitary Apoplexy
+C0032002	Pituitary Diseases
+C0032019	Pituitary Neoplasms
+C0032026	Pityriasis Rosea
+C0032027	Pityriasis Rubra Pilaris
+C0032044	Placenta Accreta
+C0032045	Disorder placental
+C0032046	Placenta Previa
+C0032051	Placental Insufficiency
+C0032064	Plague
+C0032087	Plant Poisoning
+C0032131	Plasmacytoma
+C0032134	Plasmapheresis
+C0032176	Platelet aggregation
+C0032181	Platelet Count measurement
+C0032197	Platelet Storage Pool Deficiency
+C0032209	Platybasia
+C0032226	Pleural Diseases
+C0032227	Pleural Effusion
+C0032229	Pleural Neoplasms
+C0032230	Pleural Rub
+C0032231	Pleurisy
+C0032238	Pleurodynia, Epidemic
+C0032241	Pleuropneumonia
+C0032266	Pneumatosis coli
+C0032268	Pneumocephalus
+C0032269	Pneumococcal Infections
+C0032273	Pneumoconiosis
+C0032284	Pneumonectomy
+C0032285	Pneumonia
+C0032290	Aspiration Pneumonia
+C0032298	Pneumonia lipoid
+C0032300	Lobar Pneumonia
+C0032302	Mycoplasma pneumonia
+C0032308	Pneumonia, Staphylococcal
+C0032310	Pneumonia, Viral
+C0032319	Pneumopericardium
+C0032320	Pneumoperitoneum
+C0032326	Pneumothorax
+C0032339	Rothmund-Thomson syndrome
+C0032343	Poisoning
+C0032357	Poland Syndrome
+C0032371	Poliomyelitis
+C0032453	Polychondritis, Relapsing
+C0032460	Polycystic Ovary Syndrome
+C0032461	Polycythemia
+C0032463	Polycythemia Vera
+C0032519	Polymenorrhea
+C0032533	Polymyalgia Rheumatica
+C0032541	Polyneuritis
+C0032568	Pseudopolyp
+C0032578	Polyploidy
+C0032580	Adenomatous Polyposis Coli
+C0032584	Polyp
+C0032586	Polyradiculopathy
+C0032587	Polyradiculoneuropathy
+C0032606	Polysubstance dependence
+C0032617	Polyuria
+C0032633	Dyshidrotic eczema
+C0032708	Disorders of Porphyrin Metabolism
+C0032739	Tuberculin test positive
+C0032749	Post-kala-azar dermal leishmaniasis
+C0032763	Postgastric surgery syndromes
+C0032768	Neuralgia, Postherpetic
+C0032776	Post-menopausal bleeding
+C0032781	Posterior nasal drip
+C0032787	Postoperative Complications
+C0032788	Postoperative Hemorrhage
+C0032796	Postpartum Amenorrhea
+C0032797	Postpartum Hemorrhage
+C0032805	Postpericardiotomy Syndrome
+C0032807	Postphlebitic Syndrome
+C0032808	Postphlebitic Ulcer
+C0032816	Post-traumatic headache
+C0032827	Potassium Deficiency
+C0032870	Poxviridae Infections
+C0032897	Prader-Willi Syndrome
+C0032914	Pre-Eclampsia
+C0032915	Preexcitation Syndrome
+C0032927	Precancerous Conditions
+C0032961	Pregnancy
+C0032962	Complications of pregnancy NOS
+C0032963	Pregnancy Complications, Cardiovascular
+C0032964	Pregnancy Complications, Hematologic
+C0032965	Pregnancy Complications, Infectious
+C0032966	Pregnancy Complications, Neoplastic
+C0032969	Pregnancy in Diabetics
+C0032987	Ectopic Pregnancy
+C0032989	Multiple pregnancy
+C0032993	Pregnancy, Prolonged
+C0032994	Pregnancy, Tubal
+C0033027	Preleukemia
+C0033036	Atrial premature complex
+C0033038	Premature Ejaculation
+C0033046	Premenstrual syndrome
+C0033054	Prenatal Exposure Delayed Effects
+C0033074	Presbycusis
+C0033075	Presbyopia
+C0033103	Pretibial myxedema
+C0033117	Priapism
+C0033129	Acanthameba infection
+C0033132	Cerebellar Degenerations, Primary
+C0033138	Primary Hypersomnia
+C0033139	Primary Insomnia
+C0033141	Cardiomyopathies, Primary
+C0033246	Proctitis
+C0033247	Proctocolitis
+C0033252	Proctosigmoiditis
+C0033300	Progeria
+C0033324	Prognathism
+C0033375	Prolactinoma
+C0033377	Ptosis
+C0033573	Prostatectomy NOS
+C0033575	Prostatic Diseases
+C0033578	Prostatic Neoplasms
+C0033579	Prostate nodule
+C0033581	prostatitis
+C0033586	Prosthesis Failure
+C0033587	Prosthesis Loosening
+C0033626	Protein Deficiency
+C0033677	Protein-Energy Malnutrition
+C0033680	Protein-Losing Enteropathies
+C0033687	Proteinuria
+C0033700	Proteus infections
+C0033740	Protozoan Infections
+C0033741	Protozoan Infections, Animal
+C0033770	Prune Belly Syndrome
+C0033771	Prurigo
+C0033774	Pruritus
+C0033775	Anal pruritus
+C0033777	Pruritus genital
+C0033778	Pruritus vulvae
+C0033785	Pseudarthrosis
+C0033788	Pseudo-Hurler Polydystrophy
+C0033790	Pseudobulbar Palsy
+C0033793	Pseudocoloboma
+C0033797	Pseudodementia
+C0033802	Pseudogout
+C0033804	Pseudohermaphroditism
+C0033805	Pseudohypoaldosteronism
+C0033806	Pseudohypoparathyroidism
+C0033817	Pseudomonas Infections
+C0033822	Pseudomyxoma Peritonei
+C0033823	Schizophrenia, Pseudoneurotic
+C0033831	Psychological pseudocyesis
+C0033835	Pseudopseudohypoparathyroidism
+C0033836	Pseudopsychopathic Schizophrenia
+C0033837	Pseudopsychosis
+C0033838	Kimura Disease
+C0033839	Pseudorabies
+C0033844	Pseudotumor
+C0033845	Pseudotumor Cerebri
+C0033847	Pseudoxanthoma Elasticum
+C0033860	Psoriasis
+C0033893	Tension Headache
+C0033922	Psychomotor Disorders
+C0033923	Psychomotor Performance
+C0033931	Psychophysiologic disorder, NOS
+C0033936	Psychoses, Alcoholic
+C0033937	Psychoses, Drug
+C0033941	Psychoses, Substance-Induced
+C0033943	Psychoses, Traumatic
+C0033948	Female orgasmic disorder
+C0033949	Male orgasmic disorder
+C0033953	Psychosexual Disorders
+C0033958	Psychosis, Brief Reactive
+C0033975	Psychotic disorder
+C0033999	Pterygium
+C0034012	Delayed Puberty
+C0034013	Precocious Puberty
+C0034040	Postpartum disorder
+C0034041	Puerperal Infection
+C0034050	Pulmonary Alveolar Proteinosis
+C0034063	Pulmonary Edema
+C0034065	Pulmonary Embolism
+C0034067	Emphysema
+C0034068	Pulmonary Eosinophilia
+C0034069	Pulmonary Fibrosis
+C0034072	Cor pulmonale
+C0034074	Pulmonary infarction
+C0034088	Pulmonary valve incompetence
+C0034089	Pulmonary Valve Stenosis
+C0034091	Pulmonary Veno-Occlusive Disease
+C0034103	Pulpitis
+C0034115	Paracentesis NOS
+C0034123	Pupil Malformations
+C0034124	Pupil disorders
+C0034139	Purine-Pyrimidine Metabolism, Inborn Errors
+C0034150	Purpura
+C0034151	Hyperglobulinemic purpura
+C0034152	Henoch-Schoenlein Purpura
+C0034155	Purpura, Thrombotic Thrombocytopenic
+C0034161	Pus
+C0034183	Pyelitis
+C0034186	Pyelonephritis
+C0034189	Pyemia
+C0034194	Pyloric Stenosis
+C0034212	Pyoderma
+C0034216	Pyonephrosis NOS
+C0034219	Alveolar pyorrhea
+C0034341	Pyruvate Carboxylase Deficiency Disease
+C0034345	Pyruvate Dehydrogenase Complex Deficiency Disease
+C0034350	Pyruvate Metabolism, Inborn Errors
+C0034359	Pyuria
+C0034362	Q Fever
+C0034372	Quadriplegia
+C0034494	Rabies (disorder)
+C0034530	Radiation injury
+C0034531	Radiation Injuries, Experimental
+C0034535	Radiation Syndrome
+C0034543	Radicular Cyst
+C0034544	Radiculitis
+C0034561	Radiation-Induced Dermatitis
+C0034606	Radioisotope scan
+C0034628	Radius Fractures
+C0034637	Raillietiniasis
+C0034642	Rales
+C0034734	Raynaud Disease
+C0034735	Raynaud Phenomenon
+C0034880	Hyperacusis
+C0034882	Rectal Diseases
+C0034884	Rectal Fistula
+C0034885	Rectal Neoplasms
+C0034886	Proctalgia
+C0034887	Rectal polyp
+C0034888	Rectal Prolapse
+C0034895	Rectovaginal Fistula
+C0034902	Pure Red-Cell Aplasia
+C0034931	Reflex Sympathetic Dystrophy
+C0034933	Abnormal reflex, NOS
+C0034935	Babinski Reflex
+C0034951	Refractive Errors
+C0034960	Refsum Disease
+C0034989	Regurgitation, Gastric
+C0034991	Rehabilitation therapy
+C0035012	Fiessinger-Leroy-Reiter syndrome
+C0035020	Relapse
+C0035021	Relapsing Fever
+C0035022	Tick-borne relapsing fever
+C0035066	Renal Artery Obstruction
+C0035067	Renal Artery Stenosis
+C0035078	Kidney Failure
+C0035085	Renal infarct
+C0035086	Renal Osteodystrophy
+C0035091	Renal Tubular Transport, Inborn Errors
+C0035110	Surgical procedure repeated
+C0035112	Reoviridae Infections
+C0035126	Reperfusion Injury
+C0035143	Repression
+C0035204	Respiration Disorders
+C0035220	Respiratory Distress Syndrome, Newborn
+C0035222	Adult respiratory distress syndrome, NOS
+C0035228	Respiratory Hypersensitivity
+C0035229	Respiratory Insufficiency
+C0035232	Diaphragmatic paralysis
+C0035234	Respiratory Sounds
+C0035235	Respiratory Syncytial Virus Infections
+C0035238	Anomalies of respiratory system, congenital
+C0035239	Respiratory therapy
+C0035242	Respiratory Tract Diseases
+C0035243	Respiratory Tract Infections
+C0035258	Restless Legs Syndrome
+C0035273	Resuscitation
+C0035288	Reticuloendotheliosis, X-linked
+C0035300	Abnormal retinal morphology
+C0035302	Retinal Artery Occlusion
+C0035304	Retinal Degeneration
+C0035305	Retinal Detachment
+C0035309	Retinal Diseases
+C0035312	Retinal Drusen
+C0035313	Retinal Dysplasia
+C0035317	Retinal haemorrhage
+C0035319	Retinal Necrosis Syndrome, Acute
+C0035320	Retinal Neovascularization
+C0035321	Retinal Perforations
+C0035326	Retinal vascular occlusion
+C0035328	Retinal Vein Occlusion
+C0035333	Retinitis
+C0035334	Retinitis Pigmentosa
+C0035335	Retinoblastoma
+C0035344	Retinopathy of Prematurity
+C0035353	Congenital retrognathism
+C0035354	Retrograde Degeneration
+C0035357	Retroperitoneal fibrosis
+C0035358	Retroperitoneal Neoplasms
+C0035369	Retroviridae Infections
+C0035372	Rett Syndrome
+C0035400	Reye Syndrome
+C0035410	Rhabdomyolysis
+C0035411	Rhabdomyoma
+C0035412	Rhabdomyosarcoma
+C0035435	Rheumatic Diseases
+C0035436	Rheumatic Fever
+C0035439	Rheumatic Heart Disease
+C0035450	Rheumatoid Nodule
+C0035455	Rhinitis
+C0035457	Rhinitis, Allergic, Perennial
+C0035459	Rhinitis, Atrophic
+C0035460	Rhinitis, Vasomotor
+C0035466	Rhinophyma
+C0035467	Rhinoplasty
+C0035468	Rhinoscleroma
+C0035508	Rhonchi
+C0035522	Rib Fractures
+C0035528	Riboflavin Deficiency
+C0035579	Rickets
+C0035585	Rickettsia Infections
+C0035613	Rift Valley Fever
+C0035615	Right aortic arch (disorder)
+C0035619	Ventricular Outflow Obstruction, Right
+C0035690	RNA Virus Infections
+C0035793	Rocky Mountain Spotted Fever
+C0035828	Romano-Ward Syndrome
+C0035851	Root Resorption
+C0035854	Rosacea
+C0035869	Rotavirus Infections
+C0035920	Rubella
+C0035921	Congenital Rubella Syndrome
+C0035934	Rubinstein-Taybi Syndrome
+C0035956	Rupture, Spontaneous
+C0036069	Saldino-Noonan Syndrome
+C0036093	Diseases of the salivary glands
+C0036095	Salivary Gland Neoplasms
+C0036114	Gastroenteritis salmonella
+C0036117	Salmonella infections
+C0036118	Salmonella Infections, Animal
+C0036130	Salpingitis
+C0036161	Sandhoff Disease
+C0036202	Sarcoidosis
+C0036203	Cutaneous sarcoidosis
+C0036205	Sarcoidosis, Pulmonary
+C0036211	Sarcoma 180
+C0036214	Sarcoma, Engelbreth-Holm-Swarm
+C0036216	Sarcoma, Experimental
+C0036219	Sarcoma, Jensen
+C0036220	Kaposi Sarcoma
+C0036221	Mast-Cell Sarcoma
+C0036262	Scabies <infestation>
+C0036280	Burn scar
+C0036285	Scarlet Fever
+C0036305	Schamberg Disease
+C0036310	Scheuermann\'s Disease
+C0036323	Schistosomiasis
+C0036329	Schistosomiasis japonica
+C0036330	Schistosomiasis mansoni
+C0036337	Schizoaffective Disorder
+C0036339	Schizoid Personality Disorder
+C0036341	Schizophrenia
+C0036343	Borderline schizophrenia
+C0036344	Schizophrenia, Catatonic
+C0036346	Schizophrenia, Childhood
+C0036347	Disorganized type schizophrenia
+C0036349	Paranoid Schizophrenia
+C0036351	Residual schizophrenia
+C0036358	Schizophreniform disorder
+C0036363	Schizotypal Personality Disorder
+C0036391	Schwartz-Jampel Syndrome
+C0036396	Sciatica
+C0036400	Scimitar Syndrome
+C0036412	Scleral Diseases
+C0036413	Scleredema Adultorum
+C0036416	Scleritis
+C0036420	Localized scleroderma
+C0036421	Scleroderma, Systemic
+C0036429	Sclerosis
+C0036439	Scoliosis
+C0036454	Scotoma
+C0036457	Scrapie
+C0036467	Scrofula
+C0036472	Scrub Typhus
+C0036474	Scurvy
+C0036489	Sea-Blue Histiocyte Syndrome
+C0036494	Seasickness
+C0036502	Sebaceous Gland Diseases
+C0036503	Sebaceous Gland Neoplasms
+C0036508	Dermatitis, Seborrheic
+C0036529	Myocardial Diseases, Secondary
+C0036572	Convulsion
+C0036600	Self-medication
+C0036601	Self Mutilation
+C0036631	Seminoma
+C0036646	Age-related cataract
+C0036651	Senile lentigo
+C0036659	Sensation Disorders
+C0036685	Septicaemia due to gram-negative organism, unspecified
+C0036686	Gram positive sepsis
+C0036689	Pharyngitis streptococcal
+C0036690	Septicemia
+C0036749	Serositis
+C0036769	Sertoli Cell Tumor
+C0036787	SERUM CHLORIDE ION TESTS
+C0036830	Serum Sickness
+C0036857	Severe mental retardation (I.Q. 20-34)
+C0036868	Sex Chromosome Aberrations
+C0036875	Disorders of Sex Development
+C0036902	Sexual Arousal Disorder
+C0036903	Sexual Aversion Disorder
+C0036916	Sexually transmitted disease
+C0036917	Sexually Transmitted Diseases, Bacterial
+C0036920	Sezary Syndrome
+C0036939	Shared Paranoid Disorder
+C0036973	Shivering
+C0036974	Shock
+C0036980	Cardiogenic shock
+C0036981	Endotoxic shock
+C0036982	Shock haemorrhagic
+C0036983	Septic Shock
+C0036986	Shock, Traumatic
+C0036992	Short Bowel Syndrome
+C0036996	Short Rib-Polydactyly Syndrome
+C0037005	Shoulder Dislocation
+C0037011	Shoulder pain
+C0037018	Shwartzman Phenomenon
+C0037019	Shy-Drager Syndrome
+C0037023	Sialadenitis
+C0037033	Sialometaplasia, Necrotizing
+C0037036	Sialorrhea
+C0037050	Sick Building Syndrome
+C0037052	Sick Sinus Syndrome
+C0037054	Sickle Cell Trait
+C0037061	Siderosis
+C0037073	Sigmoid Neoplasms
+C0037074	Sigmoiditis
+C0037088	Signs and Symptoms
+C0037089	Signs and Symptoms, Digestive
+C0037090	Respiratory symptom
+C0037116	Silicosis
+C0037140	B Virus Infection
+C0037157	Simple cyst
+C0037176	Single-Gene Defects
+C0037188	Sinoatrial Block
+C0037195	Sinus headache
+C0037198	Sinus Thrombosis, Intracranial
+C0037199	Sinusitis
+C0037205	Sirenomelia
+C0037221	Situs Inversus
+C0037231	Sjogren-Larsson Syndrome
+C0037268	Skin Abnormalities
+C0037271	Skin Aging
+C0037274	Dermatologic disorders
+C0037275	Skin Diseases, Vesiculobullous
+C0037277	Skin Diseases, Genetic
+C0037278	Skin Diseases, Infectious
+C0037284	Skin lesion
+C0037285	Skin Manifestations
+C0037286	Skin Neoplasms
+C0037287	Skin nodule
+C0037290	Skin Pigmentation
+C0037293	Skin tag
+C0037297	Skin grafts
+C0037299	Skin Ulcer
+C0037301	Skin Wrinkling
+C0037304	Skull fracture
+C0037315	Sleep apnea syndrome
+C0037316	Sleep Deprivation
+C0037317	Disturbance in sleep behavior
+C0037320	Night terrors
+C0037354	Smallpox
+C0037361	Smell Perception
+C0037383	Sneezing
+C0037384	Snoring
+C0037431	Social problem
+C0037578	Soft Tissue Injuries
+C0037579	Soft Tissue Neoplasms
+C0037650	Psychogenic disorder NOS
+C0037661	Somatostatinoma
+C0037672	Somnambulism
+C0037753	Sparganosis
+C0037763	Spasm
+C0037768	Spasmophilia
+C0037769	Spasms, Infantile
+C0037771	Paraparesis, Spastic
+C0037772	Spastic Paraplegia
+C0037773	Spastic Paraplegia, Hereditary
+C0037789	Specific reading disorder
+C0037822	Speech disorder
+C0037826	Speech Perception
+C0037856	Spermatic Cord Torsion
+C0037859	Spermatocele
+C0037887	Sphenopalatine Neuralgia
+C0037889	Hereditary spherocytosis
+C0037899	Sphingolipidoses
+C0037917	Spina Bifida Cystica
+C0037921	Spinal ataxia
+C0037926	Compression of spinal cord
+C0037928	Disease of spinal cord
+C0037929	Spinal Cord Injuries
+C0037930	Spinal Cord Neoplasms
+C0037932	Curvature of spine
+C0037933	Spinal Diseases
+C0037937	Vertebral injury
+C0037939	Spinal Neoplasms
+C0037944	Spinal Stenosis
+C0037952	Spinocerebellar Degeneration
+C0037974	Spirochaetales Infections
+C0037995	Splenectomy
+C0037997	Spleen disorders
+C0037998	Splenic Infarction
+C0037999	Splenic Neoplasms
+C0038000	Splenic Rupture
+C0038002	Splenomegaly
+C0038012	Spondylitis
+C0038013	Ankylosing spondylitis
+C0038015	Spondyloepiphyseal Dysplasia
+C0038016	Spondylolisthesis
+C0038018	Spondylolysis
+C0038019	Spondylosis
+C0038020	Spondylosis Deformans
+C0038034	Sporotrichosis
+C0038041	Spotted Fever Group Rickettsiosis
+C0038048	Sprains and Strains
+C0038054	Sprue, Tropical
+C0038131	Stammering
+C0038160	Staphylococcal Infections
+C0038165	Staphylococcal Scalded Skin Syndrome
+C0038166	Staphylococcal Skin Infections
+C0038187	Starvation
+C0038218	Status Asthmaticus
+C0038219	Status Dysraphicus
+C0038220	Status Epilepticus
+C0038238	Steatorrhea
+C0038271	Stereotyped Behavior
+C0038273	Stereotypic Movement Disorder
+C0038279	Sterility, Postpartum
+C0038325	Stevens-Johnson Syndrome
+C0038340	Sting Injury
+C0038353	Gastric dilatation
+C0038354	Gastric disorder
+C0038356	Stomach Neoplasms
+C0038358	Gastric ulcer
+C0038362	Stomatitis
+C0038363	Aphthous Stomatitis
+C0038364	Stomatitis, Denture
+C0038366	Stomatitis, Herpetic
+C0038368	Stomatognathic Diseases
+C0038379	Strabismus
+C0038395	Streptococcal Infections
+C0038433	Streptozotocin Diabetes
+C0038435	Stress
+C0038436	Post-Traumatic Stress Disorder
+C0038441	Stress Disorders, Traumatic
+C0038443	Stress, Psychological
+C0038449	Arterial stenosis NOS
+C0038450	Stridor
+C0038454	Cerebrovascular accident
+C0038457	Stromal Dystrophies, Corneal
+C0038459	Strongyle Infections, Equine
+C0038463	Strongyloidiasis
+C0038476	Supernumerary structure
+C0038478	Struma Ovarii
+C0038505	Sturge-Weber Syndrome
+C0038506	Stuttering
+C0038522	Subacute Sclerosing Panencephalitis
+C0038525	Subarachnoid Hemorrhage
+C0038531	Subclavian steal syndrome
+C0038536	Subcutaneous emphysema
+C0038538	Subdural effusion
+C0038539	Empyema, Subdural
+C0038557	Submandibular Gland Diseases
+C0038579	Substance Abuse, Intravenous
+C0038580	Substance Dependence
+C0038586	Substance Use Disorders
+C0038587	Substance Withdrawal Syndrome
+C0038604	Subungual exostoses
+C0038605	Subungual hyperkeratosis
+C0038644	Sudden infant death syndrome
+C0038663	Suicide attempt
+C0038732	Sulfhemoglobinemia
+C0038814	Sunburn
+C0038826	Superinfection
+C0038828	Superior mesenteric artery syndrome
+C0038833	Superior Vena Cava Syndrome
+C0038834	Superior Vena Cava Thrombosis
+C0038862	Suppurative inflammation
+C0038868	Progressive supranuclear palsy
+C0038870	Neuralgia, Supraorbital
+C0038874	Supratentorial Neoplasms
+C0038902	Female genital operation
+C0038903	Lung operation NOS
+C0038940	Surgical Wound Dehiscence
+C0038941	Postoperative wound infection
+C0038981	Swayback
+C0038986	Sweat Gland Diseases
+C0038987	Sweat Gland Neoplasms
+C0038990	Sweating
+C0038994	Sweating, Gustatory
+C0038999	Swelling
+C0039010	Swine Vesicular Disease
+C0039023	Sycosis
+C0039070	Syncope
+C0039075	Syndactyly
+C0039082	Syndrome
+C0039093	Congenital abnormal Synostosis
+C0039101	Sarcoma, Synovial
+C0039103	Synovitis
+C0039106	Pigmented villonodular synovitis
+C0039128	Syphilis
+C0039131	Syphilis, Congenital
+C0039144	Syringomyelia
+C0039223	Tabes Dorsalis
+C0039231	Tachycardia
+C0039232	AV nodal re-entry tachycardia
+C0039234	Tachycardia, Ectopic Atrial
+C0039235	Tachycardia, Ectopic Junctional
+C0039236	Tachycardia, Paroxysmal
+C0039239	Sinus Tachycardia
+C0039240	Supraventricular tachycardia
+C0039242	Tachyphylaxis
+C0039254	Taeniasis
+C0039263	Takayasu Arteritis
+C0039273	Talipes cavus
+C0039292	Tangier Disease
+C0039319	Tarsal tunnel syndrome
+C0039338	Taste Disorders
+C0039373	Tay-Sachs Disease
+C0039445	Hereditary hemorrhagic telangiectasia
+C0039446	Telangiectasis
+C0039483	Giant Cell Arteritis
+C0039494	Temporomandibular Joint Disorders
+C0039496	Temporomandibular Joint Dysfunction Syndrome
+C0039503	Tendinitis
+C0039504	Tendon Injuries
+C0039516	Tennis Elbow
+C0039520	Tenosynovitis
+C0039538	Teratoma
+C0039584	Testicular Diseases
+C0039585	Androgen-Insensitivity Syndrome
+C0039590	Testicular Neoplasms
+C0039591	Pain in testicle
+C0039614	Tetanus
+C0039621	Tetany
+C0039685	Fallot\'s tetralogy
+C0039726	Thalamic Diseases
+C0039730	Thalassemia
+C0039743	Thanatophoric Dysplasia
+C0039747	Thecoma
+C0039751	Theft
+C0039841	Thiamine Deficiency
+C0039870	Thinness
+C0039971	Thirst
+C0039978	Thoracic Diseases
+C0039980	Traumatic chest injury NOS
+C0039981	Thoracic Neoplasms
+C0039984	Thoracic Outlet Syndrome
+C0039991	Thoracotomy
+C0040015	Thrombasthenia
+C0040021	Thromboangiitis Obliterans
+C0040028	Thrombocythemia, Essential
+C0040034	Thrombocytopenia
+C0040038	Thromboembolism
+C0040046	Thrombophlebitis
+C0040053	Thrombosis
+C0040100	Thymoma
+C0040115	Thymus Hyperplasia
+C0040127	Thyroid Crisis
+C0040128	Thyroid Diseases
+C0040136	Thyroid Neoplasm
+C0040137	Thyroid Nodule
+C0040145	Thyroidectomy
+C0040147	Thyroiditis
+C0040149	Subacute thyroiditis
+C0040156	Thyrotoxicosis
+C0040185	Tibial Fractures
+C0040188	Tic
+C0040213	Costochondritis
+C0040247	Tinea
+C0040249	White Piedra
+C0040250	Tinea Capitis
+C0040252	Body tinea
+C0040259	Tinea pedis
+C0040261	Onychomycosis
+C0040262	Tinea Versicolor
+C0040264	Tinnitus
+C0040332	Tobacco Dependence
+C0040336	Tobacco Use Disorder
+C0040405	Computerised tomogram
+C0040409	Tongue Diseases
+C0040411	Tongue Neoplasms
+C0040412	Fissured tongue
+C0040416	Tonic Pupil
+C0040422	Tonsillar Neoplasms
+C0040423	Tonsillectomy
+C0040425	Tonsillitis
+C0040427	Tooth Abnormalities
+C0040433	Tooth Crowding
+C0040434	Discoloration of tooth
+C0040435	Tooth Diseases
+C0040436	Tooth erosion
+C0040437	Tooth eruption
+C0040440	Tooth extraction
+C0040441	Tooth fracture
+C0040456	Tooth impacted
+C0040457	Tooth, Supernumerary
+C0040458	Unerupted tooth
+C0040460	Toothache
+C0040479	Torsade de pointes
+C0040485	Torticollis
+C0040517	Gilles de la Tourette syndrome
+C0040524	Septic Toxemia
+C0040553	Toxocariasis
+C0040558	Toxoplasmosis
+C0040560	Toxoplasmosis, Congenital
+C0040561	Ocular Toxoplasmosis
+C0040580	Tracheal Diseases
+C0040582	Tracheal Neoplasms
+C0040583	Tracheal Stenosis
+C0040584	Tracheitis
+C0040586	Tracheobronchitis
+C0040588	Tracheo-oesophageal fistula
+C0040590	Tracheostomy
+C0040592	Trachoma
+C0040702	Transient Tic Disorder
+C0040715	Chromosomal translocation
+C0040732	Transplant
+C0040759	Congenital Transposition
+C0040761	Transposition of Great Vessels
+C0040771	Transurethral prostatectomy
+C0040774	Transvestism
+C0040797	Traumatic haemorrhage
+C0040799	Subcutaneous emphysema
+C0040809	Refusal of treatment by patient
+C0040820	Trematode Infections
+C0040822	Tremor
+C0040827	Saturnine Tremor
+C0040896	Trichinellosis
+C0040921	Trichomonas Infections
+C0040923	Trichomonas Vaginitis
+C0040938	Trichophytosis
+C0040947	Trichostrongyloidiasis
+C0040953	Trichotillomania
+C0040954	Infection by Trichuris trichiura
+C0040961	Tricuspid valve incompetence
+C0040962	Tricuspid Valve Prolapse
+C0040963	Tricuspid Valve Stenosis
+C0040997	Trigeminal Neuralgia
+C0041105	Trismus
+C0041107	Trisomy
+C0041182	Trophoblastic Neoplasms
+C0041188	Tropical pyomyositis
+C0041207	Common truncus
+C0041227	Trypanosomiasis
+C0041228	African Trypanosomiasis
+C0041234	Chagas Disease
+C0041295	Tuberculoma
+C0041296	Tuberculosis
+C0041307	Bovine tuberculosis
+C0041309	Cutaneous tuberculosis
+C0041311	Tuberculosis, Female Genital
+C0041312	Tuberculosis gastrointestinal NOS
+C0041313	Tuberculosis liver
+C0041315	Tuberculosis, Laryngeal
+C0041316	Lymph Node Tuberculosis
+C0041318	Tuberculosis, Meningeal
+C0041321	Tuberculosis, Miliary
+C0041324	Tuberculosis, Osteoarticular
+C0041325	Peritoneal tuberculosis
+C0041326	Pleural Tuberculosis
+C0041327	Tuberculosis, Pulmonary
+C0041328	Tuberculosis, Renal
+C0041330	Tuberculosis, Spinal
+C0041341	Tuberous Sclerosis
+C0041343	Tubo-ovarian abscess
+C0041349	Nephritis, Tubulointerstitial
+C0041351	Tularemia
+C0041364	Tumor Lysis Syndrome
+C0041408	Turner Syndrome
+C0041409	Turner Syndrome, Male
+C0041428	Twins, Conjoined
+C0041466	Typhoid Fever
+C0041471	TYPHUS
+C0041472	Endemic Flea-Borne Typhus
+C0041582	Ulcer
+C0041601	Ulna fracture
+C0041651	Uncomplicated alcohol withdrawal
+C0041657	Loss of consciousness
+C0041667	Underweight
+C0041671	Attention Deficit Disorder
+C0041672	Undifferentiated somatoform disorder
+C0041674	Unemployment
+C0041696	Unipolar Depression
+C0041747	Unintended pregnancy
+C0041755	Adverse drug reaction
+C0041782	Deficiency anemias
+C0041825	Tympanic membrane disorder
+C0041834	Erythema
+C0041848	Unspecified idiopathic peripheral neuropathy
+C0041849	Infectious and parasitic diseases, unspecified
+C0041909	Upper gastrointestinal haemorrhage
+C0041912	Upper respiratory infection NOS
+C0041948	Uremia
+C0041952	Ureterolithiasis
+C0041954	Ureteral Diseases
+C0041955	Ureteral Neoplasms
+C0041956	Ureteral obstruction
+C0041959	Ureteritis
+C0041960	Ureterocele
+C0041969	Urethral Diseases
+C0041971	Urethral Neoplasms
+C0041972	Urethral Obstruction
+C0041974	Urethral stenosis
+C0041976	Urethritis
+C0042018	Calculus urinary
+C0042021	Urinary fistula
+C0042023	Increased frequency of micturition
+C0042024	Urinary Incontinence
+C0042025	Stress urinary incontinence
+C0042029	Urinary tract infection
+C0042035	Micturition disorder
+C0042063	Congenital genitourinary abnormality
+C0042065	Genitourinary Neoplasms
+C0042075	Urinary tract disorder
+C0042076	Urologic Neoplasms
+C0042109	Urticaria
+C0042111	Urticaria Pigmentosa
+C0042131	Uterine Diseases
+C0042133	Uterine Fibroids
+C0042134	Uterine haemorrhage
+C0042135	Uterine atony
+C0042136	Uterine infection NOS
+C0042138	Uterine Neoplasms
+C0042139	Uterine perforation
+C0042140	Uterine Prolapse
+C0042143	Uterine Rupture
+C0042162	Uveal Neoplasms
+C0042164	Uveitis
+C0042165	Anterior uveitis
+C0042166	Uveitis, Intermediate
+C0042167	Uveitis, Posterior
+C0042170	Uveomeningoencephalitic Syndrome
+C0042171	Uveoparotid Fever
+C0042237	Malignant Vaginal Neoplasm
+C0042251	Vaginal Diseases
+C0042253	Vaginal fistula
+C0042256	Pruritus of vagina
+C0042258	Vaginal Neoplasms
+C0042267	Vaginitis
+C0042331	Migraine Variant
+C0042341	Varicocele
+C0042344	Varicose Ulcer
+C0042345	Varicose Veins
+C0042373	Vascular disease
+C0042376	Vascular headache
+C0042381	Vascular operation
+C0042384	Vasculitis
+C0042386	Vasculitis, Hemorrhagic
+C0042420	Syncope vagovagal
+C0042454	Velopharyngeal Insufficiency
+C0042484	Venous Engorgement
+C0042485	Venous Insufficiency
+C0042487	Venous Thrombosis
+C0042510	Ventricular Fibrillation
+C0042512	Ventricular Outflow Obstruction
+C0042514	Tachycardia, Ventricular
+C0042548	Plantar wart
+C0042560	Vertebral Artery Insufficiency
+C0042568	Vertebrobasilar insufficiency
+C0042571	Vertigo
+C0042580	Vesico-Ureteral Reflux
+C0042582	Vesicovaginal Fistula
+C0042594	Vestibular Diseases
+C0042656	Neuralgia, Vidian
+C0042693	Violence
+C0042721	Hepatitis viral
+C0042749	Viraemia
+C0042755	Abnormal Virilization
+C0042769	Virus Diseases
+C0042781	Visceral Myopathy
+C0042782	Visceromegaly
+C0042790	Disorder of vision
+C0042798	Low Vision
+C0042842	Vitamin A Deficiency
+C0042847	Vitamin B 12 Deficiency
+C0042850	Unspecified vitamin B deficiency
+C0042870	Vitamin D Deficiency
+C0042875	Vitamin E Deficiency
+C0042879	Vitamin K Assay
+C0042880	Vitamin K Deficiency
+C0042900	Vitiligo
+C0042903	Vitrectomy
+C0042907	Vitreous detachment
+C0042909	Vitreous Hemorrhage
+C0042928	Vocal Cord Paralysis
+C0042929	Vocal cord polyp
+C0042940	Disorder of voice
+C0042951	Volkmann Contracture
+C0042961	Intestinal Volvulus
+C0042963	Vomiting
+C0042974	von Willebrand Disease
+C0042994	Vulval disorder
+C0042995	Vulvar Neoplasms
+C0042996	Vulvitis
+C0042998	Vulvovaginitis
+C0043019	Lateral Medullary Syndrome
+C0043020	Wallerian Degeneration
+C0043037	Common wart
+C0043046	Wasting disease
+C0043049	Water Intoxication
+C0043065	Water-Electrolyte Imbalance
+C0043084	Weaning
+C0043094	Weight Gain
+C0043096	Weight decreased
+C0043102	Weil Disease
+C0043116	HMN (Hereditary Motor Neuropathy) Proximal Type I
+C0043117	Idiopathic thrombocytopenic purpura
+C0043119	Werner Syndrome
+C0043121	Wernicke Encephalopathy
+C0043124	West Nile Fever
+C0043144	Wheezing
+C0043145	Whiplash injury to neck
+C0043154	Dental White Spot
+C0043167	Pertussis
+C0043168	Whooping cough due to unspecified organism
+C0043194	Wiskott-Aldrich Syndrome
+C0043202	Wolff-Parkinson-White Syndrome
+C0043207	Wolfram Syndrome
+C0043208	Wolman Disease
+C0043241	Wound infection
+C0043246	Laceration
+C0043250	Injury wounds
+C0043251	Wounds and Injuries
+C0043252	Gun shot wound
+C0043253	Nonpenetrating Wounds
+C0043254	Wounds, Penetrating
+C0043255	Stab wound
+C0043324	Juvenile Xanthogranuloma
+C0043325	Xanthomatosis
+C0043345	Xeroderma
+C0043346	Xeroderma Pigmentosum
+C0043349	Xerophthalmia
+C0043352	Xerostomia
+C0043387	Yawning
+C0043388	Yaws
+C0043395	Yellow Fever
+C0043407	Yersinia infections
+C0043459	Zellweger Syndrome
+C0043515	Zollinger-Ellison syndrome
+C0043528	Zoonoses
+C0043541	Zygomycosis
+C0078888	Accelerated Idioventricular Rhythm
+C0078911	AIDS-Associated Nephropathy
+C0078917	Albinism, Ocular
+C0078918	Albinism, Oculocutaneous
+C0078921	Albinism, Tyrosinase-Negative
+C0078922	Albinism, Tyrosinase-Positive
+C0078923	Albinism, Yellow-Mutant
+C0078981	Arachnoid cyst
+C0078982	Arhinencephaly
+C0079027	Intraoperative bleeding
+C0079035	Bradyarrhythmia
+C0079037	Branchial Clefts-Congenital disorder
+C0079102	Cerebral Thrombosis
+C0079136	Cockayne-Touraine Disease
+C0079153	Hyperkeratosis, Epidermolytic
+C0079154	Congenital Nonbullous Ichthyosiform Erythroderma
+C0079218	Desmoid tumour
+C0079221	Determination of Death
+C0079238	Gastrointestinal fistulae
+C0079293	Epidermolysis Bullosa Acquisita
+C0079294	Epidermolysis Bullosa Dystrophica
+C0079295	Epidermolysis Bullosa Herpetiformis Dowling-Meara
+C0079297	Epidermolysis Bullosa Progressiva
+C0079298	Epidermolysis Bullosa Simplex
+C0079299	Epidermolysis Bullosa Simplex Kobner
+C0079301	Epidermolysis Bullosa, Junctional
+C0079352	Congenital torticollis
+C0079474	Hallopeau-Siemens Disease
+C0079485	Heart Valve Prolapse
+C0079487	Helicobacter Infections
+C0079504	Hermanski-Pudlak Syndrome
+C0079541	Holoprosencephaly
+C0079581	Hypochlorhydria
+C0079583	Ichthyosiform Erythroderma, Congenital
+C0079584	Ichthyosis Vulgaris
+C0079588	Ichthyosis, X-Linked
+C0079626	Insect Sting
+C0079661	Klein's Syndrome
+C0079680	Lentivirus Infections
+C0079683	Herlitz Disease
+C0079731	B-Cell Lymphomas
+C0079740	High Grade Lymphoma (neoplasm)
+C0079741	Lymphoma, Intermediate-Grade
+C0079744	Diffuse Large B-Cell Lymphoma
+C0079745	Lymphoma, Follicular
+C0079746	Immunoblastic Large-Cell Lymphoma
+C0079747	Low Grade Lymphoma (neoplasm)
+C0079748	Precursor cell lymphoblastic lymphoma
+C0079757	Diffuse Mixed-Cell Lymphoma
+C0079758	Lymphoma, Mixed-Cell, Follicular
+C0079765	Lymphoma, Small Cleaved-Cell, Follicular
+C0079770	Lymphoma, Small Noncleaved-Cell
+C0079772	Lymphomas non-Hodgkin's T-cell
+C0079773	Lymphoma, T-Cell, Cutaneous
+C0079774	Lymphoma, T-Cell, Peripheral
+C0079840	Milk Allergy
+C0079864	Murine Acquired Immunodeficiency Syndrome
+C0079924	Oligohydramnios
+C0079943	Oral Fistula
+C0079989	Parathyroidectomy
+C0080024	Piebaldism
+C0080032	Pleural Effusion, Malignant
+C0080040	Postpoliomyelitis Syndrome
+C0080107	Respiratory Tract Fistula
+C0080151	Simian Acquired Immunodeficiency Syndrome
+C0080159	Vesicular Skin Diseases
+C0080174	Spina Bifida Occulta
+C0080178	Spina Bifida
+C0080179	Spinal fracture
+C0080194	Muscle strain
+C0080203	Tachyarrhythmia
+C0080218	Tethered Cord Syndrome
+C0080233	Tooth Loss
+C0080274	Urinary Retention
+C0080276	Disorder of the genitourinary system
+C0080310	Left Ventricular Function
+C0080333	Weber-Cockayne Syndrome
+C0085073	Prosthesis-Related Infection
+C0085074	Granuloma Annulare
+C0085076	Breast reconstruction
+C0085077	Acute febrile neutrophilic dermatosis
+C0085078	Lysosomal Storage Diseases
+C0085082	Fungaemia
+C0085083	Ovarian Hyperstimulation Syndrome
+C0085084	Motor Neuron Disease
+C0085090	Lymphoma, AIDS-Related
+C0085094	Closed head injuries
+C0085096	Peripheral Vascular Diseases
+C0085106	Familial benign pemphigus
+C0085109	Corneal Neovascularization
+C0085110	Severe Combined Immunodeficiency
+C0085111	Ankle Injuries
+C0085119	Foot Ulcer
+C0085128	Cardiac output increased
+C0085129	Bronchial Hyperreactivity
+C0085131	Gangliosidosis GM1
+C0085132	Mucopolysaccharidosis VII
+C0085134	Cessation of smoking
+C0085136	Central nervous system neoplasm
+C0085138	Choroid Plexus Neoplasms
+C0085159	Seasonal Affective Disorder
+C0085160	Hidradenitis
+C0085162	Pancreaticoduodenectomy
+C0085164	Leukemia, Feline
+C0085166	Bacterial Vaginosis
+C0085167	Granular cell tumor
+C0085179	Eosinophilia-Myalgia Syndrome
+C0085183	Neoplasms, Second Primary
+C0085207	Diabetes, Gestational
+C0085215	Ovarian Failure, Premature
+C0085220	Cerebral Amyloid Angiopathy
+C0085222	Psoas abscess
+C0085232	Pharyngo-oesophageal diverticulum
+C0085253	Adult-Onset Still Disease
+C0085258	Yang Deficiency
+C0085261	Proteus Syndrome
+C0085269	Plasma Cell Granuloma, Pulmonary
+C0085270	Orbital Pseudotumor
+C0085271	Self injurious behaviour
+C0085273	Erythema Infectiosum
+C0085278	Antiphospholipid Syndrome
+C0085280	Alagille Syndrome
+C0085281	Addictive Behavior
+C0085292	Stiff-Person Syndrome
+C0085293	Hepatitis E
+C0085298	Death, Sudden, Cardiac
+C0085306	Feline infectious peritonitis
+C0085307	Embolism and Thrombosis
+C0085308	Ciliophora Infections
+C0085311	Diffuse cutaneous leishmaniasis
+C0085315	Toxoplasmosis, Cerebral
+C0085383	Hypocapnia
+C0085388	Intracranial Tuberculoma
+C0085389	Bacillaceae Infections
+C0085390	Li-Fraumeni Syndrome
+C0085394	Serratia infections
+C0085395	Ureaplasma infections
+C0085396	Neisseriaceae Infections
+C0085397	Pasteurellaceae Infections
+C0085399	Ehrlichiosis
+C0085400	Neurofibrillary degeneration (morphologic abnormality)
+C0085404	POEMS Syndrome
+C0085407	Microsporidia infection
+C0085409	Polyendocrinopathies, Autoimmune
+C0085411	Angiodysplasia
+C0085412	Encephalitozoonosis
+C0085413	Polycystic Kidney, Autosomal Dominant
+C0085417	Epilepsy, Complex Partial
+C0085423	Gram-Negative Bacterial Infections
+C0085426	Gram-Positive Bacterial Infections
+C0085434	Angiomatosis, Bacillary
+C0085435	Arthritis, Reactive
+C0085436	Meningitis, Cryptococcal
+C0085437	Meningitis, Bacterial
+C0085438	Meningitis, Fungal
+C0085511	Tooth Demineralization
+C0085532	Angiogram coronary
+C0085541	Epilepsy, Frontal Lobe
+C0085543	Epilepsia Partialis Continua
+C0085547	Phenylketonuria, Maternal
+C0085548	Autosomal Recessive Polycystic Kidney Disease
+C0085555	Hospice care
+C0085559	Intensive care
+C0085568	Buruli Ulcer
+C0085569	Acidosis hyperchloraemic
+C0085570	Alkalosis hypokalaemic
+C0085574	Palindromic rheumatism
+C0085576	Iron-Refractory Iron Deficiency Anemia
+C0085577	Normocytic anemia
+C0085578	Thalassemia Minor
+C0085580	Essential Hypertension
+C0085581	Restrictive lung disease
+C0085582	Retrobulbar Neuritis
+C0085583	Choreoathetosis
+C0085584	Encephalopathies
+C0085592	Heat Cramps
+C0085593	Chills
+C0085594	Fever with chills
+C0085595	Body odor
+C0085602	Polydipsia
+C0085605	Liver Failure
+C0085606	Micturition urgency
+C0085608	Volume blood decreased
+C0085610	Sinus bradycardia
+C0085611	Atrial arrhythmia
+C0085612	Ventricular arrhythmia
+C0085614	Atrioventricular block first degree
+C0085615	Bundle branch block right
+C0085616	Vasospasm
+C0085617	Arterial spasm
+C0085619	Orthopnea
+C0085620	Flaccid paralysis
+C0085621	Spastic paralysis
+C0085622	Monoplegia
+C0085623	Akinesia
+C0085624	Burning sensation
+C0085625	Hypoalgesia
+C0085628	Stupor
+C0085631	Agitation
+C0085632	Apathy
+C0085633	Mood swings
+C0085635	Photopsia
+C0085636	Photophobia
+C0085637	Oculogyric crisis
+C0085639	Fall
+C0085641	Rash pustular
+C0085642	Livedo reticularis
+C0085648	Synovial Cyst
+C0085649	Oedema peripheral
+C0085650	Purpura Fulminans
+C0085652	Pyoderma Gangrenosum
+C0085653	Pyogenic granuloma
+C0085654	Injection site granuloma
+C0085655	Polymyositis
+C0085656	Eczema nummular
+C0085659	Erythema marginatum
+C0085660	Aseptic necrosis
+C0085661	Onycholysis
+C0085662	Macrocytosis
+C0085663	Plasmacytosis
+C0085666	Spider naevus
+C0085668	Secondary carcinoma
+C0085669	Acute leukaemia
+C0085677	Alcoholic Neuropathy
+C0085679	Hyperchloraemia
+C0085680	Hypochloraemia
+C0085681	Hyperphosphatemia
+C0085682	Hypophosphatemia
+C0085684	Foot Drop
+C0085688	Breast engorgement
+C0085692	Cystitis haemorrhagic
+C0085693	Acute appendicitis NOS (disorder)
+C0085694	Cholecystitis chronic NOS
+C0085695	Chronic gastritis
+C0085696	Chronic prostatitis
+C0085697	Chronic pyelonephritis
+C0085699	Cardiac cirrhosis
+C0085700	Chondromalacia
+C0085702	Monocytosis
+C0085704	Abdominal exploration
+C0085740	Mendelson Syndrome
+C0085742	Injuries, Acute Brain
+C0085750	Adenosis of Breast
+C0085758	Aganglionosis, Colonic
+C0085762	Alcohol abuse
+C0085786	Hamman-Rich syndrome
+C0085808	Mycotic aneurysm
+C0085810	Anguilluliasis
+C0085819	Antibiotic-Associated Colitis
+C0085859	Polyglandular Type I Autoimmune Syndrome
+C0085860	Autoimmune Syndrome Type II, Polyglandular
+C0085916	Bouillaud Disease
+C0085920	Brachial Neuralgia
+C0085923	soft neurological signs
+C0085932	Bullous Dermatitis
+C0085933	Infections, Bunyavirus
+C0085988	Cephalo-pelvic disproportion
+C0085996	Child Development Deviations
+C0085997	Child Development Disorders, Specific
+C0086025	Codependency
+C0086066	Acute Coryza
+C0086103	Decayed, Missing, and Filled Teeth
+C0086132	Depressive symptom
+C0086133	Depressive Syndrome
+C0086138	Device failure NOS
+C0086168	Dissociation
+C0086170	Divorced
+C0086181	Intravenous Drug Abuse
+C0086182	Drug Abuse, Parenteral
+C0086189	Drug Withdrawal Symptoms
+C0086196	Eczema, Infantile
+C0086209	Emotional Stress
+C0086227	Enterobiasis
+C0086236	Epilepsy, Atonic
+C0086237	Epilepsy, Cryptogenic
+C0086238	Secondary generalized epilepsy
+C0086240	Epilepsy, Simple Partial
+C0086241	Epilepsy, Tonic
+C0086254	Essential Polyarteritis
+C0086335	Ganser Syndrome
+C0086367	Gonadotropin-Resistant Ovary Syndrome
+C0086370	Granuloma Gangraenescens
+C0086395	Hearing Loss, Extreme
+C0086404	Experimental Hepatoma
+C0086405	Hereditary Sensory Radicular Neuropathy
+C0086431	Hurler-Scheie Syndrome
+C0086432	Hyalinosis, Segmental Glomerular
+C0086437	Joint laxity
+C0086438	Hypogammaglobulinaemia
+C0086439	Hypokinesia
+C0086441	Hysterical Neuroses
+C0086445	Idiopathic Membranous Glomerulonephritis
+C0086447	Ileal Pouches
+C0086448	Ileoanal Pouches
+C0086457	Industrial Dermatosis
+C0086468	Prenatal Injuries
+C0086501	Keratoma
+C0086511	Knee arthroplasty
+C0086523	Laryngeal Paralysis
+C0086525	Lassitude
+C0086533	Leiomyoma, Epithelioid
+C0086540	Leishmaniasis, New World
+C0086541	Urban cutaneous leishmaniasis
+C0086543	Cataract
+C0086546	Nodular leprosy
+C0086565	Abnormal hepatic function
+C0086588	Marasmus
+C0086626	Minamata Disease
+C0086640	Psychotic Mood Disorders
+C0086647	Mucopolysaccharidosis III
+C0086648	MPS III B
+C0086649	MPS III C
+C0086650	MPS III D
+C0086651	Mucopolysaccharidosis, MPS-IV-A
+C0086652	Mucopolysaccharidosis type IVB
+C0086660	Assassination
+C0086664	Myelocele
+C0086666	Myocardial Preinfarction Syndrome
+C0086691	Neoplasm Metastasis, Unknown Primary
+C0086692	Benign Neoplasm
+C0086696	Neoplasms, Therapy-Associated
+C0086703	War Neurosis
+C0086743	Osteoarthrosis Deformans
+C0086768	Pancreatic Cholera
+C0086769	Panic attack
+C0086774	Cold paroxysmal hemoglobinuria
+C0086789	Periadenitis Mucosa Necrotica Recurrens
+C0086795	Pfaundler-Hurler Syndrome
+C0086815	Plantar Ulcer
+C0086818	Platelet transfusion
+C0086873	Pseudopelade
+C0086898	Recrudescence
+C0086922	Rheumatoid Purpura
+C0086942	Rous Sarcoma
+C0086981	Sicca Syndrome
+C0087012	Ataxia, Spinocerebellar
+C0087031	Juvenile-Onset Still Disease
+C0087086	Thrombus
+C0087111	Therapeutic procedure
+C0087135	Unknown Primary Tumors
+C0087169	Withdrawal Symptoms
+C0149504	Encephalopathy, Toxic
+C0149507	Cellulitis orbital
+C0149508	Eustachian tube obstruction
+C0149512	Acute sinusitis
+C0149514	Acute bronchitis
+C0149516	Chronic sinusitis
+C0149517	Chronic tonsillitis
+C0149519	Chronic Persistent Hepatitis
+C0149520	Acute Cholecystitis
+C0149521	Pancreatitis, Chronic
+C0149523	Acute cystitis
+C0149530	Congenital heart block
+C0149531	Pelvic fractures
+C0149612	Exercise electrocardiogram abnormal
+C0149613	Acute mastitis
+C0149614	Adnexal mass
+C0149622	Neurogenic Urinary Bladder, Atonic
+C0149630	Bicuspid aortic valve
+C0149640	Cecum Carcinoma
+C0149642	Cervical lymphadenitis
+C0149645	Cervical myelopathy
+C0149649	Cholesterol Embolism
+C0149651	Clubbing
+C0149654	Conduct Disorder
+C0149662	Toe deformities NOS
+C0149670	Disorder of carbohydrate metabolism
+C0149671	Dribbling of urine
+C0149676	Enzyme Deficiency
+C0149678	Epstein-Barr Virus Infections
+C0149684	Colon polypectomy
+C0149696	Food intolerance
+C0149697	Foot Injuries
+C0149699	Fibula fracture
+C0149700	Obstruction gastric
+C0149704	Gingivostomatitis
+C0149707	Haematospermia
+C0149708	Hepatitis B surface antibody positive
+C0149709	Hepatitis B surface antigen positive
+C0149720	Abuse of laxatives
+C0149721	Hypertrophy, Left Ventricular
+C0149722	Hutchinson's Melanotic Freckle
+C0149725	Lower respiratory tract infection
+C0149726	Pulmonary mass
+C0149727	Abnormality of the lymph nodes
+C0149732	Muscle rupture
+C0149736	Mass of neck
+C0149738	neurological pain
+C0149741	Breast discharge
+C0149744	Oral lesion
+C0149745	Mouth ulceration
+C0149746	Orthostasis
+C0149750	Colectomy partial
+C0149754	Cellulitis of periorbital region
+C0149756	Fasciitis, Plantar
+C0149766	Purpura senile
+C0149770	Rectal abscess
+C0149771	Rectocele
+C0149772	Abnormal salivary gland morphology
+C0149774	Scrotal mass
+C0149778	Soft Tissue Infection
+C0149779	Somatization
+C0149781	Pneumothorax spontaneous
+C0149782	Squamous cell carcinoma of lung
+C0149783	Steroid therapy
+C0149793	Amaurosis Fugax
+C0149801	Sepsis due to urinary tract infection
+C0149821	ACUTE ALCOHOL WITHDRAWAL
+C0149825	Hypertrophy of adenoids
+C0149826	Gastric adenoma
+C0149836	Atrophic vulvovaginitis
+C0149840	Senile Tremor
+C0149841	Benign recurrent intrahepatic cholestasis
+C0149844	Brain contusion
+C0149854	Cerebellar haemorrhage
+C0149860	Fractured coccyx
+C0149869	Spasmodic Croup
+C0149870	De Quervain Disease
+C0149871	Deep Vein Thrombosis
+C0149875	Primary dysmenorrhea
+C0149877	Hypoglycaemic encephalopathy
+C0149881	Epididymo-orchitis
+C0149886	Seizure, Febrile, Simple
+C0149887	Slipped Capital Femoral Epiphyses
+C0149892	Gingival abscess
+C0149893	Secondary glaucoma
+C0149896	Primary gout
+C0149904	Cholestatic hepatitis
+C0149910	Intermittent joint effusion
+C0149911	Humoral hypercalcemia of malignancy (disorder)
+C0149922	Lichen Simplex Chronicus
+C0149925	Small cell carcinoma of lung
+C0149927	Hamartoma of lung
+C0149931	Migraine Disorders
+C0149937	Acute interstitial nephritis
+C0149939	Obstructive nephropathy
+C0149940	Sciatic nerve neuropathy
+C0149951	Ovarian Fibromata
+C0149955	Annular pancreas
+C0149958	Complex partial seizures
+C0149977	Pulled elbow
+C0149978	Adenocarcinoma of rectum
+C0149985	Syphilis, secondary
+C0149992	Tracheal injury
+C0150041	Feeling hopeless
+C0150042	Functional urinary incontinence
+C0150045	Urge Incontinence
+C0150055	Chronic pain
+C0150063	Feeling powerless
+C0150080	Social Communication Disorder
+C0150088	Hemi-neglect
+C0150450	Altered state of consciousness
+C0150457	Anticoagulant therapy
+C0150496	Cardiac monitoring
+C0150543	Detoxification NOS
+C0150841	muscle pain or weakness
+C0150988	Sclerodactyly
+C0150993	Pitting of nails
+C0151190	Palpable purpura
+C0151205	Periorbital edema
+C0151236	Conduction system abnormalities
+C0151241	Atrial myxoma
+C0151260	Oesophageal hypomotility
+C0151273	Biopsy kidney abnormal
+C0151281	Genital ulceration
+C0151293	Chronic Headache
+C0151295	Mononeuritis Multiplex
+C0151311	Cranial nerve palsies
+C0151313	Peripheral sensory neuropathy
+C0151315	Neck stiffness
+C0151317	Chronic infectious disease
+C0151332	Active tuberculosis
+C0151379	Rheumatoid factor positive
+C0151435	Arthritis enteropathic
+C0151436	Hypersensitivity vasculitis
+C0151445	Primary Raynaud Phenomenon
+C0151449	Primary Sjögren\'s syndrome
+C0151450	Secondary Sjögren\'s syndrome
+C0151463	Abscess of breast
+C0151464	Injection site abscess
+C0151465	Renal abscess
+C0151467	Addisonian crisis
+C0151468	Thyroid adenoma
+C0151472	Albumin globulin ratio abnormal
+C0151474	Alcohol intolerance
+C0151476	Alkalosis hypochloraemic
+C0151477	Hormone level abnormal
+C0151479	Amylase increased
+C0151480	Anti-nuclear factor positive
+C0151482	Anaemia folate deficiency
+C0151489	Arterial malformation
+C0151490	Congenital central nervous system anomaly
+C0151491	Congenital musculoskeletal anomalies
+C0151500	Anticholinergic syndrome
+C0151505	Application site reaction
+C0151511	Atrophy of breast
+C0151512	Injection site atrophy
+C0151514	Skin atrophy
+C0151516	Thyroid Hypoplasia
+C0151517	Atrioventricular block complete
+C0151521	Overgrowth bacterial
+C0151526	Premature Birth
+C0151529	Bleeding time prolonged
+C0151536	Bronchostenosis
+C0151538	Buccoglossal syndrome
+C0151539	Blood urea increased
+C0151541	Capillary fragility increased
+C0151544	Gastrointestinal carcinoma
+C0151546	Oral Cavity Carcinoma
+C0151559	Central nervous system depression (disorder)
+C0151563	Coagulation time prolonged
+C0151564	Cogwheel Rigidity
+C0151565	Hemorrhagic colitis
+C0151569	Coombs direct test positive
+C0151571	Corneal lesion
+C0151572	Corneal reflex decreased
+C0151574	Cough decreased
+C0151576	Elevated creatine kinase
+C0151577	Creatinine renal clearance decreased
+C0151579	Crystalluria
+C0151584	Injection site cyst
+C0151585	Deafness Permanent
+C0151588	Deafness transitory
+C0151594	Diarrhoea haemorrhagic
+C0151596	Tongue discolouration
+C0151598	Drug level decreased
+C0151599	Drug level increased
+C0151601	Conjunctival oedema
+C0151602	Facial swelling
+C0151603	Anasarca
+C0151604	Genital edema
+C0151605	Injection site swelling
+C0151609	Scrotal oedema
+C0151610	Edema of the tongue
+C0151611	Electroencephalogram abnormal
+C0151614	Electrolyte depletion
+C0151620	Hypertensive Encephalopathy
+C0151622	Endometrial disorder
+C0151623	Enterocolitis haemorrhagic
+C0151625	Enzyme abnormality
+C0151626	Necrolysis epidermal
+C0151628	Epiphyses premature fusion
+C0151629	Fixed eruption
+C0151631	Low erythrocyte sedimentation rate
+C0151632	ESR raised
+C0151636	Premature ventricular contractions
+C0151638	Fanconi like syndrome
+C0151639	Decreased fertility in females
+C0151640	Decreased fertility in males
+C0151644	Fibrin increased
+C0151650	Kidney fibrosis
+C0151654	Myocardial fibrosis
+C0151659	Intestinal gangrene NOS
+C0151662	Gamma-glutamyltransferase increased
+C0151664	Gastrointestinal perforation
+C0151665	Globulins decreased
+C0151667	Globulins increased
+C0151669	Increased antibody level in blood
+C0151671	Glucose tolerance decreased
+C0151683	Neutrophil count increased
+C0151684	Granuloma skin
+C0151685	Growth accelerated
+C0151686	Growth retardation
+C0151691	Decreased circulating high-density lipoprotein levels
+C0151692	Impaired healing
+C0151693	Adrenal haemorrhage
+C0151694	Haemorrhage of colon
+C0151698	Injection site haemorrhage
+C0151699	Intracranial Hemorrhage
+C0151701	Pulmonary haemorrhage
+C0151702	Muscle haemorrhage
+C0151705	Retroperitoneal haemorrhage
+C0151713	Hyperchlorhydria
+C0151714	Hypermagnesaemia
+C0151717	Skin hypertrophy
+C0151718	Hypocholesterolaemia
+C0151721	Hypogonadism male
+C0151723	Hypomagnesaemia
+C0151726	Injection site hypersensitivity
+C0151728	Immunoglobins decreased
+C0151729	Immunoglobulins increased
+C0151730	Drug effect increased
+C0151731	Hepatic infarction
+C0151734	Injection site inflammation
+C0151735	Injection site reaction
+C0151738	Large intestine perforation
+C0151739	Small intestinal perforation NOS
+C0151740	Increased intracranial pressure
+C0151744	Myocardial Ischemia
+C0151746	Abnormal renal function
+C0151747	Renal tubular disorder
+C0151749	Laboratory test interference
+C0151757	Lenticular pigmentation
+C0151763	Hepatocellular injury
+C0151766	Abnormal results of liver function studies
+C0151767	Liver tenderness
+C0151772	Manic psychosis
+C0151773	Bone marrow depression
+C0151775	Injection site mass
+C0151778	Megakaryocytes increased
+C0151779	Cutaneous Melanoma
+C0151785	Disease of mucous membrane
+C0151786	Muscle Weakness
+C0151787	Myeloid maturation arrest
+C0151788	Eosinophilic myocarditis
+C0151790	Nasal septum disorder
+C0151795	Injection site necrosis
+C0151798	Hepatic necrosis
+C0151799	Skin necrosis
+C0151811	Nodule subcutaneous
+C0151814	Coronary artery occlusion
+C0151815	Mesenteric occlusion
+C0151818	Opisthotonus
+C0151821	Accidental overdose
+C0151824	Biliary colic
+C0151825	Bone pain
+C0151826	Retrosternal pain
+C0151827	Eye pain
+C0151828	Injection site pain
+C0151830	Urethral pain
+C0151846	Periosteal Disorder
+C0151849	Alkaline phosphatase raised
+C0151854	Abnormal platelets
+C0151857	Pleocytosis
+C0151859	Polyserositis
+C0151860	Acquired porencephaly
+C0151861	Porphyruria
+C0151864	Disorder of pregnancy
+C0151865	Pregnancy test false positive
+C0151872	Prothrombin level increased
+C0151874	Fungal infection of lung
+C0151878	Long QT Syndrome
+C0151879	Electrocardiogram QT shortened
+C0151888	Hyporeflexia
+C0151889	Hyperreflexia
+C0151891	Retinal depigmentation
+C0151900	Serum iron raised
+C0151904	Aspartate aminotransferase increased
+C0151905	Alanine aminotransferase increased
+C0151907	Discoloration of skin
+C0151908	Dry skin
+C0151911	Generalized Spasms
+C0151924	Small intestine stenosis
+C0151934	Hypogeusia
+C0151936	Disorder of tendon
+C0151937	Rupture of tendon
+C0151940	Hypocalcemic tetany
+C0151942	Arterial thrombosis
+C0151945	Cerebral venous thrombosis
+C0151946	Pulmonary thrombosis
+C0151947	Pulmonary artery thrombosis
+C0151950	Deep thrombophlebitis
+C0151966	Duodenal ulcer haemorrhage
+C0151970	Oesophageal ulcer
+C0151971	Intestinal ulcer
+C0151974	Perforated intestinal ulcer
+C0151977	Small intestine ulcer
+C0151989	Abnormal urination
+C0151990	Cylindruria
+C0151994	Enlarged uterus
+C0151998	Uterine spasm
+C0152002	Angitis kidney
+C0152006	Vitreous opacities
+C0152008	Vulvovaginal disorder
+C0152009	White blood cell abnormality
+C0152010	Withdrawal bleed
+C0152013	Adenocarcinoma of Lung
+C0152014	Atrophy of pancreas
+C0152018	Esophageal carcinoma
+C0152020	Gastroparesis
+C0152021	Congenital heart disease
+C0152025	Polyneuropathies
+C0152026	Retinal Vasculitis
+C0152027	Sensory Disorders
+C0152029	Sinus congestion
+C0152030	Skin irritation
+C0152031	Joint swelling
+C0152032	Urinary hesitation
+C0152066	Lobomycosis
+C0152068	Echinococcus granulosus infection
+C0152072	Ovale malaria
+C0152074	Ethiopian cutaneous leishmaniasis
+C0152078	Pelvic congestion
+C0152081	Pustular psoriasis
+C0152084	Jaccoud\'s syndrome
+C0152086	Traumatic arthropathy
+C0152087	Crystal arthropathies
+C0152089	Postlaminectomy syndrome
+C0152093	Hypermobility syndrome
+C0152095	Patau syndrome
+C0152096	Complete trisomy 18 syndrome
+C0152097	Disease of diaphragm
+C0152099	Postcholecystectomy syndrome
+C0152101	Hypoplastic Left Heart Syndrome
+C0152105	Hypertensive heart disease
+C0152107	Dressler's syndrome
+C0152109	Juvenile Spinal Muscular Atrophy
+C0152110	Meralgia paraesthetica
+C0152112	Foster-Kennedy Syndrome
+C0152113	Rheumatic Chorea
+C0152115	Lingual-Facial-Buccal Dyskinesia
+C0152116	Spasmodic torticollis
+C0152124	Confusion, Reactive
+C0152128	Drug withdrawal syndrome
+C0152132	Hypertensive Retinopathy
+C0152134	Internuclear ophthalmoplegia
+C0152136	Low Tension Glaucoma
+C0152138	Glaucomatocyclitic crisis
+C0152150	Twin pregnancy
+C0152154	Prolonged labour
+C0152155	Threatened labor
+C0152156	Obstructed labour NOS
+C0152159	Uterine hypotonus
+C0152164	Cyclic vomiting syndrome
+C0152169	Renal colic
+C0152171	Idiopathic pulmonary hypertension
+C0152173	Ventricular flutter
+C0152174	Psychalgia
+C0152177	Trigeminal Nerve Disorder
+C0152179	Vagus Nerve Disorder
+C0152181	Hypoglossal Nerve Disorder
+C0152183	Explosive personality disorder
+C0152191	Central scotoma
+C0152196	Spasm of accommodation
+C0152198	Accommodation disorder
+C0152200	Achromatopsia
+C0152203	Strabismus, Comitant
+C0152204	Monocular Esotropia
+C0152205	Alternating esotropia
+C0152206	Monocular Exotropia
+C0152207	Alternating Exotropia
+C0152216	Esophoria
+C0152217	Exophoria
+C0152219	Cyclophoria
+C0152221	Paralytic strabismus
+C0152222	Parinaud Syndrome
+C0152223	Mechanical Strabismus
+C0152227	Excessive tearing
+C0152230	Cholinergic urticaria
+C0152233	Congenital ankyloblepharon
+C0152234	Iniencephaly
+C0152236	Talipes valgus
+C0152237	Talipes Calcaneovalgus
+C0152240	Uterus bilocularis
+C0152244	Bone Cysts, Aneurysmal
+C0152245	Extravasation of urine
+C0152252	Anterior synechiae
+C0152253	Posterior synechiae
+C0152255	Pinguecula
+C0152256	Disuse osteoporosis
+C0152259	Cataract secondary to ocular disorder
+C0152264	Familial erythrocytosis
+C0152266	Mixed Cellularity Hodgkin Lymphoma
+C0152267	Hodgkin lymphoma, lymphocyte depletion
+C0152268	Hodgkin's disease nodular sclerosis
+C0152271	Subacute lymphoid leukemia
+C0152276	Granulocytic Sarcoma
+C0152277	Incisional drainage
+C0152413	Pneumonia respiratory syncytial viral
+C0152415	Ankyloglossia
+C0152417	Congenital aortic valve stenosis
+C0152419	Interrupted aortic arch
+C0152421	Macrotia
+C0152422	Congenital aphakia
+C0152423	Congenital small ears
+C0152424	Common ventricle
+C0152426	Craniorachischisis
+C0152427	Polydactyly
+C0152436	Hymen, Imperforate
+C0152438	Sprengel deformity
+C0152439	Retinoschisis
+C0152441	Madelung Deformity
+C0152443	Urethral diverticulum
+C0152445	Gallbladder oedema
+C0152447	Urethral discharge
+C0152451	Chronic glomerulonephritis
+C0152454	Symblepharon
+C0152455	Keratomalacia
+C0152456	Gallbladder cholesterolosis
+C0152457	Kayser-Fleischer ring
+C0152458	Leukocoria
+C0152459	Linear atrophy
+C0152486	Salmonella sepsis
+C0152491	Salmonella osteomyelitis
+C0152517	Enteritis due to specified virus
+C0152545	Primary tuberculosis
+C0152915	Acute miliary tuberculosis
+C0152936	Plague, Septicemic
+C0152964	Streptococcal sepsis
+C0152965	Staphylococcal bacteraemia
+C0152966	Pneumococcal sepsis
+C0152972	Pseudomonal sepsis
+C0152973	Serratia sepsis
+C0153014	Non-arthropod borne lymphocytic choriomeningitis
+C0153062	Viral exanthemata, unspecified
+C0153064	Encephalomyelitis, Western Equine
+C0153066	Murray valley encephalitis
+C0153092	Mumps meningitis
+C0153113	Acute Peripheral Vestibulopathy
+C0153132	Neurosyphilis, Juvenile
+C0153167	Neurosyphilis, Asymptomatic
+C0153232	Meningitis leptospiral
+C0153249	Black piedra
+C0153251	Respiratory moniliasis
+C0153252	Systemic candida
+C0153254	Endocarditis candida
+C0153261	Histoplasma capsulatum Infection
+C0153340	Cancer of Lip
+C0153349	Malignant neoplasm of tongue
+C0153350	Malignant tumor of base of tongue
+C0153351	Malignant neoplasm of dorsal surface of tongue
+C0153356	malignant tumor of lingual tonsil
+C0153362	Malignant neoplasm of other major salivary glands
+C0153368	Malignant neoplasm of floor of mouth
+C0153373	Malignant neoplasm of cheek mucosa
+C0153381	Malignant neoplasm of mouth
+C0153382	Malignant neoplasm of oropharynx
+C0153392	Malignant neoplasm of nasopharynx
+C0153398	Hypopharyngeal Cancer
+C0153405	Malignant neoplasm of pharynx
+C0153421	Malignant neoplasm of body of stomach
+C0153422	Malignant tumor of lesser curve of stomach
+C0153423	Malignant tumor of greater curve of stomach
+C0153425	Malignant tumor of small intestine
+C0153426	Malignant neoplasm of duodenum
+C0153436	Malignant neoplasm of sigmoid colon
+C0153437	Malignant neoplasm of cecum
+C0153439	Malignant neoplasm of ascending colon
+C0153446	Malignant neoplasm of anus
+C0153452	Gallbladder neoplasms malignant
+C0153453	Malignant tumor of extrahepatic bile duct
+C0153458	malignant neoplasm of head of pancreas
+C0153459	Malignant neoplasm of body of pancreas
+C0153460	Malignant neoplasm of tail of pancreas
+C0153463	Malignant neoplasm of other specified sites of pancreas
+C0153465	Retroperitoneal cancer
+C0153467	Malignant neoplasm of peritoneum, unspecified
+C0153470	Malignant neoplasm of spleen
+C0153474	Nasal sinus cancer
+C0153491	Malignant neoplasm of middle lobe, bronchus or lung
+C0153492	Malignant neoplasm of lower lobe, bronchus or lung
+C0153493	Malignant neoplasm of other parts of bronchus or lung
+C0153500	Malignant neoplasm of heart
+C0153504	Malignant tumor of mediastinum
+C0153519	Malignant neoplasm of connective and other soft tissue, site unspecified
+C0153529	Malignant melanoma of lip
+C0153535	Malignant melanoma of skin of upper limb
+C0153536	Malignant melanoma of skin of lower limb
+C0153555	Malignant neoplasm of other specified sites of female breast
+C0153560	Kaposi\'s sarcoma of skin
+C0153562	Kaposi\'s sarcoma of palate
+C0153567	Uterine Cancer
+C0153572	Malignant Placental Neoplasm
+C0153574	Malignant Uterine Corpus Neoplasm
+C0153579	Malignant neoplasm of fallopian tube
+C0153594	Malignant neoplasm of testis
+C0153601	Malignant neoplasm of penis
+C0153614	Malignant neoplasm of ureteric orifice
+C0153618	Malignant neoplasm of renal pelvis
+C0153619	Malignant neoplasm of ureter
+C0153633	Malignant neoplasm of brain
+C0153640	Malignant neoplasm of cerebellum
+C0153646	Malignant neoplasm of spinal cord
+C0153653	Malignant tumor of parathyroid gland
+C0153658	Malignant neoplasm of endocrine gland
+C0153661	Malignant neoplasm of thorax
+C0153662	Malignant neoplasm of abdomen
+C0153676	Metastases to lung
+C0153677	Metastases to the mediastinum
+C0153678	Metastases to pleura
+C0153685	Metastases to kidney
+C0153687	Metastases to skin
+C0153690	Bone cancer metastatic
+C0153792	Hodgkin's disease stage III
+C0153886	Acute myeloid leukemia in remission
+C0153888	Chronic myeloid leukemia in remission
+C0153942	Benign neoplasm of esophagus
+C0153943	Benign neoplasm of stomach
+C0153999	Benign neoplasm of uterus
+C0154007	Benign neoplasm of testis
+C0154009	Benign neoplasm of prostate
+C0154017	Benign bladder neoplasm NOS
+C0154034	Benign neoplasm of spinal cord
+C0154038	Benign neoplasm of thyroid gland
+C0154040	Benign neoplasm of adrenal gland
+C0154041	Parathyroid tumour benign
+C0154045	Benign neoplasm of aortic body and other paraganglia
+C0154051	Hemangioma of retina
+C0154059	Carcinoma in situ of esophagus
+C0154060	Carcinoma in situ of stomach
+C0154061	Stage 0 Carcinoma of Colon
+C0154064	Carcinoma in situ of anus
+C0154073	Carcinoma in situ of skin
+C0154084	Breast cancer in situ
+C0154088	Carcinoma in situ of prostate
+C0154089	Carcinoma in situ of penis
+C0154091	Carcinoma in situ of bladder
+C0154129	Neoplastic disease of uncertain behavior
+C0154141	Thyrotoxicosis with toxic single thyroid nodule
+C0154143	Toxic multinodular goiter
+C0154162	Riedel's thyroiditis
+C0154199	Diseases of thymus gland
+C0154207	Other specified disorders of adrenal gland
+C0154208	Disorder of endocrine ovary
+C0154209	Hyperestrogenism
+C0154246	Urea Cycle Disorders, Inborn
+C0154251	Lipid Metabolism Disorders
+C0154271	Hypercarotinemia
+C0154319	Other specified senile psychotic conditions
+C0154333	Subacute Delirium
+C0154409	Recurrent major depressive episodes
+C0154437	Atypical depressive disorder
+C0154455	Other anxiety states
+C0154536	Amphetamine or related acting sympathomimetic abuse
+C0154564	Specific disorders of sleep of non-organic origin
+C0154575	Rumination disorder
+C0154588	Adjustment disorder with mixed anxiety and depressed mood
+C0154629	Other specified manifestations of hyperkinetic syndrome
+C0154639	Meningitis streptococcal
+C0154640	Meningitis staphylococcal
+C0154659	Toxic Encephalitis
+C0154661	Intraspinal abscess
+C0154671	Degenerative brain disorder
+C0154674	Symptomatic torsion dystonia
+C0154675	Fragments of torsion dystonia
+C0154676	Organic writer\'s cramp
+C0154681	Anterior Horn Cell Disease
+C0154682	Lateral Sclerosis
+C0154693	Flaccid hemiplegia
+C0154694	Hemiplegia, Spastic
+C0154695	Diplegic Infantile Cerebral Palsy
+C0154697	Cerebral Palsy, Quadriplegic, Infantile
+C0154698	Monoplegic Infantile Cerebral Palsy
+C0154723	Migraine with Aura
+C0154724	Cerebral cysts
+C0154728	Meningeal disorder
+C0154731	Glossopharyngeal Neuralgia
+C0154742	Other lesions of median nerve
+C0154743	Ulnar Neuropathies
+C0154748	Lesion of Sciatic Nerve
+C0154756	Polyneuropathy idiopathic progressive
+C0154769	Myopathy toxic
+C0154777	Degenerative disorders of globe
+C0154778	Myopia, Degenerative
+C0154822	Serous retinal detachment
+C0154823	Retinal defect
+C0154828	Traction detachment of retina
+C0154830	Proliferative diabetic retinopathy
+C0154832	Exudative retinopathy
+C0154833	Retinal vascular disorder
+C0154835	Retinal telangiectasia
+C0154841	Central retinal vein occlusion
+C0154850	Cystoid macular retinal degeneration
+C0154856	Retinal lattice degeneration
+C0154860	Hereditary retinal dystrophy
+C0154863	Vitreoretinal dystrophy
+C0154874	Neuroretinitis
+C0154916	Iris neovascularization
+C0154920	Pigmentary iris degeneration
+C0154933	Adhesions of iris, unspecified
+C0154936	Pupillary abnormality
+C0154946	Acute angle-closure glaucoma
+C0154947	Anatomical narrow angle glaucoma
+C0154971	Presenile cataract
+C0155002	Sudden visual loss
+C0155003	Blindness transient
+C0155015	Color Blindness, Red
+C0155016	Color Blindness, Red-Green
+C0155017	Color Blindness, Blue
+C0155018	Acquired color blindness
+C0155072	Mooren\'s ulcer
+C0155078	Photokeratitis
+C0155091	Corneal abscess NOS
+C0155094	Corneal pannus
+C0155100	Peripheral opacity of cornea
+C0155111	Bullous keratopathy
+C0155116	Descemet\'s membrane fold
+C0155118	Corneal degeneration
+C0155119	Recurrent erosion of cornea
+C0155120	Corneal Dystrophy, Band-Shaped
+C0155127	Familial Amyloid Polyneuropathy, Type V
+C0155164	Conjunctival scar
+C0155169	Ocular hyperaemia
+C0155177	Eczema eyelids
+C0155210	Eyelid Xanthoma
+C0155223	Dacryoadenitis
+C0155241	Lacrimal mucocele
+C0155259	Tenonitis
+C0155285	Orbital cyst
+C0155287	Visual pathway disorders
+C0155288	Papilledema Associated with Increased Intracranial Pressure
+C0155299	Coloboma of optic disc
+C0155300	Pseudopapilledema
+C0155303	Toxic optic neuropathy
+C0155305	Optic Neuropathy, Ischemic
+C0155306	Optic nerve sheath haemorrhage
+C0155320	Blindness cortical
+C0155338	Total ophthalmoplegia
+C0155339	Brown Tendon Sheath Syndrome
+C0155344	Spasm of Conjugate Gaze
+C0155359	Scleral staphyloma
+C0155365	Vitreous disorder
+C0155366	Vitreous degeneration
+C0155380	Dissociated Nystagmus
+C0155388	Disorders of external ear
+C0155411	Exostosis of external ear canal
+C0155428	Otosalpingitis
+C0155490	Middle Ear Cholesteatoma
+C0155501	Vertigo, Peripheral
+C0155502	Benign Paroxysmal Positional Vertigo
+C0155503	Central Nervous System Origin Vertigo
+C0155508	Viral labyrinthitis
+C0155533	Subjective tinnitus
+C0155534	Objective tinnitus
+C0155536	Paracousis
+C0155540	Ear discharge
+C0155550	Neural hearing loss
+C0155552	Hearing Loss, Mixed Conductive-Sensorineural
+C0155567	Rheumatic aortic stenosis
+C0155568	Rheumatic aortic regurgitation
+C0155601	Hypertensive heart and renal disease
+C0155616	Secondary hypertension
+C0155626	Acute myocardial infarction
+C0155668	Old myocardial infarction
+C0155672	Cor pulmonale acute
+C0155675	Pulmonary arteriovenous fistula
+C0155676	Pulmonary artery aneurysm
+C0155686	Acute myocarditis
+C0155699	Cardiomyopathy in other diseases classified elsewhere
+C0155707	Trifascicular block
+C0155708	Other specified conduction disorders
+C0155712	Chordae tendinae rupture
+C0155713	Papillary muscle rupture
+C0155728	Other specified transient cerebral ischemias
+C0155730	Nonruptured cerebral aneurysm
+C0155733	Aortic atherosclerosis
+C0155747	Splenic artery aneurysm
+C0155760	Rupture of artery
+C0155765	Disease of capillaries
+C0155773	Portal vein thrombosis
+C0155789	Oesophageal varices haemorrhage
+C0155800	Chronic hypotension
+C0155826	Chronic nasopharyngitis
+C0155840	Nasal turbinate hypertrophy
+C0155860	Pneumonia due to Pseudomonas
+C0155862	Pneumonia, Pneumococcal
+C0155866	Inhalational anthrax
+C0155867	Pneumonia aspergilla
+C0155870	Pneumonia and influenza
+C0155877	Allergic asthma
+C0155880	Intrinsic asthma
+C0155889	Mushroom Worker's Lung
+C0155909	Mediastinal abscess
+C0155912	Pulmonary Alveolar Microlithiasis
+C0155919	Acute pulmonary oedema
+C0155947	Dentofacial anomaly
+C0155955	Exostosis of jaw
+C0155964	Atrophic glossitis
+C0156104	Inguinal hernia, obstructive
+C0156133	Umbilical hernia, obstructive
+C0156140	Hernia obstructive
+C0156147	Crohn's disease of large bowel
+C0156149	Gastrointestinal tract vascular insufficiency
+C0156181	Peritoneal adhesion
+C0156183	Anorectal stricture
+C0156185	Abscess intestinal
+C0156189	Cirrhosis and chronic liver disease
+C0156214	Gallbladder obstruction
+C0156215	Gallbladder perforation
+C0156221	Acute glomerulonephritis
+C0156247	Kidney small
+C0156257	Calculus of kidney and ureter
+C0156259	Hypertrophy of kidney
+C0156263	Ureteric fistula
+C0156272	Enterovesical fistula
+C0156273	Bladder Diverticulum
+C0156279	Urethral syndrome
+C0156290	Prostatic abscess
+C0156296	Atrophy of prostate
+C0156308	Penile oedema
+C0156309	Organic erectile dysfunction
+C0156312	Atrophy of testis
+C0156318	Breast fibrosis
+C0156339	Vulval ulceration
+C0156344	Endometriosis of ovary
+C0156349	Prolapse of female genital organs
+C0156353	Uterovaginal prolapse
+C0156369	Uterine Polyp
+C0156372	Asherman Syndrome
+C0156394	Enlarged clitoris
+C0156404	Irregular Menstruation
+C0156543	Abortion
+C0157733	Abnormality of the hair
+C0157738	Chronic skin ulcer
+C0157741	Idiopathic urticaria
+C0157742	Urticaria due to cold and heat
+C0157743	Vibratory urticaria
+C0157749	Arthropathy associated with infection
+C0157843	Infective arthritis of shoulder region
+C0157844	Unspecified infective arthritis involving upper arm
+C0157845	Unspecified infective arthritis involving forearm
+C0157846	Unspecified infective arthritis involving hand
+C0157847	Unspecified infective arthritis, pelvic region and thigh
+C0157848	Unspecified infective arthritis involving lower leg
+C0157849	Unspecified infective arthritis, ankle and foot
+C0157917	Pauciarticular juvenile rheumatoid arthritis
+C0157946	Osteoarthrosis, localized, not specified whether primary or secondary
+C0158026	Monarthritis
+C0158113	Contracture of joint of hand
+C0158118	Contracture of multiple joints
+C0158252	Intervertebral disc disorder
+C0158266	Intervertebral Disc Degeneration
+C0158280	Cervical spinal stenosis
+C0158281	Cervicobrachial syndrome
+C0158288	Lumbar spinal stenosis
+C0158300	Adhesive Capsulitis
+C0158322	Calcaneal spur
+C0158328	Trigger finger
+C0158337	Synovial rupture
+C0158350	Tendinous contracture
+C0158353	Infectious Myositis
+C0158360	Fibromatosis, Plantar
+C0158369	Swelling of limb
+C0158371	Acute osteomyelitis, site unspecified
+C0158447	Idiopathic osteoporosis
+C0158454	Fracture malunion
+C0158458	Acquired hallux valgus
+C0158461	Acquired claw toe
+C0158465	Acquired cubitus valgus
+C0158485	Acquired genu varum
+C0158489	Acquired clubfoot
+C0158538	Other congenital anomalies of nervous system
+C0158543	Congenital cystic eyeball
+C0158551	Embryonal nuclear cataract (disorder)
+C0158564	Congenital vitreous anomaly
+C0158570	Vascular anomaly
+C0158617	Congenital aortic valve incompetence
+C0158619	Congenital mitral valve incompetence
+C0158629	Congenital anomaly of aortic arch
+C0158634	Partial anomalous pulmonary venous connection
+C0158641	Congenital cystic lung
+C0158646	Cleft lip and palate
+C0158663	Tongue absent
+C0158667	Aplasia of Lacrimal and Salivary Glands
+C0158683	Polycystic liver disease
+C0158687	Congenital genital malformation
+C0158698	Congenital anomalies of urinary system
+C0158713	Bilateral congenital dislocation of hip
+C0158731	Congenital pectus carinatum
+C0158733	Hand polydactyly
+C0158734	Polydactyly of toes
+C0158738	Syndactyly of toes with fusion of bones
+C0158761	Radioulnar Synostosis
+C0158775	Congenital anomaly of spine
+C0158779	Cervical rib
+C0158782	Anomalies of diaphragm, congenital
+C0158850	Fetal Malnutrition
+C0158915	Macrosomia
+C0158935	Pneumonia NOS congenital
+C0158940	Transient tachypnoea of the newborn
+C0158944	Infections specific to perinatal period
+C0158945	Congenital cytomegalovirus infection
+C0158962	Hemolytic disease of fetus OR newborn due to RhD isoimmunization
+C0158981	Neonatal diabetes mellitus
+C0158983	Neonatal thyrotoxicosis
+C0158986	Hypoglycaemia neonatal
+C0158995	Congenital anemia
+C0158996	Anemia of prematurity
+C0159020	Convulsions in the newborn
+C0159023	Feeding problems in newborn
+C0159028	General symptom
+C0159039	Spontaneous bruising
+C0159047	Symbolic dysfunction, unspecified
+C0159054	Abnormal sputum
+C0159056	Abnormal chest sound
+C0159059	Visible peristalsis
+C0159060	Abnormal bowel sounds
+C0159066	Abdominal rigidity
+C0159069	Glucose tolerance test abnormal
+C0159075	Chyluria
+C0159076	Biliuria
+C0159102	Nerve stimulation tests NOS abnormal
+C0159104	Electrooculogram abnormal
+C0159125	Culture NOS positive
+C0159321	Facial bones fracture
+C0159658	Clavicle fracture
+C0159667	Scapula fracture
+C0159849	Patella fracture
+C0159877	Ankle Fractures
+C0159941	Traumatic dislocation of joint of wrist
+C0159970	Knee Dislocation
+C0160345	Gastrointestinal injury
+C0160390	Liver injury
+C0160405	Splenic injury
+C0160420	Renal injury NOS
+C0160680	Carotid Artery Injuries
+C0160966	Buttock crushing
+C0161398	Optic Nerve Injuries
+C0161408	Facial Nerve Injuries
+C0161457	Median nerve injury
+C0161458	Ulnar nerve injury
+C0161467	Sciatic nerve injury
+C0161479	Nerve injury
+C0161768	Mechanical complication due to intrauterine contraceptive device
+C0161801	Complications of transplanted lung
+C0161802	Complications of bone marrow transplant
+C0161803	Complications of transplanted pancreas
+C0162119	Haemoglobin decreased
+C0162154	Atrophic scar
+C0162164	Pulmonary valve stenosis congenital
+C0162275	Ketonuria
+C0162279	Choroidal detachment
+C0162281	Corneal deposit
+C0162283	Nephrogenic Diabetes Insipidus
+C0162285	Edema of eyelid
+C0162286	Burn of esophagus
+C0162287	Abnormal faeces
+C0162291	Retinal ischaemia
+C0162292	External Ophthalmoplegia
+C0162296	Polyarthralgia
+C0162297	Respiratory arrest
+C0162298	Joint stiffness
+C0162299	Thyroid cyst
+C0162301	Calculus urethral
+C0162309	Adrenoleukodystrophy
+C0162311	Androgenetic Alopecia
+C0162316	Anemia, Iron-Deficiency
+C0162323	Polyarthritis
+C0162351	Contact hypersensitivity
+C0162359	Christ-Siemens-Touraine syndrome
+C0162361	Hidrotic Ectodermal Dysplasia
+C0162385	Intertrochanteric Fractures
+C0162386	Subtrochanteric Fractures
+C0162387	Trochanteric Fractures
+C0162423	Heat rash
+C0162429	Malnutrition
+C0162442	Parapsoriasis en Plaques
+C0162473	Auriculotemporal Syndrome
+C0162482	Uterine inversion
+C0162510	Caroli Disease
+C0162526	AIDS-Related Opportunistic Infections
+C0162529	Colitis ischaemic
+C0162530	Porphyria, Erythropoietic
+C0162531	Coproporphyria, Hereditary
+C0162532	Variegate Porphyria
+C0162533	Porphyrias, Hepatic
+C0162534	Prion Diseases
+C0162538	Immunoglobulin A deficiency (disorder)
+C0162539	IgG Deficiency disorder
+C0162549	Akathisia, Tardive
+C0162550	Akathisia, Drug-Induced
+C0162557	Acute hepatic failure
+C0162563	Cardiac ablation
+C0162565	Acute intermittent porphyria
+C0162566	Porphyria Cutanea Tarda
+C0162568	Erythropoietic Protoporphyria
+C0162569	Hepatoerythropoietic Porphyria
+C0162576	Anisakiasis
+C0162577	Angioplasty
+C0162578	Thrombectomy
+C0162625	Secernentea Infections
+C0162626	Ascaridida Infections
+C0162627	Skin Diseases, Bacterial
+C0162628	Skin Diseases, Viral
+C0162635	Angelman Syndrome
+C0162638	Apoptosis
+C0162643	Treatment failure
+C0162651	Gastric outlet obstruction
+C0162666	Mitochondrial Encephalomyopathies
+C0162668	Megaconial Myopathies
+C0162669	Pleoconial Myopathies
+C0162670	Mitochondrial Myopathies
+C0162671	MELAS Syndrome
+C0162672	MERRF Syndrome
+C0162674	Chronic progressive external ophthalmoplegia
+C0162677	Caliciviridae Infections
+C0162678	Neurofibromatoses
+C0162679	Leukaemic infiltration
+C0162699	Tick-Borne Infections
+C0162700	Tick-Borne Diseases
+C0162739	HELLP Syndrome
+C0162770	Right Ventricular Hypertrophy
+C0162809	Kallmann Syndrome
+C0162810	Cicatrix, Hypertrophic
+C0162818	Skin Diseases, Papulosquamous
+C0162819	Skin Diseases, Vascular
+C0162820	Dermatitis, Allergic Contact
+C0162823	Dermatitis, Irritant
+C0162824	Dermatitis, Photoallergic
+C0162830	Dermatitis, Phototoxic
+C0162834	Hyperpigmentation
+C0162835	Hypopigmentation
+C0162836	Hidradenitis Suppurativa
+C0162838	Porokeratosis, Palmoplantar
+C0162839	Porokeratosis
+C0162848	Lichenoid Eruptions
+C0162849	Lichen Nitidus
+C0162850	Habermann's Disease
+C0162851	Chronic lichenoid pityriasis
+C0162852	Pityriasis Lichenoides et Varioliformis Acuta
+C0162853	Pityriasis Lichenoides
+C0162855	Mucinoses
+C0162869	Aneurysm ruptured
+C0162870	Iliac Aneurysm
+C0162871	Aortic Aneurysm, Abdominal
+C0162872	Aortic Aneurysm, Thoracic
+C0175167	Acneform eruptions
+C0175683	Citrullinemia
+C0175691	Dubowitz syndrome
+C0175692	Johanson-Blizzard syndrome
+C0175693	Russell-Silver syndrome
+C0175694	Smith-Lemli-Opitz Syndrome
+C0175695	Sotos' syndrome
+C0175696	Congenital cleft larynx and Opitz-Frias syndrome
+C0175697	Van der Woude syndrome
+C0175699	Saethre-Chotzen Syndrome
+C0175700	Multiple synostosis syndrome
+C0175701	Aarskog syndrome
+C0175702	Williams Syndrome
+C0175703	Thrombocytopenia-Absent Radius Syndrome
+C0175704	LEOPARD Syndrome
+C0175707	Asplenia Syndrome
+C0175708	Chronic rheumatic heart disease
+C0175709	Centronuclear myopathy
+C0175713	Aicardi's syndrome
+C0175754	Agenesis of corpus callosum
+C0175755	Congenital absent nipple
+C0175778	Larsen syndrome
+C0175816	Cold Hemagglutinin Disease
+C0175948	Infantilism
+C0176866	Haemorrhoid operation
+C0177646	Finger amputation
+C0178238	Intestinal infectious disease (disorder)
+C0178264	Central nervous system inflammation
+C0178282	Hernia of abdominal cavity
+C0178298	Skin and subcutaneous tissue disorders
+C0178316	Upper limb fracture
+C0178324	Injury to blood vessels of unspecified site
+C0178391	Breast prosthesis implantation
+C0178414	Prostatic specific antigen decr.
+C0178415	Prostatic specific antigen increased
+C0178416	Hypoplastic anaemia
+C0178417	Anhedonia
+C0178421	Fibroadenoma of breast
+C0178426	Potter's syndrome
+C0178468	Autoimmune thyroid disease
+C0178540	Cerebral Hypoxia-Ischemia
+C0178583	Decerebration
+C0178650	Gammopathy
+C0178664	Glomerulosclerosis
+C0178703	Hypertrophic osteoarthropathy
+C0178782	Orofacial Pain
+C0178824	Reactive Hyperemia
+C0178829	Reproductive tract disorder
+C0178850	Intervertebral disc injury
+C0178874	Tumor Progression
+C0178879	Urinary obstruction unspecified
+C0184554	Disuse syndrome
+C0184567	Acute onset pain
+C0184937	Removal of foreign body NOS
+C0185131	Bone operation
+C0185132	Joint operation NOS
+C0185134	Tendon operation
+C0185169	Tendon sheath incision
+C0185188	Fasciotomy
+C0185216	Sequestrectomy
+C0185221	Bone debridement
+C0185240	Bone lesion excision
+C0185304	Synovectomy
+C0185314	Removal of internal fixation
+C0185373	Open reduction of fracture
+C0185496	Closed fracture manipulation
+C0185566	Mandibulectomy
+C0185773	Neck surgery
+C0185908	Spinal operation
+C0186193	Hip arthroplasty
+C0186321	Shoulder operation
+C0186399	Arm amputation
+C0186662	Shoulder arthroplasty
+C0186666	Rotator cuff repair
+C0187064	Wrist operation NOS
+C0187769	Knee operation
+C0188412	Ankle operation
+C0188413	Foot operation
+C0188602	Toe amputation
+C0188605	Foot amputation
+C0188970	Nasal operation NOS
+C0189476	Chest tube insertion
+C0189477	Aspiration pleural cavity
+C0189485	Biopsy lung
+C0189497	Lung lobectomy
+C0189557	Pleurodesis
+C0189660	Arterial repair
+C0189661	Aneurysm repair
+C0189771	Rashkind procedure
+C0189817	Cardiac pacemaker insertion
+C0189852	Pacemaker battery replacement
+C0189965	Atrial septal defect repair
+C0190065	Heart valve operation
+C0190173	Heart valve replacement NOS
+C0190188	Coronary artery surgery
+C0190211	Coronary angioplasty
+C0191237	Pericardial drainage
+C0191322	Skin lesion excisions
+C0191342	Wound debridement
+C0192189	Pharyngeal operation NOS
+C0192259	Esophageal operation NOS
+C0192389	Oesophageal dilatation
+C0192398	Gastric operation NOS
+C0192573	Intestinal operation NOS
+C0192601	Small intestinal resection
+C0192711	Intestinal anastomosis
+C0192775	Ileostomy closure
+C0192817	Colon operation NOS
+C0192866	Sigmoidectomy
+C0192871	Colectomy total
+C0192881	Ileocolectomy
+C0192993	Colostomy closure
+C0193062	Proctectomy
+C0193373	Liver operation
+C0193388	Biopsy liver
+C0193438	Gallbladder operation NOS
+C0193446	Cholelithotomy
+C0193769	Thyroid operation
+C0193959	Adenotonsillectomy
+C0194053	Renal surgery
+C0194073	Biopsy kidney
+C0194102	Renal stone removal
+C0194361	Bladder operation NOS
+C0194475	Bladder repair
+C0194501	Urinary bladder suspension
+C0194790	Prostate surgery
+C0195488	Ovarian cystectomy
+C0195495	Salpingo-oophorectomy bilateral
+C0195775	Brain operation
+C0196544	Peripheral nerve operation NOS
+C0196576	Carpal tunnel decompression
+C0197213	Blepharoplasty
+C0197489	Glaucoma surgery
+C0198010	Ear operation
+C0198482	Abdominal operation
+C0198542	Abdominoplasty
+C0199242	Thrombosis prophylaxis
+C0199451	Continuous positive airway pressure
+C0199470	Mechanical ventilation
+C0199962	Packed red blood cell transfusion
+C0200462	Fibrin D dimer
+C0200633	Neutrophil count
+C0200635	Lymphocyte Count measurement
+C0200637	Monocyte count procedure
+C0200638	Eosinophil count procedure
+C0200641	Blood basophil count (lab test)
+C0200665	Platelet mean volume determination (procedure)
+C0201278	Antibody measurement (procedure)
+C0201534	Antiphospholipid antibodies measurement
+C0201544	Prostate specific antigen measurement
+C0201657	C-reactive protein measurement
+C0201660	Rheumatoid Factor Measurement
+C0201836	Alanine aminotransferase
+C0201850	Alkaline phosphatase measurement
+C0201874	Amino acids measurement
+C0201888	Angiotensin converting enzyme measurement
+C0201896	Arylsulfatase B measurement
+C0201899	Aspartate aminotransferase
+C0201910	Beta-2-microglobulin measurement
+C0201925	Calcium measurement
+C0201929	Carbohydrate measurement
+C0201968	Cortisol Measurement
+C0201973	Creatine kinase measurement
+C0201975	Blood creatinine
+C0201976	Creatinine measurement, serum (procedure)
+C0201983	Dehydroepiandrosterone sulfate measurement (procedure)
+C0202022	Follicle stimulating hormone measurement
+C0202035	Gamma-glutamyltransferase
+C0202054	Glycosylated haemoglobin
+C0202071	Homovanillic acid measurement
+C0202098	Insulin measurement
+C0202100	Insulin C-peptide measurement
+C0202105	Transferrin measurement
+C0202106	Unsaturated iron binding capacity measurement
+C0202115	Lactic acid measurement
+C0202117	Low density lipoprotein
+C0202123	Luteinizing hormone measurement
+C0202142	Myoglobin urine
+C0202159	Parathyroid hormone measurement
+C0202174	blood phenylalanine measurement by Guthrie microbiologic assay
+C0202177	Phospholipid measurement
+C0202178	Phosphorus measurement
+C0202202	Protein measurement
+C0202217	Serotonin measurement
+C0202218	Sex hormone binding globulin measurement
+C0202230	Thyroid stimulating hormone measurement
+C0202231	Thyroxine measurement
+C0202236	Triglycerides measurement
+C0202239	Uric acid measurement (procedure)
+C0202251	Vitamin B6 measurement
+C0202252	VITAMIN B12 MEASUREMENT
+C0204147	Wisdom teeth removal
+C0204324	Dental operation
+C0204600	Drug detoxification
+C0204854	Aspiration joint
+C0205204	Scab
+C0205255	Imprisonment
+C0205622	Microinvasive tumor
+C0205641	Adenocarcinoma, Basal Cell
+C0205642	Adenocarcinoma, Oxyphilic
+C0205643	Carcinoma, Cribriform
+C0205644	Carcinoma, Granular Cell
+C0205645	Adenocarcinoma, Tubular
+C0205646	Adenoma, Basal Cell
+C0205647	Follicular adenoma
+C0205648	Adenoma, Microcystic
+C0205649	Adenoma, Monomorphic
+C0205650	Papillary adenoma
+C0205651	Adenoma, Trabecular
+C0205671	Infections, Arenavirus
+C0205682	Waist-Hip Ratio
+C0205695	Carcinoid, Goblet Cell
+C0205696	Anaplastic carcinoma
+C0205697	Carcinoma, Spindle-Cell
+C0205698	Undifferentiated carcinoma
+C0205699	Carcinomatosis
+C0205700	Asymmetric Septal Hypertrophy
+C0205707	Sprue
+C0205710	Alpers Syndrome (disorder)
+C0205711	Pelizaeus-Merzbacher Disease
+C0205713	Roussy-Levy Syndrome (disorder)
+C0205721	Infections, Hospital
+C0205730	Hereditary Opalescent Dentin (disorder)
+C0205734	Diabetes, Autoimmune
+C0205747	Familial Atypical Multiple Mole-Melanoma
+C0205748	Dysplastic naevus
+C0205765	Chronic Cystic Mastitis
+C0205766	Myxofibroma
+C0205768	Subependymal Giant Cell Astrocytoma
+C0205769	Myxopapillary ependymoma
+C0205770	Choroid Plexus Papilloma
+C0205788	Histiocytoid hemangioma
+C0205789	Hemangioma, Intramuscular
+C0205792	Enterocele
+C0205815	Leiomyosarcoma, Epithelioid
+C0205816	Leiomyosarcoma, Myxoid
+C0205822	Hibernoma
+C0205823	Pleomorphic Lipoma
+C0205824	Liposarcoma, Dedifferentiated
+C0205825	Liposarcoma, Pleomorphic
+C0205828	Cavernous lymphangioma
+C0205833	Medullomyoblastoma
+C0205834	Meningiomas, Multiple
+C0205851	Germ cell tumor
+C0205852	Neoplasms, Embryonal and Mixed
+C0205854	Glandular Neoplasms
+C0205858	General Paralysis
+C0205874	Papilloma, Squamous Cell
+C0205875	Papillomatosis
+C0205882	Infections, Parvovirus
+C0205898	Pinealoblastoma
+C0205929	Anal Fistula
+C0205944	Sarcoma, Epithelioid
+C0205945	Sarcoma, Spindle Cell
+C0205969	Thymic Carcinoma
+C0205990	Vaginal prolapse
+C0206019	AIDS encephalopathy
+C0206042	Fatal Familial Insomnia
+C0206044	Infections, Calicivirus
+C0206051	Photoallergy
+C0206061	Pneumonia, Interstitial
+C0206062	Lung Diseases, Interstitial
+C0206063	Radiation Pneumonitis
+C0206064	Microvascular Angina
+C0206067	Focal Epithelial Hyperplasia
+C0206068	Parasystole
+C0206081	Hyperandrogenism
+C0206083	Central pontine myelinolysis
+C0206085	Kleine-Levin Syndrome
+C0206093	Neuroectodermal neoplasm
+C0206094	Neuroectodermal Tumor, Melanotic
+C0206115	WAGR Syndrome
+C0206138	CREST Syndrome
+C0206139	Lichen Planus, Oral
+C0206141	Idiopathic Hypereosinophilic Syndrome
+C0206142	Eosinophilic leukemia
+C0206143	Loeffler's Endocarditis
+C0206145	Stunned Myocardium
+C0206146	Myocardial Stunning
+C0206157	Myopathies, Nemaline
+C0206159	Postmenopause
+C0206160	Reticulocytosis
+C0206161	Reticulocyte count (procedure)
+C0206171	Community-Acquired Infections
+C0206172	Diabetic Foot
+C0206178	Cytomegalovirus Retinitis
+C0206180	Ki-1+ Anaplastic Large Cell Lymphoma
+C0206182	Lymphomatoid Papulosis
+C0206186	Leukoplakia, Hairy
+C0206239	Cubital tunnel syndrome
+C0206245	Amyloid Neuropathies, Familial
+C0206247	Amyloid Neuropathies
+C0206260	Angiogranuloma
+C0206307	Canavan Disease
+C0206368	Exfoliation Syndrome
+C0206504	Tympanic Membrane Perforation
+C0206525	Tuberculosis, Drug-Resistant
+C0206526	Tuberculosis, Multidrug-Resistant
+C0206586	Endolymphatic Hydrops
+C0206604	Arterivirus Infections
+C0206608	Flavivirus Infections
+C0206611	Pestivirus Infections
+C0206613	Paramyxoviridae Infections
+C0206617	Cardiovirus Infections
+C0206620	Cystic lymphangioma
+C0206622	Adenomyoma
+C0206623	Adenosquamous carcinoma
+C0206624	Hepatoblastoma
+C0206625	Malignant Mixed Tumor
+C0206627	Mixed Tumor, Mullerian
+C0206628	Mesoblastic Nephroma
+C0206629	Pulmonary Blastoma
+C0206630	Endometrial Stromal Sarcoma
+C0206631	Lipomatous neoplasm
+C0206633	Angiomyolipoma
+C0206634	Liposarcoma, Myxoid
+C0206635	Myelolipoma
+C0206636	Chondromatosis
+C0206637	Mesenchymal Chondrosarcoma
+C0206638	Giant Cell Tumor of Bone
+C0206639	Neoplasms, Bone Tissue
+C0206640	Ossifying Fibroma
+C0206641	Osteochondromatosis
+C0206642	Parosteal Osteosarcoma
+C0206643	Neoplasms, Fibrous Tissue
+C0206644	Fibrous histiocytoma
+C0206646	Fibromatosis, Abdominal
+C0206647	Dermatofibrosarcoma
+C0206648	Myofibromatosis
+C0206649	Neoplasms, Fibroepithelial
+C0206650	Fibroadenoma
+C0206651	Clear Cell Sarcoma of Soft Tissue
+C0206653	Angiomyoma
+C0206654	Leiomyomatosis
+C0206655	Alveolar rhabdomyosarcoma
+C0206656	Embryonal Rhabdomyosarcoma
+C0206657	Alveolar Soft Part Sarcoma
+C0206658	Smooth Muscle Tumor
+C0206659	Embryonal Carcinoma
+C0206660	Germinoma
+C0206661	Gonadoblastoma
+C0206663	Neuroectodermal Tumor, Primitive
+C0206664	Teratocarcinoma
+C0206666	Trophoblastic Tumor, Placental Site
+C0206667	Adrenal adenoma
+C0206669	Hepatic adenoma
+C0206671	Eccrine acrospiroma
+C0206674	Adenoma, Villous
+C0206675	Adenomatoid Tumor
+C0206676	Adenomatosis, Pulmonary
+C0206677	Adenomatous Polyps
+C0206680	Mesothelioma, Cystic
+C0206681	Adenocarcinoma, Clear Cell
+C0206682	Adenocarcinoma, Follicular
+C0206683	Papillary and follicular adenocarcinoma
+C0206684	Sebaceous Adenocarcinoma
+C0206685	Acinar Cell Carcinoma
+C0206686	Adrenocortical carcinoma
+C0206687	Carcinoma, Endometrioid
+C0206692	Carcinoma, Lobular
+C0206693	Medullary carcinoma
+C0206694	Mucoepidermoid Carcinoma
+C0206695	Carcinoma, Neuroendocrine
+C0206696	Carcinoma, Signet Ring Cell
+C0206698	Cholangiocarcinoma
+C0206699	Cystadenocarcinoma, Mucinous
+C0206700	Cystadenocarcinoma, Papillary
+C0206701	Cystadenocarcinoma, Serous
+C0206702	Klatskin Tumor
+C0206703	Carcinoma, Giant Cell
+C0206704	Carcinoma, Large Cell
+C0206706	Carcinoma, Verrucous
+C0206708	Cervical Intraepithelial Neoplasia
+C0206709	Cystadenoma, Serous
+C0206710	Basal Cell Neoplasm
+C0206711	Pilomatrixoma
+C0206712	Mucoepidermoid Tumor
+C0206713	Papilloma, Intraductal
+C0206715	Neoplasms, Neuroepithelial
+C0206716	Ganglioglioma
+C0206717	Esthesioneuroblastoma, Olfactory
+C0206718	Ganglioneuroblastoma
+C0206719	Central Neurocytoma
+C0206720	Squamous Cell Neoplasms
+C0206721	Inverted Papilloma
+C0206723	Sertoli-Leydig Cell Tumor
+C0206724	Sex Cord-Gonadal Stromal Tumors
+C0206725	Subependymal Glioma
+C0206726	gliosarcoma
+C0206727	Nerve Sheath Tumors
+C0206728	Neurofibroma, Plexiform
+C0206729	Neurofibrosarcoma
+C0206730	Neurothekeoma
+C0206731	Angiofibroma
+C0206732	Epithelioid hemangioendothelioma
+C0206733	Strawberry nevus of skin
+C0206734	Hemangioblastoma
+C0206735	Melanoma, Amelanotic
+C0206736	Blue naevus
+C0206737	Nevus, Intradermal
+C0206739	Epithelioid and spindle cell nevus
+C0206743	Rhabdoid Tumor
+C0206744	T-Lymphocytopenia, Idiopathic CD4-Positive
+C0206750	Coronavirus Infections
+C0206751	Rhabdoviridae Infections
+C0206752	Alphavirus Infections
+C0206754	Neuroendocrine Tumors
+C0206762	Limb Deformities, Congenital
+C0206769	Nevi and Melanomas
+C0220597	Adult Hodgkin Lymphoma
+C0220603	Childhood Brain Neoplasm
+C0220605	Adult Non-Hodgkin Lymphoma
+C0220611	Childhood Rhabdomyosarcoma
+C0220612	Childhood Non-Hodgkin Lymphoma
+C0220613	Adult Soft Tissue Sarcoma
+C0220615	Adult Acute Myeloblastic Leukemia
+C0220620	Gastrointestinal Carcinoid Tumor
+C0220621	Childhood Acute Myeloid Leukemia
+C0220624	Adult Brain Neoplasm
+C0220630	Adult Liver Carcinoma
+C0220633	Uveal melanoma
+C0220636	Malignant neoplasm of salivary gland
+C0220641	Lip and Oral Cavity Carcinoma
+C0220644	Childhood Hodgkin Lymphoma
+C0220645	Childhood Soft Tissue Sarcoma
+C0220647	Carcinoma of unknown primary
+C0220648	Renal Pelvis and Ureter Urothelial Carcinoma
+C0220650	Brain cancer metastatic
+C0220654	Meningeal Carcinomatosis
+C0220656	Malignant ascites
+C0220658	Pfeiffer Syndrome
+C0220659	Acrodysostosis
+C0220662	ARTHROGRYPOSIS, DISTAL, TYPE 1
+C0220663	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder)
+C0220664	BRACHYDACTYLY, TYPE D
+C0220666	ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
+C0220668	Congenital contractural arachnodactyly
+C0220669	Familial benign neonatal epilepsy
+C0220681	Goldenhar Syndrome with Ipsilateral Radial Defect
+C0220685	Achondrogenesis type 2
+C0220687	KBG syndrome
+C0220690	Macrocephaly, benign familial
+C0220692	Maxillonasal dysplasia, Binder type
+C0220693	Microcephaly autosomal dominant
+C0220695	Neurofibromatosis, type 4, of Riccardi
+C0220697	POLYDACTYLY, POSTAXIAL
+C0220701	RETINITIS PIGMENTOSA 1
+C0220702	SCHIZOPHRENIA 1 (disorder)
+C0220704	Shprintzen syndrome
+C0220708	VATER Association
+C0220710	Medium-chain acyl-coenzyme A dehydrogenase deficiency
+C0220711	Long chain acyl-CoA dehydrogenase deficiency
+C0220721	CATARACT 46, JUVENILE-ONSET
+C0220722	Cerebrooculofacioskeletal Syndrome 1
+C0220723	CHOANAL ATRESIA, POSTERIOR
+C0220724	CONSTRICTING BANDS, CONGENITAL
+C0220726	Diastrophic dysplasia
+C0220730	Fryns syndrome
+C0220743	Childhood hypophosphatasia (disorder)
+C0220744	Multiple gastrointestinal atresias (disorder)
+C0220748	Cartilage-hair hypoplasia
+C0220754	Biotinidase Deficiency
+C0220756	Niemann-Pick Disease, Type C
+C0220763	Vagina absent
+C0220765	Weaver-Like Syndrome
+C0220766	Congenital hypoplasia of adrenal gland
+C0220767	Craniofrontonasal dysplasia
+C0220769	FG syndrome
+C0220775	RUSSELL-SILVER SYNDROME, X-LINKED
+C0220810	Congenital defects
+C0220847	Hepatitis C virus
+C0220870	Lightheadedness
+C0220981	Metabolic acidosis
+C0220982	Ketoacidosis
+C0220983	Metabolic alkalosis
+C0220987	Hereditary orotic aciduria
+C0220988	Xanthinuria
+C0220989	Acquired partial lipodystrophy
+C0220991	Rotor Syndrome
+C0220992	Histidinemia
+C0220993	Cystathioninuria
+C0220994	Hyperammonemia
+C0220996	Infantile scurvy
+C0220998	Hypothalamic hypothyroidism
+C0221002	Hyperparathyroidism, Primary
+C0221005	Mauriac\'s syndrome
+C0221011	Malignant Atrophic Papulosis
+C0221013	Mastocytosis, Systemic
+C0221014	Reactive systemic amyloidosis
+C0221016	Red blood cell disorder
+C0221018	Hereditary sideroblastic anemia
+C0221019	Sickle cell-beta-thalassemia
+C0221021	Microangiopathic haemolytic anaemia
+C0221023	Cyclic neutropenia
+C0221025	Kasabach-Merritt syndrome
+C0221026	X-linked agammaglobulinemia
+C0221028	Neonatal thrombocytopenia (disorder)
+C0221030	Hyperviscosity syndrome
+C0221032	Familial generalized lipodystrophy
+C0221033	Trisomy X syndrome
+C0221036	Acrodermatitis enteropathica
+C0221043	Liddle Syndrome
+C0221045	Cardiac failure high output
+C0221046	Syncope, Carotid Sinus
+C0221047	Bradycardia-tachycardia syndrome
+C0221052	Chronic berylliosis
+C0221054	Welander Distal Myopathy
+C0221055	Paramyotonia Congenita (disorder)
+C0221056	Adult type dermatomyositis
+C0221057	Dejerine-Roussy Syndrome
+C0221058	Ophthalmoplegic migraine
+C0221060	Mobius Syndrome
+C0221061	Behr syndrome
+C0221065	Subacute Combined Degeneration
+C0221069	Anterior Spinal Artery Syndrome
+C0221074	Depression, Postpartum
+C0221075	Reactive psychosis
+C0221100	Hangover
+C0221106	Alkalemia
+C0221123	Transfusion Reaction
+C0221147	Platelet production decreased
+C0221150	Odynophagia
+C0221151	Projectile vomiting
+C0221155	Systolic hypertension
+C0221161	Shallow breathing
+C0221163	Motor Disorders
+C0221165	Diplegia
+C0221166	Paraparesis
+C0221168	Podagra
+C0221169	Hemiballismus
+C0221170	Muscular stiffness
+C0221182	Chordee
+C0221184	Bitemporal Hemianopia
+C0221185	Xanthopsia
+C0221198	Lesion
+C0221199	Abnormal palmar creases
+C0221200	Koplik spots
+C0221201	Rash macular
+C0221203	Rash vesicular
+C0221204	Lytic lesion
+C0221207	Urticaria due to cold
+C0221209	Pelvic kidney
+C0221210	Congenital malrotation of intestine
+C0221214	Vascular ring
+C0221215	Common atrioventricular canal
+C0221217	Neck webbing
+C0221219	Ectopic pancreas
+C0221226	Distended umbilical veins
+C0221227	Centriacinar Emphysema
+C0221228	Comedone
+C0221232	Welt
+C0221237	Angular cheilitis
+C0221238	Mesangial proliferative glomerulonephritis
+C0221239	Glomerulonephritis rapidly progressive
+C0221243	Necrolytic migratory erythema
+C0221244	Dandruff
+C0221245	Fissure in skin
+C0221248	Gouty tophus
+C0221252	Eruptive xanthoma
+C0221253	Xanthoma tendinosum
+C0221255	Calcification metastatic
+C0221259	Trichiasis
+C0221260	Dystrophia unguium
+C0221261	Koilonychia
+C0221262	Poliosis
+C0221263	Cafe au lait spots
+C0221264	Cheilosis
+C0221265	Microcytosis
+C0221269	Pseudolymphoma
+C0221270	Acanthosis
+C0221271	Elastosis perforans serpiginosa
+C0221273	Juvenile polyp
+C0221276	Relative erythrocytosis
+C0221277	Atypical lymphocytes
+C0221278	Anisocytosis
+C0221281	Poikilocytosis
+C0221287	Combined Hepatocellular Carcinoma and Cholangiocarcinoma
+C0221290	Chondromyxoid fibroma
+C0221292	Basophilic leukemia
+C0221333	Hypouricaemia
+C0221345	Nail discolouration
+C0221347	Acrocyanosis
+C0221352	Syndactyly of fingers
+C0221353	Horseshoe Kidney
+C0221354	Frontal bossing
+C0221355	Macrocephaly
+C0221356	Brachycephaly
+C0221357	Brachydactyly
+C0221358	Long narrow head
+C0221360	Congenital absence of diaphragm
+C0221363	Bifid nose
+C0221365	Double ureter
+C0221369	Acquired Camptodactyly
+C0221373	Claw hand
+C0221376	Hydrosalpinx (disease)
+C0221391	Melanosis coli
+C0221392	Atrophic Vaginitis
+C0221395	Erythropenia
+C0221405	Pituitary cachexia
+C0221406	Pituitary ACTH Hypersecretion
+C0221409	Anemia, hereditary spherocytic hemolytic
+C0221423	Illness (finding)
+C0221436	Melanoderma
+C0221468	Vitamin D-dependent rickets
+C0221470	Aphagia
+C0221473	Blindness, Hysterical
+C0221480	Recurrent depression
+C0221500	Effects of heat
+C0221505	Lesion of brain
+C0221512	Stomach ache
+C0221629	Proximal muscle weakness
+C0221706	Road traffic accident
+C0221714	Injection site infection
+C0221715	Intestinal carcinoma
+C0221717	Contact lens intolerance
+C0221725	Bronchial obstruction
+C0221727	Oesophageal pain
+C0221731	Periportal sinus dilatation
+C0221732	Mouth plaque
+C0221738	Nonspecific reaction
+C0221742	Serum sickness-like reaction
+C0221743	Skin reaction
+C0221745	Depression suicidal
+C0221752	Blood urine
+C0221757	alpha 1-Antitrypsin Deficiency
+C0221759	Brachial Plexus Neuritis
+C0221760	brain cyst
+C0221763	Chronic cystitis
+C0221764	Chronic psychosis
+C0221765	Chronic schizophrenia
+C0221766	Diastasis recti
+C0221773	Hyperamylasaemia
+C0221775	Lumbar disc disease
+C0221776	Oral pain
+C0221777	Nontoxic goiter
+C0221780	Rectal discharge
+C0221782	Uterine mass
+C0221785	Pain in wrist
+C0227791	Vaginal Discharge
+C0229197	Retinal fold (finding)
+C0231170	Disability NOS
+C0231218	Malaise
+C0231221	Asymptomatic
+C0231230	Fatigability
+C0231246	Failure to gain weight
+C0231247	Weight loss poor
+C0231254	Body mass index increased
+C0231255	Body mass index decreased
+C0231274	Intolerant of heat
+C0231311	Jet Lag Syndrome
+C0231337	Senility
+C0231341	Premature ageing
+C0231367	Activity intolerance
+C0231397	Anticipatory anxiety
+C0231441	Immobile
+C0231450	Abnormal extension
+C0231451	Hyperextension
+C0231471	Abnormal posture
+C0231474	Decerebrate posture
+C0231519	Gegenhalten
+C0231521	Decorticate Rigidity
+C0231528	Myalgia
+C0231529	Tendon pain
+C0231530	Muscle twitch
+C0231531	Muscle fibrillation
+C0231554	Osteoid formation disorder
+C0231557	Abnormal bone formation
+C0231592	Joint crepitation
+C0231608	Girdle pain
+C0231616	Beevor's sign
+C0231617	Catch - Finding of sensory dimension of pain
+C0231666	Wrist-Drop
+C0231678	Ulnar deviation of the wrist
+C0231679	Ulnar deviation of the fingers
+C0231686	Gait, Unsteady
+C0231687	Gait spastic
+C0231688	Gait, Shuffling
+C0231689	Gait, Athetotic
+C0231690	Titubation
+C0231691	Cerebellar gait
+C0231693	Charcot Gait
+C0231694	Gait, Festinating
+C0231695	Cerebellar ataxic gait
+C0231696	Gait, Hemiplegic
+C0231698	Gait, Scissors
+C0231706	Circling gait
+C0231710	Buttock pain
+C0231712	Waddling gait
+C0231730	Trendelenburg sign
+C0231749	Knee pain
+C0231780	Heel pain
+C0231785	Carpopedal spasm
+C0231791	Toeing-in
+C0231796	respiratory abnormalities
+C0231807	Dyspnea on exertion
+C0231819	Air trapping
+C0231835	Tachypnea
+C0231837	Respiratory rate decreased
+C0231856	Breath sounds abnormal
+C0231871	Whispering pectoriloquy
+C0231912	Nocturnal cough
+C0231918	Nose symptoms
+C0231919	Nasal dryness
+C0231926	Resp gas exchange disorder NOS
+C0232058	Apnoea neonatal
+C0232066	Induced apnea
+C0232070	Foreign body aspiration
+C0232100	Exsanguination
+C0232118	Pulsus paradoxus
+C0232119	Pulsus trigeminus
+C0232121	Pulsus alternans
+C0232132	Weak arterial pulse
+C0232144	Radial pulse abnormal
+C0232168	Ventricular dyskinesia
+C0232180	Cardiac shunt
+C0232196	Cardiac pacemaker malfunction
+C0232197	Cardiac fibrillation
+C0232200	Gallop rhythm
+C0232201	Sinus rhythm
+C0232208	Nodal rhythm
+C0232216	Ventricular escape rhythm
+C0232255	Innocent murmur
+C0232257	Systolic murmur, NOS
+C0232258	Pansystolic murmur
+C0232262	Diastolic murmur, NOS
+C0232263	Early diastolic murmur
+C0232265	Presystolic murmur
+C0232267	Pericardial friction rub
+C0232286	Precordial pain
+C0232292	Chest tightness
+C0232347	No-Reflow Phenomenon
+C0232352	Vascular insufficiency
+C0232359	Increased capillary filling time
+C0232370	Florid red complexion (finding)
+C0232409	Hair growth abnormal
+C0232431	Cold sweat
+C0232461	Increased appetite
+C0232462	Decrease in appetite
+C0232466	Feeding difficulties
+C0232474	Increased peristalsis
+C0232475	Decreased peristalsis
+C0232476	Absent peristalsis
+C0232480	Geophagia
+C0232487	Abdominal discomfort
+C0232488	Abdominal colic
+C0232491	Chronic abdominal pain
+C0232492	Abdominal pain upper
+C0232493	Epigastric pain
+C0232495	Abdominal pain lower
+C0232498	Abdominal tenderness
+C0232503	Umbilical bleeding
+C0232513	Premature tooth loss
+C0232534	Globus sensation
+C0232567	Hypergastrinaemia
+C0232599	Vomiting bile
+C0232600	Self-induced vomiting
+C0232602	Retching
+C0232694	Hyperactive bowel sounds
+C0232696	Bowel sounds absent
+C0232717	Rectal sensation
+C0232720	Faeces pale
+C0232721	Bulky stool
+C0232726	Rectal tenesmus
+C0232744	Decreased liver function
+C0232766	Asterixis
+C0232769	Abnormal gallbladder function
+C0232770	Gallbladder non-functioning
+C0232799	Grey Turner's sign
+C0232831	Impairment of urinary concentration
+C0232841	Bladder dysfunction
+C0232849	Bladder pain
+C0232854	Slowing of urinary stream
+C0232861	Discharge from penis
+C0232865	Functional proteinuria
+C0232867	Orthostatic proteinuria
+C0232894	Pneumatouria
+C0232910	Teratogenesis
+C0232939	Primary physiologic amenorrhea
+C0232940	Secondary physiologic amenorrhea
+C0232942	Cryptomenorrhea
+C0232943	Intermenstrual heavy bleeding
+C0232981	Arrest of spermatogenesis
+C0232982	Complete spermatogenic arrest
+C0232983	Incomplete spermatogenic arrest
+C0233122	Uterine dysfunction
+C0233187	Braxton Hicks contractions
+C0233189	Goodell's sign
+C0233191	Hegar's sign
+C0233200	Cullen's sign
+C0233205	Halo sign
+C0233256	Foetal malpresentation
+C0233315	Premature birth of newborn
+C0233397	Psychological symptom
+C0233401	Psychiatric symptom
+C0233407	Disorientation
+C0233414	Disturbance in attention
+C0233415	Distractibility
+C0233459	Emotional disorder
+C0233467	Inappropriate affect
+C0233469	Blunted affect
+C0233471	Flat affect
+C0233472	Affect lability
+C0233475	Euthymic mood
+C0233477	Dysphoria
+C0233479	Elevated mood
+C0233480	Hyperirritability
+C0233481	Worried
+C0233483	Free-floating anxiety
+C0233485	Apprehension
+C0233488	Feeling despair
+C0233494	Tension
+C0233496	Aversion
+C0233497	Insecurity
+C0233514	Abnormal behavior
+C0233519	Suspiciousness
+C0233522	Inappropriate behavior
+C0233523	Antisocial behavior
+C0233526	Offensive aggression
+C0233528	Asocial behaviour
+C0233532	Maladaptive behavior associated with physical illness
+C0233558	Temper tantrum
+C0233565	Bradykinesia
+C0233571	Excitement
+C0233576	Mannerism
+C0233585	Foot tapping
+C0233593	Eye poking
+C0233607	Catatonic stupor
+C0233608	Catatonic Rigidity
+C0233610	Negativism in catatonia
+C0233612	Waxy flexibility
+C0233613	Echopraxia
+C0233622	Ritual compulsion
+C0233629	Thinking and speaking disturbances
+C0233632	Thinking abnormal
+C0233636	Disorder of form of thought
+C0233647	Neologism
+C0233648	Word salad
+C0233651	Perseveration
+C0233652	Palinopsia
+C0233657	Flight of ideas
+C0233660	Thought blocking
+C0233681	Delusion of grandeur
+C0233684	Delusion of guilt
+C0233687	Thought insertion
+C0233689	Delusion of infidelity
+C0233693	Pseudologia fantastica
+C0233697	Obsessions
+C0233715	Speech impairment
+C0233718	Pressure of speech
+C0233720	Poverty of speech
+C0233726	Aprosodia
+C0233729	Coprolalia
+C0233730	Swearing
+C0233746	Perceptual disturbance
+C0233750	Hysterical amnesia
+C0233754	Derealisation
+C0233759	Hallucinations, Elementary
+C0233762	Auditory hallucinations
+C0233763	Hallucination, visual
+C0233765	Hallucination, olfactory
+C0233766	Hallucinations, Gustatory
+C0233767	Hallucination, tactile
+C0233769	Micropsia
+C0233771	Macropsia
+C0233773	Hallucinations, Hypnagogic
+C0233774	Hallucinations, Somatic
+C0233775	Hallucinations, Mood Congruent
+C0233776	Hallucinations, Mood Incongruent
+C0233777	Hallucinosis
+C0233794	Memory impairment
+C0233795	Amnesia, Anterograde
+C0233796	Temporary Amnesia
+C0233800	Confabulation
+C0233818	Judgement impaired
+C0233824	Lack of insight
+C0233844	Clumsiness
+C0233849	Personality Traits
+C0233949	Sexual nondevelopment
+C0233973	Painful erection
+C0234022	Anorgasmia
+C0234047	Ejaculation delayed
+C0234119	Neuromuscular blockade
+C0234131	Motor dysfunction
+C0234132	Pyramidal sign
+C0234133	Extrapyramidal sign
+C0234143	Neurological muscle weakness
+C0234144	Dysgraphia
+C0234146	Absent reflex
+C0234162	Cerebellar Dysmetria
+C0234164	Past pointing (finding)
+C0234166	Hyperexplexia
+C0234179	Brudzinski's sign
+C0234180	Chvostek sign
+C0234181	Trousseau's sign
+C0234182	Gowers sign
+C0234190	Hypesthesia, Thermal
+C0234192	Feeling cold
+C0234213	Sensory denervation disorder
+C0234215	Discomfort
+C0234221	Acroparesthesia
+C0234222	Sensation of pressure
+C0234229	Deep pain
+C0234230	Pain, Burning
+C0234233	Sore to touch
+C0234235	Tissue sensitivity
+C0234238	Ache
+C0234241	Indifference to pain
+C0234243	Central pain
+C0234244	Tissue Pain
+C0234245	Visceral Pain
+C0234246	Rebound tenderness
+C0234247	Neuralgia, Atypical
+C0234249	Neuralgia, Stump
+C0234250	Pain, Referred
+C0234251	Inflammatory pain
+C0234252	Mechanical pain
+C0234253	Rest pain
+C0234254	Radiating pain
+C0234255	Night pain
+C0234297	Taste Disorder, Primary
+C0234298	Taste Disorder, Primary, Sweet
+C0234299	Taste Disorder, Primary, Salt
+C0234300	Taste Disorder, Primary, Bitter
+C0234302	Taste Disorder, Anterior Tongue
+C0234303	Taste Disorder, Secondary
+C0234304	Taste Disorder, Secondary, Sweet
+C0234305	Taste Disorder, Secondary, Salt
+C0234306	Taste Disorder, Secondary, Bitter
+C0234319	Taste Disorder, Posterior Tongue
+C0234329	Motor Disorder, Vagus Nerve
+C0234331	Sensory Disorder, Vagus Nerve
+C0234357	Adiadochokinesis
+C0234362	Synkinesis
+C0234366	Ataxic
+C0234369	Trembling
+C0234370	Persistent Tremor
+C0234371	Continuous Tremor
+C0234372	Intermittent Tremor
+C0234373	Fine Tremor
+C0234374	Coarse Tremor
+C0234375	Massive Tremor
+C0234376	Action Tremor
+C0234377	Passive Tremor
+C0234378	Static Tremor
+C0234379	Resting Tremor
+C0234381	Darkness Tremor
+C0234387	Cerebral disorder
+C0234421	Consciousness, NOS
+C0234425	Level of consciousness
+C0234428	Disturbance of consciousness
+C0234435	Syncope, Tussive
+C0234437	Postural syncope
+C0234439	Semicoma
+C0234447	Narcosis
+C0234455	Sleep Drunkenness
+C0234458	Abnormal dreams
+C0234461	aphasic
+C0234462	Aphasia, Ageusic
+C0234469	Aphasia, Global
+C0234471	Associative aphasia
+C0234472	Aphasia, Functional
+C0234473	Jargon aphasia
+C0234474	Aphasia, Graphomotor
+C0234476	Aphasia, Intellectual
+C0234477	Kussmaul Aphasia
+C0234482	Aphasia, Semantic
+C0234484	Aphasia, Syntactical
+C0234488	Paraphasia
+C0234497	Amusia
+C0234501	Auditory agnosia
+C0234502	Visual Agnosia
+C0234503	Agnosia for Smell
+C0234504	Agnosia for Taste
+C0234505	Tactile Agnosia
+C0234506	Time Agnosia
+C0234507	Anosognosia
+C0234509	Finger Agnosia
+C0234510	Ideational Agnosia
+C0234511	Body-image agnosia
+C0234512	Prosopagnosia
+C0234516	Speech dysfunction
+C0234517	Anarthria speech disorder
+C0234518	Slurred speech
+C0234520	Apraxic
+C0234523	Apraxia, Ideomotor
+C0234526	Ideational Apraxia
+C0234527	Apraxia, Motor
+C0234529	Dressing Apraxia
+C0234533	Generalised seizure
+C0234535	Clonic convulsion
+C0234542	Epileptic aura
+C0234543	Postictal state
+C0234544	Postictal paralysis
+C0234547	Drug withdrawal convulsions
+C0234629	Abnormal color vision
+C0234632	Reduced visual acuity
+C0234656	Pain around eye
+C0234664	Lid lag
+C0234665	Eyelid retraction
+C0234668	Argyll-Robertson pupil (finding)
+C0234708	Intraocular pressure increased
+C0234757	Vertigo, Brain Stem
+C0234784	Reflex, Gag, Absent
+C0234804	Harsh voice quality
+C0234853	Facial grimacing
+C0234860	Weak cry
+C0234861	Cri du chat
+C0234866	Barking cough
+C0234894	Dermatitis acneiform
+C0234906	Annular Erythema
+C0234913	Rash erythematous
+C0234916	Rash follicular
+C0234918	Morbilliform rash
+C0234919	Rash papulosquamous
+C0234920	Papulovesicular rash
+C0234922	Rash scaly
+C0234925	Greasy skin
+C0234930	Skin odour abnormal
+C0234935	Acute urticaria
+C0234936	Application site oedema
+C0234944	Injection site anaesthesia
+C0234952	Oropharyngeal spasm
+C0234953	Tongue spasm
+C0234958	Muscle degeneration
+C0234959	Panarteritis
+C0234962	Pulmonary vasculitis
+C0234964	Poor balance (finding)
+C0234967	Choreoathetoid movements
+C0234972	Convulsive disorder
+C0234974	Simple Partial Seizures
+C0234976	Convulsive threshold lowered
+C0234979	Dysdiadochokinesis
+C0234985	Mental deterioration
+C0234987	Dizziness postural
+C0234988	Dizziness exertional
+C0234996	Gait, Rigid
+C0235000	Gait, Broadened
+C0235002	Head discomfort
+C0235013	Hypervigilance
+C0235014	Fontanelle bulging
+C0235025	Peripheral motor neuropathy
+C0235026	Neuritis, Sensory
+C0235031	Neurologic Symptoms
+C0235032	Neurotoxicity
+C0235044	Paresthesia, Distal
+C0235050	Tingling of skin
+C0235062	Neuromuscular Blockade
+C0235063	Respiratory Depression
+C0235064	Neonatal respiratory depression
+C0235065	Neonatal respiratory arrest
+C0235066	Peripheral scotoma
+C0235068	Scintillating scotoma
+C0235074	Tongue paralysis
+C0235078	Tremor, Perioral
+C0235081	Tremor, Limb
+C0235082	Tremor, Muscle
+C0235083	Nerve Tremors
+C0235086	Muscle contractions involuntary
+C0235095	Visual field constriction
+C0235108	Feeling tense
+C0235109	Mental distress
+C0235113	Emotional poverty
+C0235136	Agitated depression
+C0235146	Euphoria
+C0235153	Hallucinations, Sensory
+C0235162	Difficulty sleeping
+C0235165	Mania acute
+C0235169	Excitability
+C0235195	Sedation
+C0235198	Unable to concentrate
+C0235204	Irrational thoughts
+C0235218	Skin warm
+C0235222	Diastolic hypertension
+C0235229	Ciliary Body Spasm
+C0235234	Dry throat
+C0235238	Cycloplegia
+C0235242	Syncope, Effort
+C0235250	Hyperemesis
+C0235259	Cataract subcapsular
+C0235266	Eye irritation
+C0235267	Eye redness
+C0235270	Keratopathy
+C0235272	Retinal damage
+C0235280	Ototoxicity
+C0235287	Dysosmia
+C0235290	Taste bitter
+C0235299	Right upper quadrant pain
+C0235309	Stomach discomfort
+C0235312	Oral mucosal eruption
+C0235315	Faeces discoloured
+C0235324	Dental swelling
+C0235325	Gastric haemorrhage
+C0235327	Small intestine gangrene
+C0235328	Obstruction colon
+C0235329	Small intestinal obstruction
+C0235338	Salivary gland pain
+C0235346	Gingival erosion
+C0235347	Tongue black
+C0235351	Tongue ulceration
+C0235357	Hypoplasia of teeth
+C0235378	Hepatotoxicity
+C0235394	Wasting
+C0235401	Abnormal glucose tolerance
+C0235416	Blood uric acid increased
+C0235419	Hyperuricemic nephropathy
+C0235430	Ketonemia
+C0235431	Blood creatinine increased
+C0235433	Fat tissue increased
+C0235437	Gravitational oedema
+C0235439	Ankle edema (finding)
+C0235453	Steroid withdrawal syndrome
+C0235472	Pulse abnormal
+C0235475	Electrocardiogram QRS complex prolonged
+C0235480	Paroxysmal atrial fibrillation
+C0235490	Peripheral ischaemia
+C0235518	Illiac artery thrombosis
+C0235522	Disorder of vein
+C0235524	Vein pain
+C0235527	Heart Failure, Right-Sided
+C0235546	Hypopnoea
+C0235547	Respiratory depth decreased
+C0235551	Laryngotracheal oedema
+C0235553	Vocal cord thickening
+C0235557	Pulmonary granuloma
+C0235560	Respiratory tract haemorrhage
+C0235567	Excessive bronchial secretion
+C0235568	Bronchorrhea
+C0235573	Haemoglobinaemia
+C0235574	Intravascular haemolysis
+C0235575	Hemolytic reaction
+C0235590	Fibrosing adenosis
+C0235592	Cervical lymphadenopathy
+C0235593	Thoracic lymphadenopathy
+C0235598	Hodgkin\'s-like
+C0235601	Hypocoagulable state
+C0235604	Qualitative platelet deficiency
+C0235618	Glomerulonephritis proliferative
+C0235620	Haemorrhage urinary tract
+C0235627	Isosthenuria
+C0235632	Loin pain
+C0235634	Costovertebral angle tenderness
+C0235639	Urine abnormality
+C0235649	Breast oedema
+C0235653	Breast cancer female
+C0235659	Foetal hypokinesia
+C0235660	Galactorrhea not associated with childbirth
+C0235673	Pregnancy on oral contraceptive
+C0235678	Vaginal odor
+C0235694	Enamel anomaly
+C0235698	Abdominal distension, gaseous
+C0235710	Chest discomfort
+C0235744	Breath holding
+C0235746	Saliva altered
+C0235752	Naevus flammeus
+C0235753	Congenital hemangioma
+C0235754	Bladder papilloma
+C0235761	Nasal septum perforation
+C0235768	Retinal artery thrombosis
+C0235774	Somnolence neonatal
+C0235777	Cyanosis neonatal
+C0235782	Gallbladder Carcinoma
+C0235787	Weight decrease neonatal
+C0235802	Pupillary reflex impaired
+C0235804	Fixed Pupils
+C0235807	Hair texture abnormal
+C0235812	Vitritis
+C0235813	Neonatal leukaemia
+C0235820	Encephalopathy neonatal
+C0235821	Therapeutic response increased
+C0235827	Therapeutic response decreased
+C0235831	Renal Cell Dysplasia
+C0235832	Congenital hernia
+C0235833	Congenital diaphragmatic hernia
+C0235834	Upper motor neurone lesion
+C0235836	Coagulation disorder neonatal
+C0235839	Fever neonatal
+C0235840	Diarrhoea neonatal
+C0235841	Neonatal feeding disorder
+C0235843	Tremor neonatal
+C0235844	Agitation neonatal
+C0235849	Stomatitis necrotising
+C0235857	Decreased lacrimation
+C0235863	Delayed delivery
+C0235864	Congenital hypertrichosis lanuginosa
+C0235874	Condition aggravated
+C0235880	Mononeuritis
+C0235883	Uterine inflammation
+C0235884	Gastric perforation
+C0235886	Leg edema
+C0235887	Peritonitis sclerosing
+C0235889	Arthritis aggravated
+C0235896	Lung infiltration
+C0235912	Hepatic haemorrhage
+C0235915	Pulmonary malformation
+C0235917	Gingival discolouration
+C0235919	Nerve root liaison
+C0235926	Granulocytopenia neonatal
+C0235927	Vestibulocerebellar ataxia
+C0235942	Abnormality of the skull
+C0235946	Cerebral atrophy
+C0235950	Zinc deficiency
+C0235952	Clostridium difficile diarrhea
+C0235956	Absence attacks
+C0235957	Muscle necrosis
+C0235964	Renal dysgenesis
+C0235969	Disorder of ejaculation
+C0235971	Alpha 1 foetoprotein increased
+C0235972	Retinal deposits
+C0235974	Pancreatic carcinoma
+C0235979	Conjunctival discolouration
+C0235980	Scleral discolouration
+C0235983	Normochromic anemia
+C0235984	Salivary duct obstruction
+C0235986	Growth hormone excess
+C0235988	Serum iron low (finding)
+C0235989	Renal interstitial fibrosis
+C0235991	Small for gestational age (disorder)
+C0235996	Elevated liver enzymes
+C0236000	Jaw pain
+C0236001	Gingival atrophy
+C0236013	Hyperosmolar state
+C0236015	Coagulation factor increased
+C0236018	Aura
+C0236023	Periodontal destruction
+C0236024	Edema of pharynx
+C0236026	Foetal valproate syndrome
+C0236033	Muscle hypertrophy
+C0236036	Oculomucocutaneous syndrome
+C0236037	Poriomania
+C0236038	Congenital hearing disorder
+C0236040	Pain in calf
+C0236048	Gastric polyps
+C0236053	Mucosal ulcer
+C0236061	Haptoglobin increased
+C0236062	Haptoglobin decreased
+C0236065	Oedema mouth
+C0236068	Swollen tongue
+C0236071	Throat tightness
+C0236072	Bronchospasm paradoxical
+C0236073	Cerebellar infarction
+C0236075	Menopausal symptom
+C0236078	Pain in scrotum
+C0236082	Vaginal pain
+C0236099	Disorder of male reproductive system
+C0236116	SLE-like symptoms
+C0236124	Gastrointestinal obstruction
+C0236127	Esophageal ulceration haemorrhag
+C0236151	Renal function test abnormal
+C0236171	Infection susceptibility increased
+C0236175	Increased IgE level
+C0236178	Intra-abdominal haemorrhage
+C0236379	ESTRONE MEASUREMENT
+C0236642	Pick disease
+C0236656	Dementia associated with alcoholism
+C0236663	Alcohol withdrawal syndrome
+C0236664	Alcohol Related Disorders
+C0236688	Cocaine delirium
+C0236701	Cocaine-induced mood disorder
+C0236720	Flashback
+C0236733	Amphetamine-Related Disorders
+C0236734	Caffeine related disorders
+C0236735	Cannabis-Related Disorder
+C0236736	Cocaine-Related Disorders
+C0236742	Phencyclidine-Related Disorders
+C0236747	Mood disorder due to a general medical condition
+C0236780	Mixed bipolar I disorder
+C0236788	Bipolar II disorder
+C0236791	Childhood disintegrative disorder
+C0236792	Asperger Syndrome
+C0236795	Dissociative Amnesia
+C0236800	Panic disorder with agoraphobia
+C0236801	Phobia, Specific
+C0236804	Amphetamine Addiction
+C0236807	Amphetamine Abuse
+C0236811	Chronobiology Disorders
+C0236812	Feeding disorder of infancy or early childhood
+C0236816	Stress Disorders, Traumatic, Acute
+C0236818	Selective Mutism
+C0236826	Expressive language disorder
+C0236828	Articulation Disorders, Developmental
+C0236845	Breathing-related sleep disorder
+C0236848	Age-related cognitive decline
+C0236964	Attention Deficit and Disruptive Behavior Disorders
+C0236969	Substance-Related Disorders
+C0236970	Alcohol-Induced Disorders
+C0237020	Dermoid cyst of ovary
+C0237053	adnexal lesion
+C0237105	Emotional stability
+C0237123	Alcohol or Other Drugs use
+C0237304	Noisy respiration
+C0237313	Pulse deficit
+C0237314	Heart rate irregular
+C0237322	Skin turgor decreased
+C0237326	Dyschezia
+C0237653	Immunologic hypersensitivity
+C0237849	Peeling of skin
+C0237873	Physiological Sexual Disorders
+C0237938	Gastrointestinal ulcer
+C0237962	Retroperitoneal abscess
+C0237967	pediatric AIDS
+C0237987	Glucose-6-phosphate dehydrogenase deficiency anemia
+C0238002	Appendiceal abscess
+C0238003	Adenocarcinoma of appendix
+C0238013	Invasive aspergillosis
+C0238015	Autonomic Dysreflexia
+C0238019	Carcinoma of extrahepatic bile duct
+C0238027	Botulism, Infantile
+C0238029	Ependymoma of brain
+C0238031	Breast Phyllodes Tumor
+C0238033	Breast cancer male
+C0238034	Intraductal papilloma of breast
+C0238044	Concentric hypertrophic cardiomyopathy
+C0238049	Adult form of celiac disease
+C0238051	Cerebral Angiitis
+C0238052	Xanthomatosis, Cerebrotendinous
+C0238056	Chorea, Senile
+C0238062	Chronic intestinal pseudo-obstruction
+C0238065	Biliary Cirrhosis, Secondary
+C0238067	Colitis, Collagenous
+C0238074	Chronic pulmonary heart disease
+C0238075	Cranial Epidural Abscess
+C0238088	Diaphragmatic rupture
+C0238093	Duodenal stenosis
+C0238096	Embolism, Paradoxical
+C0238097	Cytomegalovirus encephalitis
+C0238106	Clostridium difficile colitis
+C0238111	Lennox Gastaut Syndrome
+C0238112	Herpes oesophagitis
+C0238113	Radiation oesophagitis
+C0238114	Leiomyoma of esophagus
+C0238115	Boerhaave syndrome
+C0238117	Eunuchism
+C0238122	Fallopian Tube Carcinoma
+C0238124	Necrotising fasciitis
+C0238132	Bronchopleural fistula
+C0238137	Gallbladder adenoma
+C0238141	Gingival Carcinoma
+C0238152	Cardiac Sarcoma
+C0238154	Extradural haematoma
+C0238156	Hematoma, Subdural, Intracranial
+C0238157	Benign hematuria
+C0238159	Hemoglobin E disease
+C0238183	Idiopathic atrophic hypothyroidism
+C0238190	Inclusion Body Myositis (disorder)
+C0238196	Small intestine carcinoma
+C0238198	Gastrointestinal Stromal Tumors
+C0238199	Volvulus of small bowel
+C0238207	Ectopic kidney
+C0238210	Malrotation of kidney
+C0238217	Kidney transplant rejection
+C0238224	Carcinoma of vocal cord
+C0238232	Polyp of larynx
+C0238239	Light chain disease
+C0238246	Haemangioma of liver
+C0238258	Lymphangitis carcinomatosa
+C0238261	Lymphedema praecox
+C0238265	Marchiafava-Bignami Disease
+C0238281	Middle Cerebral Artery Syndrome
+C0238284	Acute mountain sickness
+C0238286	Mucolipidosis Type IV
+C0238288	Muscular Dystrophy, Facioscapulohumeral
+C0238294	MYOCARDITIS, ACTIVE
+C0238298	Myxoedema coma
+C0238300	Stenosis of nasolacrimal duct
+C0238301	Cancer of Nasopharynx
+C0238304	Chronic interstitial nephritis
+C0238305	Sickle cell nephropathy
+C0238309	Ischaemic neuropathy
+C0238324	Ovarian Germ Cell Tumor
+C0238334	Pancreatic abscess
+C0238339	Hereditary pancreatitis
+C0238348	Squamous cell carcinoma of penis
+C0238357	Hyperkalemic periodic paralysis
+C0238358	Hypokalemic periodic paralysis
+C0238374	PITUITARY ADENOMA, NON-SECRETING
+C0238376	Pneumocephalus, Traumatic
+C0238378	Desquamative interstitial pneumonia
+C0238394	Female Pseudohermaphroditism
+C0238395	Male Pseudohermaphroditism
+C0238397	Pulmonary artery stenosis
+C0238399	Pulmonary lymphangiomyomatosis
+C0238402	Pycnodysostosis
+C0238410	Renal Pelvis Urothelial Carcinoma
+C0238418	Scrotal abscess
+C0238421	Selenium deficiency
+C0238425	Hemoglobin SS disease with crisis
+C0238434	Epidural Abscess, Spinal
+C0238436	Sternal fracture
+C0238441	Subglottic stenosis
+C0238448	Testicular embryonal carcinoma
+C0238451	Teratoma of testis
+C0238454	Cavernous sinus thrombosis
+C0238457	Renal vein thrombosis
+C0238461	Anaplastic thyroid cancer
+C0238462	Medullary carcinoma of thyroid
+C0238463	Papillary thyroid cancer
+C0238472	TOXOPLASMOSIS, CHRONIC
+C0238478	Transient erythroblastopenia of childhood
+C0238489	TUNGSTEN-CARBIDE DISEASE
+C0238502	Urethral prolapse
+C0238506	Congenital posterior urethral valves
+C0238517	Vaginal clear cell adenocarcinoma
+C0238518	Squamous cell carcinoma of the vagina
+C0238521	VENTRICULAR SEPTAL DEFECT, LARGE
+C0238525	Sarcoma of vulva
+C0238528	Infection by Yersinia enterocolitica
+C0238545	Right upper quadrant abdominal mass
+C0238551	Left lower quadrant pain
+C0238552	Left upper quadrant pain
+C0238569	Abdominal rebound tenderness
+C0238577	Abdominal wall defect
+C0238590	Acrogeria
+C0238591	Adactyly
+C0238614	Exposure to allergen
+C0238621	Aminoaciduria
+C0238634	Anal inflammation
+C0238637	Anal pain
+C0238644	Anemia, severe
+C0238650	ankle arthritis
+C0238651	Ankle clonus
+C0238656	Ankle pain
+C0238663	Antimitochondrial antibody positive
+C0238665	Antithrombin III decreased
+C0238669	Aortic root dilatation
+C0238694	Peripheral arthritis
+C0238705	Left atrial hypertrophy
+C0238729	Axillary mass
+C0238738	Spasm of back muscles
+C0238775	Bladder mass
+C0238790	bone destruction
+C0238792	Bone lesion
+C0238801	Bone marrow megaloblastic (finding)
+C0238844	Respiratory sounds decreased
+C0238874	Antineutrophil cytoplasmic antibody positive
+C0238990	Acute lower respiratory tract infection
+C0239043	Difficulty chewing
+C0239055	CHRONIC CRYPTOSPORIDIOSIS
+C0239062	Circumoral oedema
+C0239067	Difficulty walking up stairs
+C0239093	Conjunctival irritation
+C0239105	Conjunctival telangiectasis
+C0239113	Coombs test positive
+C0239119	Lenticonus
+C0239134	Productive cough
+C0239137	Coxa valga
+C0239138	Hip joint varus deformity - observation
+C0239154	High pitched cry
+C0239161	Dactylitis
+C0239174	Late tooth eruption
+C0239181	Intermittent diarrhea
+C0239182	Watery diarrhoea
+C0239211	Oedema auricular
+C0239233	Early satiety
+C0239234	Low set ears
+C0239266	Pain in elbow
+C0239281	Epiglottic oedema
+C0239293	Oesophageal haemorrhage
+C0239295	Candidiasis of the esophagus
+C0239296	Oesophageal obstruction
+C0239325	Extensor Rigidity
+C0239337	Deformity of limb
+C0239340	Edema of lower extremity
+C0239375	Numbness of limbs
+C0239377	Arm pain, NOS
+C0239399	Short extremities
+C0239454	Erythema of eyelid
+C0239479	Round face
+C0239488	Facial erythema
+C0239511	Numbness of face
+C0239548	Fasciculation of tongue
+C0239549	Fat intolerance
+C0239571	Fetor hepaticus
+C0239574	Low grade fever
+C0239576	Fibrin degradation products increased
+C0239589	Pain in finger
+C0239594	Short finger
+C0239598	Swelling of finger
+C0239649	Numbness of foot
+C0239676	High forehead
+C0239719	Genital erythema
+C0239725	Genital pain
+C0239729	Genital rash
+C0239735	Gingival erythema
+C0239739	Gingival pain
+C0239740	Gingivitis ulcerative
+C0239761	Gonadal hypoplasia
+C0239777	Color Blindness, Green
+C0239779	Grimacing
+C0239783	Groin pain
+C0239801	Blonde hair
+C0239803	Red hair
+C0239804	White hair
+C0239815	Hand clenching
+C0239816	Hand dermatitis
+C0239830	Hand muscle atrophy
+C0239831	Hand muscle weakness
+C0239832	Numbness of hand
+C0239833	Hand pain
+C0239842	Tremor of hands
+C0239849	Harlequin Fetus
+C0239882	Head tremor
+C0239888	Headache recurrent
+C0239894	HEART DISPLACEMENT
+C0239935	Haematocrit increased
+C0239937	Microscopic hematuria
+C0239941	Persistence of hemoglobin F
+C0239946	Fibrosis, Liver
+C0239948	Hepatitis A antibody positive
+C0239949	Hepatojugular reflux
+C0239954	Hip deformity NOS
+C0239978	Frequent bowel movements
+C0239981	Hypoalbuminaemia
+C0239984	Increased IgA level
+C0239989	IgM deficiency
+C0239998	Recurrent infections
+C0240007	Groin lump
+C0240017	Intercostal muscle weakness
+C0240059	Intraventricular haemorrhage
+C0240063	Coloboma of iris
+C0240066	Iron deficiency
+C0240083	Abnormal joint morphology
+C0240094	Joint tenderness
+C0240095	Joint warmth
+C0240116	Hyperactive patellar reflex
+C0240164	Squamous Papilloma of the Larynx
+C0240173	Shift to the left
+C0240182	Leukonychia
+C0240211	Lip swelling
+C0240223	Hepatic displacement
+C0240225	Hepatic mass
+C0240231	Fractures of the long bones
+C0240273	Tender lymph node
+C0240278	Lymphatic obstruction
+C0240302	Masseter Muscle Spasm
+C0240309	Hyperplasia of midface
+C0240310	Hypoplasia of the maxilla
+C0240318	Mediastinal mass
+C0240322	Menstruation delayed
+C0240327	Metallic taste
+C0240340	Microdontia (disorder)
+C0240352	Morning nausea
+C0240379	Open mouth (finding)
+C0240382	Mouth swelling
+C0240406	Murphy's sign positive
+C0240412	Muscle hematoma
+C0240414	Hypoplasia of muscle
+C0240417	Muscle mass
+C0240421	Progressive muscle weakness
+C0240444	Pachyonychia
+C0240449	Nasal sinus drainage
+C0240479	Neck muscle weakness
+C0240515	Nipple pain
+C0240521	Nipple tenderness
+C0240538	Convex nasal ridge
+C0240543	Bulbous nose
+C0240547	Deformity of the nose
+C0240595	Rotary Nystagmus
+C0240602	opioid use
+C0240608	Osler's node
+C0240611	Ovarian mass
+C0240621	Palatal oedema
+C0240635	Byzanthine arch palate
+C0240671	Activated partial thromboplastin time prolonged
+C0240679	Pelvic girdle muscle atrophy
+C0240682	Pelvic girdle pain
+C0240691	Mass of penis
+C0240698	Penile ulceration
+C0240701	Small penis
+C0240709	Pericardial constriction
+C0240717	Perineal pain
+C0240720	Perineal ulceration
+C0240733	Peroneal muscle weakness
+C0240735	Personality change
+C0240773	Plantar erythema
+C0240783	Increased circulating renin level
+C0240802	Pregnancy test positive
+C0240803	Primary cerebral lymphoma
+C0240805	Prodrome
+C0240811	Prostate infection
+C0240812	Prostatic pain
+C0240821	Pseudomembrane
+C0240822	Pseudoparalysis
+C0240840	Pulse pressure decreased
+C0240872	Rectal fissure
+C0240880	Rectoperineal fistula
+C0240896	Fundus coloboma
+C0240897	Retinal exudates
+C0240903	Rheumatoid Vasculitis
+C0240912	Vertical Talus
+C0240914	Romberg\'s sign positive
+C0240928	Salt craving
+C0240941	Pruritus of scalp
+C0240952	Dysarthria, Scanning
+C0240953	Winged scapula
+C0240972	Scrotal erythema
+C0240991	Ataxia, Sensory
+C0240995	Increased serum androstenedione
+C0240997	Decreased serum ceruloplasmin
+C0241005	Creatine phosphokinase serum increased
+C0241011	Low serum estradiol levels
+C0241012	Decreased serum ferritin
+C0241013	Increased serum ferritin
+C0241042	Shoulder stiff
+C0241054	Skin bullae
+C0241057	Burning sensation of skin
+C0241060	Cyst of skin
+C0241074	Hyperextensible skin
+C0241075	Induration of skin
+C0241128	Nikolsky sign
+C0241136	Pain of skin
+C0241144	Petechiae
+C0241148	Cutaneous plaque
+C0241157	pustule
+C0241158	Scar Tissue
+C0241165	Thick skin
+C0241166	Skin tightness
+C0241178	Velvety skin
+C0241181	Fragile skin
+C0241185	Smooth muscle antibodies positive
+C0241210	Speech Delay
+C0241235	Purulent sputum
+C0241237	Difficulty standing
+C0241240	Tall stature
+C0241254	Mucous stools
+C0241262	Strawberry tongue
+C0241266	Subcutaneous abscess
+C0241267	Absence of subcutaneous fat
+C0241310	Suprapubic pain
+C0241351	Testicular cyst
+C0241353	Testicular mass
+C0241355	Small testicle
+C0241358	Increased testosterone
+C0241390	Thrombin time prolonged
+C0241395	Spatulate thumbs
+C0241397	Triphalangeal thumb
+C0241416	Pain in toe
+C0241423	Atrophy of tongue
+C0241424	Tongue biting
+C0241426	Burning tongue
+C0241438	Tongue nodules
+C0241442	Protrusion of tongue
+C0241521	Ulnar deviation of hand
+C0241558	Urethral haemorrhage
+C0241577	Elevated urinary catecholamines
+C0241582	Culture urine positive
+C0241619	Vaginal cyst
+C0241633	Vaginal dryness
+C0241654	Abnormality of the heart valves
+C0241657	Abnormality of the vasculature
+C0241669	Venous occlusion
+C0241688	Peripheral visual field loss
+C0241697	Vitamin B12 decreased
+C0241698	Vitamin B12 increased
+C0241700	Voice Fatigue
+C0241703	High pitched voice
+C0241705	Strangury
+C0241706	Faecal vomiting
+C0241727	walking pain
+C0241729	Weight fluctuation
+C0241742	Wound haemorrhage
+C0241760	Wrist swelling
+C0241772	Reflex, Deep Tendon, Absent
+C0241775	Organic aciduria
+C0241790	Congenital pulmonary arteriovenous malformation
+C0241816	Global brain atrophy
+C0241831	Cerebral salt-wasting syndrome
+C0241832	Cerebrovascular Insufficiency
+C0241868	acute aortic dissection
+C0241873	Eczema impetiginous
+C0241876	Obstructive emphysema
+C0241880	Endometriosis of pelvis
+C0241883	Epstein-Barr virus antibody positive
+C0241902	Grunting
+C0241908	Hematuria, Benign Familial
+C0241910	Autoimmune Chronic Hepatitis
+C0241911	Chronic non-A non-B hepatitis
+C0241913	Halothane Hepatitis
+C0241932	X-linked hypogammaglobulinemia
+C0241934	Hypomania
+C0241950	Intestinal infarction
+C0241961	Angiomyolipoma of kidney
+C0241981	Impairment of balance
+C0241982	Bulla of lung
+C0241984	Honeycomb lung
+C0242006	Myelofibrosis due to another disorder
+C0242013	Sciatic Neuritis
+C0242032	Pancreatitis, Acute Edematous
+C0242036	Paraplegia, Ataxic
+C0242038	Juvenile Paresis
+C0242073	Pulmonary congestion
+C0242084	Ruptured cerebral aneurysm
+C0242089	Serology positive
+C0242129	Thrombotic stroke
+C0242147	Acute urinary tract infection
+C0242172	Pelvic Inflammatory Disease
+C0242183	Jaundice, Hemolytic
+C0242184	Hypoxia
+C0242186	Agrammatism
+C0242216	Biliary calculi
+C0242217	Calcium Pyrophosphate Dihydrate Deposition
+C0242225	Color blindness
+C0242231	Coronary Stenosis
+C0242287	Isaacs syndrome
+C0242292	McCune-Albright Syndrome
+C0242301	furuncle
+C0242338	HTLV Infections
+C0242339	Dyslipidemias
+C0242341	Sexual Infantilism
+C0242342	Sheehan Syndrome
+C0242343	Panhypopituitarism
+C0242350	Erectile dysfunction
+C0242354	Congenital Disorders
+C0242362	Disk, Herniated
+C0242363	Islet Cell Tumor
+C0242379	Lung neoplasm malignant
+C0242380	Libman-Sacks Disease
+C0242381	Lyme Arthritis
+C0242383	Age related macular degeneration
+C0242387	Mandibulofacial Dysostosis
+C0242404	Myofibroblastoma
+C0242420	Retinal Edema
+C0242422	Parkinsonian Disorders
+C0242423	Ramsay Hunt Paralysis Syndrome
+C0242426	Chylopericardium
+C0242429	Sore Throat
+C0242453	Prostatism
+C0242459	Loeffler\'s syndrome
+C0242461	Nonthrombocytopenic purpura NOS
+C0242473	Anus Prolapse
+C0242488	Acute Lung Injury
+C0242490	Enthesopathy
+C0242497	Intestinal schistosomiasis
+C0242510	Drug usage
+C0242513	Paroxysmal Reciprocal Tachycardia
+C0242514	Tachycardia, Reciprocating
+C0242520	Chronic thyroiditis
+C0242526	Gonadal Dysgenesis, 45,X
+C0242528	Azotaemia
+C0242551	Leprosy, Macular
+C0242552	Leprosy, Neural
+C0242567	Opsoclonus
+C0242583	Bare Lymphocyte Syndrome
+C0242584	Autoimmune thrombocytopenia
+C0242594	Residual Cancer
+C0242596	Neoplasm, Residual
+C0242597	Leukocyte-Adhesion Deficiency Syndrome
+C0242621	Isochromosomes
+C0242640	Multiple-drug resistance
+C0242644	Brown-Sequard syndrome
+C0242645	Blue toe syndrome
+C0242647	Lymphoma, B-Cell, Marginal Zone
+C0242656	Disease progression
+C0242666	Protein S Deficiency
+C0242669	Placenta, Retained
+C0242670	Persistent Vegetative State
+C0242684	Hypodynamia
+C0242698	Ventricular Dysfunction, Left
+C0242699	Bone Demineralization, Pathologic
+C0242700	Outerspace sickness
+C0242706	Hyperoxia
+C0242707	Right ventricular dysfunction
+C0242723	Parasitemia
+C0242770	BOOP
+C0242784	Food interaction
+C0242785	Food-Drug Interactions
+C0242786	High risk pregnancy
+C0242787	Malignant neoplasm of male breast
+C0242788	Breast Neoplasms, Male
+C0242852	Proliferative vitreoretinopathy
+C0242855	Congenital atresia of pulmonary valve
+C0242875	Interventricular septum rupture
+C0242891	Tooth Injuries
+C0242966	Systemic Inflammatory Response Syndrome
+C0242973	Ventricular Dysfunction
+C0242979	Muscle Fatigue
+C0242992	Multiple Chemical Sensitivity
+C0242993	Nephropathia Epidemica
+C0242994	Hantavirus Infections
+C0242997	Impotence, Arteriogenic
+C0242998	Impotence, Venogenic
+C0243000	Impotence, Vasculogenic
+C0243001	Abdominal Abscess
+C0243002	Congenital tricuspid valve atresia
+C0243010	Encephalitis viral
+C0243025	Hantavirus Pulmonary Syndrome
+C0243026	Sepsis
+C0243038	Carcinoma, Lewis Lung
+C0243050	Cardiovascular Abnormalities
+C0243057	Stomatognathic System Abnormalities
+C0243065	Aplasia
+C0243066	Atresia
+C0259743	Autosomal recessive SCID
+C0259744	dysproteinemia
+C0259749	Autonomic neuropathy
+C0259756	Jarisch-Herxheimer reaction
+C0259768	Wound dehiscence
+C0259770	Epithelial inclusion cyst
+C0259771	Steatocystoma multiplex
+C0259779	Fibrous Dysplasia
+C0259781	Compound nevus of skin
+C0259782	Telangiectatic osteosarcoma
+C0259783	mixed gliomas
+C0259785	Malignant Meningioma
+C0259786	Rhabdoid meningioma
+C0259799	Punctate keratitis
+C0259813	Drop Attack
+C0259817	Xerosis
+C0260037	Multiple tumors
+C0260662	Hearing problem
+C0260701	Dependence on respirator
+C0262361	Growth abnormality
+C0262365	Mammogram abnormal
+C0262374	Anal stenosis
+C0262376	anxiety generalized
+C0262380	Asymptomatic bacteriuria
+C0262385	Autonomic nervous system imbalance
+C0262393	Bladder prolapse
+C0262395	Borderline hypertension
+C0262397	Breast tenderness
+C0262401	Carcinoma of ampulla of Vater
+C0262404	Cerebellar degeneration
+C0262405	Cerebral dysfunction
+C0262407	cervical abnormality
+C0262414	Cervical vertebral fracture
+C0262421	Chronic urinary tract infection
+C0262424	CNS DEGENERATION
+C0262428	Collagen-vascular disease
+C0262431	Compression fracture of vertebral column
+C0262436	Cardiac valvular dysplasia, X-linked
+C0262444	Abnormality of the dentition
+C0262469	Embolic stroke
+C0262478	Wrinkled face
+C0262493	Gallbladder polyp
+C0262497	Global Amnesia
+C0262527	Intermittent abdominal pain
+C0262538	Ligament rupture
+C0262544	Lumbar vertebral fracture
+C0262564	Anterolateral Myocardial Infarction
+C0262565	Anteroseptal Myocardial Infarction
+C0262576	Nerve paralysis
+C0262578	Night cramps
+C0262584	Carcinoma, Small Cell
+C0262586	Osteopenia/osteoporosis
+C0262587	Parathyroid Adenoma
+C0262591	Pelvic adhesions
+C0262593	Peripheral Nerve Injuries
+C0262605	Presbyoesophagus
+C0262613	Renal mass
+C0262621	Abnormality of the sacroiliac joint
+C0262627	Seroma
+C0262630	Reduced concentration span
+C0262650	Abnormality of the thymus
+C0262655	Recurrent urinary tract infection
+C0262657	Uterine atrophy
+C0262659	Vagina Carcinoma
+C0262918	Extraocular muscle paresis
+C0262923	Protein urine
+C0262929	Cardiac myxoma
+C0262935	Brain Embolism
+C0262972	Acute dermatitis
+C0262974	Subacute dermatitis
+C0262975	Chronic dermatitis
+C0262977	Achromia of skin
+C0262984	Spongiotic dermatitis
+C0262985	Dermatitis psoriasiform
+C0262988	Cutaneous vasculitis
+C0263006	Perifolliculitis
+C0263008	Skin fibrosis
+C0263009	Sclerosis of the skin
+C0263011	Septal panniculitis
+C0263105	Abdominal wall abscess
+C0263107	Chest wall abscess
+C0263109	Groin abscess
+C0263111	Perineal abscess
+C0263218	Pyogenic granuloma of skin
+C0263222	Chronic eczema
+C0263224	Flexural atopic dermatitis
+C0263313	Pemphigus Foliaceus
+C0263314	Pemphigus and fogo selvagem
+C0263324	Erythema toxicum neonatorum
+C0263338	Chronic urticaria
+C0263347	Urticaria medicamentosa
+C0263352	Urticaria papular
+C0263353	Prurigo nodularis
+C0263355	Rash scarlatiniform
+C0263357	Erythema gyratum repens
+C0263361	Psoriasis vulgaris
+C0263367	Köbner phenomenon
+C0263370	Small plaque parapsoriasis
+C0263372	Gianotti-Crosti Syndrome
+C0263383	Keratosis pilaris
+C0263386	Ichthyosis acquired
+C0263390	Scleromyxedema
+C0263400	Segmental hyalinizing vasculitis
+C0263401	Cutis marmorata
+C0263402	Telangiectasia macularis eruptiva perstans
+C0263409	Linear Scleroderma
+C0263415	Actinic elastosis
+C0263417	Cutis verticis gyrata
+C0263419	Reactive perforating collagenosis
+C0263420	Hyperkeratosis lenticularis perstans
+C0263421	Acrodermatitis atrophicans chronica
+C0263428	Burnett Schwartz Berberian syndrome
+C0263429	Atrophoderma vermiculatum
+C0263437	Acne infantile
+C0263442	Acne Conglobata
+C0263443	Acne pustular
+C0263445	Acne fulminans
+C0263449	Dermatitis, Perioral
+C0263454	Chloracne
+C0263472	Bromhidrosis
+C0263473	Chromhidrosis
+C0263477	Female pattern alopecia (disorder)
+C0263485	Clastothrix
+C0263487	Trichostasis spinulosa
+C0263489	Pili annulati
+C0263490	Brittle hair
+C0263491	Pili Torti
+C0263492	Ingrown hair
+C0263498	Premature canities
+C0263504	Alopecia totalis
+C0263505	Alopecia universalis
+C0263519	Anagen effluvium
+C0263523	Micronychia (disorder)
+C0263530	Longitudinal split nail
+C0263532	Leukonychia punctata
+C0263534	Beau's lines
+C0263535	Muehrcke's lines
+C0263536	Hypertrophy of nail
+C0263537	Onychogryposis
+C0263538	Clubbing of nail
+C0263540	Onychomadesis
+C0263548	Pyramidal disease
+C0263560	Chronic ulcer of lower extremity
+C0263579	Pigmented hairy epidermal nevus
+C0263580	Ichthyosis hystrix
+C0263606	Early radiation dermatitis
+C0263625	Subcutaneous calcification
+C0263627	Calcinosis universalis
+C0263628	Tumoral calcinosis
+C0263630	Hypertrophic disorder of skin, unspecified
+C0263634	Excessive granulation tissue
+C0263641	Epithelial hyperplasia of skin
+C0263661	Disorder of skeletal system
+C0263662	Disseminated eosinophilic collagen disease
+C0263664	Generalized morphea
+C0263666	Dermatomyositis, Childhood Type
+C0263675	Chronic arthropathy
+C0263678	Acute arthritis
+C0263680	Chronic arthritis
+C0263725	Haemophilic arthritis
+C0263746	Osteoarthritis of the hand
+C0263776	Coxitis
+C0263779	Interphalangeal osteoarthritis
+C0263780	Bouchard's node
+C0263845	Articular calcification
+C0263859	Acquired Hyperostosis Syndrome
+C0263870	Intervertebral disc space narrowing
+C0263874	Degeneration of lumbar intervertebral disc
+C0263884	Cervical neuritis
+C0263888	Back disorder
+C0263898	Radiculitis lumbosacral
+C0263905	Atlantoaxial subluxation
+C0263907	Capsulitis
+C0263912	Rotator cuff syndrome
+C0263925	Iliac crest spur
+C0263945	Synovial disorders
+C0263946	Bursal disorders
+C0263949	Proliferative synovitis
+C0263962	Olecranon bursitis
+C0263976	Ligament disorders
+C0263978	Disorder of soft tissue
+C0263984	Polymyositis Ossificans
+C0263992	Exertional rhabdomyolysis (disorder)
+C0264000	Knuckle pads
+C0264009	Osteodystrophy
+C0264010	Hepatic osteodystrophy
+C0264080	Juvenile osteoporosis
+C0264097	Calcaneal apophysitis
+C0264112	Vertebral wedging
+C0264122	Atrophy, Disuse
+C0264133	Acquired flat foot
+C0264142	Spade-like hand
+C0264162	Camptocormia
+C0264169	Saddle nose
+C0264172	Barrel chest
+C0264184	Degenerative spondylolisthesis
+C0264219	Acute respiratory disease
+C0264220	Chronic disease of respiratory system
+C0264222	Acute upper respiratory infection
+C0264265	Nasal necrosis
+C0264267	Nasal ulcer
+C0264268	Nasal septum ulceration
+C0264292	Pharyngeal abscess
+C0264303	Laryngomalacia
+C0264308	Laryngeal ulceration
+C0264309	Vocal cord disorder NOS
+C0264314	Vocal cord inflammation
+C0264324	Calcification of trachea
+C0264344	Bronchitis bacterial
+C0264346	Fetid chronic bronchitis
+C0264352	Bronchial ulceration
+C0264353	Bronchomalacia
+C0264361	Traction bronchiectasis
+C0264362	Bronchocele
+C0264372	Bronchiolectasis
+C0264383	Organising pneumonia
+C0264393	Panacinar Emphysema
+C0264408	Childhood asthma
+C0264413	Asthma late onset
+C0264423	Asthma, Occupational
+C0264478	Sequoiosis
+C0264480	Bakers\' asthma
+C0264487	Chronic nonspecific lung disease
+C0264490	Acute respiratory failure
+C0264492	Chronic respiratory failure
+C0264511	Lymphoid interstitial pneumonia
+C0264515	Pneumonia necrotising
+C0264517	Pulmonary necrosis
+C0264523	Pulmonary ossification
+C0264541	Pleural calcification
+C0264542	Pleural adhesion
+C0264544	Adhesion of lung
+C0264545	Thickening of pleura
+C0264550	Pleural effusion associated with pulmonary infection
+C0264558	Tension Pneumothorax
+C0264573	Mediastinal fibrosis
+C0264576	Mediastinal shift
+C0264588	Spasmodic dysphonia
+C0264598	Spastic Aphonia
+C0264599	Aphonia Paralytica
+C0264600	Voice Disorder, Neurologic
+C0264609	Organic Tremor Dysphonia
+C0264611	Apraxia of Phonation
+C0264614	Hypernasality
+C0264618	Hyponasality syndrome
+C0264628	Mutism, Conversion
+C0264638	Low-renin essential hypertension
+C0264639	High-renin essential hypertension
+C0264641	Endocrine hypertension
+C0264652	Hypertensive heart failure
+C0264656	Cardiovascular renal disease
+C0264657	Renal sclerosis with hypertension
+C0264683	Coronary artery atheroma
+C0264684	Arteritis coronary
+C0264686	Coronary artery embolism
+C0264694	Chronic myocardial ischemia
+C0264695	Subendocardial ischaemia
+C0264714	Acute heart failure
+C0264716	Cardiac failure chronic
+C0264732	Cardiac dilatation
+C0264733	Dilatation ventricular
+C0264734	Atrial dilatation
+C0264757	Rheumatic disease of heart valve
+C0264766	Rheumatic mitral stenosis
+C0264774	Mitral and aortic incompetence
+C0264789	Familial cardiomyopathy
+C0264797	Dilated cardiomyopathy secondary to viral myocarditis
+C0264863	Subacute endocarditis
+C0264866	Endocarditis noninfective
+C0264878	Heart valve stenosis
+C0264879	Heart valve incompetence
+C0264882	Tricuspid valve disease NOS
+C0264885	Myxoid transformation of mitral valve
+C0264886	Conduction disorder
+C0264893	Nodal arrhythmia
+C0264897	Accessory Atrioventricular Bundle (disorder)
+C0264906	Atrioventricular block second degree
+C0264909	Defect conduction intraventricular
+C0264912	Left anterior fascicular block
+C0264913	Left posterior fascicular block
+C0264914	Bifascicular block
+C0264916	Bundle branch block bilateral
+C0264936	Secondary pulmonary hypertension
+C0264939	Systemic Vasculitis
+C0264941	Thromboangiitis
+C0264955	Idiopathic arterial calcification of infancy
+C0264956	Atheroma
+C0264963	Femoral artery aneurysm
+C0264969	Aneurysm of celiac artery
+C0264984	Arterial thrombosis (limbs)
+C0264992	Polyarteritis
+C0264995	Occlusion of artery (disorder)
+C0265000	Ischaemic ulcer
+C0265004	Aortic dilatation
+C0265010	Ruptured thoracic aortic aneurysm
+C0265012	Ruptured abdominal aortic aneurysm
+C0265026	Capillary thrombosis
+C0265031	Haemorrhoidal haemorrhage
+C0265050	Vena cava thrombosis
+C0265072	Inferior vena cava syndrome
+C0265097	Basilar Artery Stenosis
+C0265099	Basilar artery thrombosis
+C0265101	Carotid artery occlusion
+C0265103	Vertebral artery stenosis
+C0265104	Vertebral artery occlusion
+C0265110	Cerebral arteriospasm
+C0265113	Progressing stroke
+C0265116	Chronic cerebral ischemia
+C0265122	Disorder of pericardium
+C0265147	Infectious pericarditis
+C0265149	Purulent pericarditis
+C0265152	Pericarditis uraemic
+C0265191	Chronic acquired lymphedema
+C0265201	De Sanctis-Cacchione syndrome
+C0265202	Seckel syndrome
+C0265205	Robinow Syndrome
+C0265210	Weaver syndrome
+C0265211	Marshall-Smith syndrome
+C0265213	Distal arthrogryposis syndrome
+C0265215	Meckel-Gruber syndrome
+C0265216	X-linked hydrocephalus syndrome
+C0265218	Neu-Laxova syndrome
+C0265219	Miller Dieker syndrome
+C0265220	Pallister-Hall syndrome
+C0265221	Walker-Warburg congenital muscular dystrophy
+C0265222	Royer Syndrome
+C0265223	Cohen syndrome
+C0265224	Freeman-Sheldon syndrome
+C0265226	Hecht syndrome (disorder)
+C0265227	Schinzel-Giedion syndrome
+C0265233	Cryptophthalmos syndrome
+C0265234	Branchio-Oto-Renal Syndrome
+C0265235	Marshall syndrome
+C0265239	Wildervanck\'s syndrome
+C0265240	Goldenhar Syndrome
+C0265241	Franceschetti-Klein syndrome
+C0265242	Otocephaly
+C0265245	Nager syndrome
+C0265246	Townes syndrome
+C0265251	Oto-Palato-digital syndrome type 1
+C0265252	Coffin-Lowry syndrome
+C0265253	Stickler syndrome (disorder)
+C0265255	Trichorhinophalangeal syndrome
+C0265257	Genee-Wiedemann syndrome
+C0265259	Popliteal pterygium syndrome
+C0265260	Chondrodysplasia, Grebe type
+C0265261	Multiple pterygium syndrome
+C0265264	Holt-Oram syndrome
+C0265265	Aase syndrome
+C0265267	Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
+C0265268	Adams Oliver syndrome
+C0265269	Lacrimoauriculodentodigital syndrome
+C0265273	Achondrogenesis type 1A
+C0265274	Achondrogenesis, type IB (disorder)
+C0265275	Jeune thoracic dystrophy
+C0265279	Kniest dysplasia
+C0265280	Spondylometaphyseal dysplasia, Kozlowski type
+C0265281	Metatropic dwarfism
+C0265282	Fibrochondrogenesis
+C0265283	Atelosteogenesis, type 1
+C0265286	Dyggve-Melchior-Clausen syndrome
+C0265287	Acromicric Dysplasia
+C0265289	Metaphyseal chondrodysplasia Schmid type
+C0265290	Metaphyseal chondrodysplasia
+C0265291	Kenny-Caffey syndrome
+C0265292	Schwartz-Lelek syndrome
+C0265293	Frontometaphyseal dysplasia
+C0265294	Metaphyseal dysplasia
+C0265295	Jansen type metaphyseal chondrodysplasia
+C0265301	Sclerosteosis
+C0265306	Greig cephalopolysyndactyly syndrome
+C0265308	Baller-Gerold syndrome
+C0265309	Leri-Weill dyschondrosteosis
+C0265312	Brachydactyly syndrome type E
+C0265313	Weill-Marchesani syndrome
+C0265316	Neurocutaneous Syndromes
+C0265319	Fibrous skin tumor of tuberous sclerosis
+C0265323	Peutz-Jeghers polyps of small bowel
+C0265325	Turcot syndrome (disorder)
+C0265326	Bannayan-Riley-Ruvalcaba Syndrome
+C0265329	Organoid Nevus Phakomatosis
+C0265331	Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
+C0265333	Tricho-dento-osseous syndrome (disorder)
+C0265334	Pachyonychia Congenita
+C0265336	Senter syndrome
+C0265338	Coffin-Siris syndrome
+C0265339	Borjeson-Forssman-Lehmann syndrome
+C0265341	Rieger syndrome
+C0265342	Cerebrocostomandibular Syndrome
+C0265343	Jarcho-Levin syndrome
+C0265344	Donohue Syndrome
+C0265345	Lymphedema distichiasis syndrome
+C0265354	CHARGE Syndrome
+C0265357	Polysplenia Syndrome
+C0265363	Urethral obstruction sequence
+C0265372	Fetal hydantoin syndrome
+C0265374	Warfarin syndrome
+C0265449	Pallister-Killian syndrome
+C0265479	Chromosome 20, trisomy
+C0265490	Trisomy 22
+C0265493	Cat eye syndrome
+C0265499	49,XXXXY Syndrome
+C0265509	Congenital anomaly of skeletal bone
+C0265513	Osteopathia striata
+C0265514	Dermatofibrosis lenticularis disseminata
+C0265529	Plagiocephaly
+C0265534	Scaphycephaly
+C0265535	Trigonocephaly
+C0265541	Cranioschisis
+C0265547	Limb reduction defect
+C0265551	Dimelia
+C0265552	Congenital macrodactylia
+C0265553	Polysyndactyly
+C0265554	Ectrodactyly
+C0265559	Acheiropodia
+C0265563	Congenital dislocation of radial head
+C0265573	Phocomelia of upper limb
+C0265581	Longitudinal deficiency of radius
+C0265593	Brachymetacarpia
+C0265594	Congenital absence of hand
+C0265596	Talipomanus
+C0265598	Manus vara
+C0265604	Mirror hands
+C0265609	Accessory carpal bones
+C0265610	Congenital clinodactyly
+C0265633	Congenital absence of tibia
+C0265635	Fibula agenesis
+C0265642	Talipes Equinovalgus
+C0265646	Talipes Calcaneovarus
+C0265654	Tarsal Coalition
+C0265656	Congenital hallux valgus
+C0265660	Syndactyly of the toes
+C0265669	Congenital dislocation of knee
+C0265673	Congenital kyphosis
+C0265677	Congenital hemivertebra
+C0265681	Supernumerary vertebra
+C0265695	Congenital fusion of ribs
+C0265696	Sternum bifidum
+C0265699	Congenital hernia of foramen of Morgagni
+C0265700	Congenital hernia of foramen of Bochdalek
+C0265706	Gastroschisis
+C0265736	Congenital anomaly of nose
+C0265740	Arrhinia
+C0265747	Congenital atresia of nasopharynx
+C0265756	Congenital atresia of larynx
+C0265766	Congenital atresia of trachea
+C0265780	Congenital absence of lung
+C0265783	Congenital hypoplasia of lung
+C0265797	Congenital emphysema
+C0265807	Acyanotic congenital heart disease
+C0265808	Cyanotic congenital heart disease
+C0265830	Anomalies of pulmonary valve, congenital
+C0265843	Congenital atresia of aortic valve
+C0265856	Hypoplasia of right heart
+C0265857	Uhl anomaly
+C0265865	Mesocardia
+C0265878	Preductal coarctation of aorta
+C0265881	Congenital hypoplasia of aortic arch
+C0265886	Overriding aorta
+C0265890	Congenital aortic stenosis
+C0265892	Aorta hypoplasia
+C0265905	Agenesis of pulmonary artery
+C0265908	Congenital atresia of pulmonary artery
+C0265910	Congenital hypoplasia of pulmonary artery
+C0265911	Pulmonary artery stenosis congenital
+C0265914	Anomalous pulmonary vein
+C0265916	Anomalous pulmonary venous drainage
+C0265931	Persistent left superior vena cava
+C0265935	Congenital arterial malformation
+C0265950	Venous malformation
+C0265961	Erythrokeratodermia variabilis
+C0265962	Ichthyosis linearis circumflexa
+C0265964	Mutilating keratoderma
+C0265965	Dyskeratosis Congenita
+C0265970	Porokeratosis, Disseminated Superficial Actinic
+C0265971	Acrokeratosis Verruciformis of Hopf
+C0265973	Vascular hamartoma of skin
+C0265974	Birthmark
+C0265978	Collagen nevus of skin
+C0265979	Fibrous Hamartoma of Infancy
+C0265985	Mongolian Spot
+C0265987	Nevus comedonicus
+C0265988	Congenital accessory skin tag
+C0265989	Congenital scar
+C0265991	Congenital hair disorder NOS
+C0265992	alopecia congenita
+C0265997	Congenital nail disorder
+C0265998	ANONYCHIA
+C0266003	Subungual fibroma
+C0266004	Knuckle pads, leuconychia and sensorineural deafness
+C0266006	Pili torti-deafness syndrome
+C0266009	Congenital absence of breast
+C0266011	Accessory nipple
+C0266013	Congenital hypoplasia of breast
+C0266015	Congenital digestive system anomalies
+C0266025	Ectopic tooth
+C0266034	Dens evaginatus
+C0266036	Macrodontia
+C0266037	Peg-shaped teeth
+C0266039	Taurodontism
+C0266050	Failure of exfoliation of primary tooth
+C0266052	Precocious exfoliation of primary tooth
+C0266054	Premature tooth eruption
+C0266060	Anterior open bite
+C0266061	Open Bite
+C0266063	Deep overbite
+C0266067	Posterior lingual occlusion of mandibular teeth
+C0266077	Mandibular retrognathism
+C0266081	Congenital maxillary hyperplasia
+C0266092	Congenital lip pits
+C0266111	Bifid tongue
+C0266121	Congenital absence of uvula
+C0266122	Cleft uvula
+C0266142	Congenital gastric anomaly
+C0266150	Congenital microgastria
+C0266153	Ectopic gastric tissue
+C0266159	Pyloric Atresia
+C0266166	Congenital duplication of intestine
+C0266174	Duodenal atresia
+C0266175	Jejunal Atresia
+C0266184	Congenital duodenal obstruction due to malrotation of intestine
+C0266196	Malrotation of colon
+C0266200	Microcolon
+C0266215	Anorectal atresia
+C0266225	Persistent cloaca
+C0266231	Ectopic anus
+C0266239	Congenital anomaly of bile ducts
+C0266249	Gallbladder anomaly congenital
+C0266251	Gallbladder, Agenesis Of
+C0266258	Congenital absence of liver
+C0266267	Congenital hypoplasia of pancreas
+C0266270	Pancreas divisum
+C0266273	Congenital absence of adrenal gland
+C0266275	Ectopic adrenal gland
+C0266276	Ectopic adrenal cortex
+C0266283	Ectopic thyroid tissue (disorder)
+C0266284	Lingual Thyroid
+C0266292	Congenital anomaly of the kidney
+C0266294	Unilateral agenesis of kidney
+C0266295	Congenital hypoplasia of kidney
+C0266298	Accessory kidney
+C0266304	Double kidney (disorder)
+C0266305	Fused Kidney
+C0266313	Allanson Pantzar McLeod syndrome
+C0266316	Congenital hydronephrosis
+C0266319	Congenital ureteric anomaly NOS
+C0266320	Impervious ureter
+C0266324	Congenital dilatation of ureter
+C0266335	Congenital bladder anomaly NOS
+C0266336	Bladder agenesis
+C0266345	Congenital urethral valve
+C0266357	Persistent umbilical sinus
+C0266360	Streak gonad
+C0266361	True Hermaphroditism (disorder)
+C0266362	Ambiguous Genitalia
+C0266365	Congenital genital malformation female
+C0266368	Congenital absence of ovary
+C0266371	Streak ovary
+C0266383	Uterine Anomalies
+C0266387	Bicornuate uterus
+C0266393	Congenital duplication of uterus
+C0266399	Infantile uterus
+C0266411	Septate vagina
+C0266423	Congenital anomaly of testis
+C0266427	Testicular regression syndrome
+C0266429	Monorchism
+C0266432	Leydig cell agenesis
+C0266435	Congenital hypoplasia of penis
+C0266444	Congenital absence of vas deferens
+C0266445	Congenital atresia of vas deferens
+C0266449	Brain malformation
+C0266452	Hemicephaly
+C0266453	Exencephaly
+C0266456	Meningoencephalocele
+C0266461	Congenital absence of part of brain
+C0266462	Congenital hypoplasia of part of brain
+C0266463	Lissencephaly
+C0266464	Polymicrogyria
+C0266468	Congenital pontocerebellar hypoplasia
+C0266470	Cerebellar Hypoplasia
+C0266476	Congenital stenosis of aqueduct of Sylvius
+C0266480	Congenital cerebral cyst
+C0266483	Pachygyria
+C0266484	Schizencephaly
+C0266487	Etat Marbre
+C0266491	Neuronal heterotopia
+C0266501	Spina bifida of cervical region
+C0266508	Rachischisis
+C0266521	Marcus Gunn phenomenon
+C0266524	Dysplasia of eye
+C0266525	Irido-corneal dysgenesis
+C0266526	Norrie disease
+C0266527	Hypoplasia of eye
+C0266537	Congenital lamellar cataract
+C0266539	Congenital total cataract
+C0266541	Microphakia
+C0266543	Persistent tunica vasculosa lentis
+C0266544	Microcornea
+C0266548	Axenfeld anomaly (disorder)
+C0266551	Congenital coloboma of iris
+C0266559	Persistent primary vitreous
+C0266564	Congenital anomaly of retina
+C0266566	Optic disc structural anomaly
+C0266568	Persistent Hyperplastic Primary Vitreous
+C0266571	Congenital retinal aneurysm
+C0266572	Congenital anomaly of eyelid
+C0266573	Congenital ptosis
+C0266574	Ablepharon
+C0266589	Congenital ear anomaly NOS (disorder)
+C0266597	External auditory canal atresia
+C0266604	Congenital aplasia of inner ear
+C0266610	Preauricular dimple
+C0266611	Accessory auricle
+C0266614	Bat ear
+C0266617	Congenital anomaly of face
+C0266619	Potter\'s facies
+C0266623	Congenital anomaly of neck
+C0266625	Congenital preauricular sinus
+C0266631	Accessory spleen
+C0266632	Ectopic spleen
+C0266642	Situs ambiguus
+C0266647	Congenital anomalies of fetus
+C0266648	Blighted ovum
+C0266652	Abnormal fetus
+C0266667	Cyclocephaly
+C0266672	Amyelencephalus
+C0266677	Synotus
+C0266692	Craniopagus
+C0266717	Acardius
+C0266752	Twin placenta
+C0266765	Placenta Increta
+C0266766	Placenta Percreta
+C0266781	Abnormal amniotic fluid
+C0266782	Abnormal yolk sac
+C0266785	Umbilical cord abnormality NOS
+C0266786	Short cord
+C0266798	Compression of umbilical cord
+C0266807	Acute gastrointestinal hemorrhage
+C0266808	Chronic gastrointestinal bleeding
+C0266813	Fecal occult blood: positive
+C0266815	Cow milk allergy
+C0266833	Visceral Myopathy, Familial
+C0266836	Infantile Colic
+C0266858	Tooth decalcification
+C0266919	Epulides
+C0266928	Rapidly progressive periodontitis
+C0266929	Chronic Periodontitis
+C0266941	Derangement of temporomandibular joint
+C0266963	Abscess jaw
+C0266981	Torus palatinus
+C0266985	Resorption of mandible
+C0266998	Oral soft tissue disorder
+C0266999	Vesicular Stomatitis
+C0267000	Pyostomatitis vegetans
+C0267003	Abscess oral
+C0267008	Erythroplakia of mouth
+C0267026	Actinic cheilitis
+C0267028	Lip pain
+C0267033	Lip ulceration
+C0267048	Glossoptosis
+C0267055	Erosive esophagitis
+C0267071	Oropharyngeal Dysphagia
+C0267072	Esophageal Dysphagia
+C0267094	Oesophagobronchial fistula
+C0267096	Oesophageal injury
+C0267111	Gastric dysplasia
+C0267112	Acute gastric mucosal erosion
+C0267158	Reflux gastritis
+C0267166	Gastroduodenitis
+C0267176	Diabetic gastroparesis
+C0267187	Intestinal metaplasia of gastric mucosa
+C0267209	Gastric varices haemorrhage
+C0267211	Gastric Antral Vascular Ectasia
+C0267356	Duodenal perforation
+C0267370	Angiodysplasia of colon
+C0267373	Intestinal haemorrhage
+C0267375	Chronic colitis
+C0267380	Crohn\'s disease of the ileum
+C0267407	Mesenteric artery embolism
+C0267410	Thrombosis mesenteric artery
+C0267412	Mesenteric Venous Thrombosis
+C0267437	Allergic diarrhea
+C0267442	Gastroenteritis radiation
+C0267446	Acute gastroenteritis
+C0267448	Eosinophilic colitis
+C0267456	Villous atrophy of intestine
+C0267465	Intestinal stenosis
+C0267466	Colonic stricture
+C0267489	Jejunal ulcer
+C0267491	Large intestinal ulcer
+C0267493	Intestinal prolapse
+C0267537	Caecitis
+C0267541	Typhlocolitis
+C0267548	Ileocolic intussusception
+C0267556	Osmotic diarrhea
+C0267557	Secretory diarrhea
+C0267561	Perianal fistula
+C0267566	Perirectal abscess
+C0267581	Rectal stenosis
+C0267596	Rectal haemorrhage
+C0267613	Appendix disorder NOS
+C0267662	Congenital chloride diarrhea
+C0267663	Congenital secretory diarrhea, sodium type (disorder)
+C0267716	Incisional hernia
+C0267725	Paraesophageal hernia
+C0267750	Acute peritonitis
+C0267756	Peritoneal abscess
+C0267770	Retractile Mesenteritis
+C0267771	Retroperitoneal mass
+C0267778	Adhesion of intestine
+C0267785	Leiomyomatosis peritonealis disseminata
+C0267792	Hepatobiliary disease
+C0267797	Acute hepatitis
+C0267809	Cirrhosis, Cryptogenic
+C0267812	Micronodular cirrhosis
+C0267818	Bile duct proliferation
+C0267821	Hepatic congestion
+C0267834	Hepatic cyst NOS
+C0267839	Hepatic amyloidosis
+C0267841	Acalculous Cholecystitis
+C0267869	Bile duct stone
+C0267898	Cholecystoduodenal Fistula
+C0267917	Acute cholangitis
+C0267918	Chronic cholangitis
+C0267924	Cholangitis suppurative
+C0267925	Bile duct stenosis
+C0267937	Acute recurrent pancreatitis
+C0267940	Pancreatitis haemorrhagic
+C0267941	Pancreatitis necrotising
+C0267951	Pancreatolithiasis
+C0267952	Fibrosis of pancreas
+C0267953	Necrosis of pancreas
+C0267954	Peripancreatic Fat Necrosis
+C0267963	Exocrine pancreatic insufficiency
+C0267964	Pancreatic acinar atrophy
+C0267971	Storage disease
+C0267988	Hyperproteinaemia
+C0267990	Adult-onset obesity
+C0268000	Body fluid retention
+C0268005	Hyposmolality syndrome
+C0268009	Hyperosmolality
+C0268016	Chronic hypokalemia
+C0268023	Chronic hyperkalemia
+C0268024	Hyperkalemia, diminished renal excretion
+C0268031	Compensated acidosis
+C0268059	Neonatal hemochromatosis
+C0268060	Juvenile hemochromatosis
+C0268066	Hepatic hemosiderosis
+C0268070	Hypocupremia
+C0268074	Indian childhood cirrhosis
+C0268079	Hyperphosphaturia
+C0268080	Hypercalcemia, Idiopathic, of Infancy
+C0268090	Manganese deficiency
+C0268095	Keshan disease
+C0268104	Disorder of purine metabolism
+C0268108	Chronic gouty arthritis
+C0268109	Chronic tophaceous gout
+C0268113	Familial juvenile gout
+C0268117	Gout, HPRT-Related
+C0268118	Xanthinuria, Type I
+C0268119	Combined molybdoflavoprotein enzyme deficiency
+C0268120	Adenine phosphoribosyltransferase deficiency
+C0268121	APRT deficiency, Japanese type
+C0268123	Muscle AMP deaminase deficiency
+C0268124	Adenosine deaminase deficiency
+C0268125	Purine-nucleoside phosphorylase deficiency
+C0268126	Adenylosuccinate lyase deficiency (disorder)
+C0268128	Orotic aciduria
+C0268130	Hereditary orotic aciduria, type 1
+C0268134	DNA Repair-Deficiency
+C0268135	Xeroderma pigmentosum, group A
+C0268136	Xeroderma pigmentosum, group B
+C0268138	Xeroderma Pigmentosum, Complementation Group D
+C0268140	Xeroderma pigmentosum, group F
+C0268141	Xeroderma pigmentosum, group G
+C0268146	Glucose-6-phosphate transport defect
+C0268147	Glycogen storage disease, type IX
+C0268149	Glycogen storage disease type X
+C0268151	Classical galactosemia
+C0268152	Classical galactosemia, homozygous Duarte-type
+C0268155	Deficiency of galactokinase
+C0268157	Galactosuria
+C0268160	Deficiency of fructokinase
+C0268162	Pentosuria
+C0268164	Primary hyperoxaluria, type I
+C0268165	Primary hyperoxaluria type 2
+C0268179	Lactase Deficiency, Congenital
+C0268181	Lactose Intolerance, Adult Type
+C0268186	Congenital glucose-galactose malabsorption
+C0268187	alpha, alpha-Trehalase deficiency
+C0268193	NADH cytochrome B5 reductase deficiency
+C0268194	Phosphoenolpyruvate carboxykinase deficiency
+C0268197	Familial lipoprotein deficiency
+C0268199	Familial apolipoprotein C-II deficiency
+C0268221	Fucosidosis Type I
+C0268222	Fucosidosis Type II
+C0268225	Aspartylglucosaminuria
+C0268226	Type I Mucolipidosis
+C0268228	Neuraminidase 1 deficiency
+C0268233	GALACTOSIALIDOSIS
+C0268237	Cytochrome-c Oxidase Deficiency
+C0268238	Triglyceride storage disease with ichthyosis
+C0268240	Pancreatic triacylglycerol lipase deficiency
+C0268241	Pancreatic colipase deficiency
+C0268242	Niemann-Pick Disease, Type A
+C0268243	Niemann-Pick Disease, Type B
+C0268247	Niemann-Pick Disease, Type D
+C0268248	Niemann-Pick Disease, Type E
+C0268250	Gaucher Disease, Type 2 (disorder)
+C0268251	Gaucher Disease, Type 3 (disorder)
+C0268252	Late-Onset Globoid Cell Leukodystrophy
+C0268255	Farber Lipogranulomatosis
+C0268262	Metachromatic Leukodystrophy due to Saposin B Deficiency
+C0268263	Multiple Sulfatase Deficiency Disease
+C0268271	Gangliosidosis, Generalized GM1, Type 1 (disorder)
+C0268272	Gangliosidosis, Generalized GM1, Type 2
+C0268273	Gangliosidosis, Generalized GM1, Type 3
+C0268274	Gangliosidoses, GM2
+C0268275	Tay-Sachs Disease, AB Variant
+C0268276	Juvenile GM 2 gangliosidosis
+C0268278	Infantile GM 2 gangliosidosis
+C0268279	Lipofuscinosis
+C0268281	Infantile neuronal ceroid lipofuscinosis
+C0268285	Adrenal hyperplasia, congenital, type 5
+C0268287	Deficiency of steroid 21-monooxygenase
+C0268288	Mild steroid 21-hydroxylase deficiency
+C0268290	Severe steroid 21-hydroxylase deficiency
+C0268292	Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
+C0268293	Corticosterone Methyl Oxidase Type I Deficiency
+C0268296	17-Hydroxysteroid Dehydrogenase Deficiency
+C0268297	Pseudovaginal Perineoscrotal Hypospadias
+C0268301	Reifenstein Syndrome
+C0268306	Unconjugated hyperbilirubinemia
+C0268307	Conjugated hyperbilirubinemia
+C0268312	Progressive intrahepatic cholestasis (disorder)
+C0268314	Cholestasis-edema syndrome, Norwegian type
+C0268318	Cholestasis of pregnancy
+C0268322	Chester-type porphyria
+C0268323	Familial porphyria cutanea tarda
+C0268328	Porphobilinogen synthase deficiency
+C0268335	Ehlers-Danlos syndrome type 1
+C0268336	Ehlers-Danlos syndrome type 2
+C0268337	Ehlers-Danlos syndrome, type 3 (disorder)
+C0268338	Ehlers-Danlos Syndrome, Type IV
+C0268341	Ehlers-Danlos syndrome type 5
+C0268342	Ehlers-Danlos syndrome type 6
+C0268344	Ehlers-Danlos syndrome 6B
+C0268345	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE
+C0268347	Ehlers-Danlos Syndrome, Type VIII
+C0268349	Joint laxity, familial
+C0268350	Cutis Laxa, Autosomal Dominant
+C0268351	Cutis Laxa, Autosomal Recessive, Type I
+C0268353	Cutis laxa, x-linked
+C0268354	De Barsy syndrome
+C0268355	Cutis Laxa, Autosomal Recessive, Type IIA
+C0268356	Osteogenesis imperfecta with blue sclerae AND normal teeth
+C0268357	Osteogenesis imperfecta, type 1A
+C0268358	Osteogenesis imperfecta, dominant perinatal lethal
+C0268360	Osteogenesis imperfecta, recessive perinatal lethal
+C0268362	Osteogenesis imperfecta type III (disorder)
+C0268363	Osteogenesis imperfecta type IV (disorder)
+C0268365	Marfanoid hypermobility syndrome
+C0268371	Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
+C0268374	Adult junctional epidermolysis bullosa (disorder)
+C0268375	Autosomal dominant epidermolysis bullosa simplex
+C0268379	Pseudocholinesterase deficiency
+C0268380	Systemic amyloidosis
+C0268381	Primary amyloidosis
+C0268382	Amyloid nephropathy
+C0268383	Familial amyloid polyneuropathy, type VI
+C0268384	Familial Amyloid Neuropathy, Portuguese Type
+C0268385	Familial Amyloid Polyneuropathy, Jewish Type
+C0268386	Amyloid Polyneuropathy, Swiss Type
+C0268389	Amyloidosis, familial visceral
+C0268390	Muckle-Wells Syndrome
+C0268392	Localized amyloidosis
+C0268393	Familial Cerebral Amyloid Angiopathy
+C0268397	Amyloidosis, Primary Cutaneous
+C0268398	Familial lichen amyloidosis
+C0268405	Hemodialysis-associated amyloidosis
+C0268406	Age-related amyloidosis
+C0268407	Cardiac amyloidosis
+C0268410	Acid Phosphatase Deficiency
+C0268412	Infantile hypophosphatasia
+C0268413	Adult hypophosphatasia (disorder)
+C0268414	Hyperphosphatasemia with bone disease
+C0268416	Enterokinase Deficiency
+C0268417	Pancreatic trypsinogen deficiency
+C0268418	Deficiency of glycerol kinase
+C0268419	Acatalasia
+C0268425	Alstrom Syndrome
+C0268435	Renal Tubular Acidosis, Type II
+C0268436	Pseudohypoaldosteronism, Type I
+C0268443	Acquired Nephrogenic Diabetes Insipidus
+C0268445	Normokalemic Periodic Paralysis
+C0268446	Thyrotoxic periodic paralysis
+C0268448	Primary hypomagnesemia (disorder)
+C0268450	Gitelman Syndrome
+C0268451	Manz syndrome
+C0268463	Persistent hyperphenylalaninemia
+C0268464	Transient hyperphenylalaninemia
+C0268465	Phenylketonuria II
+C0268467	Hyperphenylalaninemia, BH4-Deficient, B
+C0268468	Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency
+C0268474	Hydroxykynureninuria
+C0268483	Tyrosinemias
+C0268486	Hereditary hypertyrosinemia
+C0268487	Tyrosine Transaminase Deficiency Disease
+C0268490	Tyrosinemia, Type I
+C0268493	Ochronotic arthritis
+C0268494	Oculocutaneous albinism type 1
+C0268495	Oculocutaneous albinism type 2
+C0268497	Brown oculocutaneous albinism
+C0268500	Yellow mutant oculocutaneous albinism
+C0268503	Autosomal recessive ocular albinism
+C0268505	Ocular albinism, type II
+C0268514	Urocanase deficiency
+C0268523	Glutamate-cysteine ligase deficiency
+C0268524	gamma-Glutamyltransferase deficiency
+C0268525	5-oxoprolinase deficiency
+C0268528	Hyperprolinemia
+C0268529	Proline dehydrogenase deficiency
+C0268531	Hydroxyprolinemia
+C0268532	Deficiency of prolidase
+C0268534	Prolinuria
+C0268540	HHH syndrome
+C0268542	Ornithine carbamoyltransferase deficiency
+C0268543	Hyperammonemia, type III
+C0268547	Argininosuccinic Aciduria
+C0268548	Hyperargininemia
+C0268553	Hyperlysinemias
+C0268555	Hyperlysinemia, Periodic
+C0268556	Saccharopinuria
+C0268559	Hyperglycinemia
+C0268560	Hyperglycinemia, Transient Neonatal
+C0268561	Hyperglycinemia, Nonketotic, Type I
+C0268562	Hyperglycinemia, Nonketotic, Type II
+C0268563	Sarcosinemia
+C0268568	Classic Maple Syrup Urine Disease
+C0268569	Intermittent Maple Syrup Urine Disease
+C0268573	Valinemia
+C0268574	Hyperleucine-Isoleucinemia
+C0268575	Isovaleryl-CoA dehydrogenase deficiency
+C0268576	Hyperleucinemia
+C0268579	Propionic acidemia
+C0268581	Holocarboxylase Synthetase Deficiency
+C0268583	Methylmalonic acidemia
+C0268594	Glutaric aciduria
+C0268595	Glutaric aciduria, type 1
+C0268596	Multiple Acyl Coenzyme A Dehydrogenase Deficiency
+C0268600	3-methylcrotonyl CoA carboxylase 1 deficiency
+C0268601	HMG CoA lyase deficiency
+C0268603	Acetyl-CoA: carboxylase deficiency
+C0268608	Deficiency of dihydrofolate reductase
+C0268609	Glutamate formiminotransferase deficiency
+C0268611	Arakawa syndrome 2
+C0268613	Disorder of sulfur-bearing amino acid metabolism
+C0268615	5,10-Methylenetetrahydrofolate reductase deficiency
+C0268616	Gamma-cystathionase deficiency
+C0268617	Homocystinaemia
+C0268618	Cystathioninemia
+C0268621	Hepatic methionine adenosyltransferase deficiency
+C0268623	Tyrosinemia, Type III
+C0268624	Sulfite oxidase deficiency
+C0268626	Juvenile nephropathic cystinosis (disorder)
+C0268630	Hyper-beta-alaninemia
+C0268631	succinic semialdehyde dehydrogenase deficiency
+C0268632	Homocarnosinosis
+C0268634	Disorder of fatty acid metabolism
+C0268635	Acyl-CoA dehydrogenase deficiency
+C0268641	Amino acid transport disorder
+C0268642	Histidinuria renal tubular defect
+C0268643	Cystinuria type 1
+C0268645	Cystinuria, type 3
+C0268646	Isolated cystinuria
+C0268647	Lysinuric Protein Intolerance
+C0268654	Iminoglycinuria
+C0268689	Vitamin D-dependent rickets, type 1
+C0268707	Uraemic encephalopathy
+C0268709	Renal tubular defect
+C0268731	Glomerulonephropathy
+C0268732	Nephritic syndrome
+C0268733	Acute nephritis
+C0268734	Acute nephropathy
+C0268742	Membranoproliferative Glomerulonephritis, Type I
+C0268743	Membranoproliferative Glomerulonephritis, Type II
+C0268747	Diffuse mesangial sclerosis (disorder)
+C0268749	Fibrillary glomerulonephritis
+C0268750	Necrotizing glomerulonephritis
+C0268757	SLE glomerulonephritis syndrome, WHO class IV
+C0268784	Myeloma kidney
+C0268785	Salt-losing nephropathy
+C0268790	Renal vascular disorder
+C0268796	Arteriolar nephrosclerosis
+C0268799	Acquired renal cystic disease
+C0268800	Simple renal cyst
+C0268837	Cystitis glandularis
+C0268842	Colovesical Fistula
+C0268849	Overactive Detrusor
+C0268855	Bladder hypertrophy
+C0268875	Urethrorectal fistula
+C0268889	Prostatic obstruction
+C0268891	Prostatic haemorrhage
+C0268919	Scrotal disorder NOS
+C0268936	Scrotal haematoma
+C0269002	Penile haemorrhage
+C0269011	Increased size of penis
+C0269018	Penis deviation
+C0269035	Ovarian abscess
+C0269050	Endomyometritis
+C0269062	Chronic cervicitis
+C0269084	Vulvar Vestibulitis
+C0269102	Endometrioma
+C0269131	Unspecified fistula involving female genital tract
+C0269133	Urethrovaginal fistula
+C0269155	Germinal inclusion cyst of ovary
+C0269188	Uterine cyst
+C0269189	Ectropion of cervix
+C0269190	Squamous metaplasia of cervix
+C0269202	Cervical cyst
+C0269209	Hydrometrocolpos
+C0269221	Vulval oedema
+C0269268	Breast induration
+C0269269	Inversion of nipple (disorder)
+C0269596	Haemorrhage in pregnancy
+C0269608	Antepartum hemorrhage
+C0269661	Unspecified vomiting of pregnancy
+C0269806	Failed induction of labour
+C0269842	Uterine hypertonus
+C0269899	Immediate Postpartum Hemorrhage
+C0269936	Puerperal sepsis
+C0269972	Postpartum cardiomyopathy
+C0269993	Suppressed lactation
+C0269995	Galactorrhea associated with childbirth
+C0270075	Perinatal disorder
+C0270191	Intraventricular hemorrhage of fetus or newborn
+C0270192	Perinatal Subarachnoid Hemorrhage
+C0270210	Lucey-Driscoll syndrome (disorder)
+C0270215	Neonatal jaundice due to delayed conjugation from breast milk inhibitor
+C0270224	Tetany, Neonatal
+C0270246	Meconium plug syndrome
+C0270254	Hydrops of placenta
+C0270274	Vomiting neonatal
+C0270327	Bedwetting
+C0270328	Diurnal enuresis
+C0270330	Speech disorder developmental
+C0270458	Severe major depression with psychotic features
+C0270496	Schizoaffective disorder bipolar type
+C0270497	Schizoaffective disorder depressive type
+C0270500	Coprophilia (disorder)
+C0270541	Rebound Insomnia
+C0270549	Generalised anxiety disorder
+C0270611	Brain Injuries
+C0270612	Leukoencephalopathies
+C0270627	Myelitis, Acute Transverse
+C0270629	Epidural Abscess
+C0270638	Cavernous Sinus Thrombophlebitis
+C0270639	Lateral Sinus Thrombosis
+C0270680	Posterior fossa compression syndrome
+C0270685	Cerebral calcification
+C0270686	Cerebral fungal infection
+C0270687	Pseudomeningocele
+C0270697	Post-Lumbar Puncture Headache
+C0270699	Neonatal maladjustment syndrome
+C0270707	Kluver-Bucy Syndrome
+C0270710	Bing-Neel syndrome
+C0270715	Degenerative Diseases, Central Nervous System
+C0270720	Hydrocephalus Ex-Vacuo
+C0270724	Infantile Neuroaxonal Dystrophy
+C0270726	Alexander Disease
+C0270730	MPTP Poisoning
+C0270733	Striatonigral Degeneration
+C0270736	Essential Tremor
+C0270742	Athetoid cerebral palsy
+C0270749	Marie Cerebellar Ataxia
+C0270755	Corticostriatal-Spinal Degeneration
+C0270763	Familial Motor Neuron Disease
+C0270764	Motor Neuron Disease, Lower
+C0270765	Myelopathic Muscular Atrophy
+C0270774	Myelomalacia
+C0270777	Spinal cord oedema
+C0270779	Acute necrotizing myelitis
+C0270780	Degenerative myelopathy
+C0270786	Binswanger Disease
+C0270790	Quadriparesis
+C0270791	Triplegia
+C0270795	Monoparesis
+C0270805	Hemiplegic cerebral palsy
+C0270807	Monoplegic Cerebral Palsy
+C0270810	Peroneal nerve palsy
+C0270814	Spastic syndrome
+C0270816	epilepsy and migraine
+C0270819	Reflex Epilepsy, Cursive (Running)
+C0270820	Gelastic Epilepsy
+C0270823	Petit mal status
+C0270824	Visual epilepsy
+C0270834	Complex partial seizure with impairment of consciousness
+C0270844	Tonic convulsion
+C0270846	Epileptic drop attack
+C0270847	Benign Focal Epilepsy, Childhood
+C0270850	Idiopathic generalized epilepsy
+C0270851	Benign neonatal epilepsy
+C0270853	Juvenile Myoclonic Epilepsy
+C0270854	Symptomatic Generalized Epilepsy
+C0270855	Early myoclonic encephalopathy
+C0270857	Epilepsy, Reflex
+C0270858	Abdominal Migraine
+C0270860	Basilar-Type Migraine
+C0270862	Hemiplegic migraine
+C0270869	Raeder Paratrigeminal Syndrome
+C0270871	Facial Myokymia
+C0270876	Facial Nerve Motor Disorders
+C0270877	Facial Nerve Sensory Disorders
+C0270894	Upper Brachial Plexus Neuropathy
+C0270895	Middle Brachial Plexus Neuropathy
+C0270896	Lower Brachial Plexus Neuropathy
+C0270897	Erb-Duchenne Paralysis
+C0270898	Klumpke Paralysis
+C0270911	Charcot-Marie-Tooth Disease, Type Ia (disorder)
+C0270912	Charcot-Marie-Tooth Disease, Type Ib
+C0270913	Charcot-Marie-Tooth disease, Type 1C
+C0270914	Hereditary Motor and Sensory-Neuropathy Type II
+C0270920	Supranuclear paralysis
+C0270921	Axonal neuropathy
+C0270922	Demyelinating polyneuropathy
+C0270933	Inflammatory neuropathy
+C0270934	Toxic neuropathy
+C0270942	Myasthenia gravis crisis
+C0270948	Neurogenic Muscular Atrophy
+C0270951	Ocular muscular dystrophy
+C0270952	Muscular Dystrophy, Oculopharyngeal
+C0270958	Kocher-Debre-Semelaigne syndrome
+C0270959	Myotonia Levior
+C0270960	Congenital myopathy (disorder)
+C0270962	Multi-core congenital myopathy
+C0270968	Limb-girdle muscular dystrophy type 2H
+C0270969	Zebra body myopathy
+C0270970	Reducing-body myopathy
+C0270971	Floppy infant
+C0270972	Cornelia De Lange Syndrome
+C0270975	Infantile encephalopathy AND lactic acidosis
+C0270984	Metabolic myopathy
+C0270992	Secondary myopathy
+C0270994	Myopathy steroid-induced
+C0270996	Eye swelling
+C0271004	Absent anterior chamber of eye
+C0271007	Phthisis bulbi
+C0271036	Retinal scar
+C0271051	Macular Edema
+C0271053	Cotton wool spots
+C0271055	Rhegmatogenous retinal detachment
+C0271073	Eales disease
+C0271084	Exudative age-related macular degeneration
+C0271085	Macular cyst
+C0271091	Retinoschisis, Juvenile, X-Linked
+C0271092	Progressive cone dystrophy (without rod involvement)
+C0271093	Stargardt's disease
+C0271097	Usher Syndrome
+C0271131	Occluded Pupils
+C0271134	Deformed Pupil
+C0271135	Ectopic pupil
+C0271141	Pupillary Paralysis
+C0271148	Secondary Open Angle Glaucoma
+C0271154	Aphakic glaucoma
+C0271160	Cataract cortical
+C0271165	Punctate cataract
+C0271178	Irvine-Gass Syndrome
+C0271183	Severe myopia
+C0271185	Metamorphopsia
+C0271186	Diplopia, Refractive
+C0271189	Topographical Agnosia
+C0271190	Diplopia, Unilateral
+C0271196	Centrocecal scotoma
+C0271197	Paracentral scotoma
+C0271198	Arcuate scotoma
+C0271200	Scotoma, Bjerrum
+C0271202	Hemianopsia, Homonymous
+C0271205	Altidudinal Hemianopia
+C0271207	Heteronymous bilateral field defects
+C0271208	Binasal hemianopia
+C0271214	Central blindness
+C0271215	Blindness, Legal
+C0271240	Blindness of one eye (disorder)
+C0271270	Oculovestibuloauditory syndrome
+C0271271	Xerotic keratitis
+C0271285	Epithelial basement membrane dystrophy
+C0271287	Schnyder crystalline corneal dystrophy
+C0271288	Corneal guttata
+C0271291	Corneal anesthesia
+C0271294	Chronic allergic conjunctivitis
+C0271298	Chemosis of conjunctiva
+C0271308	Blepharitis allergic
+C0271321	Madarosis
+C0271335	Orbital congestion
+C0271344	Compression of optic nerve
+C0271355	Abducens Nerve Diseases
+C0271364	Manifest vertical squint
+C0271370	Partial Third-Nerve Palsy
+C0271371	Total Third-Nerve Palsy
+C0271373	Claude Syndrome
+C0271375	Fourth cranial nerve paresis
+C0271379	Convergence Insufficiency
+C0271380	Convergence Excess
+C0271381	Skew Deviation
+C0271382	Periodic Alternating Nystagmus
+C0271383	Symptomatic Nystagmus
+C0271384	Spontaneous Ocular Nystagmus
+C0271385	Horizontal Nystagmus
+C0271386	Vertical Nystagmus
+C0271387	Rebound Nystagmus
+C0271388	Pendular Nystagmus
+C0271389	Jerk Nystagmus
+C0271390	Nystagmus, End-Position
+C0271396	Paroxysmal Ocular Dyskinesia
+C0271397	Pseudoophthalmoplegia
+C0271412	Bleeding from ear
+C0271429	Acute otitis media
+C0271441	Chronic otitis media
+C0271453	Serous otitis media
+C0271454	Chronic purulent otitis media
+C0271468	Eustachian tube disorder
+C0271474	Mastoid disorders
+C0271514	Low frequency deafness
+C0271527	Cryptogenic sexual precocity
+C0271528	Isosexual precocious puberty
+C0271547	Overproduction of growth hormone
+C0271561	Growth hormone deficiency
+C0271567	Isolated Growth Hormone Deficiency, Type II
+C0271568	Laron Syndrome
+C0271574	Empty Sella Syndrome, Primary
+C0271577	Isolated gonadotropin deficiency
+C0271578	Female hypogonadism syndrome
+C0271582	Isolated lutropin deficiency (disorder)
+C0271583	ACTH Deficiency, Isolated
+C0271586	Prolactin Deficiency, Isolated
+C0271623	Hypogonadotropic hypogonadism
+C0271629	Mullerian inhibiting factor deficiency
+C0271633	Disorder of endocrine pancreas
+C0271638	Type 2 diabetes mellitus in obese
+C0271642	Fibrocalculous pancreatic diabetes
+C0271650	Glucose Intolerance
+C0271673	Symmetric Diabetic Proximal Motor Neuropathy
+C0271674	Asymmetric Diabetic Proximal Motor Neuropathy
+C0271676	Polyradiculopathy, Abdominal
+C0271678	Diabetic Mononeuropathy
+C0271680	Diabetic Polyneuropathies
+C0271681	Sensory polyneuropathy
+C0271682	Mixed sensory-motor polyneuropathy
+C0271683	Polyneuropathy, Motor
+C0271685	Diabetic Amyotrophy
+C0271686	Diabetic Autonomic Neuropathy
+C0271689	Insulin Receptor, Defect in
+C0271690	Type 2 diabetes mellitus with acanthosis nigricans
+C0271694	Familial partial lipodystrophy
+C0271695	Rabson-Mendenhall Syndrome
+C0271706	Hyperplasia of pancreatic islet beta cell
+C0271708	Fasting Hypoglycemia
+C0271710	Reactive hypoglycemia
+C0271713	Ketotic hypoglycemia
+C0271714	Hypoglycemia, leucine-induced
+C0271725	Iatrogenic Cushing\'s disease
+C0271728	Secondary hyperaldosteronism
+C0271737	Addison\'s disease due to autoimmunity
+C0271738	Hypocortisolism secondary to another disorder
+C0271742	Glucocorticoid deficiency with achalasia
+C0271749	Abnormality of cortisol-binding globulin
+C0271750	Adrenal calcification
+C0271761	Non-toxic multinodular goiter
+C0271789	Hypothyroidism, Congenital, Nongoitrous, 4
+C0271790	Subclinical hypothyroidism
+C0271791	Severe hypothyroidism
+C0271795	Transient hypothyroidism
+C0271801	Central hypothyroidism
+C0271814	Silent thyroiditis
+C0271815	Postpartum Thyroiditis
+C0271820	Thyroid hemorrhage
+C0271826	Iodide transport defect
+C0271829	Pendred\'s syndrome
+C0271836	X-linked reduction of thyroxine-binding globulin
+C0271844	Parathyroid hyperplasia
+C0271846	Familial hyperparathyroidism
+C0271858	Tertiary hyperparathyroidism
+C0271862	Idiopathic parathyroidism
+C0271865	Autoimmune hypoparathyroidism
+C0271885	Hypothalamic obesity
+C0271886	Hypothalamic Pseudopuberty
+C0271893	Autoimmune pancytopenia
+C0271899	Normochromic normocytic anaemia
+C0271901	Microcytic hypochromic anemia (disorder)
+C0271902	Microcytic normochromic anemia
+C0271907	Acquired aplastic anemia
+C0271930	Anaemia of pregnancy
+C0271932	Anemia of chronic renal failure
+C0271933	Congenital dyserythropoietic anemia, type I
+C0271934	Congenital dyserythropoietic anemia, type III
+C0271972	Thiamine-responsive megaloblastic anemia
+C0271979	beta-Thalassemia
+C0271980	beta^0^ Thalassemia
+C0271985	Delta-Beta Thalassemia
+C0271986	delta beta^0^ Thalassemia
+C0271987	^A^gamma delta beta^0^ thalassemia
+C0271990	delta-Thalassemia
+C0271991	delta^0^ Thalassemia
+C0271994	Hereditary persistence of fetal hemoglobin thalassemia
+C0272002	alpha^0^ Thalassemia
+C0272003	alpha^+^ Thalassemia, deletion type
+C0272005	Hemoglobin Bart\'s hydrops syndrome
+C0272027	Pyridoxine-responsive sideroblastic anemia
+C0272048	stomatocytic anemia
+C0272051	Xerocytosis
+C0272052	Rh Deficiency Syndrome
+C0272066	Glycogen Storage Disease XII
+C0272080	Hemoglobin D disease
+C0272082	Hemoglobin E trait
+C0272084	Hemoglobin SD disease
+C0272085	Sickle cell-hemoglobin E disease
+C0272087	Congenital Methemoglobinemia
+C0272105	Anemia due to infection
+C0272118	Warm autoimmune hemolytic anemia
+C0272126	Evans syndrome
+C0272132	Drug-induced hemolytic anemia
+C0272137	Tn Syndrome
+C0272138	Erythroblastosis
+C0272139	Erythrocytosis due to low atmospheric pressure
+C0272144	Erythrocytosis due to tissue hypoxemia
+C0272157	Disorder of neutrophils
+C0272160	Chronic neutrophilia
+C0272167	Reticular dysgenesis
+C0272170	Shwachman syndrome
+C0272173	Myelokathexis
+C0272175	Immune neutropenia
+C0272176	Alloimmune neonatal neutropenia
+C0272178	Drug-induced neutropenia
+C0272183	Qualitative abnormality of granulocyte
+C0272187	Congenital leukocyte adherence deficiency
+C0272191	eosinophilic syndrome
+C0272192	Familial eosinophilia
+C0272199	Familial Hemophagocytic Lymphocytosis
+C0272203	Indolent Systemic Mastocytosis
+C0272210	Mononucleosis syndrome
+C0272214	Persistent lymphocytosis
+C0272220	Chronic granulomatous disease, type II
+C0272229	Congenital immunodeficiency disease
+C0272236	Hyperimmunoglobulin M syndrome
+C0272238	Transient hypogammaglobulinemia of infancy
+C0272240	Disorder of complement
+C0272241	Complement abnormality
+C0272242	Complement deficiency disease
+C0272249	Polyclonal gammopathy
+C0272272	Systemic fibrinogenolysis
+C0272274	Familial hemorrhagic diathesis
+C0272275	Heparin-induced thrombocytopenia type II
+C0272278	Congenital thrombocytopenia
+C0272285	Heparin-induced thrombocytopenia
+C0272286	Thrombocytopenia due to platelet alloimmunization
+C0272290	Drug-induced immune thrombocytopenia
+C0272292	Acute idiopathic thrombocytopenic purpura
+C0272293	Chronic idiopathic thrombocytopenic purpura
+C0272296	Thrombocytopenia due to sequestration
+C0272302	Gray Platelet Syndrome
+C0272315	Coagulation factor deficiency
+C0272317	Hereditary factor II deficiency disease
+C0272320	Hereditary factor VII deficiency disease
+C0272322	Severe hereditary factor VIII deficiency disease
+C0272323	Moderate hereditary factor VIII deficiency disease
+C0272324	Mild hereditary factor VIII deficiency disease
+C0272325	Factor 8 deficiency, acquired
+C0272339	Prekallikrein deficiency
+C0272340	High molecular weight kininogen deficiency
+C0272342	Familial multiple factor deficiency syndrome, type I
+C0272350	Dysfibrinogenemia, Congenital
+C0272355	von Willebrand disease, type IIC
+C0272356	von Willebrand disease, type IID
+C0272362	Acquired von Willebrand\'s disease
+C0272363	ANTICOAGULANT DISORDERS
+C0272375	Antithrombin III Deficiency
+C0272380	Tonsillar disorder
+C0272386	Hypertrophy of tonsils
+C0272387	Hyperplasia of tonsils
+C0272392	Tonsillar ulcer
+C0272394	Disorder of lymph node
+C0272398	Dermatopathic lymphadenitis
+C0272401	Virchow\'s node (disorder)
+C0272407	Splenic cyst
+C0272412	Splenic abscess
+C0272416	Splenic vein thrombosis
+C0272423	Ear injury
+C0272426	Mouth injury
+C0272567	Fracture of multiple ribs
+C0272774	Foot fracture
+C0272945	Brain Lacerations
+C0273058	Traumatic intracranial bleeding
+C0273115	Lung Injury
+C0273163	Pancreatic injury
+C0273482	Compression injury of nerve
+C0273545	Superficial injury of eye
+C0274285	Hypothermia, Accidental
+C0274294	Chronic mountain sickness
+C0274306	Cutaneous anaphylaxis
+C0274312	Graft complication
+C0274417	Haemodialysis complication
+C0274418	Peritoneal dialysis complication
+C0274430	Vaccination complication
+C0274435	Transfusion reaction
+C0274456	Accidental poisoning
+C0274576	Poisoning by fluorouracil
+C0274702	Cholinergic syndrome
+C0274714	Adrenergic syndrome
+C0274859	Inorganic Mercury Poisoning
+C0274860	Mercury Poisoning, Organic
+C0274861	Arsenic Poisoning, Inorganic
+C0274862	Nervous System, Organic Arsenic Poisoning
+C0274869	Heavy Metal Poisoning
+C0275522	Asymptomatic Infections
+C0275524	Coinfection
+C0275544	Congenital infectious disease
+C0275547	Balanitis circinata
+C0275551	Primary bacterial peritonitis
+C0275553	Bacterial cholangitis
+C0275572	Dermatophilosis due to Dermatophilus congolensis
+C0275578	Nocardia asteroides Infection
+C0275583	Pulmonary Nocardiosis
+C0275590	Food poisoning due to Clostridium perfringens
+C0275594	Infection due to Brucella suis
+C0275619	Infection due to Clostridium perfringens
+C0275683	Meningoencephalitis, Listeria
+C0275706	Mycobacterium kansasii infection
+C0275708	Mycobacterium marinum Infection
+C0275778	Lyme carditis
+C0275804	Streptococcal tonsillitis
+C0275814	Streptococcal lymphadenitis of swine
+C0275904	Tuberculosis, Central Nervous System
+C0275911	Tuberculosis of intestines
+C0275919	Tuberculous ascites
+C0275982	Campylobacter gastroenteritis
+C0276035	Glasser\'s disease
+C0276044	Contagious bovine pleuropneumonia
+C0276084	Osteomyelitis bacterial
+C0276088	Escherichia coli septicemia
+C0276089	Pneumonia due to Escherichia coli
+C0276093	edema disease
+C0276096	Mastitis-metritis-agalactia syndrome
+C0276138	Myocarditis viral NOS
+C0276139	Pericarditis viral NOS
+C0276141	Bronchitis viral
+C0276143	Viral sore throat
+C0276156	Pneumonia adenoviral
+C0276199	Canarypox (disorder)
+C0276223	Recurrent herpes simplex
+C0276225	Congenital herpes simplex infection
+C0276226	Encephalitis, Herpes Simplex
+C0276248	Herpes zoster disseminated
+C0276252	Cytomegalovirus hepatitis
+C0276253	Cytomegaloviral pneumonia
+C0276259	Lymphocystis disease
+C0276262	Verruca plana
+C0276275	Disease due to Parvoviridae
+C0276289	Zika Virus Infection
+C0276333	Pneumonia parainfluenzae viral
+C0276340	Respiratory syncytial virus bronchiolitis
+C0276357	Swine influenza
+C0276430	Enterovirus meningitis
+C0276434	Acute type A viral hepatitis
+C0276447	Rhinovirus infection
+C0276496	Familial Alzheimer Disease (FAD)
+C0276501	Human immunodeficiency virus II infection
+C0276527	Pneumonia associated with AIDS
+C0276535	AIDS with Kaposi\'s sarcoma
+C0276548	HIV encephalitis
+C0276609	Acute hepatitis B
+C0276622	Acute viral hepatitis
+C0276623	Chronic viral hepatitis
+C0276638	Pseudoscarlatina
+C0276640	Transmissible mink encephalopathy
+C0276647	Pericarditis fungal
+C0276648	Fungal endocarditis
+C0276651	Aspergilloma
+C0276653	Invasive Pulmonary Aspergillosis
+C0276665	Pulmonary paracoccidioidomycosis
+C0276667	Disseminated coccidioidomycosis
+C0276680	Infection by Candida albicans
+C0276684	Balanitis candida
+C0276688	Pneumonia cryptococcal
+C0276721	Phaeohyphomycosis
+C0276742	Kerion celsi
+C0276758	Fusariosis
+C0276883	Zoonotic form of cutaneous leishmaniasis
+C0276908	Infection by Pneumocystis jirovecii (disorder)
+C0276919	Intestinal nematode infection
+C0276926	Schistosoma hematobium infection
+C0277004	Opisthorchis felineus Infection
+C0277005	Opisthorchis viverrini Infection
+C0277066	Cysticercus cellulosae Infection
+C0277337	Infection by Polymorphus
+C0277355	Flea Infestation
+C0277524	Infectious colitis
+C0277525	Infectious gastroenteritis
+C0277527	Epidemic diarrhea
+C0277528	Traveler\'s diarrhea
+C0277550	Endemic Diseases
+C0277585	Drug intolerance
+C0277589	Death of unknown cause
+C0277638	Accidental death
+C0277792	Pathognomonic sign
+C0277794	Extreme exhaustion
+C0277799	Intermittent fever
+C0277807	Exercise lack of
+C0277820	Clasp-Knife Spasticity
+C0277821	Extrapyramidal Rigidity
+C0277827	Early fontanel closure
+C0277828	Delayed closure of cranial sutures
+C0277834	Kehr's sign
+C0277839	Hoffman's Reflex
+C0277848	Hoover's sign
+C0277849	Psoas sign
+C0277850	Reflex, Pendular
+C0277855	Laryngeal dyspnoea
+C0277858	Breath sounds absent
+C0277873	Nasal flaring
+C0277883	Blood pressure systolic abnormal
+C0277884	Blood pressure systolic increased
+C0277885	Blood pressure systolic decreased
+C0277889	Blood pressure diastolic increased
+C0277890	Blood pressure diastolic decreased
+C0277896	Central venous pressure increased
+C0277899	Pulse absent
+C0277910	Ejection murmur
+C0277913	Graham Steell murmur
+C0277919	Post thrombotic syndrome
+C0277925	Peripheral coldness
+C0277927	Musset's sign
+C0277934	Aortic bruit
+C0277942	Butterfly rash
+C0277959	Coarse hair
+C0277960	Dry hair
+C0277961	Greasy hair
+C0277964	Subcutaneous crepitus
+C0277969	Abdominal pain through to back
+C0277976	Rovsing's sign
+C0277977	Murphy's sign
+C0277978	Obturator sign
+C0277986	Gingival oedema
+C0278007	Normal bowel habits
+C0278008	Altered bowel function
+C0278016	Faeces hard
+C0278024	Residual urine
+C0278026	Aciduria
+C0278034	Cloudy urine
+C0278045	Urine odour abnormal
+C0278061	Abnormal mental state
+C0278076	Behavioral tic
+C0278079	Psychological addiction
+C0278080	Physical addiction
+C0278097	Abnormal male sexual function
+C0278106	Ejaculation failure
+C0278107	Painful ejaculation
+C0278110	Crossed hemiplegia
+C0278114	Paraplegia, Cerebral
+C0278115	Paraplegia, Spinal
+C0278118	Paraparesis, Cerebral
+C0278119	Paraparesis, Spinal
+C0278124	Absent tendon reflex
+C0278131	Plantar reflex
+C0278134	Absence of sensation
+C0278140	Severe pain
+C0278141	Excruciating pain
+C0278144	Dull pain
+C0278145	Stabbing pain
+C0278147	Radicular pain
+C0278148	Throbbing pain
+C0278151	Facial spasm
+C0278152	Hemifacial Spasm
+C0278155	Taste-blindness
+C0278161	Ataxia, Motor
+C0278184	Scanning speech
+C0278193	Reflex Epilepsy, Reading
+C0278198	Reflex Epilepsy, Musicogenic
+C0278210	Problem of visual accommodation
+C0278211	Reflex, Corneal, Absent
+C0278217	Von Graefe sign
+C0278218	Kocher's sign
+C0278234	Cherry red spot
+C0278314	Nephrostomy
+C0278474	Colon cancer stage I
+C0278479	Colon cancer stage II
+C0278480	Colon cancer stage III
+C0278484	Colon cancer stage IV
+C0278485	Breast cancer stage I
+C0278486	Breast cancer stage II
+C0278487	Stage III Breast Cancer AJCC v6
+C0278488	Breast cancer stage IV
+C0278489	Stage IIIA Breast Carcinoma
+C0278493	Breast cancer recurrent
+C0278495	Malignant neoplasm of stomach stage I
+C0278498	Malignant neoplasm of stomach stage IV
+C0278502	recurrent gastric cancer
+C0278504	Non-small cell lung cancer stage I
+C0278505	Non-small cell lung cancer stage II
+C0278506	Non-small cell lung cancer stage III
+C0278510	Childhood Medulloblastoma
+C0278511	Osteosarcoma localised
+C0278512	Metastatic osteosarcoma
+C0278513	Stage IIIB Breast Carcinoma
+C0278517	Non-small cell lung cancer recurrent
+C0278519	Recurrent Childhood Acute Lymphoblastic Leukemia
+C0278544	Stage II Rectal Cancer
+C0278553	Colon cancer recurrent
+C0278554	Rectal cancer recurrent
+C0278556	Anal cancer recurrent
+C0278562	Esophageal neoplasm metastatic
+C0278569	Mycosis fungoides stage II
+C0278577	Cervix carcinoma stage III
+C0278579	Cervix carcinoma recurrent
+C0278582	Cervical carcinoma stage IB
+C0278583	Cervical carcinoma stage IIB
+C0278584	Cervix cancer metastatic
+C0278586	Ewing's sarcoma metastatic
+C0278590	Ewing's sarcoma recurrent
+C0278592	Adult Angiosarcoma
+C0278595	Adult Fibrosarcoma
+C0278600	Childhood Brain Stem Glioma
+C0278601	Inflammatory Breast Carcinoma
+C0278607	Adult Leiomyosarcoma
+C0278608	Adult Liposarcoma
+C0278619	Extramedullary Plasmacytoma
+C0278620	refractory plasma cell neoplasm
+C0278622	Adult Malignant Peripheral Nerve Sheath Tumor
+C0278653	Optic Nerve Glioma, Childhood
+C0278660	Adult Synovial Sarcoma
+C0278678	Metastatic Renal Cell Cancer
+C0278681	metastatic parathyroid cancer
+C0278685	Ovarian epithelial cancer stage I
+C0278686	Ovarian epithelial cancer stage II
+C0278687	Ovarian cancer stage III
+C0278688	Stage IV Ovarian Carcinoma
+C0278689	Ovarian cancer recurrent
+C0278694	Disseminated neuroblastoma
+C0278695	Neuroblastoma recurrent
+C0278701	Adenocarcinoma gastric
+C0278704	Malignant Childhood Neoplasm
+C0278716	recurrent Wilms\' tumor and other childhood kidney tumors
+C0278717	Intraocular retinoblastoma
+C0278719	Extraocular retinoblastoma
+C0278721	Adult Lymphoblastic Lymphoma
+C0278722	DS Stage I Plasma Cell Myeloma
+C0278725	Small cell lung cancer limited stage
+C0278726	Small cell lung cancer extensive stage
+C0278727	Small cell lung cancer recurrent
+C0278752	Mesothelioma malignant advanced
+C0278764	Adult Burkitt Lymphoma
+C0278769	Chronic lymphocytic leukaemia stage 3
+C0278779	Osteosarcoma recurrent
+C0278785	Recurrent Adult Acute Lymphoblastic Leukemia
+C0278787	relapsing chronic myelogenous leukemia
+C0278791	Chronic lymphocytic leukaemia refractory
+C0278798	Ca endometrium stage I
+C0278801	Ca endometrium stage IV
+C0278802	Recurrent Endometrial Cancer
+C0278803	Adenocarcinoma of small intestine
+C0278804	Adenocarcinoma of duodenum
+C0278823	Ca bladder stage II
+C0278827	Bladder cancer recurrent
+C0278828	Stage IV Bladder Cancer AJCC v6
+C0278835	Prostate cancer stage II
+C0278836	Stage III Prostate Carcinoma
+C0278837	Prostate cancer stage IV
+C0278838	Prostate cancer recurrent
+C0278846	Thymoma malignant invasive
+C0278851	Metastatic papillary thyroid carcinoma
+C0278861	Recurrent Thyroid Carcinoma
+C0278864	Growth Hormone-Producing Pituitary Gland Neoplasm
+C0278865	Pituitary tumour recurrent
+C0278874	Adult Ependymoma
+C0278875	Adult Craniopharyngioma
+C0278876	Adult Medulloblastoma
+C0278877	adult meningioma
+C0278878	Adult Glioblastoma
+C0278879	Childhood Burkitt Lymphoma
+C0278880	Stage I Cutaneous Melanoma AJCC v6
+C0278881	stage II melanoma
+C0278882	Stage III Cutaneous Melanoma AJCC v6
+C0278883	Metastatic melanoma
+C0278884	Melanoma recurrent
+C0278952	Nasopharyngeal cancer recurrent
+C0278983	Non-small cell lung cancer stage IIIA
+C0278984	Non-small cell lung cancer stage IIIB
+C0278987	Non-small cell lung cancer metastatic
+C0278996	Head and neck cancer
+C0279000	Liver and Intrahepatic Biliary Tract Carcinoma
+C0279068	Childhood Solid Neoplasm
+C0279070	Adult Oligodendroglioma
+C0279084	Kaposi\'s sarcoma classical type
+C0279530	Bone cancer
+C0279543	Philadelphia chromosome positive chronic myelogenous leukemia
+C0279546	Adult Undifferentiated Pleomorphic Sarcoma
+C0279549	Philadelphia chromosome negative chronic myelogenous leukemia
+C0279550	Adult Rhabdomyosarcoma
+C0279557	Adenosquamous cell lung cancer
+C0279563	Lobular carcinoma in situ of breast
+C0279565	Invasive Lobular Breast Carcinoma
+C0279583	Childhood T Acute Lymphoblastic Leukemia
+C0279584	Childhood B Acute Lymphoblastic Leukemia
+C0279592	Adult T Acute Lymphoblastic Leukemia
+C0279593	Adult B Acute Lymphoblastic Leukemia
+C0279602	Fibroblastic osteosarcoma
+C0279603	Chondroblastic osteosarcoma
+C0279606	Childhood Hepatocellular Carcinoma
+C0279607	Adult Hepatocellular Carcinoma
+C0279609	blastema predominant Wilms\' tumor
+C0279612	Childhood Embryonal Rhabdomyosarcoma
+C0279613	Childhood Alveolar Rhabdomyosarcoma
+C0279622	Small cell osteosarcoma
+C0279625	Adult Acute Promyelocytic Leukemia with PML-RARA
+C0279626	Oesophageal squamous cell carcinoma stage unspecified
+C0279627	Adult Acute Myelomonocytic Leukemia
+C0279628	Adenocarcinoma Of Esophagus
+C0279632	Adult Acute Megakaryoblastic Leukemia
+C0279633	intestinal adenocarcinoma of the stomach
+C0279637	Anal cancer
+C0279639	Mucinous adenocarcinoma of colon
+C0279641	Childhood Acute Promyelocytic Leukemia with PML-RARA
+C0279644	Childhood Acute Myelomonocytic Leukemia
+C0279646	Childhood Acute Monocytic Leukemia
+C0279650	Childhood Acute Megakaryoblastic Leukemia
+C0279651	Gallbladder adenocarcinoma
+C0279661	Acinar cell carcinoma of pancreas
+C0279663	Serous cystadenocarcinoma ovary
+C0279671	Cervical Squamous Cell Carcinoma
+C0279672	Cervical Adenocarcinoma
+C0279674	Small cell carcinoma of the cervix
+C0279680	Bladder transitional cell carcinoma
+C0279681	Bladder Squamous Cell Carcinoma
+C0279682	Bladder Adenocarcinoma
+C0279702	Clear cell renal cell carcinoma
+C0279705	Thymoma, type B3
+C0279708	Testicular yolk sac tumour
+C0279709	testicular embryonal carcinoma and teratoma
+C0279734	pituitary eosinophilic adenoma
+C0279735	TSH secreting adenoma
+C0279746	Adenocarcinoma of salivary gland
+C0279751	Adenoid cystic carcinoma of salivary gland
+C0279759	Progesterone receptor assay positive
+C0279763	endometrial adenoacanthoma
+C0279765	Endometrial Clear Cell Adenocarcinoma
+C0279780	Hairy cell leukaemia recurrent
+C0279818	Laryngeal cancer recurrent
+C0279821	metastatic pheochromocytoma
+C0279822	recurrent pheochromocytoma
+C0279980	Extraosseous Ewings sarcoma-primitive neuroepithelial tumor
+C0279982	Childhood Synovial Sarcoma
+C0279986	Childhood Leiomyosarcoma
+C0279987	Childhood Malignant Peripheral Nerve Sheath Tumor
+C0280028	Refractory anemia with excess blasts in transformation (clinical)
+C0280089	Carcinoid tumor of lung
+C0280099	Adult Solid Neoplasm
+C0280100	Solid Neoplasm
+C0280131	Ovarian Teratoma
+C0280135	Ovarian germ cell tumour mixed
+C0280141	Acute Undifferentiated Leukemia
+C0280201	stage, Kaposi\'s sarcoma
+C0280216	stage, neuroblastoma
+C0280217	stage, non-small cell lung cancer
+C0280218	stage, bladder cancer
+C0280220	stage, ovarian epithelial cancer
+C0280222	stage, pancreatic cancer
+C0280232	stage, cervical cancer
+C0280242	stage, rectal cancer
+C0280248	stage, chronic lymphocytic leukemia
+C0280251	stage, chronic myelogenous leukemia
+C0280252	stage, colon cancer
+C0280253	stage, gastric cancer
+C0280255	stage, endometrial cancer
+C0280280	stage, prostate cancer
+C0280297	lip and oral cavity squamous cell carcinoma
+C0280302	Squamous cell carcinoma of lip
+C0280306	Verrucous carcinoma of oral cavity
+C0280313	Oropharyngeal Squamous Cell Carcinoma
+C0280317	Squamous cell carcinoma of tonsil
+C0280321	Hypopharyngeal Squamous Cell Carcinoma
+C0280324	Laryngeal Squamous Cell Carcinoma
+C0280333	Squamous Cell Carcinoma of the Nasal Cavity
+C0280391	Squamous cell carcinoma of the hypopharynx stage IV
+C0280427	Adult T-cell lymphoma/leukaemia recurrent
+C0280440	Catheter management
+C0280449	secondary acute myeloid leukemia
+C0280451	de novo myelodysplastic syndromes
+C0280474	Childhood Glioblastoma
+C0280475	Childhood Oligodendroglioma
+C0280630	Uterine Carcinosarcoma
+C0280631	Leiomyosarcoma of uterus
+C0280634	Adult Acute Monocytic Leukemia
+C0280725	Adult Cholangiocarcinoma
+C0280745	secondary myelodysplastic syndromes
+C0280746	Sarcoma of ovary
+C0280781	Adult Pilocytic Astrocytoma
+C0280783	Juvenile Pilocytic Astrocytoma
+C0280785	Diffuse Astrocytoma
+C0280788	Anaplastic Ependymoma
+C0280793	Mixed Oligodendroglioma-Astrocytoma
+C0280801	Grade III Meningioma
+C0280803	Central nervous system lymphoma
+C0280856	Squamous cell carcinoma of vulva
+C0280962	Bone Marrow Suppression
+C0281241	AIDS-related primary CNS lymphoma
+C0281267	bilateral breast cancer
+C0281328	Adult Subependymoma
+C0281361	Adenocarcinoma of pancreas
+C0281373	Respiratory papilloma
+C0281479	Primary Systemic Amyloidosis
+C0281508	Desmoplastic Small Round Cell Tumor
+C0281658	Intraocular Lymphoma
+C0281663	breast cancer and pregnancy
+C0281773	Acute glaucoma
+C0281774	Acute psychosis
+C0281778	Anal abscess
+C0281784	Benign Meningioma
+C0281788	Biventricular hypertrophy
+C0281790	Bone fistula
+C0281803	Endotracheal intubation complication
+C0281839	Oesophageal rupture
+C0281842	Abnormality of the fallopian tube
+C0281856	Generalized aches and pains
+C0281860	Wound haematoma
+C0281863	Hepatitis C antibody positive
+C0281890	Laryngeal web
+C0281899	Prolapsed lumbar disc
+C0281913	Muscle swelling
+C0281914	Musculoskeletal deformity
+C0281961	Recurrent hernia
+C0281964	Renal artery arteriosclerosis
+C0281966	Abnormality of the reproductive system
+C0281967	Retinal infarction
+C0281980	Skin injury NOS
+C0281981	Skin mass
+C0281982	Skin swelling
+C0282005	Scrotal swelling
+C0282008	Dilation of the thoracic aorta
+C0282015	Pneumothorax traumatic
+C0282102	Chondrodysplasia punctata, X-linked dominant type
+C0282124	Near-Death Experience
+C0282126	Depression, Neurotic
+C0282160	Aplasia Cutis Congenita
+C0282192	Hemorrhagic Fever, Bolivian
+C0282193	Iron Overload
+C0282201	Phosphate Diabetes
+C0282207	Cronkhite-Canada Syndrome
+C0282208	Injuries, Surgical
+C0282209	IUD migration
+C0282220	Amaurotic Familial Idiocy
+C0282309	Actinic reticuloid
+C0282310	Dermatitis, Actinic
+C0282312	Bubonic Plague
+C0282313	Condition, Preneoplastic
+C0282350	Sexual abuse
+C0282402	Hormone replacement therapy
+C0282488	Cystitis, Interstitial
+C0282492	Sneddon Syndrome
+C0282507	Heat Stress Disorders
+C0282512	Landau-Kleffner Syndrome
+C0282513	Primary Progressive Aphasia (disorder)
+C0282525	Adrenoleukodystrophy, Neonatal
+C0282526	Hyperpipecolic Acidemia
+C0282527	Infantile Refsum Disease (disorder)
+C0282528	Peroxisomal Disorders
+C0282529	Chondrodysplasia Punctata, Rhizomelic
+C0282548	Leukostasis
+C0282550	Persian Gulf Syndrome
+C0282577	Congenital Disorders of Glycosylation
+C0282606	Myomatous neoplasm
+C0282607	Vascular Neoplasms
+C0282609	Bone Marrow Neoplasms
+C0282612	Prostatic Intraepithelial Neoplasia
+C0282631	Facies
+C0282643	Smith-Lemli-Opitz Syndrome, Type I
+C0282644	Smith-Lemli-Opitz Syndrome, Type II
+C0282666	Very Low Birth Weight
+C0282667	Infant, Very Low Birth Weight
+C0282677	Burkholderia Infections
+C0282687	Hemorrhagic Fever, Ebola
+C0300933	Phycomycosis
+C0300946	Alymphocytosis
+C0300948	Caudal Regression Syndrome
+C0302129	Achromatopsia 1
+C0302142	Deformity
+C0302180	Condyloma
+C0302254	Juvenile cataract
+C0302269	Ostectomy
+C0302280	Adrenogenital Syndrome
+C0302295	Eruption
+C0302314	Xanthoma
+C0302319	Porokeratosis, Linear
+C0302329	Malignant lymphoma centroblastic, diffuse
+C0302332	Poisoning syndrome
+C0302356	incomplete anencephaly, hemicrania
+C0302358	Disease caused by Shigella dysenteriae
+C0302359	Disease caused by Shigella flexneri
+C0302360	Disease caused by Shigella boydii
+C0302361	Disease caused by Shigella sonnei
+C0302362	Brucella melitensis infection
+C0302369	Alcohol Withdrawal Hallucinosis
+C0302467	Congenital anomaly of aorta, unspecified
+C0302486	Erythrophagocytosis
+C0302497	Retrobulbar Hemorrhage
+C0302501	Mandibular hyperplasia
+C0302507	Parainfluenza Virus Infections
+C0302592	Carcinoma of cervix
+C0302809	Fulminant hepatitis
+C0302810	Uremia syndrome
+C0302813	Lactase deficiency
+C0302823	Crime victims
+C0302826	Expressed Emotion
+C0302840	Toxic thyroid adenoma
+C0302845	Mean cell volume increased
+C0302847	major affective disorder
+C0302858	Protein-losing gastroenteropathy
+C0302859	Euthyroid Goiter
+C0302872	MYELOMA, ENDOTHELIAL
+C0302874	Depressive personality disorder
+C0302883	SMITH DISEASE
+C0302885	Testicular dysgenesis
+C0302892	Congenital porencephaly
+C0302894	Stucco keratosis
+C0311213	Dermatitis verrucosa
+C0311223	Frozen shoulder
+C0311237	Goniodysgenesis
+C0311245	Congenital cystic kidney disease
+C0311249	Cryptophthalmos
+C0311251	Simple buphthalmos
+C0311277	Obesity, Abdominal
+C0311298	Propionic acidemia, type II
+C0311334	Generalized convulsive epilepsy
+C0311335	Grand Mal Status Epilepticus
+C0311337	Morton's neuralgia
+C0311338	Fundus Albipunctatus
+C0311343	Membranous conjunctivitis
+C0311361	Adenomatous goiter
+C0311364	Anemia due to decreased red cell production
+C0311368	Idiopathic eosinophilia
+C0311370	Lupus anticoagulant disorder
+C0311375	Arsenic Poisoning
+C0311389	Nonspecific urethritis
+C0311394	Difficulty walking
+C0311468	Blood bilirubin increased
+C0312413	Overflow incontinence of urine
+C0312414	Menstrual spotting
+C0312416	Morning sickness
+C0312420	Hypersexuality
+C0312422	Blackout
+C0312854	Extravascular Hemolysis
+C0314657	Genetic Predisposition to Disease
+C0314719	Dry eye
+C0332447	Morphologically abnormal structure (morphologic abnormality)
+C0332461	Patch
+C0332477	Erythematous plaque
+C0332534	Induration
+C0332544	Abnormal weight gain
+C0332561	Fibrous nodule
+C0332563	Papule
+C0332573	Macule
+C0332579	Lividity
+C0332599	Abnormal facies
+C0332601	Cushingoid
+C0332606	Elfin facies
+C0332615	Myopathic facies
+C0332687	Burns second degree
+C0332712	Fracture, spiral
+C0332743	Fracture delayed union
+C0332758	Avulsion fracture
+C0332768	Joint Subluxations
+C0332790	Osseous ankylosis
+C0332792	Dislocation, multiple
+C0332798	Open wound
+C0332853	Anastomosis
+C0332875	Congenital webbing
+C0332877	Congenital premature fusion
+C0332878	Congenital contracture
+C0332885	Congenital stenosis
+C0332886	Coarctation
+C0332887	Congenital hypertrophy
+C0332890	Congenital hemihypertrophy
+C0332909	Congenital unilateral absence
+C0332910	bilateral agenesis
+C0332915	Congenital failure of fusion
+C0333007	Congenital pigmentation
+C0333008	Congenital hypopigmentation
+C0333027	Microlithiasis
+C0333033	Fecalith
+C0333047	Recession
+C0333062	Hernia sac
+C0333068	Flexion contracture
+C0333099	Fusiform Aneurysm
+C0333106	Bleeding varices
+C0333113	Sacculation
+C0333128	Open comedone
+C0333133	Mucus cast
+C0333138	Stasis
+C0333139	Pneumatosis
+C0333140	Cyst rupture NOS
+C0333145	Haemorrhagic cyst
+C0333157	Colloid Cysts
+C0333160	Air cyst
+C0333161	Pseudocyst
+C0333183	Partial stenosis
+C0333186	Restenosis
+C0333203	Occlusive thrombus
+C0333205	Mural thrombus
+C0333209	Platelet thrombus
+C0333222	Septic embolus
+C0333233	Active Hyperemia
+C0333240	Acute edema
+C0333243	Pitting edema
+C0333244	Transient edema
+C0333245	Massive edema
+C0333258	Lymphorrhoea
+C0333262	Vesicle (morphologic abnormality)
+C0333271	Bloody discharge
+C0333274	Purulent discharge
+C0333286	Splinter haemorrhages
+C0333291	Bleeding ulcer
+C0333292	Perforated ulcer NOS
+C0333293	Healing ulcer
+C0333294	Recurrent ulcer
+C0333295	Acute ulcer
+C0333297	Chronic ulcer
+C0333304	Neuropathic ulcer
+C0333307	Superficial ulcer
+C0333313	Primary sequestrum
+C0333314	Secondary sequestrum
+C0333349	Nonsuppurative inflammation
+C0333355	Inflammatory disease of mucous membrane
+C0333371	Abscess rupture
+C0333376	Munro microabscess
+C0333419	Sarcoid type granuloma
+C0333440	Hyaline body
+C0333454	Granulovacuolar degeneration
+C0333457	Segmental demyelination
+C0333458	Retrograde Degeneration, Transneuronal
+C0333463	Senile Plaques
+C0333467	Cytopathic effect
+C0333472	Epidermolysis
+C0333494	Phlebosclerosis
+C0333495	Intercapillary glomerulosclerosis
+C0333497	Segmental glomerulosclerosis
+C0333512	Caseous necrosis
+C0333516	Tumour necrosis
+C0333519	Caries (morphologic abnormality)
+C0333525	Maceration
+C0333536	Dry gangrene
+C0333549	Haemorrhagic infarction
+C0333559	Infarction, Lacunar
+C0333577	Cholesterosis
+C0333582	Dystrophic calcification
+C0333616	Postinflammatory hyperpigmentation
+C0333628	Xanthosis
+C0333641	Atrophic
+C0333650	Fat atrophy NOS
+C0333662	Hemiatrophy
+C0333693	Triploidy syndrome
+C0333704	Chromosome Breaks
+C0333751	Muscle fiber atrophy
+C0333864	Giant platelet (morphologic abnormality)
+C0333873	Squamous intraepithelial lesion
+C0333875	High-Grade Squamous Intraepithelial Lesions
+C0333912	Hypochromasia
+C0333913	Achromasia
+C0333942	Polychromasia
+C0333979	Secondary hyperplasia
+C0333980	Focal Nodular Hyperplasia
+C0333983	Hyperplastic Polyp
+C0333992	Acanthoma, Clear Cell
+C0333997	Lymphoid hyperplasia
+C0334013	Phrynoderma
+C0334036	Apocrine metaplasia
+C0334037	Intestinal metaplasia
+C0334040	Extraskeletal ossification
+C0334041	Osteoma cutis
+C0334044	Dysplasia
+C0334050	Adenosis
+C0334054	cystic disease
+C0334067	Non-ossifying fibroma
+C0334082	Epidermal naevus
+C0334083	Connective tissue nevus, NOS
+C0334092	Hamartomatous polyp
+C0334106	Bowenoid papulosis
+C0334108	Multiple polyps
+C0334113	Eosinophilic granulomatous polyp
+C0334121	Inflammatory Myofibroblastic Tumor
+C0334139	Microglial nodules
+C0334157	Synechia
+C0334163	Fibrous bands
+C0334166	Pseudoainhum
+C0334192	Endometrial atrophy
+C0334230	Malignant tumor, fusiform cell type
+C0334233	Pleomorphic carcinoma
+C0334240	Combined small cell carcinoma
+C0334244	Papillary squamous cell carcinoma
+C0334245	Intraepithelial Squamous Cell Carcinoma
+C0334246	Metastatic squamous cell carcinoma
+C0334247	Squamous cell carcinoma, keratinizing
+C0334252	Squamous cell carcinoma, microinvasive
+C0334254	Lymphoepithelial carcinoma
+C0334263	Trichilemmoma
+C0334265	Transitional Cell Neoplasm
+C0334266	Transitional cell papilloma, benign
+C0334267	Transitional cell carcinoma in situ
+C0334268	Schneiderian papilloma
+C0334274	Papillary transitional cell carcinoma
+C0334276	Adenocarcinoma in Situ
+C0334277	Adenocarcinoma, metastatic
+C0334279	Adenocarcinoma, intestinal type
+C0334280	Carcinoma, diffuse type
+C0334281	Insulinoma, malignant
+C0334286	Bile duct cystadenocarcinoma
+C0334287	Fibrolamellar Hepatocellular Carcinoma
+C0334291	tubular adenomas and adenocarcinomas
+C0334292	Tubular adenoma
+C0334294	Multiple adenomatous polyps
+C0334296	Solid carcinoma
+C0334299	Carcinoid tumor no ICD-O subtype
+C0334307	Tubulovillous adenoma
+C0334309	Adenocarcinoma in tubulovillous adenoma
+C0334317	Cystadenofibroma
+C0334328	Microfollicular adenoma
+C0334331	Juxtaglomerular tumor
+C0334337	Endometrioid adenoma
+C0334342	Skin appendage adenoma
+C0334347	Eccrine spiradenoma
+C0334348	Hidradenoma Papilliferum
+C0334355	Serous cystadenoma, borderline malignancy
+C0334357	Papillary cystic tumor
+C0334359	Papillary serous cystadenocarcinoma
+C0334361	Serous surface papillary carcinoma
+C0334365	Mucinous cystic tumor of borderline malignancy
+C0334368	Mucin-producing adenocarcinoma
+C0334369	Comedocarcinoma, noninfiltrating
+C0334371	Secretory breast carcinoma
+C0334381	Non-infiltrating lobular carcinoma
+C0334384	Infiltrating duct and lobular carcinoma
+C0334385	Inflammatory carcinoma
+C0334398	Malignant Ovarian Thecoma
+C0334400	Sclerosing stromal tumor
+C0334401	Malignant Granulosa Cell Tumor
+C0334409	Leydig cell tumor, benign
+C0334416	Parasympathetic paraganglioma
+C0334419	Pheochromocytoma, malignant
+C0334421	Glomangioma
+C0334424	Nodular melanoma
+C0334428	Fibrous papule of nose
+C0334431	Melanocytoma
+C0334432	Nonpigmented nevus
+C0334438	Superficial spreading malignant melanoma of skin
+C0334439	Malignant desmoplastic melanoma
+C0334443	Epithelioid Cell Melanoma
+C0334444	Spindle Cell Melanoma
+C0334447	Malignant blue nevus of skin
+C0334448	Cellular Blue Nevus
+C0334454	Dermatofibrosarcoma Protuberans, Myxoid
+C0334459	Infantile fibrosarcoma
+C0334460	Elastofibroma
+C0334463	Histiocytoma, Malignant Fibrous
+C0334464	Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)
+C0334467	Fibrolipoma
+C0334471	Round cell liposarcoma
+C0334474	Spindle cell lipoma
+C0334475	Lipoblastomatosis
+C0334477	Cellular leiomyoma
+C0334480	Pleomorphic Rhabdomyosarcoma
+C0334482	Fetal rhabdomyoma
+C0334485	Endometrial stromal nodule
+C0334486	Low Grade Endometrial Stromal Sarcoma
+C0334488	Clear cell sarcoma of kidney
+C0334489	Pancreatoblastoma
+C0334491	Benign Mesenchymoma
+C0334492	Malignant mesenchymal tumor
+C0334494	Proliferating Brenner Tumor
+C0334505	Synovial sarcoma, spindle cell
+C0334507	Synovial sarcoma, biphasic
+C0334509	Clear cell sarcoma, of tendons and aponeuroses
+C0334513	Sarcomatoid Mesothelioma
+C0334515	Mesothelioma, biphasic, malignant
+C0334517	Spermatocytic seminoma
+C0334518	Polyembryoma
+C0334520	Teratoma, Malignant
+C0334524	Mixed Germ Cell Tumor
+C0334525	Struma ovarii, malignant
+C0334526	Strumal carcinoid
+C0334529	Hydatidiform Mole, Partial
+C0334533	Arteriovenous hemangioma
+C0334538	Epithelioid hemangioendothelioma, malignant
+C0334541	Hemangiopericytoma, benign
+C0334542	Hemangiopericytoma, Malignant
+C0334551	Myxoid chondrosarcoma
+C0334552	Malignant Giant Cell Tumor of Bone
+C0334553	Giant Cell Tumor of Soft Tissue
+C0334557	Odontogenic tumor, benign
+C0334558	Malignant odontogenic tumor
+C0334565	Adenoameloblastoma
+C0334567	Malignant Ameloblastoma
+C0334572	Ameloblastic fibroma
+C0334574	Calcifying Epithelial Odontogenic Tumor
+C0334576	Gliomatosis cerebri
+C0334578	Papillary ependymoma
+C0334579	Anaplastic astrocytoma
+C0334580	Protoplasmic astrocytoma
+C0334581	Gemistocytic astrocytoma
+C0334582	Fibrillary Astrocytoma
+C0334583	Pilocytic Astrocytoma
+C0334584	Spongioblastoma
+C0334586	Pleomorphic Xanthoastrocytoma
+C0334587	Astroblastoma
+C0334588	Giant Cell Glioblastoma
+C0334590	Anaplastic Oligodendroglioma
+C0334595	Ganglioneuromatosis
+C0334596	Medulloepithelioma
+C0334600	Retinoblastoma, differentiated
+C0334605	Meningothelial meningioma
+C0334606	Fibrous Meningioma
+C0334607	Psammomatous Meningioma
+C0334608	Angiomatous Meningioma
+C0334609	Hemangioblastic Meningioma
+C0334610	Hemangiopericytic Meningioma
+C0334611	Transitional Meningioma
+C0334616	Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation
+C0334619	HODGKIN\'S AND NON-HODGKIN\'S LYMPHOMA
+C0334633	Malignant lymphoma - lymphoplasmacytic
+C0334634	Lymphoma, Mantle-Cell
+C0334635	Malignant lymphoma - centrocytic
+C0334636	Malignant lymphoma, mixed small and large cell, diffuse
+C0334638	Malignant lymphomatous polyposis
+C0334660	Angioendotheliomatosis
+C0334663	Histiocytic sarcoma
+C0334664	Mast Cell Neoplasm
+C0334674	Acute panmyelosis with myelofibrosis
+C0334685	Chief cell adenocarcinoma
+C0334689	C cell tumor
+C0334695	Endometrial Stromal Tumors
+C0334699	Malignant myoepithelioma
+C0337210	Gait, Stumbling
+C0337308	Leg amputation
+C0337428	Fibrinogen assay
+C0337432	Androstenedione measurement
+C0337434	Estradiol measurement
+C0337437	Glucagon measurement
+C0337438	Glucose measurement
+C0337446	Tyrosine measurement
+C0337616	Educational problem
+C0337629	Economic problem NOS
+C0337664	Smoker
+C0337677	Moderate drinker
+C0338070	Childhood Cerebral Astrocytoma
+C0338078	Non-Functioning Pituitary Gland Neoplasm
+C0338106	Adenocarcinoma of colon
+C0338113	Uterine Corpus Sarcoma
+C0338237	Antibiotic therapy
+C0338401	Encephalitis enteroviral
+C0338418	Encephalitis, Acute Necrotizing
+C0338430	Limbic Encephalitis
+C0338437	Neurocysticercosis
+C0338451	Frontotemporal dementia
+C0338455	Dementia of frontal lobe type
+C0338457	Aphasia, Progressive
+C0338460	Argyrophilic grain disease
+C0338462	Semantic Dementia
+C0338468	Tic Disorders, Vocal
+C0338473	Neuroaxonal Dystrophies
+C0338474	Central nervous system demyelination
+C0338478	Idiopathic Myoclonic Epilepsy
+C0338479	Symptomatic Myoclonic Epilepsy
+C0338480	Common Migraine
+C0338483	Migraine with Prolonged Aura
+C0338484	Familial Hemiplegic Migraine
+C0338486	Migraine Aura without Headache
+C0338488	Alternating hemiplegia of childhood
+C0338489	Status Migrainosus
+C0338495	Sleep Apnea, Mixed Central and Obstructive
+C0338502	Hypoplasia of the optic nerve
+C0338503	Septo-Optic Dysplasia
+C0338507	Non-arteritic ischemic optic neuropathy
+C0338508	Optic Atrophy 1
+C0338512	Optic Nerve Avulsion
+C0338538	Ulnar Neuritis
+C0338551	Leprosy neuropathy
+C0338567	Horner's syndrome pupil
+C0338573	Cerebral venous sinus thrombosis
+C0338575	Sagittal Sinus Thrombosis
+C0338582	Sporadic Cerebral Amyloid Angiopathy
+C0338585	Carotid artery dissection
+C0338586	Vertebral Artery Dissection
+C0338591	Amnesia, Transient Global
+C0338596	Spastic cerebral palsy
+C0338597	Choroid plexus cyst
+C0338614	Psychotic episodes
+C0338630	Senile Paranoid Dementia
+C0338644	Delirium of Mixed Origin
+C0338650	Catatonia, Organic
+C0338656	Cognitive Dysfunction
+C0338657	Age-associated memory impairment
+C0338666	Substance abuser
+C0338715	Drug-induced depressive state
+C0338791	Psychoactive substance-induced withdrawal syndrome
+C0338818	Morbid jealousy
+C0338822	Cycloid psychosis
+C0338831	Mania
+C0338900	Psychasthenic neurosis
+C0338902	Writer\'s cramp neurosis
+C0338908	Mixed anxiety and depressive disorder
+C0338938	Hypochondriacal pain
+C0338986	Atypical autism
+C0339002	Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
+C0339005	Conduct disorder, childhood-onset type
+C0339063	Cellulitis of eyelid
+C0339089	Eyelid injury
+C0339115	Sebaceous adenocarcinoma of eyelid
+C0339143	Graves Ophthalmopathy
+C0339164	Seasonal allergic conjunctivitis
+C0339182	Ankyloblepharon
+C0339229	Superior limbic keratoconjunctivitis
+C0339268	Arcus juvenilis
+C0339271	Salzmann nodular dystrophy
+C0339273	Corneal dystrophy, Lattice type 3
+C0339277	Corneal Dystrophy, Juvenile Epithelial of Meesmann
+C0339278	Reis-Bucklers\' corneal dystrophy
+C0339284	Polymorphous corneal dystrophy
+C0339289	Corneal injuries
+C0339293	Corneal Perforation
+C0339303	Corneal graft rejection
+C0339304	Neoplasm of cornea
+C0339315	Anterior uveitis idiopathic
+C0339383	Chorioretinopathy
+C0339402	Birdshot chorioretinitis
+C0339434	Choroidal effusion
+C0339462	Macular retinoschisis
+C0339467	Proliferative retinopathy
+C0339470	Visually threatening diabetic retinopathy
+C0339471	Diabetic maculopathy
+C0339477	Lipidemia retinalis
+C0339495	Cilioretinal artery occlusion
+C0339499	Central retinal vein occlusion - juvenile
+C0339505	Venous retinal branch occlusion
+C0339508	Hereditary macular dystrophy
+C0339510	Vitelliform Macular Dystrophy
+C0339512	Bull\'s eye macular dystrophy
+C0339513	Dominant drusen
+C0339525	Autosomal dominant retinitis pigmentosa
+C0339526	Autosomal recessive retinitis pigmentosa
+C0339527	Leber Congenital Amaurosis
+C0339528	X-linked retinitis pigmentosa
+C0339530	Progressive cone-rod dystrophy
+C0339534	Usher syndrome type 2
+C0339535	Night blindness, congenital stationary
+C0339537	Cone monochromatism
+C0339539	Familial Exudative Vitreoretinopathies
+C0339541	Goldmann-Favre syndrome (disorder)
+C0339543	Epiretinal Membrane
+C0339546	Retinal Pigment Epithelial Detachment
+C0339555	Congenital hypertrophy of retinal pigment epithelium
+C0339562	Amyloid of vitreous
+C0339573	Glaucoma, Primary Open Angle
+C0339576	Glaucoma due to combination of mechanisms
+C0339578	Corticosteroid-induced glaucoma
+C0339623	Primary Esotropia
+C0339624	Secondary Esotropia
+C0339635	Primary Exotropia
+C0339636	Secondary Exotropia
+C0339640	Dissociated vertical deviation
+C0339648	Strabismus fixus
+C0339651	Horizontal gaze palsy
+C0339652	Vertical gaze palsy
+C0339662	Afferent Pupillary Defect
+C0339681	Index myopia
+C0339682	Regular astigmatism - corneal
+C0339693	Internal Ophthalmoplegia
+C0339696	Anisometropic amblyopia
+C0339730	Blindness, Acquired
+C0339753	External ear cellulitis NOS
+C0339780	Syncopal Vertigo
+C0339789	Congenital deafness
+C0339805	Cat allergy (disorder)
+C0339807	House dust allergy
+C0339864	Bifid epiglottis
+C0339901	Acute respiratory infections
+C0339904	Lung disease with systemic sclerosis
+C0339916	Viral upper respiratory tract infection
+C0339941	Acute viral bronchiolitis
+C0339952	Secondary bacterial pneumonia
+C0339959	Pneumonia chlamydial
+C0339961	Fungal pneumonia
+C0339968	Neonatal pneumonia
+C0339985	Idiopathic bronchiectasis
+C0339997	Asbestos pleurisy
+C0340014	Chylothorax, congenital
+C0340030	Pleural plaque
+C0340037	Young Syndrome
+C0340044	Acute exacerbation of chronic obstructive airways disease
+C0340076	Asthmatic pulmonary eosinophilia
+C0340100	High altitude pulmonary edema
+C0340161	Hematomediastinum
+C0340164	Lofgrens syndrome
+C0340169	Simple pneumoconiosis
+C0340170	Complicated pneumoconiosis
+C0340194	Hypoxemic Respiratory Failure
+C0340214	Tracheal fistula
+C0340220	Tracheal hemorrhage
+C0340221	Tracheal obstruction
+C0340228	Acquired Subglottic Stenosis
+C0340231	Tracheobronchomalacia
+C0340238	Bronchial infection
+C0340256	Sepsis-associated lung injury
+C0340274	Gestational hypertension
+C0340278	Atrial hypertrophy
+C0340279	Ventricular hypertrophy
+C0340288	Angina, Stable
+C0340293	Anterior myocardial infarction
+C0340324	Silent myocardial infarction
+C0340354	Q fever endocarditis
+C0340364	Familial mitral valve prolapse
+C0340375	Subaortic stenosis
+C0340420	Cardiac glycogenosis
+C0340425	Hypertrophic cardiomyopathy without obstruction
+C0340427	Familial dilated cardiomyopathy
+C0340429	Familial restrictive cardiomyopathy (disorder)
+C0340434	Dystrophic cardiomyopathy
+C0340464	Extrasystoles
+C0340477	Re-entrant atrioventricular tachycardia
+C0340485	Familial ventricular tachycardia
+C0340486	Induced ventricular tachycardia
+C0340489	Lone atrial fibrillation
+C0340491	Familial sick sinus syndrome
+C0340493	Paroxysmal familial ventricular fibrillation
+C0340515	Myocardial depression
+C0340517	Atrial thrombosis
+C0340520	Athlete\'s heart
+C0340529	Complications of transplanted heart
+C0340530	Heart transplant rejection
+C0340542	Sporadic primary pulmonary hypertension
+C0340543	Familial primary pulmonary hypertension
+C0340544	Pulmonary arterial hypertension induced by drug
+C0340548	Pulmonary capillary hemangiomatosis
+C0340552	High altitude pulmonary hypertension
+C0340557	Atherosclerotic renal artery stenosis
+C0340563	Upper limb ischemia
+C0340566	Critical lower limb ischemia
+C0340569	Internal Carotid Artery Stenosis
+C0340600	Femoral artery embolism
+C0340608	Renal artery thrombosis
+C0340613	Arterial aneurysm
+C0340629	Aortic aneurysm without mention of rupture NOS
+C0340630	Aortic Aneurysm, Thoracoabdominal
+C0340639	Carotid artery aneurysm
+C0340642	Anterior Spinal Artery Dissection
+C0340643	Aortic dissection
+C0340647	Distal aortic dissection
+C0340648	Coronary artery dissection
+C0340652	Arterial injury
+C0340654	Arterial haemorrhage
+C0340664	Coronary artery perforation
+C0340726	Embolism venous
+C0340753	Venous stenosis
+C0340756	Pulmonary vein stenosis
+C0340766	Venous hypertension
+C0340770	Venous injury
+C0340771	Venous haemorrhage
+C0340775	Varicose vein ruptured
+C0340782	Hyperplastic lymph node
+C0340785	Atypical mycobacterial lymphadenitis
+C0340803	Capillary malformation (disorder)
+C0340804	Hereditary vascular fragility
+C0340828	Capillary-venous malformation
+C0340834	Hennekam lymphangiectasia lymphedema syndrome
+C0340848	PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE
+C0340850	Neurally mediated syncope
+C0340854	Syncope, Situational
+C0340855	Syncope, Micturition
+C0340861	Pulseless electrical activity
+C0340865	Anaphylactoid reaction
+C0340895	Vascular graft thrombosis
+C0340896	Vascular graft infection
+C0340907	Arteriovenous fistula occlusion
+C0340908	Arteriovenous fistula stenosis
+C0340909	Arteriovenous fistula thrombosis
+C0340957	Congenital deficiency of intrinsic factor
+C0340968	Deficiency of pyruvate kinase
+C0340969	Uridine monophosphate hydrolase deficiency
+C0340970	Congenital neutropenia
+C0340971	Autoimmune neutropenia
+C0340978	May-Hegglin anomaly
+C0340979	Cryoglobulinemic purpura
+C0340987	Splenic atrophy
+C0340990	Bone marrow transplant rejection
+C0341007	Alveolar ridge abnormality
+C0341012	Oral herpes
+C0341038	Jaw Keratocyst
+C0341047	Hypertrophy of parotid gland
+C0341059	Lip pit
+C0341106	Eosinophilic esophagitis
+C0341109	Fungal oesophagitis
+C0341163	Gastric ulcer perforation
+C0341164	Gastric ulcer haemorrhage
+C0341177	Gastric erosions
+C0341189	Reactive gastritis
+C0341217	Dieulafoy's vascular malformation
+C0341225	Gastric Hamartoma
+C0341245	Duodenitis haemorrhagic
+C0341268	Disorder of small intestine
+C0341281	Ulcerative jejunitis
+C0341299	Collagenous Sprue
+C0341305	Autoimmune enteropathy
+C0341306	Microvillus inclusion disease
+C0341318	Enterocutaneous Fistula
+C0341335	Cytomegaloviral colitis
+C0341365	Colonic fistula
+C0341395	Perianal Crohn\'s disease
+C0341402	Rectal perforation
+C0341429	Colon gangrene
+C0341439	Chronic liver disease
+C0341461	Idiopathic acute pancreatitis
+C0341471	Idiopathic chronic pancreatitis
+C0341472	Obstructive chronic pancreatitis
+C0341486	Cystadenoma of pancreas
+C0341491	Pancreatic duct obstruction
+C0341503	Bacterial peritonitis
+C0341505	Chemical peritonitis
+C0341512	Retroperitoneal haematoma
+C0341562	Gastrointestinal anastomotic leak
+C0341698	Atrophy of kidney
+C0341702	Acquired Fanconi syndrome
+C0341703	Adult Fanconi syndrome
+C0341706	Glycinuria
+C0341742	Acute retention of urine
+C0341750	Urinary bladder haemorrhage
+C0341751	Bladder necrosis
+C0341787	Bifid scrotum
+C0341803	Endometrial ablation
+C0341823	Epithelial tumor of ovary
+C0341851	Condyloma acuminata of vulva
+C0341858	Adenomyosis
+C0341862	Hypothalamic amenorrhea
+C0341869	Subfertility, Female
+C0341934	Transient hypertension of pregnancy
+C0342095	Breast haematoma
+C0342114	Diffuse goiter
+C0342122	Toxic diffuse goiter
+C0342123	Thyrotoxicosis due to Graves\' disease
+C0342127	Toxic nodular goiter
+C0342136	Autonomous thyroid function
+C0342138	Thyrotoxicosis in pregnancy
+C0342153	Congenital thyroid hypoplasia
+C0342155	Congenital hypothyroidism with ectopic thyroid
+C0342162	Compensated hypothyroidism
+C0342185	Hyperthyroxinemia, Familial Dysalbuminemic
+C0342190	C-cell hyperplasia of thyroid
+C0342191	Familial dyshormonogenetic goiter
+C0342194	Thyroid Dyshormonogenesis 3
+C0342195	Thyroid Dyshormonogenesis 4
+C0342196	Thyroid Dyshormonogenesis 5
+C0342198	Thyrotoxicosis due to pituitary thyroid hormone resistance
+C0342199	Iodine deficiency syndrome
+C0342200	Endemic Cretinism
+C0342208	Multinodular goiter
+C0342245	Diabetic eye disease NOS
+C0342257	Complications of Diabetes Mellitus
+C0342273	Transient neonatal diabetes mellitus
+C0342276	Maturity onset diabetes mellitus in young
+C0342277	Diabetes mellitus autosomal dominant type II (disorder)
+C0342278	Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
+C0342282	Multiple synostoses syndrome 1
+C0342283	Hyperproinsulinemia
+C0342286	Woodhouse Sakati syndrome
+C0342287	Thiamine responsive megaloblastic anemia syndrome
+C0342288	Insulin-dependent diabetes mellitus secretory diarrhea syndrome
+C0342289	Diabetes-deafness syndrome maternally transmitted (disorder)
+C0342302	Brittle diabetes
+C0342311	Neuroglycopenia
+C0342317	Hypoglycaemia unawareness
+C0342326	Tumor-induced hypoglycemia
+C0342335	Insulin resistance in diabetes
+C0342336	Insulin resistance - type A
+C0342342	Idiopathic Hypoparathyroidism
+C0342344	Hypoparathyroidism - X-linked
+C0342345	Hypoparathyroidism - autosomal dominant
+C0342346	Pseudohypoparathyroidism and pseudopseudohypoparathyroidism
+C0342369	Somatotroph hyperplasia
+C0342376	Panhypopituitarism - X-linked
+C0342381	Idiopathic growth hormone deficiency
+C0342384	Idiopathic hypogonadotropic hypogonadism
+C0342386	Follicle stimulating hormone deficiency
+C0342388	Adrenocorticotropic hormone (ACTH) deficiency (disorder)
+C0342394	Familial central diabetes insipidus
+C0342396	Idiopathic hypopituitarism
+C0342405	Pituitary infarction
+C0342406	Pituitary haemorrhage
+C0342409	Hypophysitis
+C0342410	Autoimmune Hypophysitis
+C0342418	Hypothalamic hamartomas
+C0342419	Pituitary mass
+C0342422	Pituitary gland enlarged
+C0342442	ACTH-dependent Cushing\'s syndrome
+C0342443	Adrenal Cushing\'s syndrome
+C0342444	Cyclical Cushing\'s syndrome
+C0342464	Salt-losing congenital adrenal hyperplasia
+C0342467	Late onset congenital adrenal hyperplasia
+C0342471	3 beta-Hydroxysteroid dehydrogenase deficiency
+C0342474	Lipoid congenital adrenal hyperplasia
+C0342482	X-linked Adrenal Hypoplasia
+C0342488	Mineralocorticoid Excess Syndrome, Apparent
+C0342491	Small adrenal gland
+C0342492	Adrenal hypertrophy or hyperplasia
+C0342494	Adrenocortical hyperplasia
+C0342495	Macronodular adrenal hyperplasia
+C0342496	Micronodular adrenal hyperplasia
+C0342500	Adrenal mass
+C0342501	Adrenal cyst
+C0342510	Ovarian dysgenesis
+C0342526	Absent testes
+C0342527	Androgen deficiency
+C0342538	Constitutional delay of growth and puberty
+C0342541	Precocious pubarche
+C0342543	Central Precocious Puberty
+C0342544	Idiopathic central precocious puberty
+C0342546	Premature adrenarche
+C0342548	Early menarche
+C0342549	Familial Testotoxicosis
+C0342552	Autoimmune endocrine disease
+C0342573	PITUITARY DWARFISM I
+C0342579	Electrolyte imbalance
+C0342592	Anion gap increased
+C0342593	Anion gap decreased
+C0342608	Amyloid Polyneuropathy, British Type (disorder)
+C0342609	Hereditary oculoleptomeningeal amyloid angiopathy
+C0342610	Hereditary cerebrovascular amyloidosis
+C0342611	Familial non-neuropathic amyloidosis
+C0342613	Danish type familial amyloid cardiomyopathy
+C0342618	Amyloid myopathy
+C0342623	Senile systemic amyloidosis
+C0342634	Neonatal hypocalcemia
+C0342637	Hypocalciuric hypercalcemia, familial, type 1
+C0342639	Familial idiopathic hypercalciuria
+C0342642	Autosomal dominant hypophosphatemic rickets
+C0342643	Autosomal recessive hypophosphatemic vitamin D refractory rickets
+C0342646	Vitamin D-Dependent Rickets, Type 2A
+C0342649	Vascular calcification
+C0342653	Acquired hypophosphatemia
+C0342680	Klein-Waardenberg\'s syndrome
+C0342683	ALBINISM, OCULOCUTANEOUS, TYPE III
+C0342684	Ocular albinism, type I
+C0342686	Aromatic amino acid decarboxylase deficiency
+C0342687	dopamine beta hydroxylase deficiency
+C0342701	Transcobalamin II deficiency
+C0342704	Deficiency of Cobalamin G
+C0342705	Folate Malabsorption, Hereditary
+C0342708	Gamma aminobutyric acid transaminase deficiency
+C0342712	Disorder of branched-chain amino acid metabolism
+C0342720	Adenosylcobalamin synthesis defect
+C0342727	3-@METHYLGLUTACONIC ACIDURIA, TYPE I
+C0342728	3-Methylglutaconic aciduria type 1
+C0342731	Deficiency of mevalonate kinase
+C0342735	Cytosolic acetoacetyl-CoA thiolase deficiency
+C0342737	3-Hydroxyisobutyric aciduria
+C0342738	Beta-Hydroxyisobutyryl CoA Deacylase Deficiency
+C0342739	Trimethylaminuria
+C0342748	Glycogen synthase deficiency
+C0342749	GLYCOGEN STORAGE DISEASE Ic
+C0342750	Glycogen storage disease type Id
+C0342751	Generalized glycogen storage disease of infants
+C0342759	Primary lactose intolerance
+C0342765	D-Glyceric aciduria
+C0342770	Fumarase deficiency
+C0342776	Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
+C0342777	Succinate-coenzyme Q reductase deficiency
+C0342778	Ubiquinone dehydrogenase deficiency
+C0342779	Complex V deficiency
+C0342782	Depletion of mitochondrial DNA
+C0342783	Deficiency of butyryl-CoA dehydrogenase
+C0342784	Pearson\'s marrow-pancreas syndrome
+C0342785	Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
+C0342788	Renal carnitine transport defect
+C0342790	Carnitine palmitoyl transferase 2 deficiency
+C0342791	Carnitine-Acylcarnitine Translocase Deficiency
+C0342792	Succinyl-CoA:3-oxoacid CoA transferase deficiency
+C0342793	Malonic aciduria
+C0342800	Inosine Triphosphatase Deficiency
+C0342801	Thiopurine S methyltranferase deficiency
+C0342803	Dihydropyrimidinase deficiency
+C0342826	3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
+C0342841	Hunter\'s syndrome, severe form
+C0342842	Hunter\'s syndrome, mild form
+C0342853	Sialuria
+C0342856	Coproporphyria
+C0342858	Homozygous acute intermittent porphyria
+C0342859	Harderoporphyria
+C0342860	Homozygous variegate porphyria
+C0342861	Uroporphyrinogen decarboxylase deficiency
+C0342869	Deficiency of acetyl-CoA acyltransferase (disorder)
+C0342870	Bifunctional peroxisomal enzyme deficiency
+C0342873	Glutaric Aciduria III
+C0342879	Primary hypercholesterolemia
+C0342880	Polygenic hypercholesterolemia
+C0342881	Familial hypercholesterolemia - homozygous
+C0342883	Cholesteryl Ester Transfer Protein Deficiency
+C0342886	Primary hypertriglyceridemia
+C0342889	Secondary hypertriglyceridemia
+C0342892	Hypolipidaemia
+C0342895	Fish-Eye Disease
+C0342898	Apolipoprotein A-I deficiency
+C0342907	Sitosterolemia
+C0342922	Dietary calcium deficiency
+C0342942	Generalized obesity
+C0342951	Hypervitaminosis
+C0342952	Hypermetabolism
+C0342953	Organ dysfunction syndrome
+C0342971	Incisional hernia repair
+C0343026	Nail infection NOS
+C0343047	Complement component 5 deficiency
+C0343052	Guttate psoriasis
+C0343055	Generalized pustular psoriasis
+C0343057	Keratosis pilaris decalvans
+C0343065	Symptomatic dermographism
+C0343068	Familial cold urticaria
+C0343073	Wooly hair
+C0343081	Livedoid vasculitis
+C0343082	Senile angioma
+C0343084	Capillary Leak Syndrome
+C0343097	Nodular Elastoidosis
+C0343101	Eosinophilic cellulitis
+C0343110	Epidermolytic palmoplantar keratoderma of Vorner
+C0343111	Naegeli syndrome
+C0343114	Woolly hair nevus
+C0343115	Skin Mastocytoma
+C0343149	Contracture of joint of foot
+C0343166	Knee joint effusion
+C0343190	Cutaneous polyarteritis nodosa
+C0343206	Hypocomplementemic urticarial vasculitis
+C0343208	Essential mixed cryoglobulinemia
+C0343239	Benign congenital hypotonia
+C0343243	Muscle abscess
+C0343263	Chondrolysis
+C0343284	Chondrodysplasia
+C0343349	Infantile gastroenteritis
+C0343353	Gastroenteritis staphylococcal
+C0343357	Gastroenteritis Escherichia coli
+C0343361	Gastroenteritis adenovirus
+C0343363	Gastroenteritis rotavirus
+C0343378	Helicobacter gastritis
+C0343380	Enteropathogenic Escherichia coli gastrointestinal tract infection
+C0343381	Verotoxigenic Escherichia coli gastrointestinal tract infection
+C0343386	Clostridium difficile infection
+C0343387	Enterocolitis, Neutropenic
+C0343401	MRSA - Methicillin resistant Staphylococcus aureus infection
+C0343404	Morganella infection
+C0343442	Listeria Cerebritis
+C0343457	Borderline tuberculoid leprosy
+C0343458	Borderline lepromatous leprosy
+C0343461	Leprosy reversal reaction
+C0343466	Type 2 lepra reaction
+C0343494	Risus sardonicus
+C0343495	Lockjaw
+C0343525	Lemierre Syndrome
+C0343528	Pontiac Fever
+C0343537	Specific viral infections
+C0343560	Congenital Varicella Syndrome
+C0343640	African Burkitt's lymphoma
+C0343641	Human papilloma virus infection
+C0343643	Facial wart
+C0343683	Neurosyphilis, Secondary
+C0343686	Neurosyphilis, Gummatous
+C0343713	Gonococcal arthritis dermatitis syndrome
+C0343723	Neonatal chlamydial conjunctivitis
+C0343729	Anal warts
+C0343731	Penile warts
+C0343751	Asymptomatic human immunodeficiency virus infection
+C0343752	Acute HIV infection
+C0343755	HIV Wasting Syndrome
+C0343758	Typhus group rickettsial disease
+C0343800	Acute Chagas\' disease
+C0343804	Chronic Chagas\' disease
+C0343856	Systemic aspergillosis
+C0343858	Chronic Necrotizing Pulmonary Aspergillosis
+C0343863	Candida infection of genital region
+C0343881	Central nervous system candidiasis
+C0343885	Chronic disseminated candidiasis
+C0343886	Gastrointestinal candidiasis
+C0343890	Disseminated cryptococcosis
+C0343898	Acute pulmonary histoplasmosis
+C0343900	Histoplasmosis disseminated
+C0343939	Trichosporon infection
+C0343951	Disseminated phaeohyphomycosis
+C0343952	Hyalohyphomycosis
+C0343953	Cutaneous Hyalohyphomycosis
+C0343954	Disseminated Hyalohyphomycosis
+C0343961	Entomophthoramycosis
+C0343968	Hepatosplenic schistosomiasis
+C0344022	Onchocercal depigmentation
+C0344096	Abscess drainage
+C0344183	Exercise anaphylaxis
+C0344191	Cerebellar decompression injury
+C0344232	Blurred vision
+C0344233	Retinal blind spot
+C0344243	See-Saw Nystagmus
+C0344262	Anterior lenticonus
+C0344263	Posterior lenticonus
+C0344290	Vitreoretinal degeneration
+C0344297	Choroidal sclerosis
+C0344304	Generalized abdominal pain
+C0344306	Intercostal neuralgia
+C0344307	Absence of pain sensation
+C0344310	Striae gravidarum
+C0344312	White forelock
+C0344315	Depressed mood
+C0344322	Inhibited sexual desire
+C0344323	Flashing
+C0344357	Nocturnal dyspnea
+C0344365	Incomplete emptying of bladder
+C0344375	Stomach cramps (finding)
+C0344386	Schistocytosis
+C0344395	Bilirubin measurement
+C0344431	Ventricular tachycardia, monomorphic
+C0344432	Ventricular tachycardia, polymorphic
+C0344452	Microprolactinoma
+C0344453	Macroprolactinoma
+C0344456	Malignant Adrenal Medulla Neoplasm
+C0344460	Carcinoma ex pleomorphic adenoma
+C0344461	Oligodendroblastoma
+C0344462	Chronic lymphoproliferative disease NOS
+C0344479	Spinal Cord Myelodysplasia
+C0344482	Hypoplasia of corpus callosum
+C0344487	Lateral meningocele
+C0344490	Sacral agenesis
+C0344505	Alacrima
+C0344509	Agenesis of punctum lacrimale
+C0344511	Atresia of nasolacrimal duct
+C0344516	Coloboma of lens
+C0344522	Congenital posterior polar cataract
+C0344523	Cataract, congenital, cerulean type 1
+C0344525	Congenital membranous cataract
+C0344529	Cornea plana
+C0344530	Congenital keratoglobus
+C0344531	Embryotoxon
+C0344539	Hypoplasia of iris
+C0344541	Persistent pupillary membranes
+C0344542	Aniridia type 1
+C0344544	Polycoria
+C0344550	Congenital retinal fold
+C0344559	Irido-corneo-trabecular dysgenesis (disorder)
+C0344600	Cardiac malposition
+C0344622	Double inlet left ventricle
+C0344692	Isomerism of atrial appendages
+C0344709	Right atrial dilatation
+C0344720	Left atrial dilatation
+C0344724	Ostium secundum atrial septal defect
+C0344730	Atrial Septal Defect Sinus Venosus
+C0344735	Partial atrioventricular canal
+C0344760	Congenital atresia of mitral valve
+C0344763	Mitral valve hypoplasia
+C0344772	Cleft leaflet of mitral valve
+C0344783	Atrioventricular septal defect and common atrioventricular junction
+C0344787	Complete atrioventricular septal defect
+C0344882	Tetralogy of Fallot with pulmonary atresia
+C0344893	Right ventricular dilatation
+C0344900	Right ventricular outflow tract obstruction
+C0344905	Left ventricular abnormality
+C0344911	Left ventricular dilatation
+C0344917	Left ventricular outflow tract obstruction
+C0344923	Multiple ventricular septal defects
+C0344925	Perimembranous ventricular septal defect
+C0344955	Ventricular septal hypertrophy
+C0344963	Pseudotruncus arteriosus
+C0344975	Pulmonary Atresia with Intact Ventricular Septum
+C0345030	Peripheral pulmonary artery stenosis
+C0345049	Ascending aorta dilatation
+C0345050	Congenital aneurysm of ascending aorta
+C0345065	Cervical aortic arch
+C0345120	Coronary ostial stenosis
+C0345140	Totally absent pericardium
+C0345200	Congenital dysmotility of small intestine
+C0345217	Cloacal exstrophy
+C0345218	Low anorectal malformation
+C0345237	Short segment Hirschsprung\'s disease
+C0345240	Total intestinal aganglionosis
+C0345244	Neuronal intestinal dysplasia
+C0345286	Abnormal liver lobulation
+C0345309	Hypoplasia of vagina
+C0345319	Cyst of hydatid of Morgagni
+C0345326	Congenital phimosis
+C0345354	Radial polydactyly
+C0345371	Hypoplasia of lower limb
+C0345375	Congenital hypoplasia of femur
+C0345382	Gorlin Chaudhry Moss syndrome
+C0345392	Congenital kyphoscoliosis
+C0345394	Hypoplasia of spine
+C0345397	Accessory rib
+C0345406	Neonatal hyperparathyroidism
+C0345407	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
+C0345408	Hereditary clubbing
+C0345419	Cutis marmorata telangiectatica congenita
+C0345427	Woolly hair, congenital
+C0345602	Parotid Gland Carcinoma
+C0345832	Neoplasm of small intestine
+C0345893	Juvenile polyposis syndrome
+C0345904	Hepatic cancer
+C0345905	Intrahepatic Cholangiocarcinoma
+C0345906	Sarcoma of liver
+C0345907	Angiosarcoma of liver
+C0345916	Neoplasm of ampulla of Vater
+C0345958	Large cell carcinoma of lung
+C0345960	Giant cell carcinoma of lung
+C0345963	Benign lung neoplasm
+C0345964	Adenoma of lung
+C0345967	Malignant mesothelioma
+C0345984	Solitary keratoacanthoma
+C0345988	Neoplasm of skin with adnexal differentiation
+C0345989	Infected sebaceous cyst
+C0345992	Pilar tumor
+C0345996	Milia
+C0346010	Birt-Hogg-Dube Syndrome
+C0346011	Fibrofolliculoma
+C0346023	Syringocystadenoma
+C0346027	Eccrine epithelioma
+C0346037	Acral Lentiginous Malignant Melanoma
+C0346040	Stage 0 Skin Melanoma
+C0346041	Tumor of dermis
+C0346046	Fibrous papule of face
+C0346053	Atypical fibroxanthoma of skin
+C0346054	Verruciform xanthoma of skin
+C0346056	Neuromuscular hamartoma
+C0346057	Cutaneous neurofibroma
+C0346064	Cutaneous leiomyoma
+C0346072	Blue rubber bleb nevus syndrome
+C0346073	Tufted angioma of skin
+C0346099	Nevus spilus
+C0346109	Malignant Mesothelioma of Peritoneum
+C0346117	Malignant Lipomatous Neoplasm
+C0346118	Benign lipomatous tumor
+C0346153	Breast Cancer, Familial
+C0346154	Malignant phyllodes tumor of breast
+C0346156	Benign breast neoplasm
+C0346158	Juvenile fibroadenoma of breast
+C0346163	Endometrioid carcinoma ovary
+C0346167	Undifferentiated carcinoma of ovary
+C0346169	Ovarian Cystadenoma
+C0346172	Mucinous cystadenoma of ovary
+C0346178	Ovarian gynandroblastoma
+C0346182	Immature teratoma of ovary
+C0346183	Ovarian Embryonal Carcinoma
+C0346185	Dysgerminoma of ovary
+C0346188	Endodermal sinus tumor of ovary
+C0346191	Carcinoma in situ of endometrium
+C0346200	Intravenous leiomyomatosis
+C0346202	Adenosquamous carcinoma of the cervix
+C0346208	Vaginal intraepithelial neoplasia
+C0346210	Vulval intraepithelial neoplasia
+C0346249	Cystadenocarcinoma of kidney
+C0346251	Sarcoma of kidney
+C0346255	Oncocytoma, renal
+C0346300	Pituitary carcinoma
+C0346302	Growth Hormone-Secreting Pituitary Adenoma
+C0346303	Thyrotroph adenoma
+C0346304	Gonadotroph adenoma
+C0346306	Pituitary microadenoma
+C0346308	Pituitary macroadenoma
+C0346324	Astrocytoma, Malignant, Optic Nerve
+C0346326	Optic Nerve Glioma
+C0346340	Adenoid cystic carcinoma of lacrimal gland
+C0346342	Carcinoma ex pleomorphic adenoma of lacrimal gland
+C0346345	Pleomorphic adenoma of lacrimal gland
+C0346359	Squamous cell carcinoma of conjunctiva
+C0346360	Malignant melanoma of conjunctiva
+C0346363	Nevus of conjunctiva
+C0346373	Malignant melanoma of iris
+C0346379	Malignant melanoma of ciliary body
+C0346388	Malignant melanoma of choroid
+C0346390	Hemangioma of choroid
+C0346396	Retinoma
+C0346402	Malignant neoplasm of adrenal cortex
+C0346421	Chronic eosinophilic leukemia
+C0346429	Multiple malignancy
+C0346627	Intestinal Cancer
+C0346629	Malignant neoplasm of large intestine
+C0346647	Malignant neoplasm of pancreas
+C0346648	Malignant tumor of exocrine pancreas
+C0346773	Malignant melanoma of ear and/or external auditory canal
+C0346782	Malignant melanoma of scalp and/or neck
+C0346903	Malignant neoplasm of cerebrum
+C0346957	Disseminated Malignant Neoplasm
+C0346967	Metastases to gastrointestinal tract
+C0346976	Metastases to pancreas
+C0346977	Metastases to spleen
+C0346979	Metastases to bone marrow
+C0346989	Metastases to peritoneum
+C0346990	Carcinomatosis of peritoneal cavity
+C0346991	Secondary malignant neoplasm of omentum
+C0346993	Metastases to breast
+C0347001	Secondary malignant neoplasm of prostate
+C0347011	Metastases to bladder
+C0347014	Nervous system metastases NOS
+C0347016	Secondary malignant neoplasm of spinal cord
+C0347019	Metastases to eye
+C0347129	Anal intraepithelial neoplasia
+C0347176	Carcinoma in situ of fallopian tube
+C0347180	Penile intraepithelial neoplasia
+C0347206	Benign tumor of salivary gland
+C0347266	Duodenal polyp
+C0347269	Benign neoplasm of intestinal tract
+C0347272	Benign neoplasm of large intestine
+C0347284	Benign pancreatic neoplasm NOS
+C0347390	Skin Papilloma
+C0347493	Cervix adenomatous polyp
+C0347509	Benign neoplasm of central nervous system
+C0347515	Spinal Meningioma
+C0347530	Base excess negative
+C0347536	Head Injury, Superficial
+C0347602	Retinal injury
+C0347630	Hepatic haematoma
+C0347634	Splenic haematoma
+C0347648	Kidney rupture
+C0347804	Acetabulum fracture
+C0347805	Ilium fracture
+C0347806	Pubis fracture
+C0347869	Epilepsy, Akinetic
+C0347915	Congenital malformation syndromes associated with short stature
+C0347925	Non-Syphilitic Argyll-Robertson Pupil
+C0347938	Hypometabolism
+C0347944	Pelvic mass
+C0347950	Asthma attack
+C0347959	Lactic acidemia
+C0348023	Spinal arteriovenous malformation
+C0348148	Early syphilis, unspecified
+C0348321	Hemophilus influenza infection
+C0348374	Malignant Central Nervous System Neoplasm
+C0348375	Malignant neoplasm of meninges
+C0348426	Benign neoplasm of meninges
+C0348447	Other specified diabetes mellitus
+C0348454	Other hypoparathyroidism
+C0348460	Other hyperaldosteronism
+C0348484	Other disorders of branched-chain amino-acid metabolism
+C0348489	Other sphingolipidosis
+C0348616	Other restrictive cardiomyopathy
+C0348617	Other cardiomyopathies
+C0348626	Other specified cardiac arrhythmias
+C0348801	Group B streptococcal pneumonia
+C0348890	Aplastic anemia, idiopathic
+C0348893	Chronic superficial gastritis
+C0348911	Placental transfusion syndrome
+C0348932	Other specified diabetes mellitus with unspecified complications
+C0348951	Imbalance of constituents of food intake
+C0348991	Cerebral Cryptococcosis
+C0349081	Dementia in Parkinson\'s disease
+C0349204	Nonorganic psychosis
+C0349208	Manic episode
+C0349217	Depressive episode, unspecified
+C0349218	Recurrent depressive disorder
+C0349231	Phobic anxiety disorder
+C0349251	Behavioral syndrome associated with physiological disturbance and physical factors
+C0349255	Nonorganic Insomnia
+C0349391	Apraxia, Verbal
+C0349398	Paranoid delusion
+C0349410	Organ failure
+C0349422	Steal syndrome
+C0349426	Ferrochelatase deficiency
+C0349453	Mass of thyroid gland
+C0349458	Cervical intraepithelial neoplasia grade 1
+C0349459	Cervical intraepithelial neoplasia grade 2
+C0349464	Wernicke-Korsakoff Syndrome
+C0349476	Congenital goiter
+C0349478	Neonatal anoxia
+C0349489	Fetal Hypoxia
+C0349506	Photosensitivity of skin
+C0349515	Amelanotic Skin Melanoma
+C0349516	Isolated aortic stenosis
+C0349529	Carcinoid tumour of the stomach
+C0349530	Early gastric cancer
+C0349532	Gastric lymphoma
+C0349533	Lymphoma of intestine
+C0349534	Carcinoma of anal margin
+C0349535	Carcinoid tumor of intestine
+C0349539	Malignant melanoma of rectum
+C0349554	Vaginal intraepithelial neoplasia grade 1
+C0349555	Vaginal intraepithelial neoplasia grade 2
+C0349557	Gestational choriocarcinoma
+C0349560	Vulval intraepithelial neoplasia grade 3
+C0349564	Fallopian tube infection
+C0349566	Squamous cell carcinoma of the tongue
+C0349571	Pleomorphic adenoma of parotid gland
+C0349578	Complex Endometrial Hyperplasia
+C0349579	Atypical Endometrial Hyperplasia
+C0349588	Short stature
+C0349604	Intracranial Meningioma
+C0349606	Central Nervous System Cysts
+C0349609	Pneumocephalus, Tension
+C0349619	Medulloblastoma of cerebellum
+C0349620	Pilocytic astrocytoma of cerebellum
+C0349622	Hemangiopericytoma of meninges
+C0349623	Primary Melanocytic Lesion of Meninges
+C0349631	Richter's syndrome
+C0349632	Splenic Marginal Zone B-Cell Lymphoma
+C0349633	Hairy cell leukemia variant
+C0349636	Pre B-cell acute lymphoblastic leukemia
+C0349637	Common acute lymphoblastic leukemia
+C0349639	Juvenile Myelomonocytic Leukemia
+C0349644	Malignant lymphoma of testis
+C0349649	Pulmonary lymphangioleiomyomatosis
+C0349653	Congenital disorder of glycosylation type 1A
+C0349658	Trichoepithelioma
+C0349667	Sarcoma of breast
+C0349675	Hypergranular promyelocytic leukemia
+C0349680	Acute bilineal leukemia
+C0349702	Corneal Scar
+C0349705	Abnormal hemoglobin finding
+C0349716	Hypoglossal Neuralgia
+C0349725	Graft infection
+C0349746	Somatic delusion
+C0349780	Ischemic myocardial dysfunction
+C0349781	Hibernating myocardium
+C0349782	Ischaemic cardiomyopathy
+C0349785	Torticollis, Psychogenic
+C0349788	Arrhythmogenic Right Ventricular Dysplasia
+C0349789	Acquired Meningocele
+C0353676	Organophosphorus Poisoning
+C0362030	Verrucous epidermal nevus
+C0362046	Prediabetes
+C0362060	Legal problem
+C0369183	Erythrocyte Mean Corpuscular Hemoglobin Test
+C0373595	Creatinine clearance measurement
+C0373598	Dehydroepiandrosterone Assay
+C0373601	Dihydrotestosterone Assay
+C0373607	Ferritin measurement
+C0373675	Magnesium measurement
+C0373680	Myoglobin measurement
+C0373705	Progesterone measurement
+C0373721	Selenium measurement
+C0373745	Vitamin A measurement
+C0373785	Thrombomodulin Assay
+C0375019	Human T-cell lymphotrophic virus, type I [HTLV-I]
+C0375021	Human immunodeficiency virus, type 2 [HIV-2] infection in conditions classified elsewhere and of unspecified site
+C0375023	Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
+C0375024	Hantavirus infection in conditions classified elsewhere and of unspecified site
+C0375071	Malignant neoplasm of vulva
+C0375206	Hemiplegia/hemiparesis
+C0375268	Acute endocarditis
+C0375346	Dental alveolar anomalies
+C0376154	Skin callus
+C0376171	Necrotizing Hemorrhagic Encephalomyelitis
+C0376175	Bell Palsy
+C0376185	Hypoaldosteronism, Hyporeninemic
+C0376186	Impetigo Contagiosa
+C0376280	Anxiety States, Neurotic
+C0376286	Avitaminosis
+C0376288	Amaurosis
+C0376297	Cardiac Death
+C0376300	Dengue Shock Syndrome
+C0376304	Gangrene, Dental Pulp
+C0376323	Congestive Ophthalmopathy
+C0376329	New Variant Creutzfeldt-Jakob Disease
+C0376338	Diagnosis, Psychiatric
+C0376356	Premenstrual Tension
+C0376358	Malignant neoplasm of prostate
+C0376359	Gronblad-Strandberg Syndrome
+C0376362	Purpura Hemorrhagica
+C0376384	Nicotine Use Disorder
+C0376405	Treatment noncompliance
+C0376407	Granulomatous Slack Skin
+C0376416	Hibernation, Myocardial
+C0376480	Gingival enlargement NOS
+C0376524	Branchio-Oculo-Facial Syndrome
+C0376532	Epilepsy, Rolandic
+C0376544	Hematopoietic Neoplasms
+C0376545	Hematologic Neoplasms
+C0376618	Endotoxemia
+C0376620	Pouchitis
+C0376628	Chromosome Breakage
+C0376634	Craniofacial Abnormalities
+C0376670	Alcoholic pancreatitis
+C0376685	Shoulder Impingement Syndrome
+C0376703	Dermatitis, Periocular
+C0376704	Clinical Capillary Leak Syndrome
+C0376710	Esophageal Hernia
+C0391816	Tietz syndrome
+C0391826	Lhermitte-Duclos disease
+C0391861	Plasma cell inflammation
+C0391869	Polycythemia due to excess erythopoetin production
+C0391870	Abnormality of red blood cells
+C0391957	idiopathic epilepsy
+C0391958	Familial Epilepsies
+C0391959	Cervical Sympathetic Dystrophy
+C0391970	Carcinoid tumor, malignant
+C0391976	Pain Disorder
+C0391996	Hepatic atrophy
+C0392003	Breast cellulitis
+C0392005	Bilateral cleft lip
+C0392006	Unilateral cleft lip
+C0392008	Anaesthetic complication
+C0392014	Trachea displaced
+C0392034	Gastrooesophagitis
+C0392039	Ovarian enlargement
+C0392077	Cardiac sarcoidosis
+C0392106	Hepatic artery thrombosis
+C0392109	Congenital tracheomalacia
+C0392110	Tracheostomy malfunction
+C0392115	Neurogenic Urinary Bladder, Uninhibited
+C0392156	Akathisia
+C0392160	Application site atrophy
+C0392162	Clammy skin
+C0392163	Corneal erosion
+C0392164	Pulmonary Cystic Fibrosis
+C0392167	Drug effect prolonged
+C0392171	Influenza-like symptoms
+C0392175	Renal haemorrhage
+C0392185	Repetitive speech
+C0392188	Abnormal rapid eye movement sleep
+C0392196	Injection site urticaria
+C0392201	Blood glucose
+C0392317	Breast infections
+C0392318	Salivary gland infection
+C0392322	Undifferentiated schizophrenia
+C0392331	Arachnophobia
+C0392378	Gingival ulceration
+C0392384	Cerebellar haematoma NOS
+C0392386	Decreased platelet count
+C0392390	Hepatitis B e antigen positive
+C0392400	Diffuse malignant mesothelioma
+C0392439	Acrodermatitis continua of Hallopeau
+C0392445	Necrobiosis Lipoidica Diabeticorum
+C0392447	Radiculitis brachial
+C0392464	Ventricular aneurysm
+C0392470	Anomalous atrioventricular excitation
+C0392475	Roberts-SC phocomelia syndrome
+C0392476	Epiphyseal dysplasia
+C0392482	Common atrium
+C0392485	Congenital diverticulum of pharynx
+C0392494	Hypertrophy of tongue papillae
+C0392514	Hereditary hemochromatosis
+C0392519	Calcium deficiency
+C0392525	Nephrolithiasis
+C0392534	Ruptured ectopic pregnancy
+C0392535	Termination of pregnancy (fetus)
+C0392548	Cauda equina syndrome
+C0392550	Hemiplegia, Infantile
+C0392557	Cataract nuclear
+C0392607	Severe combined immunodeficiency due to adenosine deaminase deficiency
+C0392618	Postoperative infection
+C0392620	Alcohol poisoning
+C0392622	Toxic effect of carbon tetrachloride
+C0392661	Infection by Dipylidium caninum
+C0392663	Infection by Wuchereria bancrofti
+C0392674	Exhaustion
+C0392676	Hyperpyrexia
+C0392678	Swallowing problem
+C0392697	Intersexuality
+C0392699	Dysaesthesia
+C0392701	Giddiness
+C0392702	Abnormal involuntary movement
+C0392704	Cortical deafness
+C0392707	Atopy
+C0392708	Ineffective erythropoiesis
+C0392775	Cystic medial necrosis of aorta
+C0392777	Poikiloderma
+C0392784	Dermatofibrosarcoma Protuberans
+C0392788	Angiocentric lymphomas
+C0392885	High density lipoprotein measurement
+C0392998	Carcinosarcoma of ovary
+C0393441	Chronic lymphocytic meningitis
+C0393442	Meningitis noninfective
+C0393444	Meningitis chemical
+C0393456	Encephalitis fungal
+C0393483	Brainstem encephalitis
+C0393484	Rasmussen Syndrome
+C0393489	Vacuolar myelopathy
+C0393519	Cerebellar Ataxia, Early Onset
+C0393520	Harding ataxia
+C0393524	Cerebellar Ataxia, Late Onset
+C0393525	Progressive cerebellar ataxia
+C0393526	Periodic ataxia
+C0393534	Paraneoplastic Cerebellar Degeneration
+C0393538	Muscular Atrophy, Spinal, Type II
+C0393540	Childhood Progressive Bulbar Palsy
+C0393541	Distal Spinal Muscular Atrophy
+C0393546	Oculopharyngeal Spinal Muscular Atrophy
+C0393547	Bulbospinal Neuronopathy
+C0393554	Amyotrophic Lateral Sclerosis With Dementia
+C0393555	Pure hereditary spastic paraplegia
+C0393556	Complicated hereditary spastic paraplegia
+C0393559	Troyer syndrome
+C0393560	Vascular Dementia, Acute Onset
+C0393561	Subcortical Vascular Dementia
+C0393570	Corticobasal degeneration
+C0393571	Multiple System Atrophy
+C0393574	Huntington Disease, Late Onset
+C0393576	Chorea Acanthocytosis Syndrome
+C0393577	Pallidal degeneration
+C0393578	Pallidoluysian degeneration
+C0393584	Benign Hereditary Chorea
+C0393588	Dystonia, Paroxysmal
+C0393590	Fahr\'s syndrome (disorder)
+C0393591	AICARDI-GOUTIERES SYNDROME
+C0393593	Dystonia
+C0393598	Idiopathic familial dystonia
+C0393601	Idiopathic non-familial dystonia
+C0393602	Isolated cervical dystonia
+C0393610	Dystonia, Diurnal
+C0393615	Familial Tremor
+C0393626	Opsoclonus-Myoclonus Syndrome
+C0393638	Hyponatraemic encephalopathy
+C0393639	Hashimoto's encephalopathy
+C0393642	Septic encephalopathy
+C0393664	Multiple Sclerosis, Acute Relapsing
+C0393665	Multiple Sclerosis, Chronic Progressive
+C0393666	Multiple Sclerosis, Progressive Relapsing
+C0393667	Extrapontine Myelinolysis
+C0393671	Frontal Epilepsy, Benign, Childhood
+C0393672	Epilepsy, Benign Psychomotor, Childhood
+C0393675	Childhood Benign Occipital Epilepsy
+C0393676	Panayiotopoulos Syndrome
+C0393679	Amygdalo-Hippocampal Epilepsy
+C0393681	Rhinencephalic Epilepsy
+C0393682	Epilepsy, Lateral Temporal
+C0393683	Epilepsy, Supplementary Motor
+C0393684	Epilepsy, Cingulate
+C0393688	Epilepsy, Opercular
+C0393691	Occipital Lobe Epilepsy
+C0393692	Chronic Progressive Epilepsia Partialis Continua
+C0393693	Benign Neonatal Epilepsy, Nonfamilial
+C0393695	Early Childhood Epilepsy, Myoclonic
+C0393697	Epilepsy with grand mal seizures on awakening (disorder)
+C0393698	Cryptogenic Infantile Spasms
+C0393699	Symptomatic Infantile Spasms
+C0393702	Myoclonic Astatic Epilepsy
+C0393703	Myoclonic Absence Epilepsy
+C0393706	Early infantile epileptic encephalopathy with suppression bursts
+C0393719	Nocturnal epilepsy
+C0393720	Reflex Epilepsy, Photosensitive
+C0393729	Immersion Related Epilepsy
+C0393734	Complex Partial Status Epilepticus
+C0393735	Headache Disorders
+C0393738	Chronic tension-type headache
+C0393739	Episodic Cluster Headache
+C0393743	Chronic Paroxysmal Hemicrania
+C0393744	Atypical Cluster Headache
+C0393754	Headache associated with sexual activity
+C0393756	Hangover from alcohol
+C0393759	Transient Insomnia
+C0393760	Initial insomnia
+C0393761	Middle insomnia
+C0393770	Delayed Sleep Phase Syndrome
+C0393774	Sleep-Related Bruxism
+C0393778	Congenital anosmia
+C0393786	Trigeminal Neuralgia, Idiopathic
+C0393787	Secondary Trigeminal Neuralgia
+C0393789	Trigeminal Neuropathy, Idiopathic
+C0393799	Miller Fisher Syndrome
+C0393807	Hereditary motor and sensory neuropathy with optic atrophy (disorder)
+C0393808	Charcot-Marie-Tooth disease, X-linked, 1
+C0393814	Hereditary liability to pressure palsies
+C0393818	Congenital hypomyelinating neuropathy
+C0393819	Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
+C0393835	Diabetic Asymmetric Polyneuropathy
+C0393847	Multifocal motor neuropathy
+C0393851	Critical illness polyneuropathy
+C0393888	Radial nerve compression
+C0393907	Axonal sensorimotor neuropathy
+C0393911	Pure Autonomic Failure
+C0393912	Segmental Autonomic Dysfunction
+C0393929	Familial infantile myasthenia
+C0393933	Pseudomyopathic myasthenia
+C0393934	Slow channel syndrome
+C0393939	Neuromuscular Junction Toxic Disorders
+C0393953	Anterior Cerebral Circulation Infarction
+C0393968	Systemic lupus erythematosus encephalitis
+C0393971	Spinal cord stroke
+C0393983	Hernia of cerebellar tonsil into foramen magnum
+C0393992	Multicystic Encephalomalacia
+C0393995	Quadriplegic cerebral palsy
+C0394003	Cerebral Palsy, Dystonic-Rigid
+C0394004	Congenital non-progressive ataxia
+C0394005	Ataxic cerebral palsy
+C0394006	Dysequilibrium syndrome
+C0394007	Cerebral Palsy, Atonic
+C0394016	Coma, Post-Head Injury
+C0394884	Catheter removal
+C0394996	Acute alcoholic intoxication
+C0395000	School refusal
+C0395003	Stage fright
+C0395005	Polydipsia psychogenic
+C0395013	Developmental Agnosia
+C0395020	Eye operation NOS
+C0395837	Stenosis of external auditory canal
+C0395866	Recurrent acute otitis media
+C0395887	Tympanosclerosis
+C0395905	Postauricular fistula
+C0395920	Migrainous vertigo
+C0395932	Recurrent Vestibular Neuritis
+C0395955	Tinnitus, Noise Induced
+C0395959	Tinnitus of Vascular Origin
+C0395971	Dominant sensorineural hearing loss
+C0395973	Recessive sensorineural hearing loss
+C0395976	Hearing loss associated with syndrome
+C0396000	Acute viral pharyngitis
+C0396051	Congenital Subglottic Stenosis
+C0396052	Acquired Laryngeal Stenosis
+C0396058	Congenital Vocal Cord Palsy
+C0396060	Congenital laryngeal adductor palsy
+C0396061	Acquired Vocal Cord Palsy
+C0396064	Bowing of vocal cord
+C0396072	Laryngeal papillomatosis
+C0396849	Mitral valve repair NOS
+C0396899	Tricuspid valve repair
+C0397450	Cardiac pacemaker replacement
+C0397942	Aortic aneurysm repair
+C0398086	Arterial stent insertion
+C0398087	Carotid artery stent insertion
+C0398349	Distal intestinal obstruction syndrome
+C0398350	Acute cardiac pulmonary edema
+C0398353	Hypercapnic respiratory failure
+C0398356	Abdominal aortic atherosclerosis
+C0398359	Trousseau's syndrome
+C0398367	Histiocytic Necrotizing Lymphadenitis
+C0398368	Lymphatic Abnormalities
+C0398561	Glucose phosphate isomerase deficiency
+C0398562	Triose phosphate isomerase deficiency
+C0398563	Deficiency of hexokinase (disorder)
+C0398564	Deficiency of adenylate kinase
+C0398568	Blood group deletion syndrome
+C0398581	T-cell lymphocytosis
+C0398593	Specific granule deficiency
+C0398595	Myeloperoxidase Deficiency
+C0398597	Histiocytic syndrome
+C0398610	Congenital von Willebrand\'s disease
+C0398620	Alpha-2-antiplasmin deficiency
+C0398621	Hypoplasminogenemia
+C0398623	Thrombophilia
+C0398625	Protein C Deficiency
+C0398626	Heparin cofactor II deficiency (disorder)
+C0398627	Inherited platelet disorder
+C0398635	Thromboxane synthetase deficiency
+C0398636	Acquired platelet disorder
+C0398639	Amegakaryocytic thrombocytopenia
+C0398641	Epstein syndrome (disorder)
+C0398642	Montreal platelet syndrome
+C0398644	Hypergammaglobulinemic Purpura of Waldenstrom
+C0398650	Immune thrombocytopenic purpura
+C0398677	Ocular sarcoidosis
+C0398680	Sarcoid myopathy
+C0398686	Primary immune deficiency disorder
+C0398689	Hyper-IgM Immunodeficiency Syndrome, Type 1
+C0398691	Hyperimmunoglobulinemia D
+C0398694	Selective immunoglobulin E deficiency
+C0398701	Immunoglobulin G2 deficiency
+C0398703	Immunoglobulin G3 deficiency
+C0398704	Immunoglobulin G4 deficiency
+C0398707	Immunoglobulin A2 deficiency
+C0398712	Anti-polysaccharide antibody deficiency
+C0398738	Leukocyte adhesion deficiency type 1
+C0398739	Congenital disorder of glycosylation, type 2C
+C0398746	Gluthathione synthetase deficiency
+C0398762	Properdin deficiency disease
+C0398764	Complement Factor D Deficiency
+C0398775	Hereditary C1 esterase inhibitor deficiency - deficient factor
+C0398776	Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
+C0398777	Complement Factor H Deficiency
+C0398782	Carboxypeptidase N Deficiency
+C0398788	Immunodeficiency syndrome, variable
+C0398791	Nijmegen Breakage Syndrome
+C0398794	Hypopigmentation-immunodeficiency disease
+C0398795	Secondary immunodeficiency
+C0398950	Periodontal operation
+C0398952	Gingival operation
+C0399352	Developmental absence of tooth
+C0399357	Talon cusp
+C0399367	Amelogenesis imperfecta local hypoplastic form
+C0399368	Amelogenesis Imperfecta, Type IB
+C0399372	Amelogenesis Imperfecta hypomaturation type
+C0399373	Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
+C0399376	Amelogenesis Imperfecta, Type III
+C0399378	Dentinogenesis imperfecta - Shield\'s type III (disorder)
+C0399379	Dentin dysplasia, type 1
+C0399380	Dentin dyspalsia, Shields type 2
+C0399385	Early tooth exfoliation
+C0399440	Hereditary gingival fibromatosis
+C0399447	Early onset periodontitis
+C0399451	Subgingival plaque
+C0399459	Oral discomfort
+C0399461	Oral mucosa erosion
+C0399474	Dysplastic oral leukoplakia
+C0399478	Smokers keratosis
+C0399496	Granulomatosis, Orofacial
+C0399526	Class III malocclusion
+C0399570	Mandibular condyle aplasia
+C0399572	Hypoplasia of mandibular condyle
+C0399605	Commissural lip pit
+C0399935	Ileectomy
+C0400076	Proctocolectomy
+C0400745	Biliary drainage
+C0400821	Colitis, Microscopic
+C0400822	Colitis, Lymphocytic
+C0400823	Neutropenic colitis
+C0400837	Simple diverticular disease of large intestine
+C0400839	Rectal ulcer
+C0400843	Mechanical ileus
+C0400847	Ileal stenosis
+C0400875	Diabetic enteropathy
+C0400877	Postoperative ileus
+C0400914	Acute hepatitis C
+C0400929	Subacute hepatic failure
+C0400936	Autoimmune liver disease
+C0400943	Cirrhosis - non-alcoholic
+C0400966	Non-alcoholic Fatty Liver Disease
+C0400968	Liver transplant rejection
+C0400979	Obstruction of biliary tree
+C0400990	Biliary cyst
+C0401013	Fungal peritonitis
+C0401116	Strangulated hernia
+C0401149	Chronic constipation
+C0401151	Chronic diarrhea
+C0401186	Removal of renal transplant
+C0403367	proliferative nephritis unspecified
+C0403379	Emphysematous pyelonephritis
+C0403383	Renal cyst infection
+C0403396	Steroid-sensitive nephrotic syndrome
+C0403397	Steroid-resistant nephrotic syndrome
+C0403399	Finnish congenital nephrotic syndrome
+C0403414	Acute post-streptococcal glomerulonephritis
+C0403416	Idiopathic crescentic glomerulonephritis
+C0403440	Thin basement membrane disease
+C0403443	Renal Failure, Progressive, with Hypertension
+C0403445	Fechtner syndrome (disorder)
+C0403447	Chronic Kidney Insufficiency
+C0403477	Medullary nephrocalcinosis
+C0403483	Renal ocular syndrome
+C0403502	Low renal threshold for glucose
+C0403518	Microalbuminuric diabetic nephropathy
+C0403528	Henoch-Schönlein nephritis
+C0403529	Anti-Glomerular Basement Membrane Disease
+C0403548	Salcedo syndrome
+C0403553	Renal dysplasia and retinal aplasia (disorder)
+C0403554	Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness
+C0403555	Ochoa syndrome
+C0403559	Dialysis disequilibrium syndrome
+C0403592	Chronic allograft nephropathy
+C0403608	Ureteric disorders
+C0403622	Primary vesicoureteric reflux
+C0403632	Cystitis noninfective
+C0403639	Chemical cystitis
+C0403645	Atonic urinary bladder
+C0403654	Bladder outflow obstruction
+C0403673	Retrograde ejaculation
+C0403719	Uric acid urolithiasis
+C0403720	X-linked recessive nephrolithiasis with renal failure
+C0403723	Candiduria
+C0403766	Acquired phimosis
+C0403800	Secondary male infertility
+C0403809	Primary spermatogenic failure
+C0403810	Oligosynaptic Infertility
+C0403812	Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa
+C0403814	Congenital bilateral aplasia of vas deferens
+C0403823	Asthenozoospermia
+C0403824	Teratozoospermia
+C0403825	Globozoospermia
+C0404445	Ovarian atrophy
+C0404478	Ovarian cyst ruptured
+C0404484	Chronic pelvic pain of female
+C0404521	Infective vaginitis
+C0404531	Hypertrophy of labia
+C0404572	Female infertility associated with anovulation
+C0405124	Umbilical cord around neck
+C0405244	Vaginal laceration
+C0405352	Biopsy breast
+C0405469	Granulomatous Mastitis
+C0405479	Nipple disorder
+C0405578	Gigantism and acromegaly
+C0405580	Adrenal cortical hypofunction
+C0405581	Testicular dysfunction
+C0405583	Tendon calcification
+C0406105	Wound abscess
+C0406185	Turf Toe
+C0406209	Photo-onycholysis
+C0406217	Actinic prurigo
+C0406305	Eosinophilic pustular folliculitis
+C0406317	Chronic small plaque psoriasis
+C0406322	Nail psoriasis
+C0406369	Lichen planus pemphigoides
+C0406438	Pterygium of nail
+C0406443	Twenty nail dystrophy
+C0406468	Loose Anagen Hair Syndrome
+C0406481	Comedonal acne
+C0406484	Sebaceous hyperplasia
+C0406486	Ocular rosacea
+C0406500	Lipodermatosclerosis
+C0406502	Hereditary benign telangiectasia (disorder)
+C0406519	Infected skin ulcer
+C0406537	Morbilliform Drug Reaction
+C0406549	Cutis laxa, acquired type
+C0406556	Hereditary acrokeratotic poikiloderma of Weary
+C0406557	Poikiloderma of Kindler
+C0406584	Acrogeria, gottron type
+C0406585	Lethal tight skin contracture syndrome (disorder)
+C0406587	Wrinkly skin syndrome
+C0406607	Insulin lipoatrophy
+C0406608	Pelvic lipomatosis
+C0406612	Encephalocraniocutaneous lipomatosis
+C0406631	Keloidalis nuchae
+C0406632	Autoimmune skin disease
+C0406645	Amyopathic dermatomyositis
+C0406650	Linear IgA Bullous Dermatosis
+C0406670	Vulvodynia
+C0406702	Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
+C0406704	Rudiger syndrome 1
+C0406707	Basan syndrome
+C0406709	Hay-Wells syndrome
+C0406716	Hypodontia and nail dysgenesis
+C0406723	Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy
+C0406726	Orofaciodigital syndrome 3
+C0406727	Orofaciodigital syndrome 4
+C0406733	Curly hair-ankyloblepharon-nail dysplasia syndrome
+C0406735	Hypoplastic enamel-onycholysis-hypohidrosis syndrome
+C0406740	Kohlschutter Tonz syndrome
+C0406756	Keratolytic winter erythema
+C0406767	Keratoderma with scleroatrophy of the extremities
+C0406775	Symmetrical dyschromatosis of extremities
+C0406778	Dermatopathia pigmentosa reticularis
+C0406803	Syringocystadenoma Papilliferum
+C0406810	Carney Complex
+C0406811	Reticulate acropigmentation of Kitamura
+C0406834	Wound secretion
+C0406845	Post-mastectomy pain
+C0407333	External fixation of fracture
+C0407713	Jaw operation
+C0408591	Intervertebral disc operation
+C0408670	Spinal decompression
+C0409208	Arthritis of hand
+C0409224	Ochronotic arthropathy
+C0409336	Flexion contracture-shoulder
+C0409338	Flexion contracture - elbow
+C0409345	Flexion contracture - wrist
+C0409346	Contracture of joint of thumb
+C0409348	Flexion contracture of proximal interphalangeal joint
+C0409354	Flexion contracture of hip
+C0409355	Flexion contracture of the knee
+C0409477	Ankylosis of the elbow joint
+C0409495	Protrusio acetabuli
+C0409497	Joint injury
+C0409651	Seropositive rheumatoid arthritis
+C0409652	Seronegative rheumatoid arthritis
+C0409667	Juvenile Chronic Polyarthritis
+C0409676	Juvenile spondyloarthropathy
+C0409679	Sero negative arthropathy
+C0409818	Chronic Infantile Neurological, Cutaneous, and Articular Syndrome
+C0409860	Rotator cuff tear arthropathy
+C0409896	Familial chondrocalcinosis
+C0409952	Idiopathic osteoarthritis
+C0409956	Osteoarthrosis of the carpometacarpal joint of the thumb
+C0409959	Osteoarthritis, Knee
+C0409962	Localized osteoarthritis
+C0409974	Lupus Erythematosus
+C0409977	Bullous systemic lupus erythematosus
+C0409979	Neonatal Systemic lupus erythematosus
+C0409980	Primary antiphospholipid syndrome
+C0410000	Overlap syndrome
+C0410005	Nodular fasciitis
+C0410158	Muscle damage
+C0410165	X-linked muscular dystrophy with abnormal dystrophin
+C0410173	Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
+C0410174	Fukuyama Type Congenital Muscular Dystrophy
+C0410179	Scleroatonic muscular dystrophy
+C0410180	Eichsfeld type congenital muscular dystrophy
+C0410189	Muscular Dystrophy, Emery-Dreifuss
+C0410190	Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
+C0410192	Muscular Dystrophy, Scapulohumeral
+C0410198	Proximal myopathy
+C0410203	X-linked centronuclear myopathy
+C0410204	Myopathy, Centronuclear, Autosomal Recessive
+C0410207	Tubular Aggregate Myopathy
+C0410214	Myopathy with Abnormal Lipid Metabolism
+C0410226	Congenital Myotonic Dystrophy
+C0410256	Muscle injury
+C0410264	Contracture of tendo achilles
+C0410266	Contracture of hamstring(s)
+C0410334	Defect of articular cartilage
+C0410422	Chronic multifocal osteomyelitis
+C0410438	Primary osteoporosis
+C0410445	Osteomalacia secondary to drug
+C0410480	Avascular Necrosis of Femur Head
+C0410528	Skeletal dysplasia
+C0410529	Hypochondroplasia (disorder)
+C0410530	Metachondromatosis
+C0410533	Osteodysplasia
+C0410536	Mesomelic dysplasia
+C0410538	Pseudoachondroplasia
+C0410539	Craniodiaphyseal dysplasia
+C0410550	Collapse of vertebra
+C0410574	Synovial Hypertrophy
+C0410606	Cervical Disc Degenerative Disorder
+C0410607	Intervertebral disc calcification
+C0410632	Schmorl\'s nodes
+C0410653	Atlantoaxial instability
+C0410702	Adolescent idiopathic scoliosis
+C0410719	Bone deformity
+C0410740	Acquired deformity of finger
+C0410787	Hereditary Connective Tissue Disorder
+C0410807	Dislocation of joint prosthesis
+C0410808	Prosthetic joint infection
+C0410916	Death neonatal
+C0410918	Tachycardia foetal
+C0410919	Bradycardia foetal
+C0410935	Wide cranial sutures
+C0410959	Fetal acidosis
+C0411765	Nail operation
+C0413252	Hypothermia
+C0419415	Birth length
+C0420948	Ultrasound antenatal screen abnormal
+C0422837	Neurological observations
+C0422850	Seizures, Somatosensory
+C0422852	Auditory seizure
+C0422853	Olfactory seizure
+C0422854	Gustatory seizure
+C0422855	Vertiginous seizure
+C0422879	CNS symptom
+C0422887	Neglect of one side of body
+C0422891	Sensory Agnosia
+C0422892	Apraxia, Gestural
+C0422943	Visual symptoms
+C0422955	Lazy eye
+C0422974	Halo vision
+C0422980	Oscillopsia
+C0422991	Altitudinal scotoma
+C0423006	Discharge from eye
+C0423061	Intermittent convergent squint
+C0423063	Comitant heterophoria
+C0423082	Hypometric saccades
+C0423083	Hypermetric saccades
+C0423086	Staring
+C0423092	Superior Oblique Myokymia
+C0423109	Upward slant of palpebral fissure
+C0423110	Downward slant of palpebral fissure
+C0423112	Short palpebral fissure
+C0423113	Telecanthus
+C0423153	Lacrimation
+C0423178	Bitot's spots
+C0423221	Globe of eye large
+C0423224	Sunken eyes
+C0423226	Corneal pigmentation
+C0423250	Corneal stromal opacities
+C0423271	Scleral hyperaemia
+C0423276	Shallow anterior chamber of eye
+C0423282	Anterior chamber cell
+C0423299	Keyhole Pupil
+C0423302	Pupil Reaction Absent
+C0423310	Wernicke Hemianopic Pupil
+C0423313	Pupillary Sector Paralysis
+C0423318	Heterochromia iridis
+C0423319	Atrophic iris
+C0423320	Iridodonesis
+C0423325	Ectropion uveae
+C0423361	Posterior Vitreous Detachment
+C0423390	Retinal artery embolism
+C0423414	Retinal flecking
+C0423428	Macular scar
+C0423431	Subretinal exudate
+C0423434	Subretinal fibrosis
+C0423463	Opticociliary vessels
+C0423572	Pins and needles
+C0423602	Foreign body sensation
+C0423618	Throbbing Headache
+C0423623	Bilateral Headache
+C0423640	Right Flank Pain
+C0423641	Left flank pain
+C0423670	Shoulder joint pain
+C0423673	Spinal pain
+C0423682	Low Back Pain, Mechanical
+C0423684	Thoracic back pain
+C0423689	Low Back Pain, Posterior Compartment
+C0423690	Facet joint syndrome
+C0423701	Urinary tract pain NOS
+C0423711	Neuralgia, Perineal
+C0423712	Neuralgia, Iliohypogastric Nerve
+C0423729	Chest pain on breathing
+C0423732	After pains
+C0423736	Scalding pain on urination
+C0423742	Pain on intercourse
+C0423756	Thickness of skin
+C0423757	Thin skin
+C0423772	Cutaneous Fistula
+C0423773	Scaly skin
+C0423775	Scurfiness of scalp
+C0423776	Palmar pit
+C0423791	Maculopapular eruption
+C0423798	Increased tendency to bruise
+C0423801	Growth of nails
+C0423807	Overcurvature of nail
+C0423808	Brachyonychia
+C0423820	Nail ridging
+C0423823	Thin nails
+C0423838	Hangnail
+C0423847	Growth of eyelashes
+C0423848	Distichiasis
+C0423867	Fine hair
+C0423898	Intellectual ability
+C0423903	Low intelligence
+C0424000	Feeling suicidal (finding)
+C0424021	Religious delusion
+C0424024	Delusional perception
+C0424068	Verbal auditory hallucinations
+C0424071	Hallucinations, Visual, Unformed
+C0424072	Hallucinations, Visual, Formed
+C0424082	Hallucinations, Hypnapompic
+C0424083	Hallucinations, Dissociative
+C0424091	Decreased interest
+C0424101	Inattention
+C0424102	Easily distracted
+C0424109	Tearfulness
+C0424139	Anxiety and fear
+C0424166	Social Anxiety
+C0424187	Fear of injection
+C0424230	Motor retardation
+C0424235	Fidgeting
+C0424290	Compulsive hoarding
+C0424295	Hyperactive behavior
+C0424296	Disinhibition
+C0424304	Inappropriate laughter
+C0424320	Teasing
+C0424323	Physical aggression
+C0424366	Self-harm
+C0424410	Excessive masturbation
+C0424421	Eating problem
+C0424448	Mask-like facies
+C0424462	Neglect of personal appearance
+C0424489	Chapped lips
+C0424503	Dysmorphic facies
+C0424551	Exercise tolerance decreased
+C0424563	Quality of sleep
+C0424574	Duration of sleep
+C0424576	Fit and well
+C0424585	Tires quickly
+C0424594	Frailty
+C0424605	Developmental delay
+C0424621	Body Fat Distribution
+C0424641	Decrease in height
+C0424678	Lean body mass
+C0424688	Small head
+C0424690	Asymmetrical skull
+C0424693	Broad skull
+C0424711	Orbital separation diminished
+C0424721	Temporomandibular joint deformity
+C0424731	Single transverse palmar crease
+C0424768	Prolonged fever
+C0424781	Spiking temperature
+C0424786	Postoperative fever
+C0424790	Rigor
+C0424810	Periorbital swelling
+C0424813	Orbital oedema
+C0424844	Lump in eyelid
+C0424939	Learning difficulties
+C0425043	Death of relative
+C0425083	Loss of employment
+C0425093	Job dissatisfaction
+C0425258	Mobility poor
+C0425402	Medical diet
+C0425442	Respiratory system finding
+C0425449	Gasping for breath
+C0425464	Thoracic breathing
+C0425465	Pursed-lip breathing
+C0425468	Use of accessory respiratory muscles
+C0425470	Intercostal retraction
+C0425481	Sighing respiration
+C0425492	Irregular breathing
+C0425574	Bounding pulse
+C0425591	Dropped beats - heart
+C0425687	Jugular venous engorgement
+C0425772	Premature development of the breasts
+C0425782	Breast size
+C0425791	Peau d'orange
+C0425795	Absent nipple (finding)
+C0425913	Uterus absent (finding)
+C0426063	Transverse presentation
+C0426209	Amniotic fluid -meconium stain
+C0426320	Absent scrotum
+C0426359	Urinary symptoms
+C0426377	Infrequent urination
+C0426390	Bladder spasm
+C0426396	Urine looks dark
+C0426414	Small nose
+C0426415	Large nose
+C0426421	Wide nose
+C0426422	Narrow nose
+C0426428	Bifid nasal tip
+C0426429	Broad nasal tip
+C0426430	Drooping nasal tip
+C0426433	Pinched nasal tip
+C0426436	Small nostrils
+C0426439	Narrow nostrils
+C0426440	Large nostrils
+C0426489	Gingival cleft
+C0426494	Wasting of tongue
+C0426498	Tongue dry
+C0426501	Short frenulum of tongue
+C0426551	Vocal cord cyst
+C0426576	Gastrointestinal symptom
+C0426587	Altered appetite
+C0426597	Fluid intake decreased
+C0426636	Defaecation urgency
+C0426732	Prostatomegaly
+C0426747	Anal haemorrhage
+C0426776	Discharge from anus
+C0426785	Intermittent torticollis
+C0426789	Short thorax
+C0426790	Narrow thorax
+C0426799	Congenital hypoplasia of clavicle
+C0426801	Broad clavicle
+C0426805	Hooked clavicle
+C0426806	Bipartite clavicle
+C0426808	Long clavicle
+C0426811	Pseudoarthrosis of clavicle
+C0426816	Absence of rib
+C0426817	Short ribs
+C0426818	Thin rib
+C0426820	Thick rib
+C0426824	Beading of ribs
+C0426826	Flared ribs
+C0426848	Sacral dimples
+C0426870	Large hand
+C0426874	Trident hand
+C0426886	Tapering fingers (finding)
+C0426891	Broad thumbs
+C0426900	Tibial torsion
+C0426901	Short leg
+C0426970	Spastic Quadriplegia
+C0426980	Motor symptoms
+C0427008	Stiffness
+C0427055	Facial Paresis
+C0427063	Shoulder girdle weakness
+C0427064	Pelvic girdle weakness
+C0427065	Distal muscle weakness
+C0427068	Monoparesis - leg
+C0427086	Involuntary movement
+C0427108	General unsteadiness
+C0427128	Rapid Fatigue of Gait
+C0427144	Toe-walking gait
+C0427149	Gait, Drop Foot
+C0427160	Parkinsonian gait
+C0427169	Marche a Petit Pas
+C0427170	Magnetic gait
+C0427177	Gait, Hysterical
+C0427184	No incoordination
+C0427190	Ataxia, Truncal
+C0427195	Muscle tension
+C0427201	Floppy Muscles
+C0427202	Muscle Tone Atonic
+C0427285	Clicking hip
+C0427305	Arthritis by pattern of joint involvement
+C0427437	Mean cell haemoglobin decreased
+C0427457	Red blood cell count decreased
+C0427458	Red blood cell count increased
+C0427460	Red cell distribution width determination
+C0427480	Elliptocytosis found
+C0427515	Neutrophil abnormality
+C0427516	Hypersegmentation
+C0427540	Blast cells present
+C0427544	Monocytopenia
+C0427565	Platelet distribution width measurement
+C0427877	Cerebrospinal fluid lymphocytosis
+C0428282	Serum creatinine low
+C0428402	Human chorionic gonadotropin measurement
+C0428419	Triiodothyronine measurement
+C0428465	Serum lipids high (finding)
+C0428474	Serum LDL cholesterol measurement
+C0428478	Serum triglycerides raised
+C0428552	CSF glucose decreased
+C0428553	CSF glucose increased
+C0428568	Fasting blood glucose measurement
+C0428580	Vitamin measurement
+C0428629	FAI - Free androgen index measurement
+C0428791	Aortic valve calcification
+C0428796	Senile sclerosis of aortic cusp
+C0428851	Dilatation of pulmonary artery, unspecified
+C0428871	Right to left cardiovascular shunt (finding)
+C0428883	Diastolic blood pressure
+C0428886	Mean arterial pressure
+C0428895	Labile blood pressure
+C0428897	Jugular venous pressure
+C0428908	Sinus node dysfunction
+C0428974	Arrhythmia supraventricular
+C0428977	Bradycardia
+C0429027	Electrocardiogram QRS complex shortened
+C0429028	Electrocardiogram QT interval
+C0429029	Electrocardiogram ST segment
+C0429059	Electrocardiogram T wave amplitude decreased
+C0429087	Electrocardiogram: P-R interval
+C0429089	Electrocardiogram Q waves
+C0429097	QRS complex feature
+C0429098	Electrocardiogram QRS complex
+C0429219	Gastrointestinal sensation
+C0429349	EMG positive sharp waves
+C0429468	Anovulatory (finding)
+C0429480	Foetal heart rate deceleration
+C0429494	Ocular axial length
+C0429702	Respiratory quotient
+C0429774	Residual urine volume
+C0430022	Diagnostic procedure NOS
+C0431108	Anaplastic Oligoastrocytoma
+C0431109	Choroid Plexus Carcinoma
+C0431111	Rhabdomyosarcoma with ganglionic differentiation
+C0431121	Clear Cell Meningioma
+C0431122	Atypical meningioma
+C0431128	Papillary craniopharyngioma
+C0431129	Adamantinous Craniopharyngioma
+C0431289	Frontal Encephalocele
+C0431349	Aprosencephaly
+C0431350	Primary microcephaly
+C0431352	Secondary microcephaly
+C0431362	Lobar Holoprosencephaly
+C0431363	Alobar Holoprosencephaly
+C0431368	Partial agenesis of corpus callosum
+C0431369	Dysgenesis of corpus callosum
+C0431370	Atrophy of corpus callosum
+C0431371	Absence of septum pellucidum
+C0431375	Classical Lissencephaly
+C0431376	Cobblestone Lissencephaly
+C0431379	Laminar heterotopia
+C0431380	Cortical Dysplasia
+C0431383	Hydranencephaly with Proliferative Vasculopathy
+C0431384	Colpocephaly
+C0431388	Microdysgenesis
+C0431391	Hemimegalencephaly
+C0431399	Familial aplasia of the vermis
+C0431401	Gillespie syndrome
+C0431406	Asymmetric crying face association
+C0431415	Lumbosacral agenesis
+C0431447	Synophrys
+C0431448	Absent eyebrow
+C0431478	Posteriorly rotated ear
+C0431483	Simple ear
+C0431498	Aberrant subclavian artery
+C0431527	Laryngeal hypoplasia
+C0431564	Lobulated tongue
+C0431565	Hamartoma of tongue
+C0431603	Ectopic liver
+C0431637	Mullerian aplasia
+C0431649	Vaginal septum
+C0431659	Hypoplasia of scrotum
+C0431663	Bilateral Cryptorchidism
+C0431664	Unilateral Cryptorchidism
+C0431692	Bilateral renal hypoplasia
+C0431693	Renal cysts and diabetes syndrome
+C0431694	Oligomeganephronic hypoplasia of kidney
+C0431716	Nephronophthisis - medullary cystic disease
+C0431718	Multiple renal cysts
+C0431766	Congenital malformation syndromes involving limbs
+C0431863	Carpal synostosis
+C0431886	Thumb in palm deformity
+C0431887	Hitch-hiker thumb
+C0431890	Hypoplasia of thumb
+C0431904	Ulnar polydactyly of fingers
+C0431943	Lower Extremity Deformities, Congenital
+C0432028	Split foot
+C0432040	Simple syndactyly of toes, first web space
+C0432055	Simple syndactyly of fingers - first web
+C0432066	Congenital malformation syndromes affecting facial appearance
+C0432072	Dysmorphic features
+C0432073	Defect of skull ossification
+C0432090	Cleft of hard palate
+C0432098	Cleft Soft Palate
+C0432103	Submucous cleft of hard palate
+C0432106	Midline facial cleft - Tessier cleft 0
+C0432122	Interfrontal craniofaciosynostosis
+C0432123	Sagittal craniosynostosis
+C0432124	Unicoronal craniosynostosis
+C0432149	Lumbar hemivertebra
+C0432152	Thoracic hemivertebra
+C0432163	Defect of vertebral segmentation
+C0432185	Aplasia of muscle
+C0432194	Schneckenbecken dysplasia
+C0432195	Short rib dysplasia
+C0432197	Short rib-polydactyly syndrome, Verma-Naumoff type
+C0432198	Short rib-polydactyly syndrome, Beemer type
+C0432201	Boomerang dysplasia
+C0432211	Spondyloepimetaphyseal disorder
+C0432214	Namaqualand hip dysplasia
+C0432215	Progressive pseudorheumatoid dysplasia
+C0432217	Wolcott-Rallison syndrome
+C0432219	Opsismodysplasia
+C0432221	Spondylometaphyseal dysplasia, \'corner fracture\' type
+C0432222	Spondyloenchondrodysplasia
+C0432225	Metaphyseal chondrodysplasia Spahr type
+C0432226	Metaphyseal anadysplasia
+C0432227	Brachyolmia Type 3
+C0432228	Brachyolmia
+C0432230	Langer Mesomelic Dysplasia Syndrome
+C0432231	Nievergelt syndrome
+C0432233	Trichorhinophalangeal dysplasia type I
+C0432235	Cranioectodermal Dysplasia
+C0432238	Bent bone dysplasia
+C0432239	Kyphomelic dysplasia
+C0432240	Stuve-Wiedemann dysplasia
+C0432242	Desbuquois syndrome
+C0432243	Spondyloepimetaphyseal Dysplasia With Joint Laxity
+C0432244	Osteodysplastic primordial dwarfism
+C0432246	Microcephalic Osteodysplastic Primordial Dwarfism, Type II
+C0432252	Osteoporosis with pseudoglioma
+C0432253	Bruck syndrome
+C0432254	Singleton Merten syndrome
+C0432255	Geroderma osteodysplastica
+C0432261	Osteopetrosis - intermediate type
+C0432262	Dysosteosclerosis
+C0432267	Tricho-thiodystrophy disorder
+C0432268	Osteopathia striata cranial sclerosis
+C0432269	Lenz Majewski hyperostotic dwarfism
+C0432272	Van Buchem disease
+C0432273	Worth disease
+C0432281	Pseudochondroplasia
+C0432282	Dysplasia epiphysealis hemimelica
+C0432283	Osteoglophonic dwarfism
+C0432284	Infantile myofibromatosis
+C0432289	Winchester syndrome (disorder)
+C0432291	Mandibuloacral dysostosis
+C0432292	Familial expansile osteolysis
+C0432302	Erythrodermic lamellar ichthyosis
+C0432306	Ichthyosis Bullosa of Siemens
+C0432307	Ichthyosis hystrix of Curth-Macklin
+C0432315	Epidermolysis bullosa simplex herpetiformis
+C0432316	Epidermolysis bullosa simplex with mottled pigmentation
+C0432317	Epidermolysis bullosa simplex, Ogna type
+C0432321	Epidermolysis bullosa, pretibial
+C0432322	Dominant dystrophic epidermolysis bullosa, albopapular type (disorder)
+C0432326	Junctional epidermolysis bullosa mitis
+C0432328	Xeroderma pigmentosum, variant form
+C0432330	Erythrokeratoderma
+C0432333	Abnormal dermatoglyphic pattern
+C0432336	Cutis laxa, recessive, type I
+C0432347	Uncombable hair syndrome
+C0432355	Hypoplasia of nipple
+C0432357	Congenital absence of breast with absent nipple
+C0432360	Neurofibromatosis type 5
+C0432361	Diffuse neurofibroma
+C0432363	Shagreen patch
+C0432365	Thalidomide embryopathy syndrome
+C0432409	Trisomy 11
+C0432411	Chromosome 9, trisomy
+C0432412	Chromosome 8, trisomy
+C0432416	Down Syndrome, Partial Trisomy 21
+C0432417	Trisomy 21, Meiotic Nondisjunction
+C0432418	Trisomy 21- mitotic nondisjunction mosaicism
+C0432442	Chromosome 18p deletion syndrome
+C0432443	Deletion of long arm of chromosome 18
+C0432470	46, XY female
+C0432474	Klinefelter\'s syndrome - male with more than two X chromosomes
+C0432475	XX males
+C0432482	Fragile X chromosome
+C0432487	Post transplant lymphoproliferative disorder
+C0432562	Malignant lymphoma of spleen
+C0433445	Burns third degree
+C0433593	Limb traumatic amputation
+C0433651	Splinter
+C0433856	Brain Injuries, Diffuse
+C0433895	Spinal Cord Contusion
+C0433900	Spinal Cord Laceration
+C0433905	Spinal Cord transection injury
+C0433992	Noise-induced temporary threshold shift
+C0434014	Diaphragmatic injury
+C0434028	Gallbladder injury
+C0434133	Bladder perforation
+C0434437	Joint sprain
+C0434514	Dislocation of vertebra
+C0434717	Dislocation of toe joint
+C0434785	Subluxation of hip joint
+C0434858	Hangman Fracture
+C0435001	Ligament injury
+C0435002	Ligament sprain
+C0435492	Fractured sacrum
+C0435630	Wrist fracture
+C0435632	Hand fracture
+C0436503	CXR abnormal
+C0436539	Computerised tomogram abnormal
+C0436540	MRI abnormal
+C0438142	Urine analysis abnormal
+C0438157	Electrocardiogram P wave abnormal
+C0438159	Electrocardiogram Q wave abnormal
+C0438167	Electrocardiogram T wave abnormal
+C0438173	Electrocardiogram QRS complex abnormal
+C0438177	Cardiac function test abnormal
+C0438184	Fundoscopy abnormal
+C0438215	Laboratory test abnormal
+C0438216	Full blood count abnormal
+C0438217	Red blood cell sedimentation rate abnormal
+C0438237	Hepatic enzyme abnormal
+C0438242	Blood urea abnormal
+C0438286	No therapeutic response
+C0438397	Skin graft failure
+C0438413	Malignant neoplasm of aortic body and other paraganglia
+C0438414	Myoclonic Encephalopathy
+C0438434	Ring scotoma
+C0438697	Crying, excessive
+C0438716	Pressure in chest
+C0438717	Transaminases increased
+C0438921	Back Pain without Radiation
+C0439053	Fatigue - symptom
+C0439857	Dependence
+C0441683	Hormone measurement
+C0441713	Chemical injury
+C0442735	Nothing
+C0442833	Arteriolar hyalinosis
+C0442840	Cardiac embolism
+C0442843	Corneal epithelial loss
+C0442856	Hypoperfusion
+C0442865	Lower motor neurone lesion
+C0442871	Microinvasive carcinoma
+C0442872	Multiple cysts
+C0442874	Neuropathy
+C0442876	Occult carcinoma
+C0442880	Periungual fibroma
+C0442887	Septal hypertrophy
+C0443306	Spastic
+C0443882	Anti-thyroid antibodies disorder
+C0444720	Circulatory arrest
+C0445347	Thickening of glomerular basement membrane
+C0447996	Maxillary torus
+C0450027	Accidental exposure
+C0451641	Urolithiasis
+C0451669	Neuropathy in association with hereditary ataxia
+C0451672	Cerebellar stroke syndrome
+C0451681	Posterior Cerebral Artery Syndrome
+C0451693	Severe combined immunodeficiency with low T- and B-cell numbers
+C0451694	Severe combined immunodeficiency with low or normal B-cell numbers
+C0451696	Major histocompatibility complex class II deficiency
+C0451697	Immunodeficiency following hereditary defective response to Epstein-Barr virus
+C0451718	Non-obstructive reflux-associated chronic pyelonephritis (disorder)
+C0451720	Nephrotic syndrome, focal and segmental glomerular lesions
+C0451819	Simple obesity
+C0451840	Erosive osteoarthrosis
+C0451948	Head Injuries, Multiple
+C0451981	Crushing Skull Injury
+C0452047	Brain Injuries, Focal
+C0452136	Conductive hearing loss, bilateral
+C0452138	Sensorineural hearing loss, bilateral
+C0452143	Paraplegia, Flaccid
+C0452147	Hypospadias, penoscrotal
+C0452148	Hypospadias, perineal
+C0452168	Hypospadias, balanic
+C0452203	Neonatal Cerebral Leukomalacia
+C0452221	Osteomyelitis of vertebra
+C0454455	Mirror movements disorder
+C0454542	Stuttering, Acquired
+C0454545	Hyperkinetic Dysphonia
+C0454555	Hypernasal voice
+C0454560	Acquired Language Disorders
+C0454573	Aphasia, Anterior
+C0454576	Aphasia, Mixed
+C0454578	Receptive aphasia (finding)
+C0454596	Dysarthria, Spastic
+C0454597	Dysarthria, Flaccid
+C0454598	Dysarthria, Mixed
+C0454599	Cerebellar dysarthria
+C0454606	Oral Dyskinesia
+C0454608	Apraxia, Oral
+C0454638	Expressive language impairment
+C0454641	Expressive language delay
+C0454642	Receptive language delay
+C0454643	Word finding difficulty (disorder)
+C0454644	Delayed speech and language development
+C0454651	Specific language impairment
+C0454653	Auditory Agnosia, Congenital
+C0454655	Semantic-Pragmatic Disorder
+C0455204	Homicidal ideation
+C0455308	Serum selenium measurement
+C0455383	FH: Depression
+C0455503	H/O: depression
+C0455715	Benedict Syndrome
+C0455716	Foville Syndrome
+C0455717	Weber Syndrome
+C0455718	Top of the Basilar Syndrome
+C0455732	Poverty of thought content
+C0455769	Energy increased
+C0455792	Small scrotum
+C0455806	Infant length
+C0455829	Waist Circumference
+C0455880	Poor stream of urine
+C0455899	Pharyngeal erythema
+C0455988	Hydrops Fetalis, Non-Immune
+C0455990	Immune Hydrops Fetalis
+C0455995	Neonatal hypotension
+C0456065	Infant, Extremely Low Birth Weight
+C0456070	Growth delay
+C0456086	Intrapartum fetal hypoxia
+C0456097	Congenital viral disease
+C0456103	Neonatal Sepsis
+C0456107	Neonatal meningitis
+C0456132	Large fontanelle
+C0456144	Cerebral dysgenesis
+C0456483	Simple Endometrial Hyperplasia
+C0456487	Peutz Jehgers polyp
+C0456495	Ear canal erythema
+C0456511	Sleep paralysis
+C0456512	Sleep Starts
+C0456516	Median Neuropathy, Proximal
+C0456673	Sputum retention
+C0456702	Severe childhood autosomal recessive muscular dystrophy
+C0456844	Light chain myeloma
+C0456861	Low grade B-cell lymphoma
+C0456863	High grade B-cell lymphoma
+C0456877	High grade T-cell lymphoma
+C0456889	Enteropathy-Associated T-Cell Lymphoma
+C0456909	Blindness
+C0456973	Hilar lymphadenopathy
+C0457013	Weyers acrofacial dysostosis
+C0457133	Muscle eye brain disease
+C0457179	Desmoplastic infantile astrocytoma
+C0457190	Xanthomatous Meningioma
+C0457193	Soft tissue mass
+C0457334	Acute monoblastic leukemia
+C0457506	Reactive thrombocytosis
+C0457521	Unicystic ameloblastoma
+C0457522	Juvenile ossifying fibroma
+C0457756	Tooth absent
+C0457775	No malocclusion
+C0457928	Bent bone dysplasia group
+C0457949	Chronic low back pain
+C0458219	Complex regional pain syndrome
+C0458224	Piriformis syndrome
+C0458247	Allodynia
+C0458256	Heavy pain
+C0458257	Pain, Splitting
+C0458259	Pain, Crushing
+C0458631	Performance anxiety
+C0458960	Peripheral neuropathic pain
+C0459888	Somatosensory Agnosia
+C0460048	Large bowel obstruction
+C0472347	Subacute Necrotizing Myelitis
+C0472369	Haemorrhagic cerebral infarction
+C0472376	Thalamus haemorrhage
+C0472377	Basal ganglia haemorrhage
+C0472381	Posterior Circulation Transient Ischemic Attack
+C0472383	Subarachnoid Hemorrhage, Spontaneous
+C0472387	Vasogenic Cerebral Edema
+C0472388	Cytotoxic Cerebral Edema
+C0472686	Continuous haemodiafiltration
+C0472713	Anemia of renal disease
+C0472761	Homozygous alpha thalassemia
+C0472762	Alpha trait thalassemia
+C0472767	Beta thalassemia intermedia
+C0472769	Hemoglobin Lepore trait
+C0472777	Hemoglobin E/beta thalassemia disease
+C0472790	Chronic non-spherocytic hemolytic anemia
+C0472792	Hemolytic anemia due to hexokinase deficiency
+C0472801	Hemophilia A carrier
+C0472802	Hereditary factor VIII deficiency disease with inhibitor
+C0472803	Hypodysfibrinogenemia
+C0472813	X-linked agammaglobulinemia with growth hormone deficiency
+C0472814	Autosomal agammaglobulinemia with absent B-cells
+C0472817	WHIM syndrome
+C0473117	Ischaemic hepatitis
+C0473118	Physiological hyperbilirubinemia (disorder)
+C0473119	Fecal peritonitis
+C0473120	Peritoneal haematoma
+C0473124	Perirenal hematoma
+C0473133	Protracted diarrhea
+C0473219	Renal hypouricemia
+C0473221	Cryoglobulinemic glomerulonephritis
+C0473236	Haematuria traumatic
+C0473237	Frank hematuria
+C0473311	Haemorrhagic ovarian cyst
+C0473508	Delayed Postpartum Hemorrhage
+C0473524	Postpancreatectomy hypoinsulinemia
+C0473527	Hypoalphalipoproteinemias
+C0473546	Vibratory angioedema
+C0473574	Inflammatory linear verrucous epidermal nevus
+C0473575	Acantholytic Dyskeratotic Epidermal Nevus
+C0473577	Eccrine nevus
+C0473579	Porokeratotic eccrine ostial and dermal duct nevus
+C0473583	Nevus elasticus
+C0473586	Michelin tire baby syndrome
+C0473878	Tenia solium infection
+C0474339	Keratinization of ocular surface
+C0474354	Optic Disc Neovascularization
+C0474355	Peripheral retinal neovascularization
+C0474366	Generalized Headache
+C0474368	Labor Pain
+C0474378	Hair colour changes
+C0474381	Chromatopsia
+C0474420	Inappropriate sexual behavior
+C0474433	Uremic fetor
+C0474444	Corneal stromal edema
+C0474454	Apnoeic attack
+C0474520	Myokymia, Generalized
+C0474535	Mean corpuscular hemoglobin concentration determination
+C0474543	Hemoglobin A2 measurement
+C0474566	Platelet hematocrit measurement
+C0474585	Feces color: tarry
+C0474679	Serum ceruloplasmin measurement
+C0474702	Sulfate measurement
+C0474807	Chromophobe tumor
+C0474808	Follicular neoplasm
+C0474809	Endometrioid tumor
+C0474819	Glomus vagale tumor
+C0474822	Benign pheochromocytoma
+C0474824	Halo nevus
+C0474855	Compound leukemias
+C0474886	Localized recessive dystrophic epidermolysis bullosa
+C0474887	Generalized dystrophic epidermolysis bullosa
+C0474892	Inherited disorder of keratinization
+C0474963	Malignant tumor of junctional zone of tongue
+C0474983	Tongue haematoma
+C0474998	Traumatic Spinal Subdural Hematoma
+C0475021	Colonic haematoma
+C0475022	Renal haematoma
+C0475059	Subdural Hematoma, Traumatic
+C0475060	Intracranial Subdural Hematoma, Traumatic
+C0475072	Traumatic cerebral hemorrhage
+C0475073	Subarachnoid Hemorrhage, Traumatic
+C0475319	Pelvic haematoma
+C0475712	Primary sleep apnea of newborn
+C0475732	Hypercalcemia, Infantile
+C0475733	Idiopathic infantile hypercalcemia - mild form
+C0475746	Light anaesthesia
+C0475765	Nasal oedema
+C0475801	Leukemia, Prolymphocytic, B-Cell
+C0475811	Disorder of keratinization
+C0475813	Alpha-thalassemia/mental retardation syndrome (301040) is an allelic disorder
+C0475858	Generalized pruritus
+C0475876	Meningocele, Traumatic
+C0476073	Papillary neoplasm
+C0476089	Endometrial cancer
+C0476122	ovarian serous tumor
+C0476147	Chondrogenic Neoplasm
+C0476171	Comminuted fracture
+C0476201	Axonotmesis
+C0476206	Giddiness
+C0476217	Head movements abnormal
+C0476226	Anesthesia of skin
+C0476227	pricking of skin
+C0476236	Developmental symptoms
+C0476237	Metabolic symptoms
+C0476241	Delayed developmental milestone
+C0476254	Dyslexia
+C0476270	Cardiovascular symptoms
+C0476273	Respiratory distress
+C0476278	Anterior chest wall pain
+C0476280	Musculoskeletal chest pain
+C0476281	Non-cardiac chest pain
+C0476287	Breath holding spell
+C0476289	Abdominal wind pain
+C0476305	Hypochondrial pain
+C0476313	Swelling of inguinal region
+C0476320	Red blood cell morphology abnormal
+C0476337	Blood gases abnorm
+C0476369	Echocardiogram abnormal
+C0476393	Scan NOS brain abnormal
+C0476397	Electroretinogram abnormal
+C0476403	Electromyogram abnormal
+C0476405	Lung function abnormal
+C0476408	Reduced vital capacity
+C0476414	Thyroid function test abnormal
+C0476419	Scan liver NOS abnormal
+C0476427	Abnormal cervical smear
+C0476431	Chromosomal analysis abnormal
+C0476434	Sputum culture positive
+C0476436	Culture wound positive
+C0476442	High antibody titer
+C0476476	Generalized hyperhidrosis
+C0476486	Generalized enlarged lymph nodes
+C0476489	Alpha 1 foetoprotein abnormal
+C0477316	Other specified coagulation defects
+C0477317	Other primary thrombocytopenia
+C0477324	Other combined immunodeficiencies
+C0477325	Immunodeficiency associated with other specified major defects
+C0477360	Other dystonia
+C0477362	Other specified extrapyramidal and movement disorders
+C0477365	Other specified degenerative diseases of nervous system
+C0477370	Other generalized epilepsy and epileptic syndromes
+C0477373	Other forms of migraine
+C0477432	Post-Traumatic Hydrocephalus
+C0477474	Dermatitis and eczema
+C0477506	Other specified nonscarring hair loss
+C0477548	Other chondrocalcinosis
+C0477611	[X]Spinal osteochondrosis, unspecified
+C0477728	Hereditary nephropathy
+C0477729	Other chronic tubulo-interstitial nephritis
+C0477971	Other reduction deformities of brain
+C0477972	Other specified congenital malformations of brain
+C0477983	Other congenital corneal malformations
+C0477984	Other congenital malformations of anterior segment of eye
+C0477991	Other branchial cleft malformations
+C0478007	Other malformations of cerebral vessels
+C0478019	Other specified congenital malformations of respiratory system
+C0478044	Other doubling of uterus
+C0478072	Other specified congenital malformations of limb(s)
+C0478074	Other congenital malformations of spine, not associated with scoliosis
+C0478077	Other osteochondrodysplasia with defects of growth of tubular bones and spine
+C0478084	Other congenital ichthyosis
+C0478085	Other epidermolysis bullosa
+C0478093	Other congenital malformation syndromes with other skeletal changes
+C0478099	Other deletions of part of a chromosome
+C0478664	Localized enlarged lymph nodes
+C0481667	Live birth
+C0483368	Human anaplasmosis due to Anaplasma phagocytophilum
+C0487852	hydatids
+C0489482	Ejection fraction
+C0489636	RR interval
+C0489980	Disseminated due to other mycobacteria
+C0494053	Neurosyphilis, Symptomatic
+C0494164	Secondary malignant neoplasm of small intestine
+C0494165	Metastases to liver
+C0494261	Combined immunodeficiency
+C0494266	Other specified immunodeficiencies
+C0494360	Lipodystrophy, not elsewhere classified
+C0494410	Nonorganic Sleep Wake Cycle Disorders
+C0494415	Anxious personality disorder
+C0494463	Alzheimer Disease, Late Onset
+C0494475	Generalised tonic-clonic seizures
+C0494491	Mononeuropathies
+C0494559	Diseases of inner ear
+C0494698	Tooth development disorder
+C0494710	Mouth cyst
+C0494853	Erythema ab igne
+C0495452	Noninfective neonatal diarrhea
+C0495499	Congenital absence, atresia and stricture of auditory canal (external)
+C0495617	Congenital scoliosis due to bony malformation
+C0496755	Malignant neoplasm of border of tongue
+C0496779	Malignant neoplasm of appendix
+C0496836	Malignant tumor of eye
+C0496870	Benign neoplasm of liver
+C0496892	Benign neoplasm of kidney
+C0496897	Benign neoplasm of eye, unspecified
+C0496899	Benign neoplasm of brain, unspecified
+C0496901	Pituitary tumour benign
+C0496905	Neoplasm of uncertain or unknown behavior of stomach
+C0496920	Neoplasm of uncertain or unknown behavior of ovary
+C0496924	Neoplasm of uncertain or unknown behavior of testis
+C0496930	Neoplasm of uncertain or unknown behavior of bladder
+C0496956	Neoplasm of uncertain or unknown behavior of breast
+C0497156	Lymphadenopathy
+C0497169	hiv-infection/aids
+C0497201	Abnormal sensation in eye
+C0497202	Abnormal ocular motility
+C0497209	Conjunctivitis infective
+C0497243	Neoplasm of cardiovascular system
+C0497247	Blood pressure increased
+C0497248	Uncomplicated hypertension
+C0497299	meningitis/encephalitis
+C0497327	Dementia
+C0497365	Rash generalised
+C0497391	atopic eczema/dermatitis (non-specific)
+C0497406	Overweight
+C0497456	Menstruation absent
+C0497481	Pain in penis
+C0497538	Benign digestive system neoplasms
+C0497550	Benign neurologic neoplasms
+C0497552	Congenital neurologic anomalies
+C0518014	Hematocrit
+C0518015	Haemoglobin
+C0518017	Blood cholesterol
+C0518018	Blood triglycerides
+C0518026	body fat percentage (physical finding)
+C0518084	Impaired self-care
+C0518085	Difficulty eating
+C0518179	Change in voice (finding)
+C0518454	Head Injury, Open
+C0518656	Chronic fatigue
+C0518948	Chlamydia trachomatis infection
+C0518964	BRONCHIAL ADENOCARCINOMA
+C0518988	Dental abscess
+C0518989	Acute diverticulitis
+C0519002	Gastrointestinal amyloidosis
+C0519030	Pneumonia due to Klebsiella pneumoniae
+C0519036	Lyme Meningoencephalitis
+C0519066	Acute Q fever
+C0519095	tuberculosis chronic pulmonary
+C0519097	Left ventricular aneurysm
+C0519826	ASSAY FOR TACROLIMUS
+C0520459	Enterocolitis, Necrotizing
+C0520463	Chronic active hepatitis
+C0520474	Aseptic Necrosis of Bone
+C0520477	Prostatic Adenoma
+C0520482	Briquet's syndrome
+C0520532	Subcutaneous haematoma
+C0520546	Pulmonary microemboli
+C0520547	Poor peripheral circulation
+C0520557	Arteriovenous malformation of liver
+C0520558	Teeth brittle
+C0520560	Oesophagitis haemorrhagic
+C0520561	Small intestinal haemorrhage
+C0520562	Intestinal dilatation
+C0520564	Ileal ulcer
+C0520571	Fibrosis of bile duct
+C0520572	Enzymopathy
+C0520573	Buffalo hump
+C0520574	Cerebrovascular amyloidosis
+C0520575	Acute pyelonephritis
+C0520587	Vulvovaginal discomfort
+C0520588	Vulvovaginal pain
+C0520589	Vulvovaginal dryness
+C0520594	Breast microcalcification
+C0520599	Neonatal hypoxia
+C0520675	Minor depressive disorder
+C0520676	Premenstrual Dysphoric Disorder
+C0520678	Postpartum psychosis
+C0520679	Sleep Apnea, Obstructive
+C0520680	Sleep Apnea, Central
+C0520683	Occupation-related stress disorder
+C0520688	Brain fag
+C0520716	Pallidopontonigral degeneration
+C0520720	Perineurial cyst
+C0520723	Periorbital haematoma
+C0520724	Retinal cyst
+C0520730	Optic nerve infarction
+C0520731	Retraction Nystagmus
+C0520736	Coombs positive haemolytic anaemia
+C0520737	Coombs negative haemolytic anaemia
+C0520739	Hereditary pyropoikilocytosis
+C0520743	Lymphadenopathy mediastinal
+C0520744	Paratracheal lymphadenopathy
+C0520745	Splenic haemorrhage
+C0520746	Pubic rami fracture
+C0520757	Delayed Emergence from Anesthesia
+C0520758	Neuromuscular block prolonged
+C0520761	Chemical poisoning
+C0520764	Gastroenteritis clostridial
+C0520767	Endocarditis staphylococcal
+C0520775	Cystitis klebsiella
+C0520788	Posttransfusion viral hepatitis
+C0520789	Progressive subcortical gliosis
+C0520796	Gastroenteritis cryptosporidial
+C0520798	Hepatic schistosomiasis
+C0520804	Non-accidental overdose
+C0520817	Physical disability
+C0520821	Pleurothotonus
+C0520823	Patellar clonus
+C0520825	Platypnea
+C0520829	Total lung capacity decreased
+C0520831	Decreased vital capacity
+C0520837	Forced expiratory volume decreased
+C0520843	Peak expiratory flow rate decreased
+C0520850	Pulmonary arterial wedge pressure increased
+C0520854	Mean arterial pressure decreased
+C0520861	Raised jugular venous pressure
+C0520863	Diastolic dysfunction
+C0520869	Cardiac index increased
+C0520870	Cardiac index decreased
+C0520877	PR interval feature
+C0520878	Electrocardiogram PR shortened
+C0520886	Electrocardiogram ST segment elevation
+C0520887	Electrocardiogram ST segment depression
+C0520888	Electrocardiogram T wave inversion
+C0520904	Postoperative Nausea
+C0520905	Post-op vomiting
+C0520909	Postoperative Nausea and Vomiting
+C0520927	Decreased fertility
+C0520933	Abnormal spermatogenesis
+C0520947	Clumsiness - motor delay
+C0520961	Drug withdrawal headache
+C0520962	Localized pain
+C0520966	Abnormal coordination
+C0520997	Thrombolysis
+C0521007	Hypophonia
+C0521008	Screaming
+C0521158	Neoplasm recurrence NOS
+C0521161	Vasculitic rash
+C0521169	Compression fracture
+C0521170	Osteoporotic Fractures
+C0521172	Eschar
+C0521173	Granulomatosis
+C0521174	Microcalcification
+C0521175	Neuropil Threads
+C0521208	Accident at home
+C0521210	Polypectomy
+C0521232	Coronary arterial stent insertion
+C0521235	Varicose vein operation NOS
+C0521300	Life support
+C0521302	Fluid replacement
+C0521464	Skin oedema
+C0521465	Toxic skin eruption
+C0521471	Systemic lupus erythematosus rash
+C0521476	Infected nail bed
+C0521478	Mucocutaneous ulcer
+C0521481	Oedema mucosal
+C0521483	Mucous membrane hyperplasia
+C0521486	Burning sensation mucosal
+C0521490	Application site irritation
+C0521491	Application site pain
+C0521492	Application site ulcer
+C0521495	Application site rash
+C0521496	Application site infection
+C0521498	Injection site irritation
+C0521500	Injection site extravasation
+C0521503	Injection site burning
+C0521504	Injection site nerve damage
+C0521505	Injection site dermatitis
+C0521506	Injection site paraesthesia
+C0521507	Injection site ulcer
+C0521508	Injection site bruising
+C0521509	Injection site induration
+C0521510	Implant site reaction
+C0521515	Calcific tendinitis
+C0521516	Polymyalgia
+C0521525	Short neck
+C0521527	Shortened trunk
+C0521530	Lung consolidation
+C0521532	Diaphragm muscle weakness
+C0521533	Atrial septal aneurysm
+C0521540	Brain stem haemorrhage
+C0521541	Brain stem ischaemia
+C0521542	Brain stem infarction
+C0521546	Congenital joint malformation
+C0521554	Congenital vesicoureteric reflux
+C0521573	Coloboma of eyelid
+C0521579	Congenital strabismus
+C0521584	Gastrointestinal tract mucosal discolouration
+C0521585	Gastrointestinal mucositis
+C0521586	Gastrointestinal mucosal necrosis
+C0521587	Gastrointestinal stenosis
+C0521591	Paraesthesia oral
+C0521592	Hypoaesthesia oral
+C0521607	Peritoneal Fibrosis
+C0521613	Pancreatic haemorrhage
+C0521614	Gallstone pancreatitis
+C0521616	Pseudoporphyria
+C0521618	Stenosis of ureter
+C0521619	Obstruction of pelviureteric junction
+C0521620	Dilatation of ureter
+C0521622	Bilateral hydronephrosis
+C0521625	Bladder telangiectasia
+C0521626	Fibrosis of urinary bladder
+C0521648	Neonatal respiratory failure
+C0521654	Motor dysfunction
+C0521657	Allergic encephalitis
+C0521659	Motor Neuron Disease, Upper
+C0521662	Hemiplegia, Transient
+C0521663	Paraparesis, Chronic Progressive
+C0521664	Acute Confusional Migraine
+C0521668	Primary Thunderclap Headache
+C0521670	Cranial nerve compression
+C0521683	Chorioretinal degeneration
+C0521686	Glaucomatous retinal degeneration
+C0521691	Generalized progressive retinal atrophy
+C0521694	Atrophic retina
+C0521707	Bilateral cataracts (disorder)
+C0521719	Clouding of corneal stroma
+C0521720	Corneal fibrosis
+C0521723	Corneal dystrophy, epithelial basement membrane
+C0521736	Lower eyelid ectropion
+C0521753	Temporary Nystagmus
+C0521754	Permanent Nystagmus
+C0521755	Unidirectional Nystagmus
+C0521756	Multidirectional Nystagmus
+C0521757	Conjugate Nystagmus
+C0521759	Convergence Nystagmus
+C0521760	Fatigable Positional Nystagmus
+C0521761	Non-Fatigable Positional Nystagmus
+C0521770	Asteroid hyalosis
+C0521785	Hearing Loss, Unilateral
+C0521787	Tinnitus, Clicking
+C0521788	Tinnitus, Leudet
+C0521793	Eighth nerve lesion (NOS)
+C0521802	Congenital atransferrinemia
+C0521819	Vaccination failure
+C0521834	Eye infection staphylococcal
+C0521839	Influenza like illness
+C0521845	Drug effect decreased
+C0521847	No drug reaction
+C0521848	Drug interaction potentiation
+C0521849	Drug interaction inhibition
+C0521853	Drug tolerance increased
+C0521854	Drug tolerance decreased
+C0521857	Increased drug resistance
+C0521858	Decreased drug resistance
+C0521987	Pre-existing disease
+C0521988	Pre-existing condition improved
+C0521991	Stress symptoms
+C0522042	Loss of control of legs
+C0522051	Acute chest pain
+C0522055	Electrocardiogram abnormal
+C0522057	Numbness of skin
+C0522060	Inadequate diet
+C0522063	Impaired gastric emptying
+C0522064	Regurgitation of food
+C0522067	Hepatic pain
+C0522070	Pancreatic symptom
+C0522125	Urethral spasm
+C0522153	Urine color abnormal
+C0522165	Feeling of relaxation
+C0522168	Morose
+C0522171	Sense of oppression
+C0522172	Feeling drunk
+C0522174	Delinquent behavior
+C0522178	Self-injurious ideation
+C0522179	Fear of death
+C0522182	Fear of disease
+C0522187	Tocophobia
+C0522192	Nocturnal fear
+C0522198	Explosive speech
+C0522205	Sexual inhibition
+C0522214	Abnormal visual evoked potential
+C0522216	Abnormal auditory evoked potential
+C0522224	Paralysed
+C0522225	Normal reflex
+C0522245	Feeling hot and cold
+C0522248	Inadequate analgesia
+C0522251	Sinus pain
+C0522253	Primary Exertional Headache
+C0522254	Analgesic Overuse Headache
+C0522255	Cervical root pain
+C0522274	Humoral immune defect
+C0522336	Eye rolling
+C0522345	Reflex, Acoustic, Abnormal
+C0522349	Vertigo, Essential
+C0522351	Positional Vertigo
+C0522357	Vertigo, Paroxysmal
+C0522359	Vertigo
+C0522560	Needle track marks
+C0522621	Sessile polyp
+C0522624	Subcutaneous panniculitis-like T-cell lymphoma
+C0522631	Acute myeloid leukemia, minimal differentiation
+C0522757	Exposure to toxic agent
+C0522776	Stent insertion NOS
+C0523353	Complement factor H measurement
+C0523354	Complement factor I measurement
+C0523357	Complement decay accelerating factor measurement
+C0523446	Acylcarnitines measurement
+C0523465	Serum albumin measurement
+C0523500	Angiotensinogen measurement
+C0523509	Apolipoprotein B Assay
+C0523511	Apolipoproteins E measurement (procedure)
+C0523522	beta-Endorphin measurement
+C0523550	Catalase measurement
+C0523560	VLDL cholesterol measurement
+C0523633	Fibronectin measurement
+C0523688	Hemopexin measurement
+C0523708	5-Hydroxyindoleacetic acid measurement
+C0523744	Lipids measurement
+C0523760	Lysine measurement
+C0523807	Oxygen saturation
+C0523912	Testosterone measurement
+C0523952	Troponin NOS
+C0523953	Cardiac troponin T measurement
+C0523957	Tryptophan measurement
+C0524368	Occupational environmental problems
+C0524489	Abscess, Amebic
+C0524524	Pseudoaphakia
+C0524528	Pervasive Development Disorder
+C0524541	Deciduoma
+C0524582	Mulibrey Nanism
+C0524587	Mean Corpuscular Volume (result)
+C0524595	Aseptic Necrosis of Femur Head
+C0524598	Fractures, Occult
+C0524610	Chronic Alcoholic Hepatitis
+C0524611	Cryptogenic Chronic Hepatitis
+C0524620	Metabolic Syndrome
+C0524631	Lymphatism
+C0524632	Status Lymphaticus
+C0524662	Opiate Addiction
+C0524679	Neuropapillitis
+C0524686	Periodontitis, Acute Nonsuppurative
+C0524687	Meningeal Plague
+C0524688	Pneumonic Plague
+C0524702	Pulmonary Thromboembolisms
+C0524722	Gastrointestinal surgery
+C0524730	Odontome
+C0524801	Retinal Neoplasms
+C0524802	Optic nerve neoplasm
+C0524812	Intracranial Hypotension
+C0524851	Neurodegenerative Diseases
+C0524861	Oral surgery NOS
+C0524909	Hepatitis B, Chronic
+C0524910	Hepatitis C, Chronic
+C0524911	Hepatitis D, Chronic
+C0524912	Hepatitis, Chronic, Drug-Induced
+C0524948	Maxillofacial Abnormalities
+C0524988	Schnitzler Syndrome
+C0525024	Prosthesis implantation
+C0525032	International normalised ratio
+C0525041	Neurobehavioral Manifestations
+C0525043	Reactive Attachment Disorder
+C0525045	Mood disorder
+C0525046	Schizophrenia Spectrum and Other Psychotic Disorders
+C0525047	Sexual and Gender Disorders
+C0541403	Neuroendocrine disease or syndrome
+C0541719	Stress polycythemia
+C0541760	Hepatic adenoma
+C0541764	Delayed bone age
+C0541772	Ammonia increased
+C0541782	Atrial standstill
+C0541794	Skeletal muscle atrophy
+C0541798	Early Awakening
+C0541813	Kussmaul respiration
+C0541820	Carbohydrate tolerance decreased
+C0541829	Blood cholinesterase decreased
+C0541832	Chromaturia
+C0541850	Cross sensitivity reaction
+C0541875	Joint destruction
+C0541907	Drug effect incomplete
+C0541912	Duodenal Cancer
+C0541923	Lip oedema
+C0541941	Erection increased
+C0541957	Fasciculation, Skeletal Muscle
+C0541979	Gamma-glutamyltransferase abnormal
+C0541985	Globulin gamma serum plasma increased result
+C0542007	Cerebral haematoma
+C0542008	Injection site haematoma
+C0542027	Hypercoagulation
+C0542028	Breast hyperplasia
+C0542035	Erythroid hypoplasia
+C0542037	Hypotriglyceridemia
+C0542044	Incoherent
+C0542052	Coronary artery insufficiency
+C0542120	Injection site nodule
+C0542141	Paralysis radial
+C0542142	Recurrent laryngeal nerve palsy
+C0542147	Jejunal perforation
+C0542149	Injection site phlebitis
+C0542165	Pseudoparkinsonism
+C0542189	Reaction time decreased
+C0542211	Postoperative renal failure
+C0542213	Positive skin test
+C0542223	Loss of speech
+C0542241	Bacterial toxaemia
+C0542271	Environmental Carcinogenesis
+C0542302	Blood Pressure Disorders
+C0542313	Sleep talking
+C0542346	Pimples
+C0542428	Hypochondrogenesis
+C0542476	Forgetful
+C0542514	Blue sclera
+C0542518	Enlarged kidney
+C0542519	Congenital absence of kidney
+C0542525	Tongue injury
+C0542571	Face oedema
+C0543467	Surgery
+C0543478	Residual Tumor
+C0543514	Glycogen Storage Disease IXB
+C0543515	Sucrase deficiency
+C0543541	HYPERGLYCINURIA (disorder)
+C0543636	Lupus erythematosus, subacute
+C0543638	Fibrosing disease
+C0543641	Megaloblastic anemia, secondary
+C0543645	Heterozygous hemoglobinopathy
+C0543663	Idiopathic Autoimmune Hemolytic Anemia
+C0543669	Neutrophilia, Hereditary
+C0543673	Fibrinolytic disorder
+C0543687	Thymic alymphoplasia
+C0543693	Neutropenia neonatal
+C0543697	Mixed cryoglobulinemia
+C0543698	Hypersensitive syndrome
+C0543699	ASA intolerant asthma
+C0543754	Klinefelter Syndrome, Variants
+C0543793	Congenital renal disorder
+C0543800	Idiopathic hypercalciuria
+C0543822	Atherosclerotic occlusive disease
+C0543858	Motor Neuron Disease, Secondary
+C0543859	Amyotrophic Lateral Sclerosis, Guam Form
+C0543874	Apraxia, oculomotor, Cogan type
+C0543888	Epileptic encephalopathy
+C0543891	Neuroleptic-Induced Tardive Dyskinesia
+C0543910	Psychosis, childhood onset
+C0543918	SCHIZOPHRENIA 10
+C0543968	Cone dysfunction syndrome
+C0543982	Glaucoma, primary
+C0543991	Chronic primary angle closure glaucoma
+C0544008	Chandler syndrome
+C0544618	Orthostatic hypertension
+C0544668	Hallucinations, Kinesthetic
+C0544679	Scotoma, Paracecal
+C0544680	Quadrantanopsia
+C0544688	Disease complication
+C0544755	Bandy legged
+C0544786	wegener\'s granuloma
+C0544791	Inflammatory fistula
+C0544795	Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp
+C0544796	Myositis, Proliferative
+C0544799	Histiocytosis, generalized eruptive
+C0544820	Hypomyelination
+C0544840	Nodular amyloidosis
+C0544848	Dystrophy, granular
+C0544852	Hypertrichosis, universal
+C0544855	Leukonychia totalis
+C0544862	Neurocutaneous melanosis
+C0544925	Axonal swelling
+C0544966	Autophagic vaculoes (finding)
+C0545034	pituitary giant
+C0545044	Acrokeratoelastoidosis of Costa
+C0545053	Advanced bone age
+C0545074	Myxoid/Round Cell Liposarcoma
+C0545080	Composite Lymphoma
+C0545081	mantle lymphoma
+C0545617	Supernumerary metacarpal bone
+C0546125	Nemaline Myopathy, Childhood Onset
+C0546126	Acute Confusional Senile Dementia
+C0546127	Mercury Poisoning, Nervous System
+C0546264	Congenital Fiber Type Disproportion
+C0546275	Hypoganglionosis
+C0546297	Hallux Varus
+C0546303	Acquired Encephalocele
+C0546343	Mucosa erosion (NOS)
+C0546389	Hepatic periportal necrosis
+C0546466	Idiopathic cardiac hypertrophy
+C0546476	Multiple self-healing squamous epithelioma
+C0546483	Lung cyst
+C0546817	Fluid overload
+C0546837	Malignant neoplasm of esophagus
+C0546878	Nodding spasm
+C0546884	Hypovolaemia
+C0546947	Choking sensation
+C0546952	Congenital facial asymmetry
+C0546953	Subacromial bursitis
+C0546956	Onychoclasis
+C0546959	Atrial tachycardia
+C0546964	Genu recurvatum
+C0546966	Monilethrix
+C0546967	Posterior embryotoxon
+C0546968	Fistula of branchial cleft
+C0546969	Preauricular Fistulae, Congenital
+C0546983	Post-Concussion Syndrome
+C0546999	Larva Migrans, Cutaneous
+C0547000	Joint lock
+C0547002	Death rattle
+C0547005	Mid-cycle bleeding
+C0547030	Visual disturbance
+C0547058	Pseudopolyposis
+C0547065	Mixed oligoastrocytoma
+C0548883	Low frustration tolerance
+C0548923	Burn infection
+C0549117	Frontal lobe syndrome
+C0549122	Relative afferent pupillary defect
+C0549123	Large tonsils (finding)
+C0549124	Embolism arterial
+C0549143	Pulmonary renal syndrome
+C0549150	Pseudofolliculitis barbae
+C0549151	Follicular keratosis
+C0549159	Infant Death
+C0549173	Congenital atresia of rectum
+C0549175	Fibromatosis colli
+C0549201	Asteatosis
+C0549202	Chapped skin
+C0549209	Feeling jittery
+C0549225	Myasthenic Syndrome
+C0549249	Depressed level of consciousness
+C0549253	Bladder dilatation
+C0549262	Rebound effect
+C0549263	Opiate withdrawal symptoms
+C0549264	Sensation of blood flow
+C0549288	Pelvic venous thrombosis
+C0549289	Thrombosis of inferior vena cava
+C0549297	Auricular swelling
+C0549306	Mesomelia
+C0549307	Morning glory syndrome
+C0549310	Vaginal mycosis
+C0549313	Bronchial irritation
+C0549315	Benign hydatidiform mole
+C0549322	Eyelid infection
+C0549338	Congenital acrochordon
+C0549348	Blood glucose false positive
+C0549357	Abdominal adhesions
+C0549358	Breast cosmetic surgery
+C0549364	Osmolar gap abnormal
+C0549368	Malignant female genital neoplasm NOS
+C0549369	Pancreatic enzymes NOS increased
+C0549371	Carcinoembryonic antigen incr.
+C0549373	Laryngeal pain
+C0549379	Recurrent cancer
+C0549385	Feeling of body temperature change
+C0549391	Bladder discomfort
+C0549393	Alcohol problem
+C0549395	Blood urea decreased
+C0549396	Breast necrosis NOS
+C0549397	Deviated nasal septum
+C0549398	Meibomianitis
+C0549399	Low density lipoprotein increased
+C0549400	Apgar score low
+C0549405	Blood pressure fluctuation
+C0549410	Hand-Foot Syndrome
+C0549414	Blast cell proliferation
+C0549418	Urine flow decreased
+C0549419	Skin fragility
+C0549423	Obstructive Hydrocephalus
+C0549430	Procedural site reaction
+C0549444	Vein discolouration
+C0549448	Haemoglobin increased
+C0549453	Traumatic haematoma
+C0549463	X-Linked Lymphoproliferative Disorder
+C0549469	System disorder of the nervous system
+C0549473	Thyroid carcinoma
+C0549475	Lipase increased
+C0549478	Device expulsion
+C0549483	Abscess bacterial NOS
+C0549487	Wrong drug administered
+C0549488	Wrong patient received medication
+C0549493	Alveolitis
+C0549523	Oropharynx (excludes nasopharynx)
+C0549536	Monocyte count decreased
+C0549543	Coagulation time NOS abnormal
+C0549544	Bleeding time abnormal
+C0549567	Pigmentation disorder
+C0549608	VEINS/LYMPHATICS
+C0549609	Dysfunction adrenal
+C0549613	Biliary tract abnormality
+C0549618	MALE GENITAL ABNORMALITIES
+C0549622	Sexual Dysfunction
+C0549634	Lipids NOS abnormal
+C0553084	Red blood cell morphology
+C0553548	Necrotizing Arteritis
+C0553558	Jackknife Seizures
+C0553573	Primary infertility
+C0553576	Systemic mycosis
+C0553580	Ewings sarcoma
+C0553581	Round cell sarcoma
+C0553586	Cafe-au-lait macules with pulmonary stenosis
+C0553604	Myotonic Disorders
+C0553624	Scotoma, Sector
+C0553647	Juvenile aponeurotic fibroma
+C0553668	Labored breathing
+C0553681	Hypofibrinogenaemia
+C0553686	Brain herniation
+C0553690	Reversible ischaemic neurological deficit
+C0553692	Brain hemorrhage
+C0553694	Oropharyngeal disorders
+C0553698	Monocyte count increased
+C0553706	High blood phosphate levels
+C0553707	Malignant epithelioma
+C0553713	BREAST PAIN FEMALE
+C0553718	Renal artery occlusion
+C0553720	Spherocytosis
+C0553721	Diminished sweating
+C0553723	Squamous cell carcinoma of skin
+C0553724	Breast disorder male
+C0553727	Muscular paralysis
+C0553730	Calcium pyrophosphate deposition disease
+C0553732	Prothrombin level decreased
+C0553737	Cervical discharge
+C0553757	Disorders of smell
+C0553767	Congenital Cerebral Palsy
+C0553824	Apraxia, developmental
+C0553891	Extubation
+C0553980	Endocardial fibrosis
+C0553982	Impaired left ventricular function
+C0554101	Villous atrophy
+C0554103	Intestinal malabsorption of fat
+C0554119	Pancreatic malabsorption
+C0554309	Prerenal uremia syndrome
+C0554393	Placental infarction
+C0554400	Lactation problem
+C0554436	Diabetic gangrene
+C0554591	Polymyositis, Idiopathic
+C0554628	Group A Streptococcal Infections
+C0554970	Pallor of optic disc
+C0554972	Large auricle
+C0554976	Bradyphrenia
+C0554978	Racing thoughts
+C0554980	Moody (finding)
+C0554985	Aggressive outburst
+C0555026	Marital problem
+C0555120	White blood cells urine positive
+C0555198	Glial tumours malignant
+C0555199	Spongioblastoma, Polar
+C0555202	Malignant lymphoma - lymphocytic, intermediate differentiation
+C0555206	Chiari malformation type II
+C0555214	Multiple lung cysts
+C0555232	pseudohermaphrodite (non-specific)
+C0555278	Cerebral metastasis
+C0555305	Head Injury, Minor
+C0555358	Morbid thoughts
+C0555724	Lip dry
+C0555971	Oral infection
+C0556280	Gross motor impairment
+C0556346	Binge Drinking
+C0556374	Drunk driving
+C0556385	Craving for alcohol
+C0557874	Global developmental delay
+C0558066	Intrusive thoughts
+C0558089	Verbal abuse
+C0558142	Inflammation of wound
+C0558148	Yellow complexion
+C0558165	Curly hair (finding)
+C0558193	Stiff limbs
+C0558242	Stretched skin
+C0558348	Bacterial gastroenteritis
+C0558353	Tongue Carcinoma
+C0558355	Tonsillar Carcinoma
+C0558356	Malignant melanoma of eye
+C0558368	Vaginal irritation
+C0558401	Skin laceration
+C0558489	Renal pain
+C0558799	Femoral bruit
+C0558844	Knee reflex absent
+C0558845	Reflex, Ankle, Absent
+C0558846	Reflex, Triceps, Absent
+C0558847	Reflex, Biceps, Absent
+C0558916	Nasal and nasal-type NK/T-cell lymphoma
+C0558919	Stress at work
+C0559031	Functional gastrointestinal disorder
+C0559106	Ventricular preexcitation
+C0559260	Congenital scoliosis
+C0559395	Luxatio Erecta
+C0559459	Sacrococcygeal teratoma
+C0559460	Adrenal neuroblastoma
+C0559469	Allergy to eggs
+C0559470	Allergy to peanuts
+C0559483	Pentalogy of Cantrell
+C0559506	Neonatal unconjugated hyperbilirubinemia
+C0559546	Adverse reaction
+C0559697	Joint dislocation reduction
+C0559902	Congenital external ear disorders
+C0559938	Ileal perforation
+C0560024	Swelling of eyelid
+C0560046	Unable to walk
+C0560346	Difficulty running
+C0561843	Memory, Episodic
+C0561921	Perineal fistula
+C0562102	Chemical burn of skin
+C0562350	Hip circumference
+C0562381	Victim of abuse
+C0562386	Victim of sexual abuse
+C0562389	Victim of child abuse
+C0562483	Persistent cough
+C0563211	Carcinoma of anal canal
+C0563238	Gastritis viral NOS
+C0563243	Poor coordination
+C0563247	Blood blister
+C0563305	IgA myeloma
+C0563306	IgG myeloma
+C0563449	Epispadias, male (disorder)
+C0563560	Weight bearing difficulty
+C0563608	Hallucinations, Formed, of People
+C0563620	Simultagnosia
+C0563621	Visual Agnosia for Objects
+C0563622	Visuospatial Agnosia
+C0563624	Position Agnosia
+C0563625	Agnosia for Pain
+C0563626	Agnosia for Temperature
+C0563632	Manifest-latent nystagmus
+C0563661	Hallucinations, Reflex
+C0564221	Difficulty talking
+C0564408	Manic mood
+C0564444	Skin wound
+C0564567	Impulsive character (finding)
+C0564622	Albumin urine present
+C0564778	Obstetric disorders
+C0565599	Maternal hypertension
+C0566602	Primary sclerosing cholangitis
+C0566620	Nasal voice
+C0566625	Unintelligible Articulation
+C0566693	Large placenta
+C0566694	Small placenta
+C0566888	Narrow sacrosciatic notch
+C0566899	Small labia majora
+C0566943	Vaginal lesion
+C0566951	Vaginal ulceration
+C0566986	Vaginal discharge problem
+C0567085	Uterine pain
+C0570562	Contrast media allergy
+C0571818	Iodine allergy
+C0573196	Overdose of cocaine
+C0574002	Edema of foot (finding)
+C0574012	Subclavian artery thrombosis
+C0574014	Axillary vein thrombosis
+C0574068	Rib pain
+C0574080	Guanidinoacetate methyltransferase deficiency
+C0574083	3-Methylglutaconic aciduria type 2
+C0574084	3-Methylglutaconic aciduria type 3
+C0574143	Liver calculus
+C0574715	Drug-induced erythema multiforme
+C0574769	Loss of scalp hair
+C0574785	Lower Urinary Tract Symptoms
+C0574908	Lesion, Superficial Radial Nerve
+C0574960	Sacroiliitis
+C0574967	Cervical spine hypermobility
+C0575010	Temporomandibular joint stiff
+C0575059	Spastic tetraparesis
+C0575064	Skeletal muscle tender
+C0575071	Gowers sign present
+C0575081	Gait abnormality
+C0575090	Balance disorder
+C0575157	Deformity of spine
+C0575158	Kyphoscoliosis
+C0575167	Deformity of neck
+C0575170	Cervical kyphosis
+C0575484	Long thorax
+C0575497	Short sternum
+C0575507	Rib deformity
+C0575518	Hypertrophy of upper limb
+C0575535	Thin clavicle
+C0575802	Small hand
+C0575803	Radial deviation of hand
+C0575805	Swelling of hand
+C0575897	Thumb deformity
+C0576091	Knee deformity
+C0576093	Knee joint valgus deformity
+C0576224	Small foot
+C0576225	Long foot
+C0576227	Narrow foot
+C0576416	Pelvic deformity NOS
+C0576456	Feeding poor
+C0576479	Neglect of left side of body
+C0576481	Brain midline shift
+C0576612	Reflex, Anal, Absent
+C0576702	Barber's chair sign
+C0576860	Narrowing of ear canal
+C0576962	Tooth problem
+C0576979	Lesion of salivary gland
+C0576995	Bleeding of pharynx
+C0576999	Tonsil absent
+C0577008	Oesophageal mass
+C0577018	Stomach mass
+C0577027	Stomach problem
+C0577034	Rectal lesion
+C0577053	Hepatic lesion NOS
+C0577066	Gallbladder enlargement
+C0577115	Faeces soft
+C0577358	Impaired driving ability
+C0577559	Mass
+C0577608	C4 complement assay (procedure)
+C0577620	Nut Hypersensitivity
+C0577627	Allergy to metals
+C0577628	Latex allergy
+C0577631	Carotid arteriosclerosis
+C0577655	Quadriceps weakness
+C0577659	Axillary pain
+C0577660	Low Back Pain, Postural
+C0577662	Allergic cough
+C0577691	Disseminated squamous cell carcinoma
+C0577698	Exercise-induced angina
+C0577730	Family stress
+C0577822	Heart sounds abnormal
+C0577866	Poor venous access
+C0578022	Finding of body mass index
+C0578026	Weight abnormal
+C0578038	Thin lips
+C0578050	Lymph node pain
+C0578159	Antibiotic-associated diarrhea
+C0578437	Ischemic foot
+C0578454	Neck swelling
+C0578455	Abscess limb
+C0578477	Duodenal polyposis
+C0578503	Abnormal vaginal bleeding
+C0578531	Skin dimple
+C0578537	Cavitation of lung
+C0578575	Dissection of proximal aorta
+C0578626	blue iris (physical finding)
+C0578682	Madarosis of eyebrow
+C0578687	Sore eye
+C0578735	Axillary lymphadenopathy
+C0578736	Inguinal lymphadenopathy
+C0578757	Normal baby
+C0578870	Chronic idiopathic urticaria
+C0578878	Inflammation of large intestine
+C0579079	Breech delivery
+C0580173	Neurogenic claudication
+C0580174	Portal hypertensive gastropathy
+C0580190	3-Phosphoglycerate dehydrogenase deficiency
+C0580316	Neutrophil count abnormal
+C0580317	Platelet count abnormal
+C0580324	Electrocardiogram ambulatory abnormal
+C0580327	Antibody test
+C0580343	Culture stool positive
+C0580359	Allergy test positive
+C0580380	Reticulocyte count abnormal
+C0580412	Prothrombin time abnormal
+C0580413	Prothrombin time shortened
+C0580417	International normalised ratio abnormal
+C0580418	Ferritin level low
+C0580419	Iron binding capacity total decreased
+C0580454	Serum testosterone level abnormal
+C0580467	C-reactive protein abnormal
+C0580531	White blood cell count abnormal
+C0580546	Blood glucose abnormal
+C0580548	Red blood cell count abnormal
+C0580550	Lymphocyte count abnormal
+C0580555	Prostatic specific antigen abnormal
+C0580560	Blood magnesium abnormal
+C0580566	Creatinine renal clearance abnormal
+C0581118	Ultrasound scan abnormal
+C0581287	Injection site erythema
+C0581289	Injection site swelling
+C0581321	Vertebral osteoporosis
+C0581342	Redundant skin
+C0581354	Recurrent sinusitis
+C0581359	Acute intestinal obstruction
+C0581362	Anorectal pain
+C0581366	Recurrent cystitis
+C0581375	Double coronary vessel disease
+C0581381	Recurrent upper respiratory tract infection
+C0581384	Chronic anemia
+C0581385	Lymph node calcification
+C0581391	Chronic depression
+C0581394	Swollen legs
+C0581874	Late insomnia
+C0581876	Crying infant
+C0581882	Transient neurological symptoms
+C0581883	Complete Hearing Loss
+C0581911	Heavy legs
+C0581912	Sensation of heaviness
+C0581942	Bronchoscopy abnormal
+C0582415	Acute asthma
+C0582591	Processing speed
+C0584837	Choanal stenosis
+C0584946	Ideas of reference
+C0584960	Factor V Leiden mutation
+C0585006	Deficiency of enoyl-CoA hydratase
+C0585051	Acute sciatica
+C0585052	Chronic sciatica
+C0585059	Fracture displacement
+C0585129	Retroperitoneal sarcoma
+C0585134	Perianal pain
+C0585186	Cutaneous hypersensitivity
+C0585187	Infected ascites
+C0585213	Minor oral aphthous ulceration
+C0585216	Alpha-Thalassemia Myelodysplasia Syndrome
+C0585229	Multiple lacunar infarcts
+C0585265	Hypoglossal Nerve Palsy
+C0585274	Periodic syndrome
+C0585362	Squamous cell carcinoma of mouth
+C0585442	Osteosarcoma of bone
+C0585474	Ewing\'s sarcoma of bone
+C0585539	X-Linked Infantile Nystagmus
+C0585540	Myoclonus, Oculopalatal
+C0585544	Downbeat nystagmus
+C0585938	Hemoglobin A1 measurement
+C0585953	Recurrent chest infections
+C0585955	Dysplasia of larynx
+C0585984	Laryngotracheomalacia
+C0586323	Alcohol Withdrawal Seizures
+C0586354	Esophageal dysplasia
+C0586358	Biliary Intraepithelial Neoplasia
+C0586364	Moderate pancreatic duct dysplasia
+C0586392	Parkinsonian tremor
+C0586407	Skin symptom
+C0586553	Raised TSH level
+C0586557	Accident at work
+C0586683	Histology site unspecified abnormal
+C0586738	Calf muscle weakness
+C0586742	Difficulty reading
+C0586989	Varicella Zoster Virus Infection
+C0587048	Upper extremity mass
+C0587050	Lower extremity mass
+C0587052	Pulmonary hilum mass
+C0587054	Numbness of finger
+C0587056	Numbness of toe
+C0587094	Breast calcifications
+C0587178	Anti-nuclear antibody measurement
+C0587240	Bone erosion
+C0587246	Muscle weakness of limb
+C0587248	Costello syndrome (disorder)
+C0587310	Blister infected
+C0588006	Mild depression
+C0588007	Moderate depression
+C0588008	Severe depression
+C0588014	Malignant neoplasm of unknown primary site
+C0589110	Postoperative deep vein thrombosis
+C0589368	Postoperative myocardial infarction
+C0589616	Genitourinary chlamydia infection
+C0595862	Vasodilatation
+C0595877	Blood glucose increased
+C0595878	Blood sodium increased
+C0595883	Blood glucose decreased
+C0595900	Blood chloride increased
+C0595901	Serum chloride level decreased (finding)
+C0595902	Blood chloride decreased
+C0595905	cortex bone disorders
+C0595916	Nephropathy toxic
+C0595929	Serum cholesterol raised
+C0595930	Blood cholesterol increased
+C0595939	Stillbirth
+C0595948	Atypical absence seizure
+C0595956	Drug exanthem
+C0595978	Idiopathic megacolon
+C0595989	Carcinoma of larynx
+C0595995	Idiopathic scoliosis
+C0596118	Aortic occlusion
+C0596131	audiogenic seizure
+C0596170	Binge eating disorder
+C0596240	Cancer Pain
+C0596263	Carcinogenesis
+C0596270	Cardiovascular Infections
+C0596298	Cerebrovascular Occlusion
+C0596321	Chemical Carcinogenesis
+C0596344	clinical anxiety
+C0596368	Gastrointestinal disorder congenital NOS
+C0596452	disabling disease
+C0596611	Gene mutation
+C0596706	Hip operation NOS
+C0596793	Intracranial haematoma
+C0596848	lipoprotein disorder
+C0596887	mathematical ability
+C0596992	myelinopathy
+C0597048	Neurogenic hypertension
+C0597124	Obstructive asymmetric septal hypertrophy
+C0597167	Islets of Langerhans hyperplasia
+C0597457	Skeletal injury
+C0597503	Spinal shock
+C0597645	Viral Carcinogenesis
+C0597647	viral leukemogenesis
+C0597745	secondary immune deficiency
+C0597853	high renin hypertension
+C0597854	renin induced hypertension
+C0597966	Juxtaglomerular cell hyperplasia
+C0597984	Biliary stricture
+C0598121	Hypoglycorrhachia
+C0598221	Hereditary protein C deficiency
+C0598226	Harlequin type ichthyosis
+C0598275	Diffuse cerebral atrophy
+C0598428	genetic hypertension
+C0598589	Inherited neuropathies
+C0598608	Hyperhomocysteinaemia
+C0598675	inborn aminoaciduria
+C0598766	Leukemogenesis
+C0598784	Dyslipoproteinemias
+C0598790	lung sarcoma
+C0598798	Lymphoid neoplasm
+C0598894	Monocytic leukemia
+C0598935	Tumor Initiation
+C0599035	Hyperornithinemia
+C0599055	Waldenstrom\'s disease
+C0599458	glycosphingolipidoses
+C0599528	beta thalassemia major anemia
+C0599973	Waardenburg Anophthalmia Syndrome
+C0599990	Blood group p phenotype (finding)
+C0600021	Nail absent (finding)
+C0600028	Loose tooth
+C0600031	Congenital absence of spleen
+C0600033	Acquired Kyphoscoliosis
+C0600039	Urinary outflow obstruction
+C0600040	Chronic interstitial cystitis
+C0600041	Infective cystitis
+C0600049	Chancre
+C0600066	Malignant Cystosarcoma Phyllodes
+C0600074	Autotomy
+C0600086	Toxic goiter
+C0600104	Compulsions
+C0600113	Stromal tumor of ovary
+C0600114	Testicular stromal tumor
+C0600123	Acute hematogenous osteomyelitis
+C0600125	Electrocardiogram PR prolongation
+C0600139	Prostate carcinoma
+C0600142	Hot flush
+C0600176	Argentaffinoma
+C0600177	Low cardiac output syndrome
+C0600178	External Carotid Artery Diseases
+C0600228	Cardio-respiratory arrest
+C0600241	heroin abuse
+C0600260	Lung Diseases, Obstructive
+C0600272	Morphine Abuse
+C0600298	Periodontosis
+C0600327	Toxic Shock Syndrome
+C0600336	Subcorneal pustular dermatosis
+C0600359	Arteriosclerotic Dementia
+C0600427	Cocaine Dependence
+C0600433	Activated Protein C Resistance
+C0600452	Hepatopulmonary Syndrome
+C0600467	Neurogenic Inflammation
+C0600498	Anticipation, Genetic
+C0600502	Vascular Hemostatic Disorders
+C0600518	Choroidal neovascularisation
+C0600519	Ventricular Remodeling
+C0600520	Left Ventricle Remodeling
+C0677050	Manganese Poisoning
+C0677055	CARCINOMA OF VULVA
+C0677483	Carcinoma testes
+C0677487	Rectocele repair
+C0677499	Radial tunnel syndrome
+C0677500	Stinging Sensation
+C0677501	Congenital Nephrogenic Diabetes Insipidus
+C0677598	Stomatocytosis Result
+C0677599	Platelet aggregation test result
+C0677600	Inspiratory stridor
+C0677607	Hashimoto Disease
+C0677608	Chorioangioma
+C0677616	Plastic surgery NOS
+C0677635	Blood viscosity measurement
+C0677658	Breast disorder female
+C0677659	Gastro-esophageal reflux disease with esophagitis
+C0677660	Emotional problems
+C0677725	Mantle cell lymphoma recurrent
+C0677776	Hereditary Breast and Ovarian Cancer Syndrome
+C0677779	hereditary Wilms\' tumor (WT1)
+C0677781	Neurofibromatosis 1 and 2 (NF1 and NF2)
+C0677865	Brain Stem Glioma
+C0677866	Brain Stem Neoplasms
+C0677886	Epithelial ovarian cancer
+C0677898	invasive cancer
+C0677932	Progressive Neoplastic Disease
+C0677936	Refractory cancer
+C0677944	Sentinel node (disorder)
+C0677948	Stage II Colorectal Cancer
+C0677949	Stage III Colorectal Cancer
+C0677950	Stage IV Colorectal Cancer
+C0677952	Hodgkin's disease stage II
+C0677958	Non-Hodgkin's lymphoma NOS stage IV
+C0677984	Locally Advanced Malignant Neoplasm
+C0678033	Metastatic uterine cancer
+C0678128	Friend leukemia
+C0678189	Hyperlipidemia, group A
+C0678199	Anemia of inadequate production
+C0678201	Terminal Ileitis
+C0678202	Regional enteritis
+C0678213	Complete hydatidiform mole
+C0678222	Breast Carcinoma
+C0678230	Congenital Epicanthus
+C0678232	Serum chloride level result
+C0678236	Rare Diseases
+C0678306	alcohol sensitivity
+C0678329	drug substitution (abuse)
+C0678356	alcohol effect
+C0678807	prenatal alcohol exposure
+C0678909	Brain Waves
+C0679048	Obsessive thoughts
+C0679136	Low self-esteem
+C0679145	Sex addiction
+C0679189	Belligerence
+C0679254	Disease recurrence NOS
+C0679272	Polydrug abuse
+C0679293	familial alcoholism
+C0679294	paternal alcoholism
+C0679309	physical symptom
+C0679360	Foodborne Disease
+C0679362	Extrapulmonary tuberculosis
+C0679378	neurodevelopmental anomaly
+C0679395	vascular ischemia
+C0679401	Vascular rupture
+C0679403	Vascular stenosis
+C0679407	Gastrointestinal dysfunction
+C0679408	Lesion of stomach
+C0679412	noninfectious hepatitis
+C0679414	alcohol flush reaction
+C0679424	iron loading anemia
+C0679427	myeloblastosis
+C0679429	Platelet dysfunction
+C0679465	Psychomotor Impairment
+C0679484	Aggressive personality
+C0680490	Drug diversion
+C0683154	drug response
+C0683303	RISK-TAKING BEHAVIOR
+C0683322	Mental impairment
+C0683342	hazardous drinking
+C0683357	Excessive drinking
+C0683369	Clouded consciousness
+C0683381	inflammatory joint disease
+C0683382	renin-dependent hypertension
+C0684219	Myokymia
+C0684249	Carcinoma of lung
+C0684256	Bacterial sepsis
+C0684275	Haemophilia
+C0684276	Hypsarrhythmia
+C0684321	Regressive behaviour
+C0684324	Deficiency of phosphoglycerate kinase
+C0684328	Reasoning
+C0684332	Macrocytosis
+C0684333	Malignant neoplasm of ventral surface of tongue
+C0684337	Ewings sarcoma-primitive neuroectodermal tumor (PNET)
+C0684338	heart overload
+C0684343	Pseudophakia
+C0684354	Benign neoplasm of sweat gland
+C0684516	Benign bone neoplasm
+C0684550	Metastases to spine
+C0684743	Malignant neoplasm of muscle
+C0684817	Metastases to neck
+C0684830	Secondary malignant neoplasm of axilla
+C0684833	Metastases to chest wall
+C0685053	Carcinoma in situ of lung
+C0685108	Lenegre\'s disease
+C0685110	Metastases to heart
+C0685201	Hemangioma of spleen
+C0685381	Congenital hypoplasia of radius
+C0685409	Camptodactyly congenital
+C0685678	Incomplete ossification of pubis
+C0685682	Single naris
+C0685684	Congenital hypoplasia of nose
+C0685695	Abnormal lung lobation
+C0685707	Muscular ventricular septum defect
+C0685775	Congenital absence of jaw
+C0685776	Congenital absence of mandible
+C0685786	Cleft mandible
+C0685787	Cleft face
+C0685828	Congenital dilatation of bladder
+C0685837	Pure Gonadal Dysgenesis, 46, XX
+C0685838	Gonadal dysgenesis XX type deafness
+C0685840	Congenital hypoplasia of ovary
+C0685869	Monophthalmos
+C0685889	Splenic Hypoplasia
+C0685891	Congenital hypoplasia of thymus
+C0685894	Congenital absence of thymus
+C0685896	Acephaly
+C0685901	Allergy to fruit
+C0685924	Adhesions of temporomandibular joint
+C0685938	Malignant neoplasm of gastrointestinal tract
+C0686112	Gallbladder cancer metastatic
+C0686346	Gender Dysphoria
+C0686347	Tardive Dyskinesia
+C0686353	Muscular Dystrophies, Limb-Girdle
+C0686377	CNS metastases
+C0686619	Lymph Node Metastasis
+C0686625	Secondary malignant neoplasm of lymph nodes of neck
+C0686715	Baylisascaris procyonis Infection
+C0686761	Lack of bone formation
+C0686770	Leser-Trelat sign
+C0687120	Nephronophthisis
+C0687131	Psychoticism
+C0687132	heavy drinking
+C0687133	Drug interaction
+C0687140	Haemangioma of skin
+C0687148	Mineral deficiency
+C0687149	Pure gonadal dysgenesis
+C0687150	Parathyroid Gland Adenocarcinoma
+C0687154	Acrocephalopolysyndactyly
+C0687707	Anorectal Diseases
+C0687713	Gastrointestinal pain
+C0687720	Central Diabetes Insipidus
+C0687751	Acanthocytosis
+C0694533	Moderate obesity
+C0694539	Chronic atrial fibrillation
+C0694549	Community acquired pneumonia
+C0694550	Recurrent pneumonia
+C0694551	Right lower quadrant pain
+C0694563	Excessive daytime somnolence
+C0694566	Atypical Mycobacterial Infection, Disseminated
+C0694571	extranodal lymphoma
+C0694575	Macular fibrosis
+C0695242	Neurogenic bowel
+C0696105	Beta carotene measurement
+C0699728	Chronic progressive chorea
+C0699731	Hereditary Chorea
+C0699734	Progressive chorea
+C0699739	Sensory Neuropathy, Hereditary
+C0699741	Benign congenital myopathy
+C0699743	Congenital muscular dystrophy (disorder)
+C0699744	Ear infection
+C0699753	Cancer Relapse
+C0699790	Colon Carcinoma
+C0699791	Stomach Carcinoma
+C0699812	Bone formation increased
+C0699815	Feeding difficulties and mismanagement
+C0699828	Serotonin syndrome
+C0699848	Disaccharidase deficiency
+C0699885	Carcinoma of bladder
+C0699889	Malignant Female Reproductive System Neoplasm
+C0699890	H/O: menorrhagia
+C0699893	Skin carcinoma
+C0699949	airway disease
+C0700031	Anxiety attack
+C0700053	Idiopathic hypertrophic subaortic stenosis
+C0700075	Motor restlessness
+C0700078	Decreased tendon reflex
+C0700095	Central neuroblastoma
+C0700101	Urethral cancer
+C0700110	Carcinoma bone
+C0700129	Incoherent speech
+C0700138	PANCREAS EXOCRINE
+C0700153	Myotonia
+C0700178	Alcoholic blackout
+C0700184	Throat irritation
+C0700185	Decalcification
+C0700198	Aspiration
+C0700199	Multiple nevi
+C0700200	Presyncope
+C0700201	Dyssomnias
+C0700208	Acquired scoliosis
+C0700225	Serum creatinine raised
+C0700251	Brachial Plexus Neuropathies
+C0700285	Addicted to drugs
+C0700292	Hypoxemia
+C0700299	Heinz Body Anemias
+C0700323	Observation of Neuromuscular Block
+C0700345	Candidiasis, Vulvovaginal
+C0700359	Organophosphate poisoning
+C0700361	Emotional distress
+C0700363	Rhythm idioventricular
+C0700367	Ependymoblastoma
+C0700379	Total iron binding capacity function
+C0700438	Sick Headaches
+C0700501	Congenital nystagmus
+C0700502	Acquired hypothyroidism
+C0700572	Mobility decreased
+C0700590	Increased sweating
+C0700594	Radiculopathy
+C0700595	Spinal Muscular Atrophies of Childhood
+C0700613	Anxiety state
+C0700632	Endodontic procedure
+C0700635	Strudwick syndrome
+C0700636	Focal nodular hyperplasia of liver
+C0700639	Pyloric Stenosis, Hypertrophic
+C0701163	Adrenogenital disorder
+C0701807	Acute anterior uveitis
+C0701811	Poor short-term memory
+C0701818	Choledocholithiasis
+C0701824	Staggering gait
+C0701826	Perinatal death
+C0701836	Thermal burn
+C0702102	Arthritis mutilans
+C0702109	Erythropoiesis abnormal
+C0702135	Primary atypical pneumonia
+C0702139	Anotia
+C0702157	Thalassemia trait
+C0702159	Constitutional aplastic anemia
+C0702163	Trichorrhexis
+C0702166	Acne
+C0702167	Atrichia
+C0702169	Acrania
+C0702176	Abscess neck
+C0702266	Basophilia
+C0728829	Congenital pes cavus
+C0728895	Absent finger
+C0728936	Disorder of circulatory system
+C0729264	Preterm premature rupture of membranes
+C0729353	Subfertility
+C0729524	Urinary tract infection bacterial
+C0729525	Genital infection bacterial
+C0729527	Bacterial oral infection
+C0729531	Viral respiratory infection
+C0729544	Central Nervous System Fungal Infections
+C0729545	Ear infection fungal
+C0729549	Gastrointestinal fungal infection
+C0729552	Genital infection
+C0729582	Floating-harbor syndrome
+C0729665	Arteriovenous graft
+C0729777	Corneal infection
+C0729847	Iliac artery stenosis
+C0729958	Lung transplant rejection
+C0730018	Foetal heart rate abnormal
+C0730277	Moderate nonproliferative diabetic retinopathy
+C0730278	Severe nonproliferative diabetic retinopathy
+C0730284	Clinically significant macular edema
+C0730285	Diabetic macular edema
+C0730290	Cone dystrophy
+C0730291	Choroidal dystrophy
+C0730292	Macular dystrophy
+C0730294	North Carolina macular dystrophy
+C0730295	BASAL LAMINAR DRUSEN (disorder)
+C0730303	Capillary hemangioma of retina
+C0730307	Cancer-Associated Retinopathy
+C0730308	Melanoma-Associated Retinopathy
+C0730309	Inherited optic neuropathy
+C0730314	Chronic central serous chorioretinopathy
+C0730321	Punctate inner choroidopathy
+C0730328	Central Serous Chorioretinopathy
+C0730330	Chloroquine retinopathy
+C0730345	Microalbuminuria
+C0730362	Disorder of macula of retina
+C0730364	Idiopathic polypoidal choroidal vasculopathy
+C0730366	Rod dystrophy
+C0730516	Colonoscopy abnormal
+C0730525	Chronic Post-Traumatic Stress Disorder
+C0730557	Emotional abuse
+C0730605	Moderate chronic obstructive pulmonary disease
+C0730607	Severe chronic obstructive pulmonary disease
+C0733680	Viral hepatitis carrier
+C0733682	Hypophosphatemic Rickets, X-Linked Dominant
+C0740083	Carcinoma of glottis
+C0740265	Acid-base disorders
+C0740268	Pelvic prolapse
+C0740277	Bile duct carcinoma
+C0740279	Cerebellar atrophy
+C0740281	Multiple allergies
+C0740289	PO2 decreased
+C0740296	Sinus polyp
+C0740299	Blood culture positive
+C0740302	5q minus syndrome
+C0740304	Chronic obstructive airways disease exacerbated
+C0740305	Biopsy bone marrow abnormal
+C0740306	Biopsy breast abnormal
+C0740307	Biopsy liver abnormal
+C0740315	Ultrasound liver abnormal
+C0740319	Physical assault
+C0740321	Catheterisation cardiac abnormal
+C0740334	Congenital hepatobiliary anomaly
+C0740335	Wrist deformity NOS
+C0740339	Throat cancer NOS
+C0740340	Amyloidosis, Familial
+C0740341	Thrombophlebitis septic
+C0740343	Mononeuropathy multiplex
+C0740345	Germ Cell Cancer
+C0740353	Scan NOS bone abnormal
+C0740355	Lumbar puncture abnormal
+C0740363	Back Pain with Radiation
+C0740372	Gastrointestinal lymphoma
+C0740376	Middle Cerebral Artery Thrombosis
+C0740380	Varicella zoster
+C0740385	Aneurysm, Middle Cerebral Artery
+C0740386	Aneurysm, Anterior Communicating Artery
+C0740387	Aneurysm, Posterior Cerebral Artery
+C0740391	Middle Cerebral Artery Occlusion
+C0740392	Infarction, Middle Cerebral Artery
+C0740394	Hyperuricemia
+C0740401	Duodenal ulcer perforation
+C0740404	Limb defects
+C0740406	Incarcerated hernia
+C0740409	Psychotic behaviour
+C0740411	Delayed gastric emptying
+C0740418	Chronic back pain
+C0740421	Postsurgical menopause
+C0740425	Altered Taste
+C0740441	Acute diarrhea
+C0740447	Diabetic peripheral neuropathy
+C0740451	Granulomatous disorder
+C0740457	Malignant neoplasm of kidney
+C0740476	Biliary carcinoma
+C0740479	Undifferentiated High Grade Pleomorphic Sarcoma of Bone
+C0740577	Acute abdominal pain
+C0740651	Abdominal symptom
+C0740656	Ultrasound abdomen abnormal
+C0740694	Abscess soft tissue
+C0740703	ABUSE NEGLECT
+C0740749	Chronic metabolic acidosis
+C0740765	Activities of daily living impaired
+C0740766	Acute pneumonia
+C0740804	Adnexal torsion
+C0740830	AIDS defining illness
+C0740832	End stage AIDS
+C0740852	Upper airway obstruction
+C0740858	Substance abuse
+C0740895	Hypochloremic metabolic alkalosis
+C0740896	Hypokalemic hypochloremic metabolic alkalosis
+C0740898	Hypokalemic metabolic alkalosis
+C0740903	allergic symptom
+C0740927	Elevated maternal serum alpha-fetoprotein
+C0740961	Amputation stump pain
+C0740985	Acute anaemia
+C0740992	anemia hemoglobin
+C0741032	Refractory angina
+C0741132	Antibody test positive
+C0741146	anxiety acute
+C0741160	Aortic aneurysm rupture
+C0741165	Aortic embolus
+C0741183	aortic stenosis symptomatic
+C0741237	arthritis symptoms
+C0741250	aspirin sensitivity
+C0741260	Adult onset asthma
+C0741270	Intermittent ataxia
+C0741281	atrial fibrillation new onset
+C0741395	back pain mechanical
+C0741439	Bandaemia
+C0741453	Bedridden
+C0741494	Elevated total bilirubin
+C0741682	Premenopausal breast cancer
+C0741796	Recurrent bronchitis
+C0741899	Poorly differentiated carcinoma
+C0741900	carcinoma sarcoma
+C0741916	Cardiac defects
+C0741921	Cardiac enzymes increased
+C0741923	cardiac event
+C0741933	cardiac symptom
+C0741949	Cardiovascular Pathology
+C0741975	carotid disease
+C0742006	Catheter infection
+C0742007	Catheter related septicaemia
+C0742028	Cerebellar vermis atrophy
+C0742034	cerebellar function
+C0742035	Cerebellar lesion NOS
+C0742038	Cerebellar signs
+C0742078	Brain mass
+C0742132	cervical cancer metastasis
+C0742186	Cervical radiculopathy
+C0742191	Cervical spinal cord atrophy
+C0742343	Acute Chest Syndrome
+C0742352	Chest wall mass
+C0742395	Cholestasis, chronic
+C0742468	Central nervous system lesion
+C0742472	Central nervous system lymphoma
+C0742545	Colonic abscess
+C0742558	colon cancer liver metastasis
+C0742597	colon (non-specific) lesion
+C0742699	Polyp of sigmoid colon
+C0742747	High-output congestive heart failure
+C0742803	Conus Medullaris Syndrome
+C0742906	C-reactive protein increased
+C0742960	cyst benign
+C0742962	Cyst removal
+C0742964	Bacterial cystitis
+C0743002	Abnormal Deep Tendon Reflex
+C0743072	Depression, psychotic
+C0743073	depression anxiety disorder
+C0743089	Perivascular dermatitis
+C0743101	developmentally delayed
+C0743140	diabetes mellitus risk
+C0743150	Diabetic ulcer
+C0743178	Intractable diarrhea
+C0743188	diarrhea persistent
+C0743244	Chronic drug abuse
+C0743295	Drug screen positive
+C0743319	Dysphagia, progressive
+C0743330	Dyspnoea at rest
+C0743332	Focal Dystonia
+C0743359	Chronic ear infection
+C0743360	Recurrent ear infections
+C0743400	Ejection fraction decreased
+C0743479	emotional dysfunction
+C0743515	endometrial polyp benign
+C0743525	Enterobacter sepsis
+C0743575	Oesophageal irritation
+C0743668	Limb injury
+C0743680	Eye oedema
+C0743728	Eyeball rupture
+C0743733	Eye laser surgery
+C0743841	Disorder characterized by fever
+C0743912	Increased ferritin
+C0744130	Diabetic foot infection
+C0744235	Fungal sepsis
+C0744301	gastric ulcer benign
+C0744310	gastritis h pylori
+C0744321	Gastrointestinal arteriovenous malformation
+C0744333	Gastrointestinal polyps
+C0744356	Abnormality of the genital system
+C0744403	Gingival infection
+C0744421	Immune-complex glomerulonephritis
+C0744466	gout tophaceous
+C0744471	Gram-negative bacteremia
+C0744483	growth hormone treatment
+C0744631	Swelling of head
+C0744641	Intermittent migraine headaches
+C0744673	heart inflammation
+C0744727	Haematocrit decreased
+C0744848	hepatitis cryptogenic
+C0744855	hepatitis immune
+C0744869	Metastatic hepatocellular carcinoma
+C0744897	Recurrent singultus
+C0745031	homicidal
+C0745091	Hypereosinophilia
+C0745103	Hyperlipoproteinemia Type IIa
+C0745106	hyperparathyroid
+C0745109	Macular hyperpigmentation
+C0745136	Hypertensive emergency
+C0745138	Hypertensive urgency
+C0745153	Hypoglycaemic episode
+C0745186	hypoventilation syndrome
+C0745228	Iliac artery occlusion
+C0745242	Immunoglobulin deficiency
+C0745287	infertility tubal factor
+C0745360	Congenital intestinal malformation NOS
+C0745411	irregular bleeding
+C0745417	ischemic pain
+C0745497	Thrombosis of internal jugular vein
+C0745527	Klebsiella bacteraemia
+C0745528	Klebsiella sepsis
+C0745581	knee symptoms
+C0745674	Dilated left ventricle
+C0745730	Multiple lipomata
+C0745744	End Stage Liver Disease
+C0745745	liver disease parenchymal
+C0745754	Hepatic granuloma
+C0746087	Small cell lung cancer metastatic
+C0746101	Bullous lung disease
+C0746102	Chronic lung disease
+C0746104	lung disease granulomatous
+C0746105	Chronic interstitial lung disease
+C0746306	lupus cutaneous
+C0746316	lymph node infected
+C0746341	Hodgkin's disease recurrent
+C0746365	malaria relapse
+C0746402	manic symptom
+C0746408	mass lesion
+C0746459	Widened mediastinum
+C0746495	Recurrent meningitis
+C0746556	metabolic disturbance
+C0746604	Mitral valve endocarditis
+C0746674	Generalized muscle weakness
+C0746706	Myelitis, Necrotizing
+C0746731	Acute myocardial ischemia
+C0746787	Cancer of Neck
+C0746857	Focal Neurologic Deficits
+C0746882	Chronic neutropenia
+C0746883	Febrile Neutropenia
+C0746926	Multiple, subcutaneous nodules
+C0746935	Medication Nonadherence
+C0746940	Nonverbal
+C0746961	Oxygen saturation decreased
+C0747078	Generalized osteopenia
+C0747085	Recurrent otitis media
+C0747102	Ovarian failure
+C0747195	pancreatitis biliary
+C0747198	pancreatitis idiopathic
+C0747249	Paranoid ideation
+C0747251	Progressive spastic paraparesis
+C0747256	Infection parasitic
+C0747273	Malignant tumour of parotid gland
+C0747479	Periodontal infection
+C0747533	Peroneal Neuropathies
+C0747548	Pharyngeal Carcinoma
+C0747551	Pharyngeal mass
+C0747556	Recurrent pharyngitis
+C0747585	Physical examination abnormal
+C0747651	Recurrent aspiration pneumonia
+C0747733	Polychondritis
+C0747739	polyglandular failure
+C0747742	polyp benign
+C0747752	Polysubstance abuse
+C0747767	Acute Post-Traumatic Stress Disorder
+C0747820	Malaria, antepartum
+C0747845	early pregnancy
+C0747918	pregnancy preterm
+C0748038	Dysarthria, Pseudobulbar
+C0748052	Erythrodermic psoriasis
+C0748055	Psychiatric decompensation
+C0748061	psychiatric hospitalization
+C0748071	psychosocial impairment
+C0748073	psychosocial stressor
+C0748140	Multiple pulmonary infections
+C0748164	Multiple Pulmonary Nodules
+C0748168	Pulmonary Pathology
+C0748179	Inactive tuberculosis of lung
+C0748199	Recurrent pyelonephritis
+C0748226	Radial Neuropathy
+C0748243	rapid ventricular response
+C0748318	Progressive renal failure
+C0748324	renal obstruction
+C0748336	Ultrasound kidney abnormal
+C0748355	Acute respiratory distress
+C0748390	Retroperitoneal lymphadenopathy
+C0748397	Reynolds syndrome
+C0748427	Right atrial enlargement
+C0748483	Salmonella bacteraemia
+C0748505	Sarcoma metastatic
+C0748536	Scleral haemorrhage
+C0748540	Scleroderma, Limited
+C0748607	Recurrent seizures
+C0748691	Shoulder weakness
+C0748694	sick sinus
+C0748720	Chronic sinus disease
+C0748725	Sinus operation NOS
+C0748726	Allergic sinusitis
+C0748830	Skull fractured base
+C0748861	Metastatic small cell carcinoma
+C0748903	spinal cord involvement
+C0749087	Subclavian vein thrombosis
+C0749095	Hematoma, Subdural, Chronic
+C0749098	Hematoma, Subdural, Acute
+C0749106	Submandibular mass
+C0749163	Supraglottic Squamous Cell Carcinoma
+C0749225	Systolic dysfunction
+C0749263	temporal pain
+C0749379	Thoracolumbar scoliosis
+C0749389	Pharyngeal lesion
+C0749398	Recurrent thromboembolic disease
+C0749420	Thyroid Agenesis
+C0749424	Thyroid Hurthle Cell Carcinoma
+C0749470	Thyroid cold nodule
+C0749474	thyroid nodule solitary
+C0749557	toe necrosis
+C0749560	Toe operation
+C0749591	tonsillopharyngitis
+C0749794	Upper Extremity Deformities, Congenital
+C0749870	Upper motor neuron signs
+C0750016	Generalized urticarial
+C0750046	Granulomatous uveitis
+C0750053	Vaginal abscess
+C0750103	vaginalis
+C0750114	VAGINOSIS
+C0750145	Occlusive vascular disease
+C0750151	Vaso-Occlusive Crisis
+C0750166	Peripheral venous disease
+C0750194	Non-sustained ventricular tachycardia
+C0750197	Sustained ventricular tachycardia
+C0750292	Malabsorption of Vitamin B12
+C0750325	Vomiting, recurrent
+C0750384	Coumarin Resistance
+C0750394	Leukopenia
+C0750403	Proximal weakness
+C0750426	Leukocytosis
+C0750433	Wound, non-healed
+C0750857	Alkaline phosphatase serum increased
+C0750863	Finding of creatine kinase level
+C0750876	Phlebitis superficial
+C0750879	Eosinophil count result
+C0750880	Monocyte count result
+C0750884	Cochlear Neuritis
+C0750885	Cochlear Nerve Diseases
+C0750886	Vestibular Nerve Diseases
+C0750887	Adrenal Cancer
+C0750888	Ageusia, Hysterical
+C0750890	Acquired Agraphia
+C0750893	Constructional Agraphia
+C0750895	Developmental Agraphia
+C0750896	Pure Agraphia
+C0750897	Autonomic Hyperactivity, Alcohol Withdrawal Associated
+C0750900	Alzheimer's Disease, Focal Onset
+C0750901	Alzheimer Disease, Early Onset
+C0750902	Amblyopia, Developmental
+C0750903	Amblyopia, Suppression
+C0750905	Amino Acid Metabolism, Inherited Disorders
+C0750906	Tactile Amnesia
+C0750907	Amnestic State
+C0750908	Pre-Ictal Amnesia
+C0750909	Retrograde Memory Loss
+C0750910	Pre-Ictal Memory Loss
+C0750915	Color Anomia
+C0750917	Aphasia, Auditory Discriminatory
+C0750918	Aphasia, Commisural
+C0750919	Aphasia, Post-Ictal
+C0750920	Aphasia, Post-Traumatic
+C0750921	Dejerine-Lichtheim Phenomenon
+C0750922	Aphasia, Ataxic
+C0750924	Functional Aphonia
+C0750927	Apraxia, Developmental Verbal
+C0750928	Apraxia, Facial-Oral
+C0750929	Arnold-Chiari Malformation, Type I
+C0750931	Arnold-Chiari Malformation, Type III
+C0750932	Arnold-Chiari Malformation, Type IV
+C0750934	Arthroscopic surgery
+C0750935	Cerebral Astrocytoma
+C0750936	Intracranial Astrocytoma
+C0750937	Ataxia, Appendicular
+C0750940	Tremor, Rubral
+C0750942	Auditory Inattention
+C0750944	Peripheral Autonomic Nervous System Diseases
+C0750945	Nervous System Diseases, Parasympathetic
+C0750946	Nervous System Diseases, Sympathetic
+C0750949	Vertebrogenic Pain Syndrome
+C0750951	Lenticulostriate Disorders
+C0750952	Biliary Tract Cancer
+C0750953	Urinary Bladder Neurogenesis
+C0750955	Neurogenic Urinary Bladder, Spastic
+C0750958	Blindness, Monocular
+C0750959	Brain Abscess, Child
+C0750960	Brain Abscess, Multiple
+C0750961	Brain Abscess, Pyogenic
+C0750962	Brain Abscess, Sterile
+C0750966	Irreversible Coma
+C0750968	Central Nervous System Metabolic Disorders
+C0750969	Vasogenic Brain Edema
+C0750970	Cytotoxic Brain Edema
+C0750974	Brain Tumor, Primary
+C0750977	Recurrent Brain Neoplasm
+C0750979	Primary malignant neoplasm of brain
+C0750986	Internal Carotid Artery Diseases
+C0750987	Arterial Diseases, Common Carotid
+C0750988	Common Carotid Artery Thrombosis
+C0750989	External Carotid Artery Thrombosis
+C0750990	Internal Carotid Artery Thrombosis
+C0750991	Status Cataplexicus
+C0750992	Catatonia, Malignant
+C0750993	Schizophreniform Catatonia
+C0750994	Cerebellar Hemiataxia
+C0750995	Benign Cerebellar Neoplasms
+C0750998	Cerebellar Neoplasms, Primary
+C0751000	Aneurysm, Anterior Cerebral Artery
+C0751001	Aneurysm, Basilar Artery
+C0751002	Aneurysm, Posterior Communicating Artery
+C0751003	Brain Aneurysm
+C0751004	Giant Intracranial Aneurysm
+C0751005	Mycotic Aneurysm, Intracranial
+C0751007	Intracranial Atherosclerosis
+C0751008	Intracranial Arteriovenous Malformation, Ruptured
+C0751010	Cerebral Infarction, Left Hemisphere
+C0751011	Cerebral Infarction, Right Hemisphere
+C0751012	Anterior Choroidal Artery Infarction
+C0751014	Subcortical Infarction
+C0751019	Carotid Circulation Transient Ischemic Attack
+C0751020	Transient Ischemic Attack, Vertebrobasilar Circulation
+C0751021	Crescendo Transient Ischemic Attacks
+C0751022	Brain Stem Ischemia, Transient
+C0751024	Cerebral Palsy, Mixed
+C0751025	Cerebral Palsy, Rolandic Type
+C0751026	Cerebrospinal Fluid Otorrhea, Traumatic
+C0751027	Cerebrospinal Fluid Otorrhea, Spontaneous
+C0751030	Cerebrospinal Fluid Rhinorrhea, Spontaneous
+C0751031	Cerebrospinal Fluid Rhinorrhea, Post-Traumatic
+C0751036	Hereditary Motor and Sensory Neuropathy Type I
+C0751037	Cockayne Syndrome, Type III
+C0751038	Cockayne Syndrome, Type II
+C0751039	Cockayne Syndrome, Type I
+C0751042	Color Blindness, Inherited
+C0751043	Monochromatopsia
+C0751050	Communication Disorders, Developmental
+C0751053	Confusion, Post-Ictal
+C0751054	Consciousness, Level Altered
+C0751055	Semiconsciousness
+C0751056	Non-epileptic convulsion
+C0751057	Complex febrile seizure
+C0751059	Cranial Neuropathies, Multiple
+C0751061	Craniopharyngioma, Child
+C0751068	Deafness, Acquired
+C0751070	Decorticate State
+C0751071	Familial Dementia
+C0751072	Frontotemporal Lobar Degeneration
+C0751074	Diabetic Neuralgia
+C0751075	Cancer of Digestive System
+C0751076	Diplopia, Cortical
+C0751077	Diplopia, Horizontal
+C0751078	Diplopia, Intermittent
+C0751079	Diplopia, Vertical
+C0751080	Polyopsia
+C0751081	Trisomy 21, Mitotic Nondisjunction
+C0751083	Duane Retraction Syndrome, Type 2
+C0751084	Duane Retraction Syndrome, Type 3
+C0751088	Dyskinesia, Medication-Induced
+C0751093	Dystonia, Limb
+C0751094	Cancer of Ear Auricle
+C0751097	Empty Sella Syndrome, Secondary
+C0751099	Encephalomyelitis, Postexanthem
+C0751100	Postinfectious Encephalomyelitis
+C0751101	Post-Vaccinal Encephalitis
+C0751105	Encephalocele, Sincipital
+C0751107	Encephalomyelitis, Inflammatory
+C0751108	Leukoencephalitis, Subacute Hemorrhagic
+C0751110	Single Seizure
+C0751111	Awakening Epilepsy
+C0751112	Subclinical Seizure
+C0751113	Uncinate Seizures
+C0751115	Digestive Epilepsy
+C0751117	Cryptogenic Tonic-Clonic Epilepsy
+C0751118	Epilepsy, Tonic-Clonic, Familial
+C0751119	Epilepsy, Tonic-Clonic, Symptomatic
+C0751120	Benign Infantile Myoclonic Epilepsy
+C0751122	Infantile Severe Myoclonic Epilepsy
+C0751123	Atonic Absence Seizures
+C0751124	Epilepsy, Absence, Atypical
+C0751131	Facial Neuritis
+C0751132	Familial Facial Neuropathy
+C0751133	Acquired Facial Neuropathy
+C0751134	Myofacial Pain Syndromes
+C0751135	Neuralgic Facial Pain
+C0751136	Facial Pain, Referred
+C0751137	Craniofacial Pain
+C0751138	Myofacial Pain
+C0751141	Facial Palsy, Upper Motor Neuron
+C0751142	Facial Palsy, Lower Motor Neuron
+C0751143	Hemifacial Paralysis
+C0751144	Fasciculation, Benign
+C0751152	Fibromyalgia, Primary
+C0751153	Fibromyalgia, Secondary
+C0751156	FRAXA Syndrome
+C0751157	FRAXE Syndrome
+C0751161	UDPglucose 4-epimerase deficiency disease
+C0751170	Acquired Gerstmann Syndrome
+C0751172	Adult Glycogen Storage Disease Type II
+C0751173	Glycogen Storage Disease Type II, Infantile
+C0751174	Glycogen Storage Disease Type II, Juvenile
+C0751175	Hallucination of Body Sensation
+C0751176	Hallucinations, Internal Body Sensation
+C0751177	Cancer of Head
+C0751181	Frontal Region Trauma
+C0751182	Occipital Region Trauma
+C0751183	Parietal Region Trauma
+C0751184	Temporal Region Trauma
+C0751185	Primary Cough Headache
+C0751186	Orthostatic Headache
+C0751187	Periorbital Headache
+C0751188	Post-dural puncture headache
+C0751189	Retro-Ocular Headache
+C0751190	Sharp Headache
+C0751191	Primary Stabbing Headache
+C0751192	Vertex Headache
+C0751194	Hematoma, Subdural, Spinal
+C0751195	Hemiplegia, Post-Ictal
+C0751197	Fulminant Hepatic Failure with Cerebral Edema
+C0751198	Hepatic Stupor
+C0751201	Neurogenic Hoarseness
+C0751202	Cystathionine beta-Synthase Deficiency Disease
+C0751203	Horner Syndrome, Acquired
+C0751204	Horner Syndrome, Central
+C0751205	Ptosis Sympathetic
+C0751206	Miosis, Innervational Defect
+C0751207	Akinetic-Rigid Variant of Huntington Disease
+C0751208	Juvenile Huntington Disease
+C0751210	Hemihydranencephaly
+C0751211	Hyperalgesia, Primary
+C0751212	Hyperalgesia, Secondary
+C0751213	Tactile Allodynia
+C0751214	Hyperalgesia, Thermal
+C0751215	Hyperesthesia, Tactile
+C0751216	Hyperesthesia, Thermal
+C0751217	Hyperkinesia, Generalized
+C0751220	Inappropriate ACTH Secretion Syndrome
+C0751226	Hypersomnia, Recurrent
+C0751227	Hypersomnolence Disorders, Primary
+C0751228	Hypersomnolence Disorders, Secondary
+C0751229	Hypersomnolence
+C0751230	Hypothalamic Dysfunction Syndromes
+C0751231	Hypothalamic Dysinhibition Syndrome
+C0751232	Hypothalamic Overactivity Syndrome
+C0751233	Hypothalamic-Adenohypophyseal Disorders
+C0751234	Hypothalamic-Neurohypophyseal Disorders
+C0751235	Pituitary Diencephalic Syndrome
+C0751249	Chronic Insomnia
+C0751250	Psychophysiological Insomnia
+C0751251	Secondary Insomnia
+C0751252	Sleep Initiation and Maintenance Disorders
+C0751254	Creutzfeldt-Jakob Disease, Familial
+C0751257	Auditory Processing Disorder, Central
+C0751262	Adult Learning Disabilities
+C0751263	Learning Disturbance
+C0751265	Learning Disabilities
+C0751267	Encephalopathy, Subacute Necrotizing, Infantile
+C0751268	Encephalopathy, Subacute Necrotizing, Juvenile
+C0751273	Infantile Globoid Cell Leukodystrophy
+C0751276	Metachromatic leukodystrophy, juvenile type
+C0751278	Metachromatic Leukodystrophy, Infant
+C0751279	Metachromatic Leukodystrophy, Adult-Type (disorder)
+C0751280	Cystic Periventricular Leukomalacia
+C0751285	Maple Syrup Urine Disease, Thiamine Responsive
+C0751291	Desmoplastic Medulloblastoma
+C0751292	Age-Related Memory Disorders
+C0751293	Memory Disorder, Semantic
+C0751294	Memory Disorder, Spatial
+C0751295	Loss of memory
+C0751297	Leptomeningeal Neoplasms
+C0751300	Intracranial Meningeal Neoplasms
+C0751301	Spinal Meningeal Neoplasms
+C0751303	Cerebral Convexity Meningioma
+C0751304	Parasagittal Meningioma
+C0751307	Meningitis, Haemophilus parainfluenzae
+C0751308	Meningitis, Haemophilus influenzae Type F
+C0751312	Experimental Pneumococcal Meningitis
+C0751313	Meningitis, Pneumococcal, Penicillin-Resistant
+C0751315	Rudimentary Meningocele
+C0751316	Acquired Meningomyelocele
+C0751322	Moyamoya Disease, Primary
+C0751323	Moyamoya Disease, Secondary
+C0751324	Multiple Sclerosis, Acute Fulminating
+C0751325	Hypertonia, Detrusor Muscle
+C0751326	Hypertonia, Infantile
+C0751327	Hypertonia neonatal
+C0751328	Hypertonia, Sphincter
+C0751329	Hypertonia, Transient
+C0751330	Unilateral Hypotonia
+C0751334	Progressive Proximal Myelopathic Muscular Atrophy
+C0751335	Scapuloperoneal Form of Spinal Muscular Atrophy
+C0751336	Distal Muscular Dystrophies
+C0751337	X-Linked Emery-Dreifuss Muscular Dystrophy
+C0751338	Mutism, Organic
+C0751339	Myasthenia Gravis, Generalized
+C0751340	Myasthenia Gravis, Ocular
+C0751341	Infectious Myelitis
+C0751342	Myelitis, Paraneoplastic
+C0751343	Myelitis, Postinfectious
+C0751344	Myelitis, Postvaccinal
+C0751345	Myelitis, Subacute Transverse
+C0751346	Demyelinative Myelitis
+C0751348	Myoclonus Simplex
+C0751349	Myoclonus, Eyelid
+C0751350	Myoclonus, Lower Extremity
+C0751351	Myoclonus, Segmental
+C0751352	Myoclonus, Nocturnal
+C0751353	Myoclonus, Upper Extremity
+C0751354	Action myoclonus
+C0751355	Polymyoclonus
+C0751356	Idiopathic Inflammatory Myopathies
+C0751357	Myositis, Focal
+C0751358	Myotonic Phenomenon
+C0751359	Percussion Myotonia
+C0751360	Becker Generalized Myotonia
+C0751362	Narcolepsy-Cataplexy Syndrome
+C0751364	Cancer, Embryonal
+C0751365	Cancer, Embryonal and Mixed
+C0751366	Radiation-Induced Cancer
+C0751367	External Nerve Compression Syndromes
+C0751368	Internal Nerve Compression Syndromes
+C0751371	Neuralgia, Ilioinguinal
+C0751372	Nerve Pain
+C0751373	Paroxysmal Nerve Pain
+C0751374	Schwannomatosis, Plexiform
+C0751376	Neuroleptic-Induced Neuroleptic Malignant Syndrome
+C0751377	Neurologic Dysfunction
+C0751378	Neurologic Signs
+C0751381	Foley-Denny-Brown Syndrome
+C0751383	Juvenile Neuronal Ceroid Lipofuscinosis
+C0751394	Cancer of Nose
+C0751395	Mixed Oligodendroglioma-Ependymoma
+C0751396	Oligodendroglioma
+C0751398	Familial Olivopontocerebellar Atrophy
+C0751401	Ophthalmoparesis
+C0751402	Optic disc disorder NOS
+C0751406	Post-Traumatic Osteoporosis
+C0751407	Pain, Migratory
+C0751408	Suffering, Physical
+C0751409	Monoparesis - arm
+C0751410	Lower Extremity Paresis
+C0751412	Painful Paresthesias
+C0751414	Parkinson Disease, Secondary Vascular
+C0751415	Atherosclerotic Parkinsonism
+C0751416	Pelvic Cancer
+C0751418	Hemisensory neglect
+C0751419	Sensory Neglect
+C0751420	Somatosensory Discrimination Disorder
+C0751421	Hemispatial Neglect
+C0751422	Hereditary Autoinflammatory Diseases
+C0751434	Classical phenylketonuria
+C0751435	Hyperphenylalaninaemia
+C0751436	Hyperphenylalaninemia, Non-Phenylketonuric
+C0751437	Adenohypophyseal Diseases
+C0751438	Posterior pituitary disease
+C0751443	Pneumocephalus, Epidural
+C0751444	Pressure Pneumocephalus
+C0751445	Encephalitis, Polio
+C0751446	Poliomyelitis, Nonpoliovirus
+C0751447	Poliomyelitis, Preparalytic
+C0751448	Polyneuropathy, Familial
+C0751449	Acquired Polyneuropathy
+C0751452	Autoimmune Demyelinating Disease, Peripheral
+C0751456	Developmental Psychomotor Disorders
+C0751457	Pupillary Sphincter Rupture
+C0751458	Efferent Pupillary Defect
+C0751460	Flaccid Quadriplegia
+C0751461	Paralysis, Spinal, Quadriplegic
+C0751462	Nerve Root Avulsion
+C0751463	Nerve root compression
+C0751466	Phonophobia
+C0751467	Auditory Hyperesthesia
+C0751468	Bulbocavernosus Reflex, Decreased
+C0751469	Bulbocavernousus Reflex Absent
+C0751470	Palmo-Mental Reflex
+C0751471	Reflex, Anal, Decreased
+C0751472	Reflex, Ankle, Abnormal
+C0751473	Reflex, Ankle, Decreased
+C0751474	Reflex, Biceps, Abnormal
+C0751475	Reflex, Biceps, Decreased
+C0751476	Reflex, Gag, Decreased
+C0751477	Reflex, Knee, Abnormal
+C0751478	Reflex, Knee, Decreased
+C0751479	Reflex, Moro, Asymmetric
+C0751480	Reflex, Triceps, Abnormal
+C0751481	Reflex, Triceps, Decreased
+C0751483	Familial Retinoblastoma
+C0751484	Sporadic Retinoblastoma
+C0751485	Reye Syndrome, Adult
+C0751486	Reye-Like Syndrome
+C0751489	Adult Sandhoff Disease
+C0751490	Infantile Sandhoff Disease
+C0751491	Juvenile Sandhoff Disease
+C0751492	Sciatica, Bilateral
+C0751494	Convulsive Seizures
+C0751495	Focal seizure
+C0751496	Seizures, Sensory
+C0751497	Special Senses Disorders
+C0751500	Petrous Sinus Thrombophlebitis
+C0751501	Intracranial Sinus Thrombophlebitis
+C0751502	Petrous Sinus Thrombosis
+C0751505	Insufficient Sleep Syndrome
+C0751506	REM Sleep Deprivation
+C0751507	Sleep Fragmentation
+C0751508	Long Sleeper Syndrome
+C0751509	Short Sleeper Syndrome
+C0751510	Sleep-Related Neurogenic Tachypnea
+C0751511	Subwakefullness Syndrome
+C0751512	Dysglossia
+C0751513	Rhinolalia
+C0751514	Verbal Fluency Disorders
+C0751515	Post-Traumatic Myelopathy
+C0751517	Intramedullary Spinal Cord Neoplasms, Primary
+C0751518	Intradural-Extramedullary Spinal Cord Neoplasms
+C0751519	Intramedullary Spinal Cord Neoplasms
+C0751522	Status Epilepticus, Subclinical
+C0751523	Non-Convulsive Status Epilepticus
+C0751524	Simple Partial Status Epilepticus
+C0751525	Convergent Comitant Strabismus
+C0751526	Strabismus, Noncomitant
+C0751527	Stuttering, Adult
+C0751528	Stuttering, Childhood
+C0751529	Stuttering, Developmental
+C0751530	Subarachnoid Hemorrhage, Aneurysmal
+C0751533	Hygroma, Subdural
+C0751534	Syncopal Episode
+C0751535	Syncope, Cardiogenic
+C0751536	Syncope, Convulsive
+C0751537	Syncope, Deglutitional
+C0751538	Syncope, Hyperventilation
+C0751539	Syncope, Stokes-Adams
+C0751540	Morvan's Disease
+C0751544	Tangier Disease Neuropathy
+C0751545	Giant Cell Aortic Arteritis
+C0751547	Juvenile Temporal Arteritis
+C0751552	Malignant neoplasm of thymus
+C0751553	Childhood Tic Disorders
+C0751554	Motor Tic Disorders
+C0751555	Post-Traumatic Tic Disorder
+C0751556	Tinnitus, Spontaneous Oto-Acoustic Emission
+C0751557	Tinnitus, Tensor Palatini Induced
+C0751558	Tinnitus, Tensor Tympani Induced
+C0751559	Pulsatile Tinnitus
+C0751560	Malignant neoplasm tonsil
+C0751562	Toxoplasmosis, Fetal
+C0751564	Pill rolling
+C0751565	Tremor, Semirhythmic
+C0751567	Trophoblastic Cancer
+C0751568	Tuberculous Hypertrophic Pachymeningitis
+C0751569	Genitourinary Cancer
+C0751571	Cancer of Urinary Tract
+C0751572	Vertebrobasilar Dolichoectasia
+C0751573	Vertigo, Intermittant
+C0751574	Bilateral Vocal Cord Paresis
+C0751575	Paralysis, Unilateral, Vocal Cord
+C0751576	Partial Paralysis (Paresis) Vocal Cords
+C0751577	Unilateral Vocal Cord Paresis
+C0751579	Spastic Dysphonia, Neurologic Adducter
+C0751583	Encephalitis, West Nile Fever
+C0751584	West Nile Fever Meningitis
+C0751585	West Nile Fever Meningoencephalitis
+C0751586	West Nile Fever Myelitis
+C0751587	CADASIL
+C0751588	Benign Supratentorial Neoplasms
+C0751589	Cancer, Supratentorial
+C0751590	Primary Supratentorial Neoplasms
+C0751594	Zellweger-Like Syndrome
+C0751595	Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease
+C0751596	Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal
+C0751597	Ataxia with Lactic Acidosis, Type I
+C0751602	Hereditary Autosomal Dominant Spastic Paraplegia
+C0751603	Autosomal Recessive Hereditary Spastic Paraplegia
+C0751604	Hereditary X-Linked Recessive Spastic Paraplegia
+C0751605	X-Linked, Spastic Paraplegia, Hereditary
+C0751606	Adult Acute Lymphocytic Leukemia
+C0751609	Smooth Pursuit Deficiency
+C0751610	Tonic Pupil, Local
+C0751611	Tonic Pupil, Neuropathic
+C0751612	Anisocoria, Physiologic
+C0751617	Semilobar Holoprosencephaly
+C0751619	Head Injury, Blunt
+C0751620	Central Nervous System Neoplasms, Primary
+C0751622	Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related
+C0751623	Second Primary Cancers
+C0751628	Malaria Meningitis
+C0751629	Toxoplasmosis, Central Nervous System
+C0751630	Intracranial Toxoplasmosis
+C0751631	Neurotoxoplasmosis
+C0751633	Carotid Artery Plaque
+C0751634	Carotid Ulcer
+C0751635	Common Carotid Artery Stenosis
+C0751636	External Carotid Artery Stenosis
+C0751637	Granulomous Cerebral Cryptococcosis
+C0751638	Pachymeningitis, Fungal
+C0751640	Cryptogenic Partial Complex Epilepsy
+C0751641	Epilepsy, Symptomatic, Partial Complex
+C0751642	Epilepsy, Anterior Fronto-Polar
+C0751643	Epilepsy, Orbito-Frontal
+C0751645	Human Transmissible Spongiform Encephalopathies, Inherited
+C0751647	Pseudoakathisia
+C0751648	Recurrent Low Back Pain
+C0751651	Mitochondrial Diseases
+C0751656	Nemaline Myopathy, Autosomal Dominant
+C0751657	Nemaline Myopathy, Autosomal Recessive
+C0751663	Canavan Disease, Familial Form
+C0751664	Canavan Disease, Neonatal
+C0751665	Canavan Disease, Sporadic Form
+C0751666	Canavan Disease, Infantile
+C0751667	Canavan Disease, Juvenile
+C0751668	Machado-Joseph Disease Type I
+C0751669	Machado-Joseph Disease Type II
+C0751670	Machado-Joseph Disease Type III
+C0751671	Machado-Joseph Disease Type IV
+C0751674	Lymphangioleiomyomatosis
+C0751675	Cerebral Primitive Neuroectodermal Tumor
+C0751676	Basal Cell Cancer
+C0751677	Ependymoastrocytoma
+C0751688	Malignant Squamous Cell Neoplasm
+C0751689	Peripheral Nerve Sheath Neoplasm
+C0751690	Malignant Peripheral Nerve Sheath Tumor
+C0751691	Perineurioma
+C0751692	Multiple Hemangioblastomas
+C0751693	Brown-Sequard's Paralysis
+C0751694	Spastic Spinal Monoplegia Syndrome
+C0751695	Post-Comatose Unawareness State
+C0751696	Post-Traumatic Vegetative State
+C0751697	Prolonged Post-Traumatic Unawareness
+C0751698	Transient Vegetative State
+C0751699	Minimally conscious state
+C0751700	Permanent Vegetative State
+C0751701	Hypokinesia, Antiorthostatic
+C0751705	Tension-Vascular Headache
+C0751706	Primary Progressive Nonfluent Aphasia
+C0751708	Peroxisomal Dysfunction, General
+C0751709	Peroxisomal Dysfunction, Multiple
+C0751710	Peroxisomal Dysfunction, Single
+C0751711	Anterior Ischemic Optic Neuropathy
+C0751712	Posterior Ischemic Optic Neuropathy
+C0751713	Inclusion Body Myopathy, Sporadic
+C0751716	Adult Neuroaxonal Dystrophy
+C0751717	Juvenile Neuroaxonal Dystrophy
+C0751718	Late Infantile Neuroaxonal Dystrophy
+C0751721	Syncope, Cerebral
+C0751722	Syncope, Malignant Neurocardiogenic
+C0751723	Syncope, Supine
+C0751724	Anterior Cervical Pain
+C0751725	Posterior Cervical Pain
+C0751726	Hemifacial Myokymia
+C0751729	Blindness, Cortical, Post-Ictal
+C0751730	Anton Syndrome
+C0751733	Degenerative Diseases, Spinal Cord
+C0751739	Basal Ganglia Cerebrovascular Disease
+C0751740	Lenticulostriate Vasculopathy
+C0751741	Putamen haemorrhage
+C0751743	Metabolic Disorder, Central Nervous System, Acquired
+C0751744	Brain Diseases, Metabolic, Acquired
+C0751747	Hyperglycinemia, Nonketotic, Type III
+C0751748	Nonketotic Hyperglycinemia
+C0751750	Argininosuccinic Acid Synthetase Deficiency Disease, Partial
+C0751751	Argininosuccinic Acid Synthetase Deficiency, Complete
+C0751753	Carbamoyl-Phosphate Synthase I Deficiency Disease
+C0751757	Hypersomnolence, Idiopathic
+C0751758	Advanced Sleep Phase Syndrome
+C0751759	Non-24 Hour Sleep-Wake Disorder
+C0751760	Shift-Work Sleep Disorder
+C0751761	Upper Airway Resistance Sleep Apnea Syndrome
+C0751762	Central Sleep Apnea, Primary
+C0751763	Central Sleep Apnea, Secondary
+C0751765	Night Terrors, Childhood
+C0751766	Night Terrors, Primary
+C0751767	Night Terrors, Secondary
+C0751768	Night Terrors, Adult
+C0751769	Sleep Bruxism, Adult
+C0751770	Sleep Bruxism, Childhood
+C0751771	Sleep Bruxism
+C0751772	REM Sleep Behavior Disorder
+C0751774	Nocturnal Myoclonus Syndrome
+C0751776	Atypical Inclusion-Body Disease
+C0751777	Familial Progressive Myoclonic Epilepsy
+C0751778	Myoclonic Epilepsies, Progressive
+C0751779	Action Myoclonus-Renal Failure Syndrome
+C0751780	Biotin-Responsive Encephalopathy
+C0751781	Dentatorubral-Pallidoluysian Atrophy
+C0751782	May-White Syndrome
+C0751783	Lafora Disease
+C0751784	Lafora Body Disease, Late Onset
+C0751785	Unverricht-Lundborg Syndrome
+C0751786	Decision Making Reflex Epilepsy
+C0751787	Reflex Epilepsy, Eating-Induced
+C0751788	Reflex Epilepsy, Visual Pattern
+C0751789	Tactile Reflex Epilepsy
+C0751790	Writing-Induced Reflex Epilepsy
+C0751791	Reflex Epilepsy, Audiogenic
+C0751792	Trauma, Nervous System
+C0751793	Craniocervical Injuries
+C0751797	Intracranial Hematoma, Traumatic
+C0751798	Cerebellar Hemorrhage, Traumatic
+C0751799	Brain Hemorrhage, Traumatic
+C0751801	Cerebral Hematoma, Traumatic
+C0751812	Coma, Post-Traumatic, Prolonged
+C0751814	Cerebrovascular Trauma
+C0751815	Carotid Artery, Internal, Dissection
+C0751816	Carotid Pseudoaneurysm
+C0751820	Facial Nerve Avulsion
+C0751821	Optic Nerve Contusion
+C0751822	Optic Nerve Transection
+C0751823	Septic Phlebitis, Sagittal Sinus
+C0751824	Sagittal Sinus Thrombophlebitis
+C0751825	Septic Phlebitis, Cavernous Sinus
+C0751829	Gait Disorder, Sensorimotor
+C0751830	Gait Disorders, Neurologic
+C0751831	Gait, Frontal
+C0751832	Gait, Widebased
+C0751836	Gait Ataxia, Sensory
+C0751837	Ataxic gait
+C0751838	Bruns apraxia of gait
+C0751839	Frontal Gait Apraxia
+C0751840	Alexia, Pure
+C0751845	Middle Cerebral Artery Embolus
+C0751846	Left Middle Cerebral Artery Infarction
+C0751847	Embolic Infarction, Middle Cerebral Artery
+C0751848	Thrombotic Infarction, Middle Cerebral Artery
+C0751849	Right Middle Cerebral Artery Infarction
+C0751850	Heavy Metal Poisoning, Nervous System
+C0751851	Arsenic Encephalopathy
+C0751852	Arsenic Induced Polyneuropathy
+C0751855	Mercury Encephalopathy
+C0751856	Mad Hatter Disease
+C0751857	Mercurial Neuroanesthenia
+C0751858	Mercury Psychosis
+C0751859	Lead Poisoning, Nervous System
+C0751860	Lead Encephalopathy, Childhood
+C0751861	Lead Poisoning, Nervous System, Childhood
+C0751864	MPTP-Induced Degeneration of the Striatum
+C0751865	Alcohol-Induced Disorders, Nervous System
+C0751868	Alcohol Withdrawal-Induced Major Motor Seizure
+C0751869	Status Epilepticus, Alcohol Withdrawal-Induced
+C0751870	Heredodegenerative Disorders, Nervous System
+C0751871	Autoimmune Diseases of the Nervous System
+C0751872	Immune Disorders, Nervous System
+C0751878	Vasculitis, Central Nervous System
+C0751879	Secondary CNS Vasculitis
+C0751880	Postzoster Arteritis
+C0751881	Primary CNS Vasculitis
+C0751882	Myasthenic Syndromes, Congenital
+C0751883	Congenital Myasthenic Syndromes, Postsynaptic
+C0751884	Congenital Myasthenic Syndromes, Presynaptic
+C0751885	Myasthenic Syndromes, Congenital, Slow Channel
+C0751886	Brain Stem Neoplasms, Primary
+C0751887	Medullary Neoplasms
+C0751888	Mesencephalic Neoplasms
+C0751889	Pontine Tumors
+C0751891	Intracranial Hemorrhage, Hypertensive
+C0751892	Cerebral Hemorrhage, Hypertensive
+C0751893	Posterior Fossa Hemorrhage
+C0751895	Vasospasm, Intracranial
+C0751898	Tic, Gestural
+C0751899	Tic, Transient
+C0751900	Tic, Motor
+C0751901	Tic, Vocal
+C0751903	Post-Ictal Memory Loss
+C0751904	Migraine with Acute Onset Aura
+C0751905	Herpetic Facial Paralysis
+C0751906	Paraparesis, Hypotonic
+C0751907	Subacute Vestibular Neuritis
+C0751908	Vestibular neuronitis
+C0751909	Vestibular Neuropathy
+C0751910	Adult Optic Nerve Glioma
+C0751912	Paraneoplastic Encephalomyelitis
+C0751913	Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated
+C0751914	Adult Pelizaeus-Merzbacher Disease
+C0751915	Pelizaeus-Merzbacher Disease, Atypical
+C0751916	Classic Pelizaeus-Merzbacher Disease
+C0751917	Pelizaeus-Merzbacher Disease, Transitional
+C0751918	Cockayne-Pelizaeus-Merzbacher Disease
+C0751919	Acquired Neuromyotonia
+C0751920	Medial Neuropathy, Distal
+C0751921	Median Nerve Neuralgia
+C0751922	Median Neuropathy
+C0751924	Neuralgia-Neuritis, Sciatic Nerve
+C0751925	Sciatic Nerve Palsy
+C0751926	Neuropathy, Common Peroneal
+C0751927	Fibular Neuropathy
+C0751928	Neuropathy, Deep Peroneal
+C0751929	Neuropathy, Superficial Peroneal
+C0751930	Femoral Neuritis
+C0751931	Femoral nerve palsy
+C0751932	Tibial Neuropathy
+C0751933	Lateral Plantar Neuropathy
+C0751934	Medial Plantar Nerve Disease
+C0751935	Tibial Neuropathy, Post-Traumatic
+C0751936	Medial Plantar Neuropathy
+C0751937	Olfactory nerve disorder
+C0751939	Superior Oblique Palsy, Neurogenic
+C0751940	Abducens Palsy, Childhood, Benign Recurrent
+C0751941	Glossopharyngeal Nerve Diseases
+C0751942	Glossopharyngeal Motor Neuropathy
+C0751943	Glossopharyngeal Nerve Sensory Neuropathy
+C0751944	Glossopharyngeal Nerve Taste Disorder
+C0751945	Hypoglossal Neuropathy
+C0751946	Neonatal Sleep Myoclonus, Benign
+C0751947	Sensory Paroxysms, Sleep
+C0751948	Sleep-Related Abnormal Swallowing Syndrome
+C0751950	Neuromuscular Junction Diseases
+C0751951	Central Core Myopathy (disorder)
+C0751952	Anterior Circulation Brain Infarction
+C0751953	Brain Infarction, Posterior Circulation
+C0751954	Venous Infarction, Brain
+C0751955	Brain Infarction
+C0751956	Acute Cerebrovascular Accidents
+C0751958	Lymphoma, Lymphocytic, Intermediate
+C0751963	Millard-Gublar Syndrome
+C0751964	Multiple Sclerosis, Primary Progressive
+C0751965	Multiple Sclerosis, Secondary Progressive
+C0751967	Multiple Sclerosis, Relapsing-Remitting
+C0751992	Fetal Weight
+C0752048	Hypocatalasemia
+C0752087	Myasthenia Gravis, Autoimmune, Experimental
+C0752088	Experimental Autoimmune Myasthenia Gravis, Passive Transfer
+C0752097	Autosomal Dominant Juvenile Parkinson Disease
+C0752098	Autosomal Dominant Parkinsonism
+C0752100	Autosomal Recessive Parkinsonism
+C0752101	Parkinsonism, Experimental
+C0752104	Familial Juvenile Parkinsonism
+C0752105	Parkinsonism, Juvenile
+C0752107	Brain Diseases, Metabolic, Inherited
+C0752109	Brain Diseases, Metabolic, Inborn
+C0752110	Central Nervous System Inborn Metabolic Diseases
+C0752120	Spinocerebellar Ataxia Type 1
+C0752121	Spinocerebellar Ataxia Type 2
+C0752122	Spinocerebellar Ataxia Type 4
+C0752123	Spinocerebellar Ataxia Type 5
+C0752124	Spinocerebellar Ataxia Type 6 (disorder)
+C0752125	Spinocerebellar Ataxia Type 7
+C0752127	Spinal Cord Vascular Diseases
+C0752128	Posterior Spinal Artery Syndrome
+C0752129	Experimental Spinal Cord Ischemia
+C0752130	Spinal Cord Ischemia
+C0752132	Infarction, Posterior Cerebral Artery
+C0752133	Embolic Infarction, Posterior Cerebral Artery
+C0752134	Thrombotic Infarction, Posterior Cerebral Artery
+C0752135	Pathological Conditions, Anatomical
+C0752137	Brain Diseases, Arterial
+C0752138	Intracranial Arterial Diseases
+C0752140	Intracranial Embolism
+C0752143	Intracranial Thrombosis
+C0752144	Brain Thrombosis
+C0752146	Analgesic Rebound Headache
+C0752147	Chronic Daily Headache
+C0752149	Headache, Intractable
+C0752150	Hypnic Headache
+C0752155	Central Nervous System Vascular Malformations
+C0752156	Dural Arteriovenous Fistula
+C0752160	Hemangioma, Cavernous, Central Nervous System
+C0752161	Cavernous Hemangioma, Extracerebral
+C0752164	Cavernous Hemangioma, Intracerebral
+C0752166	Bardet-Biedl Syndrome
+C0752180	Central Nervous System Bacterial Infections
+C0752196	Ballismus
+C0752197	Adult-Onset Dystonias
+C0752198	Adult-Onset Idiopathic Focal Dystonias
+C0752199	Adult-Onset Idiopathic Torsion Dystonias
+C0752200	Autosomal Dominant Familial Dystonia
+C0752201	Autosomal Recessive Familial Dystonia
+C0752202	Childhood Onset Dystonias
+C0752203	Dystonia, Primary
+C0752205	Dystonia, Secondary
+C0752206	Dystonias, Sporadic
+C0752207	Familial Dystonia
+C0752208	Pseudodystonia
+C0752210	Dyskinesias, Paroxysmal
+C0752216	Pseudobulbar Mutism
+C0752219	Diffuse Axonal Injury
+C0752234	Encephalopathy, Lyme Disease
+C0752235	Lyme Neuroborreliosis
+C0752236	Lyme Disease Mononeuritis Multiplex
+C0752237	Central Nervous System Lyme Disease
+C0752238	Lyme Meningoradiculitis
+C0752239	Lyme Polyradiculitis
+C0752240	Lyme Polyradiculopathy
+C0752241	Peripheral Nervous System Lyme Disease
+C0752244	Rathke Cleft Cysts
+C0752251	Muscle Disease Manifestations
+C0752252	Neuromuscular Manifestations
+C0752255	Impairment, Light Touch Sensation
+C0752256	Pain Sensation Diminished
+C0752257	Pinprick Sensation Diminished
+C0752258	Position Sense Disorders
+C0752260	Proprioceptive Disorders
+C0752261	Thermal Sensation Disorders
+C0752262	Somatosensory Disorders
+C0752266	Hypovolemic
+C0752282	Congenital Structural Myopathy
+C0752285	Hypersomnia, Post-Traumatic
+C0752286	Sleep State Misperception
+C0752287	Sleep Disorders, Intrinsic
+C0752288	Adjustment Sleep Disorder
+C0752289	Environmental Sleep Disorder
+C0752291	Limit-Setting Sleep Disorder
+C0752292	Nocturnal Eating-Drinking Syndrome
+C0752293	Sleep Disorders, Extrinsic
+C0752297	Nocturnal Sleep Head Banging
+C0752298	Movement Disorders, Rhythmic Nocturnal
+C0752299	Sleep Wake Transition Disorders
+C0752300	Somnolescent Starts
+C0752303	Urological Manifestations
+C0752304	Hypoxic-ischaemic encephalopathy
+C0752305	Anoxic-Ischemic Encephalopathy
+C0752306	Anoxia-Ischemia, Brain
+C0752307	Anoxia-Ischemia, Cerebral
+C0752308	Hypoxia-Ischemia, Brain
+C0752323	Focal Clonic Seizures
+C0752324	Focal Tonic Seizures
+C0752332	Lupus Vasculitis, Central Nervous System
+C0752334	Lupus Meningoencephalitis
+C0752335	Neuropsychiatric lupus
+C0752341	Aspergillosis, Nervous System Invasive
+C0752342	Neuroaspergillosis
+C0752347	Lewy Body Disease
+C0752350	Embryo Death
+C0752351	Embryo Loss
+C0752353	Atrophy, Muscular, Spinobulbar
+C0752355	Myotonia Fluctuans (disorder)
+C0795687	Cerebral artery thrombosis
+C0795688	Subarachnoid Hemorrhage, Intracranial
+C0795690	Congenital omphalocele
+C0795692	Hyperlactacidaemia
+C0795693	Skeletal malformation
+C0795796	Chromosome 1, monosomy 1p
+C0795801	trisomy 2
+C0795803	Chromosome 2, trisomy 2p
+C0795809	Chromosome 3, trisomy 3q
+C0795816	Chromosome 6, monosomy 6q
+C0795820	Chromosome 7, trisomy 7p
+C0795821	Chromosome 7, trisomy 7q
+C0795824	Chromosome 8, monosomy 8p
+C0795825	Chromosome 8, trisomy 8p
+C0795830	CHROMOSOME 9p DELETION SYNDROME
+C0795833	Kleefstra Syndrome
+C0795836	Chromosome 10, monosomy 10p
+C0795839	Chromosome 10, monosomy 10q
+C0795841	Jacobsen Distal 11q Deletion Syndrome
+C0795842	chromosome 11q duplication syndrome
+C0795845	Chromosome 12, 12p trisomy
+C0795846	Chromosome 12, trisomy 12q
+C0795856	Trisomy 15
+C0795858	Chromosome 15q, trisomy
+C0795864	Smith-Magenis syndrome
+C0795865	Chromosome 17, trisomy 17p
+C0795875	Chromosome 21 monosomy
+C0795878	Monosomy 22
+C0795887	Complex Glycerol Kinase Deficiency
+C0795888	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4
+C0795889	Allan-Herndon-Dudley syndrome (AHDS)
+C0795898	Cleft Palate-Lateral Synechia Syndrome
+C0795902	Coloboma, cleft lip-palate and mental retardation syndrome
+C0795905	Cantu syndrome
+C0795907	CONOTRUNCAL ANOMALY FACE SYNDROME
+C0795910	COWCHOCK SYNDROME
+C0795915	Winter Shortland Temple syndrome
+C0795917	Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type
+C0795927	Deafness, congenital onychodystrophy, recessive form
+C0795934	Digitorenocerebral Syndrome
+C0795940	Filippi syndrome
+C0795942	Fitzsimmons-Guilbert syndrome
+C0795949	Galloway Mowat syndrome
+C0795950	Corpus callosum agenesis neuronopathy
+C0795953	MASA SYNDROME (disorder)
+C0795956	Chylomicron retention disease
+C0795996	STRIATONIGRAL DEGENERATION, INFANTILE (disorder)
+C0795998	JACKSON-WEISS SYNDROME
+C0796000	Multiple non-ossifying fibromatosis
+C0796003	Juberg-Marsidi syndrome
+C0796004	Kabuki make-up syndrome
+C0796012	Krause-Kivlin syndrome
+C0796013	Zimmerman Laband syndrome
+C0796016	Microphthalmia, syndromic 1
+C0796019	SPASTIC PARAPLEGIA 23 (disorder)
+C0796021	Lowry Wood syndrome
+C0796022	Lujan Fryns syndrome
+C0796028	ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
+C0796031	Malouf syndrome
+C0796032	Malpuech facial clefting syndrome
+C0796033	MARDEN-WALKER SYNDROME
+C0796037	Martsolf syndrome
+C0796055	Mercaptolactate-Cysteine Disulfiduria
+C0796059	Oculopalatoskeletal syndrome
+C0796063	microcephaly-digital anomalies syndrome
+C0796068	Oculodigitoesophagoduodenal syndrome
+C0796070	MICROPHTHALMIA, SYNDROMIC 7
+C0796074	MOHR-TRANEBJAERG SYNDROME
+C0796081	Myhre syndrome
+C0796083	Najjar syndrome
+C0796085	Nance-Horan syndrome
+C0796089	LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
+C0796093	Odontoonychodermal dysplasia
+C0796094	Blepharophimosis syndrome Ohdo type
+C0796095	Opitz trigonocephaly syndrome
+C0796113	Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
+C0796117	Pitt-Rogers-Danks Syndrome
+C0796121	Primrose syndrome
+C0796122	Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome
+C0796124	Proud Syndrome
+C0796126	AICARDI-GOUTIERES SYNDROME 1
+C0796133	Ramon Syndrome
+C0796135	Renpenning syndrome 1
+C0796137	3C syndrome
+C0796147	Acrocallosal Syndrome
+C0796149	Scott Syndrome
+C0796154	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
+C0796159	Mental retardation Smith Fineman Myers type
+C0796160	MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE
+C0796173	Spondyloperipheral dysplasia short ulna
+C0796176	STUVE-WIEDEMANN SYNDROME
+C0796179	Teebi syndrome
+C0796182	Acromelic frontonasal dysplasia
+C0796184	Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence
+C0796195	Waisman syndrome
+C0796200	Wieacker-Wolff syndrome
+C0796202	Wittwer syndrome
+C0796205	SPINOCEREBELLAR ATAXIA, X-LINKED 1
+C0796206	Atkin syndrome
+C0796207	MENTAL RETARDATION, X-LINKED 2 (disorder)
+C0796208	MENTAL RETARDATION, X-LINKED 3
+C0796215	Mental Retardation, X-Linked 9
+C0796218	MENTAL RETARDATION, X-LINKED 12
+C0796220	MENTAL RETARDATION, X-LINKED 14
+C0796221	MENTAL RETARDATION, X-LINKED 15
+C0796222	Mental Retardation, X-Linked 16
+C0796224	MENTAL RETARDATION, X-LINKED 18
+C0796225	Mental Retardation, X-Linked 19
+C0796226	MENTAL RETARDATION, X-LINKED 20
+C0796229	MENTAL RETARDATION, X-LINKED 23
+C0796232	Bohring syndrome
+C0796237	Mental Retardation, X-Linked 30
+C0796241	MENTAL RETARDATION, X-LINKED 34 (disorder)
+C0796242	MENTAL RETARDATION, X-LINKED 35
+C0796244	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED (disorder)
+C0796249	Mental Retardation, X-Linked 47
+C0796250	PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME
+C0796254	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
+C0796274	Brown-Vialetto-Van Laere syndrome
+C0796275	Brunner Syndrome
+C0796279	Carnevale syndrome
+C0796280	Acromegaloid facial appearance syndrome
+C0796418	Visual Pathway Glioma
+C0796466	Refractory cytopenia with multilineage dysplasia
+C0796548	Metastatic tumors of the Ewing\'s family
+C0796563	Localized Malignant Neoplasm
+C0796611	Newly Diagnosed Childhood Ependymoma
+C0805083	Amphetamines positive
+C0807173	Opiates positive
+C0809935	Chromosome 18, trisomy 18q
+C0809936	Branchio-skeleto-genital syndrome
+C0809983	Schizophrenia and related disorders
+C0810006	Acute cerebrovascular disease
+C0810031	alcohol-related liver disease
+C0810032	Pancreatic disorders (not diabetes)
+C0810320	Cystitis and urethritis
+C0810364	Cleft Lip with or without Cleft Palate
+C0812413	Malignant Pleural Mesothelioma
+C0812435	Chromosome 11p deletion syndrome
+C0812437	Oculo-dento-digital syndrome
+C0812454	Ulnar nerve palsy
+C0812470	Incomplete abortion
+C0813142	Circadian Rhythm Disorders
+C0813147	Stage I Endometrial Carcinoma
+C0813148	Metastatic Endometrial Carcinoma
+C0813178	Bewilderment
+C0813217	Expressionless face
+C0814138	upper GI cancer
+C0814152	Viral hepatitis, type G
+C0814154	Alcohol Related Neurodevelopmental Disorder
+C0814161	impaired motor coordination
+C0815107	psychological distress
+C0815123	neurobehavioral problems
+C0836911	Exposure to communicable disease
+C0836924	Thrombocytosis
+C0840564	Urinary bladder rupture
+C0840927	Neurologic neglect syndrome
+C0842860	Biliary dilatation
+C0846967	Acanthoma
+C0847033	Allergic oedema
+C0847092	Blood autoimmune disorders
+C0847403	Infective tenosynovitis
+C0847614	Nasal allergies
+C0848034	Low IQ
+C0848076	Myeloma, malignant
+C0848084	Renal necrosis
+C0848237	acute stress
+C0848309	Rhinitis perennial
+C0848377	Abdominal injury NOS
+C0848454	Uterine carcinoma
+C0848538	fluid retention in lung
+C0848548	hypertensive nephropathy
+C0848558	Hypospadias
+C0848648	Fungal rash
+C0848666	Spots in front of eyes
+C0848676	Subfertility, Male
+C0848765	Hearing disability
+C0848771	neurological disability
+C0848860	endocrine carcinoma
+C0849640	skin damage
+C0849668	peri-menopausal
+C0849748	caruncle
+C0849784	Bacterial diarrhoea
+C0849796	Ear congestion
+C0849835	Lip haemorrhage
+C0849907	Ear pruritus
+C0849916	Generalised erythema
+C0849918	Eyelids pruritus
+C0849925	Ventricular failure
+C0849963	Feeling nervous
+C0849970	Feeling tired
+C0850024	Gluten sensitivity
+C0850149	Dry cough
+C0850170	Mole excision
+C0850572	Adenomatous polyp of colon
+C0850610	Abnormal test result
+C0850638	Infected bite
+C0850639	premalignant lesion
+C0850666	Infection caused by Helicobacter pylori
+C0850672	hereditary anemia
+C0850674	Twitching eye
+C0850703	Frequent falls
+C0850705	Acquired Toxoplasmosis
+C0850715	Abnormality of blood and blood-forming tissues
+C0850741	Smoker\'s lung
+C0850758	Pelvic pain female
+C0850803	Anaphylaxis (non medication)
+C0850826	Localized skin lesion
+C0850918	Degeneration of spine
+C0851043	Lipids NOS increased
+C0851122	Rotator Cuff Injuries
+C0851135	In situ cancer
+C0851140	Carcinoma in situ of uterine cervix
+C0851162	Infections of musculoskeletal system
+C0851238	Breast lump removal
+C0851265	Learning problems
+C0851302	Hypoglycemic shock
+C0851536	Administration site reaction
+C0851578	Sleep disorder
+C0851689	Ectopic hormone secretion syndromes associated with neoplasias
+C0851693	Hormone secreting pituitary neoplasms
+C0851807	Aspergillus infection
+C0851848	Aeromonas infections
+C0851881	Enterococcal infection
+C0851883	Neisseria infections
+C0851886	Pneumocystis Infections
+C0851887	Adenoviral infections
+C0851979	Oesophageal infections
+C0851980	Peritoneal infections
+C0852036	Gestational hypertension
+C0852077	Blood Coagulation Disorders, Inherited
+C0852110	Viral lower respiratory tract infections
+C0852283	Respiratory Distress Syndrome
+C0852312	Gender disorders
+C0852336	Immune Hemolytic Anemia
+C0852361	Skin haemorrhage
+C0852413	Abnormal muscle tone
+C0852421	Acute polyneuropathy
+C0852566	Sleep phase rhythm disturbances
+C0852624	Extranodal marginal zone B-cell lymphoma (MALT type)
+C0852625	Injection site erythema
+C0852630	CNS ventriculitis
+C0852640	Oropharyngeal cancer stage unspecified
+C0852650	Contraindication to vaccination
+C0852654	21-hydroxylase deficiency
+C0852683	Glomerular vascular disorder
+C0852685	Abnormal palmar/plantar creases
+C0852694	Cartilage injury
+C0852700	Reticulocyte count decreased
+C0852710	Oxygen saturation increased
+C0852711	Hand and foot syndrome secondary to sickle cell anaemia
+C0852713	Pituitary tumour removal
+C0852720	Visual acuity reduced transiently
+C0852728	Partial pressure O2 abnormal NOS
+C0852733	Completed Suicide
+C0852740	Malignant breast lump removal
+C0852741	Bunion operation
+C0852792	Blood cortisol decreased
+C0852793	Blood cortisol increased
+C0852795	Blood insulin increased
+C0852810	Blood creatinine decreased
+C0852833	Tooth repair
+C0852839	Bone trimming
+C0852853	Pulmonary arterial pressure increased
+C0852866	Cervical cord compression
+C0852869	Elbow deformity NOS
+C0852870	PO2 increased
+C0852874	Moraxella infections
+C0852875	Eye allergy
+C0852879	Pulmonary alveolar haemorrhage
+C0852882	Radiation mucositis
+C0852902	Forced expiratory volume abnormal
+C0852903	On and off phenomenon
+C0852908	Drug ineffective
+C0852909	Blood bicarbonate decreased
+C0852911	Blood alkaline phosphatase increased
+C0852913	Blood amylase increased
+C0852919	Animal scratch
+C0852921	Blood fibrinogen increased
+C0852925	Gastrointestinal necrosis
+C0852926	Blood amylase decreased
+C0852932	Arthropod sting
+C0852940	Cytotoxic cardiomyopathy
+C0852943	Aortic valve disease mixed
+C0852946	Ventricle rupture
+C0852949	Arteriopathic disease
+C0852955	Protein C decreased
+C0852956	Cerebral arteriovenous malformation haemorrhagic
+C0852958	Jugular vein thrombosis
+C0852962	Complication of delivery
+C0852964	Shunt occlusion
+C0852973	Ventricular hypoplasia
+C0852975	Congenital cerebellar ataxia
+C0852983	Decreased lipid
+C0852995	Injection site pruritus
+C0853011	Diabetic hyperglycaemic coma
+C0853012	Blood growth hormone decreased
+C0853013	Diverticular perforation
+C0853015	Blood growth hormone increased
+C0853017	Blood human chorionic gonadotropin increased
+C0853018	Blood thyroid stimulating hormone decreased
+C0853019	Blood thyroid stimulating hormone increased
+C0853020	Blood oestrogen increased
+C0853021	Blood oestrogen decreased
+C0853023	Blood parathyroid hormone increased
+C0853024	Blood parathyroid hormone decreased
+C0853026	Porphyria non-acute
+C0853028	Blood pH decreased
+C0853030	Macroamylasemia
+C0853034	Blood creatine phosphokinase increased
+C0853036	Lentigo maligna stage unspecified
+C0853040	Reaction to drug excipients
+C0853049	Exercise test abnormal
+C0853050	Blood acid phosphatase increased
+C0853057	Ductus arteriosus stenosis foetal
+C0853060	Blood pH increased
+C0853062	Vascular resistance systemic decreased
+C0853068	Decreased glomerular filtration rate
+C0853079	Delusion of replacement
+C0853084	High density lipoprotein increased
+C0853085	Decreased LDL
+C0853086	Very low density lipoprotein increased
+C0853087	Nail abnormality
+C0853089	Intentional self-injury
+C0853105	Penis carcinoma
+C0853109	Malignant polyp removal
+C0853117	Blood testosterone decreased
+C0853118	Blood testosterone increased
+C0853121	Blood corticotrophin increased
+C0853122	Blood corticotrophin decreased
+C0853123	Blood luteinising hormone increased
+C0853124	Blood follicle stimulating hormone increased
+C0853126	Blood antidiuretic hormone increased
+C0853130	Blood thyroid stimulating hormone
+C0853141	Therapeutic response unexpected
+C0853142	CD4 lymphocytes decreased
+C0853144	Drug level NOS below therapeutic
+C0853149	Blood lactate dehydrogenase increased
+C0853150	Nerve conduction studies abnormal
+C0853154	Foetal arrhythmia
+C0853162	Blood alkaline phosphatase
+C0853176	Peak expiratory flow rate abnormal
+C0853193	Bipolar I disorder
+C0853198	Gastroenteritis yersinia
+C0853204	No adverse effect
+C0853206	Alcohol interaction
+C0853208	Mesenteric artery stenosis
+C0853224	Activated partial thromboplastin time shortened
+C0853225	International normalised ratio increased
+C0853226	International normalised ratio decreased
+C0853228	Serum ferritin abnormal
+C0853237	Hypothalamo-pituitary disorder
+C0853240	Mobius II syndrome
+C0853255	Femoral arterial stenosis
+C0853257	Myoglobin blood increased
+C0853277	Pseudo-Bartter syndrome
+C0853314	Soft tissue inflammation
+C0853326	Dyspnea exacerbated
+C0853327	Penile size reduced
+C0853336	Corneal infiltrates
+C0853339	Reperfusion arrhythmia
+C0853347	Venous thrombosis limb
+C0853348	Arthropod bite
+C0853351	CSF red blood cell count positive
+C0853356	Virus urine test positive
+C0853359	Acid-base balance abnoraml
+C0853373	Fungal abscess central nervous system
+C0853374	Romberg test positive
+C0853384	Blood creatine phosphokinase MB
+C0853415	Biopsy bone abnormal
+C0853435	Biopsy lung abnormal
+C0853441	Biopsy muscle abnormal
+C0853474	Biopsy skin abnormal
+C0853480	Multiple gated acquisition scan abnormal
+C0853482	Triple vessel bypass graft
+C0853483	Quadruple vessel bypass graft
+C0853500	Endoscopy upper gastrointestinal tract abnormal
+C0853501	Scan NOS abdomen abnormal
+C0853504	Angiogram NOS abnormal
+C0853523	Arteriogram coronary abnormal
+C0853526	Ultrasound Doppler abnormal
+C0853529	X-ray NOS face and mouth abnormal
+C0853538	Limb X-ray NOS abnormal
+C0853546	Positron emission tomogram abnormal
+C0853549	Renal scan NOS abnormal
+C0853562	Scan NOS myocardial perfusion abnormal
+C0853577	CSF glucose abnormal
+C0853586	CSF protein abnormal
+C0853595	Blood cholesterol abnormal
+C0853597	Blood corticotrophin abnormal
+C0853598	Blood cortisol abnormal
+C0853602	Immunodeficiency congenital
+C0853605	High density lipoprotein abnormal
+C0853608	Blood insulin abnormal
+C0853611	Low density lipoprotein abnormal
+C0853618	Blood parathyroid hormone abnormal
+C0853619	Local swelling
+C0853620	Blood prolactin abnormal
+C0853624	Blood testosterone abnormal NOS
+C0853625	Blood thyroid stimulating hormone abnormal
+C0853629	Blood triglycerides abnormal
+C0853633	Activated partial thromboplastin time abnormal
+C0853643	Concomitant disease aggravated
+C0853644	Eosinophil count abnormal
+C0853649	Full blood count decreased
+C0853655	Mean cell volume abnormal
+C0853662	Oestrogen deficiency
+C0853674	Oxygen saturation abnormal
+C0853675	Spirometry abnormal
+C0853677	Ventilation/perfusion scan abnormal
+C0853692	Blood triglycerides increased
+C0853697	Neutrophil count decreased
+C0853698	Lymphocyte count increased
+C0853700	Application site erythema
+C0853701	Blood immunoglobulin G increased
+C0853702	Blood immunoglobulin A increased
+C0853703	Blood immunoglobulin M increased
+C0853704	Blood immunoglobulin M decreased
+C0853705	Blood immunoglobulin G decreased
+C0853706	Blood immunoglobulin A decreased
+C0853708	SLE arthritis
+C0853712	Biopsy site unspecified abnormal
+C0853714	Application site pruritus
+C0853716	Basophil count increased
+C0853718	Reticulocyte count increased
+C0853719	CSF culture positive
+C0853727	Small intestinal ulcer bleeding
+C0853737	Blood bicarbonate increased
+C0853742	Blood carbon monoxide increased
+C0853746	Blood creatinine abnormal
+C0853748	Blood electrolytes NOS abnormal
+C0853749	Blood magnesium increased
+C0853750	Blood magnesium decreased
+C0853754	Blood osmolarity increased
+C0853755	Blood osmolarity decreased
+C0853759	Blood potassium abnormal
+C0853760	Blood potassium increased
+C0853761	Blood potassium decreased
+C0853772	Blood calcium abnormal
+C0853776	Blood albumin increased
+C0853777	Blood albumin decreased
+C0853779	Blood albumin abnormal
+C0853782	Blood creatine phosphokinase abnormal NOS
+C0853784	Blood iron increased
+C0853785	Blood iron decreased
+C0853786	Blood sodium abnormal
+C0853787	Blood lactate dehydrogenase abnormal NOS
+C0853800	Contrast media reaction
+C0853811	Croup infectious
+C0853813	Local reaction
+C0853828	Post inflammatory pigmentation change
+C0853834	Blood immunoglobulin E increased
+C0853840	Norepinephrine increased
+C0853844	Nodal osteoarthritis
+C0853846	Poisoning deliberate
+C0853847	Pathogen resistance
+C0853848	Infection in an immunocompromised host
+C0853852	Cystitis escherichia
+C0853853	Pneumonia haemophilus
+C0853856	Staphylococcal abscess
+C0853857	Cellulitis staphylococcal
+C0853858	Streptococcal abscess
+C0853860	Sepsis pasteurella
+C0853875	Myoglobin urine present
+C0853877	Fistula of genitourinary tract
+C0853878	Autoantibody positive
+C0853879	Invasive carcinoma of breast
+C0853880	Drug specific antibody present
+C0853885	Blood electrolytes decreased
+C0853888	Hypocomplementaemia
+C0853890	Blood gastrin increased
+C0853891	Tumour flare
+C0853892	Catabolic state
+C0853893	Device interaction
+C0853895	Mental disorder NOS due to a general medical condition
+C0853897	Diabetic Cardiomyopathies
+C0853905	CD4/CD8 ratio decreased
+C0853908	Oropharyngeal swelling
+C0853918	Diabetes with hyperosmolarity
+C0853936	Complication of device removal
+C0853939	Oral mucosal discolouration
+C0853942	Tongue blistering
+C0853945	Oral mucosal blistering
+C0853946	Pain aggravated
+C0853956	Blood creatine phosphokinase MB abnormal
+C0853958	Blood creatine phosphokinase MB increased
+C0853959	Device breakage
+C0853960	Bacterial disease carrier
+C0853966	Wheelchair user
+C0853970	Large intestinal stenosis
+C0853973	Blood gonadotrophin increased
+C0853979	Acoustic stimulation tests abnormal
+C0853986	Lymphocyte count decreased
+C0853998	Pupillary light reflex tests abnormal
+C0854011	Visual acuity tests abnormal
+C0854021	Abnormal visual field test
+C0854028	Blood copper decreased
+C0854029	Blood creatine increased
+C0854030	Blood creatine decreased
+C0854032	Blood creatine abnormal
+C0854035	Blood lactic acid decreased
+C0854043	Blood pyruvic acid decreased
+C0854044	Blood selenium increased
+C0854050	Glomerular filtration rate abnormal
+C0854056	Urine osmolarity increased
+C0854058	pH urine increased
+C0854060	Increased total iron binding capacity
+C0854062	Blood fibrinogen decreased
+C0854069	Tumour pain
+C0854076	Distal ileal obstruction syndrome
+C0854077	Diabetic retinal oedema
+C0854078	Diabetic end stage renal disease
+C0854082	Blood prolactin increased
+C0854084	Necrotising fasciitis streptococcal
+C0854092	Septic arthritis staphylococcal
+C0854095	Drug level altered
+C0854097	Hypoaesthesia eye
+C0854100	Nitrogen balance negative
+C0854104	Eosinophil count decreased
+C0854107	Haemorrhage subcutaneous
+C0854109	Epilepsy congenital
+C0854110	Insulin resistant diabetes
+C0854111	Blood triglycerides decreased
+C0854113	Mucosal dryness
+C0854114	Corneal epithelium defect
+C0854118	Respiratory tract irritation
+C0854119	Appendicitis perforated
+C0854121	Gastrointestinal motility disorder
+C0854122	Rectal ulcer haemorrhage
+C0854134	Blood bilirubin unconjugated increased
+C0854135	Pseudomonas aeruginosa infection
+C0854141	Renal aneurysm
+C0854142	Aortic thrombosis
+C0854145	Feeding disorder NOS
+C0854146	Blood test abnormal
+C0854148	Cells in urine
+C0854153	Metabolic function test abnormal
+C0854155	Immunology test abnormal
+C0854157	Antimicrobial susceptibility test resistant
+C0854161	Personality change due to a general medical condition
+C0854171	Temperature regulation disorder NOS
+C0854178	Metastases to adrenals
+C0854193	Cognitive deterioration
+C0854196	Hepatobiliary neoplasm
+C0854198	Metastases to abdominal cavity
+C0854211	Bacterial keratitis
+C0854231	Anastomotic ulcer haemorrhage
+C0854238	Diverticulum intestinal haemorrhagic
+C0854239	Diverticulitis intestinal haemorrhagic
+C0854240	Abdominal hernia NOS, obstructive
+C0854242	Gastrointestinal angiodysplasia
+C0854243	Gastrointestinal angiodysplasia haemorrhagic
+C0854248	Pneumonia due to Gram negative bacteria
+C0854254	Respiratory fume inhalation disorder NOS
+C0854268	Foetal damage
+C0854269	Amniotic cavity disorder
+C0854275	Umbilical cord vascular disorder
+C0854279	Basal ganglion degeneration
+C0854286	Eyelid function disorder
+C0854297	Head deformity
+C0854303	Limb discomfort
+C0854326	Escherichia infections
+C0854327	Bacillus infection
+C0854345	Pneumonia herpes viral
+C0854351	Renal failure neonatal
+C0854358	Purulence NOS
+C0854359	Insulin autoimmune syndrome
+C0854362	Aldolase increased
+C0854365	Breast discolouration
+C0854367	Soliloquy
+C0854369	Apallic syndrome
+C0854372	Mastication disorder
+C0854373	Lip discolouration
+C0854375	Mucosa haemorrhage NOS
+C0854379	Haemoconcentration
+C0854380	Blood insulin decreased
+C0854381	Genital haemorrhage NOS
+C0854382	Libido disorder
+C0854384	Beta-N-acetyl-D-glucosaminidase increased
+C0854385	Violence-related symptom
+C0854387	Cardiolipin antibody positive
+C0854388	Caustic injury
+C0854391	Aortic injury
+C0854404	Iatrogenic injury
+C0854407	Investigation NOS abnormal
+C0854416	Pulmonary vascular disorders
+C0854425	Sputum discoloured
+C0854431	Injection site vesicles
+C0854434	Angiosclerosis
+C0854438	Blepharal pigmentation
+C0854441	Gastric mucosal lesion NOS
+C0854443	Vascular fragility
+C0854453	Escherichia sepsis
+C0854456	Cellulitis gangrenous
+C0854482	Device leakage
+C0854504	Enterococcal bacteraemia
+C0854506	Urinary tract infection enterococcal
+C0854530	Human herpesvirus 6 infection
+C0854532	Myopericarditis
+C0854567	Complications of transplant surgery
+C0854569	Failure to anastomose
+C0854571	Reocclusion
+C0854629	Allogenic bone marrow transplantation therapy
+C0854630	Autologous bone marrow transplantation therapy
+C0854631	Cord blood transplant therapy
+C0854676	Implant failure
+C0854688	Anesthetic complication cardiac NOS
+C0854692	Anaesthetic complication pulmonary
+C0854693	Anaesthetic complication neurological
+C0854696	Malignant melanoma in situ
+C0854699	Trichomegaly
+C0854701	Complications of maternal exposure to therapeutic drugs
+C0854706	Neonatal infection
+C0854723	Retinal Dystrophies
+C0854725	Cyanopsia
+C0854727	Intracranial tumour haemorrhage
+C0854739	Advanced sleep phase
+C0854740	Delayed sleep phase
+C0854750	Colorectal cancer recurrent
+C0854754	Lip and/or oral cavity cancer
+C0854761	Oesophageal carcinoma recurrent
+C0854771	Stage I Esophageal Squamous Cell Carcinoma
+C0854775	Pancreatic carcinoma metastatic
+C0854776	Pancreatic carcinoma non-resectable
+C0854778	Pancreatic carcinoma resectable
+C0854792	Bile duct cancer resectable
+C0854794	Hepatic cancer recurrent
+C0854799	B precursor type acute leukaemia
+C0854802	Chronic lymphocytic leukaemia recurrent
+C0854819	Anaplastic large cell lymphomas T- and null-cell types
+C0854821	Anaplastic large cell lymphoma T- and null-cell types refractory
+C0854826	T-cell lymphoma recurrent
+C0854831	T-cell lymphoma stage IV
+C0854866	Non-Hodgkin's lymphoma NOS recurrent
+C0854867	Non-Hodgkin\'s lymphoma refractory
+C0854868	Non-Hodgkin\'s lymphoma transformed recurrent
+C0854893	Angiosarcoma non-metastatic
+C0854906	Benign Schwannoma
+C0854912	Pineal germinoma
+C0854914	Retinoblastoma bilateral
+C0854915	Retinoblastoma unilateral
+C0854917	Rhabdoid Tumor of the Kidney
+C0854937	Ovarian germ cell cancer NOS stage II
+C0854954	Ovarian germ cell teratoma benign
+C0854976	Large cell carcinoma of the respiratory tract stage unspecified
+C0854985	Adenocarcinoma of lung, stage I
+C0854986	Lung adenocarcinoma stage II
+C0854987	Adenocarcinoma of lung, stage III
+C0854988	Adenocarcinoma of lung, stage IV
+C0854995	Paranasal Sinus Cancer
+C0855002	Lung carcinoma cell type unspecified recurrent
+C0855004	Lung carcinoma cell type unspecified stage III
+C0855005	Ca lung stage IV
+C0855009	Peripheral neuroepithelioma of bone
+C0855012	Chondrosarcoma metastatic
+C0855054	Fibrosarcoma metastatic
+C0855056	Metastatic leiomyosarcoma
+C0855069	Recurrent Rhabdomyosarcoma
+C0855070	Synovial sarcoma metastatic
+C0855071	Synovial sarcoma non-metastatic
+C0855073	Undifferentiated (Embryonal) Sarcoma
+C0855082	Refractory Hodgkin Lymphoma
+C0855089	B-cell lymphoma recurrent
+C0855090	B-cell lymphoma refractory
+C0855094	B-cell lymphoma stage IV
+C0855095	B-cell small lymphocytic lymphomas
+C0855104	Burkitt's lymphoma recurrent
+C0855109	Burkitt's lymphoma stage IV
+C0855111	Diffuse large B-cell lymphoma recurrent
+C0855112	Diffuse large B-cell lymphoma refractory
+C0855114	Diffuse large B-cell lymphoma stage II
+C0855115	Diffuse large B-cell lymphoma stage III
+C0855116	Diffuse large B-cell lymphoma stage IV
+C0855117	Follicle centre lymphomas, follicular grade I, II, III
+C0855119	Follicle centre lymphoma, follicular grade I, II, III refractory
+C0855131	Lymphoplasmacytoid lymphomas/immunocytomas
+C0855138	Mantle cell lymphoma refractory
+C0855139	Monocytoid B-cell lymphoma
+C0855146	B Lymphoblastic Lymphoma
+C0855153	Primary mediastinal large B-cell lymphoma recurrent
+C0855173	Placental Choriocarcinoma
+C0855197	Malignant Testicular Germ Cell Tumor
+C0855217	Lack of spontaneous speech
+C0855221	Jealous delusion
+C0855223	Hallucinations, mixed
+C0855228	Eating disorder symptom
+C0855235	Feelings of worthlessness
+C0855236	Disturbance in social behaviour NOS
+C0855237	Social avoidant behaviour
+C0855239	DNA antibody positive
+C0855240	Trance
+C0855242	Disturbance in sexual arousal
+C0855246	Abnormal sleep-related event
+C0855247	Sleep attacks
+C0855249	Sleep disorder due to general medical condition, insomnia type
+C0855256	Somatoform disorder pregnancy
+C0855264	Delusional disorder, unspecified type
+C0855265	Bacteria stool identified
+C0855266	Bacteria NOS blood identified
+C0855270	Bacteria NOS sputum identified
+C0855278	Gram stain positive
+C0855289	pH body fluid NOS decreased
+C0855296	Aspiration bone marrow abnormal
+C0855304	Glycosylated haemoglobin decreased
+C0855322	Pulse pressure abnormal NOS
+C0855323	Pulse pressure increased
+C0855327	Ejection fraction abnormal
+C0855329	Electrocardiogram change
+C0855333	Electrocardiogram QT corrected interval prolonged
+C0855335	Electrocardiogram ST segment abnormal
+C0855337	Electrocardiogram T wave peaked
+C0855338	Gallop rhythm present
+C0855359	Cerebrospinal fluid WBC positive
+C0855389	Renin decreased
+C0855390	Renin increased
+C0855401	Coagulation factor V level decreased
+C0855407	Coagulation factor VII level decreased
+C0855411	Coagulation factor VIII level decreased
+C0855412	Coagulation factor VIII level increased
+C0855415	Coagulation factor X level decreased
+C0855429	Fibrin D dimer increased
+C0855436	Prothrombin time ratio decreased
+C0855437	Prothrombin time ratio increased
+C0855472	Blood alkaline phosphatase NOS decreased
+C0855476	Blood lactate dehydrogenase decreased
+C0855512	Sperm motility abnormal
+C0855513	Spermatozoa progressive motility decreased
+C0855521	Semen volume decreased
+C0855530	Urine sodium decreased
+C0855559	Scan NOS abnormal
+C0855565	Beta 2 microglobulin increased
+C0855573	Beta 2 microglobulin urine increased
+C0855577	Complement factor NOS low
+C0855588	Blood immunoglobulin M abnormal
+C0855603	Apolipoprotein A-I decreased
+C0855618	Alanine aminotransferase decreased
+C0855619	Alanine aminotransferase abnormal NOS
+C0855622	Aspartate aminotransferase decreased
+C0855623	Aspartate aminotransferase abnormal NOS
+C0855625	Bilirubin conjugated increased
+C0855644	Blood uric acid decreased
+C0855661	Ionized calcium increased
+C0855662	Calcium ionized decreased
+C0855704	Vital dye staining cornea present
+C0855740	Abnormal platelet function
+C0855742	Abnormal platelet morphology
+C0855748	Ammonia abnormal
+C0855756	Protein total abnormal
+C0855758	Protein total increased
+C0855774	Inspiratory capacity decreased
+C0855775	Pulmonary function test decreased
+C0855786	Mean cell haemoglobin concentration decreased
+C0855787	Mean cell haemoglobin concentration increased
+C0855789	Mean cell haemoglobin increased
+C0855790	Decreased mean corpuscular volume
+C0855791	Increased mean corpuscular volume
+C0855795	Red blood cell schistocytes present
+C0855835	Drug specific antibody absent
+C0855842	Hepatitis C RNA positive
+C0855856	Intradermal test negative
+C0855901	Blood ethanol increased
+C0855919	Analgesic drug level NOS above therapeutic
+C0855922	Antibiotic level NOS above therapeutic
+C0855925	Antidepressant drug level above therapeutic
+C0855931	Cardioactive drug level above therapeutic
+C0855932	Cardioactive drug level NOS below therapeutic
+C0855934	Chemotherapeutic drug level NOS above therapeutic
+C0855978	Blood folate decreased
+C0855979	Blood folate increased
+C0855987	Basophil count decreased
+C0856003	Neutrophil morphology abnormal
+C0856005	Neutrophil Pelger-Huet anomaly present
+C0856049	Peripheral embolism
+C0856050	Diet refusal
+C0856053	Leukemia secondary
+C0856054	Mental status changes
+C0856069	Vasculitis gastrointestinal
+C0856120	Multiple sclerosis relapse
+C0856150	Spinal haematoma
+C0856151	Fat redistribution
+C0856152	Buccal mucosal roughening
+C0856166	Sutre rupture
+C0856169	Endothelial dysfunction
+C0856554	Hepatic cancer metastatic
+C0856561	Opium addiction
+C0856597	Pulmonary alveolitis
+C0856600	Cell count NOS CSF increased
+C0856604	Rubber sensitivity
+C0856706	Hepatitis B positive
+C0856727	Cholesterol gallstones
+C0856738	Triple vessel disease
+C0856742	Post MI
+C0856747	Aneurysm of ascending aorta
+C0856761	Budd-Chiari Syndrome
+C0856823	Undifferentiated type acute leukemia
+C0856825	Acute graft versus host disease
+C0856830	Calcium pyrophosphate arthropathy
+C0856863	Broad-based gait
+C0856875	Diabetic ketoacidotic hyperglycemic coma
+C0856892	Livedoid
+C0856900	Sarcoma of skin
+C0856901	Retinol Deficiency
+C0856904	Allergy to fish
+C0856948	Glomerular filtration rate increased
+C0856975	Autistic behavior
+C0856977	Childhood aggression
+C0857007	Hyperbilirubinaemia neonatal
+C0857069	Chronic candidiasis
+C0857071	Stomach churning
+C0857087	Dizzy spells
+C0857112	Bilateral glaucoma
+C0857116	Gross obesity
+C0857122	Hyponatraemic
+C0857144	Metastatic pain
+C0857172	Persistent dry cough
+C0857177	Arthritic pains
+C0857276	Patellar subluxation
+C0857305	Thrombocytopenic purpura
+C0857345	Late onset epilepsy
+C0857379	Abnormality of the pinna
+C0857460	Increased number of platelets
+C0857490	Granulocyte count
+C0857494	Unresponsive to stimuli
+C0857501	Acute schizophrenia
+C0857502	Slow response to stimuli
+C0857516	Floppy
+C0857576	Abnormality of thyroid physiology
+C0857737	Vaginal yeast
+C0857797	Drug administered at inappropriate site
+C0857801	Inappropriate schedule of drug administration
+C0857804	Transmission of drug via semen
+C0857812	Sickle cell-beta^+^-thalassemia
+C0857828	Infection in the elderly
+C0857836	JC virus infection
+C0857860	Staphylococcus aureus endocarditis
+C0857862	Staphylococcus Aureus Pneumonia
+C0857898	Abnormal circulating aldosterone
+C0857973	Elevated circulating parathyroid hormone level
+C0858004	Influenza A virus infection
+C0858213	vascular aneurysm
+C0858240	Blood luteinising hormone decreased
+C0858252	Breast adenocarcinoma
+C0858259	Nasal discomfort
+C0858277	angina symptom
+C0858318	Plasmodium falciparum infection
+C0858321	Plasmodium vivax infection
+C0858342	PCO2 decreased
+C0858343	PCO2 increased
+C0858346	Gastrointestinal ulcer perforation
+C0858355	Addicted to cocaine
+C0858516	Subacute combined cord degeneration
+C0858527	Electrocardiogram PQ interval prolonged
+C0858598	Taste salty
+C0858599	Taste sour
+C0858600	Taste sweet
+C0858617	Posterior subcapsular cataract
+C0858618	Dyschromatopsia
+C0858621	Blindness, Cortical, Transient
+C0858635	Pharyngolaryngeal pain
+C0858668	Micturition frequency decreased
+C0858677	Nephritis allergic
+C0858684	Facial telangiectasia
+C0858734	Insulin hypoglycemia
+C0858744	Infection induced
+C0858751	Lip blister
+C0858765	Vascular pain
+C0858794	Application site warmth
+C0858797	Instillation site pain
+C0858804	Mucosal pain
+C0858821	Liver palpable subcostal
+C0858833	Endometrial hypertrophy
+C0858853	Impulsive aggression
+C0858864	Spot pigmented
+C0858867	Reticulocytopenia
+C0858906	Infection pyogenic
+C0858911	Blood pressure immeasurable
+C0858934	Injection site warmth
+C0859032	Moaning
+C0859055	Oedema vascular
+C0859078	Maternal drugs affecting foetus
+C0859088	Oral discharge
+C0859943	Hereditary allergy
+C0859974	Neonatal intestinal obstruction
+C0859976	Idiopathic achalasia of esophagus
+C0860006	Hypotonic dehydration
+C0860011	CPK decreased
+C0860013	Hepatitis B antibody positive
+C0860020	Hyperplastic cholecystopathy
+C0860029	Vaginal Yeast Infections
+C0860158	Leydig Cell Hypoplasia
+C0860159	Partial androgen resistance
+C0860160	Diabetes mellitus inadequate control
+C0860163	Diabetic gastropathy
+C0860168	Distal colitis
+C0860204	Cholestatic liver disease
+C0860207	Drug-Induced Liver Disease
+C0860210	Granulomatous liver disease
+C0860218	ABO incompatibility
+C0860239	Catheter related infection
+C0860439	Mottled pigmentation
+C0860499	Conjunctival follicles
+C0860514	Dreamy state
+C0860515	Freezing of gait
+C0860552	Retinal pigment epitheliopathy
+C0860554	Spinal column stenosis
+C0860556	Tongue movement disturbance
+C0860564	Retinoic acid syndrome
+C0860580	Medullary carcinoma of breast
+C0860594	Malignant melanoma, metastatic
+C0860603	Anxiety symptoms
+C0860609	Inappropriate crying
+C0860634	Psychogenic coma
+C0860659	Aloof
+C0860689	Spinal X-ray abnormal
+C0860700	Prothrombin level abnormal
+C0860711	Carbon dioxide low
+C0860713	Carbon dioxide increased
+C0860796	Differential white blood cell count abnormal
+C0860805	Urine ketone body present
+C0860811	Antidiuretic hormone abnormality
+C0860829	CSF white blood cell count increased
+C0860850	Estradiol low
+C0860851	Oestradiol increased
+C0860864	Decreased albumin
+C0860867	Albumin globulin ratio decreased
+C0860892	Alpha 1 globulin increased
+C0860896	Monoclonal immunoglobulin present
+C0860901	Protein total decreased
+C0860904	IgE deficiency
+C0861020	Insulin C-peptide decreased
+C0861021	Insulin C-peptide increased
+C0861099	Analgesic drug level NOS increased
+C0861103	Antidepressant drug level increased
+C0861111	Cardioactive drug level increased
+C0861112	Cardioactive drug level decreased
+C0861113	Chemotherapeutic drug level increased
+C0861143	Granulocyte count decreased
+C0861145	Granulocyte count increased
+C0861352	Lobular Neoplasia
+C0861727	Pancreatic adenocarcinoma metastatic
+C0861772	Rectal cancer stage IV
+C0861876	Recurrent Hepatocellular Carcinoma
+C0862030	Precursor B-lymphoblastic lymphoma/leukemia
+C0862039	Precursor B-lymphoblastic lymphoma stage II
+C0862196	Mycosis fungoides/Sezary syndrome NOS
+C0862312	Epithelioid mesothelioma, malignant
+C0862448	Stage IV Renal Cell Cancer
+C0862506	Borderline ovarian tumour
+C0862636	Adenocarcinoma of the prostate metastatic
+C0862802	Recurrent lung cancer
+C0862824	Lung cancer stage I
+C0862878	Dedifferentiated chondrosarcoma
+C0862889	Superficial basal cell carcinoma
+C0863029	Ewing\'s tumour localised
+C0863070	Catheter site related reaction
+C0863084	Skin discomfort
+C0863087	Decreased immune responsiveness
+C0863106	Afebrile seizure
+C0863129	AGEP
+C0863158	Drug level above therapeutic
+C0863159	Meningitis herpes
+C0863170	Foreign body trauma
+C0863194	Hepatoma resectable
+C0863745	Vascular bypass graft
+C0864052	Ureteral stent insertion
+C0864632	dmac
+C0864813	Sporothrix schenckii Infection
+C0865214	Autosomal recessive agammaglobulinemia
+C0865236	Acute intravascular hemolysis
+C0865245	progressive anemia
+C0865274	High-oxygen-affinity hemoglobin
+C0865275	Polycythemia due to fall in plasma volume
+C0865276	Polycythemia due to high altitude
+C0865424	Adult attention deficit hyperactivity disorder
+C0865474	Parkinsonism or Parkinson\'s disease NOS
+C0865475	Idiopathic Parkinsonism or Parkinson\'s disease
+C0865476	Primary Parkinsonism or Parkinson\'s disease
+C0865681	Chronic myocarditis
+C0865800	asthma with copd
+C0865998	Segmental Ileitis
+C0866036	Postoperative peritoneal adhesions
+C0866187	Renal embolism
+C0866188	Renal thrombosis
+C0866588	lupus erythematodes
+C0866718	Shoulder deformity
+C0867389	Chronic graft versus host disease
+C0868847	Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM
+C0868908	Pancolitis
+C0869083	Other specified congenital malformation syndromes, not elsewhere classified in ICD10CM
+C0869147	Neonatal hyperthyroidism
+C0869256	Mixed urinary incontinence
+C0869474	Acalculia
+C0869523	Carditis
+C0869532	Beta thalassemia minor
+C0870082	Hyperkeratosis
+C0871189	Psychotic symptom
+C0871215	Reading Disabilities
+C0871388	social stress
+C0871470	Systolic Pressure
+C0871610	winter depression
+C0872054	latent infection
+C0872084	Sarcopenia
+C0872218	MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
+C0872380	Food craving
+C0872410	Posturing
+C0876926	Brain damage (traumatic)
+C0876973	Infectious disease of lung
+C0876991	Histiocytosis haematophagic
+C0876993	Cardiac ventricular thrombosis
+C0876994	Cardiotoxicity
+C0876998	Intracardiac thrombus
+C0876999	Tumour marker increased
+C0877009	Muscle fibrosis
+C0877011	Concomitant disease progression
+C0877013	Restrictive pulmonary disease
+C0877015	Pelvic Organ Prolapse
+C0877017	Generalized tonic-clonic seizures with focal onset
+C0877020	Anti-erythropoietin antibody positive
+C0877024	Schimke immunoosseous dysplasia
+C0877027	Joint range of motion decreased
+C0877038	Electrocardiogram poor R-wave progression
+C0877040	Fear of falling
+C0877042	Graft loss
+C0877046	Infection of tooth
+C0877047	Occult blood positive
+C0877048	Oral fungal infection
+C0877052	Congenital choroid plexus cyst
+C0877055	Acute generalised exanthematous pustulosis
+C0877056	Hypoglycaemic seizure
+C0877061	Epiduritis
+C0877064	Cerebral ventricle dilatation
+C0877065	Anticonvulsant drug level below therapeutic
+C0877072	Cytomegalovirus chorioretinitis
+C0877077	Myocardial haemorrhage
+C0877079	Superinfection lung
+C0877087	Nail bed bleeding
+C0877089	Vaginal mucosal blistering
+C0877093	Vena cava filter insertion
+C0877094	Application site haemorrhage
+C0877095	Application site haematoma
+C0877096	Application site paraesthesia
+C0877097	Application site vesicles
+C0877098	Application site dryness
+C0877104	Retinal toxicity
+C0877107	Sinobronchitis
+C0877111	Ovarian adenoma
+C0877112	Leukoencephalomyelitis
+C0877113	Scar pain
+C0877115	Anti factor VIII antibody positive
+C0877117	Cytomegalovirus gastritis
+C0877119	Cytomegalovirus oesophagitis
+C0877121	AIDS related complication
+C0877122	Denture wearer
+C0877126	Application site inflammation
+C0877127	Application site papules
+C0877128	Application site pustules
+C0877131	Urinary tract infection fungal
+C0877134	Hernia pain
+C0877144	Spontaneous penile erection
+C0877145	Drug level NOS fluctuating
+C0877148	Pharyngotonsillitis
+C0877149	Patellofemoral Pain Syndrome
+C0877153	Neutropenic sepsis
+C0877154	Visual brightness
+C0877157	Pancreas transplant rejection
+C0877161	Drug exposure during pregnancy
+C0877165	Phalangeal hypoplasia
+C0877167	Psychomotor skills impaired
+C0877168	Haematocrit abnormal
+C0877169	Neonatal hyponatraemia
+C0877171	Blood alkaline phosphatase abnormal
+C0877172	Hematoma, Epidural, Spinal
+C0877173	Food aversion
+C0877185	Viral load decreased
+C0877186	Viral load NOS increased
+C0877192	Lipodystrophy acquired
+C0877203	Respiratory tract infection viral
+C0877208	Peripartum cardiomyopathy
+C0877211	General physical health deterioration
+C0877213	Implantable defibrillator insertion
+C0877214	Intestinal villi atrophy
+C0877217	Abasia
+C0877219	Drug clearance decreased
+C0877221	Decreased erythroid precursor production
+C0877223	Intestinal stoma site bleeding
+C0877225	Bone density decreased
+C0877232	Peripheral swelling
+C0877237	Traumatic fracture
+C0877242	Pyroglutamate increased
+C0877243	Increased serum serotonin
+C0877244	Angiotensin converting enzyme increased
+C0877248	Adverse event NOS
+C0877254	Bone marrow tumour cell infiltration
+C0877266	Upper respiratory tract inflammation
+C0877272	Enterocolitis viral NOS
+C0877275	Spinal cord infection
+C0877277	Mycobacterium chelonei infection
+C0877282	Precancerous cells present
+C0877297	Metastases to muscle
+C0877298	Blood homocysteine increased
+C0877302	Insulin-requiring type 2 diabetes mellitus
+C0877303	Post procedural pain
+C0877305	Postoperative wound complication
+C0877306	Iris hyperpigmentation
+C0877307	Pseudophaeochromocytoma
+C0877309	Renal impairment neonatal
+C0877314	Blood glucose fluctuation
+C0877318	Medical device implantation
+C0877320	Renal cyst ruptured
+C0877321	Vascular bypass dysfunction NOS
+C0877322	Muscle tightness
+C0877324	Urinary sediment present
+C0877325	Anal sphincter atony
+C0877326	Bone infarction
+C0877328	Blood HIV RNA increased
+C0877331	Abnormal clotting factor
+C0877334	Arterial stenosis limb
+C0877336	Blood bilirubin decreased
+C0877337	Tongue haemorrhage
+C0877338	Breast discomfort
+C0877341	Coronary revascularisation
+C0877359	Increased liver function tests
+C0877365	Infusion site erythema
+C0877369	Terminal state
+C0877371	Antiphospholipid antibodies positive
+C0877373	Advanced cancer
+C0877374	Drug name confusion
+C0877379	Peripheral pulse decreased
+C0877388	Cerebral haemangioma
+C0877398	Anaemia postoperative
+C0877400	Vertebral lesion
+C0877401	Sensorimotor disorder NOS
+C0877406	Performance status decreased
+C0877407	Paradoxical drug reaction
+C0877417	Cytomegalovirus enterocolitis
+C0877424	Disseminated cytomegaloviral infection
+C0877425	Pancreatic mass
+C0877429	Anaemia of malignant disease
+C0877430	Asthma chronic
+C0877437	Corrective lens user
+C0877445	Candidemia
+C0877451	C-reactive protein decreased
+C0877510	Precancerous skin lesion
+C0877517	Blood phosphorus decreased
+C0877521	Chronic synovitis
+C0877536	Fetal heart rate disorder NOS
+C0877550	Carcinomatous ascites
+C0877564	Lymphohistiocytosis
+C0877566	Oropharyngitis fungal
+C0877567	Mycobacterium fortuitum infection
+C0877568	Incision site abscess
+C0877578	Treatment related secondary malignancy
+C0877584	Tumour haemorrhage
+C0877635	Cytomegalovirus viraemia
+C0877639	Gingival blister
+C0877643	Neonatal anuria
+C0877644	Atrial pressure increased
+C0877645	Urinary bladder polyp
+C0877661	Application site burn
+C0877678	Liver graft loss
+C0877690	Renal graft loss
+C0877781	Hemicrania
+C0877792	Circadian rhythm sleep disorder
+C0877848	Distorted hearing
+C0877849	Askin\'s tumor
+C0877854	Cerebral Arteriosclerosis
+C0877855	Cerebral Embolism and Thrombosis
+C0878486	Arteriolosclerosis
+C0878500	Intraepithelial Neoplasia
+C0878520	beta Thalassemia, heterozygous
+C0878521	Beta thalassemia trait
+C0878544	Cardiomyopathies
+C0878555	Diffuse panbronchiolitis
+C0878575	Peripheral demyelination
+C0878576	Posterior Leukoencephalopathy Syndrome
+C0878588	Sphincter of Oddi dysfunction
+C0878624	lung cavity
+C0878627	Mucosal neuromas
+C0878631	pathergy
+C0878638	Abnormality of the tongue
+C0878649	Gastric hyperplastic polyp
+C0878654	Autoimmune oophoritis
+C0878659	Disproportionate short stature
+C0878660	Proportionate short stature
+C0878666	Analbuminemia
+C0878670	McLeod phenotype
+C0878672	Increased urinary urate
+C0878675	Erdheim-Chester Disease
+C0878676	6-pyruvoyl-tetrahydropterin synthase deficiency
+C0878677	Glycogen Storage Disease Type IIb
+C0878681	Dent's disease
+C0878682	Ceruloplasmin deficiency
+C0878683	Pituitary Dwarfism Type 3
+C0878684	SHORT syndrome
+C0878693	Conjunctivochalasis
+C0878705	Synovial Plica Syndrome
+C0878773	Overactive Bladder
+C0878787	Growth failure
+C0879257	Hereditary Papillary Renal Carcinoma
+C0879615	Stromal Neoplasm
+C0883301	Catheter placement
+C0887799	Posterior Choroidal Artery Infarction
+C0887800	Psychogenic Inversion of Circadian Rhythm
+C0887801	Abscess, Tubercular, Intracranial
+C0887833	Carcinoma, Pancreatic Ductal
+C0887850	Polycystic Kidney, Type 1 Autosomal Dominant Disease
+C0887866	Monckeberg Medial Calcific Sclerosis
+C0887898	Experimental Lung Inflammation
+C0887900	Upper Aerodigestive Tract Neoplasms
+C0917713	Becker Muscular Dystrophy
+C0917715	Hajdu-Cheney Syndrome
+C0917716	Pulmonic Plague
+C0917730	Female sterility
+C0917731	Male sterility
+C0917796	Optic Atrophy, Hereditary, Leber
+C0917798	Cerebral ischaemia
+C0917799	Hypersomnia
+C0917800	Epilepsy, Myoclonic, Infantile
+C0917801	Insomnia
+C0917804	Arteriovenous Malformations, Cerebral
+C0917805	Transient Cerebral Ischemia
+C0917807	Haemophilus influenzae Meningitis Type B
+C0917808	Vegetative State
+C0917811	Nerve Entrapment
+C0917812	Tetanilla
+C0917813	Spina Bifida, Open
+C0917814	Aphasia, Expressive
+C0917816	Mental deficiency
+C0917817	Neurofibromatosis 3
+C0917890	Pineocytoma
+C0917967	Pupillary Functions, Abnormal
+C0917981	Progressive Muscular Atrophy
+C0917990	Acro-Osteolysis
+C0917996	Cerebral Aneurysm
+C0919267	ovarian neoplasm
+C0919308	Decreased Intraocular Pressure-Associated Papilledema
+C0919532	Genomic Instability
+C0919560	Arterial stent occlusion
+C0919561	Congenital pyelocaliectasis
+C0919562	Faecal volume increased
+C0919567	Uterine contractions during pregnancy
+C0919568	Impatience
+C0919569	Airway complication of anaesthesia
+C0919572	Agitation postoperative
+C0919578	Idiosyncratic drug reaction
+C0919579	Oculocephalogyric reflex absent
+C0919582	Sudden onset of sleep
+C0919590	Injection site cellulitis
+C0919591	Urogenital haemorrhage
+C0919592	Hypothermia neonatal
+C0919593	Injection site coldness
+C0919596	Consciousness fluctuating
+C0919597	Fear of eating
+C0919600	Application site hyperaesthesia
+C0919603	Application site urticaria
+C0919605	Paroxysmal arrhythmia
+C0919613	Enterochromaffin cell hyperplasia
+C0919616	Oral mucosa atrophy
+C0919620	Electrocardiogram ST-T change
+C0919624	Pregnancy of partner
+C0919625	Blood phosphorus increased
+C0919626	Thirst decreased
+C0919631	Upper Extremity Deep Vein Thrombosis, Primary
+C0919636	Spinal fusion surgery
+C0919639	Faecal volume decreased
+C0919642	Ureteral necrosis
+C0919643	Urine calcium increased
+C0919644	Blast crisis in myelogenous leukaemia
+C0919648	Spleen congestion
+C0919655	Oxygen supplementation
+C0919659	Oropharyngeal candidiasis
+C0919663	Miscarriage of partner
+C0919671	Subileus
+C0919677	Protein C measurement
+C0919678	Protein S measurement
+C0919679	Double stranded DNA antibody
+C0919690	Skin ulcer haemorrhage
+C0919691	Anastomotic leak
+C0919700	Spinal fusion acquired
+C0919702	Ventricular hypokinesia
+C0919706	Cytomegalovirus antibody positive
+C0919710	Cytomegalovirus antigen positive
+C0919713	Creatinine renal clearance increased
+C0919714	Retinal vascular thrombosis
+C0919715	Lupus-like syndrome
+C0919718	Calcification of mitral valve
+C0919727	Intraoperative Awareness
+C0919728	Unwanted awareness during anaesthesia
+C0919737	Platelet aggregation inhibition
+C0919738	White blood cells urine
+C0919746	Engraftment syndrome
+C0919747	Cytokine storm
+C0919750	Nodule on extremity
+C0919752	Anti-insulin antibody
+C0919755	Congenital pulmonary hypertension
+C0919758	Vitamin D measurement
+C0919765	Vitamin D increased NOS
+C0919766	Vitamin D decreased NOS
+C0919767	Vitamin D abnormal NOS
+C0919768	Extremity contracture
+C0919777	Band neutrophil count increased
+C0919785	Decreased transferrin saturation
+C0919786	Transferrin saturation increased
+C0919791	Aspiration bronchial
+C0919792	Walking aid user
+C0919794	Itching scar
+C0919796	Groin infection
+C0919799	Heparin-induced thrombocytopenia test
+C0919806	Joint prosthesis user
+C0919808	Hearing aid user
+C0919818	Anti-neutrophil cytoplasmic antibody positive vasculitis
+C0919819	Drug screen negative
+C0919822	Postoperative thrombosis
+C0919823	Cytolytic hepatitis
+C0919860	Sinusitis aspergillus
+C0919866	Eye naevus
+C0919872	Transmission of drug via breast milk
+C0919873	Prescribed overdose
+C0919874	Post procedural haemorrhage
+C0919875	Therapy non-responder
+C0919876	Therapy responder
+C0919879	Intestinal fistula infection
+C0919882	Incision site haemorrhage
+C0919883	Puncture site haemorrhage
+C0919884	Arterial restenosis
+C0919887	Drug ineffective for unapproved indication
+C0919888	Protein S decreased
+C0919890	Hyperfibrinogenemia
+C0919892	Blood pressure inadequately controlled
+C0919894	Nasal mucosal disorder
+C0919895	Foetal heart rate decreased
+C0919907	Pleural infection
+C0919909	Tonic clonic movements
+C0919913	Nasal odour
+C0919914	Postoperative abscess
+C0919924	Pulmonary toxicity
+C0919936	Therapy naive
+C0919938	Anastomotic stenosis
+C0919939	Graft thrombosis
+C0919947	Thoracic vertebral fracture
+C0919974	Abulia
+C0919976	Renal cancer metastatic
+C0919980	VIIth nerve paralysis
+C0919986	Infusion site oedema
+C0919988	Metastatic bronchial carcinoma
+C0919989	Metastatic renal carcinoma
+C0919997	Thickened Achilles tendon
+C0920016	Adnexa uteri cyst
+C0920028	Leukaemia recurrent
+C0920064	Refractoriness to platelet transfusion
+C0920086	Limb operation NOS
+C0920103	Haematotoxicity
+C0920111	Urine bilirubin increased
+C0920129	Dental prosthesis user
+C0920150	Complement factor C3 decreased
+C0920156	Biliary sepsis
+C0920163	Idiopathic thrombocytopenia
+C0920165	Vascular access complication
+C0920166	Catheter site haemorrhage
+C0920171	Foreign body sensation in eyes
+C0920182	Pneumonia Pseudomonas aeruginosa
+C0920184	Fundic gland polyp
+C0920186	Hepatic artery stenosis
+C0920187	Congenital neuropathy
+C0920193	Photodermatosis
+C0920211	Paternal drugs affecting foetus
+C0920239	Blood urea nitrogen/creatinine ratio increased
+C0920257	Urine leukocyte esterase positive
+C0920263	Wound drainage
+C0920267	Platelet aggregation measurement
+C0920269	Microsatellite Instability
+C0920289	Sluggishness
+C0920296	Developmental reading disorder
+C0920299	Overriding toe
+C0920350	Autoimmune thyroiditis
+C0920372	Carcinogenesis, Radiation
+C0920420	cancer recurrence
+C0920424	Cancer surgery
+C0920506	Environment-Related Malignant Neoplasm
+C0920563	Insulin Sensitivity
+C0920569	Hepatic ischaemia
+C0920646	Ischemia of kidney
+C0920652	skin irritant
+C0920715	Myocardial hypoxia
+C0920776	hormone related neoplasm/cancer
+C0935681	Non-Hematologic Malignancy
+C0935909	Breast Carcinoma Metastatic in the Skin
+C0936016	Testicular Feminization
+C0936186	Gastrointestinal disorder NOS postoperative
+C0936215	Vitamin B 6 Deficiency
+C0936223	Metastatic Prostate Carcinoma
+C0936227	Abnormal loss of weight
+C0936243	HIV-1-Associated Cognitive Motor Complex
+C0936244	Developmental Gerstmann's Syndrome
+C0936247	Brain Embolism and Thrombosis
+C0936248	Chondroma
+C0936250	Eczema Herpeticum
+C0936251	Polyradiculitis
+C0936254	Polyradiculoneuritis
+C0936256	Lysine Alpha-Ketoglutarate Reductase Deficiency Disease
+C0936261	Brain Thrombus
+C0936263	Cerebral Thrombus
+C0936273	Familial Amyloid Polyneuropathy, Type IV
+C0936282	Blastoma
+C0940282	Gastrointestinal polyp haemorrhage
+C0940607	Colon Lipoma
+C0940747	Pancreatic duct stenosis
+C0940937	precancerous lesions
+C0941057	Ulcerative colitis, quiescent
+C0947622	Cholecystolithiasis
+C0947751	Vascular inflammations
+C0947912	Myasthenias
+C0947999	Blood urine present
+C0948002	Crystal urine present
+C0948008	Ischaemic stroke NOS
+C0948011	Cervix haemorrhage uterine
+C0948013	Blood viscosity increased
+C0948014	Red cell distribution width increased
+C0948016	Soft tissue haemorrhage
+C0948021	B-lymphocyte count decreased
+C0948023	Urine phosphorous concentration above normal
+C0948027	Pharmaceutical product complaint
+C0948031	Primary Graft Dysfunction
+C0948036	Gastric ulcer helicobacter
+C0948037	Cytomegalovirus gastroenteritis
+C0948044	Myeloma recurrence
+C0948046	Delayed engraftment
+C0948048	Malignant neoplasm progression
+C0948049	Urine amphetamine positive
+C0948050	Small bowel angioedema
+C0948052	Allergy to chemicals
+C0948055	Carbohydrate antigen 15-3 increased
+C0948056	Carbohydrate antigen 19-9 increased
+C0948060	Iridocele
+C0948070	Rhinalgia
+C0948074	Mitral valve sclerosis
+C0948075	Anal infection
+C0948085	Corneal defect
+C0948086	Intestinal mucosal hypertrophy
+C0948087	Haematoma infection
+C0948089	Acute Coronary Syndrome
+C0948094	Laziness
+C0948099	Cytomegalovirus test positive
+C0948100	Cytomegalovirus test
+C0948101	Gastrointestinal tract adenoma
+C0948109	Idiopathic neutropenia
+C0948116	Intestinal cyst NOS
+C0948118	Oral fibroma
+C0948120	Hepatic siderosis
+C0948158	Pulmonary sepsis
+C0948160	Pancreas infection
+C0948162	Bone marrow oedema
+C0948163	Leukoaraiosis
+C0948165	Bile duct stent insertion
+C0948168	Bone marrow toxicity
+C0948176	Blood beta-D-glucan increased
+C0948183	Myelocytosis
+C0948185	Lumbar spine flattening
+C0948186	Cervical spine flattening
+C0948187	Tracheomalacia
+C0948192	Primary infection NOS
+C0948201	Alloimmunisation
+C0948204	Citrobacter infection
+C0948205	Enterobacter infection
+C0948209	Intestinal adenocarcinoma
+C0948214	Lymphatic system neoplasm NOS
+C0948216	Ovarian adenocarcinoma
+C0948218	Pharyngeal polyp
+C0948221	Pyelocaliectasis
+C0948224	Stenotrophomonas infection
+C0948230	Hepatic artery occlusion
+C0948231	Lip erosion
+C0948233	Febrile infection
+C0948234	Anogenital dysplasia
+C0948236	Tongue eruption
+C0948240	Thyroxine free decreased
+C0948241	Thyroxine free increased
+C0948242	Foetal cystic hygroma
+C0948245	Cytokine release syndrome
+C0948246	Drug screen false positive
+C0948249	Femoral artery occlusion
+C0948256	Immunosuppressant drug level decreased
+C0948257	Immunosuppressant drug level NOS increased
+C0948264	Neuroborreliosis
+C0948266	Latent tetany
+C0948268	Haemodynamic instability
+C0948273	Foetal cardiac disorder
+C0948276	Shunt malfunction NOS
+C0948279	Beta haemolytic streptococcal infection
+C0948294	Eyelid margin crusting
+C0948296	Ear discomfort
+C0948299	Application site discharge
+C0948300	Application site scab
+C0948303	Carcinoma of peritoneum
+C0948331	Eosinophil percentage increased
+C0948332	Neutrophil percentage decreased
+C0948333	Neutrophil percentage increased
+C0948338	Monocyte percentage decreased
+C0948339	Monocyte percentage increased
+C0948340	Lymphocyte percentage increased
+C0948343	Transfusion-Related Acute Lung Injury
+C0948344	Escherichia urinary tract infection
+C0948345	Full blood count increased
+C0948347	Nephroangiosclerosis
+C0948348	Tumour associated fever
+C0948349	Respiratory tract congestion
+C0948352	Injury asphyxiation
+C0948353	Markedly reduced dietary intake
+C0948355	Myocardial bridging
+C0948361	Impaired work ability
+C0948368	Kaufman-McKusick syndrome
+C0948374	Large intestinal ulcer haemorrhage
+C0948376	Electrocardiogram ST-T segment abnormal
+C0948379	Impaired insulin secretion
+C0948380	Colorectal cancer metastatic
+C0948381	Semen discolouration
+C0948384	Cerebral hygroma
+C0948387	Secondary Adrenal Insufficiency
+C0948388	Dilatation intrahepatic duct acquired
+C0948393	Oedematous pancreatitis
+C0948395	Gastrointestinal hypermotility
+C0948404	Nitritoid reaction
+C0948425	Large intestinal haemorrhage
+C0948436	Gastrostomy tube insertion
+C0948437	Bone marrow dysplasia
+C0948441	Venoocclusive disease
+C0948444	Mitochondrial DNA mutation
+C0948447	Chromosomal mutation NOS
+C0948455	Suture insertion
+C0948470	Diaphragmalgia
+C0948474	Mycotic allergy
+C0948480	Coronary Restenosis
+C0948483	Unexpected therapeutic drug effect
+C0948484	Anal discomfort
+C0948485	Cytomegalovirus gastrointestinal infection
+C0948486	Acquired oesophageal web
+C0948521	Oral pruritus
+C0948522	Ocular vascular disorder
+C0948525	Musculoskeletal stiffness
+C0948537	Dental prosthesis placement
+C0948540	Arterial therapeutic procedure
+C0948549	Medical device removal
+C0948553	Lesion excision
+C0948558	Intra-aortic balloon placement
+C0948573	Emergency care examination
+C0948579	Bacteria NOS urine identified
+C0948585	Hydroxyprolinuria
+C0948586	Protein urine present
+C0948588	Lymphangiosis carcinomatosa
+C0948591	Oligodipsia
+C0948594	Musculoskeletal discomfort
+C0948595	Ocular discomfort
+C0948596	Paranasal sinus discomfort
+C0948599	Candida pneumonia
+C0948605	Therapeutic response delayed
+C0948610	Abdominal strangulated hernia
+C0948611	Sight disability
+C0948627	Cancer of lymph node
+C0948643	Hyperuricosuria
+C0948657	Carbohydrate antigen 125 increased
+C0948680	Adenocarcinoma of liver
+C0948689	Hepatosplenic candidiasis
+C0948691	Cerebral aspergillosis
+C0948692	Necrotising colitis
+C0948693	Postoperative drainage
+C0948699	Abdominal wall cyst
+C0948701	Metastases to thorax
+C0948702	Upper respiratory fungal infection NOS
+C0948715	Infusion related reaction
+C0948738	Lactobacillus infection
+C0948740	Hypoplasia of the pituitary gland
+C0948750	Salivary gland carcinoma
+C0948770	No reaction on previous exposure to drug
+C0948775	High weight
+C0948779	Gastrointestinal hypomotility
+C0948780	Rhinosinusitis
+C0948805	Dialysis device complication
+C0948806	Catheter related complication
+C0948807	Hepatic impairment
+C0948814	Catheter site oedema
+C0948815	Catheter site erythema
+C0948816	Catheter site hematoma
+C0948817	Catheter site inflammation
+C0948818	Catheter site phlebitis
+C0948819	Catheter site pruritus
+C0948820	Catheter site rash
+C0948824	Haemorrhagic anaemia
+C0948836	Nasal turbinate abnormality
+C0948839	Epstein-Barr virus antigen positive
+C0948853	Euthymia
+C0948856	Orgasmic sensation decreased
+C0948857	Electrocardiogram repolarisation abnormality
+C0948862	Detachment of retinal pigment epithelium
+C0948896	Primary hypogonadism
+C0948908	Nephrotoxic serum nephritis
+C0948920	Tuberculoma of central nervous system
+C0948936	Carotid artery bypass
+C0948968	Osteomyelofibrosis
+C0948976	Leukaemia cutis
+C0948978	Catheter site cellulitis
+C0948979	Catheter site drainage
+C0948981	Delusional disorder, persecutory type
+C0948991	Injection site discolouration
+C0949039	Lymphoid tissue hyperplasia
+C0949044	Lymphocyte percentage decreased
+C0949059	Large intestine polyp
+C0949070	Upper respiratory tract congestion
+C0949082	Meningorrhagia
+C0949083	Hospital acquired pneumonia
+C0949089	Spinal rod insertion
+C0949091	Candida sepsis
+C0949103	Catheter site pain
+C0949116	Congenital hypoplastic anemia
+C0949173	Delayed menarche
+C0949272	IIeocolitis
+C0949331	Gonadal Agenesis
+C0949367	Neonatal Diseases and Abnormalities
+C0949445	Cervical Dystonia
+C0949496	Luft Disease
+C0949505	Porokeratosis, Punctate
+C0949506	Porokeratosis of Mibelli
+C0949541	Hurthle Cell Tumor
+C0949570	Wheat Hypersensitivity
+C0949595	Gonadal Dysgenesis, 46,XX
+C0949658	Cardiomyopathy, Hypertrophic, Familial
+C0949664	Tauopathies
+C0949690	Spondylarthritis
+C0949691	Spondylarthropathies
+C0949804	Polyomavirus Infections
+C0949855	Electron Transport Chain Deficiencies, Mitochondrial
+C0949856	Oxidative Phosphorylation Deficiencies
+C0949857	Mitochondrial Respiratory Chain Deficiencies
+C0950121	Denys-Drash Syndrome
+C0950122	Frasier Syndrome
+C0950123	Genetic Diseases, Inborn
+C0950124	Disease due to Papilloma virus
+C0969687	Autosomal Chromosome Disorders
+C0971858	Arthritis, Collagen-Induced
+C0973461	Dysphasia
+C0993582	Arthritis, Experimental
+C0994344	Rheumatoid lung
+C0994516	Type 1 Duane Retraction Syndrome
+C0995195	Anoxia of brain
+C1095922	Wound decomposition
+C1095923	Febrile bone marrow aplasia
+C1095926	Amimia
+C1095927	Narcotic intoxication
+C1095929	Coronary artery reocclusion
+C1095971	Blood pressure orthostatic
+C1095973	Blood pressure orthostatic abnormal
+C1095974	Blood pressure orthostatic decreased
+C1095979	Progressive multiple sclerosis
+C1095982	Drug half-life increased
+C1095988	Brain natriuretic peptide increased
+C1095991	Brain natriuretic peptide abnormal
+C1095995	Atrial natriuretic peptide increased
+C1096000	Bronchopulmonary disease
+C1096001	Application site swelling
+C1096020	Secretion discharge
+C1096034	Infusion site induration
+C1096035	Infusion site pain
+C1096036	Infusion site warmth
+C1096037	Venous angioma of brain
+C1096045	Human immunodeficiency virus transmission
+C1096049	Infusion site swelling
+C1096061	Gastrointestinal cancer metastatic
+C1096063	Drug Resistant Epilepsy
+C1096064	Drug chemical incompatibility
+C1096066	Drug therapeutic incompatibility
+C1096071	Type III immune complex mediated reaction
+C1096081	Bone swelling
+C1096082	Oesophageal discomfort
+C1096083	Extraocular muscle disorder
+C1096086	Deformity of lower limb
+C1096091	Infusion site pruritus
+C1096093	Prosthesis user
+C1096099	Iris transillumination defect
+C1096103	Cardiac assistance device user
+C1096106	Wound complication
+C1096115	Wound necrosis
+C1096116	Acquired haemophilia
+C1096117	Off label use
+C1096119	Cardiac valve replacement complication
+C1096121	Skeleton dysplasia
+C1096123	B-lymphocyte abnormalities
+C1096124	Meniscus injury
+C1096141	Anti-insulin antibody positive
+C1096142	Anti-insulin antibody increased
+C1096150	Ubiquinone decreased
+C1096151	Sinus tarsi syndrome
+C1096154	Kinsbourne Syndrome
+C1096155	Macrophage Activation Syndrome
+C1096168	Chromosome 17 trisomy
+C1096176	Mitochondrial toxicity
+C1096184	West Nile viral infection
+C1096185	Dacryostenosis acquired
+C1096187	Implant site haemorrhage
+C1096188	Puncture site reaction
+C1096189	Type II hypersensitivity
+C1096194	Lipoprotein (a) increased
+C1096195	Thyroglobulin increased
+C1096197	Immune reconstitution syndrome
+C1096198	Agonal rhythm
+C1096201	Pilonidal cyst congenital
+C1096202	Lipoprotein (a) measurement
+C1096216	Oestrogen receptor assay positive
+C1096225	Vessel puncture site haemorrhage
+C1096227	Wound evisceration
+C1096228	Laryngeal discomfort
+C1096229	Listeria encephalitis
+C1096239	Stenotrophomonas sepsis
+C1096242	Clostridium difficile sepsis
+C1096243	Central line infection
+C1096244	Intestinal resection
+C1096246	Acid fast bacilli infection
+C1096248	Alternaria infection
+C1096249	Aortic calcification
+C1096252	Cardiac discomfort
+C1096253	Cardiac infection
+C1096254	Citrobacter sepsis
+C1096256	Cryptococcal cutaneous infection
+C1096257	Dental discomfort
+C1096258	Enterobacter pneumonia
+C1096260	Enterococcal sepsis
+C1096262	Escherichia bacteraemia
+C1096266	Alpha haemolytic streptococcal infection
+C1096267	Injection site discomfort
+C1096272	Vanishing bile duct syndrome
+C1096274	Corneal thinning
+C1096275	Increased viscosity of bronchial secretion
+C1096278	Anterior chamber inflammation
+C1096282	Medication residue
+C1096293	Macroangiopathy
+C1096294	Maxillofacial operation
+C1096295	Anticonvulsant drug level above therapeutic
+C1096300	Genital burning sensation
+C1096302	Vertebral column mass
+C1096303	Lipase abnormal
+C1096304	Blood phosphorus abnormal
+C1096307	Splenic lesion
+C1096309	Myolipoma
+C1096311	Mucosal discolouration
+C1096333	Meniscus operation
+C1096335	Radiculomyelopathy
+C1096340	Dysphemia
+C1096341	Injection site pustule
+C1096343	Infusion site reaction
+C1096350	Cardiac stress test abnormal
+C1096352	Pancreatic enlargement
+C1096354	Umbilical erythema
+C1096355	Electrocardiogram U-wave abnormality
+C1096358	Intervertebral disc compression
+C1096359	Vertebral osteophyte
+C1096367	Increased mean platelet volume
+C1096368	Decreased mean platelet volume
+C1096386	Biliary cancer metastatic
+C1096388	Arteriovenous fistula site complication
+C1096389	Arteriovenous fistula site haemorrhage
+C1096392	Arteriovenous graft site infection
+C1096393	Body fat disorder
+C1096400	Haemorrhagic transformation stroke
+C1096418	Peripheral revascularisation
+C1096443	Urine protein/creatinine ratio increased
+C1096444	Altered visual depth perception
+C1096448	Bronchopneumopathy
+C1096452	Neonatal Early-Onset Sepsis
+C1096458	Vascular occlusion
+C1096460	Infusion site phlebitis
+C1096488	Hereditary factor IX deficiency disease without inhibitor
+C1096506	Free prostate-specific antigen increased
+C1096527	Mosaic trisomy 8 syndrome
+C1096532	Vascular pseudoaneurysm ruptured
+C1096536	Thoracic cavity drainage
+C1096546	Congenital bowing of long bones
+C1096561	Myocardial calcification
+C1096563	Post procedural discomfort
+C1096582	Campylobacter jejuni infection
+C1096584	Chlamydia pneumoniae Infections
+C1096610	Corneal crystalline deposits
+C1096616	Contralateral breast cancer
+C1096618	Peritoneal lesion
+C1096624	Periumbilical pain
+C1096633	Phalangeal agenesis
+C1096654	Cardiac fibroma
+C1096657	Prostate examination abnormal
+C1096658	Urine phosphorus increased
+C1096660	Ehlers-Danlos syndrome type IX
+C1096666	Thyroid cancer metastatic
+C1096667	Lymph node cancer metastatic
+C1096671	Arteriovenous fistula site infection
+C1096691	BK virus infection
+C1096699	Urine albumin/creatinine ratio increased
+C1096701	Medical device discomfort
+C1096704	Blood erythropoietin increased
+C1096709	Amylase abnormal
+C1096710	Lactescent serum
+C1096714	Infusion site infection
+C1096715	Testicular cancer metastatic
+C1096717	Pain during injection
+C1096902	Infantile Sialic Acid Storage Disease
+C1096903	Sialic Acid Storage Disease, Finnish Type (disorder)
+C1112155	Hereditary non-polyposis colorectal cancer syndrome
+C1112157	Intrauterine infection
+C1112160	Gastrooesophageal cancer
+C1112161	Perianal erythema
+C1112173	Transient psychosis
+C1112174	Panencephalitis
+C1112176	Autonomic failure syndrome
+C1112180	Refusal of treatment by relative
+C1112181	Arterial bypass operation
+C1112182	Parkinsonian rest tremor
+C1112200	Accidental needle stick
+C1112209	Intraabdominal Infections
+C1112210	Catheter site infection
+C1112211	Hepatic infection
+C1112213	Cholestasis in newborn
+C1112214	Vulvovaginal pruritus
+C1112228	Drug delivery device implantation
+C1112251	Feeding tube complication
+C1112256	Peripheral sensorimotor neuropathy
+C1112257	Oral pustule
+C1112261	Gaze palsy
+C1112271	Implantable defibrillator malfunction
+C1112273	Meniscus removal
+C1112276	Postoperative thoracic procedure complication
+C1112277	Bone formation decreased
+C1112278	Body height below normal
+C1112298	Ear, nose and throat examination abnormal
+C1112303	Facial wasting
+C1112306	Adenoviral hepatitis
+C1112313	Gastrointestinal mucosal disorder
+C1112316	Salivary gland mass
+C1112318	Meconium stain
+C1112320	Temperature intolerance
+C1112341	Connective tissue inflammation
+C1112346	Prostate induration
+C1112347	T-lymphocyte count increased
+C1112353	Medical device complication
+C1112356	Bronchial dysplasia
+C1112363	Underdose
+C1112364	Human polyomavirus infection
+C1112366	Eyelid irritation
+C1112368	Hernial eventration
+C1112369	Paranasal sinus hypersecretion
+C1112371	Anterior chamber pigmentation
+C1112375	Cataract operation complication
+C1112386	Cardiac ventricular disorder
+C1112389	Implantable defibrillator replacement
+C1112391	Vascular procedure complication
+C1112395	Lymph node palpable
+C1112413	Peripheral artery aneurysm
+C1112417	Bone marrow myelogram abnormal
+C1112419	Hepatitis C positive
+C1112421	Lung infection pseudomonal
+C1112423	Post procedural bile leak
+C1112424	Post procedural urine leak
+C1112425	Blood ketone body increased
+C1112429	Interferon gamma receptor deficiency
+C1112433	Thromboembolic stroke
+C1112434	Aortic bypass
+C1112436	QRS axis abnormal
+C1112440	Cardiac valve vegetation
+C1112442	Female sexual dysfunction
+C1112443	Male sexual dysfunction
+C1112446	Wound closure
+C1112469	Cytomegalovirus syndrome
+C1112470	Infusion site inflammation
+C1112474	Small cell carcinoma of esophagus
+C1112480	Mediastinal haemorrhage
+C1112483	Anastomotic haemorrhage
+C1112486	Aggressive Systemic Mastocytosis
+C1112488	Bradycardia neonatal
+C1112499	Breath alcohol test positive
+C1112511	Dehydroepiandrosterone decreased
+C1112513	Vestibulitis
+C1112522	Bronchial oedema
+C1112525	Gastrointestinal ulcer haemorrhage
+C1112530	Leukoplakia of oral mucosa, incl tongue
+C1112537	Neurological examination abnormal
+C1112565	Pneumatosis intestinalis
+C1112570	Paraneoplastic pemphigus
+C1112584	Anti-erythrocyte antibody positive
+C1112601	Hypertonic dehydration
+C1112613	Neonatal tachypnoea
+C1112616	Loss of proprioception
+C1112629	Adenoviral haemorrhagic cystitis
+C1112640	Adenoidal disorder
+C1112654	Peripheral artery dissection
+C1112666	Respiratory dyskinesia
+C1112667	Ocular retrobulbar haemorrhage
+C1112668	Cardiac septal hypertrophy
+C1112671	Blood ketone body
+C1112705	Nuclear non-senile cataract
+C1112709	non-gonococcal urethritis (NGU)
+C1112712	Haematology test abnormal
+C1112718	Maternal condition affecting foetus
+C1112726	CD8 lymphocytes decreased
+C1112734	Gastric infection
+C1112746	Hepatic lymphoma
+C1112758	Infective exacerbation of chronic obstructive airways disease
+C1112762	Blood methaemoglobin present
+C1112768	Anterior subcapsular cataract
+C1112773	Post procedural diarrhoea
+C1112776	Thyroid hyperplasia
+C1112782	Malignant melanoma of skin of trunk, except scrotum
+C1112789	Rectal spasm
+C1112797	Nasal mucosal discoloration
+C1134719	Invasive Ductal Breast Carcinoma
+C1135120	Breakthrough Pain
+C1135161	Stage 4S neuroblastoma
+C1135188	Critical illness myopathy
+C1135191	Heart Failure, Systolic
+C1135194	Chronic systolic heart failure
+C1135196	Heart Failure, Diastolic
+C1135361	Persistent pulmonary hypertension
+C1135745	Meningitis, Meningococcal, Serogroup A
+C1135746	Meningitis, Meningococcal, Serogroup B
+C1135747	Meningitis, Meningococcal, Serogroup C
+C1135773	Acquired Metabolic Diseases, Nervous System
+C1135812	Patellar Dislocation
+C1135868	Gestational Trophoblastic Neoplasms
+C1135869	Hemorrhagic Septicemia, Viral
+C1135993	Wasting Disease, Chronic
+C1136033	Cutaneous Mastocytosis
+C1136041	Familial Acoustic Neuroma
+C1136042	Neuroma, Acoustic, Bilateral
+C1136043	Schwannoma, Acoustic, Bilateral
+C1136082	Embryo Disintegration
+C1136084	Plasma cell dyscrasia
+C1136085	Monoclonal Gammapathies
+C1136135	Water Stress
+C1136148	Heel Spur Syndrome
+C1136179	Hammer Toe
+C1136209	Meningitis, Meningococcal, Serogroup Y
+C1136210	Meningitis, Meningococcal, Serogroup W-135
+C1136249	Mental Retardation, X-Linked
+C1136321	HIV-Associated Lipodystrophy Syndrome
+C1136382	Sclerocystic Ovaries
+C1136393	Delayed Onset Post-Traumatic Stress Disorder
+C1137478	Retinoschisis, Degenerative
+C1138421	Spider Veins
+C1138434	Genetic Diseases, X-Linked
+C1140680	Malignant neoplasm of ovary
+C1140710	Cerebral Cavernous Hemangioma
+C1140716	Hypoxic Brain Damage
+C1141861	Procedural complication
+C1141862	Therapy regimen changed
+C1141863	Lymphocyte transformation test positive
+C1141868	Computerised tomogram abdomen abnormal
+C1141869	Computerised tomogram thorax abnormal
+C1141877	Anticonvulsant drug level increased
+C1141880	Bone density increased
+C1141881	Multiple drug overdose
+C1141882	Pharyngitis bacterial
+C1141885	Sclerosing encapsulating peritonitis
+C1141889	Transplant evaluation
+C1141890	Congenital long QT syndrome
+C1141891	Ear tube insertion
+C1141893	Muscle enzyme increased
+C1141900	Rheumatoid factor increased
+C1141905	Bone callus excessive
+C1141907	Lactate pyruvate ratio increased
+C1141926	Abdominal sepsis
+C1141927	Wound sepsis
+C1141928	Anastomotic complication
+C1141929	Gastrointestinal oedema
+C1141930	Post procedural complication
+C1141933	Multi-organ disorder
+C1141936	Purple glove syndrome
+C1141938	Ocular icterus
+C1141940	Intestine transplant rejection
+C1141948	Troponin increased
+C1141949	Troponin I increased
+C1141954	Allergy to arthropod sting
+C1141959	ECG signs of myocardial ischaemia
+C1141999	Tongue carcinoma stage IV
+C1142005	Biliary ischaemia
+C1142009	Artificial crown procedure
+C1142011	Orchitis noninfective
+C1142012	Infusion site abscess
+C1142015	Blood bilirubin abnormal
+C1142025	Stage IV Esophageal Squamous Cell Carcinoma
+C1142027	Anti-platelet antibody positive
+C1142028	Peripheral nerve palsy
+C1142029	Necrotizing granulomatous lymphadenitis
+C1142032	Mycobacterium avium complex immune restoration disease
+C1142034	Tandem gait test abnormal
+C1142047	Bacterial culture positive
+C1142052	Cranial sutures widening
+C1142053	Poor sucking reflex
+C1142060	Total cholesterol/HDL ratio decreased
+C1142074	Leukaemic infiltration hepatic
+C1142075	Negative thoughts
+C1142077	Sinusitis fungal
+C1142080	Injection site stinging
+C1142081	Chronic lymphocytic leukaemia transformation
+C1142087	Vitamin B1 increased
+C1142098	Vitamin E Assay
+C1142105	Fungus serology test positive
+C1142109	Sopor
+C1142110	Abdominal compartment syndrome
+C1142111	Eyelash discolouration
+C1142112	Eyelash thickening
+C1142113	Hyperalbuminaemia
+C1142114	Bone marrow necrosis
+C1142115	Enterocolitis infectious
+C1142117	Adnexa uteri pain
+C1142127	Pneumococcal bacteraemia
+C1142132	Carnitine deficiency
+C1142133	Adnexa uteri mass
+C1142135	Muscle relaxant therapy
+C1142137	General physical condition abnormal
+C1142138	Hypotonic urinary bladder
+C1142139	Drug reaction with eosinophilia and systemic symptoms
+C1142140	Pseudomonal bacteraemia
+C1142145	Bile duct necrosis
+C1142152	Heart valve calcification
+C1142154	Victim of homicide
+C1142158	Hepatic vein occlusion
+C1142159	Intentional misuse
+C1142160	Application site discolouration
+C1142162	Injection site scar
+C1142163	Intestinal mass
+C1142166	Brugada Syndrome
+C1142167	Blood stem cell harvest failure
+C1142168	Neonatal aspiration
+C1142169	Acute myeloid leukaemia recurrent
+C1142170	Scedosporium infection
+C1142172	Incision site complication
+C1142175	Shunt thrombosis
+C1142176	Medical device pain
+C1142186	Corynebacterium sepsis
+C1142248	Pseudomononucleosis
+C1142249	Infected cyst
+C1142253	Arthrofibrosis
+C1142256	Cardiac perforation
+C1142257	Incision site pain
+C1142262	Intestinal edema
+C1142272	Neutrophilic dermatosis
+C1142274	Nevus cell nevus
+C1142275	Poor quality drug administered
+C1142276	Renal anemia
+C1142294	Troponin T increased
+C1142300	Clostridium colitis
+C1142305	Melanonychia
+C1142307	Paratubal Cyst
+C1142332	Glasgow coma scale abnormal
+C1142347	Stage IV Esophageal Adenocarcinoma
+C1142349	Eyelid pain
+C1142379	Neurotmesis
+C1142397	Myoglobinaemia
+C1142399	Anti factor V antibody positive
+C1142412	Vasodilation procedure
+C1142423	Bacteremia due to Staphylococcus aureus
+C1142427	Clostridium bacteraemia
+C1142428	Enterobacter bacteraemia
+C1142430	Psychogenic seizure
+C1142436	Sundowning
+C1142438	Serratia bacteraemia
+C1142446	Bicytopenia
+C1142448	Apraxia of eyelid
+C1142459	Application site scar
+C1142463	Blood stem cell transplant failure
+C1142464	Gastrointestinal ischaemia
+C1142470	Suture related complication
+C1142492	Postinfarction angina
+C1142498	Application site excoriation
+C1142499	Gastrointestinal toxicity
+C1142503	Anticonvulsant drug level decreased
+C1142520	Nail pigmentation
+C1142533	Smooth philtrum
+C1142536	Pneumonia due to methicillin resistant Staphylococcus aureus
+C1142550	Native valve endocarditis
+C1142553	Primary HIV infection
+C1142567	Joint abscess
+C1144799	Hypertensive cardiomyopathy
+C1145628	Autonomic nervous system disorders
+C1145670	Respiratory Failure
+C1148477	Deafness, Sudden
+C1148522	Acoustic Trauma
+C1148551	X-Linked Dyskeratosis Congenita
+C1153706	Endometrial adenocarcinoma
+C1154610	sensory perception of bitter taste
+C1154706	response to antibiotic
+C1167654	Acute prerenal failure
+C1167659	Lower respiratory tract inflammation
+C1167660	Medical device change
+C1167661	Cerebral vasoconstriction
+C1167662	Diabetic foetopathy
+C1167663	Biloma
+C1167664	Situs ambiguous
+C1167665	Band neutrophil percentage increased
+C1167668	Peripheral occlusive disease
+C1167669	Blood chromogranin A increased
+C1167674	Cerebrosclerosis
+C1167675	Application site folliculitis
+C1167677	Infrequent bowel movements
+C1167679	Oxygen consumption decreased
+C1167681	Oxygen consumption increased
+C1167683	Acquired diaphragmatic eventration
+C1167685	Infusion site bruising
+C1167709	Epidermal necrosis
+C1167712	Corneal diameter increased
+C1167713	Decreased corneal diameter
+C1167716	Stage I Gallbladder Carcinoma
+C1167720	Pancreatic carcinoma stage I
+C1167724	Hepatic cancer stage IV
+C1167725	Stage IV Pancreatic Cancer
+C1167727	Postrenal failure
+C1167728	Viral haemorrhagic cystitis
+C1167731	Infected lymphocele
+C1167732	Pleuropericarditis
+C1167745	Extremity necrosis
+C1167749	Removal of transplanted organ
+C1167752	Graft ischaemia
+C1167760	Bacterial test positive
+C1167761	Fungal screen positive
+C1167762	Viral screen positive
+C1167764	Skin neoplasm excision
+C1167765	Wound infection staphylococcal
+C1167766	Wound infection pseudomonas
+C1167767	Gallbladder necrosis
+C1167779	Neutropenic infection
+C1167781	Abdominal cavity drainage
+C1167782	Lung hyperinflation
+C1167791	Skin toxicity
+C1167792	Bacterial pyelonephritis
+C1167794	Cytology abnormal
+C1167795	Peritoneal fluid analysis abnormal
+C1167797	Synovial fluid analysis abnormal
+C1167798	Stool analysis abnormal
+C1167836	Insulin-like growth factor decreased
+C1167837	Insulin-like growth factor increased
+C1167841	Obesity surgery
+C1167842	Tobacco withdrawal symptoms
+C1167849	Drug clearance increased
+C1167854	Implant site infection
+C1167863	Retinogram abnormal
+C1167866	Renal lymphocele
+C1167868	Perinephric collection
+C1167870	Graft dysfunction
+C1167886	CSF test abnormal
+C1167896	Anti-GAD antibody positive
+C1167905	Candida serology positive
+C1167912	Coagulation factor measurement
+C1167918	Increased CSF lactate
+C1167945	Infusion site rash
+C1167946	Pacemaker generated rhythm
+C1167947	Pacemaker complication
+C1167958	Jugular vein distension
+C1167959	Device ineffective
+C1167962	Cytogenetic analysis abnormal
+C1167963	Myoglobin blood present
+C1167965	Urine output increased
+C1167981	Pharyngeal hypoaesthesia
+C1167983	Blood urea nitrogen/creatinine ratio decreased
+C1168015	Base excess increased
+C1168016	Base excess decreased
+C1168018	B-lymphocyte count increased
+C1168019	Blood alcohol increased
+C1168034	Gastric pH decreased
+C1168036	Head circumference abnormal
+C1168040	Hepatitis B DNA assay positive
+C1168060	Light chain analysis increased
+C1168064	Left ventricular end-diastolic pressure increased
+C1168086	Antipsychotic drug level above therapeutic
+C1168087	Antipsychotic drug level below therapeutic
+C1168088	Parvovirus B19 serology positive
+C1168114	Pulmonary arterial pressure decreased
+C1168116	Pulmonary arterial pressure abnormal
+C1168119	Right ventricular systolic pressure increased
+C1168134	Anti-thyroid antibody positive
+C1168144	Anticoagulation drug level above therapeutic
+C1168145	Subtherapeutic INR
+C1168153	Arterial calcification
+C1168170	Poor dental condition
+C1168175	Incision site haematoma
+C1168198	Recurrent respiratory papillomatosis
+C1168239	Asymmetry of the ears
+C1168250	Laryngopharyngeal Reflux
+C1168263	Central Hypogonadism
+C1168266	Radiation dysphagia
+C1168279	Melalgia
+C1168305	Corneal melt
+C1168323	Renal cyst haemorrhage
+C1168327	High-Grade Prostatic Intraepithelial Neoplasia
+C1168328	Low Grade Prostatic Intraepithelial Neoplasia
+C1168401	Squamous cell carcinoma of head and neck
+C1168430	c-ANCA increased
+C1168438	Protein C antigen measurement
+C1168443	Pseudocholinesterase Measurement
+C1168474	Anti-SS-A antibody positive
+C1175175	Severe Acute Respiratory Syndrome
+C1175743	SARS coronavirus
+C1176475	Carcinoma, Ductal
+C1184919	Thoracic kyphosis
+C1184923	Lumbar hyperlordosis
+C1185616	Hair whorls
+C1187006	Mucosal vesicle NOS
+C1253936	Joint effusion
+C1257752	Infant Malnutrition
+C1257753	Child Malnutrition
+C1257763	Overnutrition
+C1257764	Child Overnutrition
+C1257765	Infant Overnutrition
+C1257796	Choledochal Cyst, Type II
+C1257797	Choledochal Cyst, Type III
+C1257798	Choledochal Cyst, Type IV
+C1257799	Choledochal Cyst, Type V
+C1257806	Chromosomal Instability
+C1257825	Genomic Stability
+C1257826	Chromosome Stability
+C1257840	Aganglionosis, Rectosigmoid Colon
+C1257843	Pseudomembranous colitis
+C1257844	Clostridium Enterocolitis
+C1257845	Enteritis, Pseudomembranous
+C1257847	Hemorrhagic Rectocolitis
+C1257848	Rectocolitis, Ulcerative
+C1257861	Colonic Inertia
+C1257869	Dysentery, Shigella dysenteriae
+C1257870	Dysentery, Shigella flexneri
+C1257871	Dysentery, Shigella boydii
+C1257872	Dysentery, Shigella sonnei
+C1257877	Pheochromocytoma, Extra-Adrenal
+C1257910	Aneuploid Cell
+C1257913	Polyploid Cell
+C1257915	Intestinal Polyposis
+C1257925	Mammary Carcinoma, Animal
+C1257931	Mammary Neoplasms, Human
+C1257958	Glucose Metabolism Disorders
+C1257960	Mannosidase Deficiency Diseases
+C1257963	Endogenous Hyperinsulinism
+C1257964	Exogenous Hyperinsulinism
+C1257965	Compensatory Hyperinsulinemia
+C1258039	Henipavirus Infections
+C1258085	Barrett Epithelium
+C1258104	Diffuse Scleroderma
+C1258215	Ileus
+C1258223	Flavobacteriaceae Infections
+C1258225	Moraxellaceae Infections
+C1258226	Psychobacter Infections
+C1258666	Ganglion cyst
+C1260325	Dendritic Cell Sarcoma, Follicular
+C1260326	Dendritic Cell Sarcoma, Interdigitating
+C1260386	Glucocorticoid-remediable aldosteronism
+C1260396	Alpha thalassemia intermedia
+C1260402	Splenic sequestration
+C1260403	prothrombin gene mutation
+C1260405	frontal dementia
+C1260871	Acetonaemia
+C1260873	Aortic valve disorder
+C1260874	Infective dermatitis
+C1260880	Rhinorrhea
+C1260881	Allergic bronchitis
+C1260883	Mural thrombus of heart
+C1260894	Hypertrophic obesity
+C1260899	Anemia, Diamond-Blackfan
+C1260903	Dysfibrinogenemia
+C1260922	Abnormal breathing
+C1260926	Abnormal pigmentation
+C1260959	Drusen
+C1260962	Megakaryocytes abnormal
+C1260965	Lipoblastoma
+C1261167	Sperm concentration
+C1261175	Pontoneocerebellar hypoplasia
+C1261281	Complications of transplanted kidney
+C1261282	Complications of transplanted liver
+C1261283	Actinomycetoma
+C1261287	Constriction, Pathologic
+C1261322	Investigations
+C1261380	Thoracic spondylosis
+C1261470	Congenital meningocele
+C1261473	Sarcoma
+C1261478	Viral load NOS
+C1261502	Finding of Mean Corpuscular Hemoglobin
+C1261504	Congenital absence of both testes
+C1261958	Respiratory tract infection fungal
+C1261959	Respiratory tract infection bacterial
+C1261962	Gastrointestinal erosion
+C1261965	Haematoma evacuation
+C1261969	Type I hyperlipidaemia
+C1261974	Lymphocyte stimulation test positive
+C1261979	Therapeutic product ineffective
+C1261981	Urticaria localised
+C1262000	Human herpes virus 6 serology positive
+C1262004	Embolic cerebral infarction
+C1262005	Ischaemic cerebral infarction
+C1262006	Bacterial sinusitis
+C1262008	Hyperphosphatasaemia
+C1262010	Post lumbar puncture syndrome
+C1262012	Bacteria urine
+C1262013	Recall phenomenon
+C1262017	Light chain analysis abnormal
+C1262018	Graft failure
+C1262020	Diffuse alveolar damage
+C1262022	Freezing phenomenon
+C1262025	Intraocular pressure test abnormal
+C1262036	Ocular toxicity
+C1262038	Post procedural nausea
+C1262041	Toxicologic test abnormal
+C1262046	Antibody test abnormal
+C1262048	Glial Scar
+C1262060	Post procedural fistula
+C1262063	Platelet function test abnormal
+C1262064	Oculogyration
+C1262070	Mass excision
+C1262087	SUNCT Syndrome
+C1262091	Lymphocytic infiltration
+C1262098	Congenital hyperthyroidism
+C1262102	Blast cell count increased
+C1262104	Urinary tract infection pseudomonal
+C1262105	Urinary tract infection staphylococcal
+C1262109	Procedural hypotension
+C1262113	Lipohypertrophy
+C1262117	Fungal keratitis
+C1262119	Unevaluable event
+C1262130	Unresponsive to pain stimuli
+C1262141	Poor quality sleep
+C1262144	Increased bronchial secretion
+C1262146	Renal salt-wasting syndrome
+C1262147	Scleroderma renal crisis
+C1262148	Grip strength decreased
+C1262150	Vulvar erosion
+C1262156	Herpes simplex serology positive
+C1262162	Oral administration complication
+C1262168	Cholecystitis infective
+C1262170	Herpes dermatitis
+C1262202	Lymphocytic alveolitis
+C1262206	Iliotibial band syndrome
+C1262256	Paranasal cyst
+C1262270	Periorbital contusion
+C1262281	Thrombosis in device
+C1262289	Dysmetabolic syndrome
+C1262296	Testicular infection
+C1262299	Oral papilloma
+C1262313	Invasive Fungal Infections
+C1262477	Weight decreased
+C1262481	Eosinophilic gastroenteritis
+C1262482	Allergic colitis
+C1262485	Electrocardiogram low voltage
+C1262535	Jaundice hepatocellular
+C1262760	Hepatitis, Drug-Induced
+C1262866	Granulocytes abnormal
+C1262886	Osteoprotegerin test
+C1263023	Macroorchidism
+C1263666	Advanced cirrhosis
+C1263722	Chronic metabolic disorder
+C1263726	Sulfatiduria
+C1263733	Uroporphyrinuria
+C1263739	Disorder of organic acid metabolism
+C1263758	Female genital tract infection
+C1263846	Attention Deficit Disorder with Hyperactivity
+C1263853	Paralytic stroke
+C1263855	Lumbar radiculopathy
+C1263857	Peripheral axonal neuropathy
+C1263858	Muscular dystrophy congenital, merosin negative
+C1263885	Neoplasm of cerebrum
+C1263886	Neoplasm of frontal lobe
+C1263887	Neoplasm of temporal lobe
+C1263960	Diabetes with coma (disorder)
+C1263988	Hemolytic disorder
+C1264000	Sickle cell-Hemoglobin O Arab disease
+C1264016	Familial polycythemia vera
+C1264031	Alloimmune thrombocytopenia
+C1264039	von Willebrand Disease, Type 1
+C1264040	von Willebrand Disease, Type 2
+C1264041	von Willebrand Disease, Type 3
+C1264047	Abdominal lymphadenopathy
+C1264190	Follicular non-Hodgkin\'s lymphoma, large cell
+C1264195	Refractory anaemia with ringed sideroblasts
+C1264422	Blister with infection
+C1264606	Persistent infection
+C1264610	Infectious peritonitis
+C1264613	Gastrointestinal infection
+C1264624	Fatal infectious mononucleosis
+C1265730	Progonoma
+C1265769	Multiple aneurysms
+C1265776	Diffuse telangiectasis
+C1265787	Single cyst
+C1265792	Chronic emphysema
+C1265833	Deep abscess
+C1265968	Hyperparakeratosis
+C1265994	Clear cell tumor
+C1265996	Large cell neuroendocrine carcinoma
+C1266002	Non-small cell carcinoma
+C1266005	Basaloid squamous cell carcinoma
+C1266009	Trichilemmocarcinoma
+C1266010	Papillary transitional cell neoplasm of low malignant potential
+C1266018	Hepatocellular carcinoma, scirrhous
+C1266025	Traditional Serrated Adenoma
+C1266029	Enterochromaffin-like cell carcinoid
+C1266032	Atypical carcinoid tumor
+C1266034	Bronchiolo-alveolar carcinoma, non-mucinous
+C1266035	Minimally Invasive Mucinous Lung Adenocarcinoma
+C1266042	Chromophobe Renal Cell Carcinoma
+C1266043	Sarcomatoid Renal Cell Carcinoma
+C1266044	Collecting Duct Carcinoma of the Kidney
+C1266045	Metanephric adenoma
+C1266047	Fetal adenocarcinoma
+C1266050	Poorly Differentiated Thyroid Carcinoma
+C1266051	Papillary microcarcinoma
+C1266065	Eccrine porocarcinoma
+C1266071	Intraductal papillary-mucinous adenoma
+C1266082	Atypical medullary carcinoma
+C1266086	Polymorphous low grade adenocarcinoma
+C1266088	Adenocarcinoma with neuroendocrine differentiation
+C1266089	Metaplastic carcinoma
+C1266090	Hepatoid adenocarcinoma
+C1266091	Thymoma, type A
+C1266095	Thymoma, type B2
+C1266099	Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation
+C1266100	Carcinoma showing thymus-like element
+C1266101	Thymic epithelial tumor
+C1266109	Large cell calcifying Sertoli cell tumor
+C1266118	Cellular fibroma
+C1266119	Solitary fibrous tumor
+C1266121	Myofibroma (morphologic abnormality)
+C1266123	Angiomyofibroblastoma
+C1266127	Histiocytoma, Angiomatoid Fibrous
+C1266128	Ossifying fibromyxoid tumor
+C1266129	Atypical Lipoma
+C1266131	Chondroid lipoma
+C1266134	Spindle cell rhabdomyosarcoma
+C1266136	Gastrointestinal stromal tumor, benign
+C1266138	Benign cystic nephroma
+C1266139	Cystic Partially Differentiated Nephroblastoma
+C1266144	Pleuropulmonary blastoma
+C1266147	Neuroendocrine carcinoma, grade 1
+C1266157	Intratubular malignant germ cells
+C1266158	Nongerminomatous Germ Cell Tumor
+C1266163	Intraosseous well differentiated osteosarcoma
+C1266165	High grade surface osteosarcoma
+C1266166	Intracortical osteosarcoma
+C1266167	Clear cell chondrosarcoma
+C1266168	Malignant tenosynovial giant cell tumor
+C1266175	Parachordoma
+C1266177	Dysembryoplastic neuroepithelial tumor
+C1266178	Gliofibroma
+C1266180	Large cell medulloblastoma
+C1266181	Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos)
+C1266184	Atypical Teratoid Rhabdoid Tumor
+C1266186	Retinoblastoma, spontaneously regressed
+C1266190	Metastatic lymphoma
+C1266194	Hodgkin\'s disease lymphocyte predominance type stage unspecified
+C1266708	Polybrominated biphenyl measurement
+C1268588	Porphyric polyneuropathy
+C1268606	Localized candidiasis
+C1268935	Congenital Thrombotic Thrombocytopenic Purpura
+C1268936	Diarrhea-associated hemolytic uremic syndrome
+C1268937	Diarrhea-negative hemolytic uremic syndrome
+C1268964	Myelodysplastic syndrome, no ICD-O subtype
+C1269683	Depressive Disorder, Major
+C1269684	Skin pigmentation - finding
+C1269955	Tumor invasion
+C1270972	Mild cognitive disorder
+C1271100	Lower limb spasticity
+C1271104	Blood pressure finding
+C1271219	Congenital ectopic pupil
+C1271398	Pigment dispersion syndrome
+C1272092	Impaired fasting glucose
+C1272174	Scotopic sensitivity
+C1272321	Autoantibody measurement
+C1272348	Disorder of vitamin B12
+C1272352	Deficiency of vitamin D3
+C1272641	Systemic arterial pressure
+C1272654	Wound treatment
+C1272657	Secondary angle-closure glaucoma - synechial
+C1272677	Benign mixed epithelial and stromal tumor of kidney
+C1273957	Upper limb spasticity
+C1273976	First myocardial infarction
+C1274103	Oncogenic osteomalacia
+C1274161	Lupus erythematosus overlap syndrome
+C1274167	IgA pemphigus
+C1274215	Autosomal recessive ichthyosis
+C1274216	Punctate palmoplantar keratoderma
+C1274224	Inherited epidermolysis bullosa
+C1274228	Chylomicronemia syndrome
+C1274233	T-lymphocyte immunodeficiency
+C1274282	Acral pseudolymphomatous angiokeratoma of children (APACHE)
+C1274310	Primary cutaneous B-cell lymphoma
+C1274320	Recurrent herpes simplex infection of eye
+C1274323	Recurrent genital herpes simplex
+C1274355	Streptococcal infection of skin
+C1274400	Primary Cutaneous Nocardiosis
+C1274408	Chronic plaque-like oral candidiasis
+C1274528	Mycetoma due to Madurella mycetomatis
+C1274594	Lichenoid actinic keratosis
+C1274648	Segmental vitiligo
+C1274743	Hyperhidrosis Palmaris Et Plantaris
+C1274789	Ligneous conjunctivitis
+C1274865	Scleroderma-like secondary cutaneous sclerosis
+C1274879	Port-wine stain with oculocutaneous melanosis
+C1274925	Skin-ache syndrome
+C1274933	Drug-Induced Stevens Johnson Syndrome
+C1274999	Skin flap necrosis
+C1275047	Radiation-induced xerostomia
+C1275074	Odonto-onycho-dermal dysplasia
+C1275078	Acrocephalopolysyndactyly type 2
+C1275081	Cardio-facio-cutaneous syndrome
+C1275091	Ichthyosis follicularis with alopecia and photophobia (IFAP)
+C1275114	Epidermolysis Bullosa Pruriginosa
+C1275122	Familial multiple trichoepitheliomata
+C1275125	Inherited disorder of porphyrin metabolism
+C1275126	TNF receptor-associated periodic fever syndrome (TRAPS)
+C1275128	Autosomal recessive hyperimmunoglobulin M syndrome
+C1275155	Multiple basal cell papillomata
+C1275217	Paget\'s disease of vulva
+C1275273	Familial Multiple Lipomatosis
+C1275275	Spindle cell liposarcoma
+C1275277	Soft tissue chondroma
+C1275278	Extraskeletal Myxoid Chondrosarcoma
+C1275282	Low-grade fibromyxoid sarcoma
+C1275321	Primary cutaneous marginal zone B-cell lymphoma
+C1275336	Hashimoto-Pritzker syndrome
+C1275345	Familial mastocytosis
+C1275417	Non-involuting congenital hemangioma
+C1275419	Desmoplastic spindle and epithelioid cell melanocytic nevus of skin
+C1275421	Rapidly involuting congenital hemangioma
+C1275465	Tumor stage mycosis fungoides
+C1275592	Funisitis
+C1275668	Melanotic medulloblastoma
+C1275684	Meibomian gland dysfunction
+C1275685	Avellino corneal dystrophy
+C1275718	Granulomatous rosacea
+C1275808	Congenital central hypoventilation
+C1275836	D - transposition of the great vessels
+C1275859	Transitional cell dysplasia
+C1276004	Bilateral superior oblique palsy
+C1276035	Pena-Shokeir syndrome type I
+C1276070	Infantile atopic dermatitis
+C1276071	Childhood atopic dermatitis
+C1276072	Adult atopic dermatitis
+C1276092	Chronic hand eczema
+C1276127	Sporadic porphyria cutanea tarda
+C1276146	Cutaneous lymphoma
+C1277187	Left ventricular systolic dysfunction
+C1277241	Delayed myelination
+C1277579	At risk of osteoporosis
+C1277709	Transferrin saturation measurement
+C1278049	Serum gamma-glutamyl transferase measurement
+C1278267	Nitrite urine present
+C1278536	Transient myocardial ischemia
+C1278797	Postnatal infection
+C1279264	Genitourinary tract infection NOS
+C1279265	Laboratory animal dander allergy (disorder)
+C1279296	Chronic leukaemia
+C1279376	Inflammatory abdominal aortic aneurysm
+C1279386	Postoperative pneumonia
+C1279412	periodic paralysis (finding)
+C1279420	Anxiety neurosis (finding)
+C1279481	X-Linked Combined Immunodeficiency Diseases
+C1279621	Tinea profunda (disorder)
+C1279945	Acute interstitial pneumonia
+C1280008	Abdominal angina
+C1280433	Lipoatrophy
+C1280469	Podoconiosis
+C1280473	Arteriovenous fistula operation
+C1280627	Cerebral haemorrhage neonatal
+C1280798	Von Willebrand disease, platelet type
+C1281300	Vascular degeneration
+C1281440	Familial obesity
+C1281901	Fatty acid measurement
+C1281914	Corneal allograft rejection
+C1281931	Nasolacrimal Duct Obstruction
+C1282227	Postoperative endophthalmitis
+C1282241	Sterile keratitis
+C1282359	Ocular Cicatricial Pemphigoid
+C1282365	Mixed type cataract
+C1282496	Metastasis from malignant tumor of prostate
+C1282609	Granulocytosis
+C1282799	Penile swelling
+C1282908	De Vaal\'s syndrome
+C1282921	Cotard's syndrome
+C1282951	Type 2 diabetes mellitus in nonobese
+C1282952	Enthesitis
+C1282968	von Willebrand Disease, Type 2A
+C1282971	von Willebrand Disease, Type 2B
+C1282974	von Willebrand disease type 2M
+C1282975	von Willebrand Disease, Type 2N
+C1282979	Transient hypoparathyroidism
+C1283048	Iron binding capacity total measurement
+C1283400	Butyrylcholinesterase deficiency
+C1283601	Deficiency of sulfatase
+C1283620	Sucrase-isomaltase deficiency, congenital
+C1283723	Deficiency of cathepsin C
+C1285162	Degenerative disorder
+C1285261	Fetal Nutrition Disorders
+C1285291	Fetal ascites
+C1285373	Respiratory disorder neonatal
+C1285498	Vegetation
+C1285577	Acute confusional state
+C1285654	Memory performance
+C1286370	Finding of odor of urine
+C1287298	Urine output
+C1288283	Atrophoderma maculatum
+C1290049	Plaque morphea
+C1290071	Oral mucosal disorder
+C1290073	Acute mucositis
+C1290140	Post-streptococcal reactive arthritis
+C1290161	Bursitis infective NOS
+C1290162	Disorder of smooth muscle
+C1290310	Neoplasm of back
+C1290332	Pharyngeal ulceration
+C1290344	Nonspecific interstitial pneumonia
+C1290386	Chronic heart disease
+C1290398	Cerebral arterial aneurysm
+C1290508	Abnormal number of teeth
+C1290511	Anodontia of Permanent Dentition
+C1290514	Familial hypodontia
+C1290537	Amelogenesis imperfecta pigmented hypomaturation type
+C1290587	Failure of tooth eruption
+C1290590	Hyperplastic tooth follicle
+C1290708	Osteomyelitis of mandible
+C1290785	Palatal disorder
+C1290807	Diarrheal disorder
+C1290854	Disorder of skull
+C1290857	Disorder of face
+C1290865	Abdominal wall disorder
+C1290871	Disorder of hand
+C1290884	Inflammatory disorder
+C1290886	Chronic inflammatory disorder
+C1290981	Body temperature abnormal
+C1290999	Froment's sign
+C1291045	Abnormal peristalsis
+C1291077	Abdominal bloating
+C1291078	Epigastric discomfort
+C1291163	Increased histidine
+C1291230	3-Hydroxyacyl-CoA Dehydrogenase Deficiency
+C1291245	Cortisone reductase deficiency
+C1291266	Deficiency of aldehyde oxidase
+C1291299	Deficiency of iodide peroxidase (disorder)
+C1291311	Deficiency of dehydrogenase
+C1291312	Deficiency of oxidase
+C1291314	Deficiency of monooxygenase
+C1291316	Deficiency of reductase
+C1291317	Deficiency of transferase
+C1291329	Transaldolase Deficiency
+C1291373	Deficiency of sedoheptulokinase
+C1291386	D-glycericacidemia
+C1291390	Deficiency of phosphorylase kinase
+C1291401	Phosphoribosylpyrophosphate synthetase deficiency
+C1291422	Deficiency of 3-oxoacid CoA-transferase
+C1291447	Deficiency of triacylglycerol lipase
+C1291463	Deficiency of phosphoserine phosphatase
+C1291490	Hyaluronidase Deficiency
+C1291512	Beta-Ureidopropionase Deficiency
+C1291557	Deficiency of lyase
+C1291560	Deficiency of glutamate decarboxylase
+C1291564	Deficiency of aromatic-L-amino-acid decarboxylase
+C1291575	Deficiency of citrate(si)-synthase
+C1291601	Deficiency of isomerase
+C1291607	Deficiency of maleylacetoacetate isomerase
+C1291609	Ribose 5-Phosphate Isomerase Deficiency
+C1291610	Deficiency of mannose-6-phosphate isomerase
+C1291611	Deficiency of glucose-6-phosphate isomerase
+C1291620	Deficiency of bisphosphoglycerate mutase
+C1292120	Extramedullary erythropoiesis
+C1292203	Landsteiner-Wiener phenotype
+C1292231	In(Lu) phenotype (finding)
+C1292753	Primary Effusion Lymphoma
+C1292754	Mediastinal (Thymic) Large B-Cell Lymphoma
+C1292758	Precursor T-cell lymphoblastic lymphoma
+C1292769	B-cell type acute leukaemia
+C1292771	Chronic myelogenous leukemia, BCR/ABL positive
+C1292772	Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
+C1292773	Acute myeloid leukemia with multilineage dysplasia
+C1292774	Acute myeloid leukemia, t(8;21) (q22;q22)
+C1292775	Acute myeloid leukemia, 11q23 abnormalities
+C1292776	Therapy-related acute myeloid leukemia and myelodysplastic syndrome
+C1292777	Aggressive natural killer-cell leukemia
+C1292778	Chronic myeloproliferative disorder
+C1292779	Myelodysplastic Syndrome with Isolated del(5q)
+C1292780	Therapy-related myelodysplastic syndrome
+C1295176	Leptin measurement
+C1295585	Decreased vibratory sense
+C1295643	Increased estradiol level
+C1295654	Decreased testosterone level
+C1295665	Thyroxine increased
+C1295666	Thyroxine decreased
+C1295668	Tri-iodothyronine increased
+C1295669	Tri-iodothyronine decreased
+C1295677	Increased glucagon level
+C1297882	Partial Trisomy
+C1297883	Radial scar
+C1298180	Single tumor
+C1298680	Occlusive stroke
+C1298681	Oxalosis
+C1298682	Shoulder arthritis
+C1298684	Autistic spectrum disorder with isolated skills
+C1298685	Chronic pain syndrome
+C1298692	Cleft lip and alveolus
+C1298695	Hypoplasia of optic disc
+C1298714	Congenital pelviureteric junction obstruction
+C1298820	Aneurysm of aortic root
+C1299240	Carcinoma of supraglottis
+C1299247	Primary malignant neoplasm of ovary and other uterine adnexa
+C1299262	Sarcoma - category (morphologic abnormality)
+C1299432	Multi vessel coronary artery disease
+C1299433	Left main coronary artery disease
+C1299539	Scrotal infection
+C1299567	Neonatal stroke
+C1299614	Non-insulin-dependent diabetes mellitus with unspecified complications
+C1299624	Postural Orthostatic Tachycardia Syndrome
+C1299694	Glaucomatous visual field defect
+C1299802	Tumor excision NOS
+C1299884	Eosinophilic myositis (disorder)
+C1300127	Perivascular Epithelioid Cell Neoplasms
+C1300202	Diaphyseal medullary stenosis with bone malignancy
+C1300256	Thanatophoric dysplasia, type 1
+C1300257	Thanatophoric dysplasia, type 2
+C1300267	Brachydactyly syndrome type B
+C1300268	Brachydactyly syndrome type C
+C1300346	Desmoplastic fibroblastoma
+C1300347	Atypical polypoid adenomyoma
+C1300585	Small cell carcinoma of prostate
+C1300682	Acute and chronic colitis
+C1300818	Necrotic tumor
+C1301034	Pancreatic intraepithelial neoplasia
+C1301145	Mast cell malignancy
+C1301149	Mast cell abnormality
+C1301193	Mucoepidermoid carcinoma, high grade
+C1301194	Salivary duct carcinoma
+C1301355	Myelodysplastic-Myeloproliferative Diseases
+C1301356	Refractory cytopenia with multilineage dysplasia and ringed sideroblasts
+C1301359	Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma
+C1301361	Post-transplant lymphoproliferative disorder, polymorphic
+C1301362	Primary Cutaneous Anaplastic Large Cell Lymphoma
+C1301363	Blastic plasmacytoid dendritic cell neoplasm
+C1301365	Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease
+C1301509	Severe visual impairment
+C1301510	Moderate visual impairment
+C1301624	Contraindication to medical treatment
+C1301700	Cardiovascular morbidity
+C1301721	Neurological morbidity
+C1301752	Respiratory morbidity
+C1301797	Induced hypothermia (finding)
+C1301937	Talipes
+C1301959	Bulbar weakness
+C1302363	Dysplasia of colon
+C1302392	Adenoma of small intestine
+C1302401	Adenoma of large intestine
+C1302454	Complex atypical endometrial hyperplasia
+C1302476	Necrotic melanoma
+C1302547	Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
+C1302645	Polyp of small intestine
+C1302652	Adenoma of rectum
+C1302746	Melanocytic neoplasm
+C1302772	Primary cutaneous lymphoma
+C1302773	Low Grade Squamous Intraepithelial Neoplasia
+C1302790	Congenital malformation syndrome
+C1302793	Cutaneous vascular malformation
+C1302808	Myopericytoma
+C1302995	Congenital Fibrosis of the Extraocular Muscles
+C1302999	Ankyloblepharon filiforme adnatum
+C1303001	Congenital euryblepharon
+C1303003	Epicanthus inversus
+C1303004	Epicanthus palpebralis
+C1303007	Brushfield spots
+C1303009	Microcoria, congenital
+C1303010	Mydriasis, Congenital
+C1303073	Nicolaides Baraitser syndrome
+C1303076	Tortuous carotid artery
+C1303192	Vertebroplasty
+C1304114	Generalized eczema
+C1304119	Chronic stable plaque psoriasis
+C1304134	Early onset psoriasis type 1
+C1304136	Onset of psoriasis in childhood (1-10 years)
+C1304140	Familial psoriasis
+C1304147	Retention hyperkeratosis
+C1304191	Autoimmune urticaria
+C1304300	Skin Nodular Basal Cell Carcinoma
+C1304306	Metastatic basal cell carcinoma
+C1304321	Eruptive melanocytic nevi
+C1304345	Occupational irritant contact dermatitis
+C1304456	Congo hemorrhagic fever
+C1304469	Localized vitiligo
+C1304470	Generalized vitiligo
+C1304508	Spindle cell hemangioma
+C1304517	Extrarenal rhabdoid tumor
+C1304641	Eye excision
+C1304746	RDW - Red blood cell distribution width result
+C1305122	Thoracoabdominal aortic aneurysm, ruptured
+C1305147	Congenital supravalvular aortic stenosis
+C1305215	Forearm fracture
+C1305409	Atypical adenoma
+C1305420	Prominent ear
+C1305740	Overbite
+C1305742	Oxygen consumption
+C1305855	Body mass index
+C1305866	Weight
+C1305868	Fibrinolysis
+C1305904	Familial hematuria
+C1305968	Eccrine dermal cylindroma
+C1306050	Primary malignant neoplasm of appendix
+C1306063	Acute left ventricular failure
+C1306065	DEVELOPMENTAL DYSPLASIA OF THE HIP 1
+C1306067	Drug-induced paranoid state
+C1306068	After-cataract
+C1306122	Oguchi disease
+C1306214	ACTH-Secreting Pituitary Adenoma
+C1306229	Dyschromatosis universalis
+C1306242	Aggressive angiomyxoma
+C1306247	Melanotic neurilemmoma
+C1306339	Mental retardation severity unspecified
+C1306341	Mental disability
+C1306459	Primary malignant neoplasm
+C1306460	Primary malignant neoplasm of lung
+C1306503	Congenital exomphalos
+C1306557	Chronic venous insufficiency
+C1306571	Hepatic Insufficiency
+C1306577	Death
+C1306587	Acute encephalopathy
+C1306589	Congenital dyserythropoietic anemia, type II
+C1306600	Radial nerve palsy
+C1306710	Facial asymmetry
+C1306726	Congenital naevus
+C1306759	Eosinophilic disorder
+C1306792	Red man syndrome
+C1306794	Wound Botulism
+C1306837	Papillary Renal Cell Carcinoma
+C1306839	Pyrophosphate arthritis
+C1306856	Megaloblastic anemia due to inborn errors of metabolism
+C1306857	Hyperglobulinemia
+C1306889	Peripheral arterial occlusive disease
+C1313885	Hereditary edema of legs
+C1313921	Urinoma
+C1313952	Respiration intermittent
+C1313961	Trichorrhexis nodosa syndrome
+C1313969	Hearing difficulty
+C1314691	Age at menarche
+C1314694	Astrocytoma, low grade
+C1317785	Tooth size discrepancy
+C1318020	Stromal keratitis
+C1318035	Platelet distribution width result
+C1318233	immunoglobulin G index
+C1318312	Serum iron measurement
+C1318315	Serum zinc measurement
+C1318500	Non-toxic nodular goiter
+C1318518	Infantile malignant osteopetrosis
+C1318520	Necrotizing vasculitis
+C1318533	Secondary polycythemia
+C1318541	Sertoli-Leydig cell tumor of intermediate differentiation
+C1318543	Fibrous histiocytoma of tendon sheath
+C1318544	M5b Acute differentiated monocytic leukemia
+C1318550	Refractory anemia with excess blasts I
+C1318551	Refractory anemia with excess blasts II
+C1318558	Congenital melanocytic nevus
+C1318660	Anti-cyclic citrullinated peptide antibody level
+C1318711	Herpes simplex type 1 infection
+C1318881	Vancomycin intermediate staphylococcus aureus infection
+C1318973	Staphylococcus aureus infection
+C1319016	Nephrogenic rest, intralobar
+C1319017	Nephrogenic rest, perilobar
+C1319018	Asthmatic bronchitis
+C1319193	Infection due to vancomycin resistant Staphylococcus aureus
+C1319200	Postoperative confusion
+C1319296	Pediatric human immunodeficiency virus infection
+C1319300	Nephroblastoma, favorable histology
+C1319314	Transitional cell carcinoma of kidney
+C1319315	Adenocarcinoma of large intestine
+C1319317	Squamous cell carcinoma of pharynx
+C1319384	Upper airway resistance syndrome
+C1319466	Barber Say syndrome
+C1319851	MRI brain abnormal
+C1319853	Asthma, Aspirin-Induced
+C1319860	Sendai virus infection
+C1320214	Invasive Streptococcus pneumoniae disease
+C1320453	Cervical Squamous Cell Carcinoma In Situ
+C1320468	Nephrogenic rest
+C1320471	Mesoblastic nephroma, cellular
+C1320474	Nuchal Rigidity
+C1320638	Bone marrow myeloid dysplasia
+C1320640	Peripheral degeneration of retina
+C1320657	Diabetes type
+C1320834	Drug-induced Hepatic Necrosis
+C1321133	Bronchial hemorrhage
+C1321275	Non-specific colitis
+C1321313	Astrocytic hamartoma
+C1321324	Bruns nystagmus
+C1321329	Slowed saccades
+C1321422	Monoblastic leukemia
+C1321427	Epithelioid Malignant Peripheral Nerve Sheath Tumor
+C1321489	Torre-Muir syndrome
+C1321546	Anaplastic large B-cell lymphoma
+C1321547	T-cell/histiocyte rich large B-cell lymphoma
+C1321551	Shprintzen-Goldberg syndrome
+C1321581	Bezoar
+C1321686	Faecaloma
+C1321756	Achalasia
+C1321757	Histiocytic leukemia
+C1321780	Hypomagnesmic tetany
+C1321782	Gestosis
+C1321809	HYPOTHYROIDISM, GOITROUS
+C1321869	Pediatric Intraocular Retinoblastoma
+C1321871	childhood acute myeloid leukemia/other myeloid malignancies
+C1321872	Stage IV Skin Melanoma
+C1321878	Desmoplastic infantile ganglioglioma
+C1321884	Atresia of vagina
+C1321898	Blood in stool
+C1321905	Minimal Brain Dysfunction
+C1321907	Congenital absence of parathyroid gland
+C1322252	Chordoid Glioma of the Third Ventricle
+C1322253	Eczema infected
+C1322281	Rhinitis seasonal
+C1322286	Thymoma, type C
+C1323099	sympathomimetic disorder
+C1323189	Dermatitis infected
+C1325847	Sensitisation
+C1327709	Rectosigmoid cancer
+C1327915	Congenital amegakaryocytic thrombocytopenia
+C1327916	REVESZ SYNDROME (disorder)
+C1327918	Oculootoradial syndrome
+C1327919	Myelocerebellar Disorder
+C1327920	Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
+C1328061	Myelodysplastic/myeloproliferative neoplasm, unclassifiable
+C1328252	Leishmaniasis, Mucocutaneous
+C1328286	Frothing at mouth
+C1328289	Bladder tamponade
+C1328291	Dysaesthesia pharynx
+C1328308	Increased upper airway secretion
+C1328315	Hypercreatininaemia
+C1328320	Multiple drug overdose accidental
+C1328321	Multiple drug overdose intentional
+C1328324	Nasal cavity mass
+C1328325	Pharyngeal erosion
+C1328327	Gastrooesophageal sphincter insufficiency
+C1328330	Biliary anastomosis complication
+C1328331	Social stay hospitalization
+C1328332	Procedural hypertension
+C1328337	Urethritis noninfective
+C1328339	Dennie-Morgan fold
+C1328348	Mitochondrial hepatopathy
+C1328349	Neuropathy ataxia and retinis pigmentosa
+C1328353	Infective spondylitis
+C1328355	Laryngoonychocutaneous syndrome
+C1328358	Pedal pulse decreased
+C1328361	Low turnover osteopathy
+C1328364	Analgesic asthma syndrome
+C1328374	Laryngitis bacterial
+C1328375	Application site discomfort
+C1328376	Injection site scab
+C1328379	Bronchoalveolar lavage abnormal
+C1328380	Acute right ventricular failure
+C1328383	Listeria sepsis
+C1328390	Viral mutation identified
+C1328393	Pregnancy with implant contraceptive
+C1328396	Pregnancy with contraceptive device
+C1328397	Transaminases abnormal
+C1328407	Acetabular dysplasia
+C1328408	Pharmaceutical product counterfeit
+C1328409	Propofol syndrome
+C1328411	Post procedural haematoma
+C1328419	Hydroxyproline increased
+C1328437	Amino acid level increased
+C1328440	Abnormality of amino acid metabolism
+C1328447	Brain stem syndrome
+C1328449	CD4 lymphocytes increased
+C1328457	Viral DNA test positive
+C1328461	Interleukin level increased
+C1328479	Carcinoma, Islet Cell
+C1328504	Hormone refractory prostate cancer
+C1328519	Retinal pigment epithelial tear
+C1328544	Tubular breast carcinoma
+C1328587	Panhypogammaglobulinemia
+C1328618	Agraphesthesia
+C1328840	Autoimmune Lymphoproliferative Syndrome
+C1328843	Autoimmune vasculitis
+C1328931	Multiple lentigines
+C1330966	Developmental Academic Disability
+C1331107	Arterial graft
+C1332051	AIDS-Related Non-Hodgkin Lymphoma
+C1332059	AIDS-Related Primary Effusion Lymphoma
+C1332078	Anaplastic large cell lymphoma, ALK negative
+C1332079	Anaplastic Large Cell Lymphoma, ALK-Positive
+C1332140	Acrofacial Dysostosis
+C1332146	Acute Adult T-Cell Leukemia/Lymphoma
+C1332153	Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome
+C1332156	Acute myelomonocytic leukemia with abnormal eosinophils
+C1332166	Adenocarcinoma of the gastroesophageal junction
+C1332167	Adenoid cystic breast carcinoma
+C1332171	Thymic Adenosquamous Carcinoma
+C1332182	Adult Anaplastic Large Cell Lymphoma
+C1332183	adult astrocytic tumors
+C1332200	Adult Diffuse Astrocytoma
+C1332201	Adult Diffuse Large B-Cell Lymphoma
+C1332206	Adult Lymphoma
+C1332212	Adult B Lymphoblastic Lymphoma
+C1332213	Adult T Lymphoblastic Lymphoma
+C1332218	Adult Type Ovarian Granulosa Cell Tumor
+C1332219	Adult Kidney Wilms Tumor
+C1332225	Aggressive Non-Hodgkin Lymphoma
+C1332228	Alcohol-Related Hepatocellular Carcinoma
+C1332243	Adenocarcinoma of ampulla of Vater
+C1332271	Perianal Squamous Intraepithelial Neoplasia
+C1332293	Angiofollicular Lymphoid Hyperplasia, Hyaline-Vascular Type
+C1332309	Anti-Basement Membrane Glomerulonephritis
+C1332314	Breast Apocrine Adenosis
+C1332316	Apocrine breast carcinoma
+C1332338	Asbestos-Related Malignant Mesothelioma
+C1332345	Atypical Adenomatous Lung Hyperplasia
+C1332347	Atypical Ductal Breast Hyperplasia
+C1332355	Autoimmune Hepatitis with Centrilobular Necrosis
+C1332442	BRCA1 Syndrome
+C1332460	Barrett\'s Adenocarcinoma
+C1332517	Benign Soft Tissue Tumor of Uncertain Differentiation
+C1332556	Biphasic Pulmonary Blastoma
+C1332575	Bone Epithelioid Hemangioma
+C1332578	Haemangioma of bone
+C1332582	Primary Lymphoma of Bone
+C1332591	Bone Surface (Peripheral) Osteosarcoma
+C1332608	Astrocytoma of brain stem
+C1332610	Brain Stem Glioblastoma
+C1332629	Breast Fibrocystic Change, Proliferative Type
+C1332632	Breast Liposarcoma
+C1332633	Breast Mucosa-Associated Lymphoid Tissue Lymphoma
+C1332655	C3 DEFICIENCY
+C1332833	Calcifying Fibrous Pseudotumor
+C1332849	Cardiac Lipoma
+C1332850	Cardiac Lymphoma
+C1332851	Cardiac Paraganglioma
+C1332852	Cardiac rhabdomyoma
+C1332860	Cauda Equina Paraganglioma
+C1332866	Adenocarcinoma of cecum
+C1332884	Central nervous system leukaemia
+C1332888	Central nervous system melanoma
+C1332899	Cerebellar Glioblastoma
+C1332900	Cerebellar hemangioblastoma
+C1332913	Cervical Endometrioid Adenocarcinoma
+C1332922	Cervical Squamous Intraepithelial Neoplasia
+C1332942	Childhood Anaplastic Large Cell Lymphoma
+C1332951	Childhood Brain Stem Neoplasm
+C1332965	Congenital Mesoblastic Nephroma
+C1332967	Childhood Diffuse Large B-Cell Lymphoma
+C1332969	Childhood Ganglioglioma
+C1332977	Childhood Leukemia
+C1332979	Childhood Lymphoma
+C1332986	Childhood Osteosarcoma
+C1332995	Childhood Pilocytic Astrocytoma
+C1332996	Childhood B Lymphoblastic Lymphoma
+C1332998	Childhood T Lymphoblastic Lymphoma
+C1333001	Childhood Renal Cell Carcinoma
+C1333003	Childhood Kidney Neoplasm
+C1333015	Childhood Kidney Wilms Tumor
+C1333032	Chronic Adult T-Cell Leukemia/Lymphoma
+C1333034	Chronic Cancer Pain
+C1333043	Chronic Myelomonocytic Leukemia-1
+C1333046	Myeloproliferative Neoplasm, Unclassifiable
+C1333063	Classical Burkitt Lymphoma
+C1333064	Classical Hodgkin\'s Lymphoma
+C1333067	Clear Cell Hepatocellular Carcinoma
+C1333071	Chordoma of clivus
+C1333084	Colon Neuroendocrine Tumor G1
+C1333085	Colon Carcinoma Metastatic in the Liver
+C1333088	Colonic hamartomatous polyps
+C1333096	Colon Mucosa-Associated Lymphoid Tissue Lymphoma
+C1333112	Colorectal Intraepithelial Neoplasia
+C1333117	Colorectal Tubular Adenoma
+C1333119	Colorectal Villous Adenoma
+C1333148	Conjunctival intraepithelial neoplasia
+C1333160	Lipoma of corpus callosum
+C1333171	Primary Cutaneous Follicle Center Lymphoma
+C1333172	Cutaneous Follicular Lymphoma
+C1333177	Lymphoproliferative Disorder of the Skin
+C1333190	Cystic Neoplasm
+C1333275	Dermal Fibroma
+C1333280	Desmoplastic melanoma
+C1333286	Diencephalic Neoplasm
+C1333292	Diffuse infiltrative lymphocytosis syndrome
+C1333294	ALK positive large B-cell lymphoma
+C1333295	Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type
+C1333296	Activated B-cell type diffuse large B-cell lymphoma
+C1333306	Distal-Type Epithelioid Sarcoma
+C1333324	Barretts esophagus with dysplasia
+C1333383	Encapsulated Thymoma
+C1333394	Endometrial intraepithelial neoplasia
+C1333396	Endometrial Squamous Cell Carcinoma
+C1333419	Liver and Intrahepatic Bile Duct Epithelial Neoplasm
+C1333430	EBV-Related Hodgkin Lymphoma
+C1333431	EBV-Related Lymphoma
+C1333443	Esophageal Basaloid Carcinoma
+C1333460	Esophageal Melanoma
+C1333468	Esophageal Squamous Intraepithelial Neoplasia
+C1333482	Exaggerated placental site
+C1333500	Extragastrointestinal Gastrointestinal Stromal Tumor
+C1333600	Hereditary Malignant Neoplasm
+C1333620	Flat Ductal Epithelial Atypia of the Breast
+C1333762	Gastric Cardia Adenocarcinoma
+C1333763	Gastric Cardia Carcinoma
+C1333768	Gastric Gastrointestinal Stromal Tumor
+C1333774	Gastric Inflammatory Myofibroblastic Tumor
+C1333782	Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
+C1333786	Gastric Precancerous Condition
+C1333789	Gastric Squamous Cell Carcinoma
+C1333791	Tubular adenocarcinoma gastric
+C1333813	Central Nervous System Germinoma
+C1333855	Grade 3 Colon Adenocarcinoma
+C1333856	Grade 3 Colorectal Adenocarcinoma
+C1333860	Grade 2 Colorectal Adenocarcinoma
+C1333866	Grade 1 Colon Adenocarcinoma
+C1333869	Pancreatic Intraepithelial Neoplasia-1
+C1333878	B-cell lymphoma unclassifiable with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma
+C1333940	Head and Neck Basaloid Carcinoma
+C1333944	Paraganglioma of head and neck
+C1333947	Heavy Chain Deposition Disease
+C1333955	Central Nervous System Hemangioblastoma
+C1333962	Hepatic Angiomyolipoma
+C1333963	Liver Neuroendocrine Tumor
+C1333964	Liver Dysplastic Nodule
+C1333967	Inflammatory pseudotumor of liver
+C1333971	Mesenchymal hamartoma of liver
+C1333976	Liver and Intrahepatic Bile Duct Neoplasm
+C1333977	Hepatitis B Virus-Related Hepatocellular Carcinoma
+C1333978	Hepatitis C Virus-Related Hepatocellular Carcinoma
+C1333979	Hepatitis Virus-Related Hepatocellular Carcinoma
+C1333984	Hepatosplenic T-cell lymphoma
+C1333985	Hereditary Clear Cell Renal Cell Carcinoma
+C1333987	Hereditary Glomangioma
+C1333989	Familial meningioma
+C1333990	Hereditary Nonpolyposis Colorectal Cancer
+C1333991	Hereditary Non-Polyposis Colon Cancer Type 2
+C1333992	Hereditary Ovarian Carcinoma
+C1333993	Hereditary Paraganglioma
+C1334003	Barretts esophagus with high grade dysplasia
+C1334011	High Grade Cervical Intraepithelial Neoplasia
+C1334015	High Grade Intraepithelial Neoplasia
+C1334030	Histiocytic and Dendritic Cell Neoplasm
+C1334054	Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma
+C1334170	Indolent Non-Hodgkin Lymphoma
+C1334177	Infiltrating Cervical Carcinoma
+C1334206	Intermediate Grade Ductal Breast Carcinoma In Situ
+C1334222	Intermediate Risk Gastrointestinal Stromal Tumor
+C1334228	Intestinal Graft Versus Host Disease
+C1334240	Intracranial Germinoma
+C1334243	Intracranial Melanoma
+C1334246	Intracranial Embryonal Tumor, Not Otherwise Specified
+C1334260	Intramuscular Myxoma
+C1334261	Intraorbital Meningioma
+C1334266	Intraurothelial Neoplasia
+C1334271	Intraventricular Meningioma
+C1334272	Invasive Apocrine Breast Carcinoma
+C1334274	Invasive Carcinoma
+C1334281	Infiltrating Bladder Urothelial Carcinoma
+C1334282	Inverted urothelial papilloma
+C1334363	Large Cell Lung Neuroendocrine Carcinoma
+C1334386	Meningeal melanoma
+C1334402	Lipomatous hemangiopericytoma
+C1334407	Localized Carcinoma
+C1334410	Localized Primitive Neuroectodermal Tumor
+C1334411	Locally Metastatic Malignant Neoplasm
+C1334413	Low Grade Ductal Breast Carcinoma In Situ
+C1334415	Low Grade Gastric Intraepithelial Neoplasia
+C1334419	Low Grade Sarcoma
+C1334452	Neuroendocrine neoplasm of lung
+C1334455	Pulmonary Sclerosing Hemangioma
+C1334466	Lymphomatous Adult T-Cell Leukemia/Lymphoma
+C1334603	Malignant Mixed Mesodermal (Mullerian) Tumor
+C1334614	Prolactin-Producing Pituitary Gland Carcinoma
+C1334615	Malignant Phyllodes Tumor of Prostate
+C1334620	Malignant Smooth Muscle Neoplasm
+C1334631	Intraductal proliferative breast lesion
+C1334633	Mature B-Cell Neoplasm
+C1334634	Mature B-Cell Non-Hodgkin Lymphoma
+C1334647	Maxillary Sinus Squamous Cell Carcinoma
+C1334655	Mediastinal Germ Cell Tumor
+C1334665	Mediastinal Lymphoma
+C1334680	Mediastinal seminoma
+C1334682	Mediastinal teratoma
+C1334687	Megakaryocytic Neoplasm
+C1334688	Megaloblastic erythroid hyperplasia
+C1334695	Meningeal Gliomatosis
+C1334699	Mesenchymal Cell Neoplasm
+C1334708	Metaplastic breast carcinoma
+C1334720	Metastatic Malignant Peripheral Nerve Sheath Tumor
+C1334753	Breast Microglandular Adenosis
+C1334763	Midgut Carcinoid Tumor
+C1334776	Soft Tissue Tumor of Uncertain Differentiation
+C1334781	Mixed Cell Type Gastrointestinal Stromal Tumor
+C1334798	Monomorphic Post-Transplant Lymphoproliferative Disorder
+C1334801	Monophasic Synovial Sarcoma
+C1334804	Motor Manifestations
+C1334807	Mucinous carcinoma of breast
+C1334811	Mucinous neoplasm
+C1334814	Thymic Mucoepidermoid Carcinoma
+C1334815	Multi-centric Castleman\'s Disease
+C1334820	Multifocal osteosarcoma
+C1334920	Adenocarcinoma of the nasal cavity
+C1334953	Neuroblastic tumors
+C1334956	Neuroepithelial, Perineurial, and Schwann Cell Neoplasm
+C1334963	Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
+C1334968	Nodular Lymphocyte Predominant Hodgkin Lymphoma
+C1334970	Medulloblastoma with extensive nodularity
+C1334971	Nodular Neoplasm
+C1334978	Non-Hereditary Clear Cell Renal Cell Carcinoma
+C1335029	Non-Neoplastic Peripheral Nervous System Disorder
+C1335051	Non-Neoplastic Urinary System Disorder
+C1335060	Non-Small Cell Adenocarcinoma
+C1335101	Occupational Malignant Neoplasm
+C1335103	Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma
+C1335107	Olfactory Groove Meningioma
+C1335110	Oligodendroglial Neoplasm
+C1335113	Opisthorchis Viverrini-Related Cholangiocarcinoma
+C1335114	Optic Nerve Astrocytoma
+C1335146	Osteogenic Neoplasm
+C1335167	Ovarian Mucinous Adenocarcinoma
+C1335168	Ovarian mucinous tumor
+C1335177	Ovarian Serous Adenocarcinoma
+C1335184	Ovarian Transitional Cell Carcinoma
+C1335299	Pancreatic Adenosquamous Carcinoma
+C1335302	Pancreatic Ductal Adenocarcinoma
+C1335356	Carcinoma ex pleomorphic adenoma of parotid gland
+C1335363	Mucoepidermoid carcinoma of parotid gland
+C1335377	Periampullary Adenocarcinoma
+C1335381	Pericardial mesothelioma
+C1335392	Pericytic Neoplasm
+C1335409	Prostate Phyllodes Tumor
+C1335433	Pleural Carcinomatosis
+C1335473	Primary chondrosarcoma of bone
+C1335475	Primary Carcinoma
+C1335483	Gastric Diffuse Large B-Cell Lymphoma
+C1335484	Gastric T-Cell Non-Hodgkin Lymphoma
+C1335512	Prostate Lymphoma
+C1335563	Proximal-Type Epithelioid Sarcoma
+C1335661	Radiation-Related Angiosarcoma
+C1335678	Carcinoid tumor of rectum
+C1335701	Recurrent Follicular Lymphoma
+C1335703	Recurrent Head and Neck Carcinoma
+C1335710	Recurrent Malignant Peripheral Nerve Sheath Tumor
+C1335712	Medulloblastoma recurrent
+C1335713	Recurrent Meningioma
+C1335723	Refractory Follicular Lymphoma
+C1335729	Refractory Neoplasm
+C1335762	Bone marrow reticulin fibrosis
+C1335903	Mucoepidermoid carcinoma of salivary gland
+C1335907	Polymorphous low grade adenocarcinoma of salivary gland
+C1335929	Schwannomatosis
+C1335931	Breast Sclerosing Adenosis
+C1335938	Secondary Chondrosarcoma
+C1335965	Signet-ring cell adenocarcinoma gastric
+C1335968	Vulvar Intraepithelial Neoplasia, Differentiated Type
+C1335971	Skeletal Muscle Neoplasm
+C1335975	Skull Base Chordoma
+C1335976	Skull Base Meningioma
+C1335996	Gastrointestinal stromal tumor of small intestine
+C1336005	Small Intestinal Neuroendocrine Neoplasm
+C1336007	Small Intestinal Sarcoma
+C1336012	Small Lymphocytic Lymphoma with Plasmacytoid Differentiation
+C1336015	Smoldering Adult T-Cell Leukemia/Lymphoma
+C1336030	Solid pseudopapillary tumour of the pancreas
+C1336048	Spinal Cord Embryonal Tumor, Not Otherwise Specified
+C1336050	Spinal Degenerative Disorder
+C1336052	Spindle Cell Neoplasm
+C1336056	Spindle Cell Type Gastrointestinal Stromal Tumor
+C1336076	Sporadic Breast Carcinoma
+C1336077	Sporadic Burkitt\'s lymphoma
+C1336078	Papillary renal cell carcinoma, sporadic
+C1336079	Squamous cell breast carcinoma
+C1336082	Thymic Squamous Cell Carcinoma
+C1336084	Squamous Lung Dysplasia
+C1336139	Stage IB Non-Small Cell Lung Carcinoma AJCC v7
+C1336145	Stage IB Squamous Cell Lung Carcinoma AJCC v7
+C1336160	Stage IIA Esophageal Squamous Cell Carcinoma AJCC v7
+C1336191	Stage IIB Osteosarcoma AJCC v7
+C1336219	Stage IIIB Cervical Carcinoma
+C1336257	Stage 3 Neuroblastoma
+C1336456	Hepatocellular carcinoma stage I
+C1336527	Carcinoma of urinary bladder, superficial
+C1336536	Supratentorial Glioblastoma
+C1336538	Supratentorial Embryonal Tumor, Not Otherwise Specified
+C1336548	Systemic Anaplastic Large Cell Lymphoma
+C1336554	T-Cell and NK-Cell Neoplasm
+C1336708	Testicular Germ Cell Tumor
+C1336733	Thalamic Neoplasm
+C1336735	Treatment related acute myeloid leukaemia
+C1336745	Thymic Lymphoma
+C1336746	Thymic Carcinoid Tumor
+C1336748	Thyroid Angiosarcoma
+C1336749	Thyroid Diffuse Large B-Cell Lymphoma
+C1336751	Thyroid Hyalinizing Trabecular Adenoma
+C1336753	Thyroid Lymphoma
+C1336820	Treatment-Induced Anemia
+C1336827	Tropical Disease
+C1336839	Type 1 Papillary Renal Cell Carcinoma
+C1336840	Papillary renal cell carcinoma type 2
+C1336841	Type A Lymphomatoid Papulosis
+C1336858	Undifferentiated Gastric Carcinoma
+C1336861	Undifferentiated Pancreatic Carcinoma
+C1336891	Urinary Bladder Inflammatory Myofibroblastic Tumor
+C1336899	Uterine Angiosarcoma
+C1336905	Endometrial Endometrioid Adenocarcinoma
+C1336921	Endometrial Serous Adenocarcinoma
+C1336939	Vaginal Leiomyoma
+C1336970	Visual Manifestations
+C1337011	Well Differentiated Pancreatic Endocrine Tumor
+C1337012	Well-differentiated papillary mesothelioma
+C1337013	Differentiated Thyroid Gland Carcinoma
+C1337014	Grade I Chondrosarcoma
+C1337035	Xanthogranulomatous cholecystitis
+C1366911	Cerebral Cavernous Malformations 1
+C1367420	Kaposiform Hemangioendothelioma
+C1367536	Nasopharyngeal Angiofibroma
+C1367554	Adamantinoma
+C1367652	BALT lymphoma
+C1367654	Marginal Zone B-Cell Lymphoma
+C1367859	Pineal parenchymal tumor of intermediate differentiation
+C1367970	Pagetoid reticulosis
+C1368019	Paget Disease
+C1368041	Pancreatic Somatostatinoma
+C1368065	Vascular purpura
+C1368066	pancreatic gastrinoma
+C1368107	Aplastic bone marrow
+C1368237	Solitary Myofibromatosis
+C1368275	Pigmented Basal Cell Carcinoma
+C1368295	Malignant basal cell tumor
+C1368355	Synostosis
+C1368404	Hypopharyngeal Carcinoma
+C1368683	Epithelioma
+C1368771	Burkitt-like lymphoma
+C1368816	Sebaceous adenoma
+C1368871	Pediatric Neoplasm
+C1368910	Mature Teratoma
+C1368911	Papillary urothelial carcinoma
+C1370419	Ovarian Granulosa Cell Tumor
+C1370446	Plasma cell myeloma recurrent
+C1370507	Cerebellar Liponeurocytoma
+C1370657	Soft tissue perineurioma
+C1370701	Clear cell hidradenoma
+C1370723	Stromal sarcoma
+C1370800	Bile duct adenocarcinoma
+C1370868	refractory CML
+C1370889	Liposarcoma, well differentiated
+C1370932	carcinoma of the renal pelvis and ureter
+C1370962	Prostate cancer stage C
+C1377610	Peritoneal Mesothelioma
+C1377665	Childhood Central Nervous System Neoplasm
+C1377785	Nasal cavity cancer
+C1377843	Periosteal Osteosarcoma
+C1377913	Pleural Mesothelioma
+C1377916	Benign vascular neoplasm
+C1378050	Oncocytic Neoplasm
+C1378511	Undifferentiated leukemia
+C1378512	Blast cell leukemia
+C1378703	Renal carcinoma
+C1382398	Increased capillary permeability (finding)
+C1383860	Cardiac Hypertrophy
+C1384353	Infestation
+C1384388	Maximum breathing capacity function
+C1384403	Cellular Ependymoma
+C1384406	Secretory meningioma
+C1384408	Microcystic meningioma
+C1384485	Delivery in a completely normal case
+C1384489	Scratch
+C1384493	Catarrh
+C1384494	Metastatic Carcinoma
+C1384495	Cardiac stress test
+C1384514	Conn Syndrome
+C1384582	Primary testicular failure
+C1384583	Congenital absence of germinal epithelium of testes
+C1384584	Generalized osteoarthritis
+C1384586	Forceps delivery
+C1384589	Tinea cruris
+C1384590	Hemangiomatosis
+C1384600	Systemic onset juvenile chronic arthritis
+C1384606	Dyspareunia
+C1384641	Cervical spondylosis
+C1384666	hearing impairment
+C1384670	Single umbilical artery
+C1385263	Deformity of face
+C1386048	Intrauterine retardation
+C1386553	Caffeine dependence
+C1387005	Penis agenesis
+C1387532	Chronic hemolytic anemia
+C1387805	Episodic paroxysmal anxiety
+C1388177	Aortic arteriosclerosis
+C1389016	ATRIOVENTRICULAR CANAL DEFECT
+C1389018	Atrioventricular Septal Defect
+C1389037	Bone atrophy
+C1389102	Atrophy of the spinal cord
+C1389113	Generalized amyotrophy
+C1389118	Peroneal muscle atrophy
+C1389280	Basal ganglia calcification
+C1389462	Pelvic cyst
+C1389473	Pelvic hypoplasia
+C1389851	Parathyroid hypoplasia
+C1390029	Anterior Fascicular Block
+C1390030	Posterior Fascicular Block
+C1390214	Internal haemorrhage
+C1390461	Bone contusion
+C1390474	Increased susceptibility to fractures
+C1391732	Cancer cachexia
+C1391997	Congenital cardiomyopathy
+C1392046	Cardiovascular insufficiency
+C1392104	Coralliform cataract
+C1392207	Central nervous system necrosis
+C1392224	Centrocytic lymphoma
+C1392616	Nonobstructive chronic pyelonephritis NOS
+C1392786	Cognitive changes
+C1393669	Congenital onychodystrophy
+C1393871	Congenital finger flexion contractures
+C1394030	Coronal hypospadias
+C1394320	Endometrial Cyst
+C1394691	Bowel diverticula
+C1394891	Intrinsic Factor Deficiency
+C1395088	Nervous system--Degeneration
+C1395512	Placental dysfunction
+C1395674	Bowel diverticulosis
+C1395852	Polydactyly preaxial type 1
+C1396126	Perioral eczema
+C1396651	Ankle deformity
+C1396772	Hypoplasia of the epiglottis
+C1397139	Calcification of falx cerebri
+C1397307	Cardiac fibrosis
+C1397523	Stapes fixation
+C1397674	Persistent foramen ovale
+C1398301	Short palate
+C1398312	Narrow palate
+C1398325	Absent auditory canals
+C1398522	Cleft palate and bilateral cleft lip
+C1399226	Ectopic rhythm
+C1399352	Paroxysmal Hemicrania
+C1399358	Hemiparkinsonism
+C1399682	Heat Fatigue
+C1399774	Excessive skin
+C1399793	skin fold (abnormality)
+C1399930	Attention deficit-hyperactivity
+C1400105	Hypertrophy of nose
+C1400201	Pituitary anomalies
+C1400252	Hypoplasia of parotid gland
+C1400417	Immune complex nephritis
+C1401084	Ovarian Insufficiency
+C1401086	obsolete Peripheral vascular insufficiency
+C1402291	Pigmented lesions
+C1402294	Primary Lesion
+C1402315	Vascular lesions
+C1403035	Subcutaneous lipoma
+C1403299	Radiohumeral dislocation
+C1403321	Ulnohumeral dislocation
+C1403880	Viral meningoencephalitis
+C1403891	Meningococcal Waterhouse-Friderichsen syndrome
+C1404059	Splenic calcification
+C1404153	Valve anomalies
+C1404521	Limb-girdle myopathy
+C1405301	Poliomyelitis, paralytic
+C1405308	Vaccine associated paralytic poliomyelitis
+C1405458	Language Problems
+C1405854	Retinitis punctata albescens (disorder)
+C1405984	Absent radius
+C1406717	Sirenomelia syndrome
+C1406835	Flexion contracture of toe
+C1406921	Thoracic dysplasia
+C1406945	Thymus enlargement
+C1407122	Graft bleeding
+C1407280	Peripheral artery thrombosis
+C1408174	Hypertrophic neuropathy of infancy
+C1408182	Hereditary motor and sensory neuropathy, types I-IV
+C1408247	Renal disease (acute) NOS
+C1408258	Kidney damage
+C1408443	Vaginal obstruction
+C1408507	Supranuclear ophthalmoplegia
+C1408532	Absent forearm
+C1408788	Absent ear
+C1408806	Calcification of the auricular cartilage
+C1409412	Periostosis
+C1409792	Coronary sinus defect
+C1410098	Cardiac arrest neonatal
+C1410400	Nontraumatic subarachnoid hemorrhage, unspecified
+C1411873	Ovulation disorder
+C1411876	Developmental arithmetic disorder
+C1411924	Eye colour change
+C1411934	Mycobacterium leprae infection
+C1411964	Mycobacterium; ulcerans (disease)
+C1411966	Clostridium; difficile (disorder)
+C1411980	Mycobacterium avium infection
+C1412000	Mesenteric vascular insufficiency
+C1412002	Atypical pneumonia
+C1412004	Tumor of the Pineal Region
+C1412014	Infiltrating duct carcinoma
+C1412036	Anal squamous cell carcinoma
+C1414017	DEAFNESS, AUTOSOMAL RECESSIVE 25
+C1414216	Dystonia 6, torsion (disorder)
+C1415817	HETEROTAXY, VISCERAL, 2, AUTOSOMAL
+C1419610	RP23 gene
+C1419614	RETINITIS PIGMENTOSA 28
+C1423873	CONE-ROD DYSTROPHY 9
+C1439256	Deformity thorax NOS
+C1439275	Disseminated carcinoma
+C1442826	Necrotising enterocolitis neonatal
+C1442835	Solar dermatitis
+C1442837	Myocardial necrosis
+C1442839	Hypervitaminosis D
+C1442861	Black eye
+C1442869	Lumbar Osteoarthritis
+C1442877	Sore skin
+C1442879	Phrenic nerve paralysis
+C1442903	Exostoses
+C1442907	Foreign body giant cell granuloma
+C1442965	Avascular necrosis of the capital femoral epiphysis
+C1442968	Anastomotic ulcer
+C1442978	Hernia of abdominal wall
+C1442981	Alcoholic liver damage
+C1442988	Rudimentary vagina
+C1443016	Estradiol level result
+C1443060	Feeling abnormal
+C1443296	Axial myopia
+C1443892	Chronic Q Fever
+C1443924	Severe diarrhea
+C1443947	Incomplete paralysis
+C1443971	Chronic esophagitis
+C1444077	Bone abscess
+C1444087	Disease due to Neisseria
+C1444565	Cardiopulmonary failure
+C1444627	Hutchinson's sign
+C1444680	Posterior capsule opacification
+C1445953	Poor eye contact
+C1445957	Serum total cholesterol measurement
+C1446219	Akinetic rigid syndrome
+C1446220	Basal ganglia infarction
+C1446648	Non-specific brain syndrome
+C1446712	Overlapping fingers
+C1446787	Cramping sensation quality
+C1449563	Cardiomyopathy, Familial Idiopathic
+C1449626	CADASILM
+C1449630	Sphincter of Oddi Stenosis
+C1449631	Gallbladder Dyskinesia
+C1449646	Primary Peritonitis
+C1449647	Secondary Peritonitis
+C1449718	Endocrine Breast Diseases
+C1449720	Adolescent Gynecomastia
+C1449721	Infant Gynecomastia
+C1449842	Pseudohypoaldosteronism, Type I, Autosomal Dominant
+C1449843	Pseudohypoaldosteronism, Type I, Autosomal Recessive
+C1449844	Pseudohypoaldosteronism, Type II
+C1449852	Erythematotelangiectatic Rosacea
+C1449853	Papulopustular Rosacea
+C1449854	Phymatous Rosacea
+C1449861	Micronuclei, Chromosome-Defective
+C1449862	Micronuclei, Genotoxicant-Induced
+C1450010	Plagiocephaly, Nonsynostotic
+C1450051	Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
+C1450052	Tibial Muscular Dystrophy
+C1452968	Androgenization
+C1455705	Pulmonary Histiocytosis X
+C1455718	Neurological ventriculitis
+C1455728	Acute fatty liver of pregnancy
+C1455734	Congenital hypoparathyroidism
+C1455780	Aortic valve sclerosis
+C1456144	Dental caries pit and fissure
+C1456145	Dental caries of smooth surface
+C1456240	Narcolepsy without cataplexy
+C1456246	Bacteroides fragilis infection in conditions classified elsewhere and of unspecified site
+C1456276	Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome)
+C1456283	Other alcohol-induced mental disorders
+C1456326	Selective mutism specific to childhood and adolescence
+C1456329	Stomach dilation procedure
+C1456332	Stimulant abuse
+C1456418	Absence of muscle
+C1456556	Heat illness
+C1456582	Vision Impairment and Blindness
+C1456624	Methamphetamine abuse
+C1456687	Polio and Post-Polio Syndrome
+C1456781	Benign melanocytic nevus
+C1456784	Paranoia
+C1456791	Clostridium sordellii Infections
+C1456792	Still\'s disease with juvenile onset and/or adult onset
+C1456822	Claudication (finding)
+C1456863	Vasoconstriction
+C1456865	Calculus of ureter
+C1456868	Diabetic foot ulcer
+C1456873	alpha^+^ Thalassemia
+C1457871	Sarcoid arthritis
+C1457883	Aggressive reaction
+C1457909	Pancreatic duct dilatation
+C1457917	Urethral dilatation
+C1458140	Bleeding tendency
+C1458142	Squamous odontogenic tumor
+C1458155	Breast Neoplasms
+C1504321	Infantile spitting up
+C1504322	Tryptase increased
+C1504327	INR fluctuation
+C1504329	Amniotic fluid volume decreased
+C1504336	Polypoidal choroidal vasculopathy
+C1504337	Vascular stent insertion
+C1504343	Acarodermatitis
+C1504346	Pruritus allergic
+C1504360	Gene mutation identification test positive
+C1504363	Body temperature fluctuation
+C1504367	Allergic respiratory symptom
+C1504368	Single functional kidney
+C1504369	Allergic respiratory disease
+C1504373	Bowel movement irregularity
+C1504376	Unresponsive to verbal stimuli
+C1504377	Hyperglycemic hyperosmolar nonketotic syndrome
+C1504379	Coagulation test abnormal
+C1504382	Pulmonary arterial medial hypertrophy
+C1504383	Radiation skin injury
+C1504389	Stem cell transplant
+C1504392	Helicobacter pylori identification test positive
+C1504403	Acute lymphocytic leukaemia recurrent
+C1504404	Hippocampal sclerosis
+C1504405	Pyramidal tract dysfunction
+C1504410	Vital functions abnormal
+C1504411	Post procedural oedema
+C1504412	Testotoxicosis
+C1504417	Pregnancy after post coital contraception
+C1504418	Similar reaction on previous exposure to drug
+C1504422	Application site hypersensitivity
+C1504424	Antipsychotic drug level increased
+C1504431	Idiopathic pneumonia syndrome
+C1504432	Congenital anomaly in offspring
+C1504434	Therapeutic response unexpected with drug substitution
+C1504435	Electrocardiogram QT interval abnormal
+C1504437	Life expectancy shortened
+C1504438	Cerebral artery stenosis
+C1504445	Implant site discharge
+C1504447	Implant site effusion
+C1504448	Implant site erosion
+C1504449	Implant site erythema
+C1504450	Implant site hematoma
+C1504451	Implant site inflammation
+C1504452	Implant site pain
+C1504455	Implant site itching
+C1504456	Implant site rash
+C1504458	Cataract operation
+C1504460	Genital erosion
+C1504463	Circulatory encephalopathy
+C1504465	Device malfunction
+C1504514	Infection by human herpesvirus 7
+C1504542	Puncture site infection
+C1504554	Meniscitis
+C1504561	Hypophagia
+C1507149	Partial chromosome Y deletion
+C1509147	Histiocytoma
+C1509148	Sclerosing hemangioma
+C1510410	Parosmia
+C1510412	Pseudoaneurysm
+C1510415	Osteosclerotic Myeloma
+C1510417	Gait Apraxia
+C1510420	Cavitation
+C1510426	choroid plexus carcinoma, childhood
+C1510428	Cerebral abscess
+C1510429	Entrapment Neuropathies
+C1510431	Superficial thrombophlebitis
+C1510432	Radiation Sickness
+C1510437	Chronic Actinic Dermatitis
+C1510446	Acute ischemic heart disease
+C1510449	Chronic iridocyclitis
+C1510450	Dysacusis
+C1510455	Acrocephalosyndactylia
+C1510456	Wernicke's aphasia
+C1510460	Orofaciodigital Syndrome I
+C1510471	Hypovitaminosis
+C1510472	Drug Dependence
+C1510475	Diverticular disorders
+C1510479	Neuralgic Amyotrophy
+C1510489	Cerebral Amyloid Angiopathy, Hereditary
+C1510497	Lens Opacities
+C1510502	Oxyphilic Adenoma
+C1510504	Fetal malnutrition without mention of light-for-dates
+C1510586	Autism spectrum disorder
+C1510885	Angiogenic Switch
+C1511104	Benign Struma Ovarii
+C1511306	Breast Diffuse Large B-Cell Lymphoma
+C1511566	Primary Cutaneous B-Cell Non-Hodgkin Lymphoma
+C1511789	Desmoplastic
+C1511934	Differentiating Neuroblastoma
+C1512127	HER2 gene amplification
+C1512259	Grade II Meningioma
+C1512260	Grade I Meningioma
+C1512409	Hepatocarcinogenesis
+C1512419	Hereditary Melanoma
+C1512431	High Grade B-Cell Non-Hodgkin\'s Lymphoma
+C1512433	Cervical high grade squamous intraepithelial lesion
+C1512508	Human herpesvirus 8 infection
+C1512709	Chronic Lymphoproliferative Disorder of NK-Cells
+C1512981	Mammary Tumorigenesis
+C1513269	Microcysts
+C1513276	Neoplasm Micrometastasis
+C1514225	Poorly Differentiated Neuroblastoma
+C1514284	Potassium Deficiency Disorder
+C1514422	Glioblastoma, IDH-Wildtype
+C1514428	Primary peritoneal carcinoma
+C1514507	Prostate Basal Cell Carcinoma
+C1514517	Prostate Stromal Proliferation of Uncertain Malignant Potential
+C1514915	Retinal hemangioblastoma
+C1515286	Testicular Intratubular Germ Cell Neoplasia, Unclassified
+C1516061	Astler-Coller B1 Rectal Carcinoma
+C1516170	Cancer Cell Growth
+C1516474	Cellular Congenital Mesoblastic Nephroma
+C1516490	Cholangiolocellular Carcinoma
+C1516669	Clonal Evolution
+C1516857	Serous Endometrial Intraepithelial Carcinoma
+C1516865	Endometrial Undifferentiated Carcinoma
+C1517444	Ganglioneuroblastoma, Intermixed
+C1517445	Ganglioneuroblastoma, Nodular
+C1517658	Cervical Keratinizing Squamous Cell Carcinoma
+C1518004	Low Grade B-Cell Non-Hodgkin\'s Lymphoma
+C1518005	Low Grade Cervical Squamous Intraepithelial Neoplasia
+C1518171	Malignant Conversion
+C1518296	Neuropathogenesis
+C1518693	Ovarian Clear Cell Adenocarcinoma
+C1518716	Ovarian gonadoblastoma
+C1518736	Ovarian Small Cell Carcinoma, Hypercalcemic Type
+C1518869	Pancreatic Intraductal Papillary-Mucinous Neoplasm
+C1519086	Pilomyxoid astrocytoma
+C1519172	Salivary Gland Carcinoma ex Pleomorphic Adenoma
+C1519176	Salivary Gland Pleomorphic Adenoma
+C1519214	Glioblastoma, IDH-Mutant
+C1519346	Skin Carcinogenesis
+C1519353	Rash papular
+C1519383	Smoking Behaviors
+C1519653	Trisomy 4
+C1519665	Tumor-Associated Process
+C1519666	Tumor-Associated Vasculature
+C1519670	Tumor Angiogenesis
+C1519675	Tumor Cell Mobility
+C1519678	Tumor Expansion
+C1519680	Tumor Immunity
+C1519689	Tumor Promotion
+C1519702	Turcot Syndrome Type 1
+C1519714	Type II Endometrial Adenocarcinoma
+C1519719	Type I Endometrial Adenocarcinoma
+C1519787	Undifferentiated Neuroblastoma
+C1521897	Mature T ALL
+C1522378	Large granular lymphocytosis
+C1522449	Radiotherapy
+C1522512	Transient Situational Disturbance
+C1524032	Depression and Suicide
+C1527168	Bonnevie-Ullrich Syndrome
+C1527197	Angioblastic Meningioma
+C1527226	CRST syndrome
+C1527231	Adrenomyeloneuropathy
+C1527249	Colorectal Cancer
+C1527258	Infantile paralysis
+C1527281	Separation anxiety disorder of childhood
+C1527284	Dental Pulp Stone
+C1527298	Dysentery, Bacillary
+C1527303	Chronic Airflow Obstruction
+C1527304	Allergic Reaction
+C1527305	Feelings
+C1527306	spasmus nutans
+C1527307	Sexual deviations or disorders
+C1527310	Ametropia
+C1527311	Brain Edema
+C1527317	Alpha-Aminoadipic Semialdehyde Deficiency Disease
+C1527320	Vertigo, Aural
+C1527330	Pyridoxine Deficiency
+C1527335	Transient Ischemic Attack, Anterior Circulation
+C1527336	Sjogren's Syndrome
+C1527337	Familial Amyloid Polyneuropathy, Appalachian Type
+C1527338	Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
+C1527340	Voice Disturbance
+C1527344	Dysphonia
+C1527347	Difficulty speaking
+C1527348	Brain Hypoxia
+C1527349	Ductal Breast Carcinoma
+C1527351	Nerve Root Disorder
+C1527352	Hepatic Form of Wilson Disease
+C1527353	Algodystrophic Syndrome
+C1527358	Phototoxicity
+C1527366	Salaam Seizures
+C1527375	Cystic Breast Disease
+C1527383	Morphea
+C1527384	Involuntary Quiver
+C1527388	Amniotic Bands
+C1527390	Neoplasms, Intracranial
+C1527393	Myocarditis, Chagas
+C1527394	Chylous Peritonitis
+C1527395	Ogilvie Syndrome
+C1527396	Fibrocystic Disease of Pancreas
+C1527402	Narcotic Dependence
+C1527403	Entamoebiasis, Hepatic
+C1527404	Female Pseudo-Turner Syndrome
+C1527405	Erythrocytosis
+C1527406	Rhizomelic pseudopolyarthritis
+C1527407	Eosinophilic Pneumonia
+C1527410	Renal rickets
+C1527411	Retinal vein thrombosis
+C1527424	Cervical Squamous Intraepithelial Neoplasia 1
+C1531394	Perinatal jaundice
+C1531500	Alpha carotene level
+C1531527	Blebitis
+C1531551	Chronic myeloid leukemia in lymphoid blast crisis
+C1531553	Dendritic cell neoplasm
+C1531608	Smoldering Multiple Myeloma
+C1531646	Central topographic island
+C1531647	Cerebral ventriculomegaly
+C1531651	Chaddock's reflex
+C1531773	Currarino triad
+C1531795	A pattern strabismus
+C1532085	Hamman's sign
+C1532237	Disorder of immune function
+C1532322	Infectious Endophthalmitis
+C1532338	Percutaneous coronary intervention
+C1532480	Hyperplastic obesity
+C1532782	Rifampicin resistant tuberculosis
+C1532790	Sarcoid uveitis
+C1533041	Primary congenital glaucoma
+C1533060	Multifocal choroiditis
+C1533161	Eccrine Poroma
+C1533163	Disorder of cellular component of blood
+C1533172	Infantile nystagmus syndrome
+C1533174	Acute myeloid leukemia, inv(16)(p13q22)
+C1533217	Methamphetamine dependence
+C1533284	Bone decalcification
+C1533568	fertility disorders
+C1533587	Hydroxymethylglutaric aciduria
+C1533592	Malignant Paraganglionic Neoplasm
+C1533618	Fat embolism as early complication of trauma (disorder)
+C1533628	Pseudo-Zellweger syndrome
+C1533651	Cell-mediated immune deficiency
+C1533674	Borderline glaucoma
+C1533685	Injection
+C1533847	Disorder of skeletal muscle
+C1535510	ADENOMAS AND ADENOCARCINOMAS
+C1535849	Application site induration
+C1535851	Implant site abscess
+C1535858	Implant site extravasation
+C1535860	Implant site hypersensitivity
+C1535864	Implant site mass
+C1535869	Implant site swelling
+C1535875	Implant site scar
+C1535882	Bacterial lower respiratory tract infections
+C1535886	Non-Hodgkin's lymphoma unspecified histology aggressive
+C1535887	Post procedural pulmonary embolism
+C1535888	Sleep disorder due to a general medical condition
+C1535889	Multimorbidity
+C1535893	Orthostatic intolerance
+C1535915	Limb crushing injury
+C1535916	Pelvic floor muscle weakness
+C1535919	Fetal chromosome abnormality
+C1535923	Clostridium difficile toxin test positive
+C1535926	Neurodevelopmental disorder
+C1535933	Cardiac valve disorders congenital
+C1535936	Vocal cord polypectomy
+C1535938	Cell marker increased
+C1535939	Pneumocystis jiroveci pneumonia
+C1535940	Incision site cellulitis
+C1535942	Polyglandular Type III Autoimmune Syndrome
+C1535948	Retinal aneurysm
+C1535950	Gastrointestinal inflammation
+C1535952	Carbon dioxide abnormal
+C1535953	Stenosis of foramen magnum
+C1535957	Genital labial adhesions
+C1535964	Cholestatic pruritus
+C1535965	Atrial conduction time prolongation
+C1535970	Blood count abnormal
+C1535972	Bone fissure
+C1535973	Bone fragmentation
+C1535975	Pelvic discomfort
+C1535976	Epiploic appendagitis
+C1535978	Hyperchylomicronemia
+C1535984	Splenic granuloma
+C1535985	Staphylococcal osteomyelitis
+C1535986	Onychalgia
+C1535987	Vascular graft complication
+C1535991	Cardiac valve abscess
+C1535996	Drug dose omission
+C1535997	Drug prescribing error
+C1535998	Incorrect route of drug administration
+C1535999	Incorrect drug dosage form administered
+C1536000	Incorrect drug administration rate
+C1536001	Incorrect drug administration duration
+C1536003	Human papilloma virus test positive
+C1536007	CSF immunoglobulin increased
+C1536009	Esophageal edema
+C1536010	Lymphoma transformation
+C1536011	Wrong technique in drug usage process
+C1536012	Drug dispensing error
+C1536013	Incorrect dosage administered
+C1536014	Accidental drug intake by child
+C1536015	Documented hypersensitivity to administered drug
+C1536016	Labeled drug-drug interaction medication error
+C1536017	Labeled drug-food interaction medication error
+C1536018	Labeled drug-disease interaction medication error
+C1536019	Intercepted medication error
+C1536020	Circumstance or information capable of leading to medication error
+C1536021	Dysbacteriosis
+C1536022	Hematidrosis
+C1536047	Lip exfoliation
+C1536052	Oral mucosal exfoliation
+C1536053	Tongue exfoliation
+C1536055	Drug administration error
+C1536085	Geographic Atrophy
+C1536145	Eyelash hyperpigmentation
+C1536220	ST Elevation Myocardial Infarction
+C1536235	Extra dose administered
+C1536451	Central areolar choroidal sclerosis
+C1536500	Deficiency of acetyl-CoA acetyltransferase
+C1536526	Bowenoid papulosis of penis
+C1536651	Arterial leg ulcer
+C1536696	Overactivity
+C1536916	Blood cholesterol decreased
+C1536999	cancer angiogenesis
+C1540600	Cerebral seizure
+C1540763	Penile blister
+C1540912	Hypereosinophilic syndrome
+C1541317	Adult Gliosarcoma
+C1541333	adult acute myeloid leukemia with inv(16)(p13;q22)
+C1541844	PRESENILE AND SENILE DEMENTIA
+C1541923	Infective endocarditis
+C1542178	Lower limb fracture
+C1542327	Fetus or newborn affected by alcohol transmitted via placenta or breast milk
+C1546338	Ankle arthroplasty
+C1557335	Ocular surface disease
+C1558931	Flu-Like Syndrome Adverse Event
+C1559154	Rash and Dermatitis Adverse Event Associated with Chemoradiation
+C1560305	Prolonged QTc interval
+C1561230	Soft tissue necrosis
+C1561549	Glomerular filtration rate finding
+C1561643	Chronic kidney disease
+C1561826	Overweight and obesity
+C1561828	Anemia in chronic kidney disease
+C1561921	Non-ST elevation (NSTEMI) myocardial infarction
+C1561982	Toxic anterior segment syndrome
+C1561989	Limbal stem cell deficiency
+C1562010	Langerhans cell histiocytosis of lung
+C1562028	Undifferentiated inflammatory arthritis
+C1562061	Microspherophakia
+C1562113	Fleck corneal dystrophy
+C1562312	Estrogen receptor positive tumor
+C1562585	Leprosy, Multibacillary
+C1562630	Congenital ectopia
+C1562689	Congenital hereditary endothelial dystrophy
+C1562761	Punctate epithelial keratitis
+C1562820	Tender point
+C1562894	Thiel-Behnke corneal dystrophy
+C1562901	Peripheral ulcerative keratitis
+C1562908	Leprosy, Paucibacillary
+C1563119	Hormone receptor positive tumor
+C1563367	Low T3-Low T4 Syndrome
+C1563666	Dysarthria, Guttural
+C1563694	Pituitary Dwarf
+C1563696	DNA Repair-Deficiency Disorders
+C1563697	Chromosome Instability Syndromes
+C1563705	Nephrogenic Diabetes Insipidus, Type I
+C1563706	Nephrogenic Diabetes Insipidus, Type II
+C1563709	Myopathic Ophthalmopathy
+C1563715	Andersen Syndrome
+C1563716	Thyroid Dysgenesis
+C1563718	Genital Infantilism
+C1563719	Kallmann Syndrome 1
+C1563720	Kallmann Syndrome 2 (disorder)
+C1563730	Abdominal Cryptorchidism
+C1563731	Inguinal Cryptorchidism
+C1563937	Atherogenesis
+C1565106	Headache Disorders, Primary
+C1565107	Headache Disorders, Secondary
+C1565171	Episodic Paroxysmal Hemicrania
+C1565249	Mobility Limitation
+C1565321	Cholera Infantum
+C1565489	Impaired renal function
+C1565662	Acute Kidney Insufficiency
+C1565885	Direct Hyperbilirubinemia, Neonatal
+C1565886	Indirect Hyperbilirubinemia, Neonatal
+C1565887	Newborn physiological jaundice
+C1565950	Posterior Fossa Meningioma
+C1565951	Sphenoid Wing Meningioma
+C1566050	Icterus Gravis Neonatorum
+C1566302	Preterm Premature Rupture of Fetal Membranes
+C1566590	Delayed Graft Function
+C1567257	Granulosa Cell Cancer
+C1567426	Unilateral Multicystic Dysplastic Kidney
+C1567427	Bilateral Multicystic Dysplastic Kidneys
+C1567435	Polycystic Kidney - body part
+C1567741	Alport Syndrome
+C1567742	Alport Syndrome, X-Linked
+C1567743	Alport Syndrome, Autosomal Dominant
+C1567744	Alport Syndrome, Autosomal Recessive
+C1568247	Usher syndrome type 1
+C1568248	Usher Syndrome, Type III
+C1568249	Usher Syndrome, Type II
+C1568272	Tendinopathy
+C1568363	Tendinosis
+C1568868	Oral Mucositis
+C1569637	Adenocarcinoma, Endometrioid
+C1571983	Involutional paraphrenia
+C1571984	Psychosis, Involutional
+C1578482	Valgus deformities of feet
+C1578691	Myxedema, Congenital
+C1579029	Chronic uremia
+C1579830	Blister of skin AND/OR mucosa
+C1579838	Sore mouth
+C1579931	Depressed - symptom
+C1608389	Autoimmune myocarditis
+C1608393	Megacystis microcolon intestinal hypoperistalsis syndrome
+C1608397	Device occlusion
+C1608399	Dark circles under eyes
+C1608408	Malignant transformation
+C1608410	Head titubation
+C1608426	Compensated cirrhosis
+C1608431	Thromboembolectomy
+C1608942	Complication of device insertion
+C1608945	Exfoliative rash
+C1608946	Haemorrhagic arteriovenous malformation
+C1608950	Device dislocation
+C1608953	Intestinal diaphragm disease
+C1608954	Infusion site extravasation
+C1608955	Mycobacterium abscessus Infection
+C1608957	Tachyphrenia
+C1608965	Drug exposure before pregnancy
+C1608967	Rhodococcus infection
+C1608985	High frequency ablation
+C1609432	manifestations of immunopathology
+C1609433	Congenital absence of kidneys syndrome
+C1609496	Eyelid exfoliation
+C1609501	Graft versus host disease in intestine
+C1609502	Portal venous gas
+C1609503	Renal artery stent placement
+C1609512	Vulvovaginal mycotic infection
+C1609515	Neutralizing antibodies positive
+C1609516	Necrotising retinitis
+C1609528	Restrictive deficit on pulmonary function testing
+C1609535	Candidiasis, Invasive
+C1609538	Latent Tuberculosis
+C1610049	Application site exfoliation
+C1610054	Graft versus host disease in liver
+C1610056	Antinuclear antibody increased
+C1610065	Urethral atresia
+C1610066	Urinary tract inflammation
+C1610068	Myocardial edema
+C1610071	Uhthoff's phenomenon
+C1610605	Graft versus host disease in skin
+C1610609	Nail growth abnormal
+C1610617	Burkholderia cepacia Infection
+C1610619	Acinetobacter bacteraemia
+C1610622	Coital bleeding
+C1610639	Incorrect storage of drug
+C1611157	Hepatic infiltration eosinophilic
+C1611162	Plateletcrit decreased
+C1611167	Waist circumference increased
+C1611170	Tumor perforation
+C1611171	Thalamic infarction
+C1611174	Post-traumatic pain
+C1611175	Device connection issue
+C1611184	Calcification of coronary artery
+C1611195	Congenital corneal dystrophy
+C1611703	Epstein-Barr virus test positive
+C1611706	Myosclerosis
+C1611708	Poor personal hygiene
+C1611713	Cerebral hyperperfusion syndrome
+C1611725	Leukemic infiltration brain
+C1611727	Nutritional condition abnormal
+C1611743	Familial (FPAH)
+C1619692	Nephrogenic Fibrosing Dermopathy
+C1619696	Bone marrow eosinophilic leukocyte count increased
+C1619700	RENAL ADYSPLASIA
+C1619701	Peritoneal perforation
+C1619702	Device related infection
+C1619711	Gastrointestinal telangiectasia
+C1619712	Procedural pain
+C1619714	Anticonvulsant drug level abnormal
+C1619716	Cystatin C measurement
+C1619718	Partner stress
+C1619738	Immune Reconstitution Inflammatory Syndrome
+C1621719	Lymphoepithelioid lymphoma (clinical)
+C1621895	Adrenal hyperplasia
+C1621920	Intermediate Maple Syrup Urine Disease
+C1621958	Glioblastoma Multiforme
+C1622345	Meretoja syndrome
+C1622434	Suxamethonium sensitivity
+C1622510	Neurocytoma
+C1623038	Cirrhosis
+C1623145	response to methotrexate
+C1623209	Okihiro Syndrome
+C1627767	Follicular mycosis fungoides
+C1628319	Lattice corneal dystrophy Type II
+C1629504	Atypical Burkitt\'s lymphoma
+C1629856	Fleisher ring
+C1631597	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
+C1636149	Macular dystrophy, corneal type 1
+C1636152	Primary cutaneous large B-cell lymphoma of the leg
+C1641846	Groenouw corneal dystrophy type I (disorder)
+C1641852	Gelatinous droplike corneal dystrophy
+C1644196	Ectopia Lentis with Ectopia of Pupil
+C1654637	androgen independent prostate cancer
+C1654921	High urine albumin levels
+C1655035	congenital muscle disorder
+C1656427	Early onset schizophrenia
+C1656590	lyssavirus infection
+C1657104	Surgical Adhesions
+C1658953	tumor vasculature
+C1659098	Complete paraplegia
+C1659989	Respiratory problem
+C1689817	Cardiomyopathy associated with another disorder
+C1690006	Lattice corneal dystrophy Type I
+C1691013	Macular corneal dystrophy Type II (disorder)
+C1691215	Penile hypospadias
+C1691221	Fungal lower respiratory tract infections
+C1691228	Cystic Kidney Diseases
+C1691230	Mitochondrial myopathy acquired
+C1691779	Sensory hearing loss
+C1691782	Epstein-Barr viremia
+C1692338	Ligament operation
+C1692871	Inflammatory polyarthritis
+C1692886	Arthritis bacterial
+C1695776	Vertebral wedging
+C1695782	Cerebral hypoperfusion
+C1695892	Infantile apnoeic attack
+C1695897	Infusion site irritation
+C1695982	Blood product transfusion dependent
+C1695984	Oesophageal food impaction
+C1696083	Oral cavity fistula
+C1696110	Vessel puncture site haematoma
+C1696114	Stubbornness
+C1696157	Gastrointestinal stoma complication
+C1696466	Hepatic calcification
+C1696469	Shin splints
+C1696485	Mini mental status examination abnormal
+C1696494	Infusion site scar
+C1696495	Infusion site vesicles
+C1696574	Application site erosion
+C1696575	Injection site discharge
+C1696684	ACTH stimulation test abnormal
+C1696685	Intentional drug misuse
+C1696701	Dermatillomania
+C1696704	Ovarian haemorrhage
+C1696708	Prehypertension
+C1696849	Dermo-hypodermitis
+C1696943	Hypoaesthesia facial
+C1696945	Burn-out syndrome
+C1696946	Polyomavirus-associated nephropathy
+C1697135	Infusion site cellulitis
+C1697438	Cystitis viral
+C1697441	Enterocolitis bacterial
+C1697450	Prominent epicanthal folds
+C1697453	Spontaneous haematoma
+C1697454	Pelvic fluid collection
+C1697537	Infusion site discolouration
+C1697538	Infusion site haemorrhage
+C1697732	Oral torus
+C1697733	Incision site erythema
+C1697746	Rectal obstruction
+C1697788	Carbon monoxide diffusing capacity decreased
+C1697943	Epidermal growth factor receptor decreased
+C1698196	Muscle weakness of upper limb
+C1698394	Acute promyelocytic leukaemia differentiation syndrome
+C1698397	Incision site infection
+C1698400	Incision site edema
+C1698446	Infusion site hematoma
+C1698447	Infusion site mass
+C1698473	Wound infection bacterial
+C1698480	Supraventricular tachyarrhythmia
+C1698484	Mucosal infection
+C1698510	Bacterial otitis media
+C1698581	Rokitansky Kuster Hauser syndrome
+C1698583	Fungal rhinitis
+C1698618	Ex-tobacco user
+C1698638	Drug dispensed to wrong patient
+C1698976	Infusion site hives
+C1698981	Lymphadenitis bacterial
+C1699045	Abscess fungal
+C1699206	Virologic failure
+C1699498	Infusion site necrosis
+C1699504	Intercepted drug dispensing error
+C1699603	Excessive eye blinking
+C1699634	HER-2 positive breast cancer
+C1699655	Ileal fistula
+C1699848	Therapy cessation
+C1701938	Associated Pulmonary Arterial Hypertension
+C1701939	Familial pulmonary arterial hypertension
+C1701940	Pneumonia, Ventilator-Associated
+C1704202	Aspermia
+C1704212	Embolus
+C1704214	Lipogranuloma
+C1704216	Basaloid carcinoma
+C1704230	Grade I Astrocytoma
+C1704231	Metastatic Malignant Neoplasm to the Leptomeninges
+C1704251	Breast Lymphoma
+C1704268	Delusion of persecution
+C1704272	Benign Prostatic Hyperplasia
+C1704273	Endometrial Polyp
+C1704274	Intrauterine adhesions
+C1704275	Pyomyositis
+C1704276	Spasmodic movement
+C1704299	Hypobetalipoproteinemia, Familial, Apolipoprotein B
+C1704315	Pyelonephritis acute necrotizing
+C1704317	Leukokeratosis
+C1704320	Glomerulonephritis minimal lesion
+C1704321	Nephrotic Syndrome, Minimal Change
+C1704323	Paget\'s Disease of the Nipple
+C1704327	Bone Sarcoma
+C1704328	Osteoblastic Osteosarcoma
+C1704330	Dental Diseases
+C1704356	Enchondroma
+C1704373	Compulsive Personality Disorder
+C1704374	Carcinoma of Endocrine Gland
+C1704375	Hypophosphatemic Rickets
+C1704376	Uterine Corpus Carcinosarcoma
+C1704377	Bright Disease
+C1704378	Heymann Nephritis
+C1704380	Distal Renal Tubular Acidosis
+C1704383	Primary Lung Lymphoma
+C1704417	Hyperlipoproteinemia Type IIb
+C1704421	Skin Pigmentation Disorder
+C1704423	Milroy Disease
+C1704429	Hypoalphalipoproteinemia, Familial
+C1704430	Urinary Schistosomiasis
+C1704431	Disorder of electrolytes
+C1704436	Peripheral Arterial Disease
+C1704453	Oncocytic Schneiderian papilloma
+C1704981	Hyperparathyroidism-Jaw Tumor Syndrome
+C1705254	Neonatal Deformity
+C1706004	Anhydrotic Ectodermal Dysplasias
+C1706410	Atopic IgE-mediated allergic disorder
+C1706412	Lipidemias
+C1706426	Intentional underdose
+C1706527	Primary intraocular non-Hodgkin malignant lymphoma
+C1706559	Cornea verticillata
+C1706595	Pachyonychia Congenita, Jadassohn Lewandowsky Type
+C1706731	Adult Extraskeletal Myxoid Chondrosarcoma
+C1706762	Aldosterone-Producing Adrenal Cortex Adenoma
+C1706827	Apocrine Carcinoma
+C1707291	NUT midline carcinoma
+C1707305	Carious Dentin
+C1707332	Cellular Myxoma
+C1707390	Chondroid Hamartoma
+C1707400	Classic medulloblastoma
+C1707439	Colorectal Mucinous Adenocarcinoma
+C1707440	Colorectal Signet Ring Cell Carcinoma
+C1707441	Colorectal Small Cell Neuroendocrine Carcinoma
+C1707444	Columnar Cell Change of the Breast
+C1707446	Columnar Cell Hyperplasia of the Breast
+C1707508	Conventional Dermatofibrosarcoma Protuberans
+C1707758	Direct Contact Transmission Infection
+C1707878	Eccrine carcinoma
+C1708045	Fetal Lung Adenocarcinoma
+C1708187	Gardner Fibroma
+C1708272	HIV lipodystrophy
+C1708349	Hereditary Diffuse Gastric Cancer
+C1708350	Hereditary Leiomyomatosis and Renal Cell Cancer
+C1708353	Hereditary Paraganglioma-Pheochromocytoma Syndrome
+C1708371	Histiocytoid Cardiomyopathy
+C1708502	Induced Cataract
+C1708550	Intimal sarcoma
+C1708554	Intraocular Infection
+C1708565	Invasive Skin Melanoma
+C1708566	Invasive Prostate Carcinoma
+C1708604	Keratocystic Odontogenic Tumor
+C1708751	Low grade myofibroblastic sarcoma
+C1708773	Lung Melanoma
+C1708776	mucinous adenocarcinoma of lung
+C1708778	mucoepidermoid carcinoma of lung
+C1708781	Lung Sarcomatoid Carcinoma
+C1709103	Myxoinflammatory fibroblastic sarcoma
+C1709166	Neoplastic C-Cell Hyperplasia
+C1709220	Desmoplastic Neurotropic Melanoma
+C1709286	Null Cell Pituitary Gland Adenoma
+C1709353	Osteofibrous Dysplasia
+C1709457	Papillary Thyroid Microcarcinoma
+C1709527	B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
+C1709569	Pleomorphic hyalinizing angiectatic tumor of soft tissue
+C1709573	Pleural Epithelioid Hemangioendothelioma
+C1709656	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
+C1709661	Primary Focal Segmental Glomerulosclerosis
+C1709780	Pyloric Gland Adenoma
+C1709781	Pyothorax-Associated Lymphoma
+C1709926	Response Evaluation Criteria in Solid Tumors
+C1710026	Sclerosing Epithelioid Fibrosarcoma
+C1710040	Secondary Focal Segmental Glomerulosclerosis
+C1710095	paranasal sinus and nasal cavity cancer
+C1710096	Sinonasal undifferentiated carcinoma
+C1710140	Sparsely Granulated Pituitary Gland Somatotroph Adenoma
+C1710499	Pleuropulmonary blastoma type III
+C1710501	Pleuropulmonary blastoma type I
+C1710547	Unilateral Breast Carcinoma
+C1710632	Vessel perforation
+C1711192	Sporadic Gastric Adenocarcinoma
+C1711276	carcinosarcoma of lung
+C1717804	Emphysema or COPD
+C1719306	Refractory cytopenia with multilineage dysplasia (RCMD)
+C1719313	Hereditary amyloid nephropathy
+C1719315	Hereditary cardiac amyloidosis
+C1719316	Inherited systemic amyloidosis
+C1719382	Acquired torsion dystonia
+C1719494	PERIODONTITIS, LOCALIZED AGGRESSIVE
+C1719495	Aggressive periodontitis, generalized
+C1719498	Generalized chronic periodontitis
+C1719528	Other stomatitis and mucositis (ulcerative)
+C1719672	Severe Sepsis
+C1719777	Hard drusen
+C1719788	Episodic ataxia type 1
+C1720008	AIDS-related small noncleaved cell lymphoma
+C1720037	Supranuclear gaze palsy
+C1720164	Central corneal thickness
+C1720180	Confluent drusen
+C1720189	Episodic Ataxia
+C1720251	Retinal pigment epithelium atrophy
+C1720275	Gonadotropin releasing factor deficiency
+C1720383	Simple ectopia lentis
+C1720416	Episodic ataxia type 2 (disorder)
+C1720430	Papillary carcinoma, clear cell
+C1720436	Under anesthesia
+C1720452	Soft drusen
+C1720470	Follicular carcinoma, widely invasive
+C1720491	Vitreous debris
+C1720505	Adult growth hormone deficiency
+C1720508	Retinal pigment epithelial abnormality
+C1720728	AIDS-related immunoblastic large cell lymphoma
+C1720771	Hydrocele
+C1720772	Hypoprebetalipoproteinemia
+C1720774	Glomerular Necrosis
+C1720775	Renal tubular necrosis
+C1720777	Functional Laterality
+C1720779	Apolipoprotein C-II Deficiency (disorder)
+C1720785	Meningitis, Pneumococcal, Recurrent
+C1720795	Acute Bacterial Prostatitis
+C1720796	Asymptomatic Inflammatory Prostatitis
+C1720797	Chronic Bacterial Prostatitis
+C1720798	Radiation-Recall Dermatitis
+C1720802	Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency
+C1720803	Glenohumeral Subluxation
+C1720811	Tumor of Rete Testis
+C1720814	Anterior Urethral Stricture
+C1720815	Posterior Urethral Stricture
+C1720816	Endometrial Diseases
+C1720821	Membranoproliferative Glomerulonephritis, Type III
+C1720824	Sudden Cardiac Arrest
+C1720830	Painful Bladder Syndrome
+C1720859	Familial Partial Lipodystrophy, Type 1
+C1720860	Familial Partial Lipodystrophy, Type 2
+C1720861	Familial Partial Lipodystrophy, Type 3
+C1720862	Congenital Generalized Lipodystrophy Type 1
+C1720863	Congenital Generalized Lipodystrophy Type 2
+C1720864	Sulfatidosis, Juvenile, Austin Type
+C1720887	Female Urogenital Diseases
+C1720894	Male Urogenital Diseases
+C1720922	Respiratory Aspiration
+C1720956	Hyper-IgM Immunodeficiency Syndrome, Type 2
+C1720957	Hyper-IgM Immunodeficiency Syndrome, Type 3
+C1720958	Hyper-IgM Immunodeficiency Syndrome, Type 5
+C1720965	Ectodermal Dysplasia 3, Anhidrotic
+C1720983	Channelopathies
+C1721005	Leukokeratosis, Hereditary Mucosal
+C1721006	Keratoderma, Palmoplantar, Epidermolytic
+C1721007	Pachyonychia Congenita, Type 2 (disorder)
+C1721017	Paraneoplastic Opsoclonus-Myoclonus Ataxia
+C1721096	Brugada ECG Pattern
+C1721098	Replication Error Phenotype
+C1723764	Chronic prostatitis - chronic pelvic pain syndrome
+C1735324	Fine motor delay
+C1735326	Enlarged uvula
+C1735330	Interleukin-2 receptor increased
+C1735336	Post procedural myocardial infarction
+C1735366	Progression of Alzheimer\'s disease
+C1735591	VACTERL Association
+C1735601	Floppy iris syndrome
+C1735603	Tenon's cyst
+C1735647	Mixed liver injury
+C1735856	Migraine with Typical Aura
+C1735901	Recurrent deep vein thrombosis
+C1735903	Chronic acidosis
+C1735914	Recurrent pulmonary embolism
+C1736136	Metapneumovirus infection
+C1736142	Vulvovaginal human papilloma virus infection
+C1736175	Progression of rheumatoid arthritis
+C1737211	Hypoglycaemic unconsciousness
+C1737214	Injection site injury
+C1737219	Acute graft versus host disease in intestine
+C1737222	Genotype drug resistance test positive
+C1737223	Hypoparathyroidism secondary
+C1737224	Post procedural swelling
+C1737225	Mesangioproliferative glomerulonephritis
+C1737250	Progression of non-small cell lung cancer
+C1737260	Recurrent mycobacterium avium complex infections
+C1737329	Dysmorphism
+C1739094	Foodborne botulism
+C1739097	Pneumobilia
+C1739098	In-stent arterial restenosis
+C1739102	Hepatobiliary scan abnormal
+C1739104	Acute graft versus host disease in liver
+C1739108	Latent Autoimmune Diabetes in Adults
+C1739111	Foetal anticonvulsant syndrome
+C1739113	Bladder transitional cell carcinoma recurrent
+C1739135	Progression of prostate cancer
+C1739363	Prostatic Hypertrophy
+C1739366	Injection site papule
+C1739370	Orthosis user
+C1739372	Acute graft versus host disease in skin
+C1739384	Angel shaped phalangoepiphyseal dysplasia
+C1739395	Takotsubo Cardiomyopathy
+C1739397	Abdominal wound dehiscence
+C1739399	Visceral congestion
+C1739405	CML progression
+C1740800	Expired drug administered
+C1740801	Exaggerated startle response
+C1740802	Post procedural sepsis
+C1741120	Temporal Lobectomy Behavior Syndrome
+C1744558	T-lymphocyte deficiency
+C1744559	Congenital ectodermal dysplasia of face
+C1744601	Abnormal heart beat
+C1760428	Suicidal behaviour
+C1761609	Aspiration pneumonitis
+C1761613	Conjunctival hyperaemia
+C1762616	Meningioma, benign, no ICD-O subtype
+C1765330	Immunoglobulins abnormal
+C1785148	RAPP-HODGKIN SYNDROME
+C1800706	Idiopathic Pulmonary Fibrosis
+C1801950	Opitz-G syndrome, type 2
+C1801959	Histiocytic medullary reticulosis (disorder)
+C1802395	Congenital muscular hypertrophy-cerebral syndrome
+C1802398	Chromosome 5, trisomy 5q
+C1806780	CSF protein increased
+C1809471	Familial benign hypercalcemia
+C1812607	Aortic aneurysm and dissection
+C1812609	Variola major
+C1820737	Temperature instability
+C1821417	RESTING HEART RATE
+C1822020	Insufficient Sleep
+C1824925	DEAFNESS, AUTOSOMAL RECESSIVE 70
+C1827170	Edema of extremity
+C1827192	Allergic fungal sinusitis
+C1827293	Carcinoma of urinary bladder, invasive
+C1827301	Extensively Drug-Resistant Tuberculosis
+C1827377	Slow acetylator due to N-acetyltransferase enzyme variant
+C1827478	Nervous tension
+C1827524	Wide spaced nipples
+C1827691	Refractory frontal lobe epilepsy
+C1827820	Fast acetylator due to N-acetyltransferase enzyme variant
+C1827841	Enzyme activity finding
+C1827849	IgE-mediated allergic asthma
+C1827894	Upper urinary tract infection
+C1827970	Neurofibroma of subcutaneous tissue
+C1827973	Barbiturate withdrawal
+C1827996	Ovarian cancer, disseminated
+C1828017	Intermittent hyperventilation
+C1828210	Macular dystrophy, concentric annular
+C1828221	Non dystrophic myotonia
+C1828256	Acute renal failure due to ischemia
+C1829460	Tongue thrusting
+C1829703	Carnitine palmitoyl transferase 1A deficiency
+C1829742	Fatty acid oxidation defects
+C1829844	Organic acidemias
+C1832097	EPIDERMAL DIFFERENTIATION COMPLEX
+C1832099	Wilms tumor and radial bilateral aplasia
+C1832108	PANCREATITIS, CHRONIC, PROTECTION AGAINST
+C1832117	Short humerus
+C1832119	Fibular hypoplasia
+C1832127	Square face
+C1832130	Pursed lips
+C1832146	Metaphyseal rarefaction
+C1832160	Abnormality of temperature regulation
+C1832162	HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY
+C1832167	Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism
+C1832168	BLOOD GROUP--FROESE
+C1832174	DOYNE HONEYCOMB RETINAL DYSTROPHY
+C1832175	Cataract, Congenital, Cerulean Type, 2
+C1832187	Deafness, Autosomal Dominant 12
+C1832200	Peroxisome biogenesis disorders
+C1832215	Athabaskan brainstem dysgenesis
+C1832216	Bosley-Salih-Alorainy Syndrome
+C1832230	Peroxisome Biogenesis Disorder, Complementation Group 4
+C1832231	Peroxisome Biogenesis Disorder, Complementation Group 6
+C1832232	Peroxisome Biogenesis Disorder, Complementation Group C
+C1832241	Agammaglobulinemia, non-Bruton type
+C1832243	CARDIOMYOPATHY, DILATED, 1D (disorder)
+C1832244	CARDIOMYOPATHY, DILATED, 1C (disorder)
+C1832273	Ribbing disease
+C1832274	Charcot-Marie-Tooth disease, Type 2D
+C1832276	Thenar muscle weakness
+C1832277	First dorsal interossei muscle weakness
+C1832278	First dorsal interossei muscle atrophy
+C1832279	Cold-induced hand cramps
+C1832321	INFLAMMATORY BOWEL DISEASE 2
+C1832322	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive
+C1832323	Failure to thrive secondary to recurrent infections
+C1832324	Recurrent opportunistic infections
+C1832334	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
+C1832338	Axonal loss
+C1832339	Intraaxonal accumulation of curvilinear profiles
+C1832342	Talipes cavus equinovarus
+C1832348	Slow-growing hair
+C1832370	MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
+C1832374	Restrictive heart failure
+C1832378	Retinitis Pigmentosa 18
+C1832386	Diabetes Mellitus, Transient Neonatal, 1
+C1832387	DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (disorder)
+C1832388	Platelet Disorder, Familial, with Associated Myeloid Malignancy
+C1832390	Van Maldergem Wetzburger Verloes syndrome
+C1832392	DIABETES MELLITUS, INSULIN-DEPENDENT, 12
+C1832394	Deafness, Autosomal Recessive 12
+C1832399	Charcot-Marie-Tooth disease, Type 4B1
+C1832409	Crisponi syndrome
+C1832425	Deafness, Autosomal Dominant 9
+C1832440	MICROPHTHALMIA, SYNDROMIC 8
+C1832446	Sparse eyebrow
+C1832451	Cranial hyperostosis
+C1832455	Hypoplastic sweat glands
+C1832466	CAPOS syndrome
+C1832471	Renal dysplasia diffuse cystic
+C1832475	Deafness, Autosomal Dominant 11
+C1832476	Deafness, Autosomal Dominant 10
+C1832525	Limb-girdle muscular dystrophy type 2F
+C1832526	CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT
+C1832529	HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION
+C1832544	DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1 (disorder)
+C1832550	Lamellar ichthyosis, type 2
+C1832560	RIPPLING MUSCLE DISEASE 2 (disorder)
+C1832567	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
+C1832585	CEREBELLAR ATAXIA, CAYMAN TYPE
+C1832586	DERMATITIS HERPETIFORMIS, FAMILIAL
+C1832587	POLYPOSIS SYNDROME, HEREDITARY MIXED, 1
+C1832588	Chromosome 11p11.2 Deletion Syndrome
+C1832589	Neuronal Intestinal Dysplasia, Type B
+C1832590	Craniosynostosis, Philadelphia Type
+C1832594	Verloes Bourguignon syndrome
+C1832597	Herniation of intervertebral nuclei
+C1832598	Narrow vertebral interpedicular distance
+C1832600	Naxos disease
+C1832603	ECG abnormality
+C1832612	Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
+C1832615	HYPERPARATHYROIDISM, NEONATAL SEVERE
+C1832648	Hypoparathyroidism familial isolated
+C1832661	ANOPHTHALMIA AND PULMONARY HYPOPLASIA
+C1832669	SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
+C1832671	Dysfunction of lateral corticospinal tracts
+C1832680	CARDIOMYOPATHY, DILATED, 1E
+C1832690	Vocal cord paresis in severe cases
+C1832702	BRACHYDACTYLY, TYPE A2
+C1832708	MULTIPLE SYNOSTOSES SYNDROME 2
+C1832736	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id
+C1832776	Hypertrophic nerve changes
+C1832812	Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation
+C1832814	Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
+C1832827	DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8
+C1832828	Deafness, Autosomal Recessive 9
+C1832830	Auditory Neuropathy, Nonsyndromic Recessive
+C1832834	Absence of acoustic reflex
+C1832841	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1
+C1832845	USHER SYNDROME, TYPE ID
+C1832855	CHOREOATHETOSIS/SPASTICITY, EPISODIC
+C1832884	Hemiplegic migraine, familial type 1
+C1832885	MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
+C1832903	MIGRAINE, SPORADIC HEMIPLEGIC
+C1832916	Timothy syndrome
+C1832918	Brody myopathy
+C1832926	EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)
+C1832931	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
+C1832932	DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder)
+C1832940	JUVENILE POLYPOSIS OF STOMACH
+C1832942	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
+C1832950	Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies
+C1832976	Cone-Rod Dystrophy 5
+C1832977	GLAUCOMA 3, PRIMARY INFANTILE, B
+C1832978	Deafness, Autosomal Recessive 7
+C1832983	Absent or minimally ossified vertebral bodies
+C1832988	Metaphyseal spurs
+C1832992	DEAFNESS, AUTOSOMAL RECESSIVE 6
+C1832998	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3
+C1833021	DEAFNESS, AUTOSOMAL DOMINANT 6
+C1833030	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC
+C1833053	Proprotein Convertase 1 3 Deficiency
+C1833054	Hypocortisolemia
+C1833058	Small intestine biopsy shows villous atrophy
+C1833102	DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
+C1833104	DIABETES MELLITUS, PERMANENT NEONATAL
+C1833118	Cataract, Pulverulent
+C1833136	Marden Walker like syndrome
+C1833142	contracture of elbow
+C1833144	Slender long bone
+C1833145	Distal ulnar hypoplasia
+C1833154	Long Qt Syndrome 4
+C1833182	Small platelet size
+C1833202	LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY
+C1833213	Hyperferritinemia, hereditary, with congenital cataracts
+C1833218	DIABETES MELLITUS, INSULIN-DEPENDENT, 8
+C1833219	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)
+C1833222	Autoamputation
+C1833225	Dystrophic toenail
+C1833229	Cataract, Congenital Zonular, with Sutural Opacities
+C1833236	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
+C1833245	Retinitis Pigmentosa 17
+C1833247	SCHIZOPHRENIA 4 (disorder)
+C1833275	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative
+C1833296	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
+C1833297	Frontal release signs
+C1833308	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
+C1833321	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL
+C1833323	Rickets of the lower limbs
+C1833324	Sparse bone trabeculae
+C1833325	Thin bony cortex
+C1833326	Generalized bone demineralization
+C1833328	Enlarged epiphyses
+C1833329	Bulging epiphyses
+C1833331	Increased serum 1,25-dihydroxyvitamin D3
+C1833340	Synostotic Posterior Plagiocephaly
+C1833362	Sleep-wake cycle disturbance
+C1833369	OROFACIAL CLEFT 3
+C1833372	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III
+C1833373	Inclusion Body Myopathy, Autosomal Recessive
+C1833382	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)
+C1833429	D-2-hydroxyglutaric aciduria
+C1833431	Subependymal cysts
+C1833434	Multifocal cerebral white matter abnormalities
+C1833448	RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO
+C1833453	Proximal Myopathy with Focal Depletion of Mitochondria
+C1833477	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
+C1833487	Varicella, Severe Recurrent
+C1833488	Infrequent generalized seizures
+C1833503	Deafness, Autosomal Dominant 4
+C1833508	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
+C1833511	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
+C1833518	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
+C1833538	OROFACIAL CLEFT 7
+C1833541	Caroli disease isolated
+C1833561	UV-Sensitive Syndrome
+C1833563	Cleft Lip, Congenital Healed
+C1833564	CONE-ROD DYSTROPHY 1 (disorder)
+C1833590	ATRIOVENTRICULAR SEPTAL DEFECT, SOMATIC
+C1833661	PAROXYSMAL EXTREME PAIN DISORDER
+C1833662	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
+C1833667	Elevated alkaline phosphatase of bone origin
+C1833683	NEPHROLITHIASIS, CALCIUM OXALATE
+C1833691	Otofaciocervical Syndrome
+C1833692	OTITIS MEDIA, SUSCEPTIBILITY TO (finding)
+C1833693	Otodental Dysplasia
+C1833699	Osteopoikilosis, Isolated
+C1833734	Carpal osteolysis
+C1833735	Osteolysis involving tarsal bones
+C1833736	Osteogenesis imperfecta, Levin type
+C1833739	Diaphyseal cortical sclerosis
+C1833752	Varying degree of multiple fractures
+C1833753	Biconcave flattened vertebrae
+C1833754	Femoral bowing present at birth, straightening with time
+C1833762	Decreased calvarial ossification
+C1833797	Optic Nerve Hypoplasia, Bilateral
+C1833798	Optic Nerve Aplasia, Bilateral
+C1833809	OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT
+C1833921	Familial medullary thyroid carcinoma
+C1833929	THYROID CARCINOMA, SPORADIC MEDULLARY
+C1833970	COLORECTAL CANCER, SOMATIC
+C1834002	Paternal anticipation bias
+C1834014	Oculopharyngodistal Myopathy
+C1834015	Progressive ptosis
+C1834034	Aplasia/Hypoplasia of the middle phalanx of the 5th finger
+C1834055	Underdeveloped nasal alae
+C1834056	Thin anteverted nares
+C1834057	Vertebral hyperostosis
+C1834060	Short middle phalanx of the 5th finger
+C1834062	3-4 toe syndactyly
+C1834118	Potato nose
+C1834120	NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME (disorder)
+C1834124	Shield chest
+C1834129	Abnormal vertebral morphology
+C1834144	Sick Sinus Syndrome 2, Autosomal Dominant
+C1834153	ALZHEIMER DISEASE, LATE-ONSET, SUSCEPTIBILITY TO
+C1834155	HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
+C1834167	Asymmetric overgrowth
+C1834176	MYELOKATHEXIS, ISOLATED
+C1834207	Ceroid Lipofuscinosis, Neuronal, Parry Type
+C1834235	NEUROFIBROMATOSIS, FAMILIAL SPINAL
+C1834236	Symmetric spinal nerve root neurofibromas
+C1834297	Inguinal freckling
+C1834304	AMYOTROPHY, HEREDITARY NEURALGIC
+C1834329	RETINITIS PIGMENTOSA 27
+C1834330	Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type
+C1834339	Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
+C1834345	Periosteal thickening of long tubular bones
+C1834372	Narcolepsy 1
+C1834383	Thickening of the lateral border of the scapula
+C1834384	Glenoid fossa hypoplasia
+C1834386	Hypoplasia of first ribs
+C1834387	Abnormal iris pigmentation
+C1834392	Disproportionate prominence of the femoral medial condyle
+C1834405	Nail dysplasia
+C1834421	Myxoid subcutaneous tumors
+C1834424	Profuse pigmented skin lesions
+C1834433	Obsessive-compulsive trait
+C1834460	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
+C1834478	MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
+C1834481	CARDIOMYOPATHY, DILATED, 1S
+C1834523	ARTHROGRYPOSIS, DISTAL, TYPE 2B
+C1834531	MYOPIA 2 (disorder)
+C1834536	Weakness of the intrinsic hand muscles
+C1834558	Myopathy, Centronuclear, Autosomal Dominant
+C1834559	Continuous Muscle Fiber Activity, Hereditary
+C1834569	Jankovic Rivera syndrome
+C1834570	Myoclonic dystonia
+C1834580	MYOCLONUS AND ATAXIA
+C1834582	MYELOPROLIFERATIVE SYNDROME, TRANSIENT
+C1834653	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
+C1834659	Muscular dystrophy, limb-girdle, type 1A
+C1834664	Nasal, dysarthic speech
+C1834671	FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B
+C1834673	Facioscapulohumeral muscular dystrophy 1a
+C1834674	Bethlem myopathy
+C1834690	Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
+C1834692	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
+C1834696	Hyporeflexia of lower limbs
+C1834703	Neuropathy, Distal Hereditary Motor, Type VIIA
+C1834711	CEREBELLOPARENCHYMAL DISORDER VI
+C1834712	Cerebellar Granule Cell Hypertrophy and Megalencephaly
+C1834728	Malignant genitourinary tract tumor
+C1834737	Cutaneous syndactyly of toes
+C1834750	CORONARY ARTERY DISEASE, MODIFIER OF
+C1834751	CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
+C1834752	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
+C1834821	METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
+C1834846	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
+C1834870	MIRROR MOVEMENTS 1
+C1834877	HOLOPROSENCEPHALY 2 (disorder)
+C1834928	Cloverleaf skull micromelia thoracic dysplasia
+C1834930	Fusion of the left and right thalami
+C1834931	Cystic renal dysplasia
+C1834953	Lumbar kyphoscoliosis
+C1834954	Coronal cleft vertebrae
+C1834961	Flattened, squared-off epiphyses of tubular bones
+C1834969	Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
+C1834975	Irregular acetabular roof
+C1834980	Metaphyseal cupping of proximal phalanges
+C1834993	Prominent supraorbital arches in adult
+C1835009	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE
+C1835039	Melanosis, Universal
+C1835042	Melanoma astrocytoma syndrome
+C1835044	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
+C1835047	MELANOMA, CUTANEOUS MALIGNANT, 1
+C1835084	Megaduodenum and-or Megacystis
+C1835093	Masticatory Muscles, Hypertrophy of
+C1835095	Macrodontia of permanent maxillary central incisor
+C1835101	Wide tufts of distal phalanges
+C1835117	Increased axial globe length
+C1835121	Premature osteoarthritis
+C1835130	Premature calcification of mitral annulus
+C1835148	Sparse lower eyelashes
+C1835157	Partial to total absence of eyelashes
+C1835171	Hypomagnesemia 2, renal
+C1835178	MACULAR DYSTROPHY, ATYPICAL VITELLIFORM
+C1835194	Thick corpus callosum
+C1835223	PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding)
+C1835228	Predominantly lower limb lymphedema
+C1835229	Onset of lymphedema around puberty
+C1835253	Hyperkeratosis over edematous areas
+C1835265	Lymphedema, microcephaly and chorioretinopathy syndrome
+C1835308	EXCESS LYMPHOCYTE LOW MOLECULAR WEIGHT DNA
+C1835309	EXCESS LMW-DNA
+C1835362	Lp(A) Deficiency, Congenital
+C1835380	Labial pseudohypertrophy
+C1835384	Loss of truncal subcutaneous adipose tissue
+C1835389	Increased intramuscular fat
+C1835390	Increased intraabdominal fat
+C1835398	LI-FRAUMENI SYNDROME 1
+C1835437	Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
+C1835442	Decreased cranial base ossification
+C1835444	Disc-like vertebral bodies
+C1835446	Severe limb shortening
+C1835450	Leri pleonosteosis
+C1835452	Hypoplastic ovary
+C1835470	Progressive sclerosis of skull base
+C1835473	Diaphyseal thickening
+C1835492	TOOTH AGENESIS, SELECTIVE, 4 (disorder)
+C1835493	Succedaneous Teeth, Agenesis Of
+C1835570	Hypoplastic cervical vertebrae
+C1835573	Multiple carpal ossification centers
+C1835574	Bipartite calcaneus
+C1835579	Rib exostoses
+C1835580	Mild postnatal growth retardation
+C1835583	Multiple long-bone exostoses
+C1835612	LACRIMAL DUCT DEFECT
+C1835614	Hereditary Hyperexplexia
+C1835662	Keratosis palmoplantaris papulosa
+C1835664	TYLOSIS WITH ESOPHAGEAL CANCER
+C1835672	Palmoplantar Keratoderma with Deafness
+C1835677	Keratoconus 1
+C1835686	Recurrent bacterial skin infections
+C1835697	Keratitis Fugax Hereditaria
+C1835698	Keratitis, hereditary
+C1835713	CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)
+C1835762	Widely-spaced maxillary central incisors
+C1835763	Vertebral body fusion
+C1835764	Vertebral arch anomaly
+C1835796	Crossed fused renal ectopia
+C1835798	Anoperineal fistula
+C1835801	Eversion of lateral third of lower eyelids
+C1835802	Thick eyelashes
+C1835807	Prominent fingertip pads
+C1835808	Kallikrein, Decreased Urinary Activity of
+C1835813	Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
+C1835817	FANCONI ANEMIA, COMPLEMENTATION GROUP N
+C1835819	PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)
+C1835820	HOLOPROSENCEPHALY 7
+C1835826	Renal Hypodysplasia, Nonsyndromic, 1
+C1835828	Invasive Pneumococcal Disease, Recurrent Isolated, 1
+C1835829	Immunodeficiency due to Defect in MAPBP-Interacting Protein
+C1835845	Mitochondrial Phosphate Carrier Deficiency
+C1835849	Congenital Disorder Of Glycosylation, Type Im
+C1835851	Ichthyosis with hypotrichosis, autosomal recessive
+C1835854	DEAFNESS, AUTOSOMAL RECESSIVE 68
+C1835865	Cone-Rod Dystrophy 11
+C1835867	WEST NILE VIRUS, SUSCEPTIBILITY TO (finding)
+C1835875	Normocytic hypoplastic anemia
+C1835881	Fluctuating hepatomegaly
+C1835882	Fluctuating splenomegaly
+C1835884	Triangular face
+C1835887	DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
+C1835888	Diarrhea 4, Malabsorptive, Congenital
+C1835894	Orofacial Cleft 9
+C1835895	RETINITIS PIGMENTOSA 33 (disorder)
+C1835896	SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
+C1835897	Retinal Cone Dystrophy 3B
+C1835905	Epilepsy, Nocturnal Frontal Lobe, Type 4
+C1835912	AICARDI-GOUTIERES SYNDROME 4
+C1835916	AICARDI-GOUTIERES SYNDROME 3
+C1835922	Aminoacylase 1 deficiency
+C1835923	Retinitis Pigmentosa 31
+C1835928	CARDIOMYOPATHY, DILATED, 1P
+C1835931	ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY
+C1835933	Glaucoma 1, Open Angle, G
+C1835934	Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
+C1835993	Loss of ability to walk in early childhood
+C1835995	Decreased activities of mitochondrial-encoded respiratory chain complexes
+C1836003	Facial diplegia
+C1836006	NANOPHTHALMOS 2 (disorder)
+C1836010	Spastic Paraplegia, Optic Atrophy, and Neuropathy
+C1836012	Hyperreflexia proximally
+C1836014	Exaggerated acoustic startle response
+C1836023	Drug Metabolism, Poor, CYP2C19-Related
+C1836027	Deafness, Autosomal Recessive 23
+C1836032	Immunoglobulin a deficiency 2
+C1836033	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
+C1836038	Poor head control
+C1836047	Long face
+C1836050	Filaminopathy, autosomal dominant
+C1836057	Muscle fiber splitting
+C1836076	Amyotrophic Lateral Sclerosis, Chmp2B-Related
+C1836080	Stickler Syndrome, Type I, Nonsyndromic Ocular
+C1836081	RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
+C1836118	LEFT VENTRICULAR NONCOMPACTION 2
+C1836122	SARCOIDOSIS, EARLY-ONSET
+C1836123	Goldberg-Shprintzen megacolon syndrome
+C1836141	Respiratory muscle weakness
+C1836149	Axial dystonia
+C1836150	Gait imbalance
+C1836151	Frontolimbic dementia
+C1836155	Myopathy, Myofibrillar, Zasp-Related
+C1836156	Progressive proximal muscle weakness
+C1836173	Generalized Epilepsy and Paroxysmal Dyskinesia
+C1836174	Involuntary dystonic or choreiform movements
+C1836182	Chondrodysplasia, acromesomelic, with genital anomalies
+C1836184	Short femoral neck
+C1836186	Fibular aplasia
+C1836187	Widened proximal tibial metaphyses
+C1836189	Radial deviation of finger
+C1836192	Aplasia/Hypoplasia involving the metacarpal bones
+C1836193	Synostosis of carpal bones
+C1836195	Short toe
+C1836199	DEAFNESS, AUTOSOMAL RECESSIVE 48
+C1836206	Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction
+C1836212	Proximal/middle symphalangism of 5th finger
+C1836213	Aplasia/Hypoplasia of the hallux
+C1836216	Symphalangism affecting the phalanges of the hallux
+C1836217	Tukel syndrome
+C1836219	Carpal bone aplasia
+C1836230	HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
+C1836255	Preeclampsia Eclampsia 4
+C1836264	Congenital bilateral ptosis
+C1836284	Epidermolysis Bullosa Simplex with Migratory Circinate Erythema
+C1836295	SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE (disorder)
+C1836296	Lower limb muscle weakness
+C1836302	Carotid Intimal Medial Thickness 1
+C1836308	Generalized joint laxity
+C1836320	Proximal femoral metaphyseal irregularity
+C1836326	Teratoid Tumor, Atypical
+C1836327	RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder)
+C1836330	ERYTHROKERATODERMIA VARIABILIS 3 (disorder)
+C1836336	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
+C1836373	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K
+C1836383	SPINOCEREBELLAR ATAXIA 27
+C1836392	Dysmetric saccades
+C1836395	SPINOCEREBELLAR ATAXIA 26
+C1836437	B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations
+C1836438	Familial neurocardiogenic syncope
+C1836439	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
+C1836440	Increased serum lactate
+C1836447	Nemaline myopathy 4
+C1836448	Nemaline myopathy 1
+C1836450	Distal lower limb muscle weakness
+C1836451	Distal lower limb amyotrophy
+C1836460	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2
+C1836472	Nemaline myopathy 6
+C1836474	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
+C1836479	Saccadic smooth pursuit
+C1836482	Li-Fraumeni Syndrome 2
+C1836485	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
+C1836508	Generalized tonic seizures
+C1836509	Hypotonic seizures
+C1836517	Senior-Loken Syndrome 5
+C1836522	Schindler Disease, Type II
+C1836525	White mater abnormalities in the posterior periventricular region
+C1836527	Distal sensory impairment of all modalities
+C1836533	Increased urinary O-linked sialopeptides
+C1836542	Depressed nasal bridge
+C1836543	Thick vermilion border
+C1836544	Schindler Disease, Type I
+C1836545	Schindler Disease, Type III
+C1836550	Loss of developmental milestones
+C1836573	GRISCELLI SYNDROME, TYPE 3
+C1836576	Silver-gray hair
+C1836589	Decreased hip abduction
+C1836599	Macrocephaly at birth
+C1836602	Bruck syndrome 2
+C1836603	Foveal Hypoplasia and Anterior Segment Dysgenesis
+C1836607	MYOTILINOPATHY
+C1836609	Progressive distal muscle weakness
+C1836623	Decreased circulating cortisol level
+C1836632	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE (disorder)
+C1836635	Loeys-Dietz Aortic Aneurysm Syndrome
+C1836646	Dermal translucency
+C1836651	Generalized arterial tortuosity
+C1836653	Ascending aortic dissection
+C1836669	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If
+C1836672	Total Hypotrichosis, Mari type
+C1836674	Short distal phalanx of the 5th finger
+C1836678	Abnormality of the middle ear ossicles
+C1836681	Erythrokeratoderma, Reticular
+C1836683	Czech dysplasia, metatarsal type
+C1836688	Narrow iliac wings
+C1836694	Striatal Degeneration, Autosomal Dominant
+C1836696	Lower limb hyperreflexia
+C1836705	Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
+C1836706	Hyperthyroidism, Nonautoimmune
+C1836721	MALARIA, MILD, SUSCEPTIBILITY TO
+C1836723	Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
+C1836724	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)
+C1836727	Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
+C1836729	Autonomic dysregulation
+C1836735	hypopigmented skin patch
+C1836736	White eyelashes
+C1836737	White eyebrow
+C1836742	Absent brainstem auditory responses
+C1836743	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1
+C1836752	Abnormal speech discrimination
+C1836756	ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)
+C1836765	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
+C1836767	Proximal lower limb amyotrophy
+C1836772	Decreased movement range in interphalangeal joints
+C1836775	Mild disease course
+C1836777	TELOMERE LENGTH, MEAN LEUKOCYTE
+C1836780	PANCREATIC AND CEREBELLAR AGENESIS
+C1836791	Tortuous cerebral arteries
+C1836797	Combined Oxidative Phosphorylation Deficiency 1
+C1836823	Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
+C1836824	Amish Infantile Epilepsy Syndrome
+C1836829	Developmental stagnation at onset of seizures
+C1836830	Developmental regression
+C1836835	Hyporeflexia of upper limbs
+C1836840	Decreased eye contact
+C1836842	Psychomotor deterioration
+C1836843	Progressive inability to walk
+C1836851	Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
+C1836852	Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
+C1836855	Vacuolated lymphocytes
+C1836860	FANCONI ANEMIA, COMPLEMENTATION GROUP J
+C1836861	FANCONI ANEMIA, COMPLEMENTATION GROUP I
+C1836868	Broad ischia
+C1836876	Pierson syndrome
+C1836890	Hypoplasia of the ciliary body
+C1836892	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3
+C1836899	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE (disorder)
+C1836904	Spastic/hyperactive bladder
+C1836906	Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
+C1836916	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
+C1836923	Gastrointestinal dysmotility
+C1836926	Bone spicule pigmentation of the retina
+C1836929	Emanuel syndrome
+C1836933	Low-set nipples
+C1836940	Thickened nuchal skin fold
+C1836996	Disproportionate tall stature
+C1837007	DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT
+C1837008	PREMATURE OVARIAN FAILURE 3 (disorder)
+C1837014	Atrial Fibrillation, Familial, 3
+C1837015	ATAXIA, SENSORY, AUTOSOMAL DOMINANT
+C1837016	Gait instability, worse in the dark
+C1837023	CATARACT, CONGENITAL, CERULEAN TYPE, 3
+C1837026	MEACHAM SYNDROME (disorder)
+C1837028	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive
+C1837029	Macular Dystrophy, Butterfly-Shaped Pigmentary, 2
+C1837065	CD8 Deficiency, Familial
+C1837066	Recurrent viral infection
+C1837073	Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy
+C1837078	Hypoplastic inferior ilia
+C1837081	Tibial bowing
+C1837082	Metaphyseal cupping
+C1837084	Short metacarpal
+C1837087	Macular pigmentary changes
+C1837091	MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
+C1837092	Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency
+C1837098	Easy fatigability
+C1837108	Decreased muscle mass
+C1837122	Myasthenic Syndrome, Congenital, Fast-Channel
+C1837142	Poor suck
+C1837148	MYOPIA 6 (disorder)
+C1837149	Alzheimer Disease 9
+C1837154	Drug Metabolism, Poor, CYP2D6-Related
+C1837173	CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5
+C1837174	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
+C1837187	MACULAR DEGENERATION, AGE-RELATED, 3
+C1837203	WAARDENBURG SYNDROME, TYPE IID
+C1837206	Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
+C1837210	OROFACIAL CLEFT 5
+C1837213	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO
+C1837217	Cleft lip, isolated
+C1837218	Cleft palate, isolated
+C1837229	Muscular Dystrophy, Congenital, Type 1D
+C1837245	Carney Complex Variant
+C1837246	Intracerebral periventricular calcifications
+C1837247	Antenatal intracerebral hemorrhage
+C1837249	Malformations of Cortical Development, Group II
+C1837251	Basal ganglia cysts
+C1837256	Macrovesicular hepatic steatosis
+C1837260	Prominent forehead
+C1837262	Increased muscle lipid content
+C1837271	Elevated serum long-chain fatty acids
+C1837273	Long-chain dicarboxylic aciduria
+C1837279	Hypoplastic toenails
+C1837315	COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
+C1837317	Alpha-B Crystallinopathy
+C1837323	Decreased Achilles reflex
+C1837341	Transposition of the Great Arteries, Dextro-Looped 1
+C1837342	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
+C1837352	Childhood onset
+C1837355	Leukodystrophy, Hypomyelinating, 2
+C1837371	Sudden Infant Death with Dysgenesis of the Testes Syndrome
+C1837379	Partial development of the penile shaft
+C1837380	Dysplastic testes
+C1837385	Poor growth
+C1837388	Abnormal pattern of respiration
+C1837396	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie
+C1837397	Severe global developmental delay
+C1837402	Flat occiput
+C1837404	High, narrow palate
+C1837406	Hypoplasia involving bones of the upper limbs
+C1837407	Ankle contracture
+C1837429	Pyruvate dehydrogenase phosphatase deficiency
+C1837431	Decreased activity of the pyruvate dehydrogenase (PDH) complex
+C1837454	SPINOCEREBELLAR ATAXIA 8
+C1837458	Impaired smooth pursuit
+C1837463	Narrow face
+C1837464	Small eyes
+C1837467	Excessive skin wrinkling on dorsum of hands and fingers
+C1837471	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
+C1837475	Insulin-Like Growth Factor I Deficiency
+C1837481	Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
+C1837482	Thoracic hypoplasia
+C1837483	Posterior rib cupping
+C1837485	Flat acetabular roof
+C1837487	Dysplastic iliac wings
+C1837496	Axonal degeneration
+C1837501	Microcephaly, Primary Autosomal Recessive, 5
+C1837503	Small cerebral cortex
+C1837512	Decreased serum complement C3
+C1837518	Spinocerebellar ataxia 25
+C1837522	Impaired pain sensation
+C1837530	AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
+C1837532	Fused labia minora
+C1837541	SPINOCEREBELLAR ATAXIA 20
+C1837549	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2
+C1837552	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)
+C1837602	Painless fractures due to injury
+C1837603	Acral ulceration and osteomyelitis leading to autoamputation of digits
+C1837610	ICHTHYOSIS PREMATURITY SYNDROME
+C1837615	Ciliary Dyskinesia, Primary, 5
+C1837618	CILIARY DYSKINESIA, PRIMARY, 3
+C1837639	Intermittent hypothermia
+C1837640	Deafness, Autosomal Dominant 28
+C1837649	Impaired ability to form peer relationships
+C1837650	Lack of spontaneous play
+C1837653	Inflexible adherence to routines or rituals
+C1837657	Spondyloepiphyseal dysplasia, Omani type
+C1837658	Gross motor development delay
+C1837670	Progressive intervertebral space narrowing
+C1837713	JOUBERT SYNDROME 3
+C1837728	AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)
+C1837731	Overfolded helix
+C1837732	Thickened helices
+C1837739	Hypertension, Diastolic, Resistance to
+C1837750	Oligodontia-Colorectal Cancer Syndrome
+C1837756	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
+C1837757	Progressive clavicular acroosteolysis
+C1837758	Bird-like facies
+C1837760	Prominent eyes
+C1837761	Narrow nasal ridge
+C1837763	Decreased adipose tissue around neck
+C1837764	Loss of subcutaneous adipose tissue in limbs
+C1837767	Loss of facial adipose tissue
+C1837770	Sparse hair
+C1837785	Prominent superficial veins
+C1837792	Insulin-resistant diabetes mellitus at puberty
+C1837795	Prominent umbilicus
+C1837799	Generalized muscular appearance from birth
+C1837802	Decreased serum leptin
+C1837805	Charcot-Marie-Tooth disease, axonal, Type 2G
+C1837811	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2
+C1837819	Cerebrofrontofacial Syndrome
+C1837822	Burn-Mckeown syndrome
+C1837826	Lower eyelid coloboma
+C1837830	Ulnar-Fibular Ray Defect and Brachydactyly
+C1837835	Bilateral talipes equinovarus
+C1837836	4-5 toe syndactyly
+C1837839	CARDIOMYOPATHY, DILATED, 1O
+C1837845	SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
+C1837857	DEAFNESS, AUTOSOMAL RECESSIVE 35
+C1837872	LEGIONNAIRE DISEASE, SUSCEPTIBILITY TO
+C1837873	LEBER CONGENITAL AMAUROSIS 9 (disorder)
+C1837884	Larsen-Like Syndrome
+C1837888	Absent nasal bridge
+C1837893	SCHIZOPHRENIA 12
+C1837899	Type I transferrin isoform profile
+C1837915	ERYTHROCYTOSIS, FAMILIAL, 2
+C1837974	Corneal Dystrophy, Lattice Type IIIA
+C1837991	Colorectal Adenomatous Polyposis, Autosomal Recessive
+C1838021	MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO, 1 (finding)
+C1838023	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3
+C1838027	Incomprehensible speech
+C1838049	Epilepsy, Nocturnal Frontal Lobe, Type 1
+C1838062	Autosomal Dominant Lateral Temporal Lobe Epilepsy
+C1838063	Auditory auras
+C1838099	ABCD syndrome
+C1838100	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
+C1838103	MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA
+C1838111	Bone marrow biopsy shows erythroid hyperplasia
+C1838114	Generalized limb muscle atrophy
+C1838162	Mesomelia-synostoses syndrome
+C1838163	OSLER-RENDU-WEBER SYNDROME 2
+C1838167	Nail bed telangiectasia
+C1838180	CODAS syndrome
+C1838186	Squared iliac bones
+C1838192	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
+C1838230	SPINAL MUSCULAR ATROPHY, TYPE IV
+C1838239	Band Heterotopia of Brain
+C1838244	TIBIAL MUSCULAR DYSTROPHY, TARDIVE
+C1838254	RIPPLING MUSCLE DISEASE 1
+C1838257	Serpentine fibula polycystic kidney syndrome
+C1838258	Osteopetrosis and infantile neuroaxonal dystrophy
+C1838259	DIABETES MELLITUS, INSULIN-DEPENDENT, 7
+C1838260	DIABETES MELLITUS, INSULIN-DEPENDENT, 5
+C1838261	DIABETES MELLITUS, INSULIN-DEPENDENT, 4
+C1838263	Deafness, Autosomal Recessive 3
+C1838280	Epiphyseal dysplasia, multiple, 1
+C1838299	Peroxisome Biogenesis Disorder, Complementation Group 14
+C1838300	Peroxisome Biogenesis Disorder, Complementation Group J
+C1838313	Pick Complex
+C1838319	Primitive reflexes (palmomental, snout, glabellar)
+C1838320	Hyperorality
+C1838327	Polycystic kidneys, severe infantile with tuberous sclerosis
+C1838329	APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
+C1838333	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
+C1838348	Oculomaxillofacial dysostosis
+C1838359	Diffuse palmoplantar keratoderma, Bothnian type
+C1838391	Limb hypertonia
+C1838416	CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY
+C1838429	Epiphyseal dysplasia, multiple, 2
+C1838437	VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL
+C1838440	ICHTHYOSIS EXFOLIATIVA
+C1838457	FANCONI ANEMIA, COMPLEMENTATION GROUP D1
+C1838492	SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
+C1838502	NANOPHTHALMOS 1
+C1838527	LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
+C1838539	CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
+C1838547	MELANOMA-PANCREATIC CANCER SYNDROME
+C1838548	OROLARYNGEAL CANCER, MULTIPLE
+C1838564	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2
+C1838568	Sacral defect and anterior sacral meningocele
+C1838569	Caudal Dysgenesis Syndrome
+C1838570	CEROID LIPOFUSCINOSIS, NEURONAL, 8
+C1838571	Ceroid Lipofuscinosis, Neuronal, 7
+C1838577	Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
+C1838578	Progressive encephalopathy
+C1838579	Pseudobulbar signs
+C1838601	Retinitis Pigmentosa 11
+C1838603	Retinitis Pigmentosa 14
+C1838604	EPILEPSY, CHILDHOOD ABSENCE, 1
+C1838608	Radial aplasia
+C1838610	Aplasia of the 1st metacarpal
+C1838612	Rhizomelic chondrodysplasia punctata, type 3
+C1838625	Warburg Sjo Fledelius syndrome
+C1838644	Stargardt disease 3
+C1838647	RETINITIS PIGMENTOSA 12 (disorder)
+C1838652	SPLIT-HAND/FOOT MALFORMATION 3
+C1838654	Nivelon Nivelon Mabille syndrome
+C1838656	Macrocytosis, Familial
+C1838657	Vitamin D Hydroxylation-Deficient Rickets, Type 1B
+C1838659	Deformed rib cage
+C1838662	Metaphyseal irregularity
+C1838663	Enlargement of the wrists
+C1838664	Enlargement of the ankles
+C1838670	Myelocytic leukemia-like syndrome, familial, chronic
+C1838681	Rapidly progressive
+C1838701	DEAFNESS, AUTOSOMAL RECESSIVE 2
+C1838702	Retinitis Pigmentosa 13
+C1838703	Bladder Exstrophy and Epispadias Complex
+C1838705	Anteriorly placed anus
+C1838779	Eiken Skeletal Dysplasia
+C1838780	Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease
+C1838818	MUSCLE STIFFNESS, PAINFUL
+C1838854	DEAFNESS, AMINOGLYCOSIDE-INDUCED
+C1838867	PARKINSON DISEASE, MITOCHONDRIAL (disorder)
+C1838868	Corticospinal tract atrophy
+C1838869	Proximal neurogenic muscle weakness
+C1838876	MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE
+C1838877	Myoglobinuria, Recurrent
+C1838916	ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
+C1838951	LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
+C1838954	STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA
+C1838979	MITOCHONDRIAL COMPLEX I DEFICIENCY
+C1838990	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL
+C1838993	Episodic vomiting
+C1839021	Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial
+C1839022	Striatonigral Degeneration, Infantile, Mitochondrial
+C1839025	Decreased light- and dark-adapted electroretinogram amplitude
+C1839028	Mitochondrial Myopathy with Diabetes
+C1839040	LEBER OPTIC ATROPHY AND DYSTONIA
+C1839042	Upper motor neuron dysfunction
+C1839071	Spermatogenic Failure, Nonobstructive, Y-Linked
+C1839073	Sertoli cell-only syndrome, Y-linked
+C1839082	MENTAL RETARDATION, X-LINKED 89
+C1839130	Dystonia 3, Torsion, X-Linked
+C1839141	Thyroxine-Binding Globulin Deficiency
+C1839161	Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
+C1839163	THROMBOCYTOPENIA 1 (disorder)
+C1839164	Thrombocytopenia, X-Linked, Intermittent
+C1839167	Intermittent thrombocytopenia
+C1839248	Broad chest
+C1839252	Hump-shaped mound of bone in central and posterior portions of vertebral endplate
+C1839254	Hypoplasia of the capital femoral epiphysis
+C1839258	SPLIT-HAND/FOOT MALFORMATION 2
+C1839259	Bulbo-Spinal Atrophy, X-Linked
+C1839264	SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
+C1839269	Duplication of renal pelvis
+C1839271	Birth length greater than 97th percentile
+C1839276	Broad secondary alveolar ridge
+C1839277	Submucous cleft lip
+C1839279	Six lumbar vertebrae
+C1839285	Two carpal ossification centers present at birth
+C1839304	Decreased number of CD4+ T cells
+C1839305	Decreased number of CD8+ T cells
+C1839323	Small chin
+C1839326	Abnormal form of the vertebral bodies
+C1839332	Rett Syndrome, Preserved Speech Variant
+C1839333	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
+C1839341	Abnormal T-wave
+C1839362	Cystic retinal degeneration
+C1839364	Progressive visual loss
+C1839413	Pyruvate Dehydrogenase E1 Alpha Deficiency
+C1839424	Increased blood alanine
+C1839436	Severe lactic acidosis
+C1839437	Chronic lactic acidosis
+C1839454	PROPERDIN DEFICIENCY, X-LINKED
+C1839455	Properdin Deficiency, Type II
+C1839456	Properdin Deficiency, Type III
+C1839458	Dysfunctional alternative complement pathway
+C1839463	TARP syndrome
+C1839507	Thick skull base
+C1839512	Limited knee flexion
+C1839530	VALPROATE SENSITIVITY
+C1839531	Protein avoidance
+C1839532	Low plasma citrulline
+C1839533	Hyperglutaminemia
+C1839541	Episodic ammonia intoxication
+C1839546	Microretrognathia
+C1839564	Jensen syndrome
+C1839566	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5
+C1839576	OPTIC ATROPHY 2 (disorder)
+C1839580	Nystagmus 1, congenital, X- linked
+C1839602	Neuropathy, Hereditary Sensory, X-Linked
+C1839603	Proximal tubulopathy
+C1839604	Renal failure in adulthood
+C1839606	Low-molecular-weight proteinuria
+C1839612	MYOPIA 1, X-LINKED
+C1839615	X-linked myopathy with excessive autophagy
+C1839630	Severe muscular hypotonia
+C1839653	Decreased cervical spine flexion due to contractures of posterior cervical muscles
+C1839666	Calf muscle pseudohypertrophy
+C1839707	AUTISM, SEVERE
+C1839728	METACARPAL 4-5 FUSION
+C1839730	Prieto X-linked mental retardation syndrome
+C1839731	11 pairs of ribs
+C1839735	MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME
+C1839736	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME
+C1839739	Thick lower lip vermilion
+C1839749	Paroxysmal bursts of laughter
+C1839758	Narrow forehead
+C1839764	Broad flat nasal bridge
+C1839765	Triangular nasal tip
+C1839767	Tented upper lip vermilion
+C1839780	FRAGILE X TREMOR/ATAXIA SYNDROME
+C1839782	Macroorchidism, postpubertal
+C1839783	Large forehead
+C1839785	Folate-dependent fragile site at Xq28
+C1839797	Deep philtrum
+C1839798	Long nose
+C1839816	Long neck
+C1839822	Anterior concavity of thoracic vertebrae
+C1839829	Short distal phalanx of finger
+C1839830	Frontal hirsutism
+C1839832	Noncompaction cardiomyopathy
+C1839839	MAJOR AFFECTIVE DISORDER 2
+C1839840	MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE
+C1839841	SPERMATOGENIC FAILURE, X-LINKED, 2
+C1839858	Periventricular cysts
+C1839860	Elevated amniotic fluid alpha-fetoprotein
+C1839865	Bicarbonaturia
+C1839866	Elevated serum acid phosphatase
+C1839874	Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
+C1839884	Leiomyomatosis, esophageal and vulval, with nephropathy
+C1839888	Decreased activity of the pyruvate dehydrogenase complex
+C1839909	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED
+C1839928	IRIS HYPOPLASIA WITH GLAUCOMA
+C1839942	Retinal fibrosis
+C1839965	Multiple impacted teeth
+C1839969	Reduced natural killer cell activity
+C1839972	Increased IgM level
+C1839988	Ichthyosis follicularis atrichia photophobia syndrome
+C1840006	Mild intrauterine growth retardation
+C1840013	Elevated 8-dehydrocholesterol
+C1840014	Elevated 8(9)-cholestenol
+C1840061	SMALL PATELLA SYNDROME
+C1840062	Hypoplasia of the lesser trochanter
+C1840068	Patellar hypoplasia
+C1840069	Sandal gap
+C1840077	Anteverted nostril
+C1840084	ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO
+C1840086	Pectoralis major hypoplasia
+C1840087	Radial ray hypoplasia
+C1840088	Limited wrist movement
+C1840089	Limited interphalangeal movement
+C1840169	CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
+C1840225	Absence of lower central incisor
+C1840235	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
+C1840236	Prominent midpalatal ridge
+C1840238	Midnasal stenosis
+C1840253	IgE RESPONSIVENESS, ATOPIC
+C1840254	ATOPY, SUSCEPTIBILITY TO (finding)
+C1840264	IMMUNE SUPPRESSION
+C1840284	LEBER CONGENITAL AMAUROSIS 11
+C1840296	Ichthyosis hystrix, Curth Macklin type
+C1840299	Hypotrichosis Simplex of Scalp
+C1840305	Absent external auditory canals
+C1840307	Distal shortening of limbs
+C1840309	Short 4th metacarpal
+C1840310	Midline facial capillary hemangioma
+C1840311	Laryngeal cleft
+C1840319	Redundant neck skin
+C1840322	ODONTOHYPOPHOSPHATASIA (disorder)
+C1840333	Barakat syndrome
+C1840334	Hypoparathyroidism, Autosomal Recessive
+C1840347	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
+C1840348	Hypocalciuric Hypercalcemia, Acquired
+C1840362	HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE (disorder)
+C1840364	THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY
+C1840365	King Denborough syndrome
+C1840372	Mixed respiratory and metabolic acidosis
+C1840374	Elevated systolic blood pressure
+C1840375	Elevated diastolic blood pressure
+C1840376	Elevated mean arterial pressure
+C1840379	Cerebellar vermis hypoplasia
+C1840380	Persistent cavum septum pellucidum
+C1840382	Abnormality of the ureter
+C1840390	Pseudohypoaldosteronism, Type IIb
+C1840391	Pseudohypoaldosteronism, Type IIc
+C1840392	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE
+C1840394	Parathyroid Adenomatosis, Familial Cystic
+C1840396	Renal hamartoma
+C1840402	HYPERPARATHYROIDISM 1
+C1840403	Parathyroid Adenoma, Familial
+C1840404	Hyperostosis Cranialis Interna
+C1840418	Thickened cortex of long bones
+C1840419	Metacarpal diaphyseal endosteal sclerosis
+C1840420	Metatarsal diaphyseal endosteal sclerosis
+C1840423	HEREDITARY RENAL CANCER ASSOCIATED 1
+C1840427	PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, WITH KNUCKLE PADS (disorder)
+C1840437	Isolated hyperchlorhidrosis
+C1840438	Orthostatic Hypotensive Disorder, Streeten Type
+C1840451	MULTICYSTIC RENAL DYSPLASIA, BILATERAL
+C1840452	Hyaloideoretinal degeneration of Wagner
+C1840457	Retinal pigment epithelial atrophy
+C1840528	HOLOPROSENCEPHALY 4 (disorder)
+C1840529	HOLOPROSENCEPHALY 3
+C1840535	Abnormality of the carpal bones
+C1840560	Hidradenitis suppurativa, familial
+C1840572	HIP DYSPLASIA, BEUKES TYPE
+C1840598	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2
+C1840644	Diaphragm, Complete Agenesis Of
+C1840646	Hepatic Adenomas, Familial
+C1841621	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
+C1841648	Short mandibular rami
+C1841651	Heme Oxygenase 1 Deficiency
+C1841658	Progressive Familial Heart Block, Type II
+C1841659	Atrioventricular nodal disease
+C1841679	Hand foot uterus syndrome
+C1841680	Longitudinal vaginal septum
+C1841684	Delayed ossification of carpal bones
+C1841685	Pseudoepiphyses
+C1841688	Short first metatarsal
+C1841721	ACHROMATOPSIA 4
+C1841739	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA, SOMATIC
+C1841816	Decreased von Willebrand factor
+C1841837	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1
+C1841972	Glucocorticoid Receptor Deficiency
+C1841973	Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance
+C1841982	BODY COMPOSITION, BENEFICIAL
+C1841984	GLOMUVENOUS MALFORMATIONS
+C1841989	Glomerulonephritis sparse hair telangiectases
+C1841990	Aplasia of the vagina
+C1841994	Decreased numbers of glomeruli
+C1842003	Subclinical abnormal liver function tests
+C1842010	Glioma of Brain, Familial
+C1842026	GLAUCOMA 1, OPEN ANGLE, E
+C1842028	GLAUCOMA 1, OPEN ANGLE, A
+C1842031	IRIDOGONIODYSGENESIS, TYPE 2
+C1842036	GIANT PIGMENTED HAIRY NEVUS
+C1842060	Prominent supraorbital ridges
+C1842062	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F
+C1842073	Prolonged Electroretinal Response Suppression
+C1842083	Abnormality of the ribs
+C1842084	Posterior rib fusion
+C1842090	Platelet Glycoprotein IV Deficiency
+C1842109	Microcephaly, Primary Autosomal Recessive, 6
+C1842124	BRANCHIOOTIC SYNDROME 3 (disorder)
+C1842127	Retinitis Pigmentosa 26
+C1842138	Progressive hearing impairment
+C1842143	Orofacial Cleft 4
+C1842149	Spondyloepiphyseal Dysplasia, Kimberley Type
+C1842153	Irregular vertebral endplates
+C1842155	Flat capital femoral epiphysis
+C1842160	MYOPATHY, MYOSIN STORAGE (disorder)
+C1842161	Scapuloperoneal weakness
+C1842162	Scapuloperoneal amyotrophy
+C1842170	Centrally nucleated skeletal muscle fibers
+C1842180	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
+C1842197	Charcot-Marie-Tooth Disease, Recessive Intermediate A
+C1842229	Broad metacarpals
+C1842231	Broad metatarsal
+C1842237	Charcot-Marie-Tooth Disease, Dominant Intermediate C
+C1842247	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
+C1842297	VENOOCCLUSIVE DISEASE AFTER BONE MARROW TRANSPLANTATION, SUSCEPTIBILITY TO
+C1842342	DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
+C1842357	Slowed Nerve Conduction Velocity, Autosomal Dominant
+C1842362	HERMANSKY-PUDLAK SYNDROME 2
+C1842364	Central hypotonia
+C1842366	Low anterior hairline
+C1842371	DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)
+C1842382	Epilepsy, Benign Neonatal, 3
+C1842398	Neutrophil Immunodeficiency Syndrome
+C1842402	TROPICAL CALCIFIC PANCREATITIS
+C1842404	Insulin-dependent but ketosis-resistant diabetes
+C1842406	Pancreatic calcification
+C1842408	increased risk of pancreatic cancer
+C1842422	Synpolydactyly 2
+C1842444	AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3 (finding)
+C1842462	CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
+C1842466	Uniparental disomy, paternal, chromosome 14
+C1842475	Retinitis Pigmentosa 7
+C1842485	ZINC IN BREAST MILK, REDUCED
+C1842486	Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc
+C1842528	Impaired Ig class switch recombination
+C1842534	DYSTONIA 18 (disorder)
+C1842552	Limb-girdle muscle atrophy
+C1842563	Heterotopia, Periventricular, Autosomal Recessive
+C1842564	Temporal epilepsy, familial
+C1842577	JOUBERT SYNDROME 2
+C1842581	Abnormality of the corpus callosum
+C1842584	Impaired saccades
+C1842586	Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux
+C1842587	Sensory axonal neuropathy
+C1842605	SCHIZOPHRENIA 11
+C1842675	AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
+C1842680	Small earlobe
+C1842687	PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
+C1842688	Hypoplasia of the brainstem
+C1842691	Diaphanospondylodysostosis
+C1842695	Absent in utero rib ossification
+C1842696	Posterior rib gap
+C1842698	Absent in utero ossification of vertebral bodies
+C1842704	GAUCHER DISEASE, PERINATAL LETHAL
+C1842710	Decreased beta-glucocerebrosidase protein and activity
+C1842714	Desquamation of skin soon after birth
+C1842763	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION
+C1842774	Hypermelanotic macule
+C1842777	Recurrent upper and lower respiratory tract infections
+C1842778	Atrial septal defect 2
+C1842797	Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like
+C1842816	RETINITIS PIGMENTOSA 30
+C1842820	Cardiac conduction abnormality
+C1842836	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii
+C1842839	HYPOTRICHOSIS 6
+C1842852	EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2
+C1842870	Chromosome 1p36 Deletion Syndrome
+C1842876	Depressed nasal ridge
+C1842878	Short 5th finger
+C1842884	Caudal Duplication Anomaly
+C1842892	Vascular abnormalities restricted to skin
+C1842898	Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
+C1842914	Adult-Onset Vitelliform Macular Dystrophy
+C1842930	Neutropenia, Nonimmune Chronic Idiopathic, Adult
+C1842937	AURAL ATRESIA, CONGENITAL
+C1842939	Deafness, Autosomal Dominant 48
+C1842979	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1
+C1842981	NEUROTICISM
+C1842983	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
+C1842984	Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
+C1843003	MITRAL VALVE PROLAPSE, MYXOMATOUS 2
+C1843004	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME
+C1843005	Absent eyelashes
+C1843013	Alzheimer disease, familial, type 3
+C1843014	Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
+C1843015	Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
+C1843028	Deafness, Autosomal Recessive 37
+C1843042	Craniolenticulosutural Dysplasia
+C1843057	Calf muscle hypertrophy
+C1843075	Charcot-Marie-Tooth Disease, Dominant Intermediate D
+C1843077	Segmental peripheral demyelination/remyelination
+C1843096	Acrocapitofemoral Dysplasia
+C1843105	Enlargement of the distal femoral epiphysis
+C1843108	Short palm
+C1843112	Broad nail
+C1843116	Bile acid synthesis defect, congenital, 1
+C1843139	Hypercholanemia, Familial
+C1843140	SEIZURES, BENIGN FAMILIAL INFANTILE, 3
+C1843146	Normal interictal EEG
+C1843153	Charcot-Marie-Tooth disease, Type 2J
+C1843156	Progressive sensorineural hearing impairment
+C1843164	Charcot-Marie-Tooth disease, demyelinating, Type 1F
+C1843168	Myelin outfoldings
+C1843169	Clusters of axonal regeneration
+C1843173	Charcot-Marie-Tooth disease, Type 2H
+C1843175	Hyperreflexia in upper limbs
+C1843180	Porokeratosis, disseminated superficial actinic 2
+C1843181	Noonan syndrome-like disorder with loose anagen hair
+C1843183	Charcot-Marie-Tooth disease, Type 4A, axonal form
+C1843187	Hoarse voice due to vocal cord paresis
+C1843211	PARKINSON DISEASE 11, AUTOSOMAL DOMINANT
+C1843225	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
+C1843228	Hypotrophy of the small hand muscles
+C1843244	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
+C1843247	Charcot-Marie-Tooth disease, Type 1D (disorder)
+C1843256	IRAK4 Deficiency
+C1843264	DYSTONIA 13, TORSION
+C1843273	Tubulointerstitial nephritis and uveitis
+C1843292	Skin Fragility-Woolly Hair Syndrome
+C1843294	Palmoplantar keratosis with erythema and scale
+C1843300	Sparse eyelashes
+C1843315	Neuronopathy, Distal Hereditary Motor, Type Viib
+C1843323	Van Buchem disease type 2
+C1843330	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
+C1843331	Generalized osteosclerosis
+C1843355	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS
+C1843359	Orthokeratosis
+C1843366	NIEMANN-PICK DISEASE, TYPE C2
+C1843367	Poor school performance
+C1843369	Vertical supranuclear gaze palsy
+C1843371	Low cholesterol esterification rates
+C1843372	Abnormal cholesterol homeostasis
+C1843373	Foam cells in visceral organs and CNS
+C1843386	Reduced delayed hypersensitivity
+C1843389	Accumulation of melanosomes in melanocytes
+C1843390	Melanin pigment aggregation in hair shafts
+C1843392	Death in childhood
+C1843418	Niemann-Pick Disease, Type F
+C1843428	Diffuse reticular or finely nodular infiltrations
+C1843463	Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
+C1843477	Epidermolysis Bullosa Simplex Superficialis
+C1843478	Lethal Congenital Contracture Syndrome 2
+C1843479	Neurogenic muscle atrophy, especially in the lower limbs
+C1843486	Degenerative vitreoretinopathy
+C1843496	Bilateral microphthalmos
+C1843504	Pontocerebellar Hypoplasia Type 1
+C1843505	Degeneration of anterior horn cells
+C1843507	Hypoplasia of the ventral pons
+C1843512	BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
+C1843517	Retinal arteriolar tortuosity
+C1843569	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE (disorder)
+C1843570	Tip-toe gait
+C1843637	Neck flexor weakness
+C1843643	Nocturnal hypoventilation
+C1843661	Spastic Paraplegia, Ataxia, And Mental Retardation
+C1843663	Urinary bladder sphincter dysfunction
+C1843677	Large sella turcica
+C1843687	ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
+C1843697	Axial muscle weakness
+C1843700	Increased variability in muscle fiber diameter
+C1843738	LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
+C1843758	Camptosynpolydactyly, Complex
+C1843761	TOENAIL DYSTROPHY, ISOLATED
+C1843791	CARDIOMYOPATHY, DILATED, 1N
+C1843792	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
+C1843793	Progressive language deterioration
+C1843807	Basal ganglia disease, biotin-responsive
+C1843808	CARDIOMYOPATHY, DILATED, 1M
+C1843815	Newfoundland Rod-Cone Dystrophy
+C1843816	Bothnia Retinal Dystrophy
+C1843832	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
+C1843851	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
+C1843852	SPINOCEREBELLAR ATAXIA WITH EPILEPSY
+C1843858	Atrophy/Degeneration involving the spinal cord
+C1843859	Sensory ataxic neuropathy
+C1843865	Vestibular dysfunction
+C1843884	SPINOCEREBELLAR ATAXIA 18
+C1843885	Progressive gait ataxia
+C1843889	GIL BLOOD GROUP
+C1843891	SPINOCEREBELLAR ATAXIA 21
+C1843892	Microsaccadic pursuit
+C1843895	Deafness, Autosomal Dominant 44
+C1843896	Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
+C1843898	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
+C1843920	COENZYME Q10 DEFICIENCY
+C1843921	Postural instability
+C1843942	Mental Retardation, Autosomal Recessive 2
+C1843983	Trapezoidal distal femoral condyles
+C1843985	Shortening of the talar neck
+C1843986	Flattening of the talar dome
+C1843995	Enteroviral hepatitis
+C1844006	Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction
+C1844007	Corticospinal tract hypoplasia
+C1844020	HETEROTAXY, VISCERAL, 1, X-LINKED
+C1844374	Persistent bleeding after trauma
+C1844376	Granulomatous Disease, Chronic, X-Linked
+C1844383	Recurrent bacterial infection
+C1844384	Recurrent fungal infections
+C1844385	Absence of bactericidal oxidative \'respiratory burst\' in phagocytes
+C1844390	Deficiency or absence of cytochrome b(-245)
+C1844394	Decreased activity of NADPH oxidase
+C1844412	Liver Glycogenosis, X-Linked, Type II
+C1844505	Pointed chin
+C1844508	Large foramen magnum
+C1844509	Antegonial notching of mandible
+C1844512	Anteriorly placed odontoid process
+C1844516	Increased density of long bone diaphyses
+C1844519	Partial fusion of carpals
+C1844520	Partial fusion of tarsals
+C1844527	Clitoral hypoplasia
+C1844529	Midclavicular aplasia
+C1844530	Midclavicular hypoplasia
+C1844537	Cleft ala nasi
+C1844548	Hypoplastic finger
+C1844554	Absent fingernail
+C1844555	Absent toenail
+C1844562	Medial flaring of the eyebrow
+C1844569	Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder
+C1844571	Increased upper to lower segment ratio
+C1844572	Curved linear dimple below the lower lip
+C1844573	Large earlobe
+C1844577	Hyperextensibility of the finger joints
+C1844579	Exudative Vitreoretinopathy, Familial, X-Linked Recessive
+C1844592	Soft skin
+C1844597	Molluscoid pseudotumors
+C1844605	Periorbital wrinkles
+C1844606	Periorbital hyperpigmentation
+C1844617	Hypoplastic-absent sebaceous glands
+C1844618	Aplasia/Hypoplastia of the eccrine sweat glands
+C1844632	Anal mucosal leukoplakia
+C1844654	X-linked Dyggve-Melchior-Clausen syndrome
+C1844662	Unexplained fevers
+C1844663	ISLETS OF LANGERHANS, ABSENCE OF
+C1844666	Immune dysregulation
+C1844677	DEAFNESS, X-LINKED 1 (disorder)
+C1844678	Progressive hearing loss stapes fixation
+C1844680	DEAFNESS-HYPOGONADISM SYNDROME
+C1844689	Pelvic bone exostoses
+C1844690	Limited knee extension
+C1844696	OTOPALATODIGITAL SYNDROME, TYPE II
+C1844702	Vertical clivus
+C1844704	Platyspondyly
+C1844706	Rudimentary fibula
+C1844709	Radial deviation of the 2nd finger
+C1844712	Nonossified fifth metatarsal
+C1844722	Unilateral breast hypoplasia
+C1844731	Hypoplastic nasal tip
+C1844734	Hemihypotrophy of lower limb
+C1844738	Axillary pterygia
+C1844749	Rib fusion
+C1844752	Butterfly vertebrae
+C1844753	Block vertebrae
+C1844776	CONE-ROD DYSTROPHY, X-LINKED, 1
+C1844777	CONE DYSTROPHY, X-LINKED, 1
+C1844806	Weight less than 3rd percentile
+C1844809	Thick nasal alae
+C1844810	Thick nasal septum
+C1844813	Widely spaced teeth
+C1844818	Lumbar kyphosis
+C1844820	Range of joint movement increased
+C1844822	Drumstick terminal phalanges
+C1844825	Hyperconvex fingernails
+C1844830	CLEFT PALATE, X-LINKED
+C1844831	Cleft Palate with Ankyloglossia
+C1844846	Stippled calcification in carpal bones
+C1844848	Tarsal stippling
+C1844853	Brachytelephalangic Chondrodysplasia Punctata
+C1844857	Short nasal septum
+C1844862	Abruzzo Erickson syndrome
+C1844865	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)
+C1844887	Catel Manzke syndrome
+C1844891	Ulnar deviation of the 2nd finger
+C1844906	Broad finger
+C1844909	Recurrent infections in infancy and early childhood
+C1844917	Intermittent lactic acidemia
+C1844923	Hypoplasia of the prostate
+C1844925	Cervical spinal canal stenosis
+C1844926	Scheuermann-like vertebral changes
+C1844934	Arthrogryposis multiplex congenita, distal, X-linked
+C1844947	Death in early childhood
+C1845019	Left ventricular septal hypertrophy
+C1845026	Neural tube defects X-linked
+C1845027	Spina Bifida, X-Linked
+C1845028	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA
+C1845029	Nonprogressive cerebellar ataxia
+C1845050	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
+C1845052	AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
+C1845053	Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth
+C1845055	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
+C1845069	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
+C1845070	Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked
+C1845073	INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder)
+C1845076	Lymphoproliferative Syndrome, X-Linked, 2
+C1845095	DEAFNESS, X-LINKED 5 (disorder)
+C1845102	Hyperekplexia and Epilepsy
+C1845105	Premature Ovarian Failure 2b
+C1845109	Exaggerated median tongue furrow
+C1845110	Central incisor gap
+C1845112	Hyperkyphosis
+C1845117	Immunodeficiency without anhidrotic ectodermal dysplasia
+C1845118	SHORT STATURE, IDIOPATHIC, X-LINKED
+C1845123	Generalized neonatal hypotonia
+C1845142	MENTAL RETARDATION, X-LINKED 91 (disorder)
+C1845144	Mental Retardation, X-Linked 92
+C1845146	Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
+C1845147	Hypoplasia of the frontal bone
+C1845151	Glycogen Storage Disease, Type IXD
+C1845155	Exercise-induced myoglobinuria
+C1845165	PARKINSON DISEASE 12
+C1845167	Dent Disease 2
+C1845168	Hypophosphatemic Rickets, X-Linked Recessive
+C1845169	Renal phosphate wasting
+C1845181	MENTAL RETARDATION, X-LINKED 78
+C1845202	Nephrogenic Syndrome of Inappropriate Antidiuresis
+C1845206	Decreased circulating renin level
+C1845235	Heterotopia, Periventricular, Ehlers-Danlos Variant
+C1845243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE
+C1845245	Lower limb hypertonia
+C1845250	Small forehead
+C1845251	Facial hypotonia
+C1845272	Prominent antihelix
+C1845274	Abnormal conjugate eye movement
+C1845285	Martin-Probst Deafness-Mental Retardation Syndrome
+C1845286	MENTAL RETARDATION, X-LINKED 82
+C1845292	FANCONI ANEMIA, COMPLEMENTATION GROUP B
+C1845293	Premature Ovarian Failure 2a
+C1845294	Ovarian Dysgenesis 2
+C1845295	Premature Ovarian Failure 4
+C1845297	MENTAL RETARDATION, X-LINKED 84
+C1845298	MENTAL RETARDATION, X-LINKED 52
+C1845333	Mental Retardation, X-Linked 45
+C1845334	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
+C1845336	AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
+C1845337	Lack of peer relationships
+C1845341	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
+C1845343	Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders
+C1845359	Spinal Muscular Atrophy, Distal, X-Linked 3
+C1845366	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance
+C1845369	Disorganization of the anterior cerebellar vermis
+C1845370	Retrocerebellar cyst
+C1845407	CONE-ROD DYSTROPHY, X-LINKED, 3
+C1845408	Contiguous Abcd1-Dxs1375e Deletion Syndrome
+C1845446	Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia
+C1845447	Cupped ears (finding)
+C1845499	MENTAL RETARDATION, X-LINKED 77
+C1845526	Mental Retardation, X-Linked 46
+C1845530	Stocco dos Santos syndrome
+C1845531	MENTAL RETARDATION, X-LINKED 81
+C1845539	AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
+C1845540	AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
+C1845543	Mental Retardation, X-Linked, with Epilepsy
+C1845546	FG SYNDROME 4 (disorder)
+C1845567	FG SYNDROME 3
+C1845576	Unilateral chest hypoplasia
+C1845604	Recurrent bacterial meningitis
+C1845609	Lymphoid depletion
+C1845667	RETINITIS PIGMENTOSA 3
+C1845668	Perisylvian syndrome
+C1845672	Mental Retardation, X-Linked 63
+C1845805	Cranial sclerosis
+C1845810	MENTAL RETARDATION, X-LINKED 42
+C1845837	Dyserythropoietic Anemia with Thrombocytopenia
+C1845847	Coarse facial features
+C1845860	MENTAL RETARDATION, X-LINKED 73
+C1845861	MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT
+C1845862	Creatine deficiency, X-linked
+C1845864	Poor hand-eye coordination
+C1845878	Irregularly spaced teeth
+C1845889	MENTAL RETARDATION, X-LINKED 53
+C1845892	Lesch-Nyhan Syndrome, Neurologic Variant
+C1845902	FG SYNDROME 2
+C1845919	Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
+C1845987	Neutropenia, Severe Congenital, X-Linked
+C1846006	Ectodermal dysplasia, hypohidrotic, with immune deficiency
+C1846008	HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC
+C1846009	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies
+C1846011	Pugilistic facies
+C1846013	Marked muscular hypertrophy
+C1846017	Progressive pes cavus
+C1846034	Euthyroid multinodular goiter
+C1846038	MENTAL RETARDATION, X-LINKED 72
+C1846046	SPASTIC PARAPLEGIA 16, X-LINKED (disorder)
+C1846055	Siderius X-linked mental retardation syndrome
+C1846058	Lubs X-linked mental retardation syndrome
+C1846059	Roifman syndrome
+C1846129	Terminal Osseous Dysplasia and Pigmentary Defects
+C1846130	Mental retardation X-linked, South African type
+C1846131	Photosensitive tonic-clonic seizures
+C1846133	Loss of ability to walk in first decade
+C1846135	Autistic features
+C1846142	HOYERAAL-HREIDARSSON SYNDROME
+C1846145	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11
+C1846148	Skeletal dysplasia coarse facies mental retardation
+C1846149	Intellectual disability, progressive
+C1846154	Anterior rib cupping
+C1846157	Cone-shaped capital femoral epiphysis
+C1846169	Myotubular Myopathy with Abnormal Genital Development
+C1846171	Lissencephaly, X-Linked, 2
+C1846172	Hydranencephaly and Abnormal Genitalia
+C1846174	Mental Retardation, X-Linked 58
+C1846175	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)
+C1846176	Hyperactive deep tendon reflexes
+C1846223	Adrenal hypoplasia
+C1846226	Mineralocorticoid insufficiency
+C1846228	Absence of pubertal development
+C1846242	Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
+C1846265	Microphthalmia, syndromic 2
+C1846266	Laterally curved eyebrow
+C1846278	MENTAL RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND HYPOGENITALISM, MICROCEPHALY, AND OBESITY (disorder)
+C1846288	Recurrent hypoglycemia
+C1846331	Juvenile-onset dystonia
+C1846339	Externally rotated hips
+C1846343	Bartter syndrome, type 3
+C1846344	Bartter Syndrome, Type 3, with Hypocalciuria
+C1846345	Hyperactive renin-angiotensin system
+C1846347	Renal salt wasting
+C1846348	Renal potassium wasting
+C1846349	Impaired reabsorption of chloride
+C1846351	Increased urinary potassium
+C1846352	Hyperchloriduria
+C1846357	Meckel syndrome type 3
+C1846367	Spinocerebellar ataxia 19
+C1846385	FOCAL CORTICAL DYSPLASIA OF TAYLOR
+C1846386	Focal Cortical Dysplasia of Taylor, Type IIa
+C1846388	CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY
+C1846389	Focal Cortical Dysplasia of Taylor, Type IIb
+C1846421	Lathosterolosis
+C1846422	Bilobate gallbladder
+C1846423	Thick upper lip vermilion
+C1846431	SMITH-MCCORT DYSPLASIA
+C1846433	Prominent sternum
+C1846434	Hypoplastic scapulae
+C1846435	Disproportionate short-trunk short stature
+C1846437	Deformed sella turcica
+C1846438	Hypoplastic facial bones
+C1846439	Hypoplasia of the odontoid process
+C1846442	Hypoplastic acetabulae
+C1846446	Delayed femoral head ossification
+C1846447	Multicentric femoral head ossification
+C1846449	Irregular epiphyses
+C1846460	Abnormality of the outer ear
+C1846462	Impaired ocular abduction
+C1846463	Impaired ocular adduction
+C1846464	Globe retraction and deviation on adduction
+C1846465	Palpebral fissure narrowing on adduction
+C1846473	Aplasia of metacarpal bones
+C1846474	Small thenar eminence
+C1846477	Pectoralis hypoplasia
+C1846478	Upper limb muscle hypoplasia
+C1846496	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
+C1846529	CONE-ROD DYSTROPHY 10
+C1846534	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1
+C1846545	Autoimmune Lymphoproliferative Syndrome Type 2B
+C1846546	Recurrent sinopulmonary infections
+C1846550	Decreased T cell activation
+C1846551	Defective B cell activation
+C1846564	SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
+C1846566	Degeneration of the lateral corticospinal tracts
+C1846574	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY
+C1846582	Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
+C1846620	Hemiclonic seizures
+C1846632	Thyroid Dyshormonogenesis 6
+C1846647	DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
+C1846648	MICROCEPHALY, AMISH TYPE (disorder)
+C1846672	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
+C1846674	Thigh hypertrophy
+C1846685	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT (disorder)
+C1846689	MOYAMOYA DISEASE 2
+C1846707	SPINOCEREBELLAR ATAXIA 17
+C1846722	Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
+C1846784	Deafness, Autosomal Recessive 30
+C1846790	JOUBERT SYNDROME 4 (disorder)
+C1846796	Anauxetic dysplasia
+C1846797	Short stature, severe disproportionate
+C1846798	Cervical subluxation
+C1846803	Small epiphyses
+C1846816	Congenital Disorder Of Glycosylation, Type IIID
+C1846821	Abnormality of coagulation
+C1846837	Aortic Aneurysm, Familial Thoracic 2
+C1846839	DEAFNESS, AUTOSOMAL RECESSIVE 31
+C1846843	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5
+C1846853	Delayed tarsal ossification
+C1846862	PARKINSON DISEASE 8 (disorder)
+C1846865	Substantia nigra gliosis
+C1846868	Parkinsonism with favorable response to dopaminergic medication
+C1846896	Deafness, Autosomal Recessive 22
+C1846911	Compensatory chin elevation
+C1846950	Short middle phalanx of finger
+C1846979	SENIOR-LOKEN SYNDROME 4
+C1846980	Senior-Loken Syndrome 3
+C1847013	NEPHRONOPHTHISIS 4
+C1847024	ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
+C1847089	USHER SYNDROME, TYPE IG
+C1847114	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5
+C1847117	Dilated fourth ventricle
+C1847132	ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
+C1847164	Morning myoclonic jerks
+C1847189	Absent scaphoid
+C1847197	Vascular Malformation, Primary Intraosseous
+C1847200	ALZHEIMER DISEASE 4
+C1847319	PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
+C1847352	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
+C1847356	Polymicrogyria, anterior to posterior gradient
+C1847383	Absence of lymph node germinal center
+C1847406	Digital Arthropathy-Brachydactyly, Familial
+C1847408	Brachytelomesophalangy
+C1847416	FRIEDREICH ATAXIA WITH RETAINED REFLEXES
+C1847425	Abnormal oral glucose tolerance
+C1847501	Glut1 Deficiency Syndrome
+C1847514	Postnatal microcephaly
+C1847515	Paroxysmal involuntary eye movements
+C1847524	Hyperopic astigmatism
+C1847529	ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3
+C1847530	ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2
+C1847532	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
+C1847540	Azoospermia, Nonobstructive
+C1847554	CILIARY DYSKINESIA, PRIMARY, 2 (disorder)
+C1847555	Hyperinsulinemic hypoglycemia, familial, 6
+C1847572	SECKEL SYNDROME 2
+C1847582	Lipodystrophy with Congenital Cataracts and Neurodegeneration
+C1847584	Distal sensory impairment
+C1847593	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4
+C1847604	Van der Woude syndrome 2
+C1847609	Deficit in phonologic short-term memory
+C1847610	Deficit in expressive language
+C1847626	Deafness, Autosomal Dominant 36
+C1847627	Dyskinesia, Familial, with Facial Myokymia
+C1847640	KUFOR-RAKEB SYNDROME
+C1847650	SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
+C1847667	CARDIOMYOPATHY, DILATED, 1L
+C1847711	NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO
+C1847720	Glycine N-Methyltransferase Deficiency
+C1847725	SPINOCEREBELLAR ATAXIA 15
+C1847730	GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding)
+C1847759	MUSCULAR DYSTROPHY, CONGENITAL, 1C
+C1847762	Cerebellar cyst
+C1847766	Shoulder girdle muscle atrophy
+C1847800	Waardenburg Syndrome Type 1
+C1847823	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
+C1847827	LIG4 Syndrome
+C1847831	POLYSUBSTANCE ABUSE, SUSCEPTIBILITY TO
+C1847835	VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
+C1847836	Oculocutaneous Albinism, Type IV
+C1847849	ICHTHYOSIS, LAMELLAR, 5
+C1847868	Generalized aminoaciduria
+C1847902	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)
+C1847903	Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia
+C1847906	Onion bulb formation
+C1847967	OVARIOLEUKODYSTROPHY
+C1847973	Persistent Polyclonal B-Cell Lymphocytosis
+C1847987	HUNTINGTON DISEASE-LIKE 2
+C1848029	Ehlers-Danlos syndrome caused by tenascin-X deficiency
+C1848030	Hypotonia-Cystinuria Syndrome
+C1848068	Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency
+C1848070	Lissencephaly and agenesis of corpus callosum
+C1848087	MENTAL RETARDATION, X-LINKED 50
+C1848097	Spondyloepimetaphyseal Dysplasia, X-Linked
+C1848103	Narrow pelvis bone
+C1848108	Long ulna
+C1848109	Long fibula
+C1848137	EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION (disorder)
+C1848138	X INACTIVATION, FAMILIAL SKEWED, 1 (disorder)
+C1848172	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
+C1848178	Female external genitalia in individual with 46,XY karyotype
+C1848182	Blind vagina
+C1848192	Absent facial hair
+C1848199	X-Linked Lissencephaly
+C1848200	SUBCORTICAL BAND HETEROTOPIA, X-LINKED
+C1848201	Subcortical Band Heterotopia
+C1848204	DEAFNESS, X-LINKED 4 (disorder)
+C1848207	Poor speech
+C1848211	Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism
+C1848213	Periventricular Heterotopia, X-Linked
+C1848214	Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia
+C1848296	DOSAGE-SENSITIVE SEX REVERSAL
+C1848336	Dent disease 1
+C1848389	Posterior pharyngeal cleft
+C1848392	Zunich neuroectodermal syndrome
+C1848395	Large for dates baby
+C1848410	Xeroderma pigmentosum, variant type
+C1848411	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E
+C1848431	Xanthine nephrolithiasis
+C1848435	WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS
+C1848446	C1-C2 subluxation
+C1848453	Poor motor coordination
+C1848456	Atypical or prolonged hepatitis
+C1848459	High nonceruloplasmin-bound serum copper
+C1848473	Whistling appearance
+C1848474	Limited jaw opening
+C1848486	Premature arteriosclerosis
+C1848488	Pierre Robin syndrome with fetal chondrodysplasia
+C1848490	Protruding eyes
+C1848514	Short fourth metatarsal
+C1848519	WAARDENBURG SYNDROME, TYPE 4A
+C1848526	Pontocerebellar Hypoplasia Type 2A
+C1848528	Extrapyramidal dyskinesia
+C1848529	Hypoplasia of the pons
+C1848530	Abnormal visual pursuit
+C1848533	Ataxia with vitamin E deficiency
+C1848534	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
+C1848538	Bulging of the costochondral junction
+C1848552	Methylmalonic Aciduria and Homocystinuria, CblD Type
+C1848553	Homocystinuria, CblD Type, Variant 1
+C1848554	Methylmalonic Aciduria, CblD Type, Variant 2
+C1848555	Hypomethioninemia
+C1848556	Decreased adenosylcobalamin
+C1848561	Methylmalonic acidemia with homocystinuria
+C1848578	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE (disorder)
+C1848579	Decreased methylmalonyl-CoA mutase activity
+C1848580	Decreased methionine synthase activity
+C1848587	Isolated hypoplasia of the right ventricle
+C1848595	Mesoaxial polydactyly
+C1848597	Central Y-shaped metacarpal
+C1848599	VACTERL Association With Hydrocephalus
+C1848600	Vater Association With Hydrocephalus
+C1848604	USHER SYNDROME, TYPE IC
+C1848606	Vestibular hypofunction
+C1848634	USHER SYNDROME, TYPE IIA
+C1848638	USHER SYNDROME, TYPE IB (disorder)
+C1848639	USHER SYNDROME, TYPE IA, FORMERLY
+C1848640	USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
+C1848641	Profound sensorineural hearing loss
+C1848651	Al Awadi syndrome
+C1848654	Broad ribs
+C1848657	Long ear
+C1848660	Aplastic pubic bones
+C1848670	Aplasia/Hypoplasia of the phalanges of the hand
+C1848671	Aplasia/Hypoplasia of the tarsal bones
+C1848673	Hypoplastic feet
+C1848678	4-Hydroxyphenylpyruvic aciduria
+C1848680	4-hydroxyphenylacetic aciduria
+C1848695	Episodic peripheral neuropathy
+C1848701	Elevated hepatic transaminases
+C1848702	Elevated urinary delta-aminolevulinic acid
+C1848736	Distal amyotrophy
+C1848745	Oliver-McFarlane syndrome
+C1848760	Increased anterioposterior diameter of thorax
+C1848765	Sparse/absent eyebrows
+C1848769	Overtubulated long bones
+C1848771	Prominent superficial blood vessels
+C1848773	Epidermal hyperkeratosis
+C1848794	Thyrotropin, Biologically Inactive
+C1848800	Thyroid defect in oxidation and organification of iodide
+C1848805	Thyroid Dyshormonogenesis 1
+C1848840	Bilateral radial aplasia
+C1848850	Nevus flammeus of the forehead
+C1848861	Hyperthreoninemia
+C1848862	Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
+C1848869	Absent external genitalia
+C1848873	Abnormality of the diaphragm
+C1848877	Peripheral pulmonary vessel aplasia
+C1848913	Tay-Sachs Disease, Juvenile
+C1848914	Hexosaminidase A Deficiency, Adult Type
+C1848915	Gm2-Gangliosidosis, Adult Chronic Type
+C1848916	Tay-Sachs Disease, Variant B1
+C1848917	Tay-Sachs Disease, Pseudo-AB Variant
+C1848918	Increased startle response
+C1848920	GM2-ganglioside accumulation
+C1848922	Hexosaminidase alpha-Subunit Deficiency (Variant B)
+C1848934	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME
+C1848947	COLD-INDUCED SWEATING SYNDROME 1
+C1848954	Generalized dystonia
+C1848957	Increased urinary sulfite
+C1848958	Decreased urinary sulfate
+C1848977	Short upper lip
+C1848980	Developmental stagnation
+C1849011	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
+C1849016	Broad femoral neck
+C1849020	Short metatarsal
+C1849025	Oval face
+C1849034	Hypoplastic iliac body
+C1849039	Metaphyseal widening
+C1849043	Soft, doughy skin
+C1849063	Short iliac bones
+C1849069	Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies
+C1849073	Fused vertebrae
+C1849075	Relative macrocephaly
+C1849089	Broad forehead
+C1849094	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3
+C1849095	Cochlear degeneration
+C1849096	Infantile onset spinocerebellar ataxia
+C1849097	Loss of ability to walk
+C1849101	Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures
+C1849115	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
+C1849121	Thin face
+C1849125	Premature graying of body hair
+C1849128	Spastic paraplegia 15, autosomal recessive
+C1849134	Impaired vibration sensation in the lower limbs
+C1849140	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE
+C1849143	Progressive truncal ataxia
+C1849146	Loss of Purkinje cells in the cerebellar vermis
+C1849148	Decreased sensory nerve conduction velocity
+C1849151	Hypermyelinated retinal nerve fibers
+C1849152	Swan neck-like deformities of the fingers
+C1849156	Spastic Ataxia
+C1849157	Resistance to Insulin-Like Growth Factor I
+C1849158	Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein
+C1849172	Frontal lobe hypoplasia
+C1849173	Periventricular gray matter heterotopia
+C1849176	Single kidney
+C1849185	Elevated 7-dehydrocholesterol
+C1849186	Severe photosensitivity
+C1849193	PEELING SKIN SYNDROME
+C1849198	Opacification of the corneal epithelium
+C1849211	Generalized hirsutism
+C1849221	Fair hair
+C1849227	Cleft of chin
+C1849236	Severe combined immunodeficiency, atypical
+C1849242	Abnormality of B cell physiology
+C1849260	Facial palsy secondary to cranial hyperostosis
+C1849263	Sclerotic scapulae
+C1849265	Overgrowth
+C1849276	Cortically dense long tubular bones
+C1849290	Snail-like ilia
+C1849292	Advanced ossification of carpal bones
+C1849293	Advanced tarsal ossification
+C1849295	Hypoplastic labia minora
+C1849300	Widely patent fontanelles and sutures
+C1849305	Aplasia/Hypoplasia of the pubic bone
+C1849307	Increased density of long bones
+C1849309	Wide distal femoral metaphysis
+C1849311	Short 1st metacarpal
+C1849314	absence of radius and ulna
+C1849316	Premature separation of centromeric heterochromatin
+C1849320	Sandhoff Disease, Adult Type
+C1849321	Sandhoff Disease, Juvenile Type
+C1849322	Sandhoff Disease, Infantile Type
+C1849324	Juvenile zonular cataracts
+C1849327	Forearm reduction defects
+C1849334	Robinow syndrome, autosomal recessive
+C1849338	Abnormality of the umbilicus
+C1849340	Long palpebral fissure
+C1849341	Triangular mouth
+C1849343	Duplication of the distal phalanx of hand
+C1849348	Richieri Costa Pereira syndrome
+C1849350	Cleft lower alveolar ridge
+C1849357	Abnormality of the aryepiglottic fold
+C1849358	Enlarged labia minora
+C1849364	Absent earlobe
+C1849366	Naris, slit-like
+C1849367	Nasal bridge wide
+C1849370	Tetraphocomelia
+C1849377	Midface capillary hemangioma
+C1849385	Rhabdomyosarcoma 1
+C1849386	Myoglobinuria, Acute Recurrent, Autosomal Recessive
+C1849387	Rh-Null, Regulator Type
+C1849392	Ridged fingernail
+C1849394	Enhanced S-Cone Syndrome
+C1849409	Knobloch syndrome
+C1849412	Macular hypoplasia
+C1849426	Absent cellular immunity
+C1849435	Renal tubular acidosis, distal, type 3
+C1849437	Mainzer-Saldino Disease
+C1849452	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
+C1849453	Rapadilino syndrome
+C1849478	Increased red cell osmotic fragility
+C1849485	Neuronal loss in the cerebral cortex
+C1849488	Increased serum pyruvate
+C1849489	Increased serum alanine
+C1849507	Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to
+C1849508	EPILEPSY, PYRIDOXINE-DEPENDENT
+C1849510	Prenatal movement abnormality
+C1849524	Pygmy (disorder)
+C1849537	Persistent open anterior fontanelle
+C1849538	Delayed eruption of primary teeth
+C1849540	Delayed eruption of permanent teeth
+C1849547	Osteolytic defects of the distal phalanges of the hand
+C1849554	LYMPHANGIECTASIA, PULMONARY, CONGENITAL
+C1849570	Progressive pulmonary function impairment
+C1849575	Absence of labia majora
+C1849577	Neck pterygia
+C1849579	Anterior clefting of vertebral bodies
+C1849580	Dysplastic patella
+C1849618	Accelerated atherosclerosis
+C1849667	Wide nasal base
+C1849677	Numerous nevi
+C1849678	Peroxisomal ACYL-COA oxidase deficiency
+C1849683	No social interaction
+C1849686	Diffuse hepatic steatosis
+C1849688	Flattened or absent electroretinogram (ERG)
+C1849695	Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency
+C1849699	Progesterone Resistance
+C1849700	Hyperphenylalaninemia with primapterinuria
+C1849706	Midgut malrotation
+C1849718	POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE
+C1849722	Polyglucosan Body Disease, Adult Form
+C1849749	Peripheral thrombosis
+C1849762	Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia
+C1849765	Absence of renal corticomedullary differentiation
+C1849766	Periportal fibrosis
+C1849779	Kowarski syndrome
+C1849792	Achromatopsia 3
+C1849813	Glycogen Storage Disease of Heart, Lethal Congenital
+C1849923	Generalized hypopigmentation
+C1849926	Phenylpyruvic acidemia
+C1849930	Persistent Mullerian duct syndrome
+C1849937	Disproportionate short-limb short stature
+C1849950	Agenesis of maxillary lateral incisor
+C1849953	Square pelvis bone
+C1849955	Limited elbow movement
+C1849993	Calcific stippling
+C1850000	Presentey Anomaly
+C1850013	Vitamin B12 deficiency caused by intestinal malabsorption
+C1850020	Bone marrow biopsy shows megaloblastic erythroid hyperplasia
+C1850040	Pelviscapular dysplasia
+C1850041	Facial hirsutism
+C1850043	Anterior rounding of vertebral bodies
+C1850044	Prominent protruding coccyx
+C1850048	Absent proximal finger flexion creases
+C1850049	Clinodactyly of the 5th finger
+C1850053	Pelizaeus-Merzbacher-like disease, autosomal recessive, 2
+C1850055	PEHO syndrome
+C1850056	PEHO-Like Syndrome
+C1850069	Undetectable visual evoked potentials
+C1850072	Tented upper lip
+C1850077	Supranuclear Palsy, Progressive, 1, Atypical
+C1850083	Irregular ossification at anterior rib ends
+C1850087	Narrow sacroiliac notch
+C1850096	Pancreatic Agenesis, Congenital
+C1850100	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
+C1850106	RAINE SYNDROME
+C1850109	Vitreoretinopathy
+C1850126	Osteopetrosis, mild autosomal recessive form
+C1850127	Osteopetrosis, Autosomal Recessive 1
+C1850134	Sandwich appearance of vertebral bodies
+C1850135	Flared metaphysis
+C1850155	TORG-WINCHESTER SYNDROME
+C1850158	Interphalangeal joint erosions
+C1850159	Widened metacarpal shaft
+C1850160	Thin metacarpal cortices
+C1850161	Widened metatarsal shaft
+C1850162	Thin metatarsal cortices
+C1850168	Bruck syndrome 1
+C1850169	OSTEOGENESIS IMPERFECTA, TYPE IX (disorder)
+C1850171	Neonatal short-limb short stature
+C1850178	Bowing of limbs due to multiple fractures
+C1850189	Large pinnae
+C1850190	Superiorly displaced ears
+C1850191	Posterior polar cataract
+C1850196	Posterior scalloping of vertebral bodies
+C1850256	Median cleft lip
+C1850259	Short tibia
+C1850293	Severe platyspondyly
+C1850303	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE
+C1850309	Mildly elevated creatine phosphokinase
+C1850318	Omodysplasia type 1
+C1850325	Labial hypoplasia
+C1850327	Bifid uterus
+C1850336	Single interphalangeal crease of fifth finger
+C1850343	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME
+C1850348	Hypodysplasia of the corpus callosum
+C1850362	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
+C1850363	Niemann-Pick Disease, Nova Scotian Type
+C1850380	NEUTROPHIL ACTIN DYSFUNCTION
+C1850383	Neuropathy, Painful
+C1850384	Neuropathy, Hereditary Sensory, Atypical
+C1850386	GIANT AXONAL NEUROPATHY 1
+C1850395	Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive
+C1850406	NAVAJO NEUROHEPATOPATHY
+C1850407	Navajo Familial Neurogenic Arthropathy
+C1850413	Reye syndrome-like episodes
+C1850415	Microvesicular hepatic steatosis
+C1850438	Postural hypotension with compensatory tachycardia
+C1850442	CEROID LIPOFUSCINOSIS, NEURONAL, 5
+C1850447	Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
+C1850451	CEROID LIPOFUSCINOSIS, NEURONAL, 1
+C1850456	Progressive microcephaly
+C1850493	Psychomotor regression, progressive
+C1850496	Neuronal loss in central nervous system
+C1850530	Flexion contractures of joints
+C1850533	Yellow subcutaneous tissue covered by thin, scaly skin
+C1850534	Edema, generalized
+C1850535	Absence of scalp hair
+C1850544	Hypernatremic dehydration
+C1850554	Atelosteogenesis type 2
+C1850555	De La Chapelle Dysplasia
+C1850558	Horizontal sacrum
+C1850568	Nakajo syndrome
+C1850569	Nemaline Myopathy 2
+C1850573	Slender build
+C1850597	Leigh Syndrome Due To Mitochondrial Complex II Deficiency
+C1850598	Leigh Syndrome due to Mitochondrial Complex III Deficiency
+C1850599	Leigh Syndrome due to Mitochondrial Complex IV Deficiency
+C1850600	Leigh Syndrome due to Mitochondrial Complex V Deficiency
+C1850601	Abnormality of brainstem morphology
+C1850625	Native American myopathy
+C1850628	Prominent columella
+C1850629	Exaggerated cupid\'s bow
+C1850630	Broad distal phalanx of finger
+C1850631	Short 3rd metacarpal
+C1850635	Atrial myxoma, familial
+C1850640	Long eyelashes in irregular rows
+C1850644	Anterior bowing of long bones
+C1850656	Firm muscles
+C1850658	Irregular femoral epiphysis
+C1850663	Muscle hypertrophy of the lower extremities
+C1850671	Myosclerosis, Autosomal Recessive
+C1850674	MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)
+C1850709	Myopathy, Hyaline Body, Autosomal Recessive
+C1850718	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE
+C1850719	Recurrent encephalopathy
+C1850722	Transient hyperlipidemia
+C1850746	Myopathy, congenital nonprogressive with Moebius and Robin sequences
+C1850764	EPILEPSY, PROGRESSIVE MYOCLONIC 2B
+C1850765	Visual auras
+C1850776	Rapidly progressive disorder
+C1850778	MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1
+C1850792	Congenital myasthenic syndrome ib
+C1850794	Proximal amyotrophy
+C1850808	Miyoshi myopathy
+C1850816	Decreased/absent ankle reflexes
+C1850830	Exercise-induced myalgia
+C1850848	Muscle fiber necrosis
+C1850853	Hyperextensibility at wrists
+C1850854	Increased laxity of ankles
+C1850855	Increased laxity of fingers
+C1850871	Hypoplasia of the pyramidal tract
+C1850889	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
+C1850900	Familial primary gastric lymphoma
+C1850938	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY
+C1850959	Corneal dystrophy, Fuchs\' endothelial, 1
+C1850961	Anterior basal encephalocele
+C1850968	Median cleft palate
+C1850970	Frontal cutaneous lipoma
+C1850985	Fragile Site 16p12
+C1850993	Foveal Hypoplasia, Isolated
+C1851059	Broad columella
+C1851085	Severe expressive language delay
+C1851095	Lumbosacral hirsutism
+C1851100	LAURIN-SANDROW SYNDROME
+C1851101	Laurin-Sandrow Syndrome, Segmental
+C1851102	Fibrosis Of Extraocular Muscles, Congenital, 1
+C1851107	Levator palpebrae superioris atrophy
+C1851108	Superior rectus atrophy
+C1851119	Dilatation of the aortic arch
+C1851120	Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia
+C1851124	Desmoid disease, hereditary
+C1851129	Progressive cervical vertebral spine fusion
+C1851130	Small cervical vertebral bodies
+C1851152	SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
+C1851184	Fibrinolytic Defect
+C1851286	Ectopia lentis isolated
+C1851303	Abnormality of the renal collecting system
+C1851310	Aplasia/hypoplasia of the femur
+C1851313	Limited shoulder movement
+C1851316	Iron Overload, Autosomal Dominant
+C1851319	FAVISM, SUSCEPTIBILITY TO
+C1851347	Familial Mediterranean Fever, Autosomal Dominant
+C1851400	Facial Hypertrichosis
+C1851402	Exudative vitreoretinopathy 1
+C1851406	Peripheral retinal avascularization
+C1851413	EXOSTOSES, MULTIPLE, TYPE II
+C1851414	Peripheral nerve compression
+C1851415	Scapular exostoses
+C1851418	Protuberances at ends of long bones
+C1851419	Madelung-like forearm deformities
+C1851430	Subcortical white matter calcifications
+C1851431	Cerebellar calcifications
+C1851443	Cerebrooculofacioskeletal Syndrome 3
+C1851479	Keratoderma palmoplantaris transgrediens
+C1851480	Greither Disease
+C1851481	Erythrokeratodermia with ataxia
+C1851504	Aortic aneurysm, familial thoracic 4
+C1851526	Ancell-Spiegler cylindromas
+C1851536	Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness
+C1851537	Fairbank disease
+C1851538	Epiphyseal Dysplasia, Ribbing Type
+C1851542	Limited hip movement
+C1851549	Benign Occipital Epilepsy
+C1851551	Mottled pigmentation of the trunk and proximal extremities
+C1851552	Discrete 2 to 5-mm hyper- and hypopigmented macules
+C1851562	Skin fragility with non-scarring blistering
+C1851573	Transient bullous dermolysis of the newborn
+C1851584	Childhood Ependymoma
+C1851585	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA
+C1851705	Confetti-like hypopigmented macules
+C1851710	LATERAL MENINGOCELE SYNDROME
+C1851712	Dural ectasia
+C1851714	Sclerosis of skull base
+C1851719	BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION
+C1851720	Adrenocortical cytomegaly
+C1851722	Overgrowth of external genitalia
+C1851731	Generalized overgrowth
+C1851733	Pancreatic hyperplasia
+C1851741	ELLIPTOCYTOSIS 2 (disorder)
+C1851789	Poor wound healing
+C1851792	Aplasia/Hypoplasia of the earlobes
+C1851797	Palmoplantar cutis gyrata
+C1851801	EDS VIIB
+C1851808	Premature delivery because of cervical insufficiency or membrane fragility
+C1851811	Hypermobility of distal interphalangeal joints
+C1851828	Cigarette-paper scars
+C1851833	Premature birth following premature rupture of fetal membranes
+C1851835	Narrow maxilla
+C1851841	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1
+C1851854	Thin dental enamel
+C1851868	Reduced tensile strength of hair
+C1851878	OROFACIAL CLEFT 8
+C1851879	Cleft Lip with or without Cleft Palate, Nonsyndromic, 8
+C1851883	Small, conical teeth
+C1851885	Progressive alopecia
+C1851897	Anterior creases of earlobe
+C1851915	Abnormal facial muscle tone
+C1851920	Dopa-Responsive Dystonia
+C1851936	Paroxysmal choreoathetosis
+C1851943	DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)
+C1851945	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
+C1851957	Diffuse Lewy Body Disease with Gaze Palsy
+C1851958	Lewy Body Variant of Alzheimer Disease
+C1851959	Fluctuations in consciousness
+C1851970	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT
+C1851971	Hypoplastic myelodysplasia
+C1851972	Reticular hyperpigmentation
+C1851988	Dorsal subluxation of ulna
+C1851996	Dwarfism tall vertebrae
+C1852020	Malattia Leventinese
+C1852021	Drusen, Radial, Autosomal Dominant
+C1852085	Digitotalar Dysmorphism
+C1852091	INSULIN RESISTANCE, SUSCEPTIBILITY TO
+C1852092	DIABETES MELLITUS, INSULIN-DEPENDENT, 2
+C1852093	Maturity-Onset Diabetes of the Young, Type 1
+C1852127	KERATOSIS PALMOPLANTARIS STRIATA II
+C1852145	Familial dermographism
+C1852146	DERMODISTORTIVE URTICARIA
+C1852148	Reticulate pigmentation of oral mucosa
+C1852150	Fingerprints, Absence of
+C1852169	Periapical bone loss
+C1852197	MAJOR AFFECTIVE DISORDER 1
+C1852222	Failure of Tooth Eruption, Primary
+C1852242	Nonarteritic anterior ischemic optic neuropathy (NAION)
+C1852267	OPTIC ATROPHY 1 AND DEAFNESS
+C1852271	Auditory neuropathy
+C1852282	DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)
+C1852289	Autoamputation of digits
+C1852296	Darier Disease, Acral Hemorrhagic Type
+C1852297	Darier Disease, Segmental
+C1852301	Plantar pits
+C1852311	Subungual hyperkeratotic fragments
+C1852324	ALDOSTERONE TO RENIN RATIO, INCREASED
+C1852372	MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
+C1852373	Mitochondrial encephalopathy
+C1852406	Cutis Gyrata Syndrome of Beare And Stevenson
+C1852407	Prominent scrotal raphe
+C1852411	Preauricular skin furrow
+C1852429	Cataract, Variable Zonular Pulverulent
+C1852438	CATARACT, COPPOCK-LIKE
+C1852464	Abnormality of the cervical spine
+C1852467	Creutzfeldt-Jakob Disease, Sporadic
+C1852470	Extrapyramidal muscular rigidity
+C1852476	Loss of facial expression
+C1852502	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
+C1852504	Misalignment of teeth
+C1852510	Craniofacial deafness hand syndrome
+C1852521	Spondylocostal Dysostosis 4, Autosomal Dominant
+C1852529	Corticosteroid-Binding Globulin Deficiency
+C1852534	Hypoplastic male external genitalia
+C1852548	Absent retinal pigment epithelium
+C1852551	Epithelial Recurrent Erosion Dystrophy
+C1852557	CORNEA PLANA 1
+C1852577	FEBRILE CONVULSIONS, FAMILIAL, 1 (disorder)
+C1852581	EPILEPSY, BENIGN NEONATAL, 2
+C1852587	EPILEPSY, BENIGN NEONATAL, 1
+C1852597	Arthrogryposis, distal, type 2E
+C1852700	Complement Component 4, Partial Deficiency Of
+C1852750	Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation
+C1852759	Papillorenal syndrome
+C1852767	Hereditary macular coloboma
+C1852795	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2
+C1852924	OI-EDS Combined Syndrome
+C1852989	Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia
+C1853063	EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL RECESSIVE
+C1853096	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
+C1853099	Cornelia de Lange Syndrome 3
+C1853100	CEREBROOCULOFACIOSKELETAL SYNDROME 4
+C1853102	Cerebrooculofacioskeletal Syndrome 2
+C1853116	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder)
+C1853118	Severe congenital neutropenia
+C1853120	Noonan Syndrome 4
+C1853124	NEPHROTIC SYNDROME, TYPE 3
+C1853136	Neutral Lipid Storage Disease with Myopathy
+C1853137	BRACHYDACTYLY-SYNDACTYLY SYNDROME
+C1853139	OPTIC ATROPHY 5 (disorder)
+C1853141	Slow decrease in visual acuity
+C1853144	Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia
+C1853147	MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
+C1853153	JOUBERT SYNDROME 6
+C1853154	Nemaline Myopathy 7
+C1853162	Osteogenesis Imperfecta Type VII
+C1853171	Multiple prenatal fractures
+C1853193	Recurrent skin infections
+C1853195	Prostate Cancer, Hereditary, 7
+C1853198	COLD-INDUCED SWEATING SYNDROME 2
+C1853202	PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
+C1853205	Glycosylphosphatidylinositol deficiency
+C1853214	RETINITIS PIGMENTOSA 35
+C1853223	Deafness, Autosomal Recessive 67
+C1853230	Aphakia, congenital primary
+C1853234	Anterior segment of eye aplasia
+C1853235	Sclerocornea
+C1853238	Conotruncal defect
+C1853241	Flat face
+C1853242	Midface retrusion
+C1853246	Everted lower lip vermilion
+C1853247	SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
+C1853249	SPINOCEREBELLAR ATAXIA 28
+C1853250	SPINOCEREBELLAR ATAXIA 23
+C1853251	Spastic Paraplegia 33, Autosomal Dominant
+C1853255	Synpolydactyly 3
+C1853256	Hyperostosis-hyperphosphatemia syndrome
+C1853258	Seborrhea-Like Dermatitis with Psoriasiform Elements
+C1853271	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY
+C1853276	Deafness, Autosomal Recessive 28
+C1853278	Bleeding Disorder Due To P2RY12 Defect
+C1853286	Erythrocytosis, Familial, 3
+C1853288	Increased red blood cell mass
+C1853296	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3
+C1853297	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION
+C1853345	Generalized Epilepsy With Febrile Seizures Plus, Type 4
+C1853354	Peeling skin syndrome, acral type
+C1853365	AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
+C1853371	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (disorder)
+C1853377	Enlarged cisterna magna
+C1853383	Tented mouth
+C1853392	Interleukin 2 Receptor, Alpha, Deficiency of
+C1853394	Gaze-evoked horizontal nystagmus
+C1853396	Primary lateral sclerosis juvenile
+C1853398	Spasticity of pharyngeal muscles
+C1853404	Spasticity of facial muscles
+C1853406	Difficulty in tongue movements
+C1853438	INFLAMMATORY BOWEL DISEASE 5
+C1853444	Heterotaxy, Visceral, 3, Autosomal
+C1853445	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
+C1853482	Pear-shaped nose
+C1853486	Widow\'s peak
+C1853487	Thick eyebrow
+C1853488	Thyroid Carcinoma, Nonmedullary 1
+C1853490	22q13.3 Deletion Syndrome
+C1853508	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2
+C1853509	Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome
+C1853513	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 1
+C1853554	Radiation induced meningioma
+C1853555	Alzheimer Disease 7
+C1853558	Jerky ocular pursuit movements
+C1853564	Developmental Delay, Epilepsy, and Neonatal Diabetes
+C1853566	Genitopatellar Syndrome
+C1853573	Hypoplastic inferior pubic rami
+C1853576	Diamond-Blackfan Anemia With Microtia And Cleft Palate
+C1853578	Neuroferritinopathy
+C1853618	Perivascular spaces
+C1853623	Fryns-Aftimos Syndrome
+C1853638	Broad neck
+C1853666	Anemia, Diamond-Blackfan, 2
+C1853698	Rippling muscle disease
+C1853701	Muscle hyperirritability
+C1853702	Muscle mounding
+C1853710	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
+C1853723	MYOPATHY, DISTAL 2
+C1853729	Weakness of vocal cord
+C1853733	HEMOCHROMATOSIS, TYPE 4
+C1853736	Congenital Disorder Of Glycosylation, Type IIB
+C1853737	Prominent occiput
+C1853738	Long eyelashes
+C1853743	Muscular hypotonia of the trunk
+C1853761	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
+C1853766	Pontocerebellar atrophy
+C1853767	Impaired distal vibration sensation
+C1853800	Familial Wilms tumor 2
+C1853829	Arthropathy, Erosive
+C1853831	Bleeding Disorder, East Texas Type
+C1853833	Parkinson Disease 6, Autosomal Recessive Early-Onset
+C1853892	Dimethylglycine Dehydrogenase Deficiency
+C1853925	Spondyloocular Syndrome, Autosomal Recessive
+C1853926	NONAKA MYOPATHY
+C1853932	Rimmed vacuoles on biopsy
+C1853934	Deposits immunoreactive to beta-amyloid protein
+C1853942	CITRULLINEMIA, TYPE II, NEONATAL-ONSET
+C1853949	MYASTHENIA, FAMILIAL INFANTILE, 1
+C1853950	Generalized hypotonia due to defect at the neuromuscular junction
+C1853952	Decreased miniature endplate potentials
+C1853959	Birdshot chorioretinopathy
+C1853965	Dermatitis, Atopic, 2
+C1853995	SEIZURES, BENIGN FAMILIAL INFANTILE, 2
+C1854021	Cataract, Central Saccular, With Sutural Opacities
+C1854023	Spinal muscular atrophy, Jerash type
+C1854058	SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE
+C1854059	AMYOTROPHIC LATERAL SCLEROSIS, TYPICAL
+C1854063	Cardiomyopathy dilated with Woolly hair and keratoderma
+C1854065	LATE-ONSET RETINAL DEGENERATION (disorder)
+C1854106	INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT
+C1854107	Hyperaldosteronism, Familial, Type II
+C1854111	Broad philtrum
+C1854113	Prominent nasal bridge
+C1854114	Short nose
+C1854128	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE II WITH DUANE RETRACTION SYNDROME
+C1854146	Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
+C1854150	Charcot-Marie-Tooth disease, Type 2B2
+C1854154	Charcot-Marie-Tooth disease, Type 2B1
+C1854158	DEAFNESS, AUTOSOMAL DOMINANT 25 (disorder)
+C1854178	ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 1
+C1854182	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
+C1854245	Basal cell carcinoma, multiple
+C1854260	LEBER CONGENITAL AMAUROSIS 6 (disorder)
+C1854273	Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia
+C1854274	DEAFNESS, NONSYNDROMIC, MODIFIER 1 (disorder)
+C1854301	Motor delay
+C1854302	Involuntary jerking movements
+C1854310	Hypotrichosis simplex
+C1854311	Cataract, posterior polar, 3
+C1854335	Epilepsy, Nocturnal Frontal Lobe, Type 3
+C1854336	PARAGANGLIOMAS 3
+C1854365	BREAST CANCER 3
+C1854368	Cardiomyopathy, Dilated, 1J
+C1854369	Spinocerebellar ataxia 14
+C1854372	Impaired vibration sensation at ankles
+C1854380	NEMALINE MYOPATHY 5
+C1854387	Type 1 muscle fiber predominance
+C1854408	Glabellar hemangioma
+C1854414	Deafness, Autosomal Recessive 10
+C1854416	MACROCEPHALY/AUTISM SYNDROME
+C1854417	Postnatal macrocephaly
+C1854418	Biparietal narrowing
+C1854442	SPLIT-HAND/FOOT MALFORMATION 4
+C1854449	Neuropathy, hereditary motor and sensory, Russe type
+C1854454	Axonal regeneration
+C1854465	TUBEROUS SCLEROSIS 1 (disorder)
+C1854466	Temtamy preaxial brachydactyly syndrome
+C1854467	Spastic paraplegia 13, autosomal dominant
+C1854488	Spinocerebellar ataxia 13
+C1854489	Limb dysmetria
+C1854495	Recurrent infection of the gastrointestinal tract
+C1854510	Abnormality of the cranial nerves
+C1854520	SEBASTIAN SYNDROME
+C1854540	Carney Complex, Type 2
+C1854568	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE (disorder)
+C1854570	Distal motor neuropathy
+C1854594	DEAFNESS, AUTOSOMAL DOMINANT 23
+C1854610	Metacarpal osteolysis
+C1854614	Metatarsal osteolysis
+C1854630	Growth Deficiency and Mental Retardation with Facial Dysmorphism
+C1854631	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
+C1854657	Limb fasciculations
+C1854664	LETHAL CONGENITAL CONTRACTURE SYNDROME 1
+C1854678	MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE
+C1854684	Congenital myopia
+C1854685	Hypoplasia of the retina
+C1854686	Uncontrolled eye movements
+C1854689	Short nasal bridge
+C1854698	Multiple Carboxylase Deficiency, Juvenile-Onset
+C1854699	Diffuse cerebellar atrophy
+C1854704	Metabolic Ketosis
+C1854718	J-shaped sella turcica
+C1854749	Proximal tapering of metacarpals
+C1854774	Dermatan sulfate excretion in urine
+C1854776	Infantile cardiomyopathy
+C1854780	Flaring of rib cage
+C1854783	Grayish enamel
+C1854785	Constricted iliac wings
+C1854786	Epiphyseal deformities of tubular bones
+C1854787	Pointed proximal second through fifth metacarpals
+C1854788	Beta-galactosidase deficiency in fibroblasts and white blood cells
+C1854827	Heparan sulfate excretion in urine
+C1854834	Dense calvaria
+C1854838	Progressive neurologic deterioration
+C1854882	Absent speech
+C1854885	Cerebral dysmyelination
+C1854888	Progressive retinal degeneration
+C1854896	Mucolipidosis III Gamma
+C1854910	Shallow acetabular fossae
+C1854912	Short long bone
+C1854913	Soft tissue swelling of interphalangeal joints
+C1854919	Severe psychomotor retardation
+C1854928	Protuberant abdomen
+C1854934	Progressive alveolar ridge hypertropy
+C1854940	Lower thoracic interpediculate narrowness
+C1854941	Beaking of vertebral bodies T12-L3
+C1854948	Varus deformity of humeral neck
+C1854952	Bullet-shaped phalanges of the hand
+C1854978	Monosomy 7 of Bone Marrow
+C1854988	Molybdenum Cofactor Deficiency, Complementation Group A
+C1854989	Molybdenum Cofactor Deficiency, Complementation Group B
+C1854990	Molybdenum Cofactor Deficiency, Complementation Group C
+C1855003	Bilateral postaxial polydactyly
+C1855008	Mitochondrial Complex II Deficiency
+C1855009	Psychomotor regression in infants
+C1855010	Progressive leukoencephalopathy
+C1855019	Psychomotor regression
+C1855020	Acute necrotizing encephalopathy
+C1855033	Mitochondrial myopathy with lactic acidosis
+C1855038	Hepatocellular necrosis
+C1855052	MICROPHTHALMIA, ISOLATED 1
+C1855055	Microcephaly with spastic quadriplegia
+C1855067	B lymphocytopenia
+C1855079	Microcephaly-Micromelia Syndrome
+C1855081	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1
+C1855091	Short proximal phalanx of thumb
+C1855100	Methylmalonyl-CoA Epimerase Deficiency
+C1855102	Methylmalonic aciduria cblB type
+C1855106	Neonatal onset
+C1855109	Methylmalonic aciduria cblA type
+C1855114	Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
+C1855115	Methylmalonic Aciduria, mut(0) Type
+C1855116	Methylmalonic Aciduria, mut(-) Type
+C1855119	Methylmalonic aciduria
+C1855126	3-Methylglutaconic Aciduria Type IV
+C1855128	Methylcobalamin Deficiency, CblG Type
+C1855171	Metaphyseal cupping of metacarpals
+C1855177	Flat glenoid fossa
+C1855179	CATARACT, ANTERIOR POLAR
+C1855185	Broad phalanx
+C1855188	Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
+C1855191	Progressive leg bowing
+C1855196	Flaring of lower rib cage
+C1855204	Cellular immunodeficiency
+C1855205	Susceptibility to chickenpox
+C1855222	Delayed proximal femoral epiphyseal ossification
+C1855229	Spondylometaphyseal dysplasia, Sedaghatian type
+C1855230	Focal lissencephaly
+C1855233	Large posterior fontanelle
+C1855239	Cone-shaped metacarpal epiphyses
+C1855240	Irregular tarsal bones
+C1855255	Pseudoarylsulfatase A Deficiency
+C1855284	Intrahepatic biliary atresia
+C1855285	Protruding ear
+C1855299	Forearm undergrowth
+C1855304	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1
+C1855305	Ter Haar syndrome
+C1855310	Megaepiphyseal dwarfism
+C1855311	Megacystis
+C1855330	Cerebral hypoplasia
+C1855331	Olfactory lobe agenesis
+C1855333	External genital hypoplasia
+C1855335	Hypoplasia of the bladder
+C1855340	Bowing of the long bones
+C1855346	MAST SYNDROME
+C1855350	Inferior vermis hypoplasia
+C1855353	Fixed facial expression
+C1855369	Maple Syrup Urine Disease, Type IA
+C1855371	MAPLE SYRUP URINE DISEASE, TYPE II
+C1855391	Tortuosity of conjunctival vessels
+C1855418	Thoracolumbar kyphosis
+C1855425	Marles Greenberg Persaud syndrome
+C1855432	Mandibulofacial Dysostosis with Mental Deficiency
+C1855433	Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive
+C1855456	PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL
+C1855457	MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding)
+C1855459	Congenital symmetrical palmoplantar keratosis
+C1855465	STARGARDT DISEASE 1 (disorder)
+C1855466	Hypomagnesemia 5, Renal, with Ocular Involvement
+C1855472	Acute lymphoblastic leukemia with lymphomatous features
+C1855480	Pulmonary lymphangiectasia
+C1855483	Progressive spastic paraplegia
+C1855496	Contiguous gene syndrome
+C1855498	Lipase deficiency combined
+C1855513	Prominent nipples
+C1855514	Severe failure to thrive
+C1855520	Hyperglycemia, Postprandial
+C1855523	Leg, Absence Deformity of, with Congenital Cataract
+C1855538	Small face
+C1855544	Enlarged metaphyses
+C1855548	Laron syndrome type 2
+C1855553	Pyruvate Dehydrogenase E3-Binding Protein Deficiency
+C1855565	Pyruvate Dehydrogenase E2 Deficiency
+C1855568	Jerky head movements
+C1855575	Very rare
+C1855577	Erythrocyte Lactate Transporter Defect
+C1855578	Exercise-induced muscle cramps
+C1855579	Exercise-induced muscle stiffness
+C1855580	Exercise-induced muscle fatigue
+C1855607	Keutel syndrome
+C1855608	Costal cartilage calcification
+C1855616	Cartilaginous ossification of nose
+C1855620	Premature fusion of phalangeal epiphyses
+C1855622	Cartilaginous ossification of larynx
+C1855627	HAIM-MUNK SYNDROME
+C1855633	Congenital palmoplantar keratosis
+C1855642	Atrophy of alveolar ridges
+C1855644	Keratoderma, Palmoplantar, Norrbotten Recessive Type
+C1855645	Keratoconus posticus circumscriptus
+C1855648	KENNY-CAFFEY SYNDROME, TYPE 1
+C1855650	Birth length less than 3rd percentile
+C1855657	Calvarial osteosclerosis
+C1855663	Kaufman oculocerebrofacial syndrome
+C1855665	Ovoid vertebral bodies
+C1855669	Absent frontal sinuses
+C1855670	Abnormality of the cornea
+C1855672	Immotile cilia
+C1855675	Arima syndrome
+C1855676	Aplasia/Hypoplasia of the cerebellar vermis
+C1855677	Brainstem dysplasia
+C1855681	Nephronophthisis, familial juvenile
+C1855685	Undetectable electroretinogram
+C1855690	Midline skin dimples over anterior/posterior fontanelles
+C1855694	Hypoplasia of the primary teeth
+C1855698	Aplasia cutis congenita of scalp
+C1855705	Jejunal Atresia with Microcephaly and Ocular Anomalies
+C1855710	Bone marrow failure
+C1855722	Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
+C1855728	Low posterior hairline
+C1855733	Neuronal intestinal pseudoobstruction
+C1855739	Indifference to Pain, Congenital, Autosomal Recessive
+C1855751	Bulbous nasal tip
+C1855752	Abnormality of T cells
+C1855755	Abnormal immunoglobulin level
+C1855758	Lateral displacement of the femoral head
+C1855772	Absent corpus callosum cataract immunodeficiency
+C1855773	Psychomotor retardation, profound
+C1855774	White matter neuronal heterotopia
+C1855781	Cutaneous anergy
+C1855789	Self-Healing Collodion Baby
+C1855792	ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1
+C1855794	Bamforth syndrome
+C1855796	Hypoproteinemia, Hypercatabolic
+C1855801	Calcium nephrolithiasis
+C1855815	Skin dimple over apex of long bone angulation
+C1855828	Vertebral clefting
+C1855840	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME
+C1855841	Hypocalcemic seizures
+C1855843	Severe intrauterine growth retardation
+C1855845	Patchy osteosclerosis
+C1855849	Bartter syndrome, antenatal , type 2
+C1855852	Large eyes
+C1855853	Impaired platelet aggregation
+C1855861	Glycogen Storage Disease 0, Liver
+C1855868	Polyglandular Deficiency Syndrome, Persian-Jewish Type
+C1855869	Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
+C1855889	Widened posterior fossa
+C1855895	Erlenmeyer flask deformity of the femurs
+C1855899	Broad first metatarsal
+C1855900	HYPERTRICHOSIS, CONGENITAL GENERALIZED
+C1855901	Congenital hypertrophy of left ventricle
+C1855923	Hyperphosphatasia with Mental Retardation
+C1855986	Hydroxylysinuria
+C1855995	L-2-HYDROXYGLUTARIC ACIDURIA
+C1855996	Psychomotor regression beginning in infancy
+C1856001	Severe demyelination of the white matter
+C1856006	Transverse vaginal septum
+C1856016	HYDROLETHALUS SYNDROME 1
+C1856017	Adrenal gland dysgenesis
+C1856019	Abnormal cortical gyration
+C1856023	Abnormality of the vagina
+C1856029	Proximal tibial hypoplasia
+C1856053	Hydranencephaly with Renal Aplasia-Dysplasia
+C1856057	Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
+C1856058	HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
+C1856059	Mthfr Deficiency, Thermolabile Type
+C1856061	Methylenetetrahydrofolate reductase deficiency
+C1856087	Biconcave vertebral bodies
+C1856113	Mowat-Wilson syndrome
+C1856115	Happy demeanor
+C1856117	Uplifted earlobe
+C1856118	Prominent nasal tip
+C1856119	Low hanging columella
+C1856121	Broad eyebrow
+C1856123	Pulmonary artery sling
+C1856127	Bile acid synthesis defect, congenital, 2
+C1856128	Hepatic venoocclusive disease with immunodeficiency
+C1856129	Thyroid lymphangiectasia
+C1856136	Conical incisor
+C1856139	Pleural lymphangiectasia
+C1856140	Pericardial lymphangiectasia
+C1856143	HEMOLYTIC UREMIC SYNDROME, TYPICAL
+C1856164	Hypertrophied alveolar ridge
+C1856184	HEMIHYPERPLASIA, ISOLATED
+C1856186	Deafness enamel hypoplasia nail defects
+C1856194	Neutral hyperaminoaciduria
+C1856202	U-Shaped upper lip vermilion
+C1856203	Microdontia of primary teeth
+C1856231	Thin calvarium
+C1856245	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
+C1856251	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I
+C1856255	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
+C1856266	Coronal craniosynostosis
+C1856273	46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related
+C1856285	Increased hepatic glycogen content
+C1856301	GSD IV, Classic Hepatic
+C1856302	GSD IV, Nonprogressive Hepatic
+C1856303	GSD IV, Neuromuscular Form, Fatal Perinatal
+C1856304	GSD IV, Neuromuscular Form, Congenital
+C1856305	GSD IV, Neuromuscular Form, Childhood
+C1856306	GSD IV, Neuromuscular Form, Adult, with Isolated Myopathy
+C1856361	Doll-like facies
+C1856399	Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to
+C1856401	Glutaric Aciduria IIA
+C1856403	Glutaric Aciduria IIB
+C1856405	Glutaric Aciduria IIC
+C1856408	Infantile encephalopathy
+C1856409	Dilation of lateral ventricles
+C1856432	Dicarboxylic aciduria
+C1856438	Hypoketotic hypoglycemia
+C1856439	GLAUCOMA 3, PRIMARY CONGENITAL, A
+C1856441	Late onset congenital glaucoma
+C1856447	Bernard-Soulier Syndrome, Type B
+C1856448	Bernard-Soulier Syndrome, Type C
+C1856465	Ghosal Hematodiaphyseal Dysplasia
+C1856468	Round, full face
+C1856471	Short metacarpals with rounded proximal ends
+C1856476	Gaucher Disease, Type Iiic
+C1856477	Slowed horizontal saccades
+C1856478	Hypometric horizontal saccades
+C1856491	Gaucher Disease, Type IIIa
+C1856492	Gaucher Disease, Type IIIb
+C1856493	Gaucher Disease, Norrbottnian Type
+C1856507	Bulbar signs
+C1856542	Prominent scalp veins
+C1856559	Decreased beta-galactosidase activity
+C1856560	Bone-marrow foam cells
+C1856565	Progressive psychomotor deterioration
+C1856599	Beaking of vertebral bodies
+C1856603	Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to
+C1856604	Late-onset spinocerebellar degeneration
+C1856637	Spatulate ribs
+C1856639	Absent/hypoplastic paranasal sinuses
+C1856641	Cervical platyspondyly
+C1856644	Absent/hypoplastic coccyx
+C1856646	Elevated sweat chloride
+C1856659	Polysplenia
+C1856660	Abnormality of the helix
+C1856661	Cloudy cornea
+C1856689	FRIEDREICH ATAXIA 1
+C1856691	Impaired proprioception
+C1856694	Areflexia of lower limbs
+C1856697	Mitochondrial malic enzyme reduced
+C1856714	Palmoplantar cutis laxa
+C1856716	Follicle-stimulating hormone deficiency, isolated
+C1856718	Fleck Retina, Familial Benign
+C1856719	Kininogen Deficiency, Total
+C1856728	Fuhrmann syndrome
+C1856732	Aplasia/Hypoplasia of the fibula
+C1856738	Fibular hypoplasia and complex brachydactyly
+C1856742	Malaligned carpal bone
+C1856746	Deformed tarsal bones
+C1856749	Aplastic/hypoplastic toenail
+C1856765	Irregular dentition
+C1856778	Widely patent coronal suture
+C1856779	Widely patent sagittal suture
+C1856780	Posterior vertebral hypoplasia
+C1856786	Hypoplastic fingernail
+C1856789	Femur bifid with monodactylous ectrodactyly
+C1856796	Estren-Dameshek Variant of Fanconi Anemia
+C1856797	Estren-Dameshek Variant of Fanconi Pancytopenia
+C1856871	Autosomal recessive facio-digito-genital syndrome
+C1856872	Down-sloping shoulders
+C1856877	Hyperextensible hand joints
+C1856883	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF
+C1856886	Hypoplastic philtrum
+C1856889	3-4 finger syndactyly
+C1856892	Facial Dysmorphism with Multiple Malformations
+C1856895	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1
+C1856897	Eunuchoidism, familial hypogonadotropic
+C1856904	Reduced pancreatic beta cells
+C1856911	Ivory epiphyses
+C1856912	Shortening of all middle phalanges of the fingers
+C1856920	Hypoplasia of the femoral head
+C1856922	Limited elbow flexion
+C1856934	Epidermolysis bullosa with pyloric atresia
+C1856953	Palmar hyperhidrosis
+C1856954	Plantar hyperkeratosis
+C1856963	Fragile nails
+C1856972	Encephaloclastic Proliferative Vasculopathy
+C1856974	PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder)
+C1856979	Deep white matter hypodensities
+C1856983	Increased CSF interferon alpha
+C1857002	Capitate-hamate fusion
+C1857005	Cone-shaped epiphyses of phalanges 2 to 5
+C1857011	Recurrent mandibular subluxations
+C1857012	Frontal open bite
+C1857013	Gingival hyperkeratosis
+C1857021	Spontaneous neonatal pneumothorax
+C1857025	Progressive congenital scoliosis
+C1857034	Ehlers-Danlos syndrome, cardiac valvular form
+C1857041	Ectodermal dysplasia, ectrodactyly, and macular dystrophy
+C1857042	Sparse scalp hair
+C1857045	Abnormality of the philtrum
+C1857048	Progressive hypotrichosis
+C1857055	Anteverted ears
+C1857069	SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
+C1857074	Absent sternal ossification
+C1857078	Mondini malformation
+C1857079	Atretic auditory canal
+C1857093	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE (disorder)
+C1857100	Dyssegmental dysplasia
+C1857101	Anisospondyly
+C1857108	Limitation of joint mobility
+C1857121	Neurodevelopmental regression
+C1857126	Parietal bossing
+C1857130	Hypoplastic mandible condyle
+C1857131	Absent paranasal sinuses
+C1857139	Abnormal metaphyseal trabeculation
+C1857144	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1
+C1857171	Episodic hyperhidrosis
+C1857175	Episodic hypertension
+C1857180	Enlargement of the costochondral junction
+C1857186	Iliac crest serration
+C1857190	Wide pubic symphysis
+C1857192	Multicentric ossification of proximal humeral epiphyses
+C1857193	Multicentric ossification of proximal femoral epiphyses
+C1857202	Frequent vomiting
+C1857206	Sparse lateral eyebrow
+C1857230	DISORGANIZATION, MOUSE, HOMOLOG OF
+C1857231	LACTASE PERSISTENCE
+C1857242	Rhizomelic chondrodysplasia punctata, type 2
+C1857243	Stippled calcification proximal humeral epiphyses
+C1857252	2,4-Dienoyl-CoA Reductase Deficiency
+C1857253	Dicarboxylicaminoaciduria
+C1857255	Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant
+C1857263	Hypertrophic auricular cartilage
+C1857276	Trichohepatoenteric Syndrome
+C1857277	Donnai-Barrow syndrome
+C1857278	Partial or complete agenesis of corpus callosum
+C1857280	Infra-orbital crease
+C1857287	Stroke-like episode
+C1857288	Limited mobility of proximal interphalangeal joint
+C1857299	RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL
+C1857316	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY
+C1857332	Deafness, Sensorineural, Autosomal-Mitochondrial Type
+C1857342	Deafness, Cochlear, with Myopia and Intellectual Impairment
+C1857344	Split-Hand-Foot Malformation With Sensorineural Hearing Loss
+C1857353	Posterior fossa cyst
+C1857355	Leigh syndrome , French Canadian type
+C1857388	Cystinuria, Type A
+C1857389	Cystinuria, Type B
+C1857390	Cystinuria, Type A-B
+C1857395	De Toni-Debre-Fanconi Syndrome
+C1857423	Cystic Kidney Disease with Ventriculomegaly
+C1857451	Acth-Independent Macronodular Adrenal Hyperplasia
+C1857453	Renal hypoplasia/aplasia
+C1857455	Extension of hair growth on temples to lateral eyebrow
+C1857456	Morphological abnormality of the middle ear
+C1857479	Short columella
+C1857482	Slender finger
+C1857483	Decreased palmar creases
+C1857484	Brachyturricephaly
+C1857485	Flat forehead
+C1857486	Low-set, posteriorly rotated ears
+C1857499	Bony paranasal bossing
+C1857500	Broad alveolar ridges
+C1857501	Facial hyperostosis
+C1857505	Club-shaped distal femur
+C1857508	Patchy sclerosis of finger phalanx
+C1857512	Temtamy syndrome
+C1857519	Malformation of the hepatic ductal plate
+C1857527	Flattened epiphysis
+C1857539	Deep palmar crease
+C1857569	CORNEAL ENDOTHELIAL DYSTROPHY 2
+C1857572	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS
+C1857574	CORNEA PLANA 2
+C1857586	CONOTRUNCAL HEART MALFORMATIONS (disorder)
+C1857587	Orstavik Lindemann Solberg syndrome
+C1857588	Amaurosis hypertrichosis
+C1857618	Achromatopsia 2
+C1857624	COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING
+C1857627	Chorioretinal dystrophy
+C1857632	Narrow palm
+C1857638	Patchy demyelination of subcortical white matter
+C1857640	Decreased nerve conduction velocity
+C1857641	Severe postnatal growth retardation
+C1857644	Retinal pigment epithelial mottling
+C1857645	Slender nose
+C1857651	Ivory epiphyses of the phalanges of the hand
+C1857652	Thymic hormone decreased
+C1857656	Prematurely aged appearance
+C1857657	Reduced subcutaneous adipose tissue
+C1857662	COACH syndrome
+C1857663	Yunis Varon syndrome
+C1857665	Aplastic clavicles
+C1857679	Sloping forehead
+C1857682	Combined Oxidative Phosphorylation Deficiency 4
+C1857690	Pulmonary arteriovenous malformation
+C1857692	Venous varicosities of celiac and mesenteric vessels
+C1857693	Arteriovenous fistulas of celiac and mesenteric vessels
+C1857697	Lip telangiectasia
+C1857699	Palate telangiectasia
+C1857704	Abnormal myelination
+C1857707	Increased cellular sensitivity to UV light
+C1857710	Progeroid facial appearance
+C1857719	Anemia, Diamond-Blackfan, 3
+C1857720	KALLMANN SYNDROME 4 (disorder)
+C1857728	Hereditary Angioedema Type III
+C1857743	LEBER CONGENITAL AMAUROSIS 12 (disorder)
+C1857744	DEAFNESS, AUTOSOMAL RECESSIVE 59
+C1857747	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
+C1857750	DEAFNESS, AUTOSOMAL RECESSIVE 66
+C1857761	Alagille Syndrome 2
+C1857762	Olivopontocerebellar hypoplasia, fetal-onset
+C1857768	Cataract, Pulverulent, Juvenile-Onset
+C1857775	Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
+C1857776	3-@METHYLGLUTACONIC ACIDURIA, TYPE V
+C1857777	Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
+C1857779	SENIOR-LOKEN SYNDROME 6
+C1857780	JOUBERT SYNDROME 5
+C1857781	Diaphragmatic Hernia 3
+C1857787	Aplasia of the inferior half of the cerebellar vermis
+C1857788	Atrophy of the dentate nucleus
+C1857790	Thoracic scoliosis
+C1857798	Immunodeficiency due to Defect in CD3-Zeta
+C1857800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
+C1857802	MORM syndrome
+C1857809	DEAFNESS, AUTOSOMAL RECESSIVE 44
+C1857811	DEAFNESS, AUTOSOMAL RECESSIVE 49
+C1857813	Macular Degeneration, Age-Related, 7
+C1857814	MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO
+C1857821	LEBER CONGENITAL AMAUROSIS 10 (disorder)
+C1857828	QT INTERVAL, VARIATION IN
+C1857829	Heart-hand syndrome, Slovenian type
+C1857845	CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
+C1857847	CELIAC DISEASE, SUSCEPTIBILITY TO, 4
+C1857853	Cataract, Congenital Nuclear, Autosomal Recessive 2
+C1857854	Proopiomelanocortin Deficiency
+C1857855	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT
+C1857941	Brooke-Spiegler syndrome
+C1857945	Hyperechogenic pancreas
+C1857949	Prominent metopic ridge
+C1857953	Deep plantar creases
+C1857970	Hypobetalipoproteinemia, Familial, 2
+C1857977	MICROHYDRANENCEPHALY
+C1858025	Spinal rigidity
+C1858028	WOLFRAM SYNDROME 2
+C1858033	Asymmetry of the thorax
+C1858036	Periorbital fullness
+C1858042	Becker Nevus Syndrome
+C1858051	NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS
+C1858054	BARDET-BIEDL SYNDROME 6
+C1858067	ASTHMA AND NASAL POLYPS
+C1858079	Osteoarthritis with Mild Chondrodysplasia
+C1858080	Retinal Dystrophy, Early Onset Severe
+C1858084	STICKLER SYNDROME, TYPE II (disorder)
+C1858085	Malar flattening
+C1858091	Long fingers
+C1858106	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT (disorder)
+C1858108	Microcephaly, Primary Autosomal Recessive, 3
+C1858116	Caudate atrophy
+C1858120	Generalized hypotonia
+C1858127	Limb-girdle muscle weakness
+C1858133	Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive
+C1858142	ICHTHYOSIS, LAMELLAR, 3
+C1858154	CARDIOMYOPATHY, DILATED, 1I
+C1858160	CRANIOSYNOSTOSIS, TYPE 2
+C1858172	Deafness, Autosomal Dominant 20
+C1858210	Tooth Agenesis, Selective, 5
+C1858262	EXUDATIVE VITREORETINOPATHY, DIGENIC
+C1858266	Bare Lymphocyte Syndrome, Type I
+C1858278	Charcot-Marie-Tooth disease, Type 4B2
+C1858279	Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
+C1858280	Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma
+C1858285	Decreased number of peripheral myelinated nerve fibers
+C1858301	LEBER CONGENITAL AMAUROSIS 5
+C1858302	Ectodermal dysplasia/ skin fragility syndrome
+C1858303	INFLAMMATORY BOWEL DISEASE 3
+C1858312	Megakaryocytopenia
+C1858328	Bile acid synthesis defect, congenital, 4
+C1858338	Neuropathy, hereditary motor and sensory, Okinawa type
+C1858351	SPINOCEREBELLAR ATAXIA 11
+C1858361	Pyogenic Arthritis, Pyoderma Gangrenosum and Acne
+C1858379	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)
+C1858380	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7 (disorder)
+C1858386	Leber Congenital Amaurosis 4
+C1858391	ATAXIA-TELANGIECTASIA-LIKE DISORDER
+C1858392	NEPHRONOPHTHISIS 3
+C1858395	Renal tubular atrophy
+C1858424	Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
+C1858427	Limited extraocular movements
+C1858430	Death in infancy
+C1858433	BREAST AND COLORECTAL CANCER, SUSCEPTIBILITY TO
+C1858438	COLORECTAL CANCER, SUSCEPTIBILITY TO
+C1858452	Thickened calvaria
+C1858477	Epilepsy, Partial, with Variable Foci
+C1858479	Spastic paraplegia 11, autosomal recessive
+C1858493	FEBRILE CONVULSIONS, FAMILIAL, 4
+C1858496	Advanced Sleep-Phase Syndrome, Familial
+C1858501	Spinocerebellar Ataxia 12
+C1858516	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE
+C1858517	SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
+C1858529	Denervation of the diaphragm
+C1858535	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder)
+C1858539	Shawl scrotum
+C1858545	Facial capillary hemangioma
+C1858556	OVERLAP CONNECTIVE TISSUE DISEASE
+C1858558	Rheumatoid Arthritis, Systemic Juvenile
+C1858562	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
+C1858565	Duplicated collecting system
+C1858569	Absence of Stensen duct
+C1858573	Sparse pubic hair
+C1858574	Sparse axillary hair
+C1858583	HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
+C1858592	Carney Triad
+C1858593	Limb-girdle muscular dystrophy, type 2E
+C1858626	Bicarbonate-wasting renal tubular acidosis
+C1858628	Increased red cell osmotic resistance
+C1858656	Short Stature, Idiopathic, Autosomal
+C1858664	HEMOCHROMATOSIS, TYPE 3
+C1858672	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
+C1858673	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
+C1858674	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
+C1858677	LEBER CONGENITAL AMAUROSIS 3 (disorder)
+C1858679	CATARACT, AUTOSOMAL DOMINANT
+C1858680	Familial encephalopathy with neuroserpin inclusion bodies
+C1858695	Chudley-Mccullough syndrome
+C1858712	Spastic paraplegia 10, autosomal dominant
+C1858717	Facial paresis, hereditary, congenital
+C1858719	Facial muscle weakness of muscles innervated by CN VII
+C1858723	Poikiloderma with Neutropenia
+C1858725	NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1
+C1858726	Congenital Cataracts, Facial Dysmorphism, And Neuropathy
+C1858729	Decreased motor nerve conduction velocity
+C1858732	Malar prominence
+C1858763	Cardiomyopathy, Dilated, 1g
+C1858804	Cerebellar Ataxia, Deafness, and Narcolepsy
+C1858805	Vohwinkel Syndrome, Variant Form
+C1858806	CONE-ROD DYSTROPHY 3 (disorder)
+C1858854	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
+C1858855	Diffuse swelling of cerebral white matter
+C1858857	Diffuse spongiform leukoencephalopathy
+C1858891	PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
+C1858915	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2
+C1858916	DEAFNESS, AUTOSOMAL DOMINANT 16
+C1858968	Autoimmune Lymphoproliferative Syndrome, Type IIA
+C1858969	Decreased lymphocyte apoptosis
+C1858970	Chronic noninfectious lymphadenopathy
+C1858972	Increase in B cell number
+C1858973	Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
+C1858974	Increased proportion of HLA DR+ and CD57+ T cells
+C1858977	Increased IgG level
+C1858980	Platelet antibody positive
+C1858981	Antineutrophil antibody positivity
+C1858990	Beta Thalassemia, Dominant Inclusion Body Type
+C1858991	Childhood Ataxia with Central Nervous System Hypomyelinization
+C1858995	Decreased circulating progesterone
+C1859014	Primary gonadal insufficiency
+C1859040	Medullary Cystic Kidney Disease Type 2
+C1859047	CYSTIC FIBROSIS MODIFIER 1
+C1859049	CCHS WITH HIRSCHSPRUNG DISEASE
+C1859062	LONG QT SYNDROME 3
+C1859069	Brittle Bone Disorder
+C1859077	Aplasia/Hypoplasia of the nails
+C1859088	COPPER TOXICOSIS, IDIOPATHIC
+C1859093	Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
+C1859098	Chorea, Benign Familial
+C1859101	Vertebral chordoma
+C1859111	Enlarged joints
+C1859115	Prominent interphalangeal joints
+C1859116	Large tarsal bones
+C1859117	Recurrent pulmonary infections
+C1859120	Anterior rib punctate calcifications
+C1859121	Sternal punctate calcifications
+C1859126	Stippled epiphyses
+C1859133	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1
+C1859135	Calcific stippling of infantile cartilaginous skeleton
+C1859148	Chondrodysplasia, blomstrand type
+C1859158	Laryngeal calcification
+C1859162	Neonatal cholestatic liver disease
+C1859178	Progressive peripheral neuropathy
+C1859194	GRISCELLI SYNDROME, TYPE 1
+C1859198	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
+C1859200	Inability to walk by childhood/adolescence
+C1859209	Klippel Feil syndrome recessive type
+C1859212	Limited neck range of motion
+C1859223	Deep longitudinal plantar crease
+C1859224	Second metatarsal posteriorly placed
+C1859228	Cerebrohepatorenal Syndrome, Variant Types
+C1859231	Hypoplastic olfactory lobes
+C1859235	Intrahepatic biliary dysgenesis
+C1859236	Prolonged neonatal jaundice
+C1859241	Elevated long chain fatty acids
+C1859252	Cerebrofaciothoracic Dysplasia
+C1859270	Slow speech
+C1859273	Dense calcifications in the cerebellar dentate nucleus
+C1859292	Triangular-shaped open mouth
+C1859298	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2
+C1859301	Cerebellar hypoplasia with endosteal sclerosis
+C1859305	Cerebellar Ataxia and Hypogonadotropic Hypogonadism
+C1859309	Syndactyly Cenani Lenz type
+C1859311	Microphthalmia, Isolated, with Cataract 2
+C1859312	CAMFAK syndrome
+C1859317	Cataract and cardiomyopathy
+C1859330	Cardiac Valvular Defect, Developmental
+C1859335	Thoracolumbar kyphoscoliosis
+C1859339	Midfrontal capillary hemangioma
+C1859341	Olivopontocerebellar hypoplasia
+C1859347	Abnormal subcutaneous fat tissue distribution
+C1859353	Candidiasis, Familial, 2
+C1859366	Hypoplastic 5th lumbar vertebrae
+C1859368	Camptodactyly of 2nd-5th fingers
+C1859372	Calcification of Joints and Arteries
+C1859376	Fused sternal ossification centers
+C1859377	Thick anterior alveolar ridges
+C1859391	Absent pubic hair
+C1859392	Absent axillary hair
+C1859399	Radial bowing
+C1859405	Bowen-Conradi syndrome
+C1859406	Borrone Di Rocco Crovato syndrome
+C1859408	BOMBAY PHENOTYPE
+C1859411	PARA-BOMBAY PHENOTYPE
+C1859442	Minimal subcutaneous fat
+C1859443	Severe generalized osteoporosis
+C1859447	Hypoplastic ischia
+C1859449	Thin long bone diaphyses
+C1859452	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
+C1859455	Small anterior fontanelle
+C1859458	Cleft vertebral arch
+C1859460	Bowed humerus
+C1859461	Femoral bowing
+C1859462	Absent knee epiphyses
+C1859470	Large basal ganglia
+C1859477	Hypoplasia of proximal radius
+C1859478	Hypoplasia of proximal fibula
+C1859480	Cone-shaped epiphyses of the phalanges of the hand
+C1859481	Abnormal finger flexion creases
+C1859486	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY
+C1859495	Episodic hemolytic anemia
+C1859499	3-methylcrotonyl CoA carboxylase 2 deficiency
+C1859506	Acute hyperammonemia
+C1859516	Episodic metabolic acidosis
+C1859518	Beta-Aminoisobutyric Acid, Urinary Excretion of
+C1859520	Progressive spasticity
+C1859523	Contractures of the joints of the lower limbs
+C1859524	Adductor longus contractures
+C1859534	Bare Lymphocyte Syndrome, Type II, Complementation Group A
+C1859535	Bare Lymphocyte Syndrome, Type II, Complementation Group B
+C1859536	Bare Lymphocyte Syndrome, Type II, Complementation Group C
+C1859537	Bare Lymphocyte Syndrome, Type II, Complementation Group D
+C1859538	Bare Lymphocyte Syndrome, Type II, Complementation Group E
+C1859541	Variable degree of villous atrophy
+C1859564	Bardet-Biedl syndrome 3
+C1859565	BARDET-BIEDL SYNDROME 7
+C1859566	BARDET-BIEDL SYNDROME 8
+C1859567	BARDET-BIEDL SYNDROME 9
+C1859568	BARDET-BIEDL SYNDROME 10
+C1859569	BARDET-BIEDL SYNDROME 11
+C1859570	BARDET-BIEDL SYNDROME 12
+C1859592	ATRICHIA WITH PAPULAR LESIONS
+C1859598	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
+C1859606	Decreased number of large peripheral myelinated nerve fibers
+C1859624	Defective B cell differentiation
+C1859648	Asthma, Nasal Polyps, And Aspirin Intolerance
+C1859678	Mental deterioration in childhood
+C1859680	Broad face
+C1859682	Hypoplastic frontal sinuses
+C1859690	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
+C1859692	Decreased cervical spine mobility
+C1859697	Enlargement of the proximal femoral epiphysis
+C1859698	Contractures of the large joints
+C1859700	Enlarged metacarpophalangeal joints
+C1859701	Enlarged interphalangeal joints
+C1859709	Kuskokwim disease
+C1859717	Depressed nasal tip
+C1859722	Arthrogryposis renal dysfunction cholestasis syndrome
+C1859726	ARTERIAL TORTUOSITY SYNDROME
+C1859727	Arterial calcification of infancy
+C1859728	Coronary Sclerosis, Medial, of Infancy
+C1859735	Arginine deficiency
+C1859736	Progressive spastic quadriplegia
+C1859768	Fused fourth and fifth metacarpals
+C1859773	Microphthalmia, Syndromic 3
+C1859774	Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System
+C1859775	Anterior pituitary hypoplasia
+C1859778	Postnatal growth retardation
+C1859807	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
+C1859817	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA
+C1859819	Impaired renal concentrating ability
+C1859828	Increased extraneuronal autofluorescent lipopigment
+C1859833	Granular osmiophilic deposits (GROD) in cells
+C1859844	LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)
+C1859846	Childhood-onset truncal obesity
+C1859860	Episodic ketoacidosis
+C1859863	Cerebral cortical neurodegeneration
+C1859877	Alopecia universalis congenita
+C1859878	Alopecia-Mental Retardation Syndrome 1
+C1859882	Pigmentation of the sclera
+C1859896	Progressive macrocephaly
+C1859923	Freckles in sun-exposed areas
+C1859966	Neutropenia, Severe Congenital, Autosomal Dominant 1
+C1859970	Hypodysfibrinogenemia, Congenital
+C1859972	ADRENOCORTICAL CARCINOMA, HEREDITARY
+C1859973	Adrenocortical Carcinoma, Pediatric
+C1859977	Adrenal Hypoplasia, Cytomegalic Type
+C1859979	Precocious puberty in males
+C1859980	Ambiguous genitalia due to virilization
+C1859995	Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
+C1859998	CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
+C1860042	Antley-Bixler Syndrome with Disordered Steroidogenesis
+C1860050	Cloverleaf skull
+C1860069	Exercise-induced myoglobinuria in adults
+C1860081	Medium chain dicarboxylic aciduria
+C1860099	Acral ulceration leading to autoamputation of digits
+C1860105	Severe short-limb dwarfism
+C1860107	Distal femoral bowing
+C1860111	Abnormally shaped carpal bones
+C1860119	Acrofacial dysostosis Rodriguez type
+C1860121	Decreased testosterone in males
+C1860127	Impaired T cell function
+C1860128	Recurrent candida infections
+C1860130	Low alkaline phosphatase
+C1860156	Lateral displacement of patellae
+C1860157	Elejalde Disease
+C1860162	Bifid distal phalanx of the thumb
+C1860164	Duplication of phalanx of hallux
+C1860176	Very short digits
+C1860179	Valgus hand deformity
+C1860182	Aplasia/Hypoplasia of metatarsal bones
+C1860191	Absent vertebral body mineralization
+C1860202	Unossified vertebral bodies
+C1860216	Progressive choreoathetosis
+C1860219	Self-mutilation of tongue and lips due to involuntary movements
+C1860224	ABLEPHARON-MACROSTOMIA SYNDROME
+C1860229	Hyperzincemia and Hypercalprotectinemia
+C1860236	Irregular hyperpigmentation
+C1860238	WOOLLY HAIR, AUTOSOMAL DOMINANT
+C1860243	Abnormal sternal ossification
+C1860244	Malrotation of small bowel
+C1860245	Cranial asymmetry
+C1860247	Prominent glabella
+C1860253	Pseudoepiphyses of the metacarpals
+C1860268	Gonadal tissue inappropriate for external genitalia or chromosomal sex
+C1860309	Chin with H-shaped crease
+C1860315	Whispering dysphonia, hereditary
+C1860320	Bone marrow hypercellularity
+C1860334	Lisch nodules
+C1860335	Axillary freckling
+C1860339	WAARDENBURG SYNDROME, TYPE IIA
+C1860344	Hypoplastic iris stroma
+C1860394	Multiple pancreatic cysts
+C1860405	Snowflake vitreoretinal degeneration
+C1860406	VITREORETINOCHOROIDOPATHY (disorder)
+C1860446	Congenital vertical talus, bilateral
+C1860449	Equinus calcaneus
+C1860450	Calcaneovalgus deformity
+C1860475	Retinal vascular tortuosity
+C1860488	Abnormality of internal carotid artery
+C1860493	Abnormality of the sternum
+C1860518	Vasculopathy, Retinal, With Cerebral Leukodystrophy
+C1860601	Flattened femoral head
+C1860606	Short proximal phalanx of finger
+C1860607	Uncombable hair
+C1860608	Pili canaliculi
+C1860614	ULNAR HYPOPLASIA
+C1860707	TUBEROUS SCLEROSIS 2 (disorder)
+C1860710	Achromatic retinal patches
+C1860711	Dental enamel pits
+C1860715	Giant cell astrocytoma
+C1860752	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
+C1860787	DOWN SYNDROME CRITICAL REGION
+C1860788	Transient Myeloproliferative Disorder of Down Syndrome
+C1860789	Leukemia, Megakaryoblastic, of Down Syndrome
+C1860791	Duodenal stenosis/atresia
+C1860796	Shallow acetabulum
+C1860808	Triosephosphate Isomerase Deficiency
+C1860816	Preauricular skin tag
+C1860819	Metopic synostosis
+C1860823	Trichorhinophalangeal Syndrome, Type III
+C1860825	Accelerated bone age after puberty
+C1860826	Coxa Magna
+C1860828	Cone-shaped epiphyses of the middle phalanges of the hand
+C1860834	Infantile muscular hypotonia
+C1860838	Large prominent ears
+C1860841	Swelling of proximal interphalangeal joints
+C1860844	Thin, sparse hair
+C1860850	Familial multiple trichodiscomas
+C1860861	TREMOR, HEREDITARY ESSENTIAL, 1
+C1860896	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
+C1860991	NOONAN SYNDROME 3
+C1861028	Esophageal atresia with or without tracheoesophageal fistula
+C1861063	TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)
+C1861065	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
+C1861099	Absence of tibia with polydactyly
+C1861101	THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT
+C1861106	Thyrotropin-Releasing Hormone Resistance, Generalized
+C1861129	Takao VCF Syndrome
+C1861141	Abnormality of the middle ear
+C1861171	THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)
+C1861172	Venous Thromboembolism
+C1861178	Thrombocytopenia Paris-Trousseau type
+C1861185	THROMBOCYTOPENIA 2 (disorder)
+C1861194	Thrombasthenia-Thrombocytopenia, Hereditary
+C1861195	Glanzmann Thrombasthenia, Autosomal Dominant
+C1861213	Wide-cupped costochondral junctions
+C1861217	Small foramen magnum
+C1861218	Hypoplastic ilia
+C1861226	Small abnormally formed scapulae
+C1861235	Forebrain Defects
+C1861238	ARTHROGRYPOSIS, DISTAL, TYPE 10
+C1861248	Fingerpad telangiectases
+C1861303	SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)
+C1861305	TARSAL-CARPAL COALITION SYNDROME
+C1861306	Synostosis of Talus and Calcaneus with Short Stature
+C1861310	Progressive fusion 2nd-5th pip joints
+C1861313	Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly
+C1861316	Radially deviated wrists
+C1861324	Short philtrum
+C1861325	Progressive conductive hearing impairment
+C1861326	Stapes ankylosis
+C1861328	Hypoplastic nasal septum
+C1861329	Spinal canal stenosis
+C1861331	Limited pronation/supination of forearm
+C1861332	Fusion of midphalangeal joints
+C1861336	Aplasia/Hypoplasia of the distal phalanges of the hand
+C1861339	Absent distal phalanges
+C1861348	Syndactyly, type v
+C1861349	Absent distal interphalangeal creases
+C1861350	Enlarged proximal interphalangeal joints
+C1861355	Syndactyly, Type IV
+C1861357	1-5 finger complete cutaneous syndactyly
+C1861360	6 metacarpals
+C1861366	SYNDACTYLY, TYPE III
+C1861373	Y-shaped metacarpals
+C1861376	2nd-5th toe middle phalangeal hypoplasia
+C1861380	Syndactyly, Type I
+C1861385	SYMPHALANGISM, PROXIMAL
+C1861388	Short 5th metacarpal
+C1861395	Small hypothenar eminence
+C1861443	Facial hemangioma
+C1861451	Stormorken Syndrome
+C1861453	Pseudohyperkalemia Cardiff
+C1861455	STOMATOCYTOSIS I
+C1861456	Stiff Skin Syndrome
+C1861457	PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY
+C1861481	Stickler syndrome, type 3
+C1861502	COLCHICINE RESISTANCE
+C1861512	Cochleosaccular degeneration of the inner ear and progressive cataracts
+C1861516	Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly
+C1861517	Abnormal facility in opposing the shoulders
+C1861519	Moderately short stature
+C1861528	Delayed mineralization of pubic bone
+C1861531	Long second metacarpal
+C1861536	Blepharo-cheilo-dontic syndrome
+C1861537	OROFACIAL CLEFT 1
+C1861538	Nonsyndromic cleft lip with or without cleft palate
+C1861544	Lower lip pit
+C1861553	Split-Hand-Foot Malformation With Long Bone Deficiency 1
+C1861556	Cirrhosis, Familial
+C1861621	Intrahepatic duct deficiency
+C1861627	Butterfly vertebral arch
+C1861630	CHLORPROPAMIDE-ALCOHOL FLUSHING
+C1861656	Retraction of lower eyelid
+C1861669	Charcot-Marie-Tooth disease and deafness
+C1861675	Cold-induced muscle cramps
+C1861678	Charcot-Marie-Tooth Disease, Axonal, Type 2a1
+C1861689	KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT
+C1861696	EAR WAX, WET/DRY
+C1861704	Anomalous rib insertion to vertebrae
+C1861708	Calcaneal epiphyseal stippling
+C1861732	SPINOCEREBELLAR ATAXIA 29
+C1861735	Dementia, familial Danish
+C1861736	SPINOCEREBELLAR ATAXIA 31 (disorder)
+C1861751	Minicore Myopathy, Moderate, with Hand Involvement
+C1861752	Multicore Myopathy, Moderate, with Hand Involvement
+C1861753	Multiminicore Disease, Moderate, with Hand Involvement
+C1861785	Cavernous Malformations of CNS and Retina
+C1861786	Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations
+C1861790	Hepatic vascular malformations
+C1861791	Retinal vascular malformation
+C1861821	CATARACT, MARNER TYPE
+C1861825	CATARACT, POSTERIOR POLAR, 1
+C1861826	Cataract, Nuclear Total
+C1861827	Cataract, Nuclear Diffuse Nonprogressive
+C1861828	Cataract, Zonular Pulverulent 1
+C1861829	Cataract microcornea syndrome
+C1861832	CATARACT, CRYSTALLINE ACULEIFORM
+C1861848	PARAGANGLIOMAS 4
+C1861861	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
+C1861862	Familial Hypertrophic Cardiomyopathy Type 4
+C1861863	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder)
+C1861864	Cardiomyopathy, Familial Hypertrophic, 2
+C1861866	Aplasia/Hypoplasia of the corpus callosum
+C1861869	Underdeveloped supraorbital ridges
+C1861872	Multiple palmar creases
+C1861873	Multiple plantar creases
+C1861884	Familial Sudden Death
+C1861901	Subacute progressive viral hepatitis
+C1861906	Breast Cancer, Familial Male
+C1861921	Cutaneous syndactyly
+C1861922	CAMPOMELIC DYSPLASIA
+C1861923	Acampomelic Campomelic Dysplasia
+C1861937	Anterior tibial bowing
+C1861975	Cafe au lait spots, multiple
+C1861983	Heart Block, Nonprogressive
+C1861984	Cardiac Conduction Defect, Nonprogressive
+C1862005	Epidermolytic Hyperkeratosis, Late-Onset
+C1862050	Cochlear malformation
+C1862052	Gustatory lacrimation
+C1862059	Supraauricular pit
+C1862066	Branchial anomaly
+C1862068	Fusion of middle ear ossicles
+C1862083	Short 4th toe
+C1862087	Mesomelic arm shortening
+C1862095	Bilateral single transverse palmar creases
+C1862096	Aplasia of the middle phalanx of the hand
+C1862102	BRACHYDACTYLY, TYPE E1
+C1862103	Brachydactyly type C
+C1862112	BRACHYDACTYLY, TYPE B1
+C1862132	Short ulnae
+C1862139	Brachymesophalangy 2 and 5
+C1862140	Brachydactyly type A3
+C1862142	Short 2nd finger
+C1862144	Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
+C1862147	Medially deviated second toe
+C1862151	BRACHYDACTYLY, TYPE A1 (disorder)
+C1862152	Aplasia/Hypoplasia of the middle phalanges of the hand
+C1862156	Thin proximal phalanges with broad epiphyses
+C1862157	Proportionate shortening of all digits
+C1862158	Terminal symphalangism of hands
+C1862159	Short proximal phalanx of hallux
+C1862170	Brachydactyly with hypertension
+C1862177	Diaphyseal medullary stenosis with malignant fibrous histiocytoma
+C1862178	Cole Carpenter syndrome
+C1862191	BLOOD GROUP--WALDNER TYPE
+C1862260	BPES, TYPE I
+C1862261	BPES, TYPE II
+C1862262	Bpes With Ovarian Failure
+C1862263	Bpes Without Ovarian Failure
+C1862264	Bpes With Duane Retraction Syndrome
+C1862265	Increased circulating gonadotropin level
+C1862304	Hamartomatous polyp of stomach
+C1862313	Short distal phalanx of the thumb
+C1862314	Basal cell nevus
+C1862322	Ovalocytosis, Malaysian-Melanesian-Filipino Type
+C1862323	Southeast Asian ovalocytosis
+C1862324	Elliptocytosis 4
+C1862359	Facial-lingual fasciculations
+C1862373	Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities
+C1862376	Abnormally prominent line of Schwalbe
+C1862382	SVEINSSON CHORIORETINAL ATROPHY
+C1862389	ATRIAL SEPTAL DEFECT 1
+C1862391	ASD I
+C1862392	Atrial Septal Defect, Secundum Type
+C1862393	ASD II
+C1862394	Atrial Fibrillation, Familial, 4
+C1862415	Cervical segmentation defect
+C1862420	Tombstone-shaped proximal phalanges
+C1862421	Widened distal phalanges
+C1862425	Prominent globes
+C1862428	Thoracic platyspondyly
+C1862463	Aryl Hydrocarbon Hydroxylase Inducibility
+C1862471	Arthrogryposis-like hand anomaly and sensorineural deafness
+C1862472	Oculomelic amyoplasia
+C1862474	Decreased facial expression
+C1862475	Abnormality of retinal pigmentation
+C1862479	Absent phalangeal crease
+C1862481	Limited wrist extension
+C1862491	Internally rotated shoulders
+C1862511	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)
+C1862556	Apolipoprotein E, Deficiency or Defect of
+C1862557	Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d
+C1862558	Familial Hyperbeta- and Prebetalipoproteinemia
+C1862560	Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis
+C1862561	Broad-Betalipoproteinemia
+C1862562	Floating-Betalipoproteinemia
+C1862591	CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
+C1862596	Familial hypobetalipoproteinemia
+C1862683	Townes-Brocks-Branchiootorenal-Like Syndrome
+C1862689	Stahl ear
+C1862693	Pseudoepiphyses of second metacarpal
+C1862697	Metatarsal synostosis
+C1862698	Aplasia/Hypoplasia of the 3rd toe
+C1862761	Increased hepatocellular carcinoma risk
+C1862839	Anterior segment mesenchymal dysgenesis
+C1862855	Sparse to absent eyelashes
+C1862862	Patchy alopecia
+C1862863	Sparse body hair
+C1862866	Ankyloblepharon filiforme adnatum and cleft palate
+C1862871	ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS
+C1862874	ANGIOTENSIN I-CONVERTING ENZYME, BENIGN SERUM INCREASE
+C1862876	STROKE, HEMORRHAGIC, SUSCEPTIBILITY TO
+C1862892	Hereditary Angioedema Type II
+C1862932	ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)
+C1862937	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1
+C1862939	AMYOTROPHIC LATERAL SCLEROSIS 1
+C1862941	Amyotrophic Lateral Sclerosis, Sporadic
+C1862968	Generalized amyloid deposition
+C1863008	Yellow-brown discoloration of the teeth
+C1863012	Amelogenesis Imperfecta, Type IV
+C1863051	ALZHEIMER DISEASE 2
+C1863052	ALZHEIMER DISEASE, FAMILIAL, 1
+C1863053	Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
+C1863061	Episodic hemiplegia
+C1863062	Episodic quadriplegia
+C1863080	ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF
+C1863081	alpha-Fetoprotein Deficiency
+C1863093	Alopecia congenita keratosis palmoplantaris
+C1863119	Dysalbuminemic Hyperthyroxinemia
+C1863184	Choroid plexus calcification
+C1863198	ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
+C1863200	Lacrimal gland hypoplasia
+C1863204	ADULT SYNDROME
+C1863224	Adenosine Triphosphate, Elevated, Of Erythrocytes
+C1863236	SCID Due to ADA Deficiency, Early-Onset
+C1863239	Partial adenosine deaminase deficiency
+C1863246	Absent specific antibody response
+C1863311	Elongated sella turcica
+C1863313	Tall lumbar vertebral bodies
+C1863314	Cervical instability
+C1863317	Crowded carpal bones
+C1863340	PITUITARY ADENOMA PREDISPOSITION (disorder)
+C1863351	Calvarial hyperostosis
+C1863353	Hypoplastic vertebral bodies
+C1863360	Radiohumeral synostosis of elbow
+C1863363	Cartilaginous trachea
+C1863370	Saethre-Chotzen Syndrome with Eyelid Anomalies
+C1863371	BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY
+C1863382	Absent first metatarsal
+C1863389	Apert-Crouzon Disease
+C1863391	Vogt Cephalodactyly
+C1863392	Abnormal morphology of the limbic system
+C1863395	Acrobrachycephaly
+C1863402	Broad distal phalanx of the thumb
+C1863403	Broad distal hallux
+C1863406	Anomalous tracheal cartilage
+C1863411	Retinal hamartoma
+C1863416	Autosomal dominant compelling helio ophthalmic outburst syndrome
+C1863423	Lumbar kyphosis in infancy
+C1863495	Aplasia cutis congenita over posterior parietal area
+C1863496	Aplasia cutis congenita on trunk or limbs
+C1863512	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE
+C1863516	Microcephaly with Simplified Gyral Pattern
+C1863534	Stargardt disease 4
+C1863551	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3
+C1863557	Young Simpson syndrome
+C1863561	Deafness, Autosomal Recessive 16
+C1863599	Hereditary Myopathy with Early Respiratory Failure
+C1863600	PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding)
+C1863616	ACROMELIC FRONTONASAL DYSOSTOSIS
+C1863634	Cone-Rod Dystrophy 7
+C1863655	Deafness, Autosomal Recessive 21
+C1863659	DEAFNESS, AUTOSOMAL DOMINANT 17
+C1863660	COCHLEOSACCULAR DEGENERATION
+C1863688	Xanthinuria, Type II
+C1863704	Spastic paraplegia 8, autosomal dominant
+C1863715	Severe B lymphocytopenia
+C1863727	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2
+C1863728	Hemophagocytic lymphohistiocytosis, familial, 4
+C1863732	Spondyloepimetaphyseal dysplasia with multiple dislocations
+C1863734	Caudal interpedicular narrowing
+C1863739	Narrow femoral neck
+C1863749	Carpal bone hypoplasia
+C1863752	Enlarged Vestibular Aqueduct
+C1863753	LIMB-MAMMARY SYNDROME
+C1863767	Light Fixation Seizure Syndrome
+C1863769	Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema
+C1863843	Neuronal intranuclear inclusion disease
+C1863844	Adult-onset citrullinemia type 2
+C1863872	Upper eyelid coloboma
+C1863878	Arhinia, choanal atresia, and microphthalmia
+C1863924	Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome
+C1863925	Nonmedullary thyroid carcinoma, with or without cell oxyphilia
+C1863926	GLAUCOMA 1, OPEN ANGLE, F (disorder)
+C1863959	Hyperthyroidism, Familial Gestational
+C1863960	Thyroid Adenoma, Hyperfunctioning
+C1863998	Peroxisome Biogenesis Disorder, Complementation Group 9
+C1863999	Peroxisome Biogenesis Disorder, Complementation Group D
+C1864002	GRACILE SYNDROME (disorder)
+C1864040	Cerebral Cavernous Malformations 3
+C1864041	CEREBRAL CAVERNOUS MALFORMATIONS 2
+C1864100	PSEUDOHYPOPARATHYROIDISM, TYPE IB
+C1864105	Low urinary cyclic AMP response to PTH administration
+C1864112	HUNTINGTON DISEASE-LIKE 1
+C1864124	SCHIZOPHRENIA 8 (disorder)
+C1864148	MECKEL SYNDROME, TYPE 2
+C1864153	SCHIZOPHRENIA 5
+C1864156	Conjunctivitis, recurrent
+C1864171	Peroxisome Biogenesis Disorder, Complementation Group 12
+C1864172	Peroxisome Biogenesis Disorder, Complementation Group G
+C1864179	Elevated serum transaminases during infections
+C1864205	Macular Degeneration, Age-Related, 1
+C1864233	ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY (disorder)
+C1864238	Prolonged miniature endplate currents
+C1864267	Endotoxin Hyporesponsiveness
+C1864275	SCHIZOPHRENIA 6 (disorder)
+C1864298	Fibular overgrowth
+C1864323	OROFACIAL CLEFT 2
+C1864356	ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
+C1864361	Lower thoracic kyphosis
+C1864364	Thoracolumbar interpediculate narrowness
+C1864365	Acromesomelia
+C1864375	Long hallux
+C1864389	PREMATURE CHROMATID SEPARATION TRAIT
+C1864399	Peroxisome Biogenesis Disorder, Complementation Group 7
+C1864436	Muenke Syndrome
+C1864445	Histiocytosis with joint contractures and sensorineural deafness
+C1864446	Retinitis Pigmentosa 25
+C1864449	Limited neck flexion
+C1864497	PSORIASIS 2
+C1864498	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE
+C1864499	Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss
+C1864567	CATARACT, POSTERIOR POLAR, 4 (disorder)
+C1864570	Insulin insensitivity
+C1864573	Iridescent posterior subcapsular cataract
+C1864580	Type 2 muscle fiber atrophy
+C1864584	Frontal balding
+C1864621	RETINITIS PIGMENTOSA 36
+C1864623	DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
+C1864648	CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL
+C1864651	GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY
+C1864652	Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
+C1864653	GLAUCOMA 1, OPEN ANGLE, M (disorder)
+C1864663	HYPOMYELINATION AND CONGENITAL CATARACT
+C1864668	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4
+C1864669	NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY
+C1864670	Neuronal Ceroid Lipofuscinosis, Congenital
+C1864689	MICROPHTHALMIA, SYNDROMIC 6 (disorder)
+C1864690	Microphthalmia, Syndromic 5
+C1864694	Complement Component 7 Deficiency
+C1864695	Giant Axonal Neuropathy, Autosomal Dominant
+C1864696	Distal limb muscle weakness due to peripheral neuropathy
+C1864711	Muscle biopsy shows dystrophic changes
+C1864715	Thenar muscle atrophy
+C1864720	MICROPHTHALMIA, ISOLATED 2
+C1864721	Microphthalmia, Isolated, with Coloboma 3
+C1864722	Microphthalmia, Cataracts, and Iris Abnormalities
+C1864723	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
+C1864729	HYPERPARATHYROIDISM 3
+C1864730	Polyposis Syndrome, Hereditary Mixed, 2
+C1864738	Corneal Dystrophy, Congenital Stromal
+C1864746	Deafness, Autosomal Recessive 53
+C1864761	Thyroid Hormone Metabolism, Abnormal
+C1864794	Abnormality of the odontoid process
+C1864795	Superior pectus carinatum
+C1864796	Pectus excavatum of inferior sternum
+C1864818	DEAFNESS, AUTOSOMAL RECESSIVE 42 (disorder)
+C1864825	Frias syndrome
+C1864826	Epidermolysis bullosa, lethal acantholytic
+C1864827	HOLOPROSENCEPHALY 5
+C1864839	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7 (disorder)
+C1864840	Combined Oxidative Phosphorylation Deficiency 3
+C1864843	Combined Oxidative Phosphorylation Deficiency 2
+C1864846	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (disorder)
+C1864849	RETINAL CONE DYSTROPHY 4
+C1864850	Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
+C1864851	Pigmented Nodular Adrenocortical Disease, Primary, 2
+C1864852	CATSHL syndrome
+C1864853	Increased vertebral height
+C1864854	Broad femoral metaphyses
+C1864861	Tumoral Calcinosis, Normophosphatemic, Familial
+C1864868	BURULI ULCER, SUSCEPTIBILITY TO
+C1864869	Night Blindness, Congenital Stationary, Autosomal Dominant 1
+C1864870	Night Blindness, Congenital Stationary, Autosomal Dominant 3
+C1864871	Chromosome 17q21.31 Deletion Syndrome
+C1864872	Spondyloepimetaphyseal dysplasia, Genevieve type
+C1864873	Testicular Microlithiasis
+C1864877	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
+C1864880	HEPATITIS B VIRUS, SUSCEPTIBILITY TO
+C1864897	Cognitive delay
+C1864900	Retinal Cone Dystrophy 3A
+C1864902	Hyperinsulinemic hypoglycemia, familial, 7
+C1864903	Hyperinsulinemic hypoglycemia
+C1864904	Exercise-induced hyperinsulinism
+C1864908	Cataract, autosomal recessive congenital 2
+C1864910	Glutamine deficiency, congenital
+C1864912	2-Methylbutyryl-CoA Dehydrogenase Deficiency
+C1864923	Northern epilepsy syndrome
+C1864947	Natural Killer Cell Deficiency, Familial Isolated
+C1864948	Hyperinsulinemic Hypoglycemia, Familial, 4
+C1864952	Hyperinsulinemic Hypoglycemia, Familial, 5
+C1864954	Fasting hyperinsulinemia
+C1864975	Osteomyelitis leading to amputation due to slow healing fractures
+C1864987	Migraine, Familial Hemiplegic, 3
+C1864996	Visceral Neuropathy, Familial, Autosomal Dominant
+C1864997	Majeed syndrome
+C1865014	Long philtrum
+C1865017	Thin upper lip vermilion
+C1865018	Short QT Syndrome 3
+C1865019	SHORT QT SYNDROME 2 (disorder)
+C1865020	Short QT Syndrome 1
+C1865027	Hypoplastic iliac wing
+C1865030	Hypoplastic pubic bone
+C1865037	Cone-shaped epiphysis
+C1865038	Broad toe
+C1865039	Cupped ribs
+C1865044	PARIETAL FORAMINA 2
+C1865045	Symmetrical, oval parietal bone defects
+C1865060	Molar tooth sign on MRI
+C1865070	SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
+C1865143	BRANCHIOOTIC SYNDROME 1
+C1865145	Congenital disorder of glycosylation type 1B
+C1865185	Spondyloepimetaphyseal Dysplasia, Shohat Type
+C1865186	Bell-shaped thorax
+C1865200	Delayed epiphyseal ossification
+C1865233	Muscular Dystrophy, Congenital, Megaconial Type
+C1865234	ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
+C1865241	Large sternal ossification centers
+C1865244	Shallow orbits
+C1865254	Distal widening of metacarpals
+C1865267	Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly
+C1865270	BARTTER SYNDROME, TYPE 4A
+C1865276	Global glomerulosclerosis
+C1865279	Fetal polyuria
+C1865285	Megalencephaly cutis marmorata telangiectatica congenita
+C1865286	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA
+C1865290	Hyperinsulinemic hypoglycemia, familial, 3
+C1865292	Nonketotic hypoglycemia
+C1865295	Auriculo-condylar syndrome
+C1865302	Cleft at the superior portion of the pinna
+C1865304	Overfolding of the superior helices
+C1865305	Hypoplastic superior helix
+C1865313	Speech articulation difficulties
+C1865318	Abnormality of the temporomandibular joint
+C1865322	MIGRAINE, FAMILIAL HEMIPLEGIC, 2
+C1865323	Migraine, Familial Basilar
+C1865332	Transient unilateral blurring of vision
+C1865343	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE
+C1865349	Ethylmalonic encephalopathy
+C1865351	Hyperintense lesions in the basal ganglia on MRI
+C1865353	Ethylmalonic aciduria
+C1865361	SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES
+C1865362	Scapulohumeral synostosis
+C1865363	Delayed ossification of pubic rami
+C1865366	Deafness, Autosomal Dominant 15
+C1865370	Severe combined immunodeficiency with sensitivity to ionizing radiation
+C1865371	SEVERE COMBINED IMMUNODEFICIENCY, ATHABASKAN-TYPE
+C1865372	Athabaskan severe combined immunodeficiency
+C1865373	SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL
+C1865377	Small lymph nodes
+C1865384	Amyotrophy, monomelic
+C1865409	Amyotrophic Lateral Sclerosis 4, Juvenile
+C1865412	Abnormal lower motor neuron morphology
+C1865416	Pallor of dorsal columns of the spinal cord
+C1865417	Diffuse axonal swelling
+C1865571	Aplasia/Hypoplasia of the ulna
+C1865572	Proximal placement of thumb
+C1865596	Desmosterolosis
+C1865597	Hypoplastic nasal bridge
+C1865598	Alveolar ridge overgrowth
+C1865614	HEMOCHROMATOSIS, TYPE 2A
+C1865616	HEMOCHROMATOSIS, TYPE 2B
+C1865639	Gracile bone dysplasia
+C1865643	Cholestasis, progressive familial intrahepatic 3
+C1865644	Plantar Lipomatosis, Unusual Facies, and Developmental Delay
+C1865695	Spondylometaphyseal dysplasia, axial
+C1865702	Joint contracture of the 5th finger
+C1865782	CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3
+C1865794	RHYNS syndrome
+C1865803	Peroxisome Biogenesis Disorder, Complementation Group 1
+C1865804	Peroxisome Biogenesis Disorder, Complementation Group E
+C1865818	DYSTONIA 7, TORSION (disorder)
+C1865819	CERVICAL DYSTONIA, PRIMARY
+C1865832	Spondyloepimetaphyseal Dysplasia, Missouri Type
+C1865833	Flared, irregular rib ends
+C1865841	Flared iliac wings
+C1865847	Ulnar bowing
+C1865864	AMYOTROPHIC LATERAL SCLEROSIS 5
+C1865866	Congenital sensorineural hearing loss
+C1865868	ALZHEIMER DISEASE 5
+C1865869	CONE DYSTROPHY 3 (disorder)
+C1865870	Deafness, Autosomal Recessive 18
+C1865871	HEMANGIOMA, CAPILLARY INFANTILE
+C1865872	NEPHRONOPHTHISIS 2
+C1865877	Renal cortical microcysts
+C1865880	Hyperkalemic metabolic acidosis
+C1865885	Usher Syndrome, Type IF
+C1865903	Long-tract signs
+C1865915	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2
+C1865916	Bilateral ptosis
+C1865918	Restrictive external ophthalmoplegia
+C1865926	Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
+C1865951	Ectodermal Dysplasia, Pure Hair-Nail Type
+C1865974	Hypomagnesemia 1, Intestinal
+C1865992	Short hallux
+C1866008	Muscular Dystrophy, Limb-Girdle, Type 2G
+C1866010	Proximal muscle weakness in lower limbs
+C1866012	Proximal muscle weakness in upper limbs
+C1866013	Proximal upper limb amyotrophy
+C1866021	Increased connective tissue
+C1866029	Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
+C1866031	Linear arrays of macular hyperkeratoses in flexural areas
+C1866032	Honeycomb palmoplantar keratoderma
+C1866039	EPISODIC ATAXIA, TYPE 5
+C1866040	DIABETES MELLITUS, INSULIN-DEPENDENT, 10
+C1866048	Severe hydrops fetalis
+C1866053	Deafness, Congenital Heart Defects, and Posterior Embryotoxon
+C1866070	OROFACIAL CLEFT 10
+C1866075	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
+C1866077	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5
+C1866078	Cataract, Zonular Pulverulent 3
+C1866079	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1
+C1866080	HIGH BONE MASS
+C1866091	Left-Right Axis Malformations
+C1866094	DEAFNESS, AUTOSOMAL RECESSIVE 15
+C1866095	Deafness, Autosomal Dominant 13
+C1866119	Autoimmune Lymphoproliferative Syndrome, Type IA
+C1866120	Autoimmune Lymphoproliferative Syndrome, Type IB
+C1866121	Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive
+C1866129	Abnormality of the cerebellum
+C1866130	Rhombencephalosynapsis
+C1866134	Wide anterior fontanel
+C1866141	Foot dorsiflexor weakness
+C1866173	BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
+C1866174	Phosphoglycerate Dehydrogenase Deficiency
+C1866176	EXUDATIVE VITREORETINOPATHY 4 (disorder)
+C1866180	Horizontal pendular nystagmus
+C1866182	Penttinen-Aula syndrome
+C1866190	Atresia of the external auditory canal
+C1866195	Downturned corners of mouth
+C1866206	Dysplastic pulmonary valve
+C1866227	Somatic mosaicism
+C1866231	Full cheeks
+C1866234	Protruding lower lip
+C1866239	Mesomelic/rhizomelic limb shortening
+C1866241	Broad foot
+C1866257	Peroxisome Biogenesis Disorder, Complementation Group K
+C1866259	Peroxisome Biogenesis Disorder, Complementation Group 13
+C1866260	Peroxisome Biogenesis Disorder, Complementation Group H
+C1866282	CEROID LIPOFUSCINOSIS, NEURONAL, 6
+C1866284	Motor deterioration
+C1866293	Retinal cone dystrophy 2
+C1866294	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1
+C1866339	Preaxial Hallucal Polydactyly
+C1866340	Peroxisome Biogenesis Disorder, Complementation Group 3
+C1866351	Peroxisome Biogenesis Disorder, Complementation Group 11
+C1866352	Peroxisome Biogenesis Disorder, Complementation Group R
+C1866398	Proteus-Like Syndrome (disorder)
+C1866422	RETINITIS PIGMENTOSA 19
+C1866423	Quebec platelet disorder
+C1866425	Yemenite deaf-blind hypopigmentation syndrome
+C1866426	T-cell immunodeficiency, congenital alopecia and nail dystrophy
+C1866430	NOVELTY SEEKING PERSONALITY TRAIT
+C1866432	OBESITY, SUSCEPTIBILITY TO
+C1866487	Prominent nasolabial fold
+C1866495	Bartter syndrome, antenatal type 1
+C1866496	Renal juxtaglomerular cell hypertrophy/hyperplasia
+C1866498	Hyperprostaglandinuria
+C1866500	Low-to-normal blood pressure
+C1866504	Photosensitive Trichothiodystrophy
+C1866505	Ichthyosis, Congenital, with Trichothiodystrophy
+C1866550	GLAUCOMA 3, PRIMARY CONGENITAL, A, DIGENIC
+C1866552	PARAGANGLIOMAS 2 (disorder)
+C1866555	Glomus tympanicum paraganglioma
+C1866558	Neural tube defect, folate-sensitive
+C1866559	Spina Bifida, Folate-Sensitive
+C1866560	IRIDOGONIODYSGENESIS, TYPE 1 (disorder)
+C1866561	Glaucoma Iridogoniodysplasia, Familial
+C1866636	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C
+C1866637	Basal lamina \'onion bulb\' formation
+C1866656	STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (disorder)
+C1866657	Congenital stapes ankylosis
+C1866675	Biconvex vertebral bodies
+C1866688	Spondylometaphyseal dysplasia, Algerian type
+C1866689	Short sacroiliac notch
+C1866700	Irregular, rachitic-like metaphyses
+C1866703	Severe carpal ossification delay
+C1866710	Delayed pubic bone ossification
+C1866730	Rhizomelia
+C1866731	Pear-shaped vertebrae
+C1866737	Lateral femoral bowing
+C1866751	Spinocerebellar tract degeneration
+C1866753	Impaired horizontal smooth pursuit
+C1866772	Abnormal nerve conduction velocity
+C1866777	Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant
+C1866785	Spheroid body myopathy
+C1866805	Unilateral narrow palpebral fissure
+C1866810	ELLIPTOCYTOSIS 3
+C1866855	Spastic paraplegia 4, autosomal dominant
+C1866863	Lower limb atrophy
+C1866927	SMITH-MAGENIS SYNDROME CHROMOSOME REGION
+C1866934	Reduced tendon reflexes
+C1866956	Aortic root dilation
+C1866959	Sella Turcica, Bridged
+C1866984	Sclerocornea, Autosomal Dominant
+C1866986	Social and occupational deterioration
+C1866993	SCHISTOSOMA MANSONI INFECTION, SUSCEPTIBILITY/RESISTANCE TO
+C1866994	Ulnar-mammary syndrome
+C1867003	Axillary apocrine gland hypoplasia
+C1867005	Scapuloperoneal Syndrome, Neurogenic, Kaeser Type
+C1867006	Restricted neck movement due to contractures
+C1867020	SCALP-EAR-NIPPLE SYNDROME
+C1867047	Systemic granulomatous disease
+C1867060	Lacrimal Puncta, Absence of
+C1867103	Limited elbow extension
+C1867114	Craniofacial disproportion
+C1867131	Broad hallux
+C1867132	Plantar crease between first and second toes
+C1867138	Upper limb postural tremor
+C1867146	Robinow Sorauf syndrome
+C1867155	RING DERMOID OF CORNEA
+C1867234	Rhabdomyosarcoma, Embryonal, 2
+C1867288	Retinomas (translucent, grayish retinal mass protruding into the vitreous)
+C1867289	Retinal calcification
+C1867299	Retinitis Pigmentosa 10
+C1867300	RETINITIS PIGMENTOSA 9
+C1867315	Retinal Nonattachment And Falciform Detachment
+C1867326	RETINAL CONE DYSTROPHY 1
+C1867327	RETINAL ARTERIES, TORTUOSITY OF
+C1867332	Reticular Dystrophy Of Retinal Pigment Epithelium
+C1867362	SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE
+C1867396	RADIAL-RENAL SYNDROME
+C1867403	Pyloric Stenosis, Infantile Hypertrophic 1
+C1867421	Elevated right atrial pressure
+C1867423	Increased pulmonary vascular resistance
+C1867424	Pulmonary artery vasoconstriction
+C1867438	PTOSIS, HEREDITARY CONGENITAL 1 (disorder)
+C1867439	Pterygium, Antecubital
+C1867440	Multiple Pterygium Syndrome, Autosomal Dominant
+C1867446	Bulging forehead
+C1867448	Multiple pterygia
+C1867450	Pseudoxanthoma Elasticum, Incomplete
+C1867467	Acholinesterasemia
+C1867468	Apnea, Postanesthetic
+C1867469	Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
+C1867470	Hypocholinesterasemia, Fluoride-Resistant, Japanese Type
+C1867487	Childhood onset short-limb short stature
+C1867494	Fragmented, irregular epiphyses
+C1867563	CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT
+C1867564	SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
+C1867610	Macrocephaly mesodermal hamartoma spectrum
+C1867616	Dermoid choristoma of eye proper
+C1867617	Hypertrophy of skin of soles
+C1867638	Warfarin-induced skin necrosis
+C1867717	SAPOSIN D (disease)
+C1867743	Premature coronary artery disease
+C1867773	CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
+C1867774	Sacral Agenesis Syndrome
+C1867775	Sacral Agenesis, Hereditary, With Presacral Mass, Anterior Meningocele, And-Or Teratoma, And Anorectal Malformation
+C1867776	Anterior sacral meningocele
+C1867801	Preaxial deficiency, postaxial polydactyly and hypospadias
+C1867864	Poor fine motor coordination
+C1867873	Failure to thrive in infancy
+C1867904	LONG QT SYNDROME 5
+C1867923	Posterior column ataxia
+C1867955	Increased incidence of hepatocellular carcinoma
+C1867968	Porphyria Cutanea Tarda, Type I
+C1867969	Porphyria, Acute Intermittent, Nonerythroid Variant
+C1867971	Acute episodes of neuropathic symptoms
+C1867981	POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1
+C1867982	KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE II
+C1867983	PORENCEPHALY, FAMILIAL
+C1868001	Polyposis Of Gastric Fundus Without Polyposis Coli
+C1868007	Precocious puberty with Sertoli cell tumor
+C1868071	Adenomatous colonic polyposis
+C1868072	Small intestine carcinoid
+C1868081	Juvenile Polyposis Coli
+C1868085	Craniofacial hyperostosis
+C1868097	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, DIGENIC
+C1868111	Polydactyly, preaxial 4
+C1868112	Crossed Polydactyly, Type I
+C1868114	POLYDACTYLY, PREAXIAL II (disorder)
+C1868117	POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA
+C1868118	Orofaciodigital syndrome 5
+C1868120	POSTAXIAL POLYDACTYLY, TYPE B
+C1868139	Medullary cystic kidney disease 1
+C1868148	Potter Type III Polycystic Kidney Disease
+C1868158	Absence of pectoralis minor muscle
+C1868170	Hypoplasia of deltoid muscle
+C1868184	Telangiectases in sun-exposed and nonexposed skin
+C1868193	PNEUMOTHORAX, PRIMARY SPONTANEOUS
+C1868251	Neonatal alloimmune thrombocytopenia (NAIT)
+C1868263	Platelet Aggregation, Spontaneous
+C1868310	Pigmented Paravenous Chorioretinal Atrophy
+C1868355	6-Phosphogluconolactonase Deficiency
+C1868393	Elevated urinary epinephrine
+C1868394	Elevated calcitonin
+C1868397	THIOUREA TASTING
+C1868398	PHENYLTHIOCARBAMIDE TASTING
+C1868399	PTC TASTING
+C1868400	PROPYLTHIOURACIL TASTING
+C1868401	PROP TASTING
+C1868414	HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
+C1868433	Normokalemic Periodic Paralysis, Potassium-Sensitive
+C1868496	Crusting erythematous dermatitis
+C1868512	Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
+C1868514	Diffuse leukoencephalopathy
+C1868524	Autonomic erectile dysfunction
+C1868527	Decreased sweating due to autonomic dysfunction
+C1868528	Orthostatic hypotension due to autonomic dysfunction
+C1868549	Marked delay in bone age
+C1868554	Irregular sclerotic endplates
+C1868556	Ovoid thoracolumbar vertebrae
+C1868569	Patterned dystrophy of retinal pigment epithelium
+C1868570	CHAR SYNDROME
+C1868571	Highly arched eyebrow
+C1868573	Distal/middle symphalangism of 5th finger
+C1868577	Patella aplasia-hypoplasia
+C1868578	Patellar aplasia
+C1868581	Patella aplasia, coxa vara, tarsal synostosis
+C1868594	Perry Syndrome
+C1868595	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
+C1868596	Atypical Parkinson Disease
+C1868597	Parietal Foramina With Cleidocranial Dysplasia
+C1868598	PARIETAL FORAMINA
+C1868599	PARIETAL FORAMINA 1
+C1868616	Parastremmatic dwarfism
+C1868619	Paramyotonia Congenita Without Cold Paralysis
+C1868623	Handgrip myotonia
+C1868633	Paragangliomas with Sensorineural Hearing Loss
+C1868649	PANIC DISORDER 1
+C1868653	Pancreatitis, Calcific
+C1868672	NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
+C1868675	PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
+C1868677	PHOTOPAROXYSMAL RESPONSE 1
+C1868678	THANATOPHORIC DYSPLASIA, TYPE I (disorder)
+C1868679	GRISCELLI SYNDROME, TYPE 2
+C1868681	DYSTONIA 12
+C1868682	Paroxysmal kinesigenic choreoathetosis
+C1868683	B-CELL MALIGNANCY, LOW-GRADE
+C1868684	EAR, PATELLA, SHORT STATURE SYNDROME
+C1868690	Hypoadrenocorticism, familial
+C1868693	Localized intraabdominal fluid collection
+C1868702	Diabetic keratopathy
+C1868709	Activation syndrome
+C1868710	Bronchial secretion retention
+C1868713	Weaning failure
+C1868718	In-stent coronary artery restenosis
+C1868720	Periventricular Nodular Heterotopia
+C1868723	Ureteric anastomosis complication
+C1868729	Prostatic calcification
+C1868733	Surgical failure
+C1868749	Myocardial strain
+C1868752	Procedural nausea
+C1868753	Procedural vomiting
+C1868755	Procedural headache
+C1868758	Superinfection bacterial
+C1868765	Joint fluid drainage
+C1868769	Anaphylactoid syndrome of pregnancy
+C1868770	Injection site recall reaction
+C1868771	Peritoneal cloudy effluent
+C1868773	Diabetic encephalopathy
+C1868776	Pseudomonas bronchitis
+C1868795	Vasoplegia syndrome
+C1868796	Procalcitonin increased
+C1868802	Central venous catheter removal
+C1868804	Elbow operation
+C1868809	Catheter thrombosis
+C1868821	Immediate post-injection reaction
+C1868822	Fistula discharge
+C1868827	Device misuse
+C1868833	Bronchial wall thickening
+C1868834	Congenital abdominal hernia
+C1868843	Injection site dryness
+C1868844	Injection site laceration
+C1868846	Injection site macule
+C1868850	Anal erosion
+C1868851	Pulmonary arterial hypertension associated with portal hypertension
+C1868853	Pulmonary arteriopathy
+C1868855	Post procedural infection
+C1868889	Irritable bowel syndrome characterized by constipation
+C1868934	Hemicephalalgia
+C1868945	Polyglobulia
+C1868998	Cytotoxic oedema
+C1868999	Cerebral microhaemorrhage
+C1869114	Weill-Marchesani Syndrome, Autosomal Recessive
+C1869115	Weill-Marchesani Syndrome, Autosomal Dominant
+C1869116	ASTHMA, SUSCEPTIBILITY TO (finding)
+C1869117	Paroxysmal nonkinesigenic dyskinesia
+C1869118	HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS
+C1869122	EHLERS-DANLOS SYNDROME, PROGEROID FORM
+C1869123	Limb-girdle muscular dystrophy type 2A
+C1873509	Hypotrichosis of the scalp
+C1876161	CEROID LIPOFUSCINOSIS, NEURONAL, 2
+C1876165	Copper-Overload Cirrhosis
+C1876166	Endemic Tyrolean Infantile Cirrhosis
+C1876171	Polyasplenia
+C1876172	VAH, AUTOSOMAL RECESSIVE
+C1876173	Heterotaxy, Visceroatrial, Autosomal Recessive
+C1876175	Ataxia-Telangiectasia Variant
+C1876181	EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS
+C1876182	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
+C1876185	Dysgnathia complex
+C1876187	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
+C1876203	Frontonasal dysplasia
+C1876214	ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
+C1879286	Hereditary bundle branch system defect
+C1879312	Agyria
+C1879321	Acute Myeloid Leukemia (AML-M2)
+C1879328	Blindness both eyes NOS (disorder)
+C1879344	Biliary papillomatosis
+C1879362	Hypertyrosinemia
+C1879526	Aberrant Crypt Foci
+C1879643	Adult Type Granulosa Cell Tumor
+C1879677	Alcohol Toxicity
+C1879828	Benign Teratoma
+C1881236	Interstitial Disease
+C1881254	Inverted Squamous Cell Papilloma
+C1881600	Malignant Vipoma
+C1881640	Patient-device incompatibility
+C1881681	Device issues
+C1881755	Product quality issue
+C1882062	Neoplastic disease
+C1882229	Ovarian Thecoma
+C1882972	Salivary Gland Low Grade Cribriform Cystadenocarcinoma
+C1883008	Serum Alanine Aminotransferase Measurement
+C1883018	Severe Aplastic Anemia
+C1883486	Uterine Corpus Cancer
+C1883694	Intraocular Medulloepithelioma
+C1883722	Stage 0a Bladder Urothelial Carcinoma
+C1947968	Carcinoma Metastatic to the Skin
+C1954751	Microdeletion syndromes
+C1955260	Female fertility
+C1955603	Deaf-Blind Disorders
+C1955634	Kaposi\'s sarcoma-associated herpesvirus infection
+C1955690	Extranodal marginal zone B-cell lymphoma
+C1955741	Glucocorticoid deficiency
+C1955743	Mineralocorticoid deficiency
+C1955760	Idiopathic normal pressure hydrocephalus (INPH)
+C1955768	Potassium sensitive periodic paralysis
+C1955779	Chronic total occlusion of coronary artery
+C1955835	Laser therapy NOS
+C1955858	Deaf-Blind Syndromes
+C1955860	Leukemia, Natural Killer Cell Large Granular Lymphocytic
+C1955861	T-Cell Large Granular Lymphocyte Leukemia
+C1955864	Sinus Arrest, Cardiac
+C1955869	Malformations of Cortical Development
+C1955870	Classical Lissencephalies and Subcortical Band Heterotopias
+C1955871	Cobblestone Complex
+C1955906	Lymphoma, Extranodal NK-T-Cell
+C1955934	Trichothiodystrophy Syndromes
+C1956089	Osteophyte
+C1956093	Paris-Trousseau Thrombocytopenia
+C1956097	Wolf-Hirschhorn Syndrome
+C1956125	Alagille Syndrome 1
+C1956130	Lymphoma, Follicular, Grade 1
+C1956131	Lymphoma, Follicular, Grade 3
+C1956132	Lymphoma, Follicular, Grade 2
+C1956147	Microlissencephaly
+C1956233	Hematoma, Basal Ganglia
+C1956234	Putaminal Hematoma
+C1956257	Pulmonary Stenosis
+C1956258	Familial Thrombotic Thrombocytopenic Purpura
+C1956260	Cavernous Angioma, Central Nervous System
+C1956261	Cerebral Venous Angioma
+C1956346	Coronary Artery Disease
+C1956349	Cerebral Amyloid Angiopathy, Genetic
+C1956390	Cranial Arteritis
+C1956391	Temporal Arteritis
+C1956410	Double Outlet Right Ventricle, Noncommitted VSD
+C1956411	Double Outlet Right Ventricle, Subaortic VSD
+C1956412	Double Outlet Right Ventricle, Subpulmonary VSD
+C1956413	Taussig-Bing Anomaly
+C1956414	Cardiac asthma
+C1956415	Paroxysmal nocturnal dyspnea
+C1959582	PTEN Hamartoma Tumor Syndrome
+C1959583	Myocardial Failure
+C1959584	Cardiac Carcinoma
+C1959586	Free Wall Rupture, Heart
+C1959587	Ventricular Free Wall Rupture
+C1959588	Angioma
+C1959589	Angioma, Cavernous
+C1959600	Obscure African cardiomyopathy
+C1959620	Dihydropyrimidine Dehydrogenase Deficiency
+C1959626	Mevalonic Aciduria
+C1959632	Plasma Cell Neoplasm
+C1959635	Parvovirus B19 (disease)
+C1959797	Allergic hepatitis
+C1959859	Acute lyme disease
+C1959897	Alcohol consumption during pregnancy
+C1960046	Mild persistent asthma
+C1960047	Moderate persistent asthma
+C1960048	Severe persistent asthma
+C1960272	Latent autoimmune diabetes mellitus in adult
+C1960396	Epidermal growth factor receptor negative non-small cell lung cancer
+C1960397	Philadelphia chromosome-positive acute lymphoblastic leukemia
+C1960398	HER2 positive breast cancer
+C1960443	Vasculitic neuropathy
+C1960447	Hypergonadotropic amenorrhea
+C1960448	Hyperammonaemic encephalopathy
+C1960458	Retinoic acid - acute promyelocytic leukemia syndrome
+C1960459	Hereditary angioedema with normal C1 esterase inhibitor activity
+C1960469	Left ventricular noncompaction
+C1960509	Epidural lipomatosis
+C1960539	Aromatase deficiency
+C1960545	Cytomegalovirus enteritis
+C1960546	Myxoma of heart
+C1960636	Dysglycemia
+C1960832	Gastric banding
+C1960870	Transformed migraine
+C1960883	Spina bifida aperta of cervical spine
+C1960925	Epidermal growth factor receptor positive non-small cell lung cancer
+C1961099	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
+C1961100	Erectile Dysfunction Adverse Event
+C1961102	Precursor Cell Lymphoblastic Leukemia Lymphoma
+C1961112	Heart Decompensation
+C1961121	Congenital vascular anomaly
+C1961835	Gaucher Disease
+C1962921	Vital Capacity Adverse Event
+C1962942	TRICHOMONAS VAGINALIS (finding)
+C1962976	Ventricular Fibrillation Adverse Event
+C1962983	Cataract Adverse Event
+C1962986	Glaucoma Adverse Event
+C1963067	Atrial Fibrillation Adverse Event
+C1963101	Encephalopathy Adverse Event
+C1963137	Hydrocephalus Adverse Event
+C1963185	Obesity Adverse Event
+C1963229	Retinal Detachment Adverse Event
+C1963674	Spinocerebellar Ataxia 10
+C1963714	Peritoneal effluent leukocyte count increased
+C1963717	Sleep-related eating disorder
+C1963718	Oculorespiratory syndrome
+C1963721	Laryngitis fungal
+C1963723	Septic arthritis streptococcal
+C1963729	Portal vein flow decreased
+C1963730	Retrograde portal vein flow
+C1963731	Thrombotic cerebral infarction
+C1963732	Hypercreatinaemia
+C1963737	Radiation necrosis
+C1963746	Abdominal wall haematoma
+C1963747	Herpes simplex hepatitis
+C1963750	Oral mucosal erythema
+C1963757	Dopamine dysregulation syndrome
+C1963759	Apparent death
+C1963761	No adverse event
+C1963762	No adverse reaction
+C1963763	Failed Back Surgery Syndrome
+C1963775	Cytarabine syndrome
+C1963781	Neurosensory hypoacusis
+C1963782	Transmission of an infectious agent via a medicinal product
+C1963783	Withdrawal of life support
+C1963786	Quality of life decreased
+C1963788	Peripheral nerve lesion
+C1963789	Genital swelling
+C1963790	Vulvovaginal burning sensation
+C1963804	Pregnancy on contraceptive
+C1963818	Gastrointestinal sounds abnormal
+C1963821	Oropharyngeal plaque
+C1963822	Mucosal pigmentation
+C1963823	Hyperlipasaemia
+C1963824	Shortened cervix
+C1963828	Uterine cervix stenosis
+C1963831	Graft versus host disease in lung
+C1963847	Coeliac artery stenosis
+C1963864	Myelodysplastic syndrome transformation
+C1963878	Bloody peritoneal effluent
+C1963897	Low birth weight baby
+C1963905	Infantile free sialic acid storage disease
+C1963944	Postoperative Vasoplegic Syndrome
+C1963946	Laryngeal dystonia
+C1964018	Vascular graft
+C1968550	Mental Retardation, X-Linked, Syndromic 13
+C1968551	Mental Retardation, X-Linked 79
+C1968552	Mental Retardation, X-Linked, With Spasticity
+C1968556	ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
+C1968561	Xeroderma Pigmentosum, Type G-Cockayne Syndrome
+C1968564	Defective DNA repair after ultraviolet radiation damage
+C1968565	Numerous pigmented freckles
+C1968574	Hypoplastic lacrimal duct
+C1968577	Progressive calcification of costochondral cartilage
+C1968592	Abnormal calcification of the carpal bones
+C1968602	Surfactant Metabolism Dysfunction, Pulmonary, 1
+C1968603	Osteopetrosis, Autosomal Recessive 5
+C1968605	Limited elbow flexion/extension
+C1968606	Limited knee flexion/extension
+C1968607	Hypoplastic distal humeri
+C1968610	Anterolateral radial head dislocation
+C1968611	Club-shaped proximal femur
+C1968618	Tubular basement membrane disintegration
+C1968619	Renal corticomedullary cysts
+C1968633	Intimal thickening in the coronary arteries
+C1968668	LEPROSY, SUSCEPTIBILITY TO, 3
+C1968689	Hyper-Immunoglobulin E Syndrome, Autosomal Recessive
+C1968699	Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate
+C1968706	Hypoplasia of the fallopian tube
+C1968729	Increased muscle glycogen content
+C1968739	Glycogen Storage Disease IIIA
+C1968740	Glycogen Storage Disease IIIB
+C1968741	Glycogen Storage Disease IIIC
+C1968742	Glycogen Storage Disease IIID
+C1968746	Gangliosidosis, Generalized GM1, Late-Infantile Type
+C1968748	Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement
+C1968782	MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
+C1968790	Axonal degeneration/regeneration
+C1968804	Plasminogen Deficiency, Type I
+C1968811	Prominent antitragus
+C1968814	Slender ulna
+C1968816	Broad fingertip
+C1968843	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
+C1968845	Primary Lateral Sclerosis, Adult, 1
+C1968848	Epilepsy, Familial Mesial Temporal Lobe
+C1968851	Pigmented micronodular adrenocortical disease
+C1968852	ACTH-independent hypercortisolemia
+C1968855	Paradoxical increased cortisol secretion on dexamethasone suppression test
+C1968949	Cakut
+C1968958	Subependymal nodules
+C1968959	Cortical tubers
+C1968999	Rib segmentation abnormalities
+C1969001	Shoulder muscle hypoplasia
+C1969024	CARDIOMYOPATHY, DILATED, 1X
+C1969029	Lissencephaly 3
+C1969032	Cataract, Autosomal Dominant, Multiple Types 1
+C1969038	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
+C1969039	Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
+C1969040	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M
+C1969052	MECKEL SYNDROME, TYPE 5
+C1969053	JOUBERT SYNDROME 7
+C1969054	Glycogen Storage Disease 0, Muscle
+C1969056	LEOPARD SYNDROME 2
+C1969057	Noonan Syndrome 5
+C1969060	Premature Ovarian Failure 5
+C1969062	Cataract, Congenital Nuclear, Autosomal Recessive 3
+C1969063	Cavitary Optic Disc Anomalies
+C1969073	Hyperchloremic metabolic acidosis
+C1969081	Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
+C1969084	Pontocerebellar Hypoplasia Type 6
+C1969086	Tyrosine Kinase 2 Deficiency
+C1969092	NEPHRONOPHTHISIS 7
+C1969093	Osteopetrosis, Autosomal Recessive 6
+C1969106	Osteopetrosis, Autosomal Recessive 4
+C1969107	Corticosteroid-Binding Globulin, Elevated
+C1969108	Macular Degeneration, Age-Related, 10
+C1969115	GALLBLADDER DISEASE 4
+C1969144	Renal cortical cysts
+C1969156	EEG with burst suppression
+C1969176	Hypoplastic pubic rami
+C1969178	Mesomelic leg shortening
+C1969181	Aplasia/Hypoplasia of the tibia
+C1969220	Depletion of components of the alternative complement pathway
+C1969222	Decreased serum complement factor H
+C1969232	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
+C1969236	Mitten deformity
+C1969237	Tapered distal phalanges of finger
+C1969238	Widely spaced toes
+C1969286	Hypoplastic distal radial epiphyses
+C1969287	Expanded phalanges with widened medullary cavities
+C1969288	Expanded metacarpals with widened medullary cavities
+C1969289	Expanded metatarsals with widened medullary cavities
+C1969291	Aortic arch calcification
+C1969292	Thoracic aorta calcification
+C1969342	PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED
+C1969343	Pulmonary Hypertension, Primary, Fenfluramine-Associated
+C1969363	Middle age onset
+C1969371	Impaired renal uric acid clearance
+C1969372	Tubulointerstitial fibrosis
+C1969386	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 9
+C1969404	Prominent frontal sinuses
+C1969408	Prominent U wave
+C1969410	Bidirectional ventricular ectopy
+C1969419	PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO
+C1969443	Trifunctional Protein Deficiency With Myopathy And Neuropathy
+C1969462	Demyelinating motor neuropathy
+C1969516	Aberrant melanosome maturation
+C1969532	Rhizomelic arm shortening
+C1969546	Thyroid follicular hyperplasia
+C1969562	Mental Retardation, Autosomal Dominant 1
+C1969572	Prolonged bleeding after dental extraction
+C1969621	DEAFNESS, AUTOSOMAL RECESSIVE 63
+C1969623	NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME
+C1969639	Cardiomyopathy, Dilated, 1w
+C1969644	Cataract, Cortical, Juvenile-Onset
+C1969645	Ataxia, Spastic, 3, Autosomal Recessive
+C1969651	Macular Degeneration, Age-Related, 9
+C1969652	BRACHYDACTYLY, TYPE B2 (disorder)
+C1969653	MUNGAN SYNDROME
+C1969655	LETHAL CONGENITAL CONTRACTURAL SYNDROME 3
+C1969657	Atrial Septal Defect 4
+C1969665	MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST
+C1969673	Forehead hyperpigmentation
+C1969675	Punctate lenticular opacities
+C1969679	Posterior wedging of vertebral bodies
+C1969680	High iliac wings
+C1969697	Repetitive compulsive behavior
+C1969722	Impaired pursuit initiation and maintenance
+C1969738	Premature loss of permanent teeth
+C1969758	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5 (disorder)
+C1969761	SEX CORD STROMAL TUMOR, SOMATIC
+C1969783	Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
+C1969785	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
+C1969796	ATAXIA, SPASTIC, 2, AUTOSOMAL RECESSIVE (disorder)
+C1969799	Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation
+C1969807	Dystonia, Focal, Task-Specific
+C1969809	Isobutyryl-CoA dehydrogenase deficiency
+C1969810	FEBRILE CONVULSIONS, FAMILIAL, 8
+C1969833	COPD, Severe Early-Onset
+C1969875	Beta-cell dysfunction
+C1969879	Limb joint contracture
+C1969893	Mental Retardation, Fra12a Type
+C1969913	Generalized hyperkeratosis
+C1969957	Creutzfeldt-Jakob Disease, Heidenhain Variant
+C1970005	Asphyxiating Thoracic Dystrophy 2
+C1970009	SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE
+C1970011	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J
+C1970021	Congenital Disorder Of Glycosylation, Type IIH
+C1970027	Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility
+C1970028	MALARIA, SUSCEPTIBILITY TO (finding)
+C1970035	PARKINSON DISEASE 6, LATE-ONSET, SUSCEPTIBILITY TO
+C1970051	METABOLIC SYNDROME, PROTECTION AGAINST
+C1970095	Cleft Palate, Isolated, And Mental Retardation
+C1970106	Bpes, Type I, Autosomal Recessive
+C1970107	ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT
+C1970109	AROMATASE EXCESS SYNDROME
+C1970112	Aplasia cutis congenita over the scalp vertex
+C1970117	Tooth Agenesis, Selective, With Orofacial Cleft
+C1970118	Hypodontia Oligodontia with Orofacial Cleft
+C1970119	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED
+C1970144	Alzheimer Disease 14
+C1970160	Epilepsy, Childhood Absence, Susceptibility To, 4
+C1970161	MECKEL SYNDROME, TYPE 4
+C1970163	RETINITIS PIGMENTOSA 37 (disorder)
+C1970167	Blue/yellow color vision defect
+C1970168	Red/green color vision defect
+C1970173	Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
+C1970180	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
+C1970187	Deafness, Sensorineural, And Male Infertility
+C1970197	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7
+C1970198	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6
+C1970199	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5
+C1970200	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
+C1970203	Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy
+C1970207	Inflammatory Bowel Disease 10
+C1970209	Alzheimer Disease 12
+C1970211	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4
+C1970224	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5
+C1970236	Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen
+C1970237	Microphthalmia, Isolated 3
+C1970238	Episodic Kinesigenic Dyskinesia 2
+C1970239	DEAFNESS, AUTOSOMAL RECESSIVE, 24
+C1970253	Phosphoserine Aminotransferase Deficiency
+C1970257	Decreased serum complement factor I
+C1970263	Recurrent meningococcal disease
+C1970269	Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress
+C1970270	Choreoathetosis And Congenital Hypothyroidism
+C1970291	Tooth Agenesis, Selective, 3
+C1970298	Progressive Familial Heart Block, Type Ib
+C1970308	Selective tooth agenesis
+C1970309	Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation
+C1970344	Congenital Disorder Of Glycosylation, Type IIF
+C1970386	Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities
+C1970414	Osteogenesis Imperfecta, Type V
+C1970416	XFE Progeroid Syndrome
+C1970431	PITT-HOPKINS SYNDROME
+C1970440	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2 (disorder)
+C1970441	CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7
+C1970456	Surfactant Metabolism Dysfunction, Pulmonary, 3
+C1970458	Osteogenesis imperfecta, type VIII
+C1970461	Externally rotated/abducted legs
+C1970463	Type 1 collagen overmodification
+C1970470	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2 (disorder)
+C1970479	Branchiootorenal Syndrome 2
+C1970483	Vesicoureteral Reflux 2
+C1970497	Crumpled long bones
+C1970501	Hypoplastic pulmonary veins
+C1970506	CILIARY DYSKINESIA, PRIMARY, 6
+C1970591	Abnormal pupillary light reflex
+C1970617	Hypoplastic spleen
+C1970625	Hypoplastic left atrium
+C1970630	Agenesis of pulmonary vessels
+C1970705	Fragile hair
+C1970712	Multiple Endocrine Neoplasia, Type IV
+C1970757	Tooth Agenesis, Selective, X-Linked, 1
+C1970777	Abnormally folded helix
+C1970808	Xeroderma Pigmentosum B-Cockayne Syndrome
+C1970816	Hypoplastic sacrum
+C1970820	Fabry Disease, Cardiac Variant
+C1970822	Mental Retardation, X-Linked, Syndromic 14
+C1970827	Phosphoribosylpyrophosphate Synthetase Superactivity
+C1970841	MENTAL RETARDATION, X-LINKED 93 (disorder)
+C1970848	Phosphoglycerate Kinase 1 Deficiency
+C1970859	Atypical Mycobacteriosis, Familial, X-Linked 2
+C1970879	ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder)
+C1970883	Peripheral sensory axonal neuropathy
+C1970887	Abnormal middle ear reflexes
+C1970943	MAJOR AFFECTIVE DISORDER 4
+C1970945	MAJOR AFFECTIVE DISORDER 6
+C1970989	Bladder catheterisation
+C1971021	Potassium depletion
+C1971624	Loss of appetite (finding)
+C1971810	Congenital cardiovascular disorder
+C1976726	Antibiotic resistant infection
+C1996989	Diarrhea due to drug
+C1997092	Hypertensive left ventricular hypertrophy
+C1997217	Low grade glioma
+C1997249	Pudendal neuralgia
+C1997262	Hypothyroidism in pregnancy
+C1997473	Autosomal aneuploidy
+C1997728	Osteomyelitis due to Staphylococcus aureus
+C1997740	Segmental dystonia
+C1997910	Citrin deficiency
+C1998028	Photoreceptor degeneration
+C1998083	Inflammatory acne
+C1998313	T wave alternans
+C1998346	Autoimmune sensorineural hearing loss
+C1999167	Elderly
+C2004345	phonological developmental disorder
+C2004435	Intestinal ischaemia
+C2004461	Bowel dysfunction
+C2004487	Vaginismus
+C2004489	Regurgitation
+C2004491	Cicatrix
+C2004493	Leukemia, B-Cell
+C2004521	Anaemia vitamin B12 deficiency
+C2004576	Vaginal Melanoma
+C2004632	aberrant right subclavian artery
+C2010560	Gastritis haemorrhagic
+C2013199	Oppositional Behavior
+C2014414	orthopedic disorders
+C2017869	sparse facial hair
+C2020284	Stickler syndrome, type 1
+C2020625	Group B Streptococcal Infection
+C2025392	Polar cataract
+C2025988	Cellulitis of upper eyelid
+C2026186	Diffuse large B-cell lymphoma of central nervous system
+C2028293	Haemophilus influenzae Type b Infection
+C2032780	Palate fistula
+C2033396	Yellow papule
+C2037047	Subretinal pigment epithelium hemorrhage
+C2044987	Cervical Glandular Intraepithelial Neoplasia
+C2047520	Mixed hyperlipidemia
+C2047937	Ill-defined disorder
+C2048011	Elevated immunoglobulin levels
+C2049069	Indolent multiple myeloma
+C2051831	Pectus excavatum
+C2053437	Full lower lip
+C2062372	Adrenal hyperplasia, bilateral
+C2062416	Sindbis virus infection
+C2062441	Influenza A
+C2062501	acute myelomonoblastic leukemia
+C2062593	Mesial temporal sclerosis
+C2062713	Progressive ophthalmoplegia
+C2062763	Benzodiazepine abuse
+C2062905	Left Main Coronary Artery Stenosis
+C2062908	Gout acute
+C2063079	chronic lyme disease
+C2063326	Right ventricular cardiomyopathy
+C2063389	Retroperitoneal liposarcoma
+C2063866	Depressive Disorder, Treatment-Resistant
+C2064402	Liver Epithelioid Hemangioendothelioma
+C2071267	Conjunctival pallor
+C2072946	computed tomography of chest: thoracic aortic aneurysm
+C2074900	Postoperative Pain, Chronic
+C2076596	Influenza A/H5N1
+C2076600	H1N1 influenza
+C2079538	Charcot-Marie-Tooth disease, Type 2A
+C2079540	Charcot-Marie-Tooth disease, Type 2C
+C2103602	Autoimmune Primary Adrenal Insufficiency
+C2108113	continuous electrocardiogram ventricular tachycardia
+C2108146	Contractures of the interphalangeal joint of the thumb
+C2112129	Postaxial foot polydactyly
+C2112532	Postmenopausal endometrium
+C2112942	Preaxial foot polydactyly
+C2114320	Premature contractions
+C2117329	x-ray of toe: polydactyly
+C2118460	Acute colitis
+C2118796	Severe recurrent major depression
+C2128203	Excessive face hair
+C2129214	Loose bowels
+C2129318	Morning vomiting
+C2129647	menstrual symptoms
+C2132198	Abnormal blistering of the skin
+C2139046	Laryngeal mass
+C2145472	Urothelial Carcinoma
+C2146481	Bilateral vocal cord paralysis
+C2168629	Lesion of scalp
+C2169794	Recurrent streptococcus pneumoniae infections
+C2169795	Recurrent bronchopulmonary infections
+C2169806	recurrent muscle twitches (symptom)
+C2170313	Renal transplant failure
+C2173677	Renal cyst
+C2176208	Retinal arteriolar constriction
+C2186740	reported urticaria (physical finding)
+C2187547	Retroperitoneal Leiomyosarcoma
+C2197691	Scrotal hypospadias
+C2198591	2-methylbutyrylglycinuria
+C2202686	Vitreous veils
+C2212006	Ovarian Small Cell Carcinoma
+C2213017	Meningeal Lymphoma
+C2215257	Acute postoperative pain
+C2216370	Cherry red spot of the macula
+C2216695	malignant neoplasm of breast stage I
+C2216702	malignant neoplasm of breast staging
+C2217035	Stage IIA Colon Cancer AJCC v7
+C2217040	malignant neoplasm of large intestine stage IV
+C2219717	menstrual periods stopped for over 6 months
+C2219848	Daytime somnolence
+C2220104	Skin blisters
+C2220255	Motor disturbances
+C2225524	Breast enlargement
+C2227090	Hyperplasia of the maxilla
+C2227134	mandibular excess (physical finding)
+C2229182	Psychomotor retardation, mild
+C2230441	Triceps weakness
+C2231324	Brucellosis, Pulmonary
+C2235773	Lip injury
+C2235909	Malformation of the nose
+C2237142	Moderate global developmental delay
+C2237660	exudative macular degeneration
+C2239120	eyelids (symptom)
+C2239176	Carcinoma, Hepatocellular
+C2239188	Burning feet syndrome
+C2239219	von Willebrand\'s factor (lab test)
+C2239222	Vascular Endothelial Growth Factor Measurement
+C2239246	Endometrial stromal sarcoma, high grade
+C2239290	Hodgkin lymphoma, nodular lymphocyte predominance
+C2239351	DEAFNESS, AUTOSOMAL RECESSIVE 74
+C2240374	Eosinophil count increased
+C2240378	cleft palate on exam
+C2242472	Bone infection
+C2242489	Oncologic complication
+C2242494	Haemorrhagic erosive gastritis
+C2242495	Abdominal wall haemorrhage
+C2242496	Parotid gland inflammation
+C2242502	Babinski reflex test
+C2242503	Gastrointestinal mucosal exfoliation
+C2242532	Reflux laryngitis
+C2242544	Congenital tricuspid valve incompetence
+C2242574	Compulsive sexual behaviour
+C2242575	Compulsive shopping
+C2242576	Oropharyngeal blistering
+C2242577	Oromandibular dystonia
+C2242579	Lingual dystonia
+C2242580	Eastern Cooperative Oncology Group performance status worsened
+C2242582	Cholestatic liver injury
+C2242585	Interstitial granulomatous dermatitis
+C2242588	Traumatic liver injury
+C2242595	Mucosal atrophy
+C2242596	Injection site vasculitis
+C2242597	Catheter site swelling
+C2242636	Inhibitory drug interaction
+C2242637	Potentiating drug interaction
+C2242638	Bacterial test
+C2242642	Engraft failure
+C2242658	Aortic dissection rupture
+C2242676	Post transplant distal limb syndrome
+C2242683	Gastroenteritis norovirus
+C2242685	Postresuscitation encephalopathy
+C2242703	Cardio-Renal Syndrome
+C2242704	Chronic myeloid leukaemia transformation
+C2242708	Hypertransaminasaemia
+C2242727	Tumour compression
+C2242737	Anorectal discomfort
+C2242816	Chronic secretory otitis media
+C2242817	Homocysteine measurement
+C2242987	Benign Mastocytoma
+C2242996	Has tingling sensation
+C2243023	Constructional apraxia
+C2243051	Large head (disorder)
+C2243080	Intestinal necrosis
+C2243086	basal cell adenocarcinoma of salivary gland
+C2243088	Gastritis erosive
+C2246682	response to vitamin
+C2265792	Skeletal muscle hypertrophy
+C2265833	response to exercise
+C2266639	Absence of eyebrow
+C2266670	ritualistic behavior (symptom)
+C2267227	Bulimia Nervosa
+C2267231	Chronic idiopathic neutropenia
+C2267233	Hypotonia neonatal
+C2314882	Reproductive tract infection
+C2314896	Familial Atypical Mole Melanoma Syndrome
+C2314994	Infarction of spinal cord
+C2315100	Pediatric failure to thrive
+C2315245	Agonal respiration
+C2315430	Orthostatic tremor
+C2315541	Diverticulum of renal calyx
+C2315667	Fetal microcephaly
+C2315717	Cryptotia
+C2315800	Oral phase dysphagia
+C2316159	Oral allergy syndrome
+C2316166	Slit ventricle syndrome
+C2316212	Cryopyrin-Associated Periodic Syndromes
+C2316401	Chronic kidney disease stage 1
+C2316787	Chronic kidney disease stage 3
+C2316810	Chronic kidney disease stage 5
+C2316832	Arachidonic acid measurement
+C2317473	Chronic kidney disease stage 4
+C2346458	ISS Stage I Plasma Cell Myeloma
+C2347126	Microscopic Polyangiitis
+C2347507	Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
+C2347613	Childhood Atypical Teratoid/Rhabdoid Tumor
+C2347747	Adult Classical Hodgkin Lymphoma
+C2347748	Adult Erythroleukemia
+C2347761	Childhood Myelodysplastic Syndrome
+C2347762	Childhood Teratoma
+C2347979	Rosette-forming glioneuronal tumor of the fourth ventricle
+C2348037	CD40 Ligand Deficiency
+C2348101	Destructive Arthritis
+C2348199	Short Qt Syndrome
+C2348239	Endolymphatic sac tumor
+C2349195	Acute Anterior Wall Myocardial Infarction
+C2349453	Familial migraine
+C2349568	Anal intraepithelial neoplasia I and II (AIN I and II) (histologically confirmed)
+C2349595	Fetal anemia
+C2349757	Iatrogenic Jakob-Creutzfeldt disease
+C2349952	Oropharyngeal Carcinoma
+C2350019	Solitary Pulmonary Nodule
+C2350035	Viral Croup
+C2350036	Postintubation Croup
+C2350037	Clinically Isolated Syndrome, CNS Demyelinating
+C2350038	Molar Incisor Hypomineralization
+C2350058	Neoplasms of Ear Auricle
+C2350059	Cancer of Ear
+C2350168	Polymorphic Reticulosis
+C2350170	Unilateral Nasal Obstruction
+C2350171	Bilateral Nasal Obstruction
+C2350233	Antley-Bixler Syndrome Phenotype
+C2350236	Idiopathic Interstitial Pneumonias
+C2350238	Lumbarsacral Spondylosis
+C2350242	Osteoarthritis, Spine
+C2350344	Chronic Lung Injury
+C2350387	Plasma Cell Granuloma, Orbital
+C2350449	Pancreatitis, Graft
+C2350529	Pulmonary Aspergillosis
+C2350530	Bronchopulmonary Aspergillosis
+C2350619	Maduromycosis
+C2350621	Eumycetoma
+C2350622	Radiation fibrosis
+C2350638	Cancer of Maxillary Sinus
+C2350873	Beryllium Disease
+C2350875	Constrictive Bronchiolitis
+C2350876	Bronchiolitis, Exudative
+C2350878	Focal Emphysema
+C2350879	Tropical Eosinophilic Pneumonia
+C2350988	Bronchiolitis, Proliferative
+C2355609	Mycetoma of foot
+C2362320	Subacute cutaneous lupus
+C2362324	Pediatric Obesity
+C2362742	Microgyria
+C2362914	clinical depression
+C2363065	Vitamin D-resistant rickets
+C2363129	Benign Rolandic Epilepsy
+C2363142	Leukemia, Prolymphocytic, T-Cell
+C2363246	Other specified congenital malformations of skin
+C2363280	Cervical auricle (disorder)
+C2363721	Drug effect delayed
+C2363723	Gastrointestinal bacterial infection
+C2363730	Oropharyngeal discomfort
+C2363731	Oropharyngeal pain
+C2363735	Vibratory sense increased
+C2363736	Unintentional weight loss
+C2363741	HIV-1 infection
+C2363744	Epstein-Barr virus associated lymphoproliferative disorder
+C2363747	Neurological decompensation
+C2363749	Hyperdynamic left ventricle
+C2363754	Neurocryptococcosis
+C2363755	Acquired Protein S Deficiency
+C2363762	Hepatitis C RNA increased
+C2363764	Hepatitis B DNA increased
+C2363768	Drug delivery system malfunction
+C2363769	Stomatococcal infection
+C2363774	Neutrophilic asthma
+C2363775	Rabbit syndrome
+C2363789	Hepatitis C virus test
+C2363829	Semen analysis abnormal
+C2363846	Intraocular pressure fluctuation
+C2363856	Stent embolization
+C2363879	Respiratory syncytial virus test positive
+C2363888	Intestinal anastomosis complication
+C2363903	Angiocentric glioma
+C2363904	Venous recanalisation
+C2363915	Cerebellar ischaemia
+C2363919	Childhood depression
+C2363925	Pleuroperitoneal communication
+C2363960	Superficial vein prominence
+C2363966	Pulmonary hypertensive crisis
+C2363967	Hepatitis C RNA fluctuation
+C2363973	Chronic thromboembolic pulmonary hypertension
+C2364016	Systemic sclerosis [scleroderma]
+C2364082	Hyposmia
+C2364111	Ageusia
+C2364135	Discomfort NOS
+C2364164	Fluid imbalance
+C2584409	Prothrombin G20210A mutation
+C2584611	Hereditary protein S deficiency
+C2584620	Thrombophilia, hereditary
+C2584688	Swelling of testicle (finding)
+C2584751	Severe hereditary factor VIII deficiency disease without inhibitor
+C2584774	Congenital hypofibrinogenemia
+C2584777	Autoimmune thrombotic thrombocytopenic purpura
+C2584778	Thrombotic thrombocytopenic purpura, acquired
+C2585231	Qualitative platelet disorder
+C2585317	Acquired thrombophilia
+C2585350	Hereditary hyperhomocysteinemia
+C2585570	Benign multiple sclerosis
+C2585575	Recurrent abdominal pain
+C2585653	Persistent atrial fibrillation
+C2585684	Heterozygous prothrombin G20210A mutation
+C2585739	Hyperreactio luteinalis
+C2585959	Homozygous protein C deficiency
+C2585960	Heterozygous protein C deficiency
+C2586012	Hereditary thrombocytopenic disorder
+C2586031	Hereditary antithrombin III deficiency
+C2586050	Oesophagitis ulcerative
+C2586160	Homozygous protein S deficiency
+C2607914	Allergic rhinitis (disorder)
+C2607929	Carney Complex, Type 1
+C2607947	Deafness unilateral
+C2608045	Trilateral Retinoblastoma
+C2608055	Hereditary Renal Cell Carcinoma
+C2608079	WARFARIN SENSITIVITY (disorder)
+C2608080	RENAL HYPOPLASIA, ISOLATED (disorder)
+C2608083	Cholestasis, benign recurrent intrahepatic 2
+C2608084	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)
+C2608086	HANGOVER, SUSCEPTIBILITY TO (finding)
+C2608087	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
+C2609041	Mechanical urticaria
+C2609047	Bone density abnormal
+C2609048	Ligament pain
+C2609050	Gastrosplenic fistula
+C2609053	JC virus test positive
+C2609055	Anastomotic fistula
+C2609056	Anti-cyclic citrullinated peptide antibody positive
+C2609059	Antisynthetase syndrome
+C2609071	Olmsted syndrome
+C2609096	Genital hypoaesthesia
+C2609105	Respiratory tract inflammation
+C2609129	Autoimmune pancreatitis
+C2609139	Gastrointestinal viral infection
+C2609146	Intramedullary rod insertion
+C2609151	Pseudoendophthalmitis
+C2609156	Inferior vena cava dilatation
+C2609162	Periprosthetic fracture
+C2609167	Prenatal screening test abnormal
+C2609176	Kounis syndrome
+C2609178	Product contamination
+C2609180	Product contamination microbial
+C2609181	Product contamination physical
+C2609183	Abnormal withdrawal bleeding
+C2609189	Device adhesion issue
+C2609190	Needle issue
+C2609191	Syringe issue
+C2609193	Product colour issue
+C2609194	Product coating issue
+C2609195	Product shape issue
+C2609196	Liquid product physical issue
+C2609198	Product odour abnormal
+C2609199	Product taste abnormal
+C2609200	Product formulation issue
+C2609201	Product solubility abnormal
+C2609205	Product size issue
+C2609206	Product deposit
+C2609208	Product lot number issue
+C2609216	Product label issue
+C2609217	Product outer packaging issue
+C2609218	Product container issue
+C2609222	Product commingling
+C2609224	Product packaging quantity issue
+C2609225	Product blister packaging issue
+C2609227	Product measured potency issue
+C2609228	Product substitution issue
+C2609229	Incorrect product storage
+C2609231	Product tampering
+C2609232	Product counterfeit
+C2609243	Product physical issues
+C2609247	Adrenal incidentaloma
+C2609259	Symphysis Pubis Dysfunction
+C2609260	Caudal dysplasia syndrome
+C2609268	Low phospholipid-associated cholelithiasis
+C2609273	Incorrect dose administered by device
+C2609282	Reticular pseudodrusen
+C2609315	Retinal angiomatous proliferation
+C2609414	Acute kidney injury
+C2613439	Extramedullary Hematopoiesis (disorder)
+C2673186	Aortic Aneurysm, Familial Thoracic 6
+C2673187	Erythrocytosis, Familial, 4
+C2673193	Brugada Syndrome 2
+C2673195	Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
+C2673196	LIPOPROTEIN GLOMERULOPATHY
+C2673198	Familial Cold Autoinflammatory Syndrome 2
+C2673200	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9 (disorder)
+C2673218	BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)
+C2673229	ADENOMATOUS POLYPOSIS COLI WITH CONGENITAL CHOLESTEATOMA
+C2673257	EPILEPSY, PROGRESSIVE MYOCLONIC 3
+C2673265	Skin-Hair-Eye Pigmentation, Variation In, 8
+C2673266	KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY
+C2673302	Urinary excretion of sialylated oligosaccharides
+C2673351	Paucity of anterior horn motor neurons
+C2673361	Increased serum beta-hexosaminidase
+C2673363	Increased serum iduronate sulfatase
+C2673375	Mucolipidosis III Alpha Beta, Atypical
+C2673377	MUCOLIPIDOSIS II ALPHA/BETA (disorder)
+C2673394	Radioulnar dislocation
+C2673395	Proximal fibular overgrowth
+C2673396	Phalangeal dislocation
+C2673401	Medial deviation of the foot
+C2673410	Small midface
+C2673427	METHEMOGLOBINEMIA TYPE IV
+C2673431	Abnormality of the periventricular white matter
+C2673441	Renal calcium wasting
+C2673443	Hypermagnesiuria
+C2673444	Hypocitraturia
+C2673462	Recurrent Staphylococcus aureus infections
+C2673477	Hypophosphatasia, Perinatal Lethal
+C2673482	Increased susceptibility to schizophrenia
+C2673497	Leydig Cell Hypoplasia, Type II
+C2673520	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
+C2673535	DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
+C2673536	Combined Cellular And Humoral Immune Defects With Granulomas
+C2673558	Increased urinary glycerol
+C2673584	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5 (disorder)
+C2673597	Congenital localized absence of skin
+C2673609	Epidermolysis bullosa inversa dystrophica
+C2673610	JEB-I
+C2673611	Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant
+C2673612	Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive
+C2673630	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
+C2673634	Ectopia Lentis, Isolated, Autosomal Recessive
+C2673635	Combined Saposin Deficiency
+C2673642	Combined Oxidative Phosphorylation Deficiency 5
+C2673646	Antenatal onset
+C2673648	Hypomagnesemia 4, Renal
+C2673653	Cuboid-shaped vertebral bodies
+C2673670	Curly eyelashes
+C2673677	Myopathy, Early-Onset, with Fatal Cardiomyopathy
+C2673700	Brisk reflexes
+C2673759	DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
+C2673760	DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
+C2673761	DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
+C2673776	Vascular tortuosity
+C2673809	Infantile nystagmus
+C2673820	Giant cell hepatitis on biopsy
+C2673866	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6 (disorder)
+C2673873	BARDET-BIEDL SYNDROME 13
+C2673874	BARDET-BIEDL SYNDROME 14 (disorder)
+C2673883	RENAL-HEPATIC-PANCREATIC DYSPLASIA
+C2673885	Renal hepatic pancreatic dysplasia Dandy Walker cyst
+C2673888	Decreased numbers of nephrons
+C2673892	Ductal plate malformation
+C2673913	Anemia, Hypochromic Microcytic, With Iron Overload
+C2673914	Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive
+C2673922	Amelogenesis Imperfecta, Hypomaturation Type, Iia1
+C2673923	Amelogenesis Imperfecta, Type Ic
+C2673929	Fundus atrophy
+C2673931	Hyperthreoninuria
+C2673946	Foveal hypoplasia (finding)
+C2673954	Absent skin pigmentation
+C2674004	VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF
+C2674009	Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma
+C2674081	Skin/Hair/Eye Pigmentation, Variation In, 7
+C2674127	LOEYS-DIETZ SYNDROME, TYPE 2A (disorder)
+C2674171	Lethal short-limbed short stature
+C2674173	Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
+C2674177	Areflexia of upper limbs
+C2674218	SPHEROCYTOSIS, TYPE 1 (disorder)
+C2674219	SPHEROCYTOSIS, HEREDITARY, 2
+C2674249	Anemia, Sideroblastic, Autosomal Dominant
+C2674252	VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1
+C2674259	NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
+C2674321	Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
+C2674322	Protein C Deficiency, Acquired
+C2674403	Scleral thickening
+C2674407	Foveoschisis
+C2674422	Seizures, intractable
+C2674432	Reduced bone mineral density
+C2674451	Anterior radial head dislocation
+C2674504	Palmoplantar Hyperkeratosis And True Hermaphroditism
+C2674512	Truncal titubation
+C2674574	Aortic aneurysm, familial thoracic 3
+C2674608	Feeding difficulties in infancy
+C2674612	Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty
+C2674616	FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
+C2674620	Fragile teeth
+C2674636	GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
+C2674640	FRACTURE, HIP, SUSCEPTIBILITY TO (finding)
+C2674665	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
+C2674695	Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
+C2674705	Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy
+C2674723	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
+C2674727	ASTROCYTOMA, LOW-GRADE, SOMATIC
+C2674737	Abnormality of finger
+C2674738	Abnormality of toe
+C2674766	Myokymia 1
+C2674838	ALCOHOL SENSITIVITY, ACUTE
+C2674876	LOEYS-DIETZ SYNDROME, TYPE 1B
+C2674949	Chromosome 3q29 Deletion Syndrome
+C2675014	Mullerian Aplasia and Hyperandrogenism
+C2675021	Narrow palpebral fissure
+C2675055	BEST VITELLIFORM MACULAR DYSTROPHY, MULTIFOCAL (disorder)
+C2675059	Refractory macrocytic anemia
+C2675066	Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
+C2675071	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12
+C2675074	Enlarged peripheral nerve
+C2675080	Li-Fraumeni-Like Syndrome
+C2675111	Abnormality of the eyelashes
+C2675112	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (finding)
+C2675113	CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO (finding)
+C2675128	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)
+C2675179	Arginine:Glycine Amidinotransferase Deficiency
+C2675183	Dyschromatosis Universalis Hereditaria 2
+C2675184	Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis
+C2675185	Kahrizi Syndrome
+C2675186	LEBER CONGENITAL AMAUROSIS 13
+C2675187	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 7 (disorder)
+C2675188	Kallmann Syndrome 6
+C2675191	Polymicrogyria, Bilateral Occipital
+C2675192	Spherocytosis, Type 5
+C2675204	Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract
+C2675207	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4
+C2675210	CONE-ROD DYSTROPHY 12 (disorder)
+C2675211	EPISODIC ATAXIA, TYPE 6 (disorder)
+C2675212	Spherocytosis, Type 4
+C2675227	Endocrine-Cerebroosteodysplasia
+C2675228	CILIARY DYSKINESIA, PRIMARY, 12
+C2675229	CILIARY DYSKINESIA, PRIMARY, 11
+C2675235	Deafness, Autosomal Recessive 1b
+C2675236	Deafness, Autosomal Dominant 2B
+C2675237	Deafness, Autosomal Dominant 3B
+C2675302	KALLMANN SYNDROME 5 (disorder)
+C2675334	Restrictive behavior, interests, and activities
+C2675336	Duplication 15q11-q13 Syndrome
+C2675369	Chromosome 22q11.2 Microduplication Syndrome
+C2675370	Capillary Malformation Without Arteriovenous Malformation
+C2675383	POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC
+C2675435	Restrictive external ophthalmoplegia, bilateral
+C2675440	Desmoid Tumor Caused By Somatic Mutation
+C2675459	Adenylate Kinase Deficiency, Hemolytic Anemia Due To
+C2675462	Convulsions, Benign Familial Infantile, 4
+C2675463	Chromosome 15q26-Qter Deletion Syndrome
+C2675470	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (finding)
+C2675471	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (finding)
+C2675473	Mental Retardation, Autosomal Dominant 5
+C2675481	COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
+C2675487	Mental Retardation, Autosomal Dominant 4
+C2675488	Mental Retardation, Autosomal Dominant 3
+C2675491	AMYOTROPHIC LATERAL SCLEROSIS 11
+C2675496	Retinitis Pigmentosa 46
+C2675508	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE
+C2675511	Diamond-Blackfan Anemia 8
+C2675512	Diamond-Blackfan Anemia 7
+C2675513	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 12
+C2675517	ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
+C2675518	Adiponectin Deficiency
+C2675519	Hypoadiponectinemia
+C2675520	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
+C2675521	BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
+C2675522	OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
+C2675525	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO
+C2675526	Neutropenia, Severe Congenital, Autosomal Recessive 4
+C2675527	Myopathy, Congenital, Compton-North
+C2675528	Spastic Paraplegia 42, Autosomal Dominant
+C2675540	Upswept frontal hair pattern
+C2675547	Slender long bones with narrow diaphyses
+C2675551	LUMBAR DISC DEGENERATION, SUSCEPTIBILITY TO (finding)
+C2675552	Retinitis Pigmentosa 7, Digenic
+C2675556	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3
+C2675557	Lumbosacral meningocele
+C2675558	Nephroblastomatosis
+C2675562	Unossified sacrum
+C2675590	True anophthalmia
+C2675609	OSTEOARTHRITIS SUSCEPTIBILITY 3
+C2675624	Giant cell hepatitis shown on biopsy
+C2675627	Acholic stool
+C2675644	Niemann-Pick Disease, Intermediate, With Visceral Involvement And Rapid Progression
+C2675646	NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)
+C2675650	Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
+C2675659	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10
+C2675664	PARATHYROID ADENOMA, SOMATIC
+C2675683	Epidermolysis Bullosa Dystrophica With Subcorneal Cleavage
+C2675730	Deafness, Congenital, and Onychodystrophy, Autosomal Dominant
+C2675746	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (disorder)
+C2675747	Coumarin Sensitivity
+C2675750	DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
+C2675767	EPIPHYSEAL DYSPLASIA, MULTIPLE, 6
+C2675780	EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL DOMINANT
+C2675858	Amelogenesis Imperfecta, Hypomaturation Type, Iia2
+C2675859	Diamond-Blackfan Anemia 5
+C2675860	Diamond-Blackfan Anemia 4
+C2675861	Lipodystrophy, Congenital Generalized, Type 3
+C2675862	Pyloric Stenosis, Infantile Hypertrophic, 5
+C2675864	DIABETES MELLITUS, INSULIN-DEPENDENT, 22 (disorder)
+C2675866	DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)
+C2675867	CILIARY DYSKINESIA, PRIMARY, 10
+C2675897	Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
+C2675904	Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome
+C2675914	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14
+C2675920	Anisopoikilocytosis
+C2675973	Open operculum
+C2675993	Pancreatic squamous cell carcinoma
+C2676023	Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant
+C2676024	CAROTENOIDS, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
+C2676026	Optic nerve dysplasia
+C2676033	Hepatoblastoma Caused By Somatic Mutation
+C2676042	Skin-Hair-Eye Pigmentation, Variation In, 4
+C2676078	WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1
+C2676079	METABOLIC SYNDROME, SUSCEPTIBILITY TO
+C2676098	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5
+C2676137	Diamond-Blackfan Anemia 1
+C2676191	PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder)
+C2676198	Increased serum insulin-like growth factor 1 {comment=HPO:probinson}
+C2676227	SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO
+C2676231	Skeletal Defects, Genital Hypoplasia, And Mental Retardation
+C2676232	Complement Component 6 Deficiency
+C2676235	CILIARY DYSKINESIA, PRIMARY, 9
+C2676243	Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism
+C2676244	Leukodystrophy, Hypomyelinating, 6
+C2676254	Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia
+C2676271	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
+C2676281	DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (disorder)
+C2676285	Bone Fragility with Contractures, Arterial Rupture, and Deafness
+C2676439	USHER SYNDROME, TYPE IIB, FORMERLY
+C2676443	Proximal radio-ulnar synostosis
+C2676465	Pontocerebellar Hypoplasia Type 2C
+C2676466	Pontocerebellar Hypoplasia Type 2B
+C2676468	SARCOIDOSIS, SUSCEPTIBILITY TO, 2
+C2676498	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 (disorder)
+C2676500	COWDEN-LIKE SYNDROME (disorder)
+C2676505	Post-angioplasty coronary artery restenosis
+C2676510	Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like
+C2676676	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
+C2676677	BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
+C2676678	OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
+C2676721	Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator
+C2676722	Hyperfibrinolysis, Familial, Due To Increased Release Of Tissue Plasminogen Activator
+C2676723	JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)
+C2676727	Chromosome 1q43-Q44 Deletion Syndrome
+C2676732	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT (disorder)
+C2676739	Chromosome 2q32-Q33 Deletion Syndrome
+C2676742	Premature Ovarian Failure 6
+C2676759	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
+C2676766	Osteopetrosis, Autosomal Recessive 7
+C2676767	CD59 Deficiency
+C2676770	Birk-Barel Mental Retardation Dysmorphism Syndrome
+C2676771	JOUBERT SYNDROME 8 (disorder)
+C2676772	Microtia, Hearing Impairment, And Cleft Palate
+C2676782	Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2
+C2676786	Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
+C2676788	JOUBERT SYNDROME 9 (disorder)
+C2676790	MECKEL SYNDROME, TYPE 6 (disorder)
+C2676832	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
+C2676833	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO
+C2676835	NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)
+C2676836	END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO (finding)
+C2676837	PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)
+C2676838	NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)
+C2676839	NEUROPATHY, DIABETIC, SUSCEPTIBILITY TO
+C2676840	LUMBAR DISC HERNIATION, SUSCEPTIBILITY TO
+C2676973	Dilatated internal auditory canal
+C2676974	Hypoplasia of the cochlea
+C2677002	Portal fibrosis shown on biopsy
+C2677065	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
+C2677078	Generalized Epilepsy With Febrile Seizures Plus, Type 6
+C2677079	Inflammatory Bowel Disease 19
+C2677086	Skin-Hair-Eye Pigmentation, Variation In, 11
+C2677087	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
+C2677088	Skin-Hair-Eye Pigmentation, Variation In, 10
+C2677091	Inflammatory Bowel Disease 17
+C2677092	MYD88 Deficiency
+C2677093	Inflammatory Bowel Disease 16
+C2677096	SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
+C2677097	SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10 (finding)
+C2677099	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
+C2677100	Inflammatory Bowel Disease 14
+C2677101	Inflammatory Bowel Disease 13
+C2677102	Chromosome 10q23 Deletion Syndrome
+C2677105	Inflammatory Bowel Disease 12
+C2677106	Atrial Fibrillation, Familial, 7
+C2677109	Leukodystrophy, Hypomyelinating, 4
+C2677123	COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
+C2677132	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)
+C2677162	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9
+C2677180	Congenital microcephaly
+C2677190	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder)
+C2677290	COLORECTAL CANCER, SUSCEPTIBILITY TO, 4
+C2677291	COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 15
+C2677294	Atrial Fibrillation, Familial, 6
+C2677299	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder)
+C2677325	RETINITIS PIGMENTOSA 29 (disorder)
+C2677326	Epileptic Encephalopathy, Early Infantile, 4
+C2677328	Cerebral hypomyelination
+C2677338	Cardiomyopathy, Dilated, 1AA
+C2677349	Epidermolysis Bullosa Simplex With Pyloric Atresia
+C2677362	Alveolar capillary dysplasia
+C2677378	Duodenal villous atrophy
+C2677434	OROFACIAL CLEFT 11
+C2677481	Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant
+C2677485	Aplasia of the sweat glands
+C2677491	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12
+C2677500	Oculoauricular Syndrome
+C2677504	AUTISM, SUSCEPTIBILITY TO, 15
+C2677506	Cardiomyopathy, Familial Hypertrophic, 11
+C2677516	RETINITIS PIGMENTOSA 41 (disorder)
+C2677524	Hypophosphatemic Rickets And Hyperparathyroidism
+C2677535	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
+C2677549	Hypouricemia, Renal, 2
+C2677550	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2
+C2677551	GOUT SUSCEPTIBILITY 2
+C2677565	AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
+C2677567	DYSTONIA 16 (disorder)
+C2677571	LUNG CANCER SUSCEPTIBILITY 2 (disorder)
+C2677576	RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1
+C2677586	Spastic Paraplegia 39, Autosomal Recessive
+C2677587	Cataract, Juvenile, With Microcornea And Glucosuria
+C2677589	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9
+C2677590	Congenital Disorder Of Glycosylation, Type In
+C2677608	Thrombocytopenia 4
+C2677613	Chromosome 15q13.3 Microdeletion Syndrome
+C2677632	Hemisacrum
+C2677637	Deafness, Autosomal Dominant 2A
+C2677643	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 13
+C2677650	Decreased activity of mitochondrial complex I
+C2677682	Rett Syndrome, Zappella Variant
+C2677713	Ichthyosis, X-Linked, Complicated
+C2677770	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
+C2677774	Age-Related Macular Degeneration type 11
+C2677792	Riddle Syndrome
+C2677793	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6
+C2677794	Stress-induced polymorphic ventricular tachycardia
+C2677821	Prostate Cancer, Hereditary, 13
+C2677843	Episodic Ataxia, Type 7
+C2677869	Abnormality of the hair shaft
+C2677877	Surfactant Metabolism Dysfunction, Pulmonary, 4
+C2677879	Hypospadias 2, X-Linked
+C2677889	Protoporphyria, Erythropoietic, X-Linked Dominant
+C2677897	SPASTIC PARAPLEGIA 34, X-LINKED (disorder)
+C2677903	Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
+C2678015	Myopathy, Reducing Body, X-Linked, Childhood-Onset
+C2678027	Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
+C2678034	MENTAL RETARDATION, X-LINKED 95
+C2678045	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS
+C2678046	Mental Retardation, X-Linked, Syndromic, Turner Type
+C2678048	Spinocerebellar Ataxia, X-Linked 5
+C2678051	MENTAL RETARDATION, X-LINKED 94 (disorder)
+C2678055	MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)
+C2678061	SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
+C2678065	Myofibrillar Myopathy
+C2678098	Hypospadias 1, X-Linked
+C2678117	Schizophrenia-like symptoms (uncommon)
+C2678155	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11
+C2678194	Mental Retardation, X-Linked, Syndromic, Christianson Type
+C2678223	Mental Retardation, X-Linked, With Panhypopituitarism
+C2678248	Mood instability
+C2678303	Hoarse cry
+C2678311	Thrombocytopenia 3
+C2678312	Three M Syndrome 1
+C2678323	C2-C3 subluxation
+C2678338	SPHEROCYTOSIS, TYPE 3 (disorder)
+C2678346	Diarrhea 3, Secretory Sodium, Congenital, Syndromic
+C2678367	Renal Tubular Dysgenesis With Choanal Atresia And Athelia
+C2678397	Aplasia of the ulna
+C2678403	UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO
+C2678408	PITUITARY HORMONE DEFICIENCY, COMBINED, 4
+C2678415	Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency
+C2678416	Hyperphenylalaninemia, Non-Pku Mild
+C2678439	CRANIOOSTEOARTHROPATHY
+C2678468	Amyotrophic Lateral Sclerosis 9
+C2678471	Lethal Arthrogryposis With Anterior Horn Cell Disease
+C2678473	CILIARY DYSKINESIA, PRIMARY, 7 (disorder)
+C2678474	CARDIOMYOPATHY, DILATED, 2A (disorder)
+C2678475	Cardiomyopathy, Dilated, 1z
+C2678476	Cardiomyopathy, Dilated, 1y
+C2678477	Brugada Syndrome 4
+C2678478	Brugada Syndrome 3
+C2678479	Prostate Cancer, Hereditary, 12
+C2678480	Chromosome 22q11.2 Deletion Syndrome, Distal
+C2678483	Long Qt Syndrome 11
+C2678484	Long Qt Syndrome 10
+C2678485	LONG QT SYNDROME 9 (disorder)
+C2678486	Temple-Baraitser Syndrome
+C2678492	Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs
+C2678493	BESTROPHINOPATHY
+C2678497	Elliptocytosis 1
+C2678503	AXENFELD-RIEGER SYNDROME, TYPE 3
+C2680446	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE
+C2681535	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1
+C2681923	RETINITIS PIGMENTOSA 2 (disorder)
+C2684859	APLASTIC ANEMIA, SUSCEPTIBILITY TO (finding)
+C2697368	Gastrointestinal irritation
+C2697503	Glucagon-like Peptide-1 measurement
+C2697636	Hyperdiploid B Acute Lymphoblastic Leukemia
+C2697638	Hypodiploid B Acute Lymphoblastic Leukemia
+C2697758	Interleukin 10 Measurement
+C2697760	Interleukin 12 Measurement
+C2697761	Interleukin 13 Measurement
+C2697764	Interleukin 16 Measurement
+C2697765	Interleukin 17 Measurement
+C2697766	Interleukin 18 Measurement
+C2697767	Interleukin 19 Measurement
+C2697774	Interleukin 25 Measurement
+C2697779	Interleukin 2 Measurement
+C2697785	Interleukin 4 Measurement
+C2697786	Interleukin 5 Measurement
+C2697787	Interleukin 7 Measurement
+C2697788	Interleukin 8 Measurement
+C2697789	Interleukin 9 Measurement
+C2697932	Loeys-Dietz Syndrome
+C2697933	Loeys-Dietz Syndrome Type 1
+C2697999	Macrophage Colony Stimulating Factor Measurement
+C2698045	Merkel Cell Polyomavirus Infection
+C2698203	Metastatic Ductal Breast Carcinoma
+C2698204	Metastatic Lobular Breast Carcinoma
+C2698259	Monoclonal B-Cell Lymphocytosis
+C2698294	High Grade B-Cell Lymphoma, Not Otherwise Specified
+C2698399	Myeloperoxidase Measurement
+C2698750	Pediatric follicular lymphoma
+C2699063	Resistin Measurement
+C2699419	Complement C3 Measurement
+C2699508	Splenic diffuse red pulp small B-cell lymphoma
+C2699510	Split-Hand/Foot Malformation
+C2699541	Cytokine Measurement
+C2699572	Dedifferentiated Solitary Fibrous Tumor
+C2699746	Syndactyly, type 2
+C2700265	Waardenburg Syndrome Type 2
+C2700366	Adiponectin Measurement
+C2700405	WAARDENBURG SYNDROME, TYPE IIE
+C2700406	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)
+C2700425	EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE
+C2700426	NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO (finding)
+C2700431	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE
+C2700438	MAJOR AFFECTIVE DISORDER 7
+C2700439	MAJOR AFFECTIVE DISORDER 8
+C2700440	MAJOR AFFECTIVE DISORDER 9
+C2700553	Omenn Syndrome
+C2700617	Irritation - emotion
+C2700620	Anorectal infection
+C2703042	malignant neoplasm of bone marrow
+C2703066	Lip dry
+C2711029	Hypothalamic-pituitary-adrenal axis dysfunction
+C2711110	Hepatitis B and hepatitis C
+C2711227	Hepatic steatosis
+C2711248	Osteonecrosis of jaw
+C2711618	Stimulant dependence
+C2711630	Combined immunodeficiency disease
+C2712122	Blood pressure normal
+C2712334	Actual Aspiration
+C2712360	Severe hypoxic ischemic encephalopathy
+C2712370	Apparent life threatening event
+C2712871	Gout attack
+C2712907	obsolete Combined hyperlipidemia
+C2712971	Enteritis due to Norovirus
+C2713319	Arylsulfatase A Deficiency
+C2713321	alpha-L-Iduronidase Deficiency
+C2713347	7-Dehydrocholesterol Reductase Deficiency
+C2713367	Abnormality, Severe Teratoid
+C2713368	Hematopoetic Myelodysplasia
+C2713392	Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
+C2713394	Haim-Monk Syndrome
+C2713442	Polyposis, Adenomatous Intestinal
+C2713443	Familial Intestinal Polyposis
+C2713447	Hyperpotassemia and Hypertension, Familial
+C2713497	Saccular Aneurysm
+C2713499	Total Hexosaminidase Deficiency
+C2713537	Deficiency of Platelet Glycoprotein 1b
+C2713546	Androgen Receptor Deficiency
+C2713615	Slow-Flow Phenomenon
+C2717739	Pulp Mummification
+C2717750	Platelet alpha-Granule Deficiency
+C2717757	Susac syndrome
+C2717759	Degenerative Intervertebral Discs
+C2717760	Alien Hand Syndrome
+C2717791	Acute Localized Exanthematous Pustulosis
+C2717792	Airway Remodeling
+C2717793	Small Airway Remodeling
+C2717794	Asthmatic Airway Remodeling
+C2717836	Steroid Sulfatase Deficiency Disease
+C2717837	Drug-Induced Liver Injury, Chronic
+C2717859	Peritoneal Sclerosis
+C2717860	Encapsulating Peritoneal Sclerosis
+C2717865	Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
+C2717866	Vestibulodynia
+C2717867	Generalized Vulvodynia
+C2717876	Propionicaciduria
+C2717884	Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
+C2717905	Hereditary Angioedema Types I and II
+C2717906	Hereditary Angioedema Type I
+C2717957	Vasoplegia
+C2717961	Thrombotic Microangiopathies
+C2717981	Poroma
+C2718001	Protein Misfolding Disorders
+C2718017	TDP-43 Proteinopathies
+C2718067	Alcoholic Steatohepatitis
+C2718068	beta-Galactosidase Deficiency
+C2718076	Fetal Mummification
+C2718078	Deficiency of Uroporphyrinogen III Synthase
+C2718128	Nasal inflammation
+C2718304	Sulfoiduronate Sulfatase Deficiency
+C2720163	Placental Steroid Sulfatase Deficiency
+C2720289	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
+C2720434	Macroencephaly
+C2720436	Fibrosis of pleura
+C2720437	Dislocation of elbow joint
+C2721559	Osmotic demyelination syndrome
+C2721566	Meniscal degeneration
+C2721575	Ischaemic nephropathy
+C2721578	Pulmonary oil microembolism
+C2721584	Product packaging issue
+C2721649	Subgaleal haematoma
+C2721655	Balamuthia Infection
+C2721670	Ultrafiltration failure
+C2721714	Peritoneal effluent abnormal
+C2721733	Mesenteritis
+C2721735	Infusion site discomfort
+C2721740	Ventilation perfusion mismatch
+C2721743	Burkholderia cepacia complex sepsis
+C2729166	Macrognathia
+C2732267	Auditory neuropathy spectrum disorder
+C2732374	Edema of dorsum of hand
+C2732473	Ductal Carcinoma In Situ with Microinvasion
+C2732618	Sessile Serrated Adenoma/Polyp
+C2732697	Autoimmune inflammation of skeletal muscle
+C2732728	Body height decreased
+C2732838	Neoplasm of skeletal system
+C2732979	Acquired long QT syndrome
+C2733049	Alpha ketoadipic aciduria
+C2733158	Cerebral Small Vessel Diseases
+C2733181	Ankle flare
+C2733326	Stemmer sign
+C2733595	Pulmonary Mycobacterium avium complex infection
+C2733623	Bone Fibrosarcoma
+C2733651	Chadwick's sign
+C2734068	Arm span
+C2739810	Lentigo maligna melanoma
+C2741638	Stress ulcer
+C2745900	Promyelocytic leukemia
+C2745924	Platelet aggregation increased
+C2745945	Juvenile-Onset Vitelliform Macular Dystrophy
+C2745948	Hyalinosis, Systemic
+C2745959	Spondyloepiphyseal dysplasia, congenita
+C2745963	Kashin-Beck Disease
+C2745997	OROFACIODIGITAL SYNDROME VI
+C2746066	Combined D-2- and L-2-hydroxyglutaric aciduria
+C2746067	Spinocerebellar ataxia 22
+C2746068	Congenital idiopathic intestinal pseudoobstruction
+C2746069	Familial ectopia lentis
+C2746083	DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder)
+C2747778	Streptococcus test positive
+C2747786	Staphylococcus test positive
+C2747793	Acute phosphate nephropathy
+C2747794	Spinal column injury
+C2747795	Vertebral foraminal stenosis
+C2747808	Coma scale abnormal
+C2747816	Complicated malaria
+C2747834	Acquired gene mutation
+C2747852	Device related sepsis
+C2747853	Injury associated with device
+C2747855	Pancreatic stent placement
+C2747864	Inflammatory marker increased
+C2747867	Intestinal haematoma
+C2747870	Device alarm issue
+C2747878	Device difficult to use
+C2747880	Cronobacter Infections
+C2747886	Stent malfunction
+C2747889	Device power source issue
+C2747891	Device capturing issue
+C2747892	Device component issue
+C2747893	Device damage
+C2747906	Product adhesion issue
+C2747922	Double stranded DNA antibody positive
+C2747952	Acinetobacter test positive
+C2747996	Stenotrophomonas test positive
+C2748013	Enterobacter test positive
+C2748014	Enterococcus test positive
+C2748017	Clostridium test positive
+C2748042	Antibiotic resistant Staphylococcus test positive
+C2748055	Hypoinsulinaemia (disorder)
+C2748057	Tongue pruritus
+C2748060	Hypopnea syndrome
+C2748069	Escherichia test positive
+C2748070	Klebsiella test positive
+C2748075	Neisseria test positive
+C2748079	Hemophilus test positive
+C2748080	Helicobacter test positive
+C2748104	Serratia test positive
+C2748110	Proteus test positive
+C2748111	Pseudomonas test positive
+C2748181	Varicella virus test positive
+C2748185	Hepatitis C virus test positive
+C2748188	Simplex virus test positive
+C2748206	Sexually inappropriate behaviour
+C2748208	Executive dysfunction
+C2748210	Human rhinovirus test positive
+C2748249	Infective exacerbation of bronchiectasis
+C2748255	Device kink
+C2748261	Mycobacterium test positive
+C2748263	Mycobacterium tuberculosis complex test positive
+C2748273	Respirovirus test positive
+C2748280	Polyomavirus test positive
+C2748316	Norovirus test positive
+C2748323	Enterovirus test positive
+C2748361	H5N1 influenza
+C2748362	Vulvovaginal erythema
+C2748371	Aspergillus test positive
+C2748374	Candida test positive
+C2748440	Sensorineural Deafness With Mild Renal Dysfunction
+C2748495	Metaphyseal Anadysplasia 1
+C2748502	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS
+C2748503	Corneal Dystrophy, Subepithelial Mucinous
+C2748505	Orofacial Cleft 12
+C2748507	INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
+C2748515	Spondyloepimetaphyseal Dysplasia, Pakistani Type
+C2748516	Spondylodysplasia And Premature Pubarche
+C2748518	Lumbar scoliosis
+C2748527	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)
+C2748531	Perifollicular fibrosis
+C2748536	Leukocyte Adhesion Deficiency, Type III
+C2748541	Brugada Syndrome 5
+C2748542	CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
+C2748544	Spondyloepimetaphyseal Dysplasia, Aggrecan Type
+C2748545	QUESTION MARK EARS, ISOLATED
+C2748552	Atrial Septal Defect 5
+C2748557	Immune dysfunction with T-cell inactivation due to calcium entry defect 2
+C2748568	Immune dysfunction with T-cell inactivation due to calcium entry defect 1
+C2748571	Isolated Growth Hormone Deficiency, Type IB
+C2748572	SeSAME syndrome
+C2748576	Renal sodium wasting
+C2748608	LEAD POISONING, SUSCEPTIBILITY TO
+C2748610	Progressive extrapyramidal movement disorder
+C2748652	Large face
+C2748653	Chubby cheeks
+C2748662	Mitchell-Riley Syndrome
+C2748801	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT
+C2748860	Hypoplastic pituitary gland
+C2748884	CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
+C2748895	Ovotesticular Disorders of Sex Development
+C2748896	46,Xy Gonadal Dysgenesis, Complete, Sry-Related
+C2748897	46,Xy True Hermaphroditism, Sry-Related
+C2748898	TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY
+C2748899	SEX-REVERSING LOCUS ON X, FORMERLY
+C2748910	Rett Syndrome, Atypical
+C2748918	Otopalatodigital Spectrum Disorder
+C2748919	Frontootopalatodigital Osteodysplasia
+C2748941	Glycogen Storage Disease, Type IXA2
+C2748958	Increased susceptibility to bacterial infections
+C2749016	Thrombophilia, X-Linked, Due To Factor Ix Defect
+C2749019	JOUBERT SYNDROME 10 (disorder)
+C2749020	Mental Retardation, X-Linked, Znf711-Related
+C2749022	Chromosome Xp11.23-P11.22 Duplication Syndrome
+C2749106	Emery-Dreifuss Muscular Dystrophy 6, X-Linked
+C2749137	Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
+C2749161	Paranasal sinus hypoplasia
+C2749240	Vater Association With Macrocephaly And Ventriculomegaly
+C2749283	Gm2-Gangliosidosis, Variant B1
+C2749345	Refsum Disease, Adult, 1
+C2749346	Refsum Disease, Adult, 2
+C2749369	Prominence of the premaxilla
+C2749463	Aplasia/Hypoplasia of the radius
+C2749477	Oculodentodigital Dysplasia, Autosomal Recessive
+C2749485	NEUROBLASTOMA, SUSCEPTIBILITY TO, 1 (disorder)
+C2749515	Collapsing glomerulopathy
+C2749559	Methemoglobinemia, Type I
+C2749560	Methemoglobinemia, Type Ii
+C2749561	Nadh-Cytochrome B5 Reductase Deficiency, Type I
+C2749562	Nadh-Cytochrome B5 Reductase Deficiency, Type Ii
+C2749582	Dumbbell-shaped long bone
+C2749602	AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA
+C2749604	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
+C2749625	Motor axonal neuropathy
+C2749656	Folate-responsive megaloblastic anemia
+C2749659	AICARDI-GOUTIERES SYNDROME 5 (disorder)
+C2749665	SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
+C2749675	Cortical gyral simplification
+C2749685	CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder)
+C2749688	Abnormal isoelectric focusing of serum transferrin
+C2749757	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1
+C2749759	Macrothrombocytopenia-Stomatocytosis, Mediterranean
+C2749861	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)
+C2749862	Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related
+C2749864	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)
+C2749872	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6
+C2749929	Musician\'s Dystonia
+C2749936	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder)
+C2749942	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5 (disorder)
+C2749982	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1
+C2749995	Intermittent generalized erythematous papular rash
+C2750027	Growth Hormone Deficiency With Pituitary Anomalies
+C2750035	Emery-Dreifuss Muscular Dystrophy 3
+C2750061	Hypokalemic Periodic Paralysis, Type 2
+C2750063	Leber Congenital Amaurosis 14
+C2750064	Retinal Dystrophy, Early-Onset Severe, Lrat-Related
+C2750065	RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED
+C2750066	Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
+C2750067	Plasminogen Activator Inhibitor-1 Deficiency
+C2750069	Lipodystrophy, Congenital Generalized, Type 4
+C2750074	Rhabdoid Tumor Predisposition Syndrome 2
+C2750075	Chondrodysplasia, Megarbane-Dagher-Melki Type
+C2750076	Miyoshi Muscular Dystrophy 3
+C2750078	Hypophosphatemic Rickets, Autosomal Recessive, 2
+C2750079	Exudative Vitreoretinopathy 5
+C2750080	Diamond-Blackfan Anemia 10
+C2750081	Diamond-Blackfan Anemia 9
+C2750082	Deafness, Autosomal Recessive 79
+C2750087	Bile Acid Malabsorption, Primary
+C2750088	HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO
+C2750090	Charcot-Marie-Tooth Disease, Axonal, Type 2n
+C2750091	Cardiomyopathy, Dilated, 1FF
+C2750103	LEPROSY, EARLY-ONSET, SUSCEPTIBILITY TO
+C2750161	Absent/shortened outer dynein arms
+C2750220	Karak Syndrome
+C2750234	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2
+C2750246	Pitt-Hopkins-Like Syndrome 1
+C2750247	Polymicrogyria, Asymmetric
+C2750285	Progeria Syndrome, Childhood-Onset
+C2750325	Oculootodental Syndrome
+C2750327	Hearing loss, sensorineural (high frequency)
+C2750355	Omodysplasia 2
+C2750404	Fibrosis of Extraocular Muscles, Congenital, 3C
+C2750405	Malignant Rhabdoid Tumor, Somatic
+C2750413	Cap Myopathy, Tpm2-Related
+C2750414	CAP MYOPATHY, TPM3-RELATED (disorder)
+C2750433	Bifid Nose With Or Without Anorectal And Renal Anomalies
+C2750440	FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
+C2750441	LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
+C2750442	Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
+C2750448	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6
+C2750450	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4
+C2750451	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3
+C2750452	Waardenburg Syndrome, Type 4c
+C2750457	Waardenburg Syndrome, Type 4b
+C2750459	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15
+C2750460	Tsc2 Angiomyolipomas, Renal, Modifier Of
+C2750466	Cardiomyopathy, Dilated, 1EE
+C2750467	Cardiomyopathy, Familial Hypertrophic, 14
+C2750471	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8
+C2750472	Cardiomyopathy, Familial Hypertrophic, 13
+C2750473	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
+C2750475	Focal Segmental Glomerulosclerosis 5
+C2750481	Factor XIII, B Subunit, Deficiency Of
+C2750509	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3
+C2750514	Factor Xiii, A Subunit, Deficiency Of
+C2750536	Nemaline Myopathy 3, With Intranuclear Rods
+C2750537	Myopathy, Actin, Congenital, With Cores
+C2750604	Median cleft lip and palate
+C2750654	Abnormal liver function tests during pregnancy, resolves postpartum
+C2750720	Cone-Rod Dystrophy 13
+C2750729	Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
+C2750732	Noonan Syndrome 6
+C2750733	LEPROSY, SUSCEPTIBILITY TO, 5
+C2750737	DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL
+C2750747	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C
+C2750748	Chromosome 17p13.3 Duplication Syndrome
+C2750771	Amelogenesis Imperfecta, Hypomaturation Type, Iia3
+C2750784	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)
+C2750785	MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
+C2750786	Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
+C2750787	Weill-Marchesani-Like Syndrome
+C2750789	RETINITIS PIGMENTOSA, CONCENTRIC (disorder)
+C2750790	CILIARY DYSKINESIA, PRIMARY, 13
+C2750791	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13
+C2750798	Polymicrogyria With Optic Nerve Hypoplasia
+C2750804	Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities
+C2750805	Chromosome 5p13 Duplication Syndrome
+C2750815	Marie Unna Hereditary Hypotrichosis 1
+C2750824	Dystransthyretinemic Euthyroidal Hyperthyroxinemia
+C2750825	NONPAPILLARY RENAL CARCINOMA 1 LOCUS
+C2750850	GLIOMA SUSCEPTIBILITY 1
+C2750887	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9
+C2750888	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6
+C2750892	EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
+C2750893	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11
+C2750894	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8
+C2750895	EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 2
+C2750913	Neuronal loss in basal ganglia
+C2750915	Basal ganglia gliosis
+C2750995	Cardiomyopathy, Dilated, 1DD
+C2751052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4
+C2751053	INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE
+C2751067	Parkinsonism-Dystonia, Infantile
+C2751083	Brugada Syndrome 8
+C2751084	Cardiomyopathy, Dilated, 1CC
+C2751088	Brugada Syndrome 7
+C2751089	Brugada Syndrome 6
+C2751090	Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency
+C2751091	Thrombophilia Due To Elevated Histidine-Rich Glycoprotein
+C2751092	Neuropathy, Hereditary Sensory And Autonomic, Type IIB
+C2751105	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder)
+C2751126	AERODIGESTIVE TRACT CANCER, SUSCEPTIBILITY TO
+C2751195	Epilepsy, Benign Neonatal, 1, And-Or Myokymia
+C2751259	Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related
+C2751260	Macrothrombocytopenia
+C2751288	Neutropenia, Severe Congenital, Autosomal Dominant 2
+C2751290	CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2
+C2751292	Hypotrichosis And Recurrent Skin Vesicles
+C2751293	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5
+C2751294	GLAUCOMA 1, OPEN ANGLE, O
+C2751295	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5
+C2751297	Tooth Agenesis, Selective, 6
+C2751306	Polycystic kidney disease, type 2
+C2751307	MICROPHTHALMIA, ISOLATED 4 (disorder)
+C2751308	CONE DYSTROPHY 4 (disorder)
+C2751309	Achromatopsia 5
+C2751310	Hyperuricemic Nephropathy, Familial Juvenile 2
+C2751312	BARTTER SYNDROME, TYPE 4B
+C2751315	Atrial Septal Defect 6
+C2751316	Glaucoma 3, Primary Congenital, D
+C2751317	46, XY Sex Reversal 5
+C2751318	Nijmegen Breakage Syndrome-Like Disorder
+C2751319	Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
+C2751320	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
+C2751321	Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis
+C2751322	Metaphyseal Anadysplasia 2
+C2751324	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3
+C2751325	46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy
+C2751427	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
+C2751431	Bifid Nose, Autosomal Dominant
+C2751478	Bifid thoracic vertebrae
+C2751479	Hypoplastic sacral vertebrae
+C2751480	Hypoplastic coccygeal vertebrae
+C2751492	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
+C2751493	Cerebral Amyloid Angiopathy, Gsn-Related
+C2751494	CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
+C2751506	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL
+C2751532	3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
+C2751536	CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
+C2751544	BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1
+C2751545	Basal Cell Carcinoma, Nonsyndromic
+C2751582	Mitochondrial respiratory chain defects
+C2751584	Neurodegeneration Due To Cerebral Folate Transport Deficiency
+C2751594	LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1
+C2751595	LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1
+C2751596	LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO
+C2751597	LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO
+C2751598	LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO
+C2751603	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10
+C2751604	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7
+C2751608	Pituitary Hormone Deficiency, Combined, 1
+C2751630	Dursun Syndrome
+C2751641	GLIOMA SUSCEPTIBILITY 3
+C2751642	GLIOMA SUSCEPTIBILITY 2
+C2751643	Glycogen Storage Disease IXC
+C2751666	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2
+C2751681	NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
+C2751682	NEUROBLASTOMA, SUSCEPTIBILITY TO, 2
+C2751683	Hirschsprung disease ganglioneuroblastoma
+C2751686	Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1
+C2751756	Febrile Convulsions, Familial, 3a
+C2751763	Retinitis Pigmentosa, Juvenile, Aipl1-Related
+C2751764	CONE-ROD DYSTROPHY, AIPL1-RELATED (disorder)
+C2751778	Generalized Epilepsy With Febrile Seizures Plus, 7
+C2751780	Retinitis Pigmentosa, Juvenile, SPATA7-Related
+C2751802	ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
+C2751803	HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2
+C2751805	EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT
+C2751807	Emery-Dreifuss Muscular Dystrophy 4
+C2751811	Spermatogenic Failure 7
+C2751812	OPTIC ATROPHY 7 (disorder)
+C2751822	Cataract, Autosomal Recessive Congenital 3
+C2751824	46, XY Disorders of Sex Development
+C2751825	PREMATURE OVARIAN FAILURE 7 (disorder)
+C2751826	Multiple Synostoses Syndrome 3
+C2751829	Ventricular Fibrillation, Paroxysmal Familial, 2
+C2751830	Long Qt Syndrome 12
+C2751831	Myopathy, Myofibrillar, Bag3-Related
+C2751842	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE
+C2751843	Leukoencephalopathy, Cystic, Without Megalencephaly
+C2751855	Hypomyelination, Global Cerebral
+C2751873	Edema of dorsum of hands and feet
+C2751898	Ventricular Fibrillation, Paroxysmal Familial, 1
+C2751938	Cerebral Palsy, Spastic Quadriplegic, 1
+C2751986	RETINITIS PIGMENTOSA 42
+C2751987	Cutis Laxa, Autosomal Recessive, Type IIB
+C2752001	Growth Retardation, Developmental Delay, Coarse Facies, And Early Death
+C2752007	Congenital Disorder of Glycosylation, Type Io
+C2752008	Spastic Paraplegia-50, Autosomal Recessive
+C2752009	White matter lesion
+C2752015	Glycogen Storage Disease XIV
+C2752027	Glycogen Storage Disease XIII
+C2752036	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6
+C2752037	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
+C2752038	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4
+C2752039	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
+C2752040	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2
+C2752041	Three M Syndrome 2
+C2752042	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
+C2752061	Cerebral Palsy, Spastic Quadriplegic, 2
+C2752062	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
+C2752067	MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3
+C2752072	Cardiomyopathy, Dilated, 1BB
+C2752073	Erythrocyte Amp Deaminase Deficiency
+C2752074	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY
+C2752081	ALPHA-2-PLASMIN INHIBITOR DEFICIENCY
+C2752089	Neuropathy, Hereditary Sensory And Autonomic, Type IIA
+C2752147	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
+C2752149	46,XY Sex Reversal 4
+C2825055	Recurrence (disease attribute)
+C2825139	Acute Myeloid Leukemia with Myelodysplasia-Related Changes
+C2825306	Treatment related leukaemia
+C2825560	S-Beta Thalassemia
+C2825742	Disseminated Juvenile Xanthogranuloma
+C2825851	Lymphotactin Measurement
+C2825856	Factor VII measurement
+C2825857	Factor VIII measurement
+C2825875	Interferon Alpha Measurement
+C2825877	Interferon Gamma Measurement
+C2825895	Granulocyte Colony Stimulating Factor Measurement
+C2825910	Stem Cell Factor Measurement
+C2826025	Mixed phenotype acute leukemia
+C2826177	Acute myeloid leukemia with mutated NPM1
+C2826318	Refractory cytopenia with unilineage dysplasia
+C2826321	Refractory Thrombocytopenia
+C2826323	Refractory Cytopenia of Childhood
+C2826330	Refractory anemia with ring sideroblasts associated with marked thrombocytosis
+C2827356	Myeloid and Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2
+C2827362	Myeloid and Lymphoid Neoplasms with FGFR1 Rearrangement
+C2827407	Infectious Otitis Media
+C2827432	Bile Acid Synthesis Defect
+C2827436	Liver Disease Associated with Cystic Fibrosis
+C2827469	Coronary Microvascular Disease
+C2827503	HFE-Associated Hereditary Hemochromatosis
+C2828150	Human Papillomavirus Positive Oropharyngeal Squamous Cell Carcinoma
+C2828721	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE
+C2829265	DEAFNESS, AUTOSOMAL RECESSIVE 86
+C2829267	DEAFNESS, AUTOSOMAL RECESSIVE 88
+C2830004	Somnolence
+C2830012	Chemical Gastritis
+C2830589	Mammographic microcalcification of breast
+C2845975	Malignant neuroendocrine tumor
+C2853903	Anaplastic diffuse large B-cell lymphoma
+C2853919	Lymphoblastic B-cell lymphoma
+C2853920	Lymphoblastic T-cell lymphoma
+C2853945	Non-follicular lymphoma
+C2854122	Acute myeloblastic leukemia with t(8;21)
+C2861580	Chronic myeloid leukemia, BCR/ABL-positive
+C2861596	AML M4 Eo with inv(16) or t(16;16)
+C2861614	AML M5b
+C2862185	Toddler's Fracture
+C2873719	Neoplasm of uncertain behavior of lymphoid, hematopoietic and related tissue, unspecified
+C2873754	Severe alpha thalassemia
+C2873755	Triple gene defect alpha thalassemia
+C2873756	Severe beta thalassemia
+C2873785	Deficiency of factor V [labile]
+C2873787	Deficiency of factor X [Stuart-Prower]
+C2873823	Polycythemia due to erythropoietin
+C2873824	Polycythemia due to stress
+C2873856	Essential cryoglobulinemia
+C2874124	Diabetes mellitus due to genetic defect in insulin action
+C2874125	Diabetes mellitus due to genetic defect in beta cell function
+C2874188	Isolated deficiency of pituitary hormone
+C2874189	Necrosis of pituitary gland (postpartum)
+C2874190	Pituitary short stature
+C2874202	Constitutional delay of puberty
+C2874270	GM2-GANGLIOSIDOSIS, ADULT
+C2874285	Mucolipidosis II [I-cell disease]
+C2874392	Alcohol dependence with withdrawal, unspecified
+C2874728	Nicotine dependence, cigarettes
+C2874859	Chronic hallucinatory psychosis
+C2875014	Acute disseminated encephalitis and encephalomyelitis (ADEM)
+C2875024	Cerebral Ventriculitis
+C2875058	Familial torsion dystonia
+C2875300	Peroneal muscular atrophy (axonal type) (hypertrophic type)
+C2875301	Dominantly inherited sensory neuropathy
+C2875311	Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
+C2875312	Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
+C2875313	Severe [Duchenne] muscular dystrophy
+C2875316	Myotubular (centronuclear) myopathy
+C2875318	Myotonic periodic paralysis (familial)
+C2875319	Normokalemic paralysis (familial)
+C2875367	Complex regional pain syndrome I, unspecified
+C2880562	Age-related cortical cataract
+C2882221	Acute pulmonary embolism
+C2887821	Left sided colitis
+C2900450	Other Creutzfeldt-Jakob disease
+C2902887	Nephrotic syndrome with focal and segmental hyalinosis
+C2902888	Nephrotic syndrome with focal and segmental sclerosis
+C2902889	Nephrotic syndrome with focal glomerulonephritis
+C2903074	Vasculogenic erectile dysfunction
+C2910100	Arnold-Chiari syndrome, type IV
+C2910117	Congenital malformation of cornea NOS
+C2910118	Congenital atresia or stricture of osseous meatus
+C2910124	Isomerism of atrial appendages with asplenia or polysplenia
+C2910126	Patent or persistent ostium secundum defect (type II)
+C2910127	Patent or persistent sinus venosus defect
+C2910157	Nonruptured congenital cerebral aneurysm
+C2910158	Congenital malformation of cerebral vessels NOS
+C2910327	Hemivertebra fusion or failure of segmentation with scoliosis
+C2910340	Asphyxiating thoracic dysplasia [Jeune]
+C2910342	Inherited keratosis palmaris et plantaris
+C2910343	Keratosis follicularis [Darier-White]
+C2919166	Autosomal dominant focal segmental glomerulosclerosis
+C2919194	Sporadic olivopontocerebellar atrophy
+C2919327	Pleomorphic lobular carcinoma in situ
+C2919341	Edema of dorsum of foot
+C2919365	Macroalbuminuric diabetic nephropathy
+C2919404	Raised low density lipoprotein cholesterol
+C2919414	Low density lipoprotein receptor mutation
+C2919575	Nonsustained Ventricular Tachycardia
+C2919706	Idiopathic rapidly progressive glomerulonephritis
+C2919755	Testicular dysgenesis syndrome
+C2919796	Glycogen storage disease type Ia
+C2919828	Chronic ulcerative colitis
+C2919861	Medullary cystic kidney disease type 1
+C2919945	Cavernous Hemangioma of Brain
+C2921081	Influenza NEC
+C2921112	Septate uterus, complete or partial
+C2921133	Fecal Soiling
+C2921138	Visuospatial deficit
+C2921627	Clinically isolated syndrome
+C2922974	Polymedication
+C2930471	Bilateral Wilms Tumor
+C2930543	Prosthesis Migration
+C2930617	Pulmonary Fibrosis - from Asbestos Exposure
+C2930618	Intersex Conditions
+C2930619	Sex Differentiation Disorders
+C2930620	Irradiation-Induced Sialadenitis
+C2930674	Human Babesiosis
+C2930745	Partial Monosomy
+C2930747	Shell Shock
+C2930748	Combat Stress Disorders
+C2930792	Familial acanthosis nigricans
+C2930797	Hepatic ductular hypoplasia
+C2930802	Familial antiphospholipid syndrome
+C2930803	Coarctation of aorta dominant
+C2930805	Sudden unexpected nocturnal death syndrome
+C2930808	Familial vascular leukoencephalopathy
+C2930812	Generalized elastolysis
+C2930820	Incontinentia pigmenti, familial male-lethal type
+C2930821	Keratitis sicca
+C2930823	XXY trisomy
+C2930826	Acute malaria
+C2930827	Chronic malaria
+C2930833	Irritable heart
+C2930839	Bilateral pheochromocytoma and islet cell adenoma of the pancreas
+C2930842	Familial pityriasis rubra pilaris
+C2930844	Hypopituitarism and septooptic \'dysplasia\'
+C2930849	Von willebrand factor, deficiency
+C2930863	Primary cortisol resistance
+C2930865	Ramer Ladda syndrome
+C2930868	Rasmussen subacute encephalitis
+C2930878	Cataract, congenital, with microcornea or slight microphthalmia
+C2930879	Cerebellar degeneration, subacute
+C2930889	Arthrogryposis multiplex congenita, distal type 2
+C2930896	Congenital thrombotic disease, due to Protein C deficiency
+C2930898	Benign essential blepharospasm
+C2930900	Beta-sarcoglycanopathy
+C2930902	Bidirectional tachycardia
+C2930922	Reginato Schiapachasse syndrome
+C2930923	N-Acetylneuraminic acid storage disease
+C2930924	Interferon gamma, receptor 1, deficiency
+C2930927	Kallmann syndrome, type 3, recessive
+C2930930	Abdominal obesity metabolic syndrome
+C2930970	Acromesomelic dysplasia Hunter-Thompson type
+C2930971	Acroosteolysis dominant type
+C2930974	Acute erythroleukemia
+C2930980	Malignant hyperthermia susceptibility type 1
+C2930984	Malignant hyperthermia susceptibility type 5
+C2930990	Maple syrup urine disease, type 1B
+C2930995	Dyschromatosis universalis hereditaria
+C2930996	Muscular dystrophy, tardive Emery-Dreifuss type, with contractures
+C2930997	Congenital disorder of glycosylation type 1C
+C2931001	Congenital disorder of glycosylation type 1G
+C2931002	Congenital disorder of glycosylation type 1H
+C2931004	Congenital disorder of glycosylation type 1J
+C2931005	Congenital disorder of glycosylation type 1K
+C2931006	Congenital disorder of glycosylation type 1L
+C2931007	Congenital disorder of glycosylation type 1X
+C2931008	Congenital disorder of glycosylation type 2A
+C2931009	Congenital disorder of glycosylation type 2D
+C2931010	Congenital disorder of glycosylation type 2E
+C2931011	Congenital disorder of glycosylation, type 2G
+C2931013	Cystinosis, benign, nonnephropathic
+C2931019	Split hand foot deformity 1
+C2931022	Amyloidosis, Cerebral, with Spongiform Encephalopathy
+C2931027	Neutropenia, severe chronic
+C2931029	Nevi flammei, familial multiple
+C2931035	Pulmonary alveolar proteinosis, congenital
+C2931037	Pancreatic cancer, adult
+C2931038	Pancreatic carcinoma, familial
+C2931039	Pancreatic islet cell tumors
+C2931042	Hawkinsinuria
+C2931046	Heart defect, tongue hamartoma and polysyndactyly
+C2931048	HEM dysplasia
+C2931058	Marfan Syndrome type 2
+C2931059	Marie Unna congenital hypotrichosis
+C2931067	Cholestasis, progressive familial intrahepatic 4
+C2931068	Desmoplastic cerebral astrocytoma of infancy
+C2931071	Dianzani autoimmune lymphoproliferative syndrome
+C2931072	Epidermolysa bullosa simplex and limb girdle muscular dystrophy
+C2931073	Collagenopathy, type 2 alpha 1
+C2931074	Cone rod dystrophy amelogenesis imperfecta
+C2931082	Familial apoceruloplasmin deficiency
+C2931092	Maternally Inherited Leigh Syndrome
+C2931093	Osteogenesis imperfecta, type 5
+C2931095	Osteogenesis imperfecta, type 7
+C2931104	Hydrolethalus syndrome
+C2931105	Hypercalciuria, childhood idiopathic
+C2931107	Myasthenic syndrome, congenital, postsynaptic slow-channel
+C2931111	Myopia, susceptibility to
+C2931112	Myostatin-related muscle hypertrophy
+C2931116	Cerebral Nocardiosis
+C2931117	Fetal megacystis
+C2931118	Megalocytic interstitial nephritis
+C2931121	Meier Blumberg Imahorn syndrome
+C2931122	Keratosis palmoplantaris striata 1
+C2931123	Keratosis palmoplantaris striata 3
+C2931132	Crigler Najjar syndrome, type 2
+C2931133	Pediatric Crohn\'s disease
+C2931134	Cutis laxa, recessive
+C2931135	Blepharophimosis syndrome type 1
+C2931136	Blepharophimosis syndrome type 2
+C2931139	Nondystrophic myotonia
+C2931141	Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency
+C2931150	Synostotic Anterior Plagiocephaly
+C2931163	Male sterility due to Y-chromosome deletions
+C2931171	Juvenile pauciarticular chronic arthritis
+C2931173	Pediatric ulcerative colitis
+C2931174	Polycystic kidney disease, type 1
+C2931187	Nephropathic cystinosis
+C2931189	Neural crest tumor
+C2931193	Prinzmetal\'s variant angina
+C2931196	Craniofacial dysostosis type 1
+C2931201	Urachal adenocarcinoma
+C2931205	Usher syndrome, type 1A
+C2931206	Usher syndrome, type 1B
+C2931207	Usher syndrome, type 1C
+C2931208	Usher syndrome, type 1D
+C2931210	Usher syndrome, type 1F
+C2931213	Usher syndrome, type 2C
+C2931216	Tetra-amelia autosomal recessive
+C2931218	Tetraamelia multiple malformations
+C2931223	6 alpha mercaptopurine sensitivity
+C2931228	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS
+C2931230	Vacuolar myopathy
+C2931244	Craniometaphyseal dysplasia, autosomal recessive type
+C2931245	Bone Marrow Failure Disorders
+C2931246	Potocki-Lupski syndrome
+C2931253	Alport syndrome, dominant type
+C2931254	Alport syndrome, recessive type
+C2931257	Alzheimer disease type 1
+C2931258	Amaurosis congenita of Leber, type 1
+C2931263	Familial cerebral cavernous malformation
+C2931268	Scapuloperoneal myopathy
+C2931276	Spastic paraplegia 17
+C2931277	Pena Shokeir syndrome Type 2
+C2931278	Phosphoenolpyruvate carboxykinase 2 deficiency
+C2931280	Perniola Krajewska Carnevale syndrome
+C2931282	Skeletal dysplasia, San Diego type
+C2931286	Warburton Anyane Yeboa syndrome
+C2931290	Welander distal myopathy, Swedish type
+C2931296	Yorifuji Okuno syndrome
+C2931297	Yusho Disease
+C2931299	ZAP70 deficiency
+C2931320	T cell immunodeficiency primary
+C2931322	T-lymphocyte count decreased
+C2931337	Chromosome 3, monosomy 3p25
+C2931347	Cardiac form of generalized glycogenosis
+C2931351	Familial myelofibrosis
+C2931352	Familial renal cell carcinoma
+C2931355	Spastic paraplegia 3, autosomal dominant
+C2931356	Spastic paraplegia type 5A, recessive
+C2931358	Muscular atrophy, spinal, infantile chronic form
+C2931364	Thrombocytopenia Robin sequence
+C2931367	Thyroid cancer, follicular
+C2931375	Temporomandibular ankylosis
+C2931379	Neonatal Torulopsis glabrata Fungemia
+C2931383	Chromosomal mosaicism due to mitotic instability
+C2931384	Moyamoya disease 1
+C2931387	Leber congenital amaurosis, type 4
+C2931395	Bulbospinal neuronopathy, X-linked recessive
+C2931401	Long QT syndrome type 3
+C2931404	Albright\'s hereditary osteodystrophy
+C2931416	Fara Chlupackova syndrome
+C2931418	Bare lymphocyte syndrome 2
+C2931426	Orofaciodigital syndrome type1
+C2931434	Paraquat lung
+C2931441	Hereditary spastic paralysis, infantile onset ascending
+C2931456	Prostate cancer, familial
+C2931459	Lynch syndrome I (site-specific colonic cancer)
+C2931461	Forney Robinson Pascoe syndrome
+C2931471	Sialuria, French type
+C2931480	Neurofibromatosis, Type 3, mixed central and peripheral
+C2931482	Neurofibromatosis-Noonan syndrome
+C2931488	Zlotogora-Ogur syndrome
+C2931498	Mental Retardation, X-Linked 1
+C2931500	Microphthalmia and mental deficiency
+C2931501	Microphthalmia associated with colobomatous cyst
+C2931505	Mixed sclerosing bone dystrophy
+C2931517	Plasmacytoma anaplastic
+C2931521	Sclerosing lymphocytic lobulitis
+C2931559	Chromosome 4q- Syndrome
+C2931574	Chromosome 5, monosomy 5q35
+C2931577	Basaran Yilmaz syndrome
+C2931585	Gaucher-like disease
+C2931588	GEMSS syndrome
+C2931596	Macrodactyly of the foot
+C2931599	Oculocutaneous albinism type 3
+C2931618	Gestational trophoblastic disease
+C2931638	Chromosome 8, monosomy 8p23 1
+C2931639	Macrophagic myofasciitis
+C2931642	Benign symmetrical lipomatosis
+C2931644	O\'Donnell Pappas syndrome
+C2931645	Ochronosis, hereditary
+C2931648	Larsen syndrome, dominant type
+C2931649	Larsen syndrome, recessive type
+C2931653	Petty Laxova Wiedemann syndrome
+C2931658	Phacomatosis pigmentokeratotica
+C2931662	Baraitser Brett Piesowicz syndrome
+C2931672	Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
+C2931673	Ceroid lipofuscinosis, neuronal 1, infantile
+C2931686	Charcot-Marie-Tooth disease, Type 1E
+C2931687	Dysferlinopathy
+C2931689	Dystrophia myotonica 2
+C2931713	Chromosome 17 deletion
+C2931716	Deafness, autosomal dominant nonsyndromic sensorineural 17
+C2931732	Familial Paget\'s disease of bone
+C2931735	Epidermolytic palmoplantar keratoderma Vorner type
+C2931739	Hirschsprung disease type 3
+C2931743	Lactate dehydrogenase deficiency type A
+C2931746	Sulfocysteinuria
+C2931753	Achromatopsia incomplete, X-linked
+C2931758	Acquired angioedema
+C2931760	Acrocallosal syndrome, Schinzel type
+C2931764	Furlong syndrome
+C2931767	Deafness, autosomal dominant nonsyndromic sensorineural 22
+C2931779	Congenital defect of skull and scalp
+C2931781	Adenosine monophosphate deaminase deficiency
+C2931782	Adrenal hyperplasia 2
+C2931783	Amelogenesis imperfecta nephrocalcinosis
+C2931784	Amyloid angiopathy
+C2931786	Amyotrophic lateral sclerosis, type 6
+C2931787	Intracardiac myxoma
+C2931788	Atypical Hemolytic Uremic Syndrome
+C2931791	Cataract Hutterite type
+C2931803	Deletion 11p13
+C2931816	Chromosome 2, monosomy 2q24
+C2931817	Chromosome 2q37 deletion syndrome
+C2931820	Inclusion body myopathy, autosomal dominant
+C2931821	Nakamura Osame syndrome
+C2931822	Nasopharyngeal carcinoma
+C2931826	Potassium aggravated myotonia
+C2931829	RDS - infants
+C2931830	Restless legs syndrome 2
+C2931832	Hyperinsulinemic hypoglycemia, familial, 1
+C2931833	Hyperinsulinemic hypoglycemia, familial, 2
+C2931835	Hyperprolinemia type 2
+C2931837	Familial hypertryptophanemia
+C2931838	Familial HDL deficiency
+C2931840	Aspartylglucosamidase (AGA) deficiency
+C2931844	Spinal muscular atrophy 4
+C2931845	Neurodegeneration with brain iron accumulation (NBIA)
+C2931847	Type I familial incomplete male pseudohermaphroditism
+C2931850	Aase Smith syndrome 2
+C2931852	Clear-cell metastatic renal cell carcinoma
+C2931854	Allergic Bronchopulmonary Mycosis
+C2931857	Double cortex
+C2931859	Acquired CJD
+C2931860	Monosomy 5p
+C2931861	Hemorrhagic hereditary nephritis
+C2931862	Familial hyperchylomicronemia syndrome
+C2931868	Catalase deficiency
+C2931870	Familial schizencephaly
+C2931872	Free sialic acid storage disease
+C2931875	Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
+C2931876	Hirschsprung disease 1
+C2931877	Preeclamptic toxemia
+C2931884	Reticuloendotheliosis, familial, with eosinophilia
+C2931887	Familial progressive supranuclear palsy
+C2931888	Pfeiffer type acrocephalosyndactyly
+C2931889	Oral-facial-digital syndrome, type 2
+C2931891	Necrotizing encephalopathy, infantile subacute, of Leigh
+C2931893	Lysosomal beta-mannosidase deficiency
+C2931894	Mucolipidosis 2
+C2931895	Pericardial constriction with growth failure
+C2931899	Papillary renal cell carcinoma, familial
+C2931915	Watermelon stomach disease
+C2931923	Hyperkeratosis of the palms and soles and esophageal papillomas
+C2931928	Mitochondrial cytopathy
+C2932678	Inherited Peripheral Neuropathy
+C2932714	Pontocerebellar Hypoplasia Type 2
+C2932715	Pseudohypoparathyroidism Type 1B
+C2932716	Pseudohypoparathyroidism Type 1C
+C2936170	Patent Ductus Arteriosus Familial
+C2936171	Familial Ebstein's Anomaly
+C2936179	Obesity, Visceral
+C2936233	Post-Exercise Hypotension
+C2936258	Peri-Implantitis
+C2936331	Sarcoglycanopathies
+C2936332	Alpha-Sarcoglycanopathies
+C2936346	22q11 Deletion Syndrome
+C2936349	Plaque, Amyloid
+C2936350	Plaque, Atherosclerotic
+C2936351	Fibroatheroma
+C2936380	Neointima
+C2936381	Neointima Formation
+C2936403	46, XX Disorders of Sex Development
+C2936406	alpha-Dystroglycanopathies
+C2936419	46, XX Testicular Disorders of Sex Development
+C2936421	Sex Chromosome Disorders of Sex Development
+C2936423	Echogenic Bowel
+C2936443	Infectious Ventriculitis
+C2936444	Pyogenic Sacroiliitis
+C2936445	Septic Sacroiliitis
+C2936458	Fasciculoventricular Accessory Pathway
+C2936459	Nodoventricular Accessory Pathway
+C2936476	Chronic hepatic failure
+C2936486	Partial Tetrasomy
+C2936502	Familial CHARGE Syndrome
+C2936659	Familial Felty's Syndrome
+C2936661	Gerstmann Syndrome 2
+C2936664	Acquired Hypogammaglobulinemia
+C2936665	Immunoglobulin Deficiency, Late-Onset
+C2936694	Swyer Syndrome
+C2936703	Familial Kleine-Levin Syndrome
+C2936718	Fetal Cerebral Ventriculomegaly
+C2936719	Mechanical Allodynia
+C2936739	Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
+C2936740	XXXY Males
+C2936741	48,XXYY Syndrome
+C2936755	Familial Waldenstrom's Macroglobulinaemia
+C2936777	Nevo syndrome (disorder)
+C2936779	Hydroxymethylbilane Synthase Deficiency
+C2936781	Generalized Myotonia of Thomsen
+C2936783	Colorectal cancer, hereditary nonpolyposis, type 1
+C2936786	Aqueductal Stenosis
+C2936791	Antley-Bixler Syndrome, Autosomal Dominant
+C2936793	Spinocerebellar ataxia 30
+C2936797	Acid cholesteryl ester hydrolase deficiency, type 2
+C2936816	Micromelic dysplasia, congenital, with dislocation of radius
+C2936826	Fumaric aciduria
+C2936827	Focal facial dermal dysplasia
+C2936833	Mycobacterium tuberculosis, susceptibility to infection by
+C2936837	Keratosis of Greither
+C2936846	Scarring alopecia
+C2936847	Acatalasemia Japanese type
+C2936848	Acatalasemia Swiss type
+C2936858	Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
+C2936859	N syndrome
+C2936860	Spastic paraplegia 25, autosomal recessive
+C2936861	Cortisol 11-beta-ketoreductase deficiency
+C2936862	Bardet-Biedl syndrome 1 (disorder)
+C2936863	Bardet-Biedl syndrome 2 (disorder)
+C2936864	Bardet-Biedl syndrome 4 (disorder)
+C2936879	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT
+C2936880	SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT (disorder)
+C2936904	Opitz GBBB Syndrome, X-Linked
+C2936907	NADH:Q(1) Oxidoreductase deficiency
+C2936913	Porphyria, South African type
+C2936914	Cirrhosis, familial, with deposition of abnormal glycogen
+C2936915	Amylo-1,6-glucosidase deficiency
+C2936921	Saccharopine dehydrogenase deficiency
+C2937220	Congenital abnormality of vein
+C2937222	Proctitis ulcerative
+C2937224	Constitutional obesity
+C2937225	Biotin deficiency disease
+C2937228	Tunnel vision
+C2937246	Overwork
+C2937288	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT
+C2937300	Congenital hereditary muscular dystrophy
+C2937319	Internal injury NOS
+C2937358	Cerebral Hemorrhage
+C2937359	Old thrombus
+C2937365	Recurrent aphthous ulcer
+C2937421	Prostatic Hyperplasia
+C2938875	Upper-airway cough syndrome
+C2938905	Central Nervous System Sensitization
+C2938912	Hyperintensity of cerebral white matter on MRI
+C2938913	Distributive shock
+C2938924	Oestrogen receptor positive breast cancer
+C2938933	Product used for unknown indication
+C2938939	Rapid correction of hyponatraemia
+C2938940	Post stroke depression
+C2938941	Infective pulmonary exacerbation of cystic fibrosis
+C2938947	Device infusion issue
+C2938960	Loss of bladder sensation
+C2938981	Limb asymmetry
+C2938983	Focal cortical dysplasia
+C2938997	Device deployment issue
+C2939014	Band sensation
+C2939039	False negative investigation result
+C2939040	False positive investigation result
+C2939062	Respiratory tract oedema
+C2939074	Bronze skin
+C2939087	Corrosive oropharyngeal injury
+C2939094	Skin sensitisation
+C2939127	Indolent ulcer
+C2939147	Feeling hot
+C2939149	Amyloid of cornea
+C2939174	Medullary cystic disease
+C2939175	Meconium ileus
+C2939186	Disturbance in mood
+C2939414	Nuclear sclerosis
+C2939416	Pectus carinatum
+C2939419	Metastatic neoplasm
+C2939420	Metastatic Neoplasm
+C2939447	Right ventricular failure
+C2939461	Myeloid neoplasm
+C2939462	Immunoglobulin deposition disease
+C2939465	Deficiency of glucose-6-phosphate dehydrogenase
+C2940785	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
+C2940786	Thyroid Hormone Resistance Syndrome
+C2945552	Attention deficit hyperactivity disorder, combined type
+C2945558	Vulvovaginitis trichomonal
+C2945566	Chronic mucus hypersecretion
+C2945586	Bladder irritability
+C2945606	Encopresis
+C2945695	Limb ischemia
+C2945698	panic symptoms
+C2945759	aggressive cancer
+C2945767	Childhood Malignant Liver Neoplasm
+C2955673	Urate nephropathy
+C2957106	headache severe
+C2959467	Tuberculous pleural effusion
+C2959547	Endometrial sarcoma
+C2960064	Low grade dysplastic nodule
+C2960065	High grade dysplastic nodule
+C2960127	Heart failure with normal ejection fraction
+C2960129	Vanishing white matter disease
+C2960725	Invasive pituitary adenoma
+C2960760	Calcification of muscle
+C2973527	Dentinogenesis imperfecta without osteogenesis imperfecta
+C2973529	Leukocytoclastic vasculitis
+C2973725	Pulmonary arterial hypertension
+C2973787	Coxiella burnetii Infection
+C2976853	Immune reconstitution inflammatory syndrome [IRIS]
+C2979982	Vaginal haemorrhage
+C2980105	Recurring skin boils
+C2981132	Shell teeth
+C2981140	Glaucoma of childhood
+C2981142	Refractory anemia, without ringed sideroblasts, without excess blasts
+C2981150	Uranostaphyloschisis
+C2981158	Loss of libido
+C2981366	Cancer Stage (Antiquated)
+C2981712	Ocular Adnexal Lymphoma
+C2981926	Stage III Cutaneous Melanoma AJCC v7
+C2982481	Stage IV Hypopharyngeal Carcinoma AJCC v7
+C2983423	Hepatocellular carcinoma stage III
+C2985171	Glioneuronal Tumor with Neuropil-Like Islands
+C2985174	Papillary glioneuronal tumor
+C2985175	Extraventricular neurocytoma
+C2985219	Papillary tumor of the pineal region
+C2985220	Anaplastic Medulloblastoma
+C2985290	Fetal Alcohol Spectrum Disorders
+C2985307	Maternal Hypotension
+C2985524	Rhabdoid Tumor Predisposition Syndrome
+C2986536	Bisphosphonate-associated osteonecrosis
+C2986550	Pituicytoma
+C2986561	Spindle Cell Oncocytoma of the Adenohypophysis
+C2986622	Cervical Intraepithelial Neoplasia Grade 2/3
+C2986658	Diffuse Intrinsic Pontine Glioma
+C2986662	Multifocal breast carcinoma
+C2986664	Multicentric Breast Carcinoma
+C2986665	Early-Stage Breast Carcinoma
+C2986691	Congenital Bone Marrow Failure Syndromes
+C2986703	Overgrowth Syndrome
+C2986717	Anti-N-Methyl-D-Aspartate Receptor Encephalitis
+C2987120	Intramucosal Adenocarcinoma
+C2987127	Digestive System Neuroendocrine Tumor
+C2987128	Digestive System Neuroendocrine Carcinoma
+C2987142	Pancreatic Intraepithelial Neoplasia-1A
+C2987143	Pancreatic Intraepithelial Neoplasia-1B
+C2987145	Pancreatic Intraepithelial Neoplasia-3
+C2987191	Pancreatic Intraductal Papillary Mucinous Neoplasm, Gastric-Type
+C2987252	Esophageal Spindle Cell Carcinoma
+C2987397	Gastric Carcinoma with Lymphoid Stroma
+C2987469	Substance-induced psychotic disorder
+C2987516	Cervix Intraepithelial Neoplasia Grade 3 AJCC v7
+C3146244	Alcohol Related Birth Defect
+C3146249	Stage IV Renal Cell Cancer AJCC v7
+C3146250	Stage III Colorectal Cancer AJCC v7
+C3146251	Stage IV Colorectal Cancer AJCC v7
+C3146252	Stage II Colorectal Cancer AJCC v7
+C3146254	Stage III Colon Cancer AJCC v7
+C3146256	Stage II Rectal Cancer AJCC v7
+C3146257	Stage II Colon Cancer AJCC v7
+C3146264	Stage IV Prostate Cancer AJCC v7
+C3146265	Prostate cancer stage D
+C3146271	Stage III Breast Cancer AJCC v7
+C3147083	DEAFNESS, AUTOSOMAL RECESSIVE 76
+C3148695	Increased urinary thiosulfate
+C3148763	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E
+C3148823	WOOLLY HAIR, AUTOSOMAL RECESSIVE 2, WITH OR WITHOUT HYPOTRICHOSIS
+C3148824	WH/HT
+C3148833	Childhood-onset short-trunk short stature
+C3148872	FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
+C3148929	USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC
+C3148959	IMINOGLYCINURIA, DIGENIC
+C3149009	DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY
+C3149074	SEIZURES, BENIGN FAMILIAL NEONATAL, 1
+C3149075	SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
+C3149083	Decreased activity of mitochondrial complex III
+C3149117	GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
+C3149223	Aplasia of the abdominal wall musculature
+C3149226	ESOPHAGEAL CANCER, ALCOHOL-RELATED, SUSCEPTIBILITY TO
+C3149237	MEN1 SOMATIC MUTATIONS
+C3149254	ESCC, SUSCEPTIBILITY TO
+C3149255	GASTRIC CARDIA ADENOCARCINOMA, SUSCEPTIBILITY TO
+C3149276	CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB
+C3149287	GASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFT PALATE
+C3149378	IMMUNODEFICIENCY, COMMON VARIABLE, 1
+C3149399	DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED
+C3149462	HYPERALPHALIPOPROTEINEMIA 1
+C3149463	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 10
+C3149517	LARYNGOSPASM, SEVERE NEONATAL EPISODIC
+C3149566	DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT
+C3149631	MELORHEOSTOSIS, ISOLATED
+C3149657	CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
+C3149695	Melorheostosis with Osteopoikilosis
+C3149706	CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
+C3149711	PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO
+C3149750	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)
+C3149841	POLYCYSTIC KIDNEY DISEASE 1
+C3149848	VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT
+C3149907	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
+C3149908	Neonatal short-trunk short stature
+C3149931	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL
+C3150077	Mild short stature
+C3150086	Aplasia/Hypoplasia of the nipples
+C3150099	ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS
+C3150127	BARDET-BIEDL SYNDROME 15
+C3150154	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB
+C3150168	SMOKING AS A QUANTITATIVE TRAIT LOCUS 3 (disorder)
+C3150169	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED
+C3150171	FTLD-TDP, TARDBP-RELATED
+C3150172	MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
+C3150191	Coloboma, Ocular, And Ichthyosis, Brain Malformations, And Endocrine Abnormalities
+C3150207	AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE
+C3150208	RETINITIS PIGMENTOSA 53
+C3150215	CHROMOSOME 6q24-q25 DELETION SYNDROME
+C3150267	Increased plasma renin activity
+C3150274	COMPLEMENT COMPONENT C1r/C1s DEFICIENCY
+C3150275	COMPLEMENT COMPONENT 2 DEFICIENCY
+C3150281	Fetal overgrowth
+C3150315	AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT
+C3150343	HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
+C3150344	HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
+C3150353	Ventral septal defect (VSD)
+C3150354	IMMUNODEFICIENCY, COMMON VARIABLE, 2
+C3150358	Increased serum prostaglandin E2
+C3150399	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITY TO
+C3150411	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2
+C3150412	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3
+C3150413	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
+C3150414	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6
+C3150415	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL IMPAIRMENT), TYPE B, 1
+C3150416	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 2
+C3150417	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3
+C3150418	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2
+C3150419	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1
+C3150546	PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
+C3150547	PANCREATIC CANCER, SUSCEPTIBILITY TO, 3
+C3150596	MONONEUROPATHY OF THE MEDIAN NERVE, MILD
+C3150607	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME
+C3150613	Long toe
+C3150617	Maturity-onset diabetes of the young, type 10
+C3150618	Maturity-onset diabetes of the young, type 11
+C3150619	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC
+C3150620	Distal upper limb muscle weakness
+C3150644	BRACHYDACTYLY, TYPE E2
+C3150649	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM
+C3150652	FANCONI RENOTUBULAR SYNDROME 2
+C3150653	FANCONI ANEMIA, COMPLEMENTATION GROUP O
+C3150654	DEAFNESS, AUTOSOMAL RECESSIVE 84A
+C3150657	BIRBECK GRANULE DEFICIENCY
+C3150658	WARSAW BREAKAGE SYNDROME
+C3150659	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
+C3150660	BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
+C3150661	OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
+C3150667	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY
+C3150672	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2
+C3150674	CHROMOSOME 15q24 DELETION SYNDROME
+C3150675	CHROMOSOME 15q24 DUPLICATION SYNDROME
+C3150677	AUTISM, SUSCEPTIBILITY TO, 16
+C3150678	OGUCHI DISEASE 2
+C3150680	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15
+C3150681	CARDIOMYOPATHY, DILATED, 1R
+C3150682	LEFT VENTRICULAR NONCOMPACTION 4
+C3150690	LEFT VENTRICULAR NONCOMPACTION 5
+C3150691	RETINITIS PIGMENTOSA 54
+C3150692	AMYOTROPHIC LATERAL SCLEROSIS 12
+C3150693	AUTISM, SUSCEPTIBILITY TO, 17
+C3150700	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20
+C3150701	CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB
+C3150702	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 16
+C3150703	FRONTONASAL DYSPLASIA 2
+C3150704	DEAFNESS, AUTOSOMAL RECESSIVE 91
+C3150705	FOXG1 syndrome
+C3150706	FRONTONASAL DYSPLASIA 3
+C3150714	FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
+C3150715	RETINITIS PIGMENTOSA 51
+C3150730	HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY
+C3150731	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 5
+C3150732	LYMPHEDEMA, HEREDITARY, IC
+C3150733	LONG QT SYNDROME 13
+C3150736	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj
+C3150738	Antibody Deficiency due to Defect in CD19
+C3150741	IMMUNODEFICIENCY, COMMON VARIABLE, 6
+C3150750	AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE
+C3150754	GLYCOGEN STORAGE DISEASE XV
+C3150755	SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
+C3150757	MICROPHTHALMIA, ISOLATED 6
+C3150773	CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME
+C3150796	NEPHRONOPHTHISIS 11
+C3150797	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
+C3150801	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7
+C3150802	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2
+C3150803	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA
+C3150805	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6
+C3150807	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1
+C3150808	RETINITIS PIGMENTOSA 55
+C3150819	RETINITIS PIGMENTOSA 56
+C3150821	RETINITIS PIGMENTOSA 57
+C3150833	OCCULT MACULAR DYSTROPHY
+C3150834	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
+C3150852	EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
+C3150874	CRANIOECTODERMAL DYSPLASIA 2
+C3150875	CHOANAL ATRESIA AND LYMPHEDEMA
+C3150876	COG5 congenital disorder of glycosylation
+C3150877	SENIOR-LOKEN SYNDROME 7
+C3150878	Primary hyperoxaluria type III
+C3150879	RETINITIS PIGMENTOSA 58
+C3150880	CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME
+C3150889	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2
+C3150891	COCOON SYNDROME
+C3150896	Hereditary sensory autonomic neuropathy type IC
+C3150897	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B
+C3150898	CARDIOMYOPATHY, DILATED, 1GG
+C3150899	PARKINSON DISEASE 5, AUTOSOMAL DOMINANT
+C3150900	METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT
+C3150901	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE
+C3150902	C1q DEFICIENCY
+C3150908	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
+C3150909	D-2-HYDROXYGLUTARIC ACIDURIA 2
+C3150910	Brain calcification Rajab type
+C3150911	GASTRIC CANCER, INTESTINAL
+C3150912	CONE-ROD DYSTROPHY 15
+C3150913	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip
+C3150914	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)
+C3150921	MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY
+C3150923	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
+C3150924	MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS
+C3150925	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE
+C3150926	Congenital dyserythropoietic anemia type IV
+C3150927	VESICOURETERAL REFLUX 3
+C3150928	NF1 Microdeletion Syndrome
+C3150931	Steep acetabular roof
+C3150933	HYPERALDOSTERONISM, FAMILIAL, TYPE III
+C3150939	BEAULIEU-BOYCOTT-INNES SYNDROME
+C3150941	RUBINSTEIN-TAYBI SYNDROME 2
+C3150942	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE
+C3150943	Long Qt Syndrome 2
+C3150953	Long Qt Syndrome 6
+C3150954	LONG QT SYNDROME 6, ACQUIRED, SUSCEPTIBILITY TO
+C3150956	LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO
+C3150958	Cardiomyopathy, Dilated, 1V
+C3150966	Supernumerary der(22)t(8;22) syndrome
+C3150967	KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
+C3150968	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6
+C3150969	MICROPHTHALMIA, ISOLATED 7
+C3150970	NOONAN SYNDROME 7
+C3150971	LEOPARD SYNDROME 3
+C3150972	NEUROPATHY, HEREDITARY SENSORY, TYPE ID
+C3150973	Progressive polyneuropathy with bilateral striatal necrosis
+C3150974	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
+C3150975	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4
+C3150983	TREACHER COLLINS SYNDROME 2
+C3150986	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7
+C3150987	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
+C3150988	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 12
+C3150989	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q
+C3150990	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY
+C3150998	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10
+C3151000	HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS
+C3151001	Retinitis Pigmentosa 4
+C3151036	CHROMOSOME 1p32-p31 DELETION SYNDROME
+C3151038	ACNE INVERSA, FAMILIAL, 3
+C3151055	ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE
+C3151056	SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
+C3151057	HETEROTAXY, VISCERAL, 4, AUTOSOMAL
+C3151058	S-adenosylhomocysteine hydrolase deficiency
+C3151059	RETINITIS PIGMENTOSA 49
+C3151060	Macular Degeneration, Age-Related, 6
+C3151061	RETINITIS PIGMENTOSA 47
+C3151062	INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS
+C3151063	MACULAR DEGENERATION, AGE-RELATED, 5
+C3151064	46,XY SEX REVERSAL 6
+C3151065	Cataract, Posterior Polar, 2
+C3151066	RETINITIS PIGMENTOSA 45
+C3151068	RETINITIS PIGMENTOSA 44
+C3151070	MACULAR DEGENERATION, AGE-RELATED, 8
+C3151071	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE
+C3151077	AORTIC ANEURYSM, FAMILIAL THORACIC 7
+C3151078	Complement Component C1s Deficiency
+C3151079	MACULAR DEGENERATION, AGE-RELATED, 12
+C3151080	COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
+C3151081	COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
+C3151082	C8 deficiency
+C3151083	Recurrent Neisserial infections
+C3151085	MASP2 Deficiency
+C3151086	Retinitis Pigmentosa 20
+C3151087	LOEYS-DIETZ SYNDROME 3
+C3151088	IMMUNODEFICIENCY 31B
+C3151097	MEIER-GORLIN SYNDROME 2
+C3151107	RETINITIS PIGMENTOSA 40 (disorder)
+C3151111	Abnormal light- and dark-adapted electroretinogram
+C3151113	MEIER-GORLIN SYNDROME 3
+C3151120	MEIER-GORLIN SYNDROME 4
+C3151126	MEIER-GORLIN SYNDROME 5
+C3151136	CILIARY DYSKINESIA, PRIMARY, 14
+C3151137	CILIARY DYSKINESIA, PRIMARY, 15
+C3151138	RETINITIS PIGMENTOSA 39 (disorder)
+C3151139	RETINITIS PIGMENTOSA 43
+C3151140	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D
+C3151147	Bile Acid Synthesis Defect, Congenital, 3
+C3151153	ADENOMA, CORTISOL-PRODUCING
+C3151184	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9
+C3151185	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY
+C3151186	NEPHRONOPHTHISIS 12
+C3151187	SECKEL SYNDROME 5
+C3151188	NEPHRONOPHTHISIS 9
+C3151189	C9 Deficiency
+C3151190	RETINITIS PIGMENTOSA 48
+C3151191	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8
+C3151192	LEBER CONGENITAL AMAUROSIS 7
+C3151193	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D
+C3151201	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME
+C3151202	LEBER CONGENITAL AMAUROSIS 8
+C3151204	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16
+C3151205	Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency
+C3151206	LEBER CONGENITAL AMAUROSIS 15
+C3151209	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
+C3151211	OSTEOGENESIS IMPERFECTA, TYPE X
+C3151218	OSTEOGENESIS IMPERFECTA, TYPE XI
+C3151221	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
+C3151222	OROFACIAL CLEFT 13
+C3151226	FICOLIN 3 DEFICIENCY
+C3151227	RETINITIS PIGMENTOSA 59
+C3151228	RETINITIS PIGMENTOSA 38 (disorder)
+C3151229	FEBRILE SEIZURES, FAMILIAL, 3B
+C3151230	DEAFNESS, AUTOSOMAL RECESSIVE 61
+C3151236	MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED
+C3151237	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction
+C3151264	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17
+C3151265	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
+C3151266	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 19
+C3151267	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
+C3151268	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4
+C3151293	CARDIOMYOPATHY, DILATED, 1HH
+C3151295	HYPOMAGNESEMIA 6, RENAL
+C3151302	Chromosome 13q14 deletion syndrome
+C3151303	Obesity, Hyperphagia, and Developmental Delay
+C3151304	CATARACT 36
+C3151343	SPINOCEREBELLAR ATAXIA 32
+C3151351	DEAFNESS, AUTOSOMAL RECESSIVE 89
+C3151355	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A
+C3151356	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION
+C3151379	OKT4 EPITOPE DEFICIENCY
+C3151380	SCHIZOPHRENIA 15
+C3151402	CANDIDIASIS, FAMILIAL, 5
+C3151403	AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+C3151404	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2
+C3151405	CANDIDIASIS, FAMILIAL, 6
+C3151406	SPERMATOGENIC FAILURE 8
+C3151407	SPERMATOGENIC FAILURE 9
+C3151409	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 3
+C3151411	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
+C3151417	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6
+C3151421	CYANOSIS, TRANSIENT NEONATAL
+C3151431	ATRIAL FIBRILLATION, FAMILIAL, 9
+C3151432	HYPOTRICHOSIS 3
+C3151433	OSTEOGENESIS IMPERFECTA, TYPE XII
+C3151434	RETINITIS PIGMENTOSA 60
+C3151440	PITUITARY HORMONE DEFICIENCY, COMBINED, 6
+C3151441	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2
+C3151442	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3
+C3151443	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2
+C3151444	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 4
+C3151445	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3
+C3151446	Nestor Guillermo progeria syndrome
+C3151460	CILIARY DYSKINESIA, PRIMARY, 16
+C3151461	LISSENCEPHALY 4
+C3151462	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14
+C3151463	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3
+C3151464	ATRIAL FIBRILLATION, FAMILIAL, 10
+C3151466	HEPATIC LIPASE DEFICIENCY (disorder)
+C3151467	Apolipoprotein C-III Deficiency
+C3151468	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1
+C3151470	AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
+C3151471	AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
+C3151476	MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)
+C3151482	HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING
+C3151495	Long upper lip
+C3151513	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
+C3151519	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3
+C3151520	Early severe fetal akinesia sequence
+C3151523	Abnormal cervical curvature
+C3151525	Hypoplastic heart
+C3151556	Abnormal iron deposition in mitochondria
+C3151568	NEPHROTIC SYNDROME, TYPE 4
+C3151609	ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS
+C3151610	ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY
+C3151617	ANTERIOR SEGMENT DYSGENESIS 7
+C3151752	NYSTAGMUS 6, CONGENITAL, X-LINKED
+C3151753	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6
+C3151781	CK SYNDROME
+C3151784	MACULAR DEGENERATION, X-LINKED ATROPHIC
+C3151853	MCLEOD SYNDROME WITH CHRONIC GRANULOMATOUS DISEASE
+C3151857	MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM
+C3151867	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
+C3151880	NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED (disorder)
+C3151897	DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
+C3151898	MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT
+C3151952	3-Methylglutaric aciduria
+C3151970	MERRF/MELAS OVERLAP SYNDROME
+C3151975	DEAFNESS, SENSORINEURAL, WITH NEUROLOGIC FEATURES
+C3152055	D-2-HYDROXYGLUTARIC ACIDURIA 1
+C3152083	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3, WITH MYOPATHY
+C3152097	AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA
+C3152102	USH1D/F, CDH23/PCDH15, DIGENIC
+C3152137	LEFT VENTRICULAR NONCOMPACTION 3
+C3152182	Anterior chamber anomalies
+C3152204	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
+C3152231	Gastrointestinal infarctions
+C3158111	response to SSRI
+C3158627	response to interferon-beta
+C3159311	BORNHOLM EYE DISEASE
+C3159322	SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE
+C3160718	PARKINSON DISEASE, LATE-ONSET
+C3160720	Cardiomyopathy, Dilated, 1u
+C3160738	FANCONI ANEMIA, COMPLEMENTATION GROUP D2
+C3160739	FANCONI ANEMIA, COMPLEMENTATION GROUP E
+C3160741	Toxicity to various agents
+C3160750	Cerebral small vessel ischaemic disease
+C3160754	Atypical femur fracture
+C3160756	Infection reactivation
+C3160761	Diabetic dyslipidaemia
+C3160764	Metastases to pelvis
+C3160771	Sperm concentration decreased
+C3160812	Gastric mucosa erythema
+C3160813	Vascular compression
+C3160814	Cannabis use
+C3160815	Intraductal papillary mucinous neoplasm
+C3160827	Exposed bone in jaw
+C3160830	Prostatic dysplasia
+C3160836	Walking distance test abnormal
+C3160846	Seizure like phenomena
+C3160855	Drug administered to patient of inappropriate age
+C3160858	Posterior reversible encephalopathy syndrome
+C3160866	Tablet physical issue
+C3160867	Capsule physical issue
+C3160909	Autoimmune arthritis
+C3160917	Bladder pain syndrome
+C3160921	Device battery issue
+C3160944	Vulvovaginal swelling
+C3161105	Neuroendocrine cell hyperplasia of infancy
+C3161106	Pulmonary interstitial glycogenosis
+C3161173	Hemoglobin H Constant Spring
+C3161174	Hemoglobin H Disease
+C3161175	Hydrops fetalis due to alpha thalassemia
+C3161220	Tuberculin (skin test) positive
+C3161259	Pilar and trichilemmal cysts
+C3161330	Profound intellectual disabilities
+C3161373	Dominant thalassemia
+C3161650	Primary immunoglobulin A nephropathy (disorder)
+C3163622	Papillary Meningioma
+C3163798	Recurrent lower respiratory tract infection
+C3163801	Abnormality of aortic arch
+C3163843	Chondrosarcoma of bone
+C3163918	Tumor thrombus
+C3163961	Dysplastic nodule
+C3163987	Endocervical adenocarcinoma in situ
+C3164096	Sarcoma of mesentery
+C3164271	Obstruction of aortic arch
+C3164344	Adult onset autosomal dominant leukodystrophy
+C3164374	Abnormality of pulmonary valve
+C3164429	Indeterminate atrial arrangement
+C3164445	Abnormality of aortic valve
+C3164456	Malignant respiratory tract neoplasm
+C3164501	Mega cisterna magna
+C3164626	Anorectal adenocarcinoma
+C3164780	Clinical sepsis
+C3164851	Palisaded myofibroblastoma
+C3164874	Dilatation of descending aorta
+C3165106	Infiltrating duct carcinoma of female breast
+C3165209	High density lipoprotein deficiency
+C3178766	Nociceptive Pain
+C3178789	Widespread Chronic Pain
+C3178801	Stroke, Lacunar
+C3178803	Social Anhedonia
+C3178804	Physical Anhedonia
+C3178805	Heterotaxy Syndrome
+C3178806	Right Atrial Isomerism
+C3178807	Left Atrial Isomerism
+C3178957	Subcutaneous Phaeohyphomycosis
+C3178958	Cutaneous Phaeohyphomycosis
+C3178973	Disseminated Fusariosis
+C3178974	Pulmonary Fusariosis
+C3178979	Subcutaneous Hyalohyphomycosis
+C3178980	Pulmonary Hyalohyphomycosis
+C3178981	Splenic Hyalohyphomycosis
+C3179021	Obsessive Hoarding
+C3179058	Corpus Callosum Malformation
+C3179194	GALNS Deficiency
+C3179196	Myofascial Trigger Point Pain
+C3179239	Osteopetrosis Autosomal Dominant Type 2
+C3179244	Pseudo Pelger-Huet Anomaly
+C3179277	Prosthesis Survival
+C3179278	Prosthesis Durability
+C3179349	Gastrointestinal Stromal Sarcoma
+C3179396	Glanzmann Thrombasthenia, Type A
+C3179450	Pott's Paraplegia
+C3179455	Niemann-Pick Disease, Type C1
+C3179502	Linear Verrucous Epidermal Nevus
+C3179508	Aplasia/Hypoplasia of the thumb
+C3179539	Congenital Deficiency of Pulmonary Surfactant Protein B
+C3203102	Idiopathic pulmonary arterial hypertension
+C3203356	Factor II deficiency
+C3203357	Bone tuberculosis
+C3203358	Hypoventilation
+C3203359	Rupture
+C3203360	Suppuration
+C3203457	Procedural haemorrhage
+C3203487	Hyperglycaemic unconsciousness
+C3203488	Suspected counterfeit product
+C3203495	Parkinsonism hyperpyrexia syndrome
+C3203509	Neuropsychiatric syndrome
+C3203514	Human chorionic gonadotropin increased
+C3203523	Seizure cluster
+C3203531	Post-traumatic neck syndrome
+C3203532	Infected dermal cyst
+C3203533	Psychological Trauma
+C3203548	Mycobacterium chelonae infection
+C3203549	Exposure during breast feeding
+C3203550	Exposure via father
+C3203551	Foetal exposure during pregnancy
+C3203552	Foetal exposure timing unspecified
+C3203553	Maternal exposure before pregnancy
+C3203554	Maternal exposure during delivery
+C3203555	Maternal exposure during pregnancy
+C3203558	Exposure via direct contact
+C3203559	Exposure via partner
+C3203562	Maternal exposure timing unspecified
+C3203574	Epstein-Barr virus associated lymphoma
+C3203622	Crystal nephropathy
+C3203644	Hyporesponsive to stimuli
+C3203645	Nasal discharge discolouration
+C3203653	IgG4 related sclerosing disease
+C3203660	Vulvovaginal rash
+C3203695	Noninfectious peritonitis
+C3203708	N-terminal prohormone brain natriuretic peptide increased
+C3203729	Periorbital haemorrhage
+C3203730	Infectious pleural effusion
+C3203733	Precordial Catch Syndrome
+C3203738	Fowler syndrome
+C3241919	Erythema Multiforme Major
+C3241936	Non-cardiogenic pulmonary oedema
+C3241937	Non-alcoholic steatohepatitis
+C3241940	Roux-en-y Anastomosis Site
+C3241942	Sore on skin
+C3241958	Myocardial Disorder
+C3245525	Familial renal glucosuria
+C3248383	Logorrhea
+C3249875	Laryngopharyngeal Cancer
+C3249880	Solar Erythema
+C3249881	Infection - suppurative
+C3250443	MYOTONIC DYSTROPHY 1
+C3251817	Condylomatous carcinoma
+C3257801	Dextrotransposition of aorta
+C3257803	Watery eyes
+C3258293	Valvular disease
+C3263719	Primary acquired melanosis
+C3263723	Injury
+C3264046	Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
+C3264382	Swine influenza virus (viruses that normally cause infections in pigs)
+C3264595	Agoraphobia without panic disorder
+C3266076	Orofacial cleft
+C3266101	22q11 partial monosomy syndrome
+C3266102	Steroid resistant nephrotic syndrome of childhood
+C3266123	Serrated polyp
+C3266164	Dropped head syndrome
+C3266262	Multiple Chronic Conditions
+C3266628	Persistent asthma
+C3266731	2-methyl-3-hydroxybutyric aciduria
+C3266843	47, XYY syndrome
+C3266863	Atypical Mycobacteriosis, Familial
+C3266898	Waardenburg Syndrome
+C3266963	Muscle oedema
+C3266969	Dialysis related complication
+C3267019	Central nervous system haemorrhage
+C3267041	Catheter site abscess
+C3267047	Autoimmune necrotizing myopathy
+C3267050	Chronic graft versus host disease in skin
+C3267051	Chronic graft versus host disease in liver
+C3267073	Autoinflammatory disease
+C3267074	Renal vascular thrombosis
+C3267094	Infected fistula
+C3267097	Narcotic bowel syndrome
+C3267104	Product quality control issue
+C3267129	Prerenal failure
+C3267136	Intercepted drug prescribing error
+C3272111	Merycism
+C3272265	Three Vessel Coronary Disease
+C3272399	Gastric Neuroendocrine Tumor
+C3272409	Gastric Neuroendocrine Carcinoma
+C3272425	Gastric Schwannoma
+C3272525	Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
+C3272528	Small Intestinal Neuroendocrine Tumor
+C3272530	Intestinal Neuroendocrine Carcinoma
+C3272610	Colorectal Neuroendocrine Tumor
+C3272793	Filiform Serrated Adenoma
+C3272797	Colon Serrated Polyposis
+C3272802	Hamartomatous polyposis
+C3272804	Rectal Tubular Adenoma
+C3272805	Colorectal Adenomatous Polyp
+C3272809	Colorectal Serrated Adenocarcinoma
+C3272820	Ulcerative Colitis-Associated Colorectal Adenocarcinoma
+C3272822	Colorectal Lymphoma
+C3272830	Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma
+C3272841	MUTYH-Associate Polyposis
+C3273009	Beta-Catenin-Activated Hepatocellular Adenoma
+C3273010	Inflammatory Hepatocellular Adenoma
+C3273019	Early Hepatocellular Carcinoma
+C3273033	Well Differentiated Hepatocellular Carcinoma
+C3273034	Moderately Differentiated Hepatocellular Carcinoma
+C3273035	Poorly Differentiated Hepatocellular Carcinoma
+C3273225	Hereditary Neurodegenerative Disorder
+C3273239	Proliferative Inflammatory Atrophy
+C3273251	Sclerosing Polycystic Adenosis
+C3273254	Arterionephrosclerosis
+C3274463	Sickle Beta 0 Thalassemia
+C3274502	Opiate Withdrawal Syndrome
+C3274515	Severe Bronchopulmonary Dysplasia
+C3274516	Single Ventricle Defect
+C3274519	Surfactant Protein C Deficiency
+C3274709	Contralateral Breast Carcinoma
+C3275069	Chronic Total Occlusion Vessel
+C3275121	One Vessel Coronary Disease
+C3275124	Biliary System Disorder
+C3275356	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS
+C3275406	INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE
+C3275408	MENTAL RETARDATION, X-LINKED 96
+C3275410	DEEP VENOUS THROMBOSIS, PROTECTION AGAINST
+C3275417	Ragged-red muscle fibers
+C3275438	AUTISM, SUSCEPTIBILITY TO, X-LINKED 5
+C3275443	MENTAL RETARDATION, X-LINKED 90 (disorder)
+C3275444	MENTAL RETARDATION, X-LINKED 88 (disorder)
+C3275445	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
+C3275447	OGDEN SYNDROME
+C3275452	Protruding upper lip
+C3275459	AMYOTROPHIC LATERAL SCLEROSIS 15, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+C3275464	MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE
+C3275476	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA
+C3275495	KABUKI SYNDROME 2
+C3275508	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
+C3275521	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
+C3275558	MENTAL RETARDATION, X-LINKED, SYNDROMIC 16
+C3275684	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1
+C3275685	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 2
+C3275686	CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY
+C3275750	ATRIOVENTRICULAR SEPTAL DEFECT 3
+C3275754	Upswept frontal hairline
+C3275758	Choriocapillaris atrophy
+C3275872	USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
+C3275898	RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO
+C3275899	Hyperechogenic kidneys
+C3275959	LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO
+C3275963	Abnormal iris vasculature
+C3275998	THROMBOCYTHEMIA 2
+C3276032	Hypoplastic areola
+C3276036	High anterior hairline
+C3276074	PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
+C3276096	ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
+C3276161	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
+C3276200	MALE GERM CELL TUMOR, SOMATIC
+C3276228	ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE
+C3276239	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1
+C3276240	LONG QT SYNDROME 2/3, DIGENIC
+C3276241	LONG QT SYNDROME 3/6, DIGENIC Disorder
+C3276246	MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO
+C3276276	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1
+C3276324	Fifth metacarpal with ulnar notch
+C3276419	USHER SYNDROME, TYPE ID/F, DIGENIC
+C3276432	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1
+C3276441	Decreased activity of mitochondrial respiratory complexes
+C3276539	CUTIS LAXA, AUTOSOMAL DOMINANT 1
+C3276549	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
+C3276551	DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH
+C3276611	Absent or delayed speech development
+C3276623	Toenail dysplasia
+C3276706	Small Fiber Neuropathy
+C3276709	Adult-onset is referred to as small fiber neuropathy
+C3276742	Fibular duplication
+C3276744	Absent tibia
+C3276815	Stiff skin
+C3276821	Thin glomerular basement membrane
+C3276941	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2
+C3276977	LEUKONYCHIA STRIATUS
+C3277019	Horizontal eyebrow
+C3277059	Congenital Bilateral Cataracts
+C3277074	BARRETT ESOPHAGUS/ESOPHAGEAL ADENOCARCINOMA
+C3277076	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT
+C3277090	CHROMOSOME 2q23.1 DELETION SYNDROME
+C3277114	Relatively short spine
+C3277116	Long coccyx
+C3277117	Caudal appendage
+C3277119	Halberd-shaped pelvis
+C3277120	Hyperplasia of the femoral trochanters
+C3277123	Dumbbell-shaped metaphyses
+C3277124	Prominent joints
+C3277126	Absent primary metaphyseal spongiosa
+C3277127	Abnormal metaphyseal vascular invasion
+C3277184	Decreased patellar reflex
+C3277187	Type 2 muscle fiber predominance
+C3277190	THROMBOCYTHEMIA 2, SOMATIC
+C3277226	Restrictive ventilatory defect
+C3277376	Multiple mitochondrial DNA deletions
+C3277418	Gastrointestinal hamartomatous polyps
+C3277426	Lack of facial subcutaneous fat
+C3277428	Severe viral infections
+C3277679	EPIDERMAL NEVUS WITH UROTHELIAL CANCER, SOMATIC
+C3277687	Central nervous system degeneration
+C3277688	Progressive forgetfulness
+C3277693	Punctate vasculitis skin lesions
+C3277697	Decreased visual acuity, progressive
+C3277700	LONG QT SYNDROME 1/2, DIGENIC (disorder)
+C3277701	VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6
+C3277723	JOUBERT SYNDROME 12
+C3277750	Absent middle phalanx of 5th finger
+C3277753	Deep-set nails
+C3277849	17,20-Lyase Deficiency, Isolated
+C3277900	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4
+C3277918	TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
+C3278004	Thymic hypoplasia or aplasia
+C3278024	Enlarged cerebellum
+C3278123	Severe hydrocephalus
+C3278138	FIBROCHONDROGENESIS 1
+C3278146	GALACTOSEMIA, DUARTE VARIANT
+C3278147	GELEOPHYSIC DYSPLASIA 1
+C3278148	BERNARD-SOULIER SYNDROME, TYPE A1
+C3278152	GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET (disorder)
+C3278153	GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET
+C3278154	GLUTARIC ACIDEMIA IIA
+C3278155	GLUTARIC ACIDEMIA IIB
+C3278156	GLUTARIC ACIDEMIA IIC
+C3278204	Dysmyelinating leukodystrophy
+C3278211	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
+C3278307	Diffuse glomerular basement membrane lamellation
+C3278322	Cerebellar dysplasia
+C3278384	HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
+C3278401	Hypopigmentation of hair
+C3278404	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS
+C3278429	Bilateral elbow dislocations
+C3278481	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1
+C3278482	DESBUQUOIS DYSPLASIA, KIM VARIANT
+C3278509	Spinal fusion
+C3278622	OROTIC ACIDURIA WITHOUT MEGALOBLASTIC ANEMIA
+C3278626	Orotic acid crystalluria
+C3278636	Neonatal insulin-dependent diabetes mellitus
+C3278658	Linear hyperpigmentation
+C3278664	LIVER FAILURE, INFANTILE, TRANSIENT
+C3278811	Thumb aplasia
+C3278865	Pigment gallstones
+C3278923	Dilated ventricles (finding)
+C3278975	Attenuation of retinal blood vessels
+C3278981	Decreased visual acuity, slowly progressive
+C3279038	Body temperature instability
+C3279090	Unilateral vertebral artery hypoplasia
+C3279092	LONG QT SYNDROME 2/5, DIGENIC (disorder)
+C3279093	LONG QT SYNDROME 2/9, DIGENIC
+C3279149	Liver dysfunction, mild
+C3279191	Arterial tortuosity
+C3279203	JOUBERT SYNDROME 11
+C3279222	Aplasia/Hypoplasia of the cerebellum
+C3279322	Progressive flexion contractures
+C3279336	Impaired gluconeogenesis
+C3279392	PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF
+C3279393	PXE, MODIFIER OF SEVERITY OF
+C3279397	Very long chain fatty acid accumulation
+C3279407	Hypoplasia of the abdominal wall musculature
+C3279409	Distal ileal atresia
+C3279437	PREGNANCY LOSS, RECURRENT, 4
+C3279439	Recurrent spontaneous abortion
+C3279470	HYPOTRICHOSIS 8
+C3279547	Hypergranulosis
+C3279550	Cryptozoospermia
+C3279564	Osteogenesis Imperfecta, Type VI
+C3279571	Ectopic posterior pituitary
+C3279575	Reticulated skin pigmentation
+C3279601	Reticular pigmentation pattern
+C3279614	BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO
+C3279627	EPILEPSY, PROGRESSIVE MYOCLONIC, 6
+C3279658	Glyoxalase deficiency
+C3279660	DEAFNESS, AUTOSOMAL RECESSIVE 29
+C3279661	alpha-2-Macroglobulin Deficiency
+C3279662	Leukotriene C4 Synthase Deficiency
+C3279664	Emberger syndrome
+C3279674	Frontoparietal polymicrogyria
+C3279675	Perisylvian polymicrogyria
+C3279690	MOYAMOYA DISEASE 5
+C3279693	ATRIAL FIBRILLATION, FAMILIAL, 11
+C3279695	ATRIAL FIBRILLATION, FAMILIAL, 12
+C3279699	Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
+C3279708	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3
+C3279716	N-ACETYLASPARTATE DEFICIENCY
+C3279722	MYOPATHY, DISTAL, 4
+C3279725	Hip flexor weakness
+C3279738	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE
+C3279743	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
+C3279748	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2
+C3279754	PSORIASIS 13, SUSCEPTIBILITY TO
+C3279756	HERMANSKY-PUDLAK SYNDROME 7
+C3279757	Chondrodysplasia with joint dislocations gPAPP type
+C3279775	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1
+C3279786	ANHAPTOGLOBINEMIA
+C3279787	HYPOHAPTOGLOBINEMIA (disorder)
+C3279790	Atrial Septal Defect 3
+C3279791	SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO
+C3279792	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
+C3279793	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8
+C3279800	KEPPEN-LUBINSKY SYNDROME
+C3279807	CRANIOECTODERMAL DYSPLASIA 3
+C3279824	Kappa-Chain Deficiency
+C3279839	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7
+C3279840	Methylmalonate Semialdehyde Dehydrogenase Deficiency
+C3279841	Pyruvate Dehydrogenase E1-Beta Deficiency
+C3279842	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2
+C3279843	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2
+C3279875	CORTICAL MALFORMATIONS, OCCIPITAL
+C3279885	Hereditary Sensory and Autonomic Neuropathy Type Ie
+C3279899	Hydrolethalus Syndrome 2
+C3279902	CHITOTRIOSIDASE DEFICIENCY
+C3279904	Lactate Dehydrogenase B Deficiency
+C3279905	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6
+C3279941	STICKLER SYNDROME, TYPE IV
+C3279947	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
+C3279948	DEAFNESS, AUTOSOMAL DOMINANT 64
+C3279964	HYPERBILIVERDINEMIA
+C3279974	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10
+C3279990	CANDIDIASIS, FAMILIAL, 7
+C3279992	PARAGANGLIOMAS 5
+C3279997	MYOPIA 21, AUTOSOMAL DOMINANT
+C3280011	BRITTLE CORNEA SYNDROME 2
+C3280020	Developmental hip dysplasia
+C3280026	HERMANSKY-PUDLAK SYNDROME 9
+C3280030	GATA2 Deficiency
+C3280031	JOUBERT SYNDROME 13
+C3280036	MECKEL SYNDROME, TYPE 10
+C3280041	RETINITIS PIGMENTOSA 61
+C3280042	RETINITIS PIGMENTOSA 62
+C3280054	GELEOPHYSIC DYSPLASIA 2
+C3280062	LEBER CONGENITAL AMAUROSIS 16
+C3280073	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES
+C3280094	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3
+C3280095	MACROCEPHALY, MACROSOMIA, AND FACIAL DYSMORPHISM SYNDROME
+C3280099	CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
+C3280100	NEPHROTIC SYNDROME, TYPE 6
+C3280112	MYASTHENIC SYNDROME, CONGENITAL, 16
+C3280113	NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
+C3280114	Glycoprotein IA Deficiency
+C3280120	BLEEDING DISORDER, PLATELET-TYPE, 11
+C3280127	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
+C3280131	Long eyebrows
+C3280133	PARKINSON DISEASE 17
+C3280153	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17
+C3280155	MECKEL SYNDROME, TYPE 9
+C3280160	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4
+C3280168	NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
+C3280182	ADAMS-OLIVER SYNDROME 2
+C3280203	WARBURG MICRO SYNDROME 3
+C3280205	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS
+C3280214	WARBURG MICRO SYNDROME 2
+C3280215	HOLOPROSENCEPHALY 11
+C3280216	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
+C3280220	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
+C3280226	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11
+C3280240	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME
+C3280265	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18
+C3280266	NARCOLEPSY 7
+C3280271	PARKINSON DISEASE 18
+C3280282	MENTAL RETARDATION, AUTOSOMAL DOMINANT 8
+C3280283	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
+C3280284	MENTAL RETARDATION, AUTOSOMAL DOMINANT 10
+C3280285	MENTAL RETARDATION, AUTOSOMAL DOMINANT 11
+C3280296	Microcephaly-capillary malformation syndrome
+C3280303	Abnormal hair whorl
+C3280309	ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY
+C3280314	Combined Malonic and Methylmalonic Aciduria
+C3280315	Platelet-Activating Factor Acetylhydrolase Deficiency
+C3280342	STICKLER SYNDROME, TYPE V
+C3280345	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 4
+C3280346	MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION
+C3280349	Peripheral vitreoretinal degeneration
+C3280358	Wolfram-Like Syndrome, Autosomal Dominant
+C3280371	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4
+C3280378	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA
+C3280381	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY
+C3280392	EDICT syndrome
+C3280402	SCLEROSTEOSIS 2
+C3280415	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
+C3280428	Alpha-Methylacyl-CoA Racemase Deficiency
+C3280442	PANCREATIC CANCER, SUSCEPTIBILITY TO, 4
+C3280443	MYOPATHY, DISTAL, TATEYAMA TYPE
+C3280452	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
+C3280471	OVARIAN DYSGENESIS 3
+C3280479	PITT-HOPKINS-LIKE SYNDROME 2
+C3280489	FEINGOLD SYNDROME 2
+C3280492	TUMOR PREDISPOSITION SYNDROME
+C3280501	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1
+C3280524	SCHIZOPHRENIA 17
+C3280526	ARTHROGRYPOSIS, DISTAL, TYPE 1B
+C3280527	PANCREATIC LIPASE DEFICIENCY
+C3280528	COLIPASE, CONGENITAL ABSENCE OF PANCREATIC
+C3280529	LIPASE AND COLIPASE, DEFICIENCY OF
+C3280530	LIPASE AND COLIPASE, CONGENITAL ABSENCE OF PANCREATIC
+C3280538	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27
+C3280556	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
+C3280574	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5
+C3280586	Mannose-Binding Protein Deficiency
+C3280587	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE
+C3280598	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY
+C3280612	NEPHRONOPHTHISIS 13
+C3280616	CRANIOECTODERMAL DYSPLASIA 4
+C3280641	Decreased serum complement C4b
+C3280642	Complement Component 4a Deficiency
+C3280644	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM
+C3280647	BACTEREMIA, SUSCEPTIBILITY TO, 2
+C3280660	ENCEPHALOPATHY, LETHAL, DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION
+C3280670	PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1
+C3280672	PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
+C3280674	PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3
+C3280679	MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET
+C3280690	ACCELERATED TUMOR FORMATION, SUSCEPTIBILITY TO
+C3280703	MYOPATHY, CENTRONUCLEAR, 3
+C3280715	GLYCEROL QUANTITATIVE TRAIT LOCUS
+C3280721	CHILBLAIN LUPUS 2
+C3280729	RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES
+C3280730	EPILEPSY, FAMILIAL TEMPORAL LOBE, 5
+C3280734	FEBRILE SEIZURES, FAMILIAL, 11
+C3280742	SYSTEMIC LUPUS ERYTHEMATOSUS 16
+C3280766	JOUBERT SYNDROME 14
+C3280768	Abnormality of the posterior cranial fossa
+C3280770	Cerebellar vermis aplasia or hypoplasia
+C3280777	VENTRICULAR SEPTAL DEFECT 1
+C3280781	ATRIOVENTRICULAR SEPTAL DEFECT 4
+C3280785	VENTRICULAR SEPTAL DEFECT 3
+C3280790	ATRIAL SEPTAL DEFECT 8
+C3280795	HYPOPLASTIC LEFT HEART SYNDROME 2
+C3280797	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P
+C3280798	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB
+C3280799	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB
+C3280800	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2
+C3280817	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
+C3280845	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E
+C3280856	ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION
+C3280866	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)
+C3280887	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES
+C3280898	JOUBERT SYNDROME 9/15, DIGENIC
+C3280899	JOUBERT SYNDROME 12/15, DIGENIC
+C3280906	JOUBERT SYNDROME 16
+C3280914	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3
+C3280939	ATRIOVENTRICULAR SEPTAL DEFECT 5
+C3280940	Unbalanced atrioventricular canal defect
+C3280943	ATRIAL SEPTAL DEFECT 9
+C3280953	HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE
+C3280965	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION
+C3280970	PORENCEPHALY 2
+C3280974	TRIGONOCEPHALY 2
+C3280976	Thrombophilia due to Thrombomodulin Defect
+C3280977	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE
+C3281027	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
+C3281029	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL
+C3281034	Multifocal seizures
+C3281044	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY
+C3281045	CONE-ROD DYSTROPHY 16
+C3281046	RETINITIS PIGMENTOSA 64
+C3281055	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM
+C3281059	Broad jaw
+C3281066	USHER SYNDROME, TYPE IIIB
+C3281084	Congenital disorder of glycosylation type 1r
+C3281089	MIRROR MOVEMENTS 2
+C3281092	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE
+C3281105	HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO
+C3281125	THROMBOCYTHEMIA 3
+C3281128	FIBROCHONDROGENESIS 2
+C3281138	CHROMOSOME 17q12 DELETION SYNDROME
+C3281153	EFAVIRENZ, POOR METABOLISM OF
+C3281154	EFAVIRENZ CENTRAL NERVOUS SYSTEM TOXICITY, SUSCEPTIBILITY TO
+C3281160	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2
+C3281191	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13
+C3281192	Infantile cerebellar and retinal degeneration
+C3281200	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS
+C3281201	MENTAL RETARDATION, AUTOSOMAL DOMINANT 12
+C3281202	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13
+C3281203	CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
+C3281215	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E
+C3281223	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME
+C3281234	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9
+C3281235	BARAITSER-WINTER SYNDROME 2
+C3281236	DYSTONIA 21
+C3281247	BENT BONE DYSPLASIA SYNDROME
+C3281288	PREECLAMPSIA/ECLAMPSIA 5
+C3281289	TRICHOHEPATOENTERIC SYNDROME 2
+C3281297	DEAFNESS, AUTOSOMAL DOMINANT 4B
+C3282903	Metastatic Carcinoma in the Liver
+C3463824	MYELODYSPLASTIC SYNDROME
+C3463897	HYDATIDIFORM MOLE, RECURRENT, 1
+C3463916	Complement Factor I (C3 inactivator) deficiency
+C3463917	Corticosterone Methyl Oxidase Type II Deficiency
+C3463918	EMBRYONAL CELL CARCINOMA
+C3463992	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
+C3468041	FANCONI ANEMIA, COMPLEMENTATION GROUP C
+C3468114	Juvenile amyotrophic lateral sclerosis
+C3468338	CARPAL TUNNEL SYNDROME, FAMILIAL
+C3468561	familial atrial fibrillation
+C3469186	HEMOCHROMATOSIS, TYPE 1
+C3469521	FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
+C3469522	BREAST CANCER, SUSCEPTIBILITY TO
+C3469524	PROSTATE CANCER, SUSCEPTIBILITY TO
+C3469526	FANCONI ANEMIA, COMPLEMENTATION GROUP F
+C3469527	fanconi anemia complementation group g
+C3469528	FANCONI ANEMIA, COMPLEMENTATION GROUP L
+C3469542	FANCONI ANEMIA, COMPLEMENTATION GROUP P
+C3469605	PSEUDOHYPOALDOSTERONISM, TYPE IID
+C3469606	PSEUDOHYPOALDOSTERONISM, TYPE IIE
+C3472608	Micropapillary carcinoma
+C3472614	Plasmablastic lymphoma
+C3472616	Mixed phenotype acute leukemia B/myeloid
+C3472621	Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement
+C3472623	Serrated adenocarcinoma
+C3472711	Spinocerebellar ataxia 36
+C3484357	HERMANSKY-PUDLAK SYNDROME 4
+C3489393	Hiatal Hernia
+C3489395	Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
+C3489396	Hypogonadism, Isolated Hypogonadotropic
+C3489398	Neuroepithelioma, Peripheral
+C3489413	Lipomatosis, Multiple
+C3489447	Hyperkalemic Periodic Paralysis Type 2
+C3489529	Tooth Agenesis, Familial
+C3489532	Cone-Rod Dystrophy 2
+C3489571	Familial Extrahepatic Biliary Atresia
+C3489572	Idiopathic Extrahepatic Biliary Atresia
+C3489626	Cerebelloparenchymal Disorder V
+C3489627	Stuttering, Familial Persistent 1
+C3489628	Thrombocytosis, Autosomal Dominant
+C3489630	Somatotrophinoma, Familial
+C3489704	Vision Disability
+C3489724	Aicardi-Goutieres Syndrome 2
+C3489725	Pseudo-TORCH syndrome
+C3489726	Geleophysic dysplasia
+C3489728	Familial intrahepatic cholestasis of pregnancy
+C3489732	Familial mesangial sclerosis
+C3489733	Oculomotor apraxia
+C3489734	Anti-plasmin deficiency, congenital
+C3489771	Keratosis Palmaris et Plantaris Familiaris
+C3489773	Medication Compliance
+C3489787	Pituitary Hormone Deficiency, Combined, 3
+C3489789	Cholestasis, Progressive Familial Intrahepatic, 2
+C3489791	Parkinson Disease, Familial, Type 1
+C3489793	46,XY Sex Reversal 3
+C3489795	Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant
+C3489796	Thyroid Hormone Resistance, Generalized, Autosomal Recessive
+C3489856	Cold Hypersensitivity
+C3492932	Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency
+C3492944	Lentiginosis Profusa
+C3493776	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1
+C3494162	Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous
+C3494181	Glomus Tumors, Familial, 1
+C3494186	Autosomal Hemophilia A
+C3494187	Factor VIII Deficiency
+C3494247	Organothiophosphonate Poisoning
+C3494248	Organothiophosphate Poisoning
+C3494358	Prodromal Symptoms
+C3494359	Prodromal States
+C3494360	Prodromal Period
+C3494361	Prodromal Stage
+C3494422	Retrognathia
+C3494423	Maxillary Retroposition
+C3494424	Maxillary Retrusion
+C3494425	Mandibular Retroposition
+C3494426	Mandibular Retrusion
+C3494489	Autoimmune polyendocrinopathy syndrome, type 1
+C3494506	Pseudohypoparathyroidism, Type Ia
+C3494522	Hypergonadotropic Ovarian Failure, X-Linked
+C3494623	Mild dementia
+C3494652	Severe dementia
+C3494934	Benign paroxysmal torticollis of infancy
+C3494976	Migrating partial seizures in infancy
+C3495144	Apraxia, Articulatory
+C3495145	Dyslalia
+C3495417	Hemifacial microsomia
+C3495421	Chromosome 18q syndrome
+C3495426	Homocysteinemia
+C3495427	Fanconi-Bickel Syndrome
+C3495436	American cutaneous leishmaniasis
+C3495438	Macular Degeneration, Age-Related, 2
+C3495439	Inflammatory disorder of breast
+C3495442	Phantom pain
+C3495483	Amish Brittle Hair Brain Syndrome
+C3495488	Axenfeld-Rieger syndrome
+C3495489	Rieger eye malformation sequence
+C3495498	Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
+C3495530	Congenital alopecia X-linked
+C3495537	Heterotaxy, Visceral, 5, Autosomal
+C3495549	Patent ductus arteriosus
+C3495551	Dihydropyrimidinuria
+C3495552	Cystathionase Deficiency
+C3495554	Homocarnosinase deficiency
+C3495555	Carnosinemia
+C3495559	Arthritis, Juvenile
+C3495566	Reflux nephropathy (disorder)
+C3495587	Night Blindness, Congenital Stationary, Type 1A
+C3495589	Jalili syndrome
+C3495591	Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
+C3495676	Anorectal Malformations
+C3495700	Atypical fracture
+C3495711	Antipsychotic drug level decreased
+C3495723	Glassy eyes
+C3495739	Faecal calprotectin increased
+C3495797	Peripheral artery stenosis
+C3495801	Granulomatosis with polyangiitis
+C3495820	Hand-eye coordination impaired
+C3495832	Rheumatic disorder
+C3495839	Suspected transmission of an infectious agent via product
+C3495842	Humidity intolerance
+C3495845	Drain placement
+C3495847	Immune reconstitution inflammatory syndrome associated tuberculosis
+C3495861	Sensitivity to weather change
+C3495874	Nonepileptic Seizures
+C3495917	Advanced breast cancer
+C3495919	Enthesitis-Related Arthritis
+C3495920	Lacrimal structural disorder
+C3495949	Locally advanced breast cancer
+C3496069	cocaine use
+C3496228	Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia
+C3496337	Idiopathic Nephrotic Syndrome
+C3496493	Galectin-3 measurement
+C3496549	Male Germ Cell Tumor
+C3501249	Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome
+C3501265	Deafness, Sensorineural, with Hypertrophic Cardiomyopathy
+C3501611	Mental Retardation, X-Linked Nonsyndromic
+C3501647	Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to
+C3501679	Bleeding Disorder due to Defective Thromboxane A2 Receptor
+C3501830	Microcephaly, Primary Autosomal Recessive, 2
+C3501835	alpha-1-Antitrypsin Deficiency, Autosomal Recessive
+C3501843	Non-medullary thyroid carcinoma
+C3501844	Familial Nonmedullary Thyroid Cancer
+C3501846	Noonan-Like Syndrome With Loose Anagen Hair
+C3501847	Night blindness, congenital stationary, type 1
+C3501848	Nephrosis, congenital
+C3501849	Mngie Without Leukoencephalopathy
+C3501854	Leukemia, Acute, X-Linked
+C3501858	Muscular Dystrophy, Limb-Girdle, Type 1D
+C3501891	Mitochondrial DNA Depletion Syndrome, Myopathic Form
+C3501912	Cerebrocostomandibular-Like Syndrome
+C3501946	Microcephaly with Chorioretinopathy, Autosomal Dominant
+C3502051	Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive
+C3502052	Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant
+C3502054	Leukodystrophy, Dysmyelinating, with Oligodontia
+C3502073	Woolly Hair, Autosomal Recessive
+C3502075	Multiple Mitochondrial Dysfunctions Syndrome
+C3502105	Dyskeratosis Congenita, Autosomal Recessive
+C3502107	Breastfeeding Jaundice
+C3502110	Homocystinuria, Pyridoxine-Responsive
+C3502131	Adrenal Insufficiency, Congenital
+C3502132	Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal
+C3502214	Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities
+C3502298	Lactic Acidosis, Fatal Infantile
+C3502353	Atrial Septal Defect with Atrioventricular Conduction Defects
+C3502417	Amyotrophic Lateral Sclerosis 10
+C3502469	Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia
+C3502492	Microcephaly with Chorioretinopathy, Autosomal Recessive
+C3502495	Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal
+C3502630	Myasthenic Syndrome due to Mutation in SCN4A
+C3502809	Generalized Epilepsy with Febrile Seizures Plus
+C3532221	Long lower third of face
+C3532222	Inflammatory cardiomyopathy
+C3532239	Mitochondrial cardiomyopathy
+C3532240	Hypertrophic mitochondrial cardiomyopathy
+C3532243	Fatal infantile mitochondrial cardiomyopathy
+C3532934	Mild expressive language delay
+C3532942	Mixed dementia
+C3532946	Moderate receptive language delay
+C3534585	Infection caused by Norovirus
+C3534591	Diabetic Heart Disease
+C3536572	End stage renal disease due to hypertension
+C3536576	Chronic myelopathy
+C3536593	Chronic cerebrovascular accident
+C3536618	Segond Fracture
+C3536663	Acute deep venous thrombosis
+C3536714	Renal dysplasia
+C3536715	AA amyloidosis
+C3536734	Hypoplastic pelvis
+C3536738	Lumbar meningomyelocele
+C3536741	Discordant ventriculoarterial connection
+C3536797	Ichthyosis Congenita II
+C3536864	Acute disseminated encephalitis
+C3536893	Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
+C3536958	Surfactant protein D measurement
+C3536983	Familial Hypophosphatemic Rickets
+C3536984	Vitamin D-Resistant Rickets, X-Linked
+C3537146	Ménière's Vertigo
+C3537179	Non-venereal endemic syphilis
+C3537440	Cystinosis, Infantile Nephropathic
+C3538946	DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
+C3538951	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA
+C3538999	DYSTONIA 23
+C3539003	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
+C3539010	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F
+C3539013	AICARDI-GOUTIERES SYNDROME 6
+C3539063	Bart\'s Hemoglobinopathy
+C3539071	NEPHRONOPHTHISIS 14
+C3539120	PROSTATE CANCER, HEREDITARY, 2
+C3539123	CEROID LIPOFUSCINOSIS, NEURONAL, 11
+C3539168	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
+C3539195	TREMOR, HEREDITARY ESSENTIAL, 4
+C3539494	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE
+C3539495	SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE
+C3539506	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE
+C3539507	SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE
+C3539781	Progressive cGVHD
+C3539878	Triple Negative Breast Neoplasms
+C3539888	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3
+C3539909	Allergic disposition
+C3539916	MYOCLONUS, FAMILIAL CORTICAL
+C3539920	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
+C3540094	INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
+C3540450	HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA
+C3540453	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F
+C3540662	Congenital Amaurosis of Retinal Origin
+C3540839	Neonatal Drug Withdrawal
+C3540844	CILIARY DYSKINESIA, PRIMARY, 20
+C3540845	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8
+C3540850	CATARACT 4, MULTIPLE TYPES
+C3540852	Rickets, X-Linked Hypophosphatemic
+C3541318	Soluble Transferrin Receptor Measurement
+C3541319	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY
+C3541456	Spondyloepiphyseal Dysplasia Tarda, X-Linked
+C3541462	HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA
+C3541471	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
+C3541474	ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE
+C3541476	MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT
+C3541517	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
+C3541518	ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
+C3541853	NEPHRONOPHTHISIS 15
+C3541994	Drug Hypersensitivity Syndrome
+C3542021	Duchenne and Becker Muscular Dystrophy
+C3542022	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS SYNDROME
+C3542024	AORTIC VALVE DISEASE 2
+C3542025	AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
+C3542026	PEROXISOME BIOGENESIS DISORDER 5B
+C3542499	Aminoacylase 2 Deficiency
+C3542500	ADH-Resistant Diabetes Insipidus
+C3542501	Acute Infective Polyneuritis
+C3542549	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
+C3542550	CILIARY DYSKINESIA, PRIMARY, 17
+C3542922	IMMUNODEFICIENCY, COMMON VARIABLE, 7
+C3543825	CILIARY DYSKINESIA, PRIMARY, 18
+C3543826	CILIARY DYSKINESIA, PRIMARY, 19
+C3543867	Collodion Fetus
+C3544060	Accidental exposure to product
+C3544075	Exposure via inhalation
+C3544092	Urgency frequency syndrome
+C3544103	Mycobacterial peritonitis
+C3544104	Exposure during pregnancy
+C3544160	Blister rupture
+C3544180	Accidental exposure to product by child
+C3544188	Exposure via ingestion
+C3544190	Exposure via body fluid
+C3544205	Ovarian clear cell carcinoma
+C3544214	Reversible cerebral vasoconstriction syndrome
+C3544263	Prescribed underdose
+C3544291	Congenital skin dimples
+C3544321	Treatment-resistant schizophrenia
+C3544346	Device use error
+C3544347	Intestinal fibrosis
+C3546653	response to reverse transcriptase inhibitor
+C3546688	response to temozolomide
+C3547186	response to ribavirin
+C3547187	response to metformin
+C3547188	response to fenofibrate
+C3548501	response to risperidone
+C3548505	response to antipsychotic drug
+C3548510	response to antineoplastic agent
+C3548532	response to alcohol
+C3548801	response to irinotecan
+C3548804	response to platelet aggregation inhibitor
+C3548806	response to anticoagulant
+C3549248	response to anticonvulsant
+C3549249	response to antidepressant
+C3549252	response to statin
+C3549253	response to gemcitabine
+C3549447	ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
+C3549448	ALZHEIMER DISEASE, PROTECTION AGAINST
+C3549544	ACAMPOMELIC CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
+C3549698	Coxa valga deformity
+C3549703	Retinal thinning
+C3549742	Breast cancer, lobular
+C3549779	Menstrual abnormalities
+C3549845	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1
+C3549874	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY
+C3550150	Recurrent thrombophlebitis
+C3550204	Mild growth deficiency
+C3550234	PEROXISOME BIOGENESIS DISORDER 2B
+C3550273	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER)
+C3550274	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 2
+C3550331	Aged leonine appearance
+C3550336	Multiple rows of eyelashes
+C3550430	Eclabion
+C3550478	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA
+C3550546	Depressed nasal root/bridge
+C3550569	Flat anterior chamber of eye
+C3550658	Maternal oligohydramnios
+C3550693	PEROXISOME BIOGENESIS DISORDER 3B
+C3550704	Abnormality of digit
+C3550789	THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
+C3550856	ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES
+C3550873	Hypoplasia of the calcaneus
+C3550875	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6
+C3550903	CORNELIA DE LANGE SYNDROME 5
+C3550904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36
+C3550913	MENTAL RETARDATION, X-LINKED, SYNDROMIC 32
+C3550921	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2
+C3550963	HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT
+C3550973	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
+C3551041	Short ear
+C3551052	Night blindness, stationary
+C3551381	PEROXISOMAL BIOGENESIS DISORDER 3B
+C3551426	Dystrophic fingernails
+C3551430	Sparse or absent eyebrows
+C3551431	Sparse or absent eyelashes
+C3551443	ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT
+C3551535	Mitral regurgitation, mild
+C3551587	ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
+C3551716	CORTISONE REDUCTASE DEFICIENCY 1
+C3551756	NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT
+C3551954	COENZYME Q10 DEFICIENCY, PRIMARY, 1
+C3552099	Respiratory insufficiency due to defective ciliary clearance
+C3552136	HYPOGONADOTROPHIC HYPOGONADISM 5 WITHOUT ANOSMIA
+C3552156	Hypoplasia of the semicircular canal
+C3552227	ACHROMATOPSIA 6
+C3552236	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7
+C3552335	MYASTHENIC SYNDROME, CONGENITAL, 12
+C3552343	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA
+C3552414	Deviation of the thumb
+C3552463	Very poor growth
+C3552484	Pseudoepiphysis of the thumb
+C3552491	AUTISM, SUSCEPTIBILITY TO, 14A
+C3552526	Metaphyseal sclerosis
+C3552552	COWDEN SYNDROME 2
+C3552553	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA
+C3552574	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
+C3552634	LYMPHOPROLIFERATIVE SYNDROME 1
+C3552713	Talipes foot deformities
+C3552821	EEG with photoparoxysmal response
+C3552824	Enhancement of the C-reflex
+C3552825	Jerk-locked premyoclonus spikes
+C3552852	RETINITIS PIGMENTOSA 65
+C3552853	Color vision defect, severe
+C3552917	Bone marrow smear shows erythroid hyperplasia
+C3553016	Peripheral retinal atrophy
+C3553029	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8
+C3553060	EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT
+C3553077	MICROPHTHALMIA, SYNDROMIC 11
+C3553078	Agenesis of pineal gland
+C3553084	Bilateral cleft palate
+C3553230	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl
+C3553247	MENTAL RETARDATION, AUTOSOMAL DOMINANT 14
+C3553248	MENTAL RETARDATION, AUTOSOMAL DOMINANT 15
+C3553249	COFFIN-SIRIS SYNDROME 4
+C3553250	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE
+C3553264	JOUBERT SYNDROME 17
+C3553270	DIARRHEA 6
+C3553288	HYPEREKPLEXIA 3
+C3553291	HYPEREKPLEXIA 2
+C3553298	UV-SENSITIVE SYNDROME 2
+C3553328	UV-SENSITIVE SYNDROME 3
+C3553330	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7
+C3553349	COENZYME Q10 DEFICIENCY, PRIMARY, 6
+C3553354	COENZYME Q10 DEFICIENCY, PRIMARY, 2
+C3553358	COENZYME Q10 DEFICIENCY, PRIMARY, 3
+C3553368	Limited hip extension
+C3553374	COENZYME Q10 DEFICIENCY, PRIMARY, 5
+C3553382	CORTISONE REDUCTASE DEFICIENCY 2
+C3553395	Microcolon on contrast enema
+C3553397	Meconium ileus on ultrasonography
+C3553404	AURICULOCONDYLAR SYNDROME 2
+C3553409	CARDIOMYOPATHY, DILATED, 2B
+C3553414	MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE
+C3553418	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT
+C3553449	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B
+C3553450	Profound global developmental delay
+C3553493	SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
+C3553494	CATARACT 38
+C3553512	IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY
+C3553517	CORNELIA DE LANGE SYNDROME 4
+C3553529	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10
+C3553538	BROWN-VIALETTO-VAN LAERE SYNDROME 2
+C3553549	POROKERATOSIS 7, MULTIPLE TYPES
+C3553571	Carbohydrate deficient glycoprotein syndrome type 2k
+C3553582	SECKEL SYNDROME 6
+C3553587	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY
+C3553597	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME
+C3553606	BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
+C3553607	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY
+C3553617	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1
+C3553622	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2
+C3553625	FACIAL PARESIS, HEREDITARY CONGENITAL, 3
+C3553636	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL
+C3553637	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2
+C3553645	MYASTHENIC SYNDROME, CONGENITAL, 13
+C3553656	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB
+C3553660	SOTOS SYNDROME 2
+C3553661	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
+C3553676	HETEROTAXY, VISCERAL, 6, AUTOSOMAL
+C3553696	Decreased visual acuity, nonprogressive
+C3553709	MYOPATHY, CENTRONUCLEAR, 4
+C3553719	AMYOTROPHIC LATERAL SCLEROSIS 18
+C3553720	CFHR5 DEFICIENCY
+C3553748	ADAMS-OLIVER SYNDROME 3
+C3553754	Absent toe
+C3553758	JOUBERT SYNDROME 18
+C3553762	LOEYS-DIETZ SYNDROME 4
+C3553764	Joint hyperflexibility
+C3553774	INTERSTITIAL NEPHRITIS, KARYOMEGALIC
+C3553785	WEILL-MARCHESANI SYNDROME 3
+C3553788	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
+C3553793	SPERMATOGENIC FAILURE 10
+C3553813	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8
+C3553816	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13
+C3553830	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
+C3553831	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES
+C3553841	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA
+C3553842	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA
+C3553843	HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA
+C3553844	HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA
+C3553846	JOUBERT SYNDROME 19
+C3553859	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
+C3553868	HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 3
+C3553869	HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 4
+C3553870	SECKEL SYNDROME 7
+C3553886	MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE
+C3553887	OSTEOGENESIS IMPERFECTA, TYPE XIII
+C3553915	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE
+C3553929	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER)
+C3553932	DEAFNESS, AUTOSOMAL RECESSIVE 98
+C3553936	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)
+C3553937	PEROXISOME BIOGENESIS DISORDER 4B
+C3553940	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)
+C3553941	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 5
+C3553942	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 10
+C3553943	T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS
+C3553944	USHER SYNDROME, TYPE IJ
+C3553947	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
+C3553948	PEROXISOME BIOGENESIS DISORDER 6B
+C3553950	PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8
+C3553951	PEROXISOME BIOGENESIS DISORDER 7B
+C3553958	METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA
+C3553959	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER)
+C3553960	PEROXISOME BIOGENESIS DISORDER 8B
+C3553961	AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED
+C3553977	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA
+C3553989	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5
+C3553999	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)
+C3554000	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)
+C3554001	PEROXISOME BIOGENESIS DISORDER 11B
+C3554002	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)
+C3554004	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)
+C3554018	SINOATRIAL NODE DYSFUNCTION AND DEAFNESS
+C3554021	HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
+C3554042	DIAMOND-BLACKFAN ANEMIA 11
+C3554046	LETHAL CONGENITAL CONTRACTURE SYNDROME 4
+C3554047	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4
+C3554055	PEROXISOME BIOGENESIS DISORDER 14B
+C3554067	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11
+C3554078	BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY
+C3554079	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12
+C3554105	PERRAULT SYNDROME 2
+C3554113	Thin toenail
+C3554117	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE
+C3554127	ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE
+C3554129	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13
+C3554159	DEAFNESS, AUTOSOMAL RECESSIVE 84B
+C3554163	DEAFNESS, AUTOSOMAL RECESSIVE 18B
+C3554168	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14
+C3554182	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15
+C3554195	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 14
+C3554209	Congenital pontocerebellar hypoplasia type 8
+C3554224	LEPTIN DEFICIENCY OR DYSFUNCTION
+C3554225	LEPTIN RECEPTOR DEFICIENCY
+C3554226	Congenital pontocerebellar hypoplasia type 7
+C3554235	JOUBERT SYNDROME 20
+C3554241	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3
+C3554246	FOCAL FACIAL DERMAL DYSPLASIA 4
+C3554247	CARPENTER SYNDROME 2
+C3554279	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2
+C3554306	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5
+C3554316	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15
+C3554321	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
+C3554330	NEPHROTIC SYNDROME, TYPE 7
+C3554343	MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
+C3554344	PHOSPHOHYDROXYLYSINURIA
+C3554349	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9
+C3554355	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10
+C3554366	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q
+C3554367	EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE
+C3554373	AUTISM, SUSCEPTIBILITY TO, 18
+C3554374	DYSTONIA 24
+C3554381	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10
+C3554385	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
+C3554398	SPINAL MUSCULAR ATROPHY, JOKELA TYPE
+C3554399	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F
+C3554409	HYPOTRICHOSIS 11
+C3554415	ARTHROGRYPOSIS, DISTAL, TYPE 5D
+C3554428	OSTEOGENESIS IMPERFECTA, TYPE XIV
+C3554439	ALAZAMI SYNDROME
+C3554446	BRACHYDACTYLY, TYPE A1, C
+C3554447	DYSTONIA 25
+C3554448	GAND SYNDROME
+C3554449	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
+C3554453	SPERMATOGENIC FAILURE 11
+C3554456	C3HEX, ABILITY TO SMELL
+C3554460	COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
+C3554462	MITOCHONDRIAL DNA DEPLETION SYNDROME 11
+C3554478	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8
+C3554496	LEFT VENTRICULAR NONCOMPACTION 7
+C3554499	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE
+C3554516	COWDEN SYNDROME 3
+C3554517	COWDEN SYNDROME 4
+C3554518	COWDEN SYNDROME 5
+C3554519	COWDEN SYNDROME 6
+C3554520	UROFACIAL SYNDROME 2
+C3554524	MICROPHTHALMIA, ISOLATED 8
+C3554534	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2
+C3554540	LYMPHOPROLIFERATIVE SYNDROME 2
+C3554568	Young adult onset
+C3554574	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9
+C3554576	FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE
+C3554587	Telangiectases of the cheeks
+C3554592	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9
+C3554593	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME
+C3554594	STEEL SYNDROME
+C3554599	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 6
+C3554605	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
+C3554606	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3
+C3554607	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4
+C3554608	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5
+C3554612	Contracture of the proximal interphalangeal joint of the 5th finger
+C3554614	Ulnar deviation of the 3rd finger
+C3554617	Adducted thumb
+C3554634	Light complexion
+C3554638	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11
+C3554649	CARDIOMYOPATHY, DILATED, 1II
+C3554654	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F
+C3554656	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5
+C3554657	LISSENCEPHALY 5
+C3554663	BLEEDING DISORDER, PLATELET-TYPE, 15
+C3554665	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA
+C3554669	Clavicular sclerosis
+C3554686	IMMUNODEFICIENCY 11
+C3554687	IL21R IMMUNODEFICIENCY
+C3554689	AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
+C3554690	ATAXIA-OCULOMOTOR APRAXIA 3
+C3554691	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES
+C3554721	Morning glory anomaly
+C3554724	Complete duplication of thumb phalanx
+C3554793	Loose anagen hair
+C3639956	Functional intestinal obstruction
+C3640053	Renal Artery Disease
+C3640999	High Grade Astrocytic Tumor
+C3641106	Congenital Bleeding Disorder
+C3642254	High Grade Ovarian Serous Adenocarcinoma
+C3642255	Low Grade Ovarian Serous Adenocarcinoma
+C3642304	Placental Malformation
+C3642345	Luminal A Breast Carcinoma
+C3642346	Luminal B Breast Carcinoma
+C3642347	Basal-Like Breast Carcinoma
+C3645536	Autosomal Recessive Centronuclear Myopathy
+C3645711	Congenital Osteopetrosis
+C3647143	Metastases to ovary
+C3647231	Oculocutaneous albinism type 4
+C3650625	Abnormal uterine bleeding
+C3658208	Dysbiosis
+C3658248	Hypertriglyceridemic Waist
+C3658266	Prostatic Cancer, Castration-Resistant
+C3658267	Prostatic Neoplasms, Castration-Resistant
+C3658290	Drug-Induced Acute Liver Injury
+C3658294	Hereditary Antithrombin Deficiency
+C3658299	Zellweger Spectrum
+C3658301	Mycoplasma-Induced Stevens-Johnson Syndrome
+C3658302	Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
+C3658339	Chemically-Induced Disorders
+C3661439	Hashimoto-Pritzger Disease
+C3661483	Partial Fetal Alcohol Syndrome
+C3661485	17p11.2 Monosomy
+C3661489	Autosomal Dominant Myotubular Myopathy
+C3661519	Hereditary Motor Neuronopathy
+C3661523	Congenital Intestinal Aganglionosis
+C3661525	Autosomal Recessive Chronic Granulomatous Disease
+C3661995	Peroneal Nerve Entrapment
+C3662011	Radial Nerve Entrapment
+C3662017	Combativeness
+C3662068	Static encephalopathy
+C3662259	Fetal anencephaly
+C3662483	Allergic sensitization
+C3662528	Discogenic pain
+C3665332	Primary hypertrophic cardiomyopathy
+C3665333	Keratitis-Ichthyosis-Deafness Syndrome
+C3665335	Cutis laxa, autosomal recessive
+C3665339	Bacterial sepsis of newborn
+C3665342	Progressive cone degeneration
+C3665346	Unspecified visual loss
+C3665347	Visual Impairment
+C3665349	Secondary hypothyroidism
+C3665358	Galactorrhea
+C3665365	Arteriosclerotic cardiovascular disease, NOS
+C3665382	2,8-Dihydroxyadenine Urolithiasis
+C3665386	Abnormal vision
+C3665388	Downy hair
+C3665418	Labile hypertension
+C3665419	intracranial glioma
+C3665425	Hemoglobin M Disease
+C3665439	Mature cataract
+C3665444	Neutrophilia
+C3665464	Dementia due to Alzheimer\'s disease (disorder)
+C3665472	Chemotherapies
+C3665473	Bilateral Deafness
+C3665488	Familial Osteochondritis Dissecans
+C3665489	Ovarian low malignant potential tumour
+C3665493	Snake bite
+C3665496	Congenital anomaly of cardiovascular system (disorder)
+C3665593	Melanocytic nevus of skin
+C3665596	Warts
+C3665624	Blood calcium decreased
+C3665628	Hypomineralization of enamel of tooth
+C3665629	Dental fluorosis
+C3665679	Undifferentiated attention deficit disorder
+C3665704	Congenital reticular ichthyosiform erythroderma
+C3665732	Metastatic Dermatofibrosarcoma Protuberans
+C3665804	Catheter site extravasation
+C3665810	Application site laceration
+C3665818	Medication residue present
+C3665834	Catheter site injury
+C3665852	Time perception altered
+C3665874	Gastrointestinal stoma output increased
+C3665887	Circumstance or information capable of leading to device use error
+C3665894	Therapy change
+C3668822	Hypermetria (finding)
+C3668935	Luteinizing Hormone Resistance, Female
+C3668940	Dmd-Associated Dilated Cardiomyopathy
+C3668942	Atelosteogenesis Type 3
+C3668943	Fatty Acid Hydroxylase-Associated Neurodegeneration
+C3668948	Circling behavior
+C3669048	Round cell tumor
+C3669121	11-Beta-hydroxylase deficiency
+C3669122	5-Alpha Reductase Deficiency
+C3669212	Progressive retinal atrophy
+C3669246	Mammary adenocarcinoma
+C3669395	X-Linked Chondrodysplasia Punctata 1
+C3670629	Orthokeratotic hyperkeratosis
+C3670925	Blood bicarbonate increased
+C3671377	Sebocystomatosis
+C3671688	Cyclic Hematopoesis
+C3671887	Hypernatriuria
+C3671888	Creatinine urine increased
+C3672035	Copper accumulation in liver
+C3683483	Autosomal Recessive Cerebellar Ataxia Type 1
+C3683791	Ataxia Neuropathy Spectrum
+C3683846	Chromosome 17p Deletion Syndrome
+C3686778	Biliary hyperplasia
+C3687801	Middle Eastern Respiratory Syndrome
+C3693482	Giant Cell Fibroblastoma
+C3694279	Middle East Respiratory Syndrome
+C3694531	GLYCOGEN STORAGE DISEASE IXa1
+C3695006	GLYCOGEN STORAGE DISEASE, TYPE IIIb
+C3695007	GLYCOGEN STORAGE DISEASE, TYPE IIIa
+C3695063	Charcot-Marie-Tooth disease type 4B3
+C3695086	Symptomatic carotid artery stenosis
+C3695127	Astrocytoma of brain
+C3695272	Oculocutaneous albinism type 6
+C3695318	Chronic kidney disease due to hypertension
+C3696376	3-Methylglutaconic Aciduria
+C3696898	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
+C3696954	Precapillary pulmonary hypertension
+C3697010	Ulcerative colitis in remission
+C3697119	Pulmonary arterial hypertension associated with congenital heart disease
+C3697137	Fibrous dysplasia of bone with intramuscular myxoma
+C3697172	Osteoporosis circumscripta
+C3697248	Short lower third of face
+C3697269	15q24 Microdeletion
+C3697670	Spinal cord myoclonus
+C3697716	Acute flaccid paralysis
+C3697776	Proliferative verrucous oral leukoplakia
+C3697893	Telangiectatic focal nodular hyperplasia
+C3697982	Pulmonary arterial hypertension associated with connective tissue disease
+C3698119	Inherited aminoaciduria
+C3698186	Cardiac channelopathy
+C3698226	Noninvasive carcinoma ex pleomorphic adenoma
+C3698239	Cerebral cortex myoclonus
+C3698348	Anti-D isoimmunization affecting pregnancy
+C3698493	Intraosseous mucoepidermoid carcinoma
+C3698507	Post-traumatic Porencephaly
+C3698541	Ohdo syndrome, Maat-Kievit-Brunner type
+C3699402	Alcohol abuse or dependence
+C3710589	Cap Myopathy
+C3710741	Torticollis, familial
+C3711125	Mitochondrial DNA Depletion Syndrome 8A
+C3711162	Metatropic Dysplasia Type 1
+C3711368	Surfactant Dysfunction
+C3711369	Succinate-Coa Ligase Deficiency
+C3711370	Spastic Paraplegia Type 7
+C3711371	Spastic Paraplegia Type 4
+C3711374	Nonsyndromic Deafness
+C3711376	Isodicentric Chromosome 15 Syndrome
+C3711377	Intranuclear Rod Myopathy
+C3711378	Inherited Thyroxine-Binding Globulin Deficiency
+C3711380	Huntington Disease-Like Syndrome
+C3711381	Hereditary Diffuse Leukoencephalopathy with Spheroids
+C3711382	Familial Acute Myeloid Leukemia with Mutated Cebpa
+C3711383	Early-Onset Glaucoma
+C3711384	Distal Hereditary Motor Neuropathy, Type II
+C3711385	Deoxyguanosine Kinase Deficiency
+C3711387	Autosomal Recessive Primary Microcephaly
+C3711388	African Hemochromatosis
+C3711389	Actin-Accumulation Myopathy
+C3711390	9q22.3 Microdeletion
+C3711531	Hdl Deficiency, Type 2
+C3711543	X-Linked Csnb
+C3711560	Pdgfrb-Associated Chronic Eosinophilic Leukemia
+C3711645	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
+C3711749	Nonsyndromic Holoprosencephaly
+C3711850	Opticospinal Multiple Sclerosis
+C3713418	Ppm-X Syndrome
+C3713420	Familial Hyperaldosteronism
+C3714042	46,XY Disorder of Sex Development Due To LH Defects
+C3714043	Trisomy Xq28
+C3714208	Blepharophimosis, Ptosis, and Epicanthus Inversus Type II
+C3714237	Trifunctional Protein Deficiency, Type 2
+C3714239	Bmpr1a-Related Juvenile Polyposis
+C3714240	Smad4-Related Juvenile Polyposis
+C3714497	Reactive airway disease
+C3714506	Meckel syndrome type 1
+C3714509	Nutrition Disorders
+C3714514	Infection
+C3714524	Fibromyxosarcoma
+C3714534	dowling-degos disease
+C3714542	Lymphoma, Diffuse
+C3714552	Weakness
+C3714580	Hypokalemic periodic paralysis type 1
+C3714581	Multicystic Dysplastic Kidney
+C3714582	Pneumonitis chemical
+C3714602	Staphylococcal toxic shock syndrome
+C3714618	Primary Hyperthyroidism
+C3714619	Insulin resistance syndrome
+C3714625	Neuropathic pain
+C3714636	Pneumonitis
+C3714644	Thymus Neoplasms
+C3714651	Follicular Variant Thyroid Gland Papillary Carcinoma
+C3714726	Breast operation NOS
+C3714731	Early childhood caries
+C3714739	Mesothelial Neoplasms
+C3714745	Malabsorption
+C3714753	RETINOSCHISIS 1, X-LINKED, JUVENILE
+C3714756	Intellectual Disability
+C3714757	Juvenile rheumatoid arthritis
+C3714758	Juvenile psoriatic arthritis
+C3714760	Drug-induced tardive dyskinesia
+C3714772	Recurrent fevers
+C3714796	Isolated somatotropin deficiency
+C3714844	Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia
+C3714873	Axenfeld-Rieger Syndrome, Type 1
+C3714896	SMITH-MCCORT DYSPLASIA 2
+C3714897	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE
+C3714899	SYMPHALANGISM, PROXIMAL, 1A
+C3714927	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
+C3714932	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
+C3714933	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY
+C3714934	MYOPATHY, MYOFIBRILLAR, 3
+C3714940	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18
+C3714941	OTOFACIOCERVICAL SYNDROME 1
+C3714942	OTOFACIOCERVICAL SYNDROME 2
+C3714945	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16
+C3714948	PACHYONYCHIA CONGENITA 3
+C3714949	PACHYONYCHIA CONGENITA 4
+C3714958	PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
+C3714976	ACTIVATED PI3K-DELTA SYNDROME
+C3714980	BARDET-BIEDL SYNDROME 17
+C3714987	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17
+C3714992	CANDIDIASIS, FAMILIAL, 8
+C3714994	CAP MYOPATHY 1
+C3714995	CARDIOMYOPATHY, DILATED, 1KK
+C3714998	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22
+C3715049	CEROID LIPOFUSCINOSIS, NEURONAL, 13
+C3715051	CRANIOSYNOSTOSIS 3
+C3715082	EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1
+C3715128	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
+C3715155	AMYOTROPHIC LATERAL SCLEROSIS 19
+C3715156	AMYOTROPHIC LATERAL SCLEROSIS 20
+C3715164	LEBER CONGENITAL AMAUROSIS 17
+C3715165	LEFT VENTRICULAR NONCOMPACTION 10
+C3715192	ANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME
+C3715199	RENAL-HEPATIC-PANCREATIC DYSPLASIA 1
+C3715216	RETINITIS PIGMENTOSA 66
+C3804986	Aplasia of paranasal sinuses
+C3804991	Benign genitourinary tract neoplasm
+C3805012	Ectopic pregnancy with contraceptive device
+C3805013	Embedded device
+C3805015	Stoma site haemorrhage
+C3805027	Anticoagulation drug level increased
+C3805050	Decreased intestinal transit time
+C3805051	Tendon discomfort
+C3805059	Foetal heart rate deceleration abnormality
+C3805066	Pulmonary pain
+C3805083	Portal fibrosis
+C3805089	Hyperfibrinolysis
+C3805143	Non-transfusion dependent thalassaemia
+C3805156	Chronic hepatitis C virus genotype 1
+C3805278	Extrahepatic Cholangiocarcinoma
+C3805349	CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
+C3805373	CATARACT 13 WITH ADULT i PHENOTYPE
+C3805375	ALBINISM, OCULOCUTANEOUS, TYPE VI
+C3805410	CATARACT 20, MULTIPLE TYPES
+C3805411	CATARACT 30
+C3805412	CATARACT 41
+C3805420	Popliteal pterygium
+C3805432	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION
+C3805450	Calf muscle hypoplasia
+C3805574	Increased fracture rate
+C3805604	FOVEAL HYPOPLASIA 1
+C3805618	CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
+C3805639	Generalized muscle hypertrophy
+C3805715	Short stepped shuffling gait
+C3805726	Medial rotation of the medial malleolus
+C3805742	Sebaceous gland tumors
+C3805764	Biceps aplasia
+C3805765	Quadriceps aplasia
+C3805839	Central hypoventilation
+C3805877	Hyperpigmentation in sun-exposed areas
+C3805879	PRECOCIOUS PUBERTY, CENTRAL, 1
+C3805887	Generalized osteoporosis with pathologic fractures
+C3805911	Increased cup-to-disc ratio
+C3805919	Recurrent intrapulmonary hemorrhage
+C3805969	Scapular muscle atrophy
+C3806125	Increased red cell hemolysis by shear stress
+C3806153	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
+C3806174	BARDET-BIEDL SYNDROME 18
+C3806178	Spotty hypopigmentation
+C3806179	Spotty hyperpigmentation
+C3806216	Neonatal breathing dysregulation
+C3806218	Episodic tachypnea
+C3806221	Giant melanosomes in melanocytes
+C3806226	Ectopic calcification
+C3806275	DEAFNESS AND MYOPIA
+C3806280	Laryngotracheal stenosis
+C3806283	Frequent fractures
+C3806285	Recurrent infections due to aspiration
+C3806286	Decreased sensitivity to hypoxemia
+C3806301	Scarring alopecia of scalp
+C3806306	Periarticular subcutaneous nodules
+C3806347	Hyperhomocystinemia
+C3806402	EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
+C3806403	Continuous spike and waves during slow sleep
+C3806415	Numerous congenital melanocytic nevi
+C3806428	Progressive vitiligo
+C3806442	Myoclonic spasms
+C3806443	Puffy cheeks
+C3806447	Increased urinary taurine
+C3806462	Apneic episodes precipitated by illness, fatigue, stress
+C3806467	Respiratory insufficiency due to muscle weakness
+C3806482	Recurrent respiratory infections
+C3806510	Horizontal ribs
+C3806516	Disproportionate shortening of the tibia
+C3806533	Tibial deviation of toes
+C3806554	Dysseborrheic dermatitis
+C3806565	XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME
+C3806579	CONGENITAL SHORT BOWEL SYNDROME, X-LINKED
+C3806583	Functional abnormality of the bladder
+C3806604	Infantile axial hypotonia
+C3806634	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION
+C3806644	Lower limb muscle hypotrophy
+C3806660	Enteroviral dermatomyositis syndrome
+C3806670	PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1
+C3806688	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm
+C3806702	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6
+C3806711	ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO
+C3806712	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18
+C3806722	PARKINSONISM WITH SPASTICITY, X-LINKED
+C3806730	MENTAL RETARDATION, X-LINKED 98
+C3806737	DEAFNESS, X-LINKED 6
+C3806742	MICROPHTHALMIA, SYNDROMIC 13
+C3806745	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED
+C3806746	MENTAL RETARDATION, X-LINKED 99
+C3806774	GROWTH RETARDATION, PRENATAL, WITH PROGRESSIVE PANCYTOPENIA AND CEREBELLAR HYPOPLASIA
+C3806917	CRANIOSYNOSTOSIS 4
+C3806932	PULMONARY VENOOCCLUSIVE DISEASE 1
+C3806961	Giant somatosensory evoked potentials
+C3807025	Intermittent episodes of respiratory insufficiency due to muscle weakness
+C3807131	Reduced renal corticomedullary differentiation
+C3807295	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT
+C3807306	Acute rhabdomyolysis
+C3807327	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1
+C3807521	AMYOTROPHIC LATERAL SCLEROSIS 21
+C3807541	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
+C3807567	PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME
+C3807591	Widening of cervical spinal canal
+C3807873	FOVEAL HYPOPLASIA 2
+C3807907	CAP MYOPATHY 2
+C3807980	Apneic episodes in infancy
+C3808012	CATARACT 23, MULTIPLE TYPES
+C3808022	Episodic abdominal pain
+C3808029	CATARACT 11 WITH MICROPHTHALMIA AND NEURODEVELOPMENTAL ABNORMALITIES
+C3808039	Nemaline bodies
+C3808046	Breathing dysregulation
+C3808107	CATARACT 33, MULTIPLE TYPES
+C3808115	CATARACT 12, MULTIPLE TYPES
+C3808145	LEFT VENTRICULAR NONCOMPACTION 9
+C3808166	MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT
+C3808184	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
+C3808249	Abnormality of the optic disc
+C3808270	Acetabular spurs
+C3808377	CATARACT 16, MULTIPLE TYPES
+C3808397	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1
+C3808403	Large fleshy ears
+C3808414	PERRAULT SYNDROME 3
+C3808494	CHROMOSOME 2p16.3 DELETION SYNDROME
+C3808553	Bone marrow failure syndrome 1
+C3808589	IMMUNODEFICIENCY 32A
+C3808620	HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7
+C3808667	EPISODIC PAIN SYNDROME, FAMILIAL, 1
+C3808739	MYASTHENIC SYNDROME, CONGENITAL, 8
+C3808786	ALBINISM, OCULOCUTANEOUS, TYPE VII
+C3808800	CATARACT 39, MULTIPLE TYPES
+C3808802	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4
+C3808820	Chronic hepatitis due to cryptospridium infection
+C3808844	OSTEOGENESIS IMPERFECTA, TYPE XV
+C3808874	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2
+C3808876	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING
+C3808889	POLYDACTYLY, POSTAXIAL, TYPE A6
+C3808899	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4
+C3808920	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2
+C3808935	CARDIOMYOPATHY, DILATED, 1JJ
+C3808940	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5
+C3808953	NEPHROTIC SYNDROME, TYPE 8
+C3808963	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4
+C3808964	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12
+C3808971	HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA
+C3808975	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA
+C3808977	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4
+C3808981	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA
+C3808983	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA
+C3808986	HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA
+C3808988	FANCONI ANEMIA, COMPLEMENTATION GROUP Q
+C3808991	NGLY1 deficiency
+C3809001	CATARACT 15, MULTIPLE TYPES
+C3809004	CATARACT 19, MULTIPLE TYPES
+C3809005	CARDIOFACIOCUTANEOUS SYNDROME 2
+C3809006	CARDIOFACIOCUTANEOUS SYNDROME 3
+C3809007	CARDIOFACIOCUTANEOUS SYNDROME 4
+C3809008	HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY
+C3809013	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2
+C3809031	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE
+C3809039	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
+C3809042	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13
+C3809049	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMAL DOMINANT
+C3809084	MYOFIBROMATOSIS, INFANTILE, 2
+C3809087	CILIARY DYSKINESIA, PRIMARY, 21
+C3809092	ADAMS-OLIVER SYNDROME 4
+C3809104	SYMPHALANGISM, PROXIMAL, 1B
+C3809105	PERRAULT SYNDROME 4
+C3809137	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R
+C3809147	DOWLING-DEGOS DISEASE 2
+C3809160	SHAHEEN SYNDROME
+C3809165	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3
+C3809173	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
+C3809181	Caused by mutation in the TBC1 domain family, member 24 gene (TBC1D24, 613577.0004)
+C3809192	PULMONARY HYPERTENSION, PRIMARY, 3
+C3809198	PULMONARY HYPERTENSION, PRIMARY, 4
+C3809199	PRECOCIOUS PUBERTY, CENTRAL, 2
+C3809209	NEMALINE MYOPATHY 8
+C3809210	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2
+C3809216	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14
+C3809221	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 14
+C3809233	NOONAN SYNDROME 8
+C3809236	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S
+C3809243	HYPOCALCEMIA, AUTOSOMAL DOMINANT 2
+C3809250	ESTROGEN RESISTANCE
+C3809272	LETHAL CONGENITAL CONTRACTURE SYNDROME 5
+C3809278	EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
+C3809288	LEFT VENTRICULAR NONCOMPACTION 8
+C3809289	CARDIOMYOPATHY, DILATED, 1LL
+C3809299	CONE-ROD DYSTROPHY 18
+C3809301	Foveal hyperpigmentation
+C3809309	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C
+C3809311	ATRIAL FIBRILLATION, FAMILIAL, 13
+C3809312	ATRIAL FIBRILLATION, FAMILIAL, 14
+C3809320	NEPHRONOPHTHISIS 16
+C3809327	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14
+C3809332	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY
+C3809339	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16
+C3809346	CARDIOMYOPATHY, DILATED, 1MM
+C3809352	MECKEL SYNDROME, TYPE 11
+C3809356	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3
+C3809369	PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2
+C3809374	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5
+C3809383	IMMUNODEFICIENCY 8
+C3809394	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
+C3809414	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3
+C3809420	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4
+C3809427	SPERMATOGENIC FAILURE 12
+C3809431	MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE
+C3809434	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2
+C3809443	MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE
+C3809454	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1
+C3809464	MYOPIA 22, AUTOSOMAL DOMINANT
+C3809468	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2
+C3809469	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3
+C3809470	EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
+C3809482	MYOPIA 23, AUTOSOMAL RECESSIVE
+C3809483	SPECIFIC LANGUAGE IMPAIRMENT 5
+C3809503	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS
+C3809513	AORTIC ANEURYSM, FAMILIAL THORACIC 8
+C3809522	INFANTILE LIVER FAILURE SYNDROME 1
+C3809523	MACULAR DEGENERATION, AGE-RELATED, 13
+C3809526	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17
+C3809536	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS
+C3809543	CILIARY DYSKINESIA, PRIMARY, 22
+C3809548	CILIARY DYSKINESIA, PRIMARY, 23
+C3809553	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
+C3809567	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS
+C3809583	IMMUNODEFICIENCY 12
+C3809592	FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
+C3809606	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17
+C3809609	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES
+C3809624	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18
+C3809634	CILIARY DYSKINESIA, PRIMARY, 24
+C3809641	CILIARY DYSKINESIA, PRIMARY, 25
+C3809645	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5
+C3809650	BAINBRIDGE-ROPERS SYNDROME
+C3809651	INFANTILE LIVER FAILURE SYNDROME 2
+C3809653	MACULAR DEGENERATION, AGE-RELATED, 14
+C3809654	MACULAR DEGENERATION, AGE-RELATED, REDUCED RISK OF
+C3809655	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R
+C3809665	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE
+C3809672	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37
+C3809684	CILIARY DYSKINESIA, PRIMARY, 26
+C3809686	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
+C3809691	SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY
+C3809701	CILIARY DYSKINESIA, PRIMARY, 27
+C3809706	CILIARY DYSKINESIA, PRIMARY, 28
+C3809710	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5
+C3809715	Spontaneous, recurrent epistaxis
+C3809719	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE
+C3809738	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME
+C3809753	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38
+C3809768	IMMUNODEFICIENCY 13
+C3809781	Cole disease
+C3809798	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8
+C3809803	MICROPHTHALMIA, SYNDROMIC 12
+C3809811	PARKINSON DISEASE 19A, JUVENILE-ONSET
+C3809819	CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO
+C3809824	PARKINSON DISEASE 20, EARLY-ONSET
+C3809827	Staring gaze
+C3809845	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2
+C3809853	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39
+C3809858	TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
+C3809872	PERIVENTRICULAR NODULAR HETEROTOPIA 6
+C3809874	LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 3
+C3809875	VAN MALDERGEM SYNDROME 2
+C3809877	SCHAAF-YANG SYNDROME
+C3809882	Hereditary sensory and autonomic neuropathy type 7
+C3809888	DIAMOND-BLACKFAN ANEMIA 12
+C3809893	EPISODIC PAIN SYNDROME, FAMILIAL, 2
+C3809899	EPISODIC PAIN SYNDROME, FAMILIAL, 3
+C3809910	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES
+C3809918	MULTIPLE FIBROADENOMAS OF THE BREAST
+C3809928	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III
+C3809950	COMPLEMENT FACTOR B DEFICIENCY
+C3809954	RETINITIS PIGMENTOSA 67
+C3809965	NEPHROTIC SYNDROME, TYPE 9
+C3809971	ASPARAGINE SYNTHETASE DEFICIENCY
+C3809991	IMMUNODEFICIENCY, COMMON VARIABLE, 10
+C3810001	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18
+C3810012	RIENHOFF SYNDROME
+C3810018	Bilateral coxa valga
+C3810023	VERHEIJ SYNDROME
+C3810041	ALZHEIMER DISEASE 18
+C3810042	MACULAR DEGENERATION, AGE-RELATED, 15
+C3810043	IMMUNODEFICIENCY 15
+C3810053	IMMUNODEFICIENCY 16
+C3810055	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19
+C3810062	Congenital disorder of glycosylation type 1w
+C3810072	Palmoplantar keratoderma Nagashima type
+C3810080	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
+C3810089	MEMORY QUANTITATIVE TRAIT LOCUS
+C3810090	L-FERRITIN DEFICIENCY
+C3810100	FANCONI RENOTUBULAR SYNDROME 3
+C3810107	IMMUNODEFICIENCY 17
+C3810127	IMMUNODEFICIENCY 18
+C3810128	IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT
+C3810129	IMMUNODEFICIENCY 18, SCID VARIANT
+C3810138	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13
+C3810147	IMMUNODEFICIENCY 19
+C3810160	SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE
+C3810161	SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT
+C3810170	DEAFNESS, AUTOSOMAL DOMINANT 56
+C3810175	SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY
+C3810185	ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
+C3810194	NEUROPATHY, HEREDITARY SENSORY, TYPE IF
+C3810200	SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY
+C3810212	JOUBERT SYNDROME 21
+C3810214	Elongated superior cerebellar peduncle
+C3810225	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41
+C3810230	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6
+C3810242	LEUKOENCEPHALOPATHY WITH ATAXIA
+C3810265	WARBURG MICRO SYNDROME 4
+C3810278	JOUBERT SYNDROME 22
+C3810283	SCHWANNOMATOSIS 2
+C3810285	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS
+C3810289	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE
+C3810294	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
+C3810295	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE
+C3810313	DOWLING-DEGOS DISEASE 4
+C3810324	MORBID OBESITY AND SPERMATOGENIC FAILURE
+C3810325	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS
+C3810326	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15
+C3810332	AURICULOCONDYLAR SYNDROME 3
+C3810342	IMMUNODEFICIENCY 20
+C3810343	SACRAL AGENESIS WITH VERTEBRAL ANOMALIES
+C3810349	ALZHEIMER DISEASE 19
+C3810350	Bone marrow failure syndrome 2
+C3810354	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4
+C3810359	RENAL HYPODYSPLASIA/APLASIA 2
+C3810363	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME
+C3810365	Central visual impairment
+C3810367	PREMATURE OVARIAN FAILURE 8
+C3810376	PREMATURE OVARIAN FAILURE 9
+C3810380	RETINITIS PIGMENTOSA 68
+C3810384	NEMALINE MYOPATHY 9
+C3810394	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE
+C3810400	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 19
+C3810401	ATRIAL STANDSTILL 2
+C3810402	ECULIZUMAB, POOR RESPONSE TO
+C3810403	MOYAMOYA DISEASE 6 WITH ACHALASIA
+C3810404	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO
+C3810405	POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE
+C3810406	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23
+C3810407	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5
+C3810445	Low-frequency sensorineural hearing impairment
+C3810451	Increased corneal thickness
+C3810471	Intercrural pterygium
+C3810484	Triceps aplasia
+C3810487	Increased urinary hypoxanthine
+C3811131	Estrogen Receptor Measurement
+C3811653	Experimental Organism Basal Cell Carcinoma
+C3811918	GRN-related frontotemporal dementia
+C3812396	Chronic idiopathic pulmonary fibrosis
+C3812408	Congenital renal cyst
+C3812686	Interleukin 1 Receptor Antagonist Measurement
+C3812899	Papillary carcinoma of the breast
+C3813158	Experimental Organism Islet Cell Adenoma Neoplasm
+C3814530	Skin Vesicle
+C3814825	Sudden Unexplained Infant Death
+C3814879	Phosphaturic mesenchymal tumor, benign
+C3815172	Interleukin 1 Beta Measurement
+C3824769	Lymphomas in children
+C3824872	Obesity in animals
+C3824901	Osteoporosis in children
+C3824909	Arthritis in animals
+C3825128	Respiratory infections in children
+C3825158	Learning disabled
+C3825201	Mitochondrial pathology
+C3825246	Diabetes in old age
+C3825272	Food allergy in infants
+C3825343	Diabetes in adolescence
+C3825353	Protozoan diseases
+C3825373	Hodgkin\'s disease in children
+C3825385	Epilepsy in adolescence
+C3825452	Depression in old age
+C3825462	Diabetes in youth
+C3825570	Tuberculosis in children
+C3825592	Thromboembolism in children
+C3825715	Rheumatic fever in children
+C3825718	Retina--Diseases
+C3825727	Respiratory allergy
+C3825816	Pneumonia in children
+C3825879	Otitis media in children
+C3825926	Nephrotic syndrome in children
+C3825939	Multiple sclerosis in children
+C3825986	Meningitis in children
+C3826044	Lymphoblastic leukemia in children
+C3826066	Leukemia in children
+C3826102	Iron deficiency anemia in children
+C3826128	Infection in children
+C3826233	Hearing impaired children
+C3826291	Gastroenteritis in children
+C3826394	Epilepsy in children
+C3826424	Neural tube--Abnormalities
+C3826452	Diarrhea in children
+C3826457	Diabetes in children
+C3826462	Depression in children
+C3826590	Chest--Tumors
+C3826591	Chest--Diseases
+C3826604	Celiac disease in children
+C3826614	Cardiac arrest in children
+C3826634	Bronchitis in children
+C3826743	Anemia in children
+C3826758	AIDS (Disease)
+C3826804	Abdominal pain in children
+C3827253	Classical Glioblastoma
+C3827961	Spontaneous Preterm Birth
+C3828416	Radiation Damage
+C3828464	Proneural Glioblastoma
+C3828476	Primary hypoparathyroidism
+C3828492	Pre-Gestational Diabetes
+C3828832	Neural Glioblastoma
+C3829122	Mesenchymal Glioblastoma
+C3829514	Intrapartum fever
+C3830362	Early Pregnancy Loss
+C3830467	Disseminated Bacillus Calmette-Guerin infection
+C3830518	Diabetic embryopathy
+C3831078	Clinical Chorioamnionitis
+C3831784	Acute monocytic/monoblastic leukemia
+C3836857	MECKEL SYNDROME, TYPE 8
+C3837219	Hoarding Disorder
+C3837958	Diabetes Mellitus, Ketosis-Prone
+C3838465	BASAL CELL CARCINOMA, SOMATIC
+C3838731	Familial hyperaldosteronism type 1
+C3838754	Congenital leptin deficiency
+C3838758	Familial hyperaldosteronism type 3
+C3838883	Phakomatosis cesioflammea
+C3838947	Invasive micropapillary carcinoma of breast
+C3838965	Microcystic stromal tumor
+C3839044	Compensated liver disease
+C3839062	Perivascular epithelioid tumor, malignant
+C3839184	Low grade serous carcinoma
+C3839280	High grade serous carcinoma
+C3839296	Phakomatosis cesiomarmorata
+C3839326	Kuskokwim syndrome
+C3839407	Edema of upper eyelid
+C3839507	Diminished ovarian reserve
+C3839524	Anemia in malignant neoplastic disease
+C3839609	Complex craniosynostosis
+C3839736	Sensitisation
+C3839741	Core binding factor acute myeloid leukemia
+C3839753	Abnormality of nail of toe
+C3839822	DICER1 syndrome
+C3839868	Cytogenetically normal acute myeloid leukemia
+C3839957	Hereditary cystatin C amyloid angiopathy
+C3840049	Dysexecutive syndrome
+C3840083	Late closure of anterior fontanel
+C3840085	Disorder of Achilles tendon
+C3840214	High-functioning autism
+C3840252	Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma
+C3841475	beta^+^ Thalassemia
+C3850071	Metabolic Side Effects of Drugs
+C3850072	Metabolic Side Effects of Substances
+C3850141	Acute-On-Chronic Liver Failure
+C3850148	Vascular Remodeling
+C3850153	Ovarian Reserve
+C3850155	Congenital Microtia
+C3850157	Metabolic Side Effects of Drugs and Substances
+C3852953	Pulmonary Arterial Remodeling
+C3852984	Acute Mesenteric Arterial Embolus
+C3852985	Occlusive Mesenteric Arterial Ischemia
+C3852986	Nonocclusive Mesenteric Ischemia
+C3852987	Acute Mesenteric Arterial Thrombosis
+C3853033	Allotriophagy
+C3853041	Severe Congenital Microcephaly
+C3853525	Fourth heart sound, S4
+C3853540	Aspirin exacerbated respiratory disease
+C3853541	Erosive duodenitis
+C3853548	Pdgfra-Associated Chronic Eosinophilic Leukemia
+C3853727	Tobacco user
+C3853779	Neonatal Alloimmune Thrombocytopenia
+C3853962	Enterovirus 71 infection
+C3854048	Erosive gastritis
+C3854173	Pre-renal acute kidney injury
+C3854181	Nevus sebaceous
+C3854283	Pharyngeal dysphagia
+C3854315	Pseudoprimary hyperaldosteronism
+C3854329	Primary mucoepidermoid carcinoma of lung
+C3854333	Narrowing
+C3854346	Expired product administered
+C3854347	Intentional product misuse
+C3854357	Therapeutic response changed
+C3854359	Multiple drug therapy
+C3854388	Hyperferritinaemia
+C3854430	Graft versus host disease in gastrointestinal tract
+C3854434	Bone marrow infiltration
+C3854443	Myocardial necrosis marker increased
+C3854603	FNAITP
+C3860213	Autoinflammatory disorder
+C3872560	Acute vascular graft rejection
+C3872662	Chronic active hepatitis C
+C3872848	Chronic pneumonitis of infancy
+C3873241	Amelogenesis imperfecta and gingival hyperplasia syndrome
+C3873302	Secondary pulmonary alveolar proteinosis
+C3873341	Primary adenocarcinoma of lung
+C3873361	Langerhans cell histiocytosis of skin
+C3873482	Chronic ulcerative stomatitis
+C3873491	Invasive meningococcal disease
+C3873513	Invasive listeriosis
+C3873531	Phagocytic immunodeficiency
+C3873533	Mycobacterial lymphadenitis
+C3873567	Chemotherapy-induced peripheral neuropathy
+C3874346	Skeletal malocclusion
+C3874381	Childhood nephrotic syndrome
+C3874414	Human metapneumovirus infection
+C3874418	Gastroduodenal disorder
+C3874835	Exudative edema
+C3875002	Idiopathic glomerulonephritis
+C3875007	Nodular thyroid disease
+C3875011	Familial hyperalphalipoproteinemia
+C3875046	Partial nephrogenic diabetes insipidus
+C3875058	Disorders of plasma protein metabolism
+C3875161	Anterior pituitary hormone deficiency
+C3875321	Inflammatory dermatosis
+C3875470	Improved exercise tolerance
+C3875492	Hypocalciuric hypercalcemia
+C3884338	Isolated Congenital Heart Block
+C3887461	Head and Neck Carcinoma
+C3887485	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
+C3887486	Interstitial lung fibrosis
+C3887487	Postaxial polydactyly type A
+C3887489	Clubbing of toes
+C3887494	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
+C3887496	Oligodactyly
+C3887497	Bifid Nose, Autosomal Recessive
+C3887498	Bifid ureter
+C3887499	Cyst - kidney
+C3887501	LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO
+C3887506	Hyperkinesia
+C3887513	Necrosis ischaemic
+C3887514	Chromophobe carcinoma
+C3887523	Very long chain acyl-CoA dehydrogenase deficiency
+C3887524	Skin Erosion
+C3887525	Keratosis Follicularis Spinulosa Decalvans, X-Linked
+C3887527	Fused cervical vertebrae
+C3887531	Keratoglobus
+C3887547	Central sleep apnea syndrome
+C3887548	Central Apnea
+C3887551	Memory dysfunction
+C3887558	Hemophagocytic Syndrome
+C3887608	HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
+C3887611	Restlessness
+C3887612	Psychomotor Agitation
+C3887633	Dandy-Walker Syndrome, Familial
+C3887638	Failure to thrive in infant
+C3887639	Autoimmune gastritis
+C3887640	Astrocytosis
+C3887641	Recurrent hepatitis
+C3887645	Job Syndrome
+C3887650	Adult Rickets
+C3887654	POLYARTERITIS NODOSA, CHILDHOOD-ONSET
+C3887658	PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT
+C3887662	Intraspinal Neoplasm
+C3887667	Retrocollis
+C3887668	Infection by larvae of Trichinella spiralis
+C3887678	Central Nervous System Embryonal Tumor, Not Otherwise Specified
+C3887688	Glare
+C3887709	Optic Neuropathy
+C3887743	WILMS TUMOR 2
+C3887755	Mountain Sickness
+C3887784	Urinary volume deficient
+C3887804	Feeling upset
+C3887873	Hearing Loss
+C3887875	Visual field defects
+C3887876	OSTEOARTHRITIS SUSCEPTIBILITY 1
+C3887877	Deficiency of glycerate kinase
+C3887892	Aortic Valve Disease 1
+C3887893	Encephalitic infection
+C3887896	Primary Adrenal Insufficiency
+C3887898	Infantile Spasm
+C3887929	DEAFNESS, AUTOSOMAL DOMINANT 27
+C3887937	CONE DYSTROPHY 5, X-LINKED
+C3887938	COLORBLINDNESS, PARTIAL, DEUTAN SERIES
+C3887939	MENTAL RETARDATION, X-LINKED 41
+C3887942	GLAUCOMA 1, OPEN ANGLE, B
+C3887947	HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1
+C3887948	HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2
+C3887949	Apparent mineralocorticoid excess
+C3887959	MENTAL RETARDATION, X-LINKED 49
+C3887964	POLYCYSTIC KIDNEY DISEASE 3, AUTOSOMAL DOMINANT
+C3887971	RETINAL DYSPLASIA, PRIMARY
+C3887972	GLYCOGEN CONTENT IN SKELETAL MUSCLE, INCREASED
+C3887980	COLORBLINDNESS, PARTIAL, PROTAN SERIES
+C3887992	THYROTROPIN-RELEASING HORMONE DEFICIENCY
+C3888001	HERMANSKY-PUDLAK SYNDROME 3
+C3888002	PULMONARY HYPERTENSION, PRIMARY, 2
+C3888004	HERMANSKY-PUDLAK SYNDROME 5
+C3888007	HERMANSKY-PUDLAK SYNDROME 6
+C3888018	Congenital Hyperinsulinism
+C3888023	Blood sodium decreased
+C3888024	Cacosmia
+C3888025	BRAIN PSEUDOATROPHY, REVERSIBLE, VALPROATE-INDUCED, SUSCEPTIBILITY TO
+C3888026	HERMANSKY-PUDLAK SYNDROME 8
+C3888031	SPINOCEREBELLAR ATAXIA 35
+C3888044	Nephrogenic Systemic Fibrosis
+C3888065	ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
+C3888081	L-2-hydroxyglutaric acidemia
+C3888085	PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS
+C3888087	Charcot-Marie-Tooth disease, Type 2I
+C3888088	SMITH-MCCORT DYSPLASIA 1
+C3888090	Early onset torsion dystonia
+C3888093	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2
+C3888097	CATARACT 21, MULTIPLE TYPES
+C3888098	Cataract, Autosomal Recessive Congenital 1
+C3888099	Autosomal dominant vitreoretinochoroidopathy
+C3888102	Frontotemporal Dementia With Motor Neuron Disease
+C3888103	Question mark ear
+C3888104	Glomerulopathy with fibronectin deposits
+C3888123	DEAFNESS, AUTOSOMAL DOMINANT 50
+C3888124	CATARACT 17, MULTIPLE TYPES
+C3888126	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 7
+C3888153	LONG QT SYNDROME 2, ACQUIRED, SUSCEPTIBILITY TO
+C3888192	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS
+C3888194	MIXED LINEAGE LEUKEMIA
+C3888196	IMPDH2 ENZYME ACTIVITY, VARIATION IN
+C3888197	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3
+C3888198	BESTROPHINOPATHY, AUTOSOMAL RECESSIVE
+C3888208	SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT
+C3888209	SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE
+C3888212	SECKEL SYNDROME 4
+C3888239	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
+C3888244	AICARDI-GOUTIERES SYNDROME 7
+C3888271	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID
+C3888307	CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
+C3888308	CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
+C3888309	CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
+C3888316	Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B
+C3888317	Sialidosis, type 2
+C3888318	Myopathy, familial idiopathic inflammatory
+C3888355	DEAFNESS, AUTOSOMAL RECESSIVE 93
+C3888385	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)
+C3888390	Cataract, Punctate, Progressive Juvenile-Onset
+C3888391	Nonnuclear polymorphic congenital cataract
+C3888401	ALBINISM, OCULOCUTANEOUS, TYPE V
+C3888417	CATARACT 5, MULTIPLE TYPES
+C3888418	Colicky Pain
+C3888435	Product use issue
+C3888631	Monogenic diabetes
+C3888668	Hemorrhagic Necrotic Pancreatitis
+C3888823	Intentional product use issue
+C3888846	Hyperosmolar Hyperglycemic State
+C3888880	Rhonchopathy
+C3888896	Wet age-related macular degeneration
+C3888924	Glycogen storage disease due to acid maltase deficiency, infantile onset
+C3888925	Pompe\'s disease adult onset
+C3888929	Cryptococcus gattii Infection
+C3889136	Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome
+C3889474	BARDET-BIEDL SYNDROME 16
+C3889475	BARDET-BIEDL SYNDROME 19
+C3889476	Benign Familial Convulsion
+C3889586	BCHE, FLUORIDE 1 PHENOTYPE
+C3889588	BCHE, FLUORIDE 2 PHENOTYPE
+C3889589	BCHE, K VARIANT PHENOTYPE
+C3889591	BCHE, J VARIANT PHENOTYPE
+C3889592	BCHE, H VARIANT PHENOTYPE
+C3889596	BCHE NEWFOUNDLAND PHENOTYPE
+C3889604	BCHE, SILENT 1 PHENOTYPE
+C3889605	BCHE CYNTHIANA PHENOTYPE
+C3889606	BCHE JOHANNESBURG PHENOTYPE
+C3889607	SPECTRIN SAINT CHAMOND PHENOTYPE
+C3889608	SPECTRIN TLEMCEN PHENOTYPE
+C3889609	SPECTRIN PROVIDENCE PHENOTYPE
+C3889636	SPINOCEREBELLAR ATAXIA 37
+C3889979	Periodic Fever Syndrome
+C3890167	MENTAL RETARDATION, X-LINKED 100
+C3890168	MENTAL RETARDATION, X-LINKED 101
+C3890176	Psoriatic Juvenile Idiopathic Arthritis
+C3890205	Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
+C3890218	SPHEROCYTOSIS, TYPE 2, AUTOSOMAL DOMINANT
+C3890352	P-Selectin Measurement
+C3890422	Post-Treatment Lyme Disease Syndrome
+C3890429	Liquid Tumor
+C3890591	NEPHRONOPHTHISIS 18
+C3890602	Bodily Pain
+C3890737	Autoinflammatory Syndrome
+C3890941	Acute Motor Axonal Neuropathy
+C3891114	HEMOGLOBIN CONSTANT SPRING PHENOTYPE
+C3891298	SUPEROXIDE DISMUTASE, ELEVATED EXTRACELLULAR
+C3891301	WILMS TUMOR, SUSCEPTIBILITY TO
+C3891448	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
+C3891452	SECKEL SYNDROME 8
+C3891556	CHROMOSOME Xq26.3 DUPLICATION SYNDROME
+C3891815	Arthritis, Suppurative
+C3891817	SARDINIAN HPFH PHENOTYPE
+C3892039	BARDET-BIEDL SYNDROME 5
+C3892044	Oligoarticular Arthritis
+C3892048	DEAFNESS, AUTOSOMAL DOMINANT 65
+C3892049	DEAFNESS, AUTOSOMAL RECESSIVE 101
+C3892050	DEAFNESS, AUTOSOMAL RECESSIVE 102
+C3893645	response to ACE inhibitor
+C3896578	Familial Colorectal Cancer Type X
+C3896643	New Onset Diabetes After Transplant
+C3896673	Familial Nonmedullary Thyroid Gland Carcinoma
+C3896960	Childhood Pre-B Acute Lymphoblastic Leukemia
+C3897045	Short Stature Homeobox Deficiency
+C3897558	Soluble Interleukin 6 Receptor Measurement
+C3897720	Renal Allograft Thrombosis
+C3897729	Refractory Childhood Hodgkin Lymphoma
+C3897752	Recurrent Childhood Glioblastoma
+C3897938	Persistent Oligoarticular Juvenile Idiopathic Arthritis
+C3897939	PERSISTENT MULLERIAN DUCT SYNDROME, TYPE I
+C3897940	PERSISTENT MULLERIAN DUCT SYNDROME, TYPE II
+C3898105	Oligoarticular Juvenile Idiopathic Arthritis
+C3898123	Nonerosive Arthritis
+C3898127	Non-Metastatic Childhood Soft Tissue Sarcoma
+C3898222	Mucosal Melanoma
+C3898224	Mouse Colon Adenocarcinoma
+C3898352	Mild Bronchopulmonary Dysplasia
+C3898580	Loeys-Dietz Syndrome Type 2
+C3898582	Localized Angiofollicular Lymphoid Hyperplasia
+C3898709	Intestinal-Type Sinonasal Adenocarcinoma
+C3898765	Keratitis caused by infection
+C3899154	Familial Testicular Germ Cell Tumor
+C3899155	Familial Neuroblastoma
+C3899192	Extended Oligoarticular Juvenile Idiopathic Arthritis
+C3899234	Experimental Organism Benign Keratoacanthoma
+C3899278	Early Rheumatoid Arthritis
+C3899281	Early Inflammatory Arthritis
+C3899369	Direct Extension
+C3899403	Decreased Concentration
+C3899405	Decreased Attention
+C3899503	Congenital hypogonadotropic hypogonadism
+C3899655	Childhood Langerhans Cell Histiocytosis
+C3899658	Childhood Gliosarcoma
+C3899716	Canine Osteosarcoma
+C3899731	Calcineurin Nephrotoxicity
+C3899764	CIC-DUX Sarcoma
+C3899844	C4 Deficiency
+C3900098	Adult Myelodysplastic Syndrome
+C3900100	Adult Langerhans Cell Histiocytosis
+C3900111	Acute motor sensory axonal neuropathy
+C3900122	Acid-Labile Subunit Deficiency
+C4011454	CATARACT 42
+C4011556	Abnormality of the eyebrow
+C4011726	MYOPATHY, TUBULAR AGGREGATE, 1
+C4011754	Nevus, Keratinocytic, Nonepidermolytic
+C4011788	Behavioral variant of frontotemporal dementia
+C4011926	WHITE SPONGE NEVUS 1
+C4011949	IMMUNODEFICIENCY 27A
+C4011974	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE
+C4012050	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1
+C4012054	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
+C4012146	DESBUQUOIS DYSPLASIA 1
+C4012268	TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE
+C4012359	Pointed tooth
+C4012395	Congenital disorder of glycosylation type 1y
+C4012409	PITUITARY ADENOMA 2, GROWTH HORMONE-SECRETING
+C4012454	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES
+C4012727	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1
+C4012790	Ataxia-Telangiectasisa-Like Disorder 1
+C4012968	Mild global developmental delay
+C4013035	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES
+C4013102	LEBER CONGENITAL AMAUROSIS 18
+C4013182	Caused by mutation in the transportin 3 gene (TNPO3, 610032.0001)
+C4013360	GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT
+C4013426	Bronchial carcinoid
+C4013429	Underdeveloped tragus
+C4013473	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
+C4013560	ATRIAL FIBRILLATION, FAMILIAL, 17
+C4013648	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL
+C4013699	ATRIAL FIBRILLATION, FAMILIAL, 16
+C4013764	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES
+C4013947	IMMUNODEFICIENCY 28
+C4013948	IMMUNODEFICIENCY 29
+C4013949	IMMUNODEFICIENCY 30
+C4013950	IMMUNODEFICIENCY 31A
+C4014233	IMMUNODEFICIENCY 22
+C4014234	CD4+ T-cell lymphopenia
+C4014239	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY
+C4014258	IMMUNODEFICIENCY, COMMON VARIABLE, 11
+C4014261	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16
+C4014269	ATRIAL FIBRILLATION, FAMILIAL, 15
+C4014283	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6
+C4014291	OOCYTE MATURATION DEFECT 1
+C4014294	DESBUQUOIS DYSPLASIA 2
+C4014310	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4
+C4014312	RETINITIS PIGMENTOSA 69
+C4014321	WHITE SPONGE NEVUS 2
+C4014339	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES
+C4014343	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42
+C4014347	PONTOCEREBELLAR HYPOPLASIA, TYPE 10
+C4014354	PONTOCEREBELLAR HYPOPLASIA, TYPE 9
+C4014361	ABDOMINAL OBESITY-METABOLIC SYNDROME 3
+C4014371	IMMUNODEFICIENCY 23
+C4014386	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43
+C4014393	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS
+C4014408	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
+C4014414	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24
+C4014419	AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome
+C4014425	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4
+C4014430	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 21
+C4014435	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
+C4014440	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8
+C4014449	SPERMATOGENIC FAILURE 13
+C4014454	SPERMATOGENIC FAILURE 14
+C4014476	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10
+C4014479	CULLER-JONES SYNDROME
+C4014488	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E
+C4014492	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23
+C4014501	CONE-ROD DYSTROPHY 19
+C4014507	NEPHROTIC SYNDROME, TYPE 10
+C4014516	DIARRHEA 7
+C4014528	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27
+C4014531	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 24
+C4014534	CILIARY DYSKINESIA, PRIMARY, 29
+C4014538	ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
+C4014540	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME
+C4014545	Tatton Brown Rahman syndrome
+C4014553	PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS
+C4014557	MYOPATHY, TUBULAR AGGREGATE, 2
+C4014563	HYPOTRICHOSIS 12
+C4014578	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5
+C4014584	BLEEDING DISORDER, PLATELET-TYPE, 18
+C4014588	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE
+C4014596	OROFACIAL CLEFT 14
+C4014605	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY
+C4014616	HYPOTRICHOSIS 13
+C4014617	IMMUNODEFICIENCY 24
+C4014621	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 25, WITH AMELOGENESIS IMPERFECTA
+C4014628	LYMPHEDEMA, HEREDITARY, ID
+C4014641	DIAMOND-BLACKFAN ANEMIA 13
+C4014648	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2
+C4014650	Abnormal mitochondrial morphology
+C4014656	CARDIOMYOPATHY, DILATED, 1NN
+C4014660	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20
+C4014668	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21
+C4014676	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2
+C4014681	RETINITIS PIGMENTOSA 70
+C4014690	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE
+C4014700	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY
+C4014708	WEBB-DATTANI SYNDROME
+C4014722	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET
+C4014733	Follicular hyperplasia
+C4014738	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2
+C4014742	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3
+C4014745	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44
+C4014762	MYOPIA 24, AUTOSOMAL DOMINANT
+C4014767	HYPERLIPOPROTEINEMIA, TYPE ID
+C4014780	OROFACIODIGITAL SYNDROME XIV
+C4014795	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
+C4014803	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2
+C4014812	SPINOCEREBELLAR ATAXIA 38
+C4014814	MYOPATHY, CENTRONUCLEAR, 5
+C4014821	PORETTI-BOLTSHAUSER SYNDROME
+C4014831	VESICOURETERAL REFLUX 8
+C4014833	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
+C4014848	NANOPHTHALMOS 4
+C4014856	CONE-ROD DYSTROPHY 20
+C4014863	IMMUNODEFICIENCY 27B
+C4014864	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45
+C4014869	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6
+C4014918	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2
+C4014925	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7
+C4014934	IMMUNODEFICIENCY 36
+C4014939	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2
+C4014942	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA
+C4014954	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE
+C4014958	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5
+C4014962	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
+C4014970	ADAMS-OLIVER SYNDROME 5
+C4014987	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME
+C4014988	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
+C4014993	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8
+C4014997	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1
+C4015009	Decreased plasma free carnitine
+C4015016	CILIARY DYSKINESIA, PRIMARY, 30
+C4015019	NEU-LAXOVA SYNDROME 2
+C4015029	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D
+C4015038	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC
+C4015050	DEAFNESS, AUTOSOMAL RECESSIVE 103
+C4015052	Vestibular areflexia
+C4015062	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22
+C4015067	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS
+C4015080	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE
+C4015095	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7
+C4015098	Hypoglycosylation of alpha-dystroglycan
+C4015119	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 26
+C4015124	MIRROR MOVEMENTS 3
+C4015128	POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE
+C4015129	46,XY SEX REVERSAL 9
+C4015130	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2
+C4015136	Recurrent bronchiolitis
+C4015141	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
+C4015146	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES
+C4015156	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE
+C4015160	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C
+C4015167	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30
+C4015172	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY
+C4015183	DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5
+C4015184	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12
+C4015186	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY
+C4015195	IMMUNODEFICIENCY 37
+C4015202	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR
+C4015203	Woolly scalp hair
+C4015214	CTLA4 Haploinsufficiency
+C4015235	PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO
+C4015242	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME
+C4015253	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9
+C4015261	POLYENDOCRINE-POLYNEUROPATHY SYNDROME
+C4015276	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4
+C4015283	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46
+C4015285	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
+C4015286	MACULAR DEGENERATION, EARLY-ONSET
+C4015293	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION
+C4015301	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17
+C4015307	PERRAULT SYNDROME 5
+C4015316	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27
+C4015323	LEUKODYSTROPHY, HYPOMYELINATING, 9
+C4015342	MACULAR DYSTROPHY, VITELLIFORM, 4
+C4015343	MACULAR DYSTROPHY, VITELLIFORM, 5
+C4015344	PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER
+C4015349	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S
+C4015357	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31
+C4015360	NEMALINE MYOPATHY 10
+C4015368	AORTIC ANEURYSM, FAMILIAL THORACIC 9
+C4015371	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT
+C4015388	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2
+C4015395	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9
+C4015405	BLEEDING DISORDER, PLATELET-TYPE, 19
+C4015409	OVARIAN DYSGENESIS 4
+C4015420	EPILEPSY, PROGRESSIVE MYOCLONIC 7
+C4015424	RETINAL DYSTROPHY AND OBESITY
+C4015436	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS
+C4015444	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47
+C4015447	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23
+C4015452	POLYGLUCOSAN BODY MYOPATHY 2
+C4015461	RUIJS-AALFS SYNDROME
+C4015465	Thoracic kyphoscoliosis
+C4015474	Chronic atrial and intestinal dysrhythmia
+C4015495	CEREBELLOFACIODENTAL SYNDROME
+C4015505	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
+C4015512	AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
+C4015513	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT
+C4015519	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
+C4015525	LISSENCEPHALY 6 WITH MICROCEPHALY
+C4015537	THROMBOCYTOPENIA 5
+C4015542	NEPHRONOPHTHISIS 19
+C4015552	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5
+C4015555	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9
+C4015557	AMELOGENESIS IMPERFECTA, TYPE IH
+C4015558	TEMPLE SYNDROME
+C4015596	MYASTHENIC SYNDROME, CONGENITAL, 15
+C4015597	MYASTHENIC SYNDROME, CONGENITAL, 14
+C4015619	EPILEPSY, PROGRESSIVE MYOCLONIC, 8
+C4015624	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES
+C4015635	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T
+C4015643	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24
+C4015671	LONG QT SYNDROME 14
+C4015686	LETHAL CONGENITAL CONTRACTURE SYNDROME 6
+C4015695	LONG QT SYNDROME 15
+C4015701	MECKEL SYNDROME 12
+C4015710	TENORIO SYNDROME
+C4015728	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET
+C4015729	PEELING SKIN SYNDROME 3
+C4015776	ANALBUMINEMIA BAGHDAD
+C4015779	PROSTATE CANCER, SOMATIC
+C4015780	ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES
+C4015781	ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
+C4015782	ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
+C4015841	XANTHELASMAS, PERIORBITAL
+C4015843	AMYLOIDOSIS, CARDIAC AND CUTANEOUS
+C4015884	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE
+C4015885	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL DOMINANT
+C4015898	RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
+C4015904	ACANTHOCYTOSIS DUE TO BAND 3 HT
+C4015919	RHD CATEGORY D-VII
+C4015920	RHD, WEAK D, TYPE I
+C4015931	CARBONIC ANHYDRASE I, GUAM
+C4015932	CARBONIC ANHYDRASE I DEFICIENCY
+C4015945	EPIDERMOLYSIS BULLOSA, PRETIBIAL, AUTOSOMAL RECESSIVE
+C4015948	OSTEOGENESIS IMPERFECTA, TYPE III/IV
+C4015949	OSTEOGENESIS IMPERFECTA, TYPE IIC
+C4015950	OSTEOGENESIS IMPERFECTA, TYPE I, MILD
+C4015951	BONE MINERAL DENSITY VARIATION QUANTITATIVE TRAIT LOCUS
+C4015965	MARSHALL/STICKLER SYNDROME
+C4015970	ESOPHAGEAL CARCINOMA, SOMATIC
+C4015977	ATRIAL FIBRILLATION, SOMATIC
+C4015984	CATARACT 9, AUTOSOMAL RECESSIVE
+C4015995	CATARACT 2, COPPOCK-LIKE
+C4016013	PORPHYRIA, ACUTE HEPATIC, DIGENIC
+C4016014	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1
+C4016019	DNA LIGASE I DEFICIENCY
+C4016020	DNA TOPOISOMERASE I, CAMPTOTHECIN-RESISTANT
+C4016022	AUTONOMIC NERVOUS SYSTEM DYSFUNCTION
+C4016025	NICOTINE DEPENDENCE, PROTECTION AGAINST
+C4016027	NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL RECESSIVE
+C4016028	DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT
+C4016037	ESTROGEN RECEPTOR MUTANT, TEMPERATURE-SENSITIVE
+C4016044	SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
+C4016051	L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE
+C4016052	MARFAN SYNDROME, SEVERE CLASSIC
+C4016053	MARFAN SYNDROME, MILD VARIABLE
+C4016054	MARFAN SYNDROME, NEONATAL
+C4016055	MARFAN SYNDROME, ATYPICAL
+C4016059	MARFAN SYNDROME, AUTOSOMAL RECESSIVE
+C4016097	FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
+C4016099	CANCER PROGRESSION AND TUMOR CELL MOTILITY
+C4016100	FMO3 ACTIVITY, DECREASED
+C4016104	HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
+C4016112	GLUCOCORTICOID RESISTANCE, CELLULAR
+C4016117	DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
+C4016131	MACROTHROMBOCYTOPENIA, FAMILIAL, BERNARD-SOULIER TYPE
+C4016139	MCCUNE-ALBRIGHT SYNDROME, SOMATIC, MOSAIC
+C4016140	PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
+C4016141	ICHTHYOSIS HISTRIX, CURTH-MACKLIN TYPE
+C4016143	VENTRICULAR TACHYCARDIA, SOMATIC
+C4016148	ALPHA-THALASSEMIA-2, NONDELETIONAL
+C4016158	ALPHA-THALASSEMIA, HMONG TYPE
+C4016178	DELTA-ZERO-THALASSEMIA, KNOSSOS TYPE
+C4016190	DELTA-PLUS-THALASSEMIA
+C4016207	HIV-1 VIREMIA, SUSCEPTIBILITY TO
+C4016211	IgG RECEPTOR I, PHAGOCYTIC, FAMILIAL DEFICIENCY OF
+C4016214	INFLAMMATORY BOWEL DISEASE 28
+C4016231	GLIOBLASTOMA MULTIFORME, SOMATIC
+C4016234	ERYTHROCYTOSIS, JAK2-RELATED, SOMATIC
+C4016235	EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE, WITH SEVERE PALMOPLANTAR KERATODERMA
+C4016236	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SEVERE PALMOPLANTAR KERATOSIS
+C4016241	HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
+C4016248	LONG QT SYNDROME, BRADYCARDIA-INDUCED
+C4016252	LEYDIG HYPOPLASIA, TYPE I
+C4016264	DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
+C4016266	CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
+C4016274	HYPOGONADOTROPIC HYPOGONADISM 10 WITHOUT ANOSMIA
+C4016279	LEPTIN DYSFUNCTION
+C4016282	BREAST CANCER, SOMATIC
+C4016285	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA
+C4016286	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE
+C4016294	PIEBALDISM WITH SENSORINEURAL DEAFNESS
+C4016297	PIEBALDISM, PROGRESSIVE
+C4016298	POSTAXIAL POLYDACTYLY, TYPE A1/B
+C4016299	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, SEVERE
+C4016301	NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA
+C4016304	PAPILLORENAL SYNDROME WITH MACULAR ABNORMALITIES
+C4016321	HEMOLYTIC ANEMIA, NONSPHEROCYTIC, AND NEUROLOGIC DEFICITS, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY
+C4016331	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB
+C4016334	MYOKYMIA 1 WITH HYPOMAGNESEMIA
+C4016345	PFEIFFER SYNDROME, TYPE III
+C4016346	CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
+C4016356	APNEA, POSTANESTHETIC, DUE TO BCHE, ATYPICAL-1
+C4016362	HYPERPRORENINEMIA, FAMILIAL
+C4016365	RH-MOD SYNDROME
+C4016366	RETINITIS PIGMENTOSA 4, AUTOSOMAL RECESSIVE
+C4016368	CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
+C4016375	SEROTONIN TRANSPORTER ACTIVITY, INCREASED/DECREASED
+C4016380	ANEMIA, NEONATAL HEMOLYTIC, FATAL AND NEAR-FATAL
+C4016381	ELLIPTOCYTOSIS 3 DUE TO SPECTRIN COSENZA
+C4016383	OBESITY, ASSOCIATION WITH
+C4016392	ADRENOCORTICAL TUMOR, SOMATIC
+C4016396	LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
+C4016397	CHRONIC MYELOID LEUKEMIA, RESISTANT TO IMATINIB
+C4016398	COSTELLO SYNDROME, SEVERE
+C4016403	BLADDER CANCER, TRANSITIONAL CELL, SOMATIC
+C4016406	COLON CANCER, ADVANCED, SOMATIC
+C4016412	TRIOSEPHOSPHATE ISOMERASE MANCHESTER
+C4016414	AMYOTROPHIC LATERAL SCLEROSIS 22 WITH FRONTOTEMPORAL DEMENTIA
+C4016415	TNF RECEPTOR BINDING, ALTERED
+C4016429	RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE DEAFNESS
+C4016430	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL, AUTOSOMAL RECESSIVE
+C4016431	CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH QUADRUPEDAL LOCOMOTION 1
+C4016435	BARDET-BIEDL SYNDROME 1/7, DIGENIC
+C4016438	GLUTARIC ACIDEMIA IIC, LATE-ONSET
+C4016440	MAPLE SYRUP URINE DISEASE, THIAMINE-RESPONSIVE, TYPE II
+C4016442	MAPLE SYRUP URINE DISEASE, CLASSIC, TYPE IB
+C4016443	IDUA PSEUDODEFICIENCY
+C4016444	GHOSAL HEMATODIAPHYSEAL SYNDROME
+C4016445	NEPHROLITHIASIS, X-LINKED RECESSIVE
+C4016452	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED
+C4016457	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
+C4016464	CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT, ATYPICAL
+C4016473	HYPOAGAMMAGLOBULINEMIA, X-LINKED
+C4016476	DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
+C4016477	INTERMEDIATE MUSCULAR DYSTROPHY
+C4016481	WISKOTT-ALDRICH SYNDROME, ATTENUATED
+C4016483	PELIZAEUS-MERZBACHER DISEASE, CONNATAL
+C4016484	PELIZAEUS-MERZBACHER DISEASE, MILD
+C4016494	EXUDATIVE VITREORETINOPATHY, X-LINKED
+C4016507	THROMBOCYTOPENIA, X-LINKED, WITH DYSERYTHROPOIETIC ANEMIA
+C4016508	THROMBOCYTOPENIA, X-LINKED, WITHOUT DYSERYTHROPOIETIC ANEMIA
+C4016579	RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITH DEAFNESS
+C4016581	ANDROGEN INSENSITIVITY, PARTIAL, WITH BREAST CANCER
+C4016599	EXERCISE INTOLERANCE, CARDIOMYOPATHY, AND SEPTOOPTIC DYSPLASIA
+C4016600	PARKINSONISM/MELAS OVERLAP SYNDROME
+C4016601	SIDEROBLASTIC ANEMIA, ACQUIRED IDIOPATHIC
+C4016602	CYTOCHROME c OXIDASE I DEFICIENCY
+C4016603	SEIZURES AND LACTIC ACIDOSIS
+C4016604	MYOTONIC DYSTROPHY-LIKE MYOPATHY
+C4016605	OPHTHALMOPLEGIA, ISOLATED
+C4016606	MITOCHONDRIAL MYOPATHY, ISOLATED
+C4016607	DYSTONIA, MITOCHONDRIAL
+C4016608	MYOPATHY, MITOCHONDRIAL, WITH DIABETES MELLITUS
+C4016610	CARDIOMYOPATHY, IDIOPATHIC DILATED, MITOCHONDRIAL
+C4016611	PIGMENTARY RETINOPATHY AND SENSORINEURAL DEAFNESS
+C4016612	CARDIOMYOPATHY, FATAL INFANTILE
+C4016613	CARDIOMYOPATHY, FATAL
+C4016614	ENCEPHALOPATHY, FAMILIAL PROGRESSIVE NECROTIZING
+C4016615	CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY
+C4016616	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH
+C4016617	SKELETAL MYOPATHY, RESPONSIVE TO RIBOFLAVIN
+C4016618	NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT
+C4016620	CARDIOMYOPATHY AND DEAFNESS
+C4016621	Mitochondrial neurogastrointestinal encephalomyopathy syndrome
+C4016623	MYOPATHY, MITOCHONDRIAL, LATE-ONSET
+C4016624	EPILEPSY, MITOCHONDRIAL
+C4016625	MERFF SYNDROME
+C4016626	MITOCHONDRIAL CYTOCHROME c OXIDASE DEFICIENCY
+C4016627	EXERCISE INTOLERANCE, MUSCLE PAIN, AND LACTIC ACIDEMIA
+C4016628	CEREBELLAR ATAXIA, CATARACT, AND DIABETES MELLITUS
+C4016629	NEUROGASTROINTESTINAL SYNDROME, MITOCHONDRIAL
+C4016630	ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL
+C4016631	EXERCISE INTOLERANCE AND COMPLEX III DEFICIENCY, SOMATIC
+C4016633	FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND DILATED CARDIOMYOPATHY
+C4016634	ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS
+C4016643	METAPHYSEAL ANADYSPLASIA 1, AUTOSOMAL DOMINANT
+C4016652	ATRIAL STANDSTILL 1, DIGENIC
+C4016655	CLEIDOCRANIAL DYSPLASIA, SEVERE, WITH OSTEOPOROSIS AND SCOLIOSIS
+C4016660	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1, SEVERE
+C4016662	ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY
+C4016663	ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY
+C4016672	PHOSPHOLIPASE A2, GROUP IV A, DEFICIENCY OF
+C4016683	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL RECESSIVE
+C4016684	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL DOMINANT
+C4016698	IMMUNODEFICIENCY 26 WITHOUT NEUROLOGIC ABNORMALITIES
+C4016705	LARON SYNDROME WITH ELEVATED SERUM GH-BINDING PROTEIN
+C4016706	LARON SYNDROME WITH UNDETECTABLE SERUM GH-BINDING PROTEIN
+C4016708	HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH EXACERBATION IN PREGNANCY
+C4016713	EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
+C4016717	CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS
+C4016741	IMMUNODEFICIENCY 32B
+C4016745	SCHWANNOMATOSIS 1, SOMATIC
+C4016746	FUNDUS ALBIPUNCTATUS, AUTOSOMAL RECESSIVE
+C4016748	CUSHING SYNDROME, ACTH-INDEPENDENT ADRENAL, SOMATIC
+C4016749	GLAUCOMA 1, OPEN ANGLE, A, AUTOSOMAL RECESSIVE
+C4016750	GLAUCOMA 1, OPEN ANGLE, A, DIGENIC
+C4016751	ANTERIOR SEGMENT ANOMALIES AND CATARACT
+C4016761	SEPTOOPTIC DYSPLASIA, MILD
+C4016768	OBESITY, SEVERE, AND TYPE II DIABETES
+C4016770	CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME
+C4016782	OBESITY, LATE-ONSET
+C4016791	SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
+C4016796	COLORECTAL CANCER WITH CHROMOSOMAL INSTABILITY
+C4016797	INFECTIONS, RECURRENT, ASSOCIATED WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS
+C4016802	RHABDOMYOSARCOMA, SOMATIC
+C4016806	LYMPHOMA, SOMATIC
+C4016809	WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET
+C4016816	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVASCULAR PULMONIC STENOSIS
+C4016819	MEGALOBLASTIC ANEMIA 1, FINNISH TYPE
+C4016834	CITRULLINEMIA, MILD
+C4016838	EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL DOMINANT
+C4016839	EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE
+C4016840	EXUDATIVE VITREORETINOPATHY 4, DIGENIC
+C4016851	BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
+C4016855	HYPOGONADOTROPIC HYPOGONADISM 20 WITHOUT ANOSMIA
+C4016868	PARAMYOTONIA CONGENITA/MYOTONIA CONGENITA
+C4016869	MYOTONIA CONGENITA, ATYPICAL, ACETAZOLAMIDE-RESPONSIVE
+C4016875	HYPOGONADOTROPIC HYPOGONADISM 8 WITHOUT ANOSMIA
+C4016880	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3
+C4016881	ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC
+C4016893	OBESITY, MILD, EARLY-ONSET
+C4016904	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC
+C4016908	BARDET-BIEDL SYNDROME 2/6, DIGENIC
+C4016911	FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS
+C4016917	CHONDROCALCINOSIS 2, SPORADIC
+C4016925	OBESITY, AGE AT ONSET OF
+C4016928	46,XY GONADAL DYSGENESIS, COMPLETE, DHH-RELATED
+C4016941	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE
+C4016942	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE
+C4016948	MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
+C4016951	BREAST CANCER, EARLY-ONSET
+C4016956	BARDET-BIEDL SYNDROME 2/4, DIGENIC
+C4016957	BARDET-BIEDL SYNDROME 1/2, DIGENIC
+C4016960	DIABETES MELLITUS, NONINSULIN-DEPENDENT, ASSOCIATION WITH
+C4016970	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5
+C4016973	NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
+C4016981	GLYCOGEN STORAGE DISEASE II, ADULT FORM
+C4016983	HYPOGONADOTROPIC HYPOGONADISM 18 WITH ANOSMIA
+C4016986	COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR
+C4016988	GM2-GANGLIOSIDOSIS, CHRONIC
+C4016991	SULFITE OXIDASE DEFICIENCY, ISOLATED
+C4016992	CHEDIAK-HIGASHI SYNDROME, CHILDHOOD TYPE
+C4016993	CHEDIAK-HIGASHI SYNDROME, ADULT TYPE
+C4017048	GALACTOSE EPIMERASE DEFICIENCY, SEVERE
+C4017056	ISOVALERIC ACIDEMIA, TYPE I
+C4017059	CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED
+C4017062	HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
+C4017065	Autosomal dominant keratitis
+C4017066	ANIRIDIA, ATYPICAL
+C4017067	FOVEAL HYPOPLASIA 1 WITH CATARACT
+C4017072	HYPOGONADOTROPIC HYPOGONADISM 3 WITHOUT ANOSMIA
+C4017074	PSORIASIS 2, PUSTULAR
+C4017084	SHORT-RIB THORACIC DYSPLASIA 10 WITHOUT POLYDACTYLY
+C4017085	SHORT-RIB THORACIC DYSPLASIA 10 WITH POLYDACTYLY
+C4017087	CYSTIC PARATHYROID ADENOMA, SOMATIC
+C4017089	LONG QT SYNDROME 1, RECESSIVE
+C4017091	ARYLSULFATASE A PSEUDODEFICIENCY
+C4017093	METACHROMATIC LEUKODYSTROPHY, LATE-ONSET
+C4017094	METACHROMATIC LEUKODYSTROPHY, SEVERE
+C4017095	ARYLSULFATASE A PSEUDODEFICIENCY, SEVERE
+C4017096	ARYLSULFATASE A PSEUDODEFICIENCY, INTERMEDIATE
+C4017102	ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY
+C4017105	NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM
+C4017106	NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM
+C4017114	GLYCOGEN STORAGE DISEASE IV, NONPROGRESSIVE HEPATIC
+C4017116	GLYCOGEN STORAGE DISEASE IV, COMBINED HEPATIC AND MYOPATHIC
+C4017117	GLYCOGEN STORAGE DISEASE IV, FATAL PERINATAL NEUROMUSCULAR
+C4017118	ADULT POLYGLUCOSAN BODY NEUROPATHY
+C4017127	CANAVAN DISEASE, MILD
+C4017152	MAPLE SYRUP URINE DISEASE, INTERMEDIATE, TYPE IA
+C4017156	MCARDLE DISEASE, MILD
+C4017161	RENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS
+C4017171	TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE
+C4017174	OBESITY, VARIATION IN
+C4017192	DOPAMINE BETA-HYDROXYLASE ACTIVITY, PLASMA
+C4017220	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 49
+C4017238	DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST
+C4017252	MUCOPOLYSACCHARIDOSIS, TYPE VI, INTERMEDIATE
+C4017253	MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE
+C4017254	MUCOPOLYSACCHARIDOSIS, TYPE VI, MILD
+C4017257	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH MENTAL RETARDATION
+C4017260	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH INTRACELLULAR INCLUSIONS
+C4017271	factor V Hong Kong phenotype
+C4017275	SPHEROCYTOSIS, TYPE 1, AUTOSOMAL RECESSIVE
+C4017279	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1, SUSCEPTIBILITY TO
+C4017280	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY
+C4017281	COPROPORPHYRIA, DIGENIC
+C4017284	BLOOD GROUP--LUTHERAN NULL
+C4017292	GALACTOSIALIDOSIS, LATE INFANTILE
+C4017293	GALACTOSIALIDOSIS, ADULT
+C4017294	GALACTOSIALIDOSIS, EARLY INFANTILE
+C4017301	ASPARTYLGLUCOSAMINURIA, FINNISH TYPE
+C4017302	HYPOGONADOTROPIC HYPOGONADISM 22 WITH ANOSMIA
+C4017305	GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA
+C4017308	HOMOCYSTINURIA, PYRIDOXINE-NONRESPONSIVE
+C4017311	TRANSCOLABAMIN II DEFICIENCY
+C4017330	LIPOMA, SOMATIC
+C4017331	ANGIOFIBROMA, SOMATIC
+C4017360	APPARENT MINERALOCORTICOID EXCESS, MILD
+C4017372	SHORT-RIB THORACIC DYSPLASIA WITHOUT POLYDACTYLY
+C4017378	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH FRACTURES
+C4017380	RETINITIS PIGMENTOSA WITHOUT SITUS INVERSUS
+C4017389	FOVEAL HYPOPLASIA 2 AND OPTIC NERVE MISROUTING WITH OR WITHOUT ANTERIOR SEGMENT DYSGENESIS
+C4017494	BETA-KNOSSOS-THALASSEMIA
+C4017510	BETA-MALAY-THALASSEMIA
+C4017522	BETA-SHOWA-YAKUSHIJI THALASSEMIA
+C4017525	BETA-PLUS-THALASSEMIA, DOMINANT
+C4017528	BETA-THALASSEMIA, LERMONTOV TYPE
+C4017537	GREEK HPFH PHENOTYPE
+C4017538	BRITISH HPFH PHENOTYPE
+C4017543	BCHE, DIBUCAINE-RESISTANT I PHENOTYPE
+C4017544	CHE*70G PHENOTYPE
+C4017545	BCHE*70G PHENOTYPE
+C4017546	BCHE ANN ARBOR PHENOTYPE
+C4017547	CHE*FS117 PHENOTYPE
+C4017548	BCHE*FS117 PHENOTYPE
+C4017549	BCHE, FLUORIDE-RESISTANT I PHENOTYPE
+C4017550	CHE*243M PHENOTYPE
+C4017551	BCHE*243M PHENOTYPE
+C4017552	BCHE, FLUORIDE-RESISTANT II PHENOTYPE
+C4017553	CHE*390V PHENOTYPE
+C4017554	BCHE*390V PHENOTYPE
+C4017555	BCHE, QUANTITATIVE K POLYMORPHISM PHENOTYPE
+C4017556	CHE*539T PHENOTYPE
+C4017557	BCHE*539T PHENOTYPE
+C4017558	BCHE, QUANTITATIVE J VARIANT PHENOTYPE
+C4017559	BCHE, QUANTITATIVE H VARIANT PHENOTYPE
+C4017560	BCHE*FS126 PHENOTYPE
+C4017564	C7 AND C6 DEFICIENCY, COMBINED SUBTOTAL
+C4017626	MITOCHONDRIAL COMPLEX IV DEFICIENCY WITH RECURRENT MYOGLOBINURIA
+C4017627	DIABETES MELLITUS, NONINSULIN-DEPENDENT, MATERNALLY TRANSMITTED
+C4017656	ALDOSTERONE-PRODUCING ADRENAL ADENOMA, SOMATIC
+C4017657	FOVEAL HYPOPLASIA 1 WITH OR WITHOUT ANTERIOR SEGMENT ANOMALIES
+C4017660	BARDET-BIEDL SYNDROME 6/10, DIGENIC
+C4017668	VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
+C4017784	HYDROCEPHALUS, X-LINKED, WITH HIRSCHSPRUNG DISEASE
+C4017829	MICROVASCULAR COMPLICATIONS OF DIABETES, PROTECTION AGAINST
+C4017844	HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, INCREASED PERINATAL TRANSMISSION OF
+C4017847	METACHROMATIC LEUKODYSTROPHY, MILD
+C4018849	Abnormal fear/anxiety-related behavior
+C4018858	J wave
+C4018860	Pituitary growth hormone cell adenoma
+C4018871	Abnormality of the respiratory system
+C4018978	Unilateral Breast Neoplasms
+C4019039	Intestinal obstruction co-occurrent and due to decreased peristalsis
+C4019167	Speech Sound Disorders
+C4019436	Antiphospholipid antibody positivity
+C4020689	Insertional polydactyly
+C4020690	Abnormality of peripheral nerve conduction
+C4020691	Partial/complete duplication of the phalanges of the hallux
+C4020694	Constricted helix type IV
+C4020695	Increased serum bile acid concentration during pregnancy, resolves
+C4020697	Giant cell hepatitis on liver biopsy
+C4020699	Congenital dermal melanocytosis
+C4020700	Intestinal hypoperistalsis
+C4020703	Cystic lung lesion
+C4020704	Sertoli cell neoplasm
+C4020705	Glomerulocystic kidney disease
+C4020707	Aplasia/Hypoplasia of the nares
+C4020709	Neoplasia of the biliary tract
+C4020713	Penile melanosis
+C4020718	Wide nasal ridge
+C4020719	Dilated cerebral perivascular spaces
+C4020726	Abnormal social interactions
+C4020730	Increased intramyocellular lipid droplets
+C4020731	Abnormality of creatine metabolism
+C4020732	Mitochondrial abnormalities
+C4020733	Abnormal acetylcarnitine profile
+C4020734	Nystagmus, continuous pendular
+C4020735	Elevated urinary vanillylmandelic acid
+C4020736	Elevated urinary homovanillic acid
+C4020737	Respiratory complex deficiency, ATPase deficiency
+C4020738	Respiratory complex III deficiency
+C4020739	Respiratory complex I deficiency
+C4020742	Familial primary hyperaldosteronism type 2
+C4020743	Glucocorticoid-remediable familial primary aldosteronism
+C4020744	Familial primary hyperaldosteronism type 1
+C4020747	Biopsy shows villous atrophy
+C4020749	Head circumference small for gestational age
+C4020753	Intimal fibrosis
+C4020755	Abnormality of fontanelles
+C4020756	Unilateral coronal craniosynostosis
+C4020757	Aplasia of the eyelids
+C4020759	Pointed incisor
+C4020765	EEG with 3-4-Hz spike waves
+C4020768	Abnormal ossification involving bones of the feet
+C4020769	Fusion of thamali
+C4020770	Hypoplasia of the premaxilla
+C4020771	Neoplasia of the skeletal system
+C4020772	Hypoplastic palate
+C4020773	Hypoplasia/agenesis of distal phalanges of toes
+C4020777	Underdeveloped brows
+C4020778	maternal hyperglycemia
+C4020779	Absence of the parotid gland
+C4020781	Fusion of the terminal and middle phalanges of the 5th finger
+C4020786	Diminished diaphragmatic motion
+C4020787	Subcoronal hypospadias
+C4020788	Xy female gonadal dysgenesis
+C4020789	Abnormal sperm development
+C4020790	Medullary sponge kidney disease
+C4020791	Absent or rudimentary fallopian tubes
+C4020792	Snail ear
+C4020793	Shell ear
+C4020794	Severe cupped ear, type III
+C4020795	Mini ear
+C4020796	Ear, grade II dysplasia
+C4020797	Microtia, second degree
+C4020798	Moderate neural deafness
+C4020799	Midthoracic hemivertebrae
+C4020800	Decreased activity of mitochondrial complex IV
+C4020801	Respiratory complex II deficiency
+C4020802	Abnormal zinc metabolism
+C4020803	Abnormal type II collagen
+C4020804	Abnormal hyaline collagen
+C4020805	Athyroidal hypothyroidism
+C4020808	Everted lower eyelids
+C4020810	White matter dysmyelination/demyelination
+C4020811	Length dependent motor neuropathy
+C4020812	Abnormality of the anterior horn cell
+C4020813	Increased gastric cancer
+C4020815	Agenesis of incisor
+C4020816	Absence of incisors
+C4020817	Crescent/chevron-shaped pulp chambers
+C4020821	Aplasia of the interphalangeal creases
+C4020824	Absence of B cells
+C4020825	Irregular capital femoral epiphysis
+C4020827	Neonatal hemolytic anemia
+C4020828	Increased spinal bone density
+C4020830	Fatty acids abnormal
+C4020835	Flared humerus
+C4020837	EMG: spontaneous, repetitive electrical activity
+C4020838	Relative short stature
+C4020839	Multiple vertebral anomalies
+C4020840	Abnormal vertebral bodies
+C4020841	EMG: decrement at repetitive stimulation
+C4020843	Abnormal urinary amino-acid findings
+C4020844	Bullet vertebral body
+C4020845	Orotidine-5-prime-phosphate decarboxylase defect
+C4020846	Prone to bacterial infection
+C4020847	Abnormality of pelvic girdle bone morphology
+C4020848	Aneurysmal disease
+C4020849	Bowed and upward slanting eyebrows
+C4020850	Generalized trichodysplasia
+C4020851	Cortical white matter abnormalities seen on MRI
+C4020852	Involvement of the corticospinal pathways
+C4020853	Ataxic tremor
+C4020854	Neuro-degenerative disease
+C4020855	Respiratory function loss
+C4020856	Terminal tremor
+C4020857	Neuronal lipopigments
+C4020858	Choreatic disease
+C4020859	Pyramidal tract disease
+C4020860	Supratentorial atrophy
+C4020861	Depressed philtrum
+C4020862	Abnormality of cells of the erythroid lineage
+C4020863	Blood platelet disease
+C4020865	Fibular polydactyly
+C4020866	Equinovalgus deformity
+C4020867	Persistant truncus arteriosus
+C4020868	Elevated heart rate
+C4020869	Abnormality of abdomen morphology
+C4020870	Abnormality of the hip joint
+C4020871	Dystonic disease
+C4020872	Cranial nerve abnormality
+C4020873	Infratentorial atrophy
+C4020874	No development of motor milestones
+C4020875	Mental and motor retardation
+C4020876	Dull intelligence
+C4020878	Diffusely thickened skin
+C4020879	Stippled pigmentation
+C4020880	Ruddy face
+C4020882	Abnormality of the backbone
+C4020883	Hypoplastic sternum
+C4020884	Anxiety disease
+C4020885	Difficulties with night vision
+C4020886	Defective or absent horizontal voluntary eye movements
+C4020887	Photodysphoria
+C4020888	Epithelial corneal erosions
+C4020889	Cornela disease
+C4020890	Notched nasal tip
+C4020891	Pinched nasal bridge
+C4020892	Capuchin ears
+C4020894	Submucous clefting
+C4020895	Genitourinary dysplasia
+C4020896	Abnormality of genital physiology
+C4020897	Uroureter
+C4020898	Overactive bladder syndrome
+C4020902	Abnormal urine alpha-ketoglutarate concentration
+C4020904	Myelin tomacula
+C4020907	Metaphyseal dappling
+C4020908	Hypointensity of cerebral white matter on MRI
+C4020911	Herpetiform corneal ulceration
+C4020912	Flared humeral metaphysis
+C4020918	Dysharmonic bone age
+C4020919	Dense metaphyseal bands
+C4020922	Enlarged fossa interpeduncularis
+C4020947	Plantar telangiectasia
+C4020948	Palmar telangiectasia
+C4020952	Fingernail dysplasia
+C4020953	Abnormality of vertebral epiphysis morphology
+C4020957	Abnormal trabecular bone morphology
+C4020958	Rough bone trabeculation
+C4020959	Abnormal pigmentation of the oral mucosa
+C4020960	Abnormality of nail color
+C4020961	Displacement of the external urethral meatus
+C4020962	Enlarged thorax
+C4020963	Absent nares
+C4020966	Abnormal vertebral ossification
+C4020968	Abnormal localization of kidney
+C4020969	Inflammatory abnormality of the eye
+C4020971	Abnormality of lower limb joint
+C4021006	Short distal phalanx of the 5th toe
+C4021020	Non-midline cleft lip
+C4021024	Muscle fiber tubular inclusions
+C4021027	Abnormality of the medullary cavity of the long bones
+C4021028	Pseudo-fractures
+C4021029	Conspicuously happy disposition
+C4021038	Abnormal circulating renin
+C4021047	Impaired visually enhanced vestibulo-ocular reflex
+C4021050	Dilated superficial abdominal veins
+C4021076	Iron accumulation in brain
+C4021081	Absent nail of hallux
+C4021082	Fatty replacement of skeletal muscle
+C4021084	Aplasia of optic nerve
+C4021085	Abnormality of brain morphology
+C4021086	Abnormal biliary tract morphology
+C4021087	Abnormal social behavior
+C4021093	Decreased serum complement C9
+C4021094	Type II transferrin isoform profile
+C4021095	Abnormal hypothalamus morphology
+C4021097	Reduced prothrombin activity
+C4021098	Abnormal natural killer morphology
+C4021099	Orthostatic tachycardia
+C4021100	Increased fibular diameter
+C4021103	Abnormality of exocrine pancreas physiology
+C4021107	Non-obstructive azoospermia
+C4021108	Anterior wedging of T12
+C4021109	Long cerebellar peduncles
+C4021111	Short 5th toe
+C4021124	Adrenocorticotropic hormone excess
+C4021133	Left ventricular noncompaction cardiomyopathy
+C4021152	Abnormal CNS myelination
+C4021154	Enlarged cochlear aqueduct
+C4021157	Generalized abnormality of skin
+C4021160	Posterior plagiocephaly
+C4021161	Multiple suture craniosynostosis
+C4021164	Bicoronal synostosis
+C4021167	Tapered toe
+C4021168	Slender toe
+C4021169	Partial absence of toe
+C4021174	Microtia, third degree
+C4021175	Microtia, first degree
+C4021186	Underdeveloped antitragus
+C4021189	Underdeveloped superior crus of antihelix
+C4021206	Chromosomal breakage induced by ionizing radiation
+C4021216	EEG with persistent abnormal rhythmic activity
+C4021217	EEG with generalized slow activity
+C4021219	Multifocal epileptiform discharges
+C4021222	Impaired temperature sensation
+C4021224	Abnormality of the twelfth cranial nerve
+C4021225	Abnormality of the eleventh cranial nerve
+C4021228	Gonadal neoplasm
+C4021232	Absent metatarsal bone
+C4021234	2-4 toe syndactyly
+C4021235	1-5 toe syndactyly
+C4021237	Nuclear pulverulent cataract
+C4021240	Elevated tissue non-specific alkaline phosphatase
+C4021241	Abnormal foot bone ossification
+C4021242	Hypoplasia of the zygomatic bone
+C4021243	Abnormality of thalamus morphology
+C4021244	Abnormal hand bone ossification
+C4021245	Patchy variation in bone mineral density
+C4021249	Anterior pituitary agenesis
+C4021250	Intracranial cystic lesion
+C4021251	Dysplasia of the femoral head
+C4021252	Abnormality of the epiphysis of the femoral head
+C4021253	Undulate clavicles
+C4021254	Cutaneous finger syndactyly
+C4021257	Aplasia of the tarsal bones
+C4021259	Limitation of knee mobility
+C4021260	Long metacarpals
+C4021262	Absent palmar crease
+C4021264	Abnormal ventricular septum morphology
+C4021292	Flexion contracture of the 4th toe
+C4021296	Flexion contracture of the 2nd toe
+C4021299	Abnormality of dentin
+C4021301	Ivory epiphyses of the distal phalanges of the hand
+C4021302	Aplasia of the proximal phalanges of the hand
+C4021305	Small epiphyses of the phalanges of the hand
+C4021326	Aplasia/Hypoplasia of the distal phalanges of the toes
+C4021333	Mesoaxial foot polydactyly
+C4021335	Short distal phalanx of hallux
+C4021337	Partial duplication of the distal phalanx of the hallux
+C4021343	Broad hallux phalanx
+C4021360	Partial duplication of the distal phalanx of the 3rd finger
+C4021365	Partial duplication of the distal phalanx of the 2nd finger
+C4021370	Duplication of thumb phalanx
+C4021371	Absent mandible
+C4021375	Attached earlobe
+C4021377	Prominent crus of helix
+C4021383	Broad middle phalanx of finger
+C4021385	Abnormality of the distal phalanx of finger
+C4021386	Abnormality of the elbow
+C4021390	Symphalangism affecting the phalanges of the hand
+C4021391	Broad phalanges of the hand
+C4021392	Fibrous syngnathia
+C4021395	Abnormality of the antihelix
+C4021398	Metacarpal synostosis
+C4021399	Finger symphalangism
+C4021418	Absent proximal phalanx of thumb
+C4021427	Complete duplication of distal phalanx of the thumb
+C4021431	Abnormality of the vestibulocochlear nerve
+C4021432	Triangular shaped proximal phalanx of the 2nd finger
+C4021435	Short middle phalanx of the 2nd finger
+C4021438	Short distal phalanx of the 2nd finger
+C4021454	Triangular epiphysis of the proximal phalanx of the 2nd finger
+C4021455	Enlarged epiphysis of the proximal phalanx of the 2nd finger
+C4021465	Pseudoepiphyses of the 2nd finger
+C4021469	Short 3rd finger
+C4021480	Pseudoepiphyses of the 3rd finger
+C4021487	Triangular epiphysis of the proximal phalanx of the 3rd finger
+C4021488	Enlarged epiphysis of the proximal phalanx of the 3rd finger
+C4021490	Triangular epiphysis of the middle phalanx of the 3rd finger
+C4021499	Short distal phalanx of the 4th finger
+C4021515	Deviation of the 5th finger
+C4021520	Abnormal cerebral artery morphology
+C4021521	Depletion of mitochondrial DNA in muscle tissue
+C4021523	Upper limb amyotrophy
+C4021524	Abnormality of adipose tissue
+C4021525	Abnormal pelvis bone ossification
+C4021526	Exercise-induced rhabdomyolysis
+C4021527	Abdominal wall muscle weakness
+C4021528	Pelvic girdle amyotrophy
+C4021533	Severe sensorineural hearing impairment
+C4021534	Adult onset sensorineural hearing impairment
+C4021535	Infantile sensorineural hearing impairment
+C4021537	Congenital conductive hearing loss
+C4021538	Mild neurosensory hearing impairment
+C4021539	Posterior helix pit
+C4021541	Anterior beaking of lumbar vertebrae
+C4021542	Recurrent loss of toenails and fingernails
+C4021545	Immunoglobulin IgG2 deficiency
+C4021546	Abnormal mitochondria in muscle tissue
+C4021547	Neutrophil inclusion bodies
+C4021548	Adrenocorticotropin receptor defect
+C4021550	Elevated circulating follicle stimulating hormone level
+C4021551	Absence of secondary sex characteristics
+C4021552	Asymptomatic hyperammonemia
+C4021553	Periodic hypokalemic paresis
+C4021554	Irregular tarsal ossification
+C4021558	Enlarged flash visual evoked potentials
+C4021559	Retinitis pigmentosa inversa
+C4021560	Posterior Y-sutural cataract
+C4021561	Electronegative electroretinogram
+C4021564	Hypoplasia of the lacrimal puncta
+C4021565	Punctate opacification of the cornea
+C4021566	Progressive cataract
+C4021567	Central heterochromia
+C4021568	Cortical pulverulent cataract
+C4021569	Central retinal vessel vascular tortuosity
+C4021570	Undetectable light- and dark-adapted electroretinogram
+C4021571	Abnormal vestibulo-ocular reflex
+C4021573	Patchy hypo- and hyperpigmentation
+C4021574	Decreased number of sweat glands
+C4021575	Diffuse palmoplantar hyperkeratosis
+C4021578	Chronic axonal neuropathy
+C4021580	Progressive extrapyramidal muscular rigidity
+C4021581	Distal upper limb amyotrophy
+C4021582	Distal peripheral sensory neuropathy
+C4021583	Impaired distal tactile sensation
+C4021584	Frontotemporal cerebral atrophy
+C4021585	Impaired distal proprioception
+C4021589	Absent glenoid fossa
+C4021591	Reduced number of intrahepatic bile ducts
+C4021592	Unilateral primary pulmonary dysgenesis
+C4021597	Delayed patellar ossification
+C4021598	Distal tibial bowing
+C4021599	Flat distal femoral epiphysis
+C4021603	Widely spaced primary teeth
+C4021605	Shortening of all middle phalanges of the toes
+C4021606	Mesoaxial hand polydactyly
+C4021607	Proximal symphalangism of hands
+C4021608	Shortening of all distal phalanges of the fingers
+C4021609	Delayed phalangeal epiphyseal ossification
+C4021610	Bilateral lung agenesis
+C4021611	Abnormality of epiphysis morphology
+C4021618	Polysyndactyly of hallux
+C4021619	Ulnar radial head dislocation
+C4021621	Absent fourth finger distal interphalangeal crease
+C4021622	2-4 toe cutaneous syndactyly
+C4021623	Neonatal epiphyseal stippling
+C4021625	Spinal stenosis with reduced interpedicular distance
+C4021626	Lethal skeletal dysplasia
+C4021627	Bilateral triphalangeal thumbs
+C4021629	Absent ossification of calvaria
+C4021630	Broad long bones
+C4021631	Abnormality of the tracheobronchial system
+C4021632	Facial telangiectasia in butterfly midface distribution
+C4021633	Patchy palmoplantar keratoderma
+C4021634	Abnormality of bone marrow cell morphology
+C4021636	Decreased serum complement factor B
+C4021637	Abnormality of the nares
+C4021638	Absent nasal septal cartilage
+C4021640	Intestinal hypoplasia
+C4021641	Absence of intrinsic factor
+C4021642	Abnormality of the Achilles tendon
+C4021643	Impairment of galactose metabolism
+C4021645	Recurrent abdominal hernia
+C4021646	Prolonged bleeding after surgery
+C4021648	Fava bean-induced hemolytic anemia
+C4021649	Short fifth metatarsal
+C4021651	Hypoplasia of the nasal bone
+C4021652	Anterior wedging of T11
+C4021654	Precocious atherosclerosis
+C4021655	Abnormality of the sense of smell
+C4021656	Abnormality of fatty-acid metabolism
+C4021657	Abnormality of bone mineral density
+C4021661	Abnormality of macrophages
+C4021664	Abnormality of the abdominal wall
+C4021681	Short distal phalanx of the 3rd finger
+C4021684	Sclerosis of hand bone
+C4021688	Ulnar metaphyseal irregularity
+C4021692	Radial metaphyseal irregularity
+C4021695	Hypoplastic radial head
+C4021723	Short middle phalanx of toe
+C4021724	Cytochrome C oxidase-negative muscle fibers
+C4021725	Reduced activity of N-acetylglucosaminyltransferase II
+C4021726	EMG: myopathic abnormalities
+C4021727	EMG: neuropathic changes
+C4021728	EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
+C4021729	Increased circulating very-low-density lipoprotein levels
+C4021730	Junctional split
+C4021731	Pyrimidine-responsive megaloblastic anemia
+C4021732	Reduced prothrombin consumption
+C4021733	Hyperlysinuria
+C4021734	Abnormality of mitochondrial metabolism
+C4021735	Abnormality of the hip bone
+C4021736	Decreased methylcobalamin
+C4021737	Chromosomal breakage induced by crosslinking agents
+C4021738	Abnormality of the pubic bone
+C4021739	Abnormality of the acetabulum
+C4021740	Increased circulating ACTH level
+C4021741	Abnormal cortical bone morphology
+C4021742	Abnormality of the humerus
+C4021743	Abnormality of the patella
+C4021744	Abnormality of the wrist
+C4021745	Abnormality of the musculature
+C4021746	Abnormality of the ilium
+C4021748	Abnormality of B cells
+C4021749	Cystic angiomatosis of bone
+C4021750	Abnormality of femur morphology
+C4021751	Recurrent Klebsiella infections
+C4021752	Recurrent Aspergillus infections
+C4021753	Abnormality of the immune system
+C4021754	Abnormality of the sella turcica
+C4021756	Thickened superior cerebellar peduncle
+C4021757	EEG with polyspike wave complexes
+C4021758	Delayed CNS myelination
+C4021759	Generalized myoclonic seizures
+C4021760	Abnormality of lung morphology
+C4021761	Morphological abnormality of the pyramidal tract
+C4021762	Abnormality of the cerebrum
+C4021767	Decreased platelet glycoprotein IIb-IIIa
+C4021768	Abnormality of metabolism/homeostasis
+C4021769	Short 2nd toe
+C4021770	Clinodactyly of toe
+C4021771	Short distal phalanx of toe
+C4021772	Bifid distal phalanx of toe
+C4021774	Camptodactyly of toe
+C4021775	High-frequency sensorineural hearing impairment
+C4021776	Abnormality of the voice
+C4021777	Abnormality of the larynx
+C4021779	Abnormality of the calf musculature
+C4021780	Abnormality of the liver
+C4021781	Abnormal nervous system electrophysiology
+C4021782	Abnormality of the fingernails
+C4021784	Interphalangeal joint contracture of finger
+C4021785	Abnormality of the metacarpal bones
+C4021786	Atypical scarring of skin
+C4021787	Abnormal diaphysis morphology
+C4021789	Abnormality of the vertebral column
+C4021790	Abnormality of the skeletal system
+C4021792	Abnormality of the clavicle
+C4021794	Abnormality of the adrenal glands
+C4021795	Abnormality of Krebs cycle metabolism
+C4021796	Renal steatosis
+C4021797	Abnormality of the thorax
+C4021798	Impaired use of nonverbal behaviors
+C4021799	Restrictive behavior
+C4021800	Abnormality of dental enamel
+C4021801	Lacrimation abnormality
+C4021803	Abnormality of the eyelid
+C4021805	Abnormality of the nasal bridge
+C4021806	Prelingual sensorineural hearing impairment
+C4021808	Abnormality of earlobe
+C4021811	Abnormality of the midface
+C4021812	Abnormality of the head
+C4021813	Oral cleft
+C4021814	Accessory oral frenulum
+C4021815	Abnormality of the palate
+C4021816	Abnormality of the gingiva
+C4021818	Abnormality of the ovary
+C4021820	Abnormality of reproductive system physiology
+C4021821	Abnormality of the urinary system
+C4021822	Abnormality of female external genitalia
+C4021823	Ambiguous genitalia, male
+C4021824	Postaxial polysyndactyly of foot
+C4021826	Abnormality of the renal tubule
+C4021828	Advanced pneumatization of the mastoid process
+C4021829	Narrow nail
+C4021830	Bilateral camptodactyly
+C4021831	Hypohidrosis or hyperhidrosis
+C4021834	Abnormality of the parietal bone
+C4021835	Sacral lipoma
+C4021837	Atypical nevi in non-sun exposed areas
+C4021843	Increased serum free triiodothyronine
+C4021845	Oromotor apraxia
+C4021847	Abnormal cartilage collagen
+C4021849	Conjunctival hamartoma
+C4021850	Increased sensitivity to ionizing radiation
+C4021852	Reduction of oligodendroglia
+C4021857	Speckled corneal dystrophy
+C4021865	Long distal phalanx of finger
+C4021875	Tall chin
+C4021881	Agenesis of lateral incisor
+C4021882	Increased serum bile acid concentration during pregnancy
+C4021883	Abnormal liver function tests during pregnancy
+C4021884	Bilateral choanal atresia/stenosis
+C4021885	Atrial cardiomyopathy
+C4021893	Nonprogressive visual loss
+C4021898	Upper limb hypertonia
+C4021899	Premature chromatid separation
+C4021900	Symmetric great toe depigmentation
+C4021902	Short corpus callosum
+C4021906	Splayed epiphyses
+C4021910	Narrow foramen obturatorium
+C4021951	Vertebral body sclerosis
+C4021953	Poorly ossified vertebrae
+C4021956	Aplasia/Hypoplasia of the eyebrow
+C4021957	Recurrent cutaneous abscess formation
+C4021959	Round ear
+C4021960	Increase in T cell count
+C4021966	Abnormality of the periungual region
+C4021967	Pancreatic aplasia
+C4021968	Aplasia/Hypoplasia of the pancreas
+C4021971	Peripheral arteriovenous fistula
+C4021972	Urogenital sinus anomaly
+C4021973	Cartilage destruction
+C4021975	Abnormality of the tonsils
+C4021976	Abnormality of the lymphatic system
+C4021977	Visceral angiomatosis
+C4021978	Abnormality of salivation
+C4021982	Abnormal eating behavior
+C4021984	Abnormality of the soft palate
+C4021985	Germ cell neoplasia
+C4021986	Hypoplasia of the ear cartilage
+C4021989	Abnormality of the thoracic spine
+C4021998	Lack of skin elasticity
+C4022001	Abnormality of the cerebral vasculature
+C4022003	Erectile abnormalities
+C4022011	Leydig cell neoplasia
+C4022012	Death in early adulthood
+C4022013	Multiple glomerular cysts
+C4022014	Maternal hyperphenylalaninemia
+C4022015	Calcification of cartilage
+C4022016	Abnormality of the preputium
+C4022018	Telangiectasia of the skin
+C4022020	Mucosal telangiectasiae
+C4022024	Upper limb asymmetry
+C4022025	Asymmetric growth
+C4022031	Abnormality of calcium-phosphate metabolism
+C4022034	Abnormality of vitamin E metabolism
+C4022035	Abnormality of vitamin D metabolism
+C4022036	Abnormality of vitamin metabolism
+C4022107	Aplasia of the middle phalanges of the toes
+C4022125	Aplasia of the phalanges of the 3rd toe
+C4022143	Unilateral cleft palate
+C4022148	Abnormality of the dentate nucleus
+C4022153	Cerebral cortical hemiatrophy
+C4022154	Cerebellar hemisphere hypoplasia
+C4022157	Muscle fiber cytoplasmatic inclusion bodies
+C4022159	Muscle fiber inclusion bodies
+C4022161	Increased endomysial connective tissue
+C4022163	Abnormality of central somatosensory evoked potentials
+C4022168	EMG: impaired neuromuscular transmission
+C4022169	EMG: myotonic discharges
+C4022173	Hyponasal speech
+C4022179	Stenosis of the medullary cavity of the long bones
+C4022180	Lipomas of the central neryous system
+C4022181	Meningeal calcification
+C4022253	Fragmented epiphyses
+C4022386	Overfriendliness
+C4022387	Recurrent hand flapping
+C4022389	Abnormality of the mesentery
+C4022395	Abnormality of the mediastinum
+C4022403	Abnormality of the substantia nigra
+C4022417	Degeneration of the striatum
+C4022432	Bilateral external ear deformity
+C4022448	Abnormal prolactin level
+C4022449	Abnormal levels of creatine kinase in blood
+C4022459	Decreased adipose tissue
+C4022490	Prominent coccyx
+C4022492	Increased mitochondrial number
+C4022496	Small posterior fossa
+C4022506	Multinucleated giant chondrocytes in epiphyseal cartilage
+C4022507	Decreased osteoclast count
+C4022510	Cervicomedullary schisis
+C4022524	Hypoplastic anterior commissure
+C4022537	Triangular tongue
+C4022538	Cervical C3/C4 vertebral fusion
+C4022544	Reduced red cell adenosine deaminase activity
+C4022546	Reduced erythrocyte 2,3-diphosphoglycerate concentration
+C4022547	Elevated red cell adenosine deaminase activity
+C4022548	Hyperplastic callus formation
+C4022554	Hyperpigmented genitalia
+C4022557	Defective T cell proliferation
+C4022560	Splanchnic vein thrombosis
+C4022565	Highly elevated creatine phosphokinase
+C4022574	Limb apraxia
+C4022575	Inertia
+C4022576	Slow pupillary light response
+C4022583	Fatiguable weakness of proximal limb muscles
+C4022587	Fatigable weakness of respiratory muscles
+C4022588	Fatigable weakness of swallowing muscles
+C4022600	Peripheral amyelination
+C4022605	Abnormal liver parenchyma morphology
+C4022625	Absent muscle fiber calpain-3
+C4022654	Abnormal testosterone level
+C4022662	Abnormality of lateral ventricle
+C4022665	Isothenuria
+C4022675	Increased female libido
+C4022676	Decreased female libido
+C4022693	Posteriorly placed anus
+C4022695	Abnormality of the labia majora
+C4022698	Acephalic spermatozoa
+C4022699	Sperm tail anomaly
+C4022707	Abnormal scrotal rugation
+C4022715	Hypoplastic female external genitalia
+C4022716	Bilateral breast hypoplasia
+C4022725	Retinal astrocytic hamartoma
+C4022729	Increased arm span
+C4022735	Cerebral white matter atrophy
+C4022738	Neurodevelopmental delay
+C4022739	Abnormal neuron morphology
+C4022744	Focal T2 hypointense basal ganglia lesion
+C4022745	Abnormal basal ganglia MRI signal intensity
+C4022747	Focal T2 hypointense brainstem lesion
+C4022748	Focal T2 hyperintense brainstem lesion
+C4022749	Abnormal brainstem MRI signal intensity
+C4022750	Thin fingernail
+C4022754	Episodic hypokalemia
+C4022756	Profound hearing impairment
+C4022758	Mild hearing impairment
+C4022766	Abnormal large intestine physiology
+C4022769	Small basal ganglia
+C4022798	Abnormal brain FDG positron emission tomography
+C4022805	Abnormal inflammatory response
+C4022808	Cerebellar agenesis
+C4022810	Abnormality of nervous system morphology
+C4022829	Abnormal urine potassium concentration
+C4022832	Mild proteinuria
+C4022845	Decreased T3/T4 ratio
+C4022846	Increased T3/T4 ratio
+C4022848	EEG with centrotemporal focal spike waves
+C4022850	Hypoplastic thumbnail
+C4022852	Absent neutrophil specific granules
+C4022855	Abnormal involuntary eye movements
+C4022858	Elevated aldolase level
+C4022864	Absence of alpha granules
+C4022866	Abnormal platelet shape
+C4022867	Spider hemangioma
+C4022868	Abnormality of circle of Willis
+C4022869	Reduced catalase activity
+C4022873	Small pituitary gland
+C4022874	Abnormal size of pituitary gland
+C4022878	Descending aortic dissection
+C4022891	Elevated hepatic iron concentration
+C4022892	Elevated transferrin saturation
+C4022895	Medial calcification of medium-sized arteries
+C4022915	Increased urine alpha-ketoglutarate concentration
+C4022916	Abnormal aldolase level
+C4022922	Abnormal enzyme/coenzyme activity
+C4022928	Decreased sialylation of O-linked protein glycosylation
+C4022933	Abnormal protein O-linked glycosylation
+C4022946	Abnormal glycosylation
+C4022947	Decreased resting energy expenditure
+C4022961	Slender proximal phalanx of finger
+C4022962	Slender distal phalanx of finger
+C4022964	Abnormality of the occipital bone
+C4022967	Hypothalamic luteinizing hormone-releasing hormone deficiency
+C4022969	Small proximal tibial epiphyses
+C4022970	Small distal femoral epiphysis
+C4022971	Hyposerinemia
+C4022973	Hypoglycinemia
+C4022977	Increased carotid artery intimal medial thickness
+C4022978	Episodic upper airway obstruction
+C4022979	Decreased muscle glycogen content
+C4022983	Abnormal ciliary motility
+C4022985	Abnormal central microtubular pair morphology of respiratory motile cilia
+C4022986	Absent inner and outer dynein arms
+C4022987	Abnormal axonemal organization of respiratory motile cilia
+C4022988	Absent inner dynein arms
+C4022989	Absent outer dynein arms
+C4022995	Sex reversal
+C4022996	Abnormal sex determination
+C4022998	Arachnoid hemangiomatosis
+C4023001	Nonmotile sperm
+C4023003	Recurrent vulvovaginal candidiasis
+C4023004	Increased serum bile acid concentration
+C4023006	Juvenile colonic polyposis
+C4023007	Increased erythrocyte protoporphyrin concentration
+C4023009	Constrictive median neuropathy
+C4023010	Hyperplastic colonic polyposis
+C4023011	Craniofacial dystonia
+C4023012	Abnormal natural killer cell physiology
+C4023013	Stereotypical body rocking
+C4023014	Stereotypical hand wringing
+C4023018	Subcortical cerebral atrophy
+C4023022	Reduced quantity of Von Willebrand factor
+C4023024	Abnormality of multiple cell lineages in the bone marrow
+C4023026	Abnormality of cells of the megakaryocyte lineage
+C4023028	Granulocytic hyperplasia
+C4023031	Abnormality of cells of the granulocytic lineage
+C4023039	Rhizomelic leg shortening
+C4023042	Abnormality of the mitochondrion
+C4023049	Abnormality of pancreas morphology
+C4023050	Abnormal mitochondrial shape
+C4023052	Ubiquitin-positive cerebral inclusion bodies
+C4023053	Cerebellar Purkinje layer atrophy
+C4023058	Abnormality of acetylcarnitine metabolism
+C4023059	Chondroitin sulfate excretion in urine
+C4023060	Keratan sulfate excretion in urine
+C4023062	Increased urinary disaccharide excretion
+C4023065	Low serum calcitriol
+C4023068	Increased urinary cortisol level
+C4023071	Hypergalactosemia
+C4023090	Impaired neutrophil bactericidal activity
+C4023093	Abnormality of neutrophil physiology
+C4023094	Ectopic ossification in ligament tissue
+C4023095	Ectopic ossification in tendon tissue
+C4023096	Ectopic ossification in muscle tissue
+C4023099	Elevated urinary dopamine
+C4023100	Aminoglycoside-induced hearing loss
+C4023101	Elevated circulating luteinizing hormone level
+C4023102	Elevated plasma citrulline
+C4023106	Obstructive azoospermia
+C4023110	Hepatic granulomatosis
+C4023113	Small vessel vasculitis
+C4023114	Anterior wedging of L2
+C4023115	3-4 finger cutaneous syndactyly
+C4023116	Hypoplastic fifth toenail
+C4023117	Decreased plasma total carnitine
+C4023118	Decreased urinary urate
+C4023119	Mesenteric artery aneurysm
+C4023122	Hypersegmentation of proximal phalanx of third finger
+C4023124	Short digit
+C4023125	Decreased activity of mitochondrial ATP synthase complex
+C4023126	Abnormal activity of mitochondrial respiratory chain
+C4023127	Toe extensor amyotrophy
+C4023133	Shortening of all phalanges of fingers
+C4023134	Flattened metacarpal heads
+C4023136	Reduced alpha/beta synthesis ratio
+C4023137	Reduced beta/alpha synthesis ratio
+C4023145	Abnormal umbilical stump bleeding
+C4023146	Abnormal platelet granules
+C4023153	Impaired thrombin-induced platelet aggregation
+C4023156	Abnormality of the wing of the ilium
+C4023157	Elevated plasma pyrophosphate
+C4023159	Reduced factor IX activity
+C4023161	Abnormal bone ossification
+C4023165	Abnormality of skeletal morphology
+C4023169	Moyamoya phenomenon
+C4023170	Abnormality of oral mucosa
+C4023171	Chin with horizontal crease
+C4023172	Broad chin
+C4023175	Submucous cleft soft palate
+C4023177	Increased cerebral lipofuscin
+C4023179	Paradoxical myotonia
+C4023180	Type 1 muscle fiber atrophy
+C4023188	Activating thyroid-stimulating hormone receptor defect
+C4023190	Thyroid hemiagenesis
+C4023205	Neoplasm of the anterior pituitary
+C4023208	Glucocortocoid-insensitive primary hyperaldosteronism
+C4023209	Dexamethasone-suppresible primary hyperaldosteronism
+C4023211	Adrenocorticotropin deficient adrenal insufficiency
+C4023222	Abnormal electrophysiology of sinoatrial node origin
+C4023237	Interrupted inferior vena cava with azygous continuation
+C4023288	Short chordae tendineae of the mitral valve
+C4023292	Imperforate tricuspid valve
+C4023317	Dichromacy
+C4023322	Macular flecks
+C4023325	Partial aniridia
+C4023327	Central opacification of the cornea
+C4023328	Abnormality of corneal stroma
+C4023330	Abnormality of Descemet\'s membrane
+C4023332	Abnormality of corneal endothelium
+C4023338	Profound sensorineural hearing impairment
+C4023351	Hyposegmentation of neutrophil nuclei
+C4023358	Maternal autoimmune disease
+C4023374	Delayed peripheral myelination
+C4023383	Narrow internal auditory canal
+C4023385	Aplasia of the semicircular canal
+C4023386	Morphological abnormality of the semicircular canal
+C4023387	Dilated vestibule of the inner ear
+C4023396	Abnormality of hair growth rate
+C4023397	Abnormal hair quantity
+C4023400	Generalized hypopigmentation of hair
+C4023401	Abnormality of hair density
+C4023402	Regional abnormality of skin
+C4023403	Arterial intimal fibrosis
+C4023406	Abnormality of upper lip vermillion
+C4023411	Hemifacial hypoplasia
+C4023418	Unicoronal synostosis
+C4023422	Long palm
+C4023430	Long-segment aganglionic megacolon
+C4023438	Recurrent mycobacterial infections
+C4023439	Absent tragus
+C4023449	Infra-orbital fold
+C4023450	Prominent eyelashes
+C4023452	Elevated C-reactive protein level
+C4023454	Metopic depression
+C4023457	Short face
+C4023470	EEG with continuous slow activity
+C4023471	EEG with abnormally slow frequencies
+C4023476	EEG with generalized epileptiform discharges
+C4023479	EEG with focal sharp slow waves
+C4023481	EEG with focal spikes
+C4023499	Generalized clonic seizures
+C4023501	Focal myoclonic seizures
+C4023511	Obtundation status
+C4023515	Dialeptic seizures
+C4023521	Chronic furunculosis
+C4023526	Abnormality of epidermal morphology
+C4023528	Abnormality of skin morphology
+C4023540	Hypomature dental enamel
+C4023546	Abnormality of canine
+C4023551	Abnormality of dental color
+C4023557	Abnormality of dental structure
+C4023558	Dentinogenesis imperfecta limited to primary teeth
+C4023560	Generalized periodontitis
+C4023566	Agenesis of premolar
+C4023574	Abnormality of circulating adrenocorticotropin level
+C4023577	Abnormality of the intrahepatic bile duct
+C4023579	Abnormality of renal excretion
+C4023583	Abnormality of iron homeostasis
+C4023591	Abnormality of circulating enzyme level
+C4023592	Abnormality of mucopolysaccharide metabolism
+C4023599	Abnormality of carbohydrate metabolism/homeostasis
+C4023607	Abnormality of the striatum
+C4023608	Abnormality of the abdominal musculature
+C4023610	Abnormality of the intrinsic pathway
+C4023616	Abnormality of immune system physiology
+C4023619	Absence of Lutheran antigen on erythrocytes
+C4023620	Blood group antigen abnormality
+C4023628	Mild fetal ventriculomegaly
+C4023636	Aplasia/Hypoplasia of the nasal bone
+C4023641	Abnormality of the upper urinary tract
+C4023650	Posterior cortical cataract
+C4023653	Abnormality of tyrosine metabolism
+C4023662	Abnormality of histidine metabolism
+C4023663	Abnormality of glutamine metabolism
+C4023673	Abnormality of branched chain family amino acid metabolism
+C4023676	Increased nuchal translucency
+C4023678	Unilateral strabismus
+C4023681	Delayed fine motor development
+C4023684	EEG with spike-wave complexes (>3.5 Hz)
+C4023687	EEG with multifocal slow activity
+C4023698	Everted upper lip vermilion
+C4023701	Impaired visuospatial constructive cognition
+C4023703	Abnormality of the Leydig cells
+C4023710	Palmar hyperkeratosis
+C4023719	Spontaneous rupture of the globe
+C4023720	Cystic lesions of the pinnae
+C4023721	Abnormal hair pattern
+C4023722	Abnormality of hair texture
+C4023728	1-5 finger syndactyly
+C4023731	4-5 finger syndactyly
+C4023734	Sutural cataract
+C4023735	Lamellar pulverulent cataract
+C4023749	Abnormality of the zygomatic bone
+C4023759	Flat nasal alae
+C4023764	Elevated alkaline phosphatase of hepatic origin
+C4023786	Elevated levels of phytanic acid
+C4023791	Abnormality of the clivus
+C4023795	Ectopic thymus tissue
+C4023796	Aplasia/Hypoplasia of the thymus
+C4023800	Limitation of movement at ankles
+C4023801	Fibular bowing
+C4023802	Hyperextensibility of the knee
+C4023803	Hypertrophy of the lower limb
+C4023808	Hyperextensibility at elbow
+C4023812	Aplasia of the bladder
+C4023814	Abnormality of the heme biosynthetic pathway
+C4023815	Oligosacchariduria
+C4023817	Aplasia/Hypoplasia of the testes
+C4023819	Abnormality of the male genitalia
+C4023824	Bifid femur
+C4023905	Abnormality of the 5th toe
+C4023909	Aplasia/Hypoplasia of the abdominal wall musculature
+C4023911	Aplasia/Hypoplasia of the breasts
+C4023915	Abnormally low-pitched voice
+C4023916	Aplasia/Hypoplasia of the tongue
+C4023918	Short hard palate
+C4023921	Oral synechia
+C4023926	Pseudoepiphyses of the proximal phalanges of the hand
+C4023931	Cone-shaped epiphyses of the proximal phalanges of the hand
+C4023965	Structural foot deformity
+C4023976	Aplasia/Hypoplasia of the middle phalanges of the toes
+C4023986	Broad phalanx of the toes
+C4023987	Aplasia/Hypoplasia of the phalanges of the toes
+C4023991	Ivory epiphyses of the toes
+C4024048	Aplasia of the distal phalanx of the hallux
+C4024054	Duplication of the proximal phalanx of the hallux
+C4024067	Bullet-shaped distal phalanx of the hallux
+C4024068	Broad distal phalanx of the hallux
+C4024076	Aplasia/hypoplasia of the 1st metatarsal
+C4024079	Aplasia/Hypoplasia of the phalanges of the hallux
+C4024082	Abnormality of the first metatarsal bone
+C4024097	Broad 1st metacarpal
+C4024098	Aplasia/Hypoplasia of the 1st metacarpal
+C4024106	Cone-shaped epiphysis of the 1st metacarpal
+C4024118	Complete duplication of the distal phalanges of the hand
+C4024136	Polydactyly affecting the 4th finger
+C4024144	Polydactyly affecting the 3rd finger
+C4024158	Abnormality of the columella
+C4024159	Aplasia/Hypoplasia involving the nose
+C4024162	Abnormality of the tragus
+C4024166	Crumpled ear
+C4024167	Abnormality of the antitragus
+C4024168	Thickened ears
+C4024171	Abnormality of secondary sexual hair
+C4024172	Abnormality of hair pigmentation
+C4024173	Aplasia of the distal phalanges of the hand
+C4024174	Broad distal phalanges of all fingers
+C4024176	Triangular shaped distal phalanges of the hand
+C4024187	Bullet-shaped middle phalanges of the hand
+C4024188	Curved distal phalanges of the hand
+C4024196	Lower limb peromelia
+C4024201	Low-output congestive heart failure
+C4024202	Reduced number of teeth
+C4024203	Aplasia of the phalanges of the hand
+C4024210	Lester\'s sign
+C4024212	Pyramidal skinfold extending from the base to the top of the nails
+C4024213	Aplasia of the pectoralis major muscle
+C4024215	Aplasia of the parotid gland
+C4024216	Tibial pseudoarthrosis
+C4024217	Spinal neurofibromas
+C4024220	Hypomelanotic macule
+C4024221	Papillary cystadenoma of the epididymis
+C4024222	Abnormality of the epididymis
+C4024223	Spinal hemangioblastoma
+C4024224	Chilblain lesions
+C4024229	Chronic CSF lymphocytosis
+C4024235	Stippling of the epiphysis of the distal phalanx of the thumb
+C4024273	Complete duplication of proximal phalanx of the thumb
+C4024276	Peripheral Schwannoma
+C4024283	Triangular shaped middle phalanx of the 2nd finger
+C4024296	Projection of scalp hair onto lateral cheek
+C4024297	Abnormality of the hairline
+C4024310	Triangular epiphysis of the middle phalanx of the 2nd finger
+C4024317	Enlarged epiphysis of the middle phalanx of the 2nd finger
+C4024318	Bracket epiphysis of the middle phalanx of the 2nd finger
+C4024345	Radial deviation of the 3rd finger
+C4024349	Triangular shaped proximal phalanx of the 3rd finger
+C4024362	Triangular shaped middle phalanx of the 3rd finger
+C4024412	Broad phalanges of the 5th finger
+C4024441	Enlarged epiphysis of the middle phalanx of the 3rd finger
+C4024473	Radial deviation of the 4th finger
+C4024507	Aplasia/Hypoplasia of the distal phalanx of the 5th finger
+C4024536	Bracket epiphysis of the middle phalanx of the 5th finger
+C4024552	Triangular shaped middle phalanx of the 5th finger
+C4024579	Osteolysis involving bones of the feet
+C4024583	Fat tissue increased
+C4024589	Aplasia/Hypoplasia of the mandible
+C4024595	Abnormal ossification involving the femoral head and neck
+C4024597	Aplasia/Hypoplasia involving the pelvis
+C4024598	Anterior open-bite malocclusion
+C4024599	Chronic oral candidiasis
+C4024601	Weakness of long finger extensor muscles
+C4024603	Atrophy of quadriceps femoris muscle
+C4024604	Amyotrophy of ankle musculature
+C4024606	Loss of gluteal subcutaneous adipose tissue
+C4024608	Necrotizing myopathy
+C4024609	Decreased activity of mitochondrial respiratory chain
+C4024610	Leg muscle stiffness
+C4024611	Nonprogressive muscular atrophy
+C4024612	Tibialis muscle weakness
+C4024613	Progressive distal muscular atrophy
+C4024615	Adipose tissue loss
+C4024617	Hypoplastic ischiopubic rami
+C4024618	Large iliac wings
+C4024620	Widened sacrosciatic notch
+C4024622	Wide capital femoral epiphyses
+C4024623	Wide proximal femoral metaphysis
+C4024628	Aplasia of the epiglottis
+C4024631	Renal hypophosphatemia
+C4024632	Gonadal dysgenesis with female appearance, male
+C4024634	Distal urethral duplication
+C4024640	Aplasia/hypoplasia of the uterus
+C4024641	Enlarged polycystic ovaries
+C4024644	Multiple small medullary renal cysts
+C4024645	Incomplete male pseudohermaphroditism
+C4024646	Aplasia/Hypoplasia of the fallopian tube
+C4024650	Congenital macroorchidism
+C4024654	Postlingual sensorineural hearing impairment
+C4024655	Underfolded superior helices
+C4024656	Absent vestibular function
+C4024660	Aplasia/Hypoplasia of the sacrum
+C4024661	Abnormality of the vertebral spinous processes
+C4024664	Moderate sensorineural hearing impairment
+C4024665	High-grade hypermetropia
+C4024667	Congenital craniofacial dysostosis
+C4024669	Asymmetry of spinal facet joints
+C4024670	Poorly ossified cervical vertebrae
+C4024672	Central vertebral hypoplasia
+C4024674	Hypoplastic spinal processes
+C4024675	C1-C2 vertebral abnormality
+C4024677	Anterior wedging of L1
+C4024678	Punctate vertebral calcifications
+C4024679	Onychogryposis of toenails
+C4024682	Hypoplastic fifth fingernail
+C4024686	Abnormality of vitamin A metabolism
+C4024689	Abnormality of the calcaneus
+C4024692	Reduced factor XIII activity
+C4024693	Factor X activation deficiency
+C4024695	Increased red cell sickling tendency
+C4024697	Elevated plasma branched chain amino acids
+C4024698	Diaminoaciduria
+C4024700	Elevated creatine kinase after exercise
+C4024701	Reduced von Willebrand factor activity
+C4024702	Reduced factor X activity
+C4024703	Impaired collagen-induced platelet aggregation
+C4024704	Elevated leukocyte alkaline phosphatase
+C4024705	Decreased activity of mitochondrial complex II
+C4024706	Spinal cord posterior columns myelin loss
+C4024709	Transient hypophosphatemia
+C4024710	Cerebellar cortical atrophy
+C4024711	Abnormality of zinc homeostasis
+C4024712	Abnormal light-adapted electroretinogram
+C4024713	Transient aminoaciduria
+C4024716	Secondary growth hormone deficiency
+C4024719	Adrenocortical hypoplasia
+C4024722	Reduced factor VII activity
+C4024723	Reduced circulating T-helper cells
+C4024726	Mucopolysacchariduria
+C4024727	Impaired epinephrine-induced platelet aggregation
+C4024728	Delayed calcaneal ossification
+C4024729	Distal tapering of metatarsals
+C4024730	Calcaneonavicular fusion
+C4024731	Flexion limitation of toes
+C4024732	Ankylosis of feet small joints
+C4024733	Abnormality of the fifth metatarsal bone
+C4024734	Low maternal serum estriol
+C4024735	Maternal virilization in pregnancy
+C4024737	Aplasia/Hypoplasia of the skin
+C4024738	Aplasia/Hypoplasia of the lens
+C4024742	Aplasia/Hypoplasia of the macula
+C4024748	Aplasia/Hypoplasia of the iris
+C4024750	Abnormality of the palpebral fissures
+C4024751	Abnormality of the extraocular muscles
+C4024753	Abnormality of the retinal vasculature
+C4024756	Abnormality of macular pigmentation
+C4024757	Malformed lacrimal ducts
+C4024758	Intraretinal exudate
+C4024759	Macular hypopigmentation
+C4024760	Progressive visual field defects
+C4024761	Retinal arteriolar occlusion
+C4024762	Pattern dystrophy of the retina
+C4024763	Optic atrophy from cranial nerve compression
+C4024765	Peripapillary chorioretinal atrophy
+C4024767	Dense posterior cortical cataract
+C4024768	Intermittent microsaccadic pursuits
+C4024769	Reticular pigmentary degeneration
+C4024772	Abnormal flash visual evoked potentials
+C4024773	Lacrimal duct aplasia
+C4024776	Reticular retinal dystrophy
+C4024779	Marginal corneal dystrophy
+C4024780	Almond-shaped palpebral fissure
+C4024784	Amyloid deposition in the vitreous humor
+C4024788	Anterior chamber synechiae
+C4024789	Nonprogressive restrictive external ophthalmoplegia
+C4024790	Adult-onset night blindness
+C4024792	Nodular corneal dystrophy
+C4024794	Horizontal supranuclear gaze palsy
+C4024795	Nongranulomatous uveitis
+C4024796	Punctate corneal dystrophy
+C4024799	Granular macular appearance
+C4024803	Posterior retinal neovascularization
+C4024804	Congenital visual impairment
+C4024809	Chorioretinal dysplasia
+C4024810	Chronic irritative conjunctivitis
+C4024811	Peripheral vitreous opacities
+C4024816	Depigmented fundus
+C4024817	Vitelliform-like macular lesions
+C4024818	Progressive night blindness
+C4024819	Abnormality of chorioretinal pigmentation
+C4024820	Large hyperpigmented retinal spots
+C4024821	Diffuse nuclear cataract
+C4024822	Lacrimal gland aplasia
+C4024825	Peripheral traction retinal detachment
+C4024826	Pigmentation anomalies of sun-exposed skin
+C4024827	Telangiectasia of extensor surfaces
+C4024828	Fine, reticulate skin pigmentation
+C4024831	Blotching pigmentation of the skin
+C4024832	Hypoproteinemic edema
+C4024836	Generalized reticulate brown pigmentation
+C4024842	Generalized bronze hyperpigmentation
+C4024843	Late onset atopic dermatitis
+C4024844	Generalized seborrheic dermatitis
+C4024848	Absent pigmentation of the ventral chest
+C4024851	Punctate palmoplantar hyperkeratosis
+C4024852	Hypopigmented skin patches on arms
+C4024853	Increased number of skin folds
+C4024855	Lack of subcutaneous fatty tissue
+C4024856	Redundant skin on fingers
+C4024859	Progressive hyperpigmentation
+C4024861	Streaks of hyperkeratosis along each finger onto the palm
+C4024862	Recurrent staphylococcal infections
+C4024863	Diffuse skin atrophy
+C4024864	Depigmentation/hyperpigmentation of skin
+C4024865	Generalized papillary lesions
+C4024867	Perifollicular hyperkeratosis
+C4024869	Generalized anhidrosis
+C4024871	Prominent veins on trunk
+C4024872	Progressive reticulate hyperpigmentation
+C4024876	Palmoplantar blistering
+C4024877	Hyperpigmented/hypopigmented macules
+C4024878	Generalized hyperpigmentation
+C4024880	Hair-nail ectodermal dysplasia
+C4024881	Few cafe-au-lait spots
+C4024882	Telangiectasia of the oral mucosa
+C4024884	Neonatal wrinkled skin of hands and feet
+C4024886	Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines
+C4024888	Asymmetric, linear skin defects
+C4024890	Excessive wrinkled skin
+C4024891	Hyperkeratosis with erythema
+C4024892	Congenital exfoliative erythroderma
+C4024896	Motor neuron atrophy
+C4024900	Atrophy/Degeneration affecting the brainstem
+C4024905	Abnormality of the pons
+C4024907	Mixed demyelinating and axonal polyneuropathy
+C4024908	Rapid neurologic deterioration
+C4024911	Acute infantile spinal muscular atrophy
+C4024912	Occipital myelomeningocele
+C4024914	Symmetric peripheral demyelination
+C4024916	Decreased number of small peripheral myelinated nerve fibers
+C4024917	Congenital encephalopathy
+C4024918	Recurrent subcortical infarcts
+C4024919	Spinocerebellar tract disease in lower limbs
+C4024920	Decreased distal sensory nerve action potential
+C4024921	Lower limb amyotrophy
+C4024922	Irregular myelin loops
+C4024923	Diffuse white matter abnormalities
+C4024924	Cerebral artery atherosclerosis
+C4024926	Focal T2 hyperintense basal ganglia lesion
+C4024927	Peripheral hypomyelination
+C4024929	Slowed slurred speech
+C4024930	Diffuse demyelination of the cerebral white matter
+C4024933	Acute demyelinating polyneuropathy
+C4024934	Cerebellar medulloblastoma
+C4024935	Subcortical dementia
+C4024936	Temporal cortical atrophy
+C4024938	Segmental peripheral demyelination
+C4024940	Cranial nerve motor loss
+C4024942	Late-onset muscular dystrophy
+C4024943	Decreased amplitude of sensory action potentials
+C4024944	Profound static encephalopathy
+C4024945	Generalized cerebral atrophy/hypoplasia
+C4024946	Focal white matter lesions
+C4024947	Symmetric lesions of the basal ganglia
+C4024948	Anterior encephalocele
+C4024949	Generalized hyperreflexia
+C4024950	Nonprogressive encephalopathy
+C4024952	Cavitation of the basal ganglia
+C4024953	Dorsal column degeneration
+C4024956	Grammar-specific speech disorder
+C4024957	Proximal spinal muscular atrophy
+C4024959	Frontoparietal cortical dysplasia
+C4024960	Unilateral polymicrogyria
+C4024961	Metachromatic leukodystrophy variant
+C4024964	Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material
+C4024965	Frontal cortical atrophy
+C4024968	Impaired thermal sensitivity
+C4024970	Thick cerebral cortex
+C4024972	Symmetrical progressive peripheral demyelination
+C4024975	Posterior leukoencephalopathy
+C4024976	Episodic generalized hypotonia
+C4024979	Ovarian papillary adenocarcinoma
+C4024981	Localized neuroblastoma
+C4024984	Diffuse leiomyomatosis
+C4024986	Congenital neuroblastoma
+C4024988	Intestinal carcinoid
+C4024989	Hereditary nonpolyposis colorectal carcinoma
+C4024990	Aplasia/Hypoplasia of the sternum
+C4024993	Aplasia/Hypoplasia of the clavicles
+C4024996	Aplasia/Hypoplasia of the lungs
+C4025000	Myocardial steatosis
+C4025001	Short chordae tendineae of the tricuspid valve
+C4025002	Pulmonic valve myxoma
+C4025003	Aortic tortuosity
+C4025004	Ventricular preexcitation with multiple accessory pathways
+C4025008	Reduced systolic function
+C4025009	Impaired myocardial contractility
+C4025010	Coat hanger sign of ribs
+C4025016	Straight clavicles
+C4025017	Fatal liver failure in infancy
+C4025018	Depletion of mitochondrial DNA in liver
+C4025019	Intrahepatic cholestasis with episodic jaundice
+C4025020	Acute hepatic steatosis
+C4025021	Increased hepatocellular lipid droplets
+C4025022	Decreased mitochondrial complex III activity in liver tissue
+C4025028	Intraalveolar nodular calcifications
+C4025031	Aplasia/hypoplasia of the humerus
+C4025033	Aplasia/Hypoplasia involving the carpal bones
+C4025034	Abnormality of femoral epiphysis
+C4025038	Abnormality of the tibial metaphysis
+C4025040	Abnormality of the femoral metaphysis
+C4025043	Abnormality of the pancreatic islet cells
+C4025044	Fixed elbow flexion
+C4025045	Irregular proximal tibial epiphyses
+C4025047	Proximal femoral metaphyseal abnormality
+C4025048	Elongated radius
+C4025049	Distal tapering femur
+C4025050	Irregular distal femoral epiphysis
+C4025052	Dumbbell-shaped femur
+C4025053	Broad long bone diaphyses
+C4025054	Agenesis of mandibular central incisor
+C4025055	Hypoplasia of the tooth germ
+C4025056	Failure of eruption of permanent teeth
+C4025057	Obliteration of the pulp chamber
+C4025058	Screwdriver-shaped incisors
+C4025059	Abnormality of primary molar morphology
+C4025060	Peg-shaped maxillary lateral incisors
+C4025062	Supernumerary maxillary incisor
+C4025065	Generalized microdontia
+C4025067	Dagger-shaped pulp calcifications
+C4025069	Multiple unerupted teeth
+C4025074	Aplasia/Hypoplasia of the 5th finger
+C4025077	Slender metacarpals
+C4025078	Tapering pointed ends of distal finger phalanges
+C4025079	Thin proximal phalanges with broad epiphyses of the hand
+C4025080	Hypersegmentation of proximal phalanx of second finger
+C4025083	Thimble-shaped middle phalanges of hand
+C4025086	Irregular metacarpals
+C4025087	Long phalanx of finger
+C4025088	Broad metacarpal epiphyses
+C4025089	Shortening of all proximal phalanges of the fingers
+C4025090	Long proximal phalanx of finger
+C4025093	Cuboidal metacarpal
+C4025094	Reduced phenylalanine hydroxylase activity
+C4025095	Hypoargininemia
+C4025096	Progressive inspiratory stridor
+C4025097	Ventilator dependence with inability to wean
+C4025098	Intermittent hyperpnea at rest
+C4025100	Abnormal respiratory motile cilium morphology
+C4025102	Abnormal renal corticomedullary differentiation
+C4025109	Abnormal hand morphology
+C4025111	Radial deviation of thumb terminal phalanx
+C4025114	Aphalangy of the hands
+C4025117	Metacarpophalangeal synostosis
+C4025119	Multiple small vertebral fractures
+C4025121	Metaphyseal enchondromatosis
+C4025122	Opposable triphalangeal thumb
+C4025132	Shortening of all distal phalanges of the toes
+C4025133	Cortical thickening of long bone diaphyses
+C4025138	Multiple skeletal anomalies
+C4025139	Fifth finger distal phalanx clinodactyly
+C4025144	Congenital foot contractures
+C4025145	Cortical irregularity
+C4025153	Dysplastic distal thumb phalanges with a central hole
+C4025155	Talocalcaneal synostosis
+C4025159	Bilateral intracranial calcifications
+C4025161	Positional foot deformity
+C4025162	Multiple digital exostoses
+C4025167	Abnormal vertebral segmentation and fusion
+C4025170	Osteoporosis of vertebrae
+C4025174	Large cafe-au-lait macules with irregular margins
+C4025175	Congenital alopecia totalis
+C4025182	Exercise-induced hemolysis
+C4025183	Macrocytic dyserythropoietic anemia
+C4025184	Spontaneous hemolytic crises
+C4025186	T-cell lymphoma/leukemia
+C4025187	Increased megakaryocyte count
+C4025189	Metopic suture patent to nasal root
+C4025192	Orbital craniosynostosis
+C4025193	Craniofacial osteosclerosis
+C4025195	Sclerotic cranial sutures
+C4025196	Recurrent systemic pyogenic infections
+C4025197	Absence of CD8+ T cells
+C4025198	Recurrent gram-negative bacterial infections
+C4025201	Reduction of neutrophil motility
+C4025202	Recurrent protozoan infections
+C4025204	Recurrent Haemophilus influenzae infections
+C4025207	Susceptibility to herpesvirus
+C4025208	Severe T-cell immunodeficiency
+C4025209	Abnormal facial expression
+C4025211	Abnormal carotid artery morphology
+C4025212	Autonomic bladder dysfunction
+C4025213	Abnormality of complement system
+C4025214	Sleepy facial expression
+C4025216	Prominent nasal septum
+C4025217	Pulmonary aterial intimal fibrosis
+C4025218	Vasculitis of large artery
+C4025226	Pectoral muscle hypoplasia/aplasia
+C4025228	Partial abdominal muscle agenesis
+C4025231	Chronic calcifying pancreatitis
+C4025232	Jejunoileal ulceration
+C4025234	Duplication of internal organs
+C4025236	Anomalous splenoportal venous system
+C4025237	Stiff interphalangeal joints
+C4025238	Generalized morning stiffness
+C4025240	Flattened metatarsal heads
+C4025244	Abnormal atrioventricular conduction
+C4025248	Dilatation of the abdominal aorta
+C4025249	Abnormality of the intervertebral disk
+C4025250	Abnormality of the sacrum
+C4025251	Abnormality of the vertebral endplates
+C4025252	Abnormal nasal morphology
+C4025253	Streaky metaphyseal sclerosis
+C4025254	Absent styloid process of ulna
+C4025255	Cone-shaped epiphyses fused within their metaphyses
+C4025257	Shortening of all phalanges of the toes
+C4025258	Polyarticular chondrocalcinosis
+C4025260	Large joint dislocations
+C4025261	Aplasia/Hypoplasia of the capital femoral epiphysis
+C4025262	Prominent styloid process of ulna
+C4025264	Recurrent cerebral hemorrhage
+C4025265	Medial calcification of large arteries
+C4025266	Dilatation of the descending thoracic aorta
+C4025269	Generalized arterial calcification
+C4025270	Arteriosclerosis of small cerebral arteries
+C4025272	Peripheral arterial stenosis
+C4025275	Generalized distal tubular acidosis
+C4025276	Congenital lactic acidosis
+C4025277	Exercise-induced lactic acidemia
+C4025278	Stress/infection-induced lactic acidosis
+C4025279	Respiratory failure requiring assisted ventilation
+C4025282	Impaired ADP-induced platelet aggregation
+C4025283	Compensated hemolytic anemia
+C4025284	Reduced protein S activity
+C4025285	Microspherocytosis
+C4025286	Recurrent thromboembolism
+C4025287	Folate-unresponsive megaloblastic anemia
+C4025288	Hypersegmentation of neutrophil nuclei
+C4025298	Effort-induced polymorphic ventricular tachycardias
+C4025301	Cervical C5/C6 vertebrae fusion
+C4025302	Anterior beaking of thoracic vertebrae
+C4025303	Enlarged vertebral pedicles
+C4025306	Anterior beaking of lower thoracic vertebrae
+C4025307	Hyperconvex vertebral body endplates
+C4025309	Supernumerary vertebral ossification centers
+C4025314	Atrophic, patchy alopecia
+C4025315	Large clumps of pigment irregularly distributed along hair shaft
+C4025316	Temporal hypotrichosis
+C4025317	Bilateral choanal atresia
+C4025318	Chronic rhinitis due to narrow nasal airway
+C4025319	Cessation of head growth
+C4025320	Craniofacial asymmetry
+C4025321	Mandibular hyperostosis
+C4025322	Prolonged brainstem auditory evoked potentials
+C4025323	Postauricular skin tag
+C4025324	Abnormality of the cheek
+C4025327	Congenital pyloric atresia
+C4025329	Abnormality of the anus
+C4025339	Abnormality of circulating leptin level
+C4025341	Abnormality of leucine metabolism
+C4025348	Abnormality of ganglioside metabolism
+C4025350	Abnormality of glycosphingolipid metabolism
+C4025356	Abnormality of the vitreous humor
+C4025358	Abnormality of reticulocytes
+C4025362	Abnormality of the gastric mucosa
+C4025368	Pseudoepiphyses of hand bones
+C4025374	Irregular ossification of hand bones
+C4025381	Osteoarthritis of the small joints of the hand
+C4025401	Irregular carpal bones
+C4025411	Midline defect of the nose
+C4025412	Midline nasal groove
+C4025414	Radial club hand
+C4025424	Abnormality of ulnar metaphysis
+C4025467	Deformed radius
+C4025491	Abnormality of the joint spaces of the elbow
+C4025548	Cortical diaphyseal thickening of the upper limbs
+C4025565	Late-onset distal muscle weakness
+C4025568	Type 1 and type 2 muscle fiber minicore regions
+C4025569	Eunuchoid habitus
+C4025570	Hypoplasia of lymphatic vessels
+C4025571	Type 1 fibers relatively smaller than type 2 fibers
+C4025572	Episodic flaccid weakness
+C4025573	Increased muscle fatiguability
+C4025574	Genetic anticipation with paternal anticipation bias
+C4025576	EMG: myotonic runs
+C4025578	Late-onset proximal muscle weakness
+C4025579	Large beaked nose
+C4025582	Reduced dihydropyrimidine dehydrogenase activity
+C4025583	Cellular metachromasia
+C4025586	Electron transfer flavoprotein-ubiquinone oxidoreductase defect
+C4025589	Positive ferric chloride test
+C4025590	Foam cells with lamellar inclusion bodies
+C4025591	Absent urinary urothione
+C4025593	Increased intracellular sodium
+C4025594	Positive regitine blocking test
+C4025596	Abnormality of connective tissue
+C4025597	Subsarcolemmal accumulations of abnormally shaped mitochondria
+C4025598	Urinary glycosaminoglycan excretion
+C4025599	Increased serum iduronate sulfatase activity
+C4025600	Reduced xanthine dehydrogenase activity
+C4025601	Delayed oxidation of acetaldehyde
+C4025602	Ornithinuria
+C4025603	Glutaric acidemia
+C4025604	Parathormone-independent increased renal tubular calcium reabsorption
+C4025607	Elevated urine pyrophosphate
+C4025608	Defective dehydrogenation of isovaleryl CoA and butyryl CoA
+C4025609	EMG: axonal abnormality
+C4025610	Peripheral dysmyelination
+C4025612	Polyclonal elevation of IgM
+C4025613	Increased rate of premature chromosome condensation
+C4025614	EMG: chronic denervation signs
+C4025615	Decreased size of nerve terminals
+C4025616	CNS hypomyelination
+C4025619	Peripheral axonal atrophy
+C4025623	Elevated intracellular cystine
+C4025624	Endopolyploidy on chromosome studies of bone marrow
+C4025625	Impaired lymphocyte transformation with phytohemagglutinin
+C4025626	Elevated urinary norepinephrine
+C4025628	Abnormal enchondral ossification
+C4025629	Elevated circulating catecholamine level
+C4025630	Abnormal bone structure
+C4025631	Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
+C4025635	Argininuria
+C4025636	Reduced orotidine 5-prime phosphate decarboxylase activity
+C4025639	Prolonged G2 phase of cell cycle
+C4025640	Deficient excision of UV-induced pyrimidine dimers in DNA
+C4025641	Decreased pyruvate carboxylase activity
+C4025644	Hypothalamic gonadotropin-releasing hormone deficiency
+C4025648	Abnormal peripheral myelination
+C4025649	Reduced factor VIII activity
+C4025650	Abnormality of lipid metabolism
+C4025651	Increased circulating cortisol level
+C4025656	Abnormality of cholesterol metabolism
+C4025659	Abnormality of the shoulder
+C4025660	Abnormality of the ankles
+C4025662	Abnormality of the ulna
+C4025663	Abnormality of tibia morphology
+C4025664	Abnormality of fibula morphology
+C4025665	Aplasia/Hypoplasia involving the central nervous system
+C4025666	Abnormality of the forearm
+C4025668	Leydig cell insensitivity to gonadotropin
+C4025669	Decreased circulating ACTH level
+C4025670	Abnormality of chromosome segregation
+C4025671	Sudden episodic apnea
+C4025672	Impaired memory B-cell generation
+C4025673	Recurrent Burkholderia cepacia infections
+C4025674	Flared femoral metaphysis
+C4025675	Abnormality of the radius
+C4025676	Abnormality of the knee
+C4025679	Stippled chondral calcification
+C4025681	Recurrent enteroviral infections
+C4025682	Recurrent Serratia marcescens infections
+C4025683	Lymph node hypoplasia
+C4025684	Recurrent abscess formation
+C4025688	Abnormality of the skull base
+C4025690	Prenatal maternal abnormality
+C4025692	Abnormality of calvarial morphology
+C4025693	Hypertension associated with pheochromocytoma
+C4025695	Right aortic arch with mirror image branching
+C4025696	Paresis of extensor muscles of the big toe
+C4025697	Gastrointestinal atresia
+C4025698	Abnormality of the peritoneum
+C4025699	Abnormality of the stomach
+C4025700	Trichodysplasia
+C4025701	Abnormality of the cerebral cortex
+C4025703	Calcification of the small brain vessels
+C4025704	Abnormality of the corticospinal tract
+C4025705	Eye of the tiger anomaly of globus pallidus
+C4025706	Abnormality of the globus pallidus
+C4025707	Abnormal motor neuron morphology
+C4025708	Cerebellar malformation
+C4025711	Abnormality of the caudate nucleus
+C4025712	Abnormality of the cerebellar vermis
+C4025713	Paroxysmal drowsiness
+C4025714	Abnormality of the autonomic nervous system
+C4025715	Abnormality of the large intestine
+C4025716	Abnormality of the duodenum
+C4025717	Abnormality of the small intestine
+C4025718	Early balding
+C4025719	Dysgenesis of the cerebellar vermis
+C4025720	Pseudobulbar behavioral symptoms
+C4025723	Abnormal upper motor neuron morphology
+C4025726	Abnormality of the pleura
+C4025728	Increased neuronal autofluorescent lipopigment
+C4025730	Renal cortical atrophy
+C4025731	Abnormal thrombosis
+C4025732	Tubulointerstitial abnormality
+C4025733	Mesangial abnormality
+C4025734	Abnormality of the scalp
+C4025735	Nonspherocytic hemolytic anemia
+C4025736	Abnormality of basophils
+C4025738	Abnormality of eosinophils
+C4025739	Acroosteolysis of distal phalanges (feet)
+C4025740	Autoamputation of foot
+C4025741	Clinodactyly of the 5th toe
+C4025742	Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)
+C4025744	Foot acroosteolysis
+C4025747	Bulbous tips of toes
+C4025749	Abnormality of the spleen
+C4025750	Abnormality of the nasopharynx
+C4025751	Abnormality of the pancreas
+C4025752	Abnormal cardiac ventricle morphology
+C4025753	Abnormality of the tricuspid valve
+C4025755	Primary atrial arrhythmia
+C4025759	Abnormality of the mitral valve
+C4025760	Primary hypercorticolism
+C4025761	Abnormality of the integument
+C4025763	Abnormality of the rib cage
+C4025773	Aplasia/Hypoplasia involving the skeletal musculature
+C4025777	Autosomal dominant contiguous gene syndrome
+C4025787	Calvarial skull defect
+C4025788	Nystagmus-induced head nodding
+C4025789	Psychotic mentation
+C4025790	Specific learning disability
+C4025792	EEG with irregular generalized spike and wave complexes
+C4025793	Brain very small
+C4025795	Short tubular bones of the hand
+C4025796	Abnormality of the fingertips
+C4025797	Abnormality of prenatal development or birth
+C4025798	Abnormalities of placenta or umbilical cord
+C4025799	Ulnar claw
+C4025800	Large central visual field defect
+C4025805	Intermittent jaundice
+C4025806	High axial triradius
+C4025808	Facial flushing after alcohol intake
+C4025810	Abnormal palmar dermatoglyphics
+C4025811	Anemic pallor
+C4025813	Abnormality of subcutaneous fat tissue
+C4025814	Abnormality of the metaphysis
+C4025815	Short diaphyses
+C4025819	Abnormality of the hypothalamus-pituitary axis
+C4025821	Anterior hypopituitarism
+C4025822	Abnormality of the parathyroid gland
+C4025823	Abnormality of the endocrine system
+C4025826	Abnormality of the urethra
+C4025828	Abnormality of the scapula
+C4025829	Abnormality of the breast
+C4025830	Peripheral axonal degeneration
+C4025831	Abnormal peripheral nervous system morphology
+C4025834	Abnormal amplitude of pattern reversal visual evoked potentials
+C4025835	Abnormality of the nasolacrimal system
+C4025836	Abnormality of the choroid
+C4025838	Abnormality of the pharynx
+C4025840	Abnormality of the sclera
+C4025841	Abnormality of saccadic eye movements
+C4025843	Abnormality of refraction
+C4025844	Chorioretinal abnormality
+C4025845	Abnormality of the iris
+C4025846	Abnormality of vision
+C4025847	Abnormality of the conjunctiva
+C4025849	Abnormality of the fovea
+C4025850	Increased adipose tissue around the neck
+C4025853	Nasal mucosa telangiectasia
+C4025857	Incomplete partition of the cochlea type II
+C4025858	Abnormality of cochlea
+C4025860	Hearing abnormality
+C4025862	Abnormality of the maxilla
+C4025863	Abnormality of the orbital region
+C4025867	Abnormality of the forehead
+C4025868	Increased facial adipose tissue
+C4025871	Abnormality of the face
+C4025872	Abnormality of the mastoid
+C4025876	Abnormality of the fontanelles or cranial sutures
+C4025878	Tongue telangiectasia
+C4025881	Abnormality of oral frenula
+C4025883	Abnormality of lower lip
+C4025884	Abnormality of upper lip
+C4025886	Severe periodontitis
+C4025887	Abnormality of the oral cavity
+C4025888	Abnormality of the menstrual cycle
+C4025891	Ambiguous genitalia, female
+C4025892	Abnormality of the labia
+C4025893	Abnormality of the clitoris
+C4025895	Abnormality of the scrotum
+C4025896	Abnormality of the penis
+C4025897	Abnormality of male external genitalia
+C4025898	Functional abnormality of male internal genitalia
+C4025899	Abnormality of male internal genitalia
+C4025900	Abnormality of female internal genitalia
+C4025901	Abnormality of body height
+C4029280	Hypotonic facies
+C4038730	Asthma-chronic obstructive pulmonary disease overlap syndrome
+C4038738	Steep mandibular plane angle
+C4038754	Gastritis cystica profunda
+C4039254	Chronic pneumonia
+C4039764	Undifferentiated spondyloarthropathy
+C4039867	Acute Hypoxemic Respiratory Failure
+C4040007	Complex regional pain syndrome of upper limb
+C4040349	Bacteremia due to Methicillin resistant Staphylococcus aureus
+C4040419	Acute Hypercapnic Respiratory Failure
+C4040601	Dream enactment behavior
+C4040739	3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
+C4040834	Inflammation of fetal umbilical artery
+C4040879	STING-associated vasculopathy with onset in infancy
+C4041080	Neurocognitive Disorders
+C4041089	Poorly differentiated sarcoma
+C4041147	Acute exacerbation of chronic obstructive bronchitis
+C4041194	Lesion of fallopian tube
+C4041558	Cone-rod synaptic disorder, congenital nonprogressive
+C4042763	Postoperative Residual Curarization
+C4042784	Feeding and Eating Disorders
+C4042891	Sleep Wake Disorders
+C4042906	Mammary Analogue Secretory Carcinoma
+C4045968	Altitude Hypoxia
+C4045991	Perihilar Cholangiocarcinoma
+C4046002	Research-Related Injuries
+C4046029	Mental Disorders, Severe
+C4048158	Convulsions
+C4048184	Trochlear Nerve Diseases
+C4048195	Autosomal dominant hypocalcemia
+C4048196	beta-Mannosidosis
+C4048199	Ulnar deviation of the hand or of fingers of the hand
+C4048228	Congenital anomaly of anterior segment of eye
+C4048234	Undifferentiated spindle cell sarcoma
+C4048262	Hydronephrosis Due To Pujo
+C4048264	Nodular regenerative hyperplasia
+C4048268	Cortical visual impairment
+C4048270	Decreased antibody level in blood
+C4048273	Chorioretinal atrophy
+C4048296	Phantom Limb Pain
+C4048297	Idiopathic retroperitoneal fibrosis
+C4048304	Undifferentiated round cell sarcoma
+C4048305	Neuroepithelioma
+C4048306	Multiple endocrine neoplasia Type 2
+C4048328	Cancer of cervix
+C4048329	Immunosuppression
+C4048549	Malignant germ cell neoplasm
+C4048610	Cardiac procedure complication
+C4048700	Sclerosing rhabdomyosarcoma
+C4048705	Hypermethioninemia
+C4048750	Sphincter of Oddi Dyskinesia
+C4048798	Complete congenital stationary night blindness
+C4048801	Scalp defect
+C4048809	SCHWANNOMATOSIS 1
+C4048833	Satyr ear
+C4049005	Cataract, total congenital with posterior sutural opacities in Heterozygotes
+C4049006	Selective IgA immunodeficiency
+C4049050	Opalescent dentin
+C4049066	Retinal dystrophy with early macular involvement
+C4049272	Tumour budding
+C4049328	Renal medullary carcinoma
+C4049342	Foot osteomyelitis
+C4049343	Combined pulmonary fibrosis and emphysema
+C4049393	Chronic hepatitis C genotype 1a
+C4049446	Neointimal hyperplasia
+C4049615	Megaureter
+C4049636	ROSE Cluster 1
+C4049650	Familial Glucocorticoid Deficiency Type 1
+C4049702	Focal Segmental Glomerulosclerosis, Not Otherwise Specified
+C4049711	Lepidic Predominant Adenocarcinoma
+C4049714	Familial Glucocorticoid Deficiency Type 2
+C4049796	Abnormality of cardiovascular system morphology
+C4049830	Focal seizures, afebril
+C4049883	Obstructive Ureterocele
+C4049919	Insulin Sensitivity Measurement
+C4049938	Physical Activity Measurement
+C4049993	Aristolochic Acid Nephropathy
+C4050064	ROSE Cluster 5
+C4050313	ROSE Cluster 2
+C4050314	ROSE Cluster 3
+C4050407	Pauci-immune Glomerulonephritis associated with Granulomatosis with Polyangiitis
+C4050504	Ectomesenchymal Chondromyxoid Tumor
+C4050627	Soluble P-Selectin Measurement
+C4053506	Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation
+C4053514	Nasal Chondromesenchymal Hamartoma
+C4053521	Hemosiderotic Fibrolipomatous Tumor
+C4053528	Cribriform Neuroepithelial Tumor
+C4053736	Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
+C4053762	Congenital Renal Hypoplasia
+C4053775	Pituitary stalk interruption syndrome
+C4053936	Thyroglobulin Deficiency
+C4054043	Secondary Peripheral Chondrosarcoma
+C4054044	Secondary Hemophagocytic Lymphohistiocytosis
+C4054076	Renal Angiomyoadenomatous Tumor
+C4054085	Refractory Childhood Acute Lymphoblastic Leukemia
+C4054120	Rat Neuroblastoma
+C4054121	Rat Insulinoma
+C4054122	Rat Adrenal Gland Pheochromocytoma
+C4054127	Radiation Nephropathy
+C4054188	Ph-Like Acute Lymphoblastic Leukemia
+C4054251	Pancreaticobiliary Malunion
+C4054287	Ovarian Microcystic Stromal Tumor
+C4054476	Monogenic Obesity
+C4054534	Meningioangiomatosis
+C4054543	Membranous Lupus Nephritis
+C4054590	Lupus Flare
+C4054726	Infant Leukemia
+C4054727	Infant Acute Lymphoblastic Leukemia
+C4054752	Hypocellular Myelodysplastic Syndrome
+C4054891	Grade III Chondrosarcoma
+C4054892	Grade II Chondrosarcoma
+C4054911	Fusion-Positive Rhabdomyosarcoma
+C4054945	Focal Segmental Glomerulosclerosis Collapsing Variant
+C4055018	Familial Atypical Hemolytic Uremic Syndrome
+C4055160	Deep Circumscribed Morphea
+C4055183	Contrast - Induced Nephropathy
+C4055342	C3 Glomerulonephritis
+C4055466	Angiosarcoma of Soft Tissue
+C4055488	Adnexal Dysplasia
+C4060446	Papilloma of breast
+C4068743	Juvenile open angle
+C4068858	Avascular retina
+C4068898	Pseudohypopyon
+C4072686	Cardiovascular disease+Pulmonary disease
+C4072820	Large bregma sutures
+C4072821	Large, late-closing fontanelle
+C4072822	Wide bregma sutures
+C4072823	Broad cranium shape
+C4072824	Wide skull shape
+C4072825	Thickened facial skin with coarse facial features
+C4072826	Skin tag on the posterior cheek
+C4072830	Asymmetry of the posterior cranium
+C4072831	Delayed closure of the soft spot on the skull
+C4072832	Distortion of face
+C4072833	Funny looking face
+C4072834	Rough hair texture
+C4072835	Kinky hair texture
+C4072836	Nappy hair texture
+C4072837	Fractured hair
+C4072838	Hypoplasia of foramen magnum
+C4072839	Abnormality of the hypophysial fossa
+C4072841	J-shaped hypophysial fossa
+C4072842	Omega shaped hypophysial fossa
+C4072844	Missing sinuses
+C4072845	Hyperplasia of hypophysial fossa
+C4072846	Large hypophysial fossa
+C4072847	HyperCalcification of skull base
+C4072848	HyperMineralization of skull base
+C4072849	Scapular weakness
+C4072850	Increased calcification of skull
+C4072851	Increased Mineralization of skull
+C4072853	Early closure of the bregma sutures
+C4072857	Focal absence of scalp tissue
+C4072858	Solitary scalp defect
+C4072863	Dull foveal reflex
+C4072867	obsolete Peripheral retinopathy
+C4072868	Paravenous chorioretinal atrophy
+C4072872	obsolete Rod-cone dystrophy
+C4072873	Limited eye motility from Duane anomaly
+C4072877	Scalp folds
+C4072878	Premaxillary retrusion
+C4072879	Small cheekbone
+C4072880	Abnormality of hair consistency
+C4072881	Abnormality of hair curl pattern
+C4072883	Abnormal craniofacial posture
+C4072884	Ciliary body coloboma
+C4072885	Increased serum testosterone level
+C4072889	Decreased circulating follicle stimulating hormone level
+C4072890	Decreased circulating luteinizing hormone level
+C4072891	Abnormal circulating follicle-stimulating hormone level
+C4072893	Increased circulating androgen level
+C4072894	Decreased circulating androgen level
+C4072897	Decreased serum insulin-like growth factor 1
+C4072902	Reduced muscle carnitine level
+C4072907	Hyperphalangy of the 2nd finger
+C4072908	Induced vaginal delivery
+C4072928	Spoken Word Recognition Deficit
+C4072940	Ossifying fibroma of the jaw
+C4072958	Abnormal multifocal electroretinogram
+C4072973	Reduced amplitude of dark-adapted bright flash electroretinogram a-wave
+C4072980	Exudative vitreoretinopathy
+C4072987	Yellow/white lesions of the macula
+C4072992	Retinal crystals
+C4072995	Difficulty adjusting from light to dark
+C4073008	Abnormal best corrected visual acuity test
+C4073079	Photoreceptor layer loss on macular OCT
+C4073083	Abnormal foveal morphology on macular OCT
+C4073099	Perifoveal ring of hyperautofluorescence
+C4073101	Hyperautofluorescent macular lesion
+C4073107	Incomplete congenital stationary night blindness
+C4073109	Blind-spot enlargment
+C4073118	Optically empty vitreous
+C4073127	Decreased adiponectin level
+C4073132	Abnormal pelvis bone morphology
+C4073134	Abnormality of the periosteum
+C4073137	Decreased serum testosterone level
+C4073143	Increased level of platelet-activating factor
+C4073145	Hyperkeratosis pilaris
+C4073146	White scaling skin
+C4073161	Abnormal circulating insulin level
+C4073162	Elevated hemoglobin A1c
+C4073167	Osteolysis involving bones of the upper limbs
+C4073168	Abnormal lactate dehydrogenase activity
+C4073171	Elevated plasma acylcarnitine levels
+C4073178	Tiger tail banding
+C4073182	Decreased carnitine level in liver
+C4073184	Thick hair
+C4073207	Bilateral facial muscle weakness
+C4073208	Abnormality of the shape of the midface
+C4073209	Maxillary prognathia
+C4073228	Abnormality of buccal mucosa
+C4073245	Abnormality of neck blood vessel
+C4073290	Abnormality of hair volume
+C4073291	Hyperplasia of foramen magnum
+C4073292	Afro-textured hair
+C4073295	Decreased levels of alpha-fetoprotein
+C4074771	Sterility, Reproductive
+C4075603	Occult chronic type B viral hepatitis
+C4075720	Severe alcohol dependence
+C4075847	Decompensated liver disease
+C4075851	Autoimmune cholangitis
+C4076240	Chronic kidney disease mineral and bone disorder
+C4076304	Dental plaque induced gingivitis
+C4076349	Chronic alcoholic liver disease
+C4076533	Encephalitis caused by tick-borne encephalitis virus
+C4076671	Prostate cancer metastatic to bone
+C4080064	Autosomal Dominant Hereditary Pancreatitis
+C4081731	Hereditary systemic amyloidosis
+C4082144	Metatarsal Valgus
+C4082167	Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome
+C4082168	Partial duplication of thumb phalanx
+C4082169	Metatarsus Varus
+C4082171	Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency
+C4082172	Porencephalic cyst
+C4082173	Porencephaly
+C4082174	Thyrotropin deficiency, isolated
+C4082197	Charcot-Marie-Tooth disease type 4
+C4082200	Rootless teeth
+C4082243	Maxillary retrognathia
+C4082299	Bulbar palsy
+C4082301	Developmental Porencephaly
+C4082304	Oligodontia
+C4082305	Deaf Mutism
+C4082761	Abnormality of limb bone morphology
+C4082764	Gastrointestinal infection
+C4082769	Chronic Traumatic Encephalopathy
+C4082933	Allergy to animal
+C4082937	Necrotizing enterocolitis in fetus OR newborn
+C4082954	Hypoplasia of right ventricle
+C4082974	Dupuytren's Disease
+C4083008	Guillain-Barre Syndrome, Familial
+C4083045	PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
+C4083046	Absent upper lateral incisors
+C4083047	MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO
+C4083048	SPONDYLOCOSTAL DYSOSTOSIS 5
+C4083050	Tooth agenesis
+C4083056	Basal cell carcinoma, nodular
+C4083076	Increased head circumference
+C4083212	Alopecia, Male Pattern
+C4083251	Trichothiodystrophy, Nonphotosensitive 1
+C4083290	Missing incisors
+C4084708	DEAFNESS, AUTOSOMAL DOMINANT 40
+C4084709	DEAFNESS, AUTOSOMAL RECESSIVE 97
+C4084712	DEAFNESS, AUTOSOMAL DOMINANT 67
+C4084821	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U
+C4084822	JOUBERT SYNDROME 23
+C4084823	MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL
+C4084840	FANCONI ANEMIA, COMPLEMENTATION GROUP T
+C4084841	JOUBERT SYNDROME 24
+C4084842	JOUBERT SYNDROME 25
+C4084843	JOUBERT SYNDROME 26
+C4084968	Hereditary Hyperekplexia
+C4085238	MYOCLONIC-ATONIC EPILEPSY
+C4085243	MEND SYNDROME
+C4085248	OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO
+C4085250	PAGET DISEASE OF BONE 6
+C4085251	PAGET DISEASE OF BONE 2, EARLY-ONSET
+C4085252	PAGET DISEASE OF BONE 3
+C4085370	Fibromatosis, Palmar
+C4085580	Carbamoyl Phosphate Synthase 1 Deficiency
+C4085582	MENTAL RETARDATION, X-LINKED 102
+C4085590	Cone-Rod Dystrophies
+C4085595	AL-RAQAD SYNDROME
+C4085597	CHOPS SYNDROME
+C4085873	LUSCAN-LUMISH SYNDROME
+C4086152	Childhood Astrocytoma
+C4086165	Childhood Neuroblastoma
+C4086607	Mouse Kidney Carcinoma
+C4086611	Mucolipidosis Type IIIA
+C4086945	Ventilatory Threshold
+C4086965	Woodchuck Hepatocellular Carcinoma
+C4087273	C3 glomerulopathy
+C4087347	Autosomal dominant cerebellar ataxia
+C4087491	End stage COPD
+C4087504	Peritoneal dissemination
+C4225153	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
+C4225154	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3
+C4225155	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY
+C4225156	MENTAL RETARDATION, AUTOSOMAL DOMINANT 34
+C4225157	FAMILIAL ADENOMATOUS POLYPOSIS 3
+C4225158	SPINOCEREBELLAR ATAXIA 41
+C4225159	REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET
+C4225160	NUDT15 deficiency
+C4225161	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3
+C4225162	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE
+C4225163	MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)
+C4225164	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
+C4225165	NEPHROTIC SYNDROME, TYPE 13
+C4225166	NEPHROTIC SYNDROME, TYPE 12
+C4225167	SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY
+C4225168	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52
+C4225169	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3
+C4225170	LEUKODYSTROPHY, HYPOMYELINATING, 13
+C4225171	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION
+C4225172	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION
+C4225173	IMMUNODEFICIENCY, COMMON VARIABLE, 13
+C4225174	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO
+C4225176	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2
+C4225177	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1
+C4225178	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA
+C4225179	COWDEN SYNDROME 7
+C4225180	EVEN-PLUS SYNDROME
+C4225181	MYOPATHY, SCAPULOHUMEROPERONEAL
+C4225182	CATARACT 45
+C4225183	BRACHYDACTYLY, TYPE A1, D
+C4225184	LYMPHATIC MALFORMATION 6
+C4225186	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
+C4225187	EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE
+C4225188	MEIER-GORLIN SYNDROME 6
+C4225189	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS
+C4225190	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp
+C4225191	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo
+C4225192	MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, WITH CARDIOMYOPATHY AND TRIANGULAR TONGUE
+C4225193	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA
+C4225194	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 3
+C4225195	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2
+C4225196	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION
+C4225197	PREIMPLANTATION EMBRYONIC LETHALITY 1
+C4225199	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 25
+C4225200	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
+C4225201	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6
+C4225202	LAMB-SHAFFER SYNDROME
+C4225203	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2
+C4225205	SPINOCEREBELLAR ATAXIA 42
+C4225206	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
+C4225208	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS
+C4225209	OROFACIAL CLEFT 15
+C4225210	OOCYTE MATURATION DEFECT 2
+C4225211	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2
+C4225212	SECKEL SYNDROME 9
+C4225213	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA
+C4225214	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3
+C4225215	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES
+C4225217	HETEROTAXY, VISCERAL, 7, AUTOSOMAL
+C4225218	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
+C4225219	IMMUNODEFICIENCY 46
+C4225220	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51
+C4225221	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
+C4225222	TAKENOUCHI-KOSAKI SYNDROME
+C4225223	TREMOR, HEREDITARY ESSENTIAL, 5
+C4225225	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2
+C4225226	COENZYME Q10 DEFICIENCY, PRIMARY, 8
+C4225227	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES
+C4225228	NEPHROTIC SYNDROME, TYPE 11
+C4225229	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES
+C4225230	CILIARY DYSKINESIA, PRIMARY, 33
+C4225231	TOOTH AGENESIS, SELECTIVE, 7
+C4225232	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE
+C4225233	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT
+C4225234	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn
+C4225235	MYASTHENIC SYNDROME, CONGENITAL, 19
+C4225236	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21
+C4225237	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5
+C4225238	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
+C4225239	DESANTO-SHINAWI SYNDROME
+C4225240	DEAFNESS, AUTOSOMAL DOMINANT 68
+C4225241	DEAFNESS, AUTOSOMAL DOMINANT 69
+C4225242	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2
+C4225243	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z
+C4225244	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y
+C4225245	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14
+C4225246	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K
+C4225247	LEUKODYSTROPHY, HYPOMYELINATING, 12
+C4225248	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME
+C4225249	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE
+C4225250	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE
+C4225251	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27
+C4225252	IMMUNODEFICIENCY 45
+C4225253	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
+C4225254	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY
+C4225255	YUAN-HAREL-LUPSKI SYNDROME
+C4225256	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 35
+C4225257	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 34
+C4225258	EPILEPSY, PROGRESSIVE MYOCLONIC, 10
+C4225259	SMITH-KINGSMORE SYNDROME
+C4225260	IMMUNODEFICIENCY 44
+C4225261	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME
+C4225262	POROKERATOSIS 9, MULTIPLE TYPES
+C4225263	SENIOR-LOKEN SYNDROME 9
+C4225265	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W
+C4225266	IMMUNODEFICIENCY 42
+C4225267	HEIMLER SYNDROME 2
+C4225268	CUTIS LAXA, AUTOSOMAL DOMINANT 3
+C4225269	CRANIOSYNOSTOSIS 6
+C4225270	KOSAKI OVERGROWTH SYNDROME
+C4225271	ADAMS-OLIVER SYNDROME 6
+C4225272	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
+C4225273	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE
+C4225274	AU-KLINE SYNDROME
+C4225275	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40
+C4225276	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME
+C4225277	IMMUNODEFICIENCY, COMMON VARIABLE, 12
+C4225278	GLIOMA SUSCEPTIBILITY 9
+C4225279	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE
+C4225280	NOONAN SYNDROME 10
+C4225281	RETINITIS PIGMENTOSA 74
+C4225282	NOONAN SYNDROME 9
+C4225283	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7
+C4225284	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6
+C4225285	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM
+C4225286	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY
+C4225287	RETINITIS PIGMENTOSA 73
+C4225288	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION
+C4225289	EPILEPSY, PROGRESSIVE MYOCLONIC, 9
+C4225290	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26
+C4225291	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9
+C4225292	THYROID CANCER, NONMEDULLARY, 5
+C4225293	THYROID CANCER, NONMEDULLARY, 4
+C4225294	HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 7
+C4225295	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS
+C4225296	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
+C4225297	ACHROMATOPSIA 7
+C4225298	DEAFNESS, AUTOSOMAL RECESSIVE 104
+C4225299	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14
+C4225300	CATARACT 44
+C4225301	OSTEOGENESIS IMPERFECTA, TYPE XVII
+C4225302	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB
+C4225303	LETHAL CONGENITAL CONTRACTURE SYNDROME 9
+C4225304	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4
+C4225305	LEUKODYSTROPHY, HYPOMYELINATING, 11
+C4225306	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V
+C4225307	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES
+C4225308	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII
+C4225309	EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY
+C4225310	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE
+C4225311	CILIARY DYSKINESIA, PRIMARY, 32
+C4225312	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2
+C4225313	BETHLEM MYOPATHY 2
+C4225314	ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2
+C4225315	RETINITIS PIGMENTOSA 72
+C4225316	EXUDATIVE VITREORETINOPATHY 6
+C4225317	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE
+C4225318	EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
+C4225319	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50
+C4225320	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 50
+C4225321	ZIMMERMANN-LABAND SYNDROME 2
+C4225322	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE
+C4225323	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME
+C4225324	CANDIDIASIS, FAMILIAL, 9
+C4225325	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4
+C4225326	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3
+C4225327	EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
+C4225328	IMMUNODEFICIENCY 40
+C4225329	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25
+C4225330	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10
+C4225331	46,XY SEX REVERSAL 10
+C4225332	LEUKODYSTROPHY, HYPOMYELINATING, 10
+C4225333	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION
+C4225334	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE
+C4225335	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6
+C4225336	DYSTONIA 27
+C4225337	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33
+C4225338	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE
+C4225339	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2
+C4225340	BRUGADA SYNDROME 9
+C4225341	DYSTONIA 26, MYOCLONIC
+C4225342	RETINITIS PIGMENTOSA 71
+C4225343	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38
+C4225344	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE
+C4225345	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G
+C4225346	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3
+C4225347	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4
+C4225348	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4
+C4225349	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA
+C4225350	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 32
+C4225351	White Sutton syndrome
+C4225352	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36
+C4225353	PARKINSON DISEASE 21
+C4225354	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35
+C4225355	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20
+C4225356	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6
+C4225357	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31
+C4225358	IMMUNODEFICIENCY 39
+C4225359	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA
+C4225360	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 30
+C4225361	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 29
+C4225362	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3
+C4225363	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
+C4225364	MYASTHENIC SYNDROME, CONGENITAL, 18
+C4225365	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13
+C4225367	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
+C4225368	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
+C4225369	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL
+C4225370	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
+C4225371	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL
+C4225372	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL
+C4225374	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL
+C4225375	MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
+C4225376	SENIOR-LOKEN SYNDROME 8
+C4225377	MYASTHENIC SYNDROME, CONGENITAL, 17
+C4225378	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY
+C4225379	LIPOYLTRANSFERASE 1 DEFICIENCY
+C4225380	SINGLETON-MERTEN SYNDROME 2
+C4225381	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS
+C4225382	COLE-CARPENTER SYNDROME 2
+C4225383	LICHTENSTEIN-KNORR SYNDROME
+C4225384	OPTIC ATROPHY 9
+C4225385	LETHAL CONGENITAL CONTRACTURE SYNDROME 8
+C4225386	LETHAL CONGENITAL CONTRACTURE SYNDROME 7
+C4225387	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT
+C4225388	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49
+C4225389	CATARACT 43
+C4225390	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5
+C4225391	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
+C4225392	COENZYME Q10 DEFICIENCY, PRIMARY, 7
+C4225393	3-methylglutaconic aciduria type 7
+C4225394	AMELOGENESIS IMPERFECTA, TYPE IF
+C4225395	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48
+C4225396	ARBOLEDA-THAM SYNDROME
+C4225397	ATAXIA-OCULOMOTOR APRAXIA 4
+C4225398	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY
+C4225399	SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES
+C4225400	INTERSTITIAL LUNG AND LIVER DISEASE
+C4225402	PREMATURE OVARIAN FAILURE 10
+C4225403	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION
+C4225404	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE
+C4225405	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL
+C4225406	NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION
+C4225408	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25
+C4225409	EPILEPSY, PROGRESSIVE MYOCLONIC, 5, FORMERLY
+C4225411	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS
+C4225412	Spondylo-ocular syndrome
+C4225413	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL
+C4225414	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24
+C4225415	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3
+C4225416	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED
+C4225417	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34
+C4225418	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
+C4225419	RITSCHER-SCHINZEL SYNDROME 2
+C4225420	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE
+C4225421	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3
+C4225422	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS
+C4225423	REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET
+C4225424	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY
+C4225425	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY
+C4225426	THYROID CANCER, NONMEDULLARY, 2
+C4225427	SINGLETON-MERTEN SYNDROME 1
+C4225428	ANEMIA, SIDEROBLASTIC, 4
+C4225429	Ehlers-Danlos syndrome classic type
+C4225431	CHROMOSOME 10p12-p11 DELETION SYNDROME
+C4225432	CHROMOSOME 2p25.3 DUPLICATION SYNDROME
+C4225433	CHROMOSOME 2p25.3 DELETION SYNDROME
+C4225434	CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL
+C4225436	RETINAL DYSTROPHY, EARLY-ONSET, WITH OR WITHOUT PITUITARY DYSFUNCTION
+C4225440	EPILEPSY, PROGRESSIVE MYOCLONIC, WITH SENSORY ATAXIC NEUROPATHY
+C4225445	PLASMINOGEN DEFICIENCY, TYPE II
+C4225503	SPERMATOGENIC FAILURE 6
+C4225591	MITOCHONDRIAL MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3 (1 patient)
+C4225596	INCONTINENTIA PIGMENTI, ATYPICAL
+C4225631	HEREDITARY HEMORRHAGIC TELANGIECTASIA 1
+C4225666	CHROMOSOME 15q14 DELETION SYNDROME
+C4225667	CHROMOSOME 16p13.2 DELETION SYNDROME
+C4225671	VATER/VACTERL ASSOCIATION
+C4227331	Cardiomyocyte hypertrophy
+C4227831	Absence of lateral incisor
+C4228227	Small thymus
+C4228933	Limited jaw mobility
+C4229090	Decreased size of facial bones
+C4229565	Loss in color vision
+C4230640	Convex nasal bridge
+C4235577	response to bleomycin
+C4237227	Obstructive sleep apnea hypopnea
+C4237343	Overweight or obesity
+C4255008	Multiple osteochondroma of long bone
+C4255010	Non-ST Elevated Myocardial Infarction
+C4255043	Microphthalmos co-occurrent with congenital ocular coloboma
+C4255079	Familial Hyperekplexia
+C4255098	Cleft tongue
+C4255193	Bilateral Vestibulopathy
+C4255213	Increased size of skull
+C4255214	Fusion of foot joint
+C4255450	Familial malignant neoplasm of pancreas
+C4266441	Thyroid tumor metastasis
+C4266451	Fetal abnormality
+C4268182	Obesity hypoventilation syndrome (OHS)
+C4268599	Food-protein induced enterocolitis syndrome
+C4268691	Tumor necrosis factor receptor associated periodic syndrome [TRAPS]
+C4268694	Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome [PFAPA]
+C4268741	Age-related sarcopenia
+C4272578	Autosomal Recessive Osteopetrosis
+C4272579	Autosomal Dominant Osteopetrosis
+C4273658	Graham Little Piccardi Lassueur syndrome
+C4273671	Inherited predisposition to essential thrombocythemia
+C4273726	Congenital dysplasia of cardiac valve
+C4273756	Hepatoportal sclerosis
+C4273897	Distal monosomy 1q
+C4273952	Folinic acid responsive seizure syndrome
+C4273958	Obesity due to melanocortin 4 receptor deficiency
+C4273964	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
+C4273970	Familial pseudohyperkalemia
+C4273988	Benign adult familial myoclonic epilepsy
+C4274029	Biliary atresia with splenic malformation syndrome
+C4274077	Autosomal recessive sideroblastic anemia
+C4274078	Hyperinsulinism due to HNF4A deficiency
+C4274079	Bile acid CoA ligase deficiency and defective amidation
+C4274080	Autosomal dominant hyperinsulinism due to SUR1 deficiency
+C4274081	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
+C4274084	Pelizaeus Merzbacher like disease
+C4274085	Syndromic recessive X-linked ichthyosis
+C4274118	Joubert syndrome with ocular defect
+C4274282	Nanophthalmia
+C4274307	Hypoplastic tibia and postaxial polydactyly syndrome
+C4274324	Genetic recurrent myoglobinuria
+C4274329	FRAXF syndrome
+C4274343	Solitary rectal ulcer syndrome
+C4274354	Severe early childhood onset retinal dystrophy
+C4274355	Autosomal dominant late onset Parkinson disease
+C4274391	Dominant beta-thalassemia
+C4274414	Epstein-Barr virus associated gastric carcinoma
+C4274665	Logopenic progressive aphasia
+C4274732	Ischio-vertebral syndrome
+C4274761	Autosomal dominant spondylocostal dysostosis
+C4274947	Multiple endocrine neoplasia type 4
+C4274986	Spinocerebellar ataxia type 31
+C4274987	Spinocerebellar ataxia type 29
+C4274988	Spinocerebellar ataxia type 28
+C4274995	Lissencephaly with cerebellar hypoplasia
+C4275003	Familial Creutzfeldt-Jakob
+C4275008	Acetazolamide responsive myotonia
+C4275023	Spinocerebellar ataxia type 10
+C4275024	Spinocerebellar ataxia type 8
+C4275029	Maternal uniparental disomy of chromosome 20
+C4275033	Syndactyly type 1
+C4275062	Intestinal epithelial dysplasia
+C4275067	Transthyretin related familial amyloid cardiomyopathy
+C4275073	Desmin related myopathy with Mallory body-like inclusions
+C4275075	Atypical Werner syndrome
+C4275079	Posterior cortical atrophy syndrome
+C4275153	Hereditary glucocorticoid resistance
+C4275164	Autosomal dominant optic atrophy plus syndrome
+C4275170	Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
+C4275179	Young onset Parkinson disease
+C4275181	Autosomal recessive limb girdle muscular dystrophy type 2A
+C4275182	Autosomal recessive limb girdle muscular dystrophy type 2D
+C4275242	Sudden sensorineural hearing loss
+C4275252	Familial spontaneous pneumothorax
+C4277521	Cerebrospinal Fluid Hypovolemia
+C4277533	Dissection, Blood Vessel
+C4277682	Chemical and Drug Induced Liver Injury
+C4277690	Ciliopathies
+C4279912	Chemically-Induced Liver Toxicity
+C4279940	Tillaux Fracture
+C4280251	Absence of a tooth
+C4280252	Diastema between maxillary central incisors
+C4280253	Increased porosity of tooth enamel
+C4280254	Sclerosis of spinal bone
+C4280256	Hypotrophic paranasal sinus
+C4280258	Asymmetry of head
+C4280259	True denticles
+C4280260	Abnormality of skull bone morphology
+C4280262	Dystrophic tooth enamel
+C4280263	Increased size of permanent maxillary central incisor
+C4280264	Premature plaque build-up in arteries
+C4280265	Hyperplasia of frontal sinus
+C4280266	Soft teeth
+C4280267	Palatal spider veins
+C4280268	Underdevelopment of facial bones
+C4280269	Noncancerous mole
+C4280272	Increased projection of maxilla
+C4280273	Hypertrophy of maxilla
+C4280284	Small, pointed teeth
+C4280285	Small, peg shaped teeth
+C4280288	Red and sore lips
+C4280289	Lesion of oral cavity
+C4280291	Nappy scalp hair texture
+C4280292	Kinky scalp hair texture
+C4280293	Afro-textured scalp hair
+C4280298	Curvature of finger
+C4280304	Curvature of digit
+C4280305	Kabuki syndrome eyelids
+C4280317	Abnormal bone maturation
+C4280318	Indented bridge of nose
+C4280319	Cleft nasal bridge
+C4280320	Hypotrophic midface
+C4280321	Decreased projection of midface
+C4280331	Abnormal shape/structure of ear
+C4280333	Recurrent sinus disease
+C4280335	Extra cusp on inside of front tooth
+C4280336	Soft tooth enamel
+C4280341	Pointed front tooth
+C4280342	Peg shaped front tooth
+C4280351	Absence of bicuspid
+C4280363	Drooping upper lip
+C4280365	Hyperplasia of columella
+C4280366	Malformation of the temporomandibular joint
+C4280367	Abnormal maturation of foot bones
+C4280368	Hypotrophic cheekbone
+C4280369	Flattening of the zygomatic bone
+C4280370	Depressed cheekbone
+C4280374	Hyperplasia of malar bones
+C4280377	Abnormality of femoral head development
+C4280378	Thickening of the scalp
+C4280379	Thin skull bone
+C4280380	Repeated speech
+C4280381	Smooth dorsum of tongue
+C4280382	Atrophy of lingual surface
+C4280383	Atrophy of dorsum of tongue
+C4280385	Hole in roof of mouth
+C4280390	Collapsed nostrils
+C4280391	Missing nose
+C4280392	Hypotrophic nose
+C4280393	Absent finger bone of the hand
+C4280395	Rounded columella
+C4280402	Abnormal maturation of the pelvis bone
+C4280404	Notch of lower alveolar process
+C4280405	Cleft of lower gingiva
+C4280406	Cleft of lower alveolar process
+C4280407	Increasing overgrowth of gum ridge
+C4280410	Delayed maturation of the head of the thigh bone
+C4280411	Delayed maturation fo pubic bone
+C4280412	Large tailbone
+C4280413	Congenital malformed nails
+C4280414	Delayed heel bone maturation
+C4280415	Irregular ankle bone maturation
+C4280417	Accelerated ankle bone maturation
+C4280418	Delayed ankle bone maturation
+C4280419	Unequal size of opening between the eyelids
+C4280421	Abnormally small eyeball on both sides
+C4280422	Bilateral nanophthalmos
+C4280423	Small condylar neck of mandible
+C4280424	Small condylar head of mandible
+C4280425	Hypotrophic mandibular condyle
+C4280426	Hypotrophic condylar process of mandible
+C4280427	Hypoplasia of condylar neck of mandible
+C4280428	Hypoplasia of condylar head of mandible
+C4280429	Underdevelopment of condylar neck of mandible
+C4280430	Failure of development of the condylar process of mandible
+C4280431	Failure of development of condylar neck of mandible
+C4280432	Failure of development of condylar head of mandible
+C4280433	Agenesis of condylar neck of mandible
+C4280434	Agenesis of condylar head of mandible
+C4280435	Absence of the condylar process of mandible
+C4280436	Absence of the condylar neck of mandible
+C4280437	Absence of the condylar head of mandible
+C4280441	Decreased pneumatization of paranasal sinus
+C4280442	Atelectasis of paranasal sinus
+C4280443	Absent bone maturation in sternum
+C4280444	Abnormality of the wide portion of the femoral bone
+C4280445	Abnormality of alveolar processes of jaw
+C4280446	Delayed bone maturation of the knee cap
+C4280447	Unerupted adult dentition
+C4280448	Narrowing of pulp chamber of tooth
+C4280454	Flattening of alveolar margin
+C4280455	Flattening of alveolar processes of jaw
+C4280456	Dysplasia of tooth enamel
+C4280457	Defective enamel matrix
+C4280460	White spot lesions of tooth enamel
+C4280461	Fluorosis of tooth enamel
+C4280466	Severe delay in maturation of wrist bone
+C4280468	Enlargement of the inner surface of the skull bones
+C4280469	Thick inner surface of the skull bones
+C4280470	Overgrowth of the inside of the skull
+C4280471	Increased ossification of the internal surface of the cranial bones
+C4280472	Hypertrophy of the internal surface of the cranial bones
+C4280476	Increased bone density in skeletal bones
+C4280477	Curvature of outermost bone of little finger
+C4280479	Increased volume of frontal sinus
+C4280480	Increased size of frontal sinus
+C4280481	Hypertrophy of frontal sinus
+C4280482	Flat back of the head
+C4280483	Thin bone of forehead
+C4280484	Hypotrophic frontal bones
+C4280485	Increased ossification of facial bones
+C4280486	Hypertrophy of facial bones
+C4280487	Enlargement of facial bones
+C4280489	Visible nasal septum
+C4280490	Low hanging nasal septum
+C4280494	Hypotrophic bridge of nose
+C4280495	Concave bridge of nose
+C4280496	Hypotrophic nasal tip
+C4280497	Aplasia of nasal tip
+C4280498	Hypertrophy of nasal tip
+C4280499	Hyperplasia of nasal tip
+C4280500	Bulbous tip of nose
+C4280501	Failure of development of nasal septal cartilage
+C4280503	Premature hardening of arteries
+C4280504	Accelerated plaque build-up in arteries
+C4280505	Hardened artery wall in small cerebral arteries
+C4280507	Episodic rapid heart beat
+C4280508	Foot crease
+C4280512	Inability to touch chin to chest
+C4280513	Eburnation of spinal bone
+C4280514	Concrete spinal bone
+C4280515	Compact spinal bone
+C4280516	Thick craniofacial bones
+C4280517	Enlargement of craniofacial bones
+C4280518	Hypertrophy of craniofacial bones
+C4280519	Increased ossification of calvarial bones
+C4280520	Enlargement of calvarial bones
+C4280521	Thick lower jaw bone
+C4280522	Excessive growth of mandibular bone
+C4280523	Increased ossification of lower jaw
+C4280524	Thick inner surface of the frontal bone
+C4280525	Enlargement of the inner surface of the frontal bone
+C4280526	Increased ossification of the internal surface of the frontal bone
+C4280527	Hypertrophy of the internal surface of the frontal bone
+C4280528	Thick skull bones
+C4280529	Excessive growth of skull bones
+C4280530	Hypertrophy of cranial bones
+C4280531	Enlargement of skull bones
+C4280532	Decreased width of the skull
+C4280533	Decreased calcification of skull
+C4280536	Accelerated wrist bone maturation
+C4280537	Absent wrist bone
+C4280538	Curvature of little finger
+C4280539	Central cleft of nose
+C4280545	Decreased size of mandibular ramus
+C4280546	False denticles
+C4280547	Infected joint
+C4280548	Hypotrophic frontal sinus
+C4280549	Decreased pneumatization of frontal sinus
+C4280554	Increased diameter of foramen magnum
+C4280555	Increased circumference of foramen magnum
+C4280557	Hypotrophic facial bones
+C4280558	Flattening of facial bones
+C4280559	Aplasia of frontal sinus
+C4280560	Increased thickness of cranium
+C4280562	Malformation of skull shape
+C4280563	Abnormality of skull shape
+C4280564	Cloverleaf cranium shape
+C4280565	Delayed maturation of end part of long bone
+C4280566	Abnormal development of end part of bone
+C4280567	Abnormal skeletal development
+C4280568	Hardened artery wall
+C4280569	Plaque build-up in arteries
+C4280570	Increased tone of facial muscles
+C4280571	Increased stiffness of facial muscles
+C4280572	Acute blood cancer
+C4280573	Communication delay
+C4280574	Problems speaking
+C4280575	Progressive brain disease
+C4280576	Difficulty making arithmetical calculations
+C4280577	Uncoordinated limb movement
+C4280578	Grey eyelashes
+C4280579	Grey eyebrow
+C4280580	Blonde eyebrow
+C4280581	Aplasia of eyebrows
+C4280582	Agenesis of eyebrows
+C4280583	Hypertrophy of forehead
+C4280584	Hyperplasia of forehead
+C4280585	Hypoplasia of columella
+C4280586	Curvature of the little toe
+C4280587	Toe curvature
+C4280590	Increased size of tooth
+C4280591	Hypertrophy of tooth
+C4280592	Hyperplasia of tooth
+C4280593	Multiple buried teeth
+C4280594	Small wrist bones
+C4280596	Calvarial defect
+C4280597	Rhomboid shaped head
+C4280598	Flattening of head
+C4280599	Delayed maturation of wrist bone
+C4280601	Xanthoma of periocular region
+C4280602	Xanthelasma of periocular region
+C4280603	Increased size of palpebral fissures
+C4280604	Speckled iris
+C4280605	Baby eczema
+C4280606	Hanging skin
+C4280607	Small wings of the pelvic girdle
+C4280609	Bone loss around tooth root
+C4280610	Abnormality of position of teeth
+C4280611	Decreased size of teeth
+C4280612	Decreased width of tooth
+C4280613	Angle class 3 malocclusion
+C4280614	Angle class 2 malocclusion
+C4280615	Defective tooth enamel
+C4280616	Large elongated pulp chamber
+C4280617	Tooth mass arch size discrepancy
+C4280618	Inadequate arch length for tooth size
+C4280619	Missing more than six teeth
+C4280620	Hypertrophy of permanent maxillary central incisor
+C4280621	Hyperplasia of permanent maxillary central incisor
+C4280622	Missing all teeth
+C4280623	Rotting teeth
+C4280624	Blind spot located at fixation point
+C4280625	Decreased size of eyeball
+C4280626	Aplasia of eyelashes
+C4280627	Failure of development of eyelashes
+C4280628	Malformation of the neck
+C4280629	Hyperplasia of nose
+C4280630	Pinched bridge of nose
+C4280633	Hypotrophic forehead
+C4280634	Hypoplasia of forehead
+C4280635	Decreased facial muscle movement
+C4280636	Hypertrophy of supraorbital ridge
+C4280637	Hypertrophy of supraorbital margins
+C4280638	Hyperplasia of supraorbital ridge
+C4280639	Hyperplasia of supraorbital margins
+C4280640	Retrusion of upper jaw bones
+C4280641	Hypotrophic maxilla
+C4280642	Deficiency of upper jaw bones
+C4280643	Decreased projection of maxilla
+C4280644	Increased size of the mandible
+C4280645	Hypertrophy of lower jaw
+C4280646	Atony of facial musculature
+C4280647	Hypertrophy of cheeks
+C4280648	Hyperplasia of cheeks
+C4280649	Facial fat hypertrophy
+C4280650	Facial fat hyperplasia
+C4280651	Hypotrophic malar bone
+C4280652	Prominent back of the head
+C4280653	Turridolichocephaly
+C4280654	Narrow skull shape
+C4280655	Narrow head shape
+C4280656	Narrow cranium shape
+C4280657	Malformation of head shape
+C4280658	Malformation of cranium shape
+C4280659	Malformation of cranial vault shape
+C4280660	Abnormality of head shape
+C4280661	Abnormality of cranium shape
+C4280662	Abnormality of cranial vault shape
+C4280664	Big calvaria
+C4280665	Wedge shaped head
+C4280666	Triangular head shape
+C4280668	Angioectasias of the tongue
+C4280669	Velopharyngeal dysfunction
+C4280670	Spider veins of the lip
+C4280671	Angioectasias of the lip
+C4280672	Decrease in jaw opening
+C4280673	Hypoplasia of lingual frenulum
+C4280674	Agenesis of parotid duct
+C4280675	Broad alveolar processes of jaw
+C4280676	Hypokinesia of the tongue
+C4280677	Idiopathic gingival hyperplasia
+C4280678	Posterior displacement of the tongue
+C4280679	Increased calcium level in kidney
+C4280686	Proximal upper limb muscle hypertrophy
+C4280701	Reduced euglobulin clot lysis time
+C4280711	Leukocyte inclusion bodies
+C4280715	Decreased level of plasminogen
+C4280733	Abnormal cardiac ventricular function
+C4280737	Large elbow
+C4280753	Orange discoloured tonsils
+C4280763	Increased C-peptide level
+C4280765	Abnormal C-peptide level
+C4280773	Increased circulating free fatty acid level
+C4280802	Pulmonary venous occlusion
+C4280803	Decreased CSF homovanillic acid
+C4280804	Percussion-induced rapid rolling muscle contractions
+C4280805	Negative nitroblue tetrazolium reduction test
+C4280806	Calcium oxalate kidney stones
+C4280807	Flattening of cranial vault
+C4280808	Abnormally small eyeball
+C4280863	Undifferentiated large cell carcinoma
+C4281559	FRONTOMETAPHYSEAL DYSPLASIA 1
+C4281601	Foot oligodactyly
+C4281741	Mesangial proliferation
+C4281771	Thin eyebrow
+C4281785	Childhood Absence Epilepsy
+C4281786	Presence of foam cells
+C4281802	Spongiform encephalopathy
+C4281993	Neonatal respiratory distress
+C4282132	Malignancy
+C4282180	Juvenile macular degeneration
+C4282398	Sialidase deficiency
+C4282399	Abnormal maturation of the hand bone
+C4282400	Polydactyly, Postaxial, Type A1
+C4282407	Sparse and thin eyebrow
+C4283893	DEAFNESS, AUTOSOMAL DOMINANT 66
+C4283894	MENTAL RETARDATION, X-LINKED 61
+C4284013	Primary cholangiocarcinoma of intrahepatic biliary tract
+C4284088	MIRAGE SYNDROME
+C4284093	FANCONI ANEMIA, COMPLEMENTATION GROUP R
+C4284414	AORTIC ANEURYSM, FAMILIAL THORACIC 10
+C4284586	Perinatal depression in mother
+C4284588	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE
+C4284592	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY
+C4284594	BAND HETEROTOPIA
+C4284595	PATENT DUCTUS ARTERIOSUS 2
+C4284790	Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1
+C4285693	HIV-associated neurocognitive disorder
+C4285709	Ligamentum flavum hypertrophy
+C4285730	Activated PI3 kinase delta syndrome
+C4285910	Obstructive sleep apnea hypopnea syndrome
+C4288013	Vulvar Adenocarcinoma of Mammary Gland Type
+C4288305	Recurrent Glioblastoma
+C4288538	Ovotesticular Differences of Sex Development
+C4288754	Metastatic Urothelial Carcinoma
+C4288927	IFN-gamma Receptor 1 Deficiency
+C4288963	Hepatitis C Virus Infection
+C4289690	Diffuse Glioma
+C4289946	B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative
+C4290046	trachomatis
+C4290088	decreased absolute neurophile count (ANC)
+C4290090	diabetes (mellitus) due to autoimmune process
+C4290091	diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction
+C4290092	idiopathic diabetes (mellitus)
+C4290094	postprocedural diabetes mellitus
+C4290095	secondary diabetes mellitus NEC
+C4293666	Myerson\'s sign
+C4293672	Abnormality of mesentery morphology
+C4293678	Glabellar reflex
+C4293686	Periventricular white matter hyperdensities
+C4293687	Congenital shortened small intestine
+C4293689	Abnormal proerythroblast morphology
+C4293700	Subcutaneous spheroids
+C4293701	Status cribrosum
+C4293708	Recurrent paroxysmal headache
+C4302111	Familial Ménière disease
+C4302243	Autoimmune pancreatitis type 1
+C4302263	Cryptogenic multifocal ulcerous stenosing enteritis
+C4302547	Dystrophic epidermolysis bullosa nails only
+C4302548	Dysspondyloenchondromatosis
+C4302669	Autosomal dominant beta2-microglobulinic amyloidosis
+C4303082	Hyperinsulinism due to uncoupling protein 2 deficiency
+C4303164	Autoimmune hepatitis type 1
+C4303475	Hyperinsulinism due to HNF1A deficiency
+C4303482	Familial Alzheimer-like prion disease
+C4303546	Brain dopamine-serotonin vesicular transport disease
+C4303593	DEND syndrome
+C4303697	Ectasia of thoracic aorta
+C4303761	Familial thrombocytosis
+C4303786	Ehlers-Danlos syndrome vascular-like type
+C4303860	Craniofacial ulnar renal syndrome
+C4304021	Autosomal dominant macrothrombocytopenia
+C4304022	Attenuated Chédiak-Higashi syndrome
+C4304505	8p11.2 deletion syndrome
+C4304514	6q terminal deletion syndrome
+C4304526	5q35 microduplication syndrome
+C4304529	5q14.3 microdeletion syndrome
+C4304532	2q23.1 microdeletion syndrome
+C4304537	2p21 microdeletion syndrome
+C4304539	20p12.3 microdeletion syndrome
+C4304540	1q44 microdeletion syndrome
+C4304578	1p21.3 microdeletion syndrome
+C4304594	16q24.3 microdeletion syndrome
+C4304667	Benign concentric annular macular dystrophy
+C4304724	Late-onset junctional epidermolysis bullosa
+C4304725	Leber plus disease
+C4304727	Sudden unexplained death in epilepsy
+C4304822	Spinocerebellar ataxia type 35
+C4304832	Primary pigmented nodular adrenocortical disease
+C4305131	Cataract glaucoma syndrome
+C4305134	Fried syndrome
+C4305140	12q14 microdeletion syndrome
+C4305151	Syndromic microphthalmia type 5
+C4305155	Isolated autosomal dominant hypomagnesemia Glaudemans type
+C4305240	14q12 microdeletion syndrome
+C4305324	Acral self-healing collodion baby
+C4305399	Wartenberg Syndrome
+C4310232	Hypercalcemia, Infantile, 1
+C4310473	Hypercalcemia, infantile, 2
+C4310613	POLYCYSTIC LIVER DISEASE 1
+C4310614	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME
+C4310616	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE
+C4310617	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS
+C4310618	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME
+C4310619	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59
+C4310620	YAO SYNDROME
+C4310621	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12
+C4310622	ANTERIOR SEGMENT DYSGENESIS 8
+C4310623	ANTERIOR SEGMENT DYSGENESIS 6
+C4310624	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6
+C4310625	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS
+C4310626	RETINITIS PIGMENTOSA 77
+C4310627	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME
+C4310628	OPTIC ATROPHY 11
+C4310629	HYDROPS FETALIS, NONIMMUNE, AND/OR ATRIAL SEPTAL DEFECT, SUSCEPTIBILITY TO
+C4310630	AMELOGENESIS IMPERFECTA, TYPE IJ
+C4310631	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS
+C4310632	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT
+C4310633	DYSTONIA 28, CHILDHOOD-ONSET
+C4310634	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES
+C4310635	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 49
+C4310636	ATRIAL FIBRILLATION, FAMILIAL, 18
+C4310637	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 48
+C4310638	TOOTH AGENESIS, SELECTIVE, 9
+C4310639	GLAUCOMA 3, PRIMARY CONGENITAL, E
+C4310640	NEPHRONOPHTHISIS 20
+C4310641	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58
+C4310643	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE
+C4310644	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES
+C4310645	MYOPATHY, MYOFIBRILLAR, 8
+C4310646	LISSENCEPHALY 8
+C4310647	SECKEL SYNDROME 10
+C4310648	UNCOMBABLE HAIR SYNDROME 3
+C4310649	UNCOMBABLE HAIR SYNDROME 2
+C4310650	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII
+C4310651	FANCONI ANEMIA, COMPLEMENTATION GROUP U
+C4310652	FANCONI ANEMIA, COMPLEMENTATION GROUP V
+C4310653	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME
+C4310654	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC
+C4310655	MYOPIA 25, AUTOSOMAL DOMINANT
+C4310656	IMMUNODEFICIENCY 49
+C4310657	CONE-ROD DYSTROPHY AND HEARING LOSS
+C4310658	MYOCLONUS, INTRACTABLE, NEONATAL
+C4310659	PREIMPLANTATION EMBRYONIC LETHALITY 2
+C4310660	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 21
+C4310661	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31
+C4310662	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
+C4310663	SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED
+C4310664	SUDDEN CARDIAC FAILURE, INFANTILE
+C4310665	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6
+C4310666	SPERMATOGENIC FAILURE 17
+C4310667	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY
+C4310668	HETEROTAXY, VISCERAL, 8, AUTOSOMAL
+C4310669	PERIVENTRICULAR NODULAR HETEROTOPIA 7
+C4310670	LETHAL CONGENITAL CONTRACTURE SYNDROME 11
+C4310671	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM
+C4310672	SHASHI-PENA SYNDROME
+C4310673	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57
+C4310674	SPERMATOGENIC FAILURE 16
+C4310675	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY
+C4310676	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT
+C4310677	HAREL-YOON SYNDROME
+C4310678	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA
+C4310679	CHITAYAT SYNDROME
+C4310680	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES
+C4310681	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2
+C4310682	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA
+C4310683	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER
+C4310684	SOTOS SYNDROME 3
+C4310685	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47
+C4310686	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY
+C4310687	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 46
+C4310688	SIFRIM-HITZ-WEISS SYNDROME
+C4310689	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES
+C4310690	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)
+C4310691	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 45
+C4310692	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
+C4310693	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET
+C4310694	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC
+C4310695	ANIRIDIA 3
+C4310696	Zhu-Tokita-Takenouchi-Kim syndrome
+C4310697	FRONTOMETAPHYSEAL DYSPLASIA 2
+C4310699	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24
+C4310700	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 44
+C4310701	OROFACIODIGITAL SYNDROME XV
+C4310702	ALAZAMI-YUAN SYNDROME
+C4310703	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56
+C4310704	RETINITIS PIGMENTOSA 76
+C4310705	JOUBERT SYNDROME 28
+C4310706	JOUBERT SYNDROME 27
+C4310707	BARDET-BIEDL SYNDROME 20
+C4310708	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3
+C4310709	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2
+C4310710	PEELING SKIN SYNDROME 5
+C4310711	MYOPATHY, MYOFIBRILLAR, 7
+C4310712	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 43
+C4310713	MACULAR DYSTROPHY, PATTERNED, 3
+C4310714	SESSILE SERRATED POLYPOSIS CANCER SYNDROME
+C4310715	THAUVIN-ROBINET-FAIVRE SYNDROME
+C4310716	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 42
+C4310717	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 41
+C4310718	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY
+C4310719	FAMILIAL ADENOMATOUS POLYPOSIS 4
+C4310720	GROWTH RETARDATION, IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND HEPATOPATHY
+C4310721	CILIARY DYSKINESIA, PRIMARY, 35
+C4310722	CILIARY DYSKINESIA, PRIMARY, 34
+C4310723	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE
+C4310724	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY
+C4310725	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B
+C4310726	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2
+C4310727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa
+C4310728	SEIZURES, BENIGN FAMILIAL INFANTILE, 5
+C4310729	NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3
+C4310730	TOOTH AGENESIS, SELECTIVE, 8
+C4310731	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y
+C4310733	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4
+C4310734	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3
+C4310735	PORTAL HYPERTENSION, NONCIRRHOTIC
+C4310736	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE
+C4310737	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 40
+C4310738	MEIER-GORLIN SYNDROME 7
+C4310739	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
+C4310740	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY
+C4310741	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4
+C4310742	COLD-INDUCED SWEATING SYNDROME 3
+C4310743	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET
+C4310744	BONE MARROW FAILURE SYNDROME 3
+C4310745	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55
+C4310746	HERMANSKY-PUDLAK SYNDROME 10
+C4310747	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5
+C4310748	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5
+C4310749	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26
+C4310750	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE
+C4310751	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS
+C4310752	DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS
+C4310753	PATENT DUCTUS ARTERIOSUS 3
+C4310754	MYOPATHY, DISTAL, 5
+C4310755	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54
+C4310756	HYPERALDOSTERONISM, FAMILIAL, TYPE IV
+C4310757	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F
+C4310758	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H
+C4310759	RETINITIS PIGMENTOSA 75
+C4310760	LETHAL CONGENITAL CONTRACTURE SYNDROME 10
+C4310761	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA
+C4310762	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38
+C4310763	SPINOCEREBELLAR ATAXIA 43
+C4310764	NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE
+C4310765	HYPERMANGANESEMIA WITH DYSTONIA 2
+C4310766	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION
+C4310767	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3
+C4310768	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
+C4310769	POLYCYSTIC LIVER DISEASE 2
+C4310770	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37
+C4310771	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43
+C4310772	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART
+C4310773	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30
+C4310774	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42
+C4310775	DEAFNESS, AUTOSOMAL DOMINANT 70
+C4310776	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
+C4310777	DEAFNESS, AUTOSOMAL RECESSIVE 105
+C4310778	YOU-HOOVER-FONG SYNDROME
+C4310779	SPERMATOGENIC FAILURE 15
+C4310780	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23
+C4310781	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22
+C4310782	PREMATURE OVARIAN FAILURE 12
+C4310783	PREMATURE OVARIAN FAILURE 11
+C4310784	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41
+C4310785	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE
+C4310786	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT
+C4310787	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION
+C4310788	COFFIN-SIRIS SYNDROME 5
+C4310789	THROMBOCYTOPENIA 6
+C4310790	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC
+C4310791	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2
+C4310792	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET
+C4310793	HEART AND BRAIN MALFORMATION SYNDROME
+C4310794	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53
+C4310796	MARFAN LIPODYSTROPHY SYNDROME
+C4310797	BLEEDING DISORDER, PLATELET-TYPE, 20
+C4310798	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4
+C4310799	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3
+C4310800	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE
+C4310801	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR
+C4310802	PARKINSON DISEASE 19B, EARLY-ONSET
+C4310803	IMMUNODEFICIENCY 51
+C4310804	WITTEVEEN-KOLK SYNDROME
+C4310805	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS
+C4310806	CATARACT 47
+C4310807	BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME
+C4310808	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1
+C4310809	ANTERIOR SEGMENT DYSGENESIS 5
+C4310810	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS
+C4310811	MEESTER-LOEYS SYNDROME
+C4310812	IMMUNODEFICIENCY 50
+C4310814	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE
+C4310815	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED
+C4310816	MENTAL RETARDATION, X-LINKED 105
+C4310817	MENTAL RETARDATION, X-LINKED 104
+C4310818	MENTAL RETARDATION, X-LINKED 103
+C4310819	IMMUNODEFICIENCY 47
+C4310820	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT
+C4310821	THYROXINE-BINDING GLOBULIN QUANTITATIVE TRAIT LOCUS
+C4310822	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY
+C4310824	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR
+C4310833	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
+C4310943	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE
+C4315130	Hippocampal atrophy
+C4315392	Brachydactyly, Type E
+C4315963	Alveolar bone loss around teeth
+C4316787	Kenny-Caffey syndrome, type 2
+C4316788	Abnormality of the intestine
+C4316791	Entamoeba histolytica Infection
+C4316810	Writer's Cramp
+C4316812	Fibrinogen Deficiency
+C4316837	Clear cell odontogenic carcinoma
+C4316870	Abnormality of the eye
+C4316878	Loss of eyelashes
+C4316881	Prescription Drug Abuse
+C4316895	Anaphylactic shock
+C4316899	Cystinosis
+C4316903	Absence Seizures
+C4316985	Cerebellar edema
+C4316995	Primary Hypothyroidism
+C4317009	Diverticular Diseases
+C4317043	Simpson-Golabi-Behmel syndrome
+C4317045	Gluten intolerance
+C4317046	Hematological abnormality
+C4317089	Infantile hemangioma
+C4317091	Trisomy 18
+C4317093	Reduced factor XI activity
+C4317107	Abnormality of the thyroid gland
+C4317109	Epileptic Seizures
+C4317112	Generalized Lipodystrophy
+C4317123	Myoclonic Seizures
+C4317124	Polynesian Bronchiectasis
+C4317146	Acid reflux
+C4317151	Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
+C4317152	Dimple chin
+C4317153	Simple partial occipital seizures
+C4317154	COLE-CARPENTER SYNDROME 1
+C4317171	Adolescent Obesity
+C4317224	Congenital disorder of glycosylation type 1q
+C4317295	Congenital disorder of glycosylation type 1s
+C4317320	Factor V deficiency
+C4317339	Juvenile Absence Epilepsy
+C4318382	Cardiac Conduction Defects
+C4318485	Giardia lamblia Infection
+C4318618	Peritoneal Surface Malignancy
+C4318844	Anaplastic sarcoma
+C4319565	Microcephalic osteodysplastic primordial dwarfism types I and III
+C4319932	BARDET-BIEDL SYNDROME 21
+C4321245	Cleft lip or lips
+C4321324	Constitutional Mismatch Repair Deficiency Syndrome
+C4321359	Reduced insulin like growth factor binding protein acid labile subunit level
+C4321477	Sickle Cell-SS Disease
+C4324314	Primary familial brain calcification
+C4324336	Hyperleukocytosis
+C4324563	Neutrophil extracellular trap formation
+C4324621	Opioid Use Disorder
+C4324656	Non-squamous non-small cell lung cancer
+C4329210	11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency
+C4329212	17-Alpha-Hydroxylase/17,20 Lyase Deficiency
+C4329279	Adipsic Diabetes Insipidus
+C4330050	Grade II Glioma
+C4331965	Medulloblastoma, WNT-Activated
+C4476521	Renal glomerular fibrosis
+C4476522	Oral soft tissue hyperplasia
+C4476523	Decreased projection of lower jaw
+C4476524	Decreased projection of mandible
+C4476525	Retrusion of lower jaw
+C4476526	High urine occult blood
+C4476527	Flat head
+C4476531	Excessive sputum secretion
+C4476534	Subperiosteal bone resorption
+C4476535	Nostril coloboma
+C4476537	Reduced intrathoracic adipose tissue
+C4476539	Glomerular subendothelial electron-dense deposits
+C4476540	Dilatation of the cerebral artery
+C4476543	Complete heart block with broad QRS complexes
+C4476544	Tubulointerstitial scarring
+C4476545	Dilatation of the ventricular cavity
+C4476546	Forgetfullness
+C4476548	Intrinsic hand muscles weakness
+C4476549	Sacrococcygeal agenesis
+C4476550	Sudden loss of muscle tone
+C4476552	Dilatation of mesenteric artery
+C4476553	Atrial septal dilatation
+C4476554	Carotid artery dilatation
+C4476595	Reduced red cell pyruvate kinase activity
+C4476602	Reduced intraabdominal adipose tissue
+C4476604	Decreased small intestinal mucosa lactase activity
+C4476614	Beaten bronze macular sheen
+C4476616	Atrophic muscularis propria
+C4476617	Autonomic visceral myopathy
+C4476618	Degenerative enteric myopathy
+C4476619	Poor visual behavior for age
+C4476632	Fragmented elastic fibers in the dermis
+C4476639	Ground-glass opacification on pulmonary HRCT
+C4476644	Segmental myoclonic seizures
+C4476649	Abnormal apolipoprotein level
+C4476719	Limbal edema
+C4476724	Abnormal cellular phenotype
+C4476725	Retinal arterial macroaneurysms
+C4476726	Pschomotor retardation
+C4476727	Erratic myoclonus
+C4476743	Anti-thyroid peroxidase antibody positivity
+C4476748	Reticular pattern on pulmonary HRCT
+C4476772	Staccato cry
+C4476775	Elevated serum 11-deoxycortisol
+C4476801	Violaceous plaque
+C4476817	Yellow-orange papule
+C4476847	Short bowel
+C4476848	Low 1-minute APGAR score
+C4477011	Thinning of Descemet membrane
+C4477027	Comedogenic acne
+C4477032	Abnormality of skeletal muscles
+C4477033	Skeletal muscle steatosis
+C4477049	Hypoplasia of the olfactory bulb
+C4477053	Decreased number of CD3+ T cells
+C4477055	Limb myoclonus
+C4477056	Constant urination
+C4477058	Fragmented sleep
+C4477059	Dilatation of celiac artery
+C4477062	Decreased activity of 3-hydroxyacyl-CoA dehydrogenase
+C4477063	Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency
+C4477081	Abnormal serum dehydroepiandrosterone level
+C4477091	Monoclonal immunoglobulin M proteinemia
+C4477095	Increased lactate dehydrogenase activity
+C4478372	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED
+C4478379	MENTAL RETARDATION, X-LINKED 106
+C4478383	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35
+C4478700	FOCAL CORTICAL DYSPLASIA, TYPE IIA
+C4478701	FOCAL CORTICAL DYSPLASIA, TYPE IIB
+C4478716	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1
+C4478940	BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS
+C4479088	MYASTHENIC SYNDROME, CONGENITAL, 22
+C4479186	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE
+C4479208	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 51
+C4479220	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2
+C4479229	HYPERPARATHYROIDISM 4
+C4479235	AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO
+C4479236	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52
+C4479246	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER
+C4479250	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA
+C4479254	PEROXISOME BIOGENESIS DISORDER 10B
+C4479260	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2
+C4479270	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT
+C4479278	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS
+C4479313	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 53
+C4479319	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54
+C4479322	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE
+C4479333	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION
+C4479344	SCLEROSING CHOLANGITIS, NEONATAL
+C4479353	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq
+C4479357	ANAUXETIC DYSPLASIA 2
+C4479376	PSEUDO-TORCH SYNDROME 2
+C4479387	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC
+C4479409	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID
+C4479410	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY
+C4479416	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY
+C4479424	DIAMOND-BLACKFAN ANEMIA 16
+C4479428	DIAMOND-BLACKFAN ANEMIA 17
+C4479431	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY
+C4479452	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES
+C4479476	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60
+C4479481	RETINITIS PIGMENTOSA 78
+C4479491	LOPES-MACIEL-RODAN SYNDROME
+C4479496	CRANIOSYNOSTOSIS 7
+C4479504	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS
+C4479510	PREMATURE OVARIAN FAILURE 13
+C4479515	BLEEDING DISORDER, PLATELET-TYPE, 21
+C4479517	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD
+C4479520	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES
+C4479526	RETINITIS PIGMENTOSA 79
+C4479534	TOWNES-BROCKS SYNDROME 2
+C4479539	ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT
+C4479548	SPECIFIC GRANULE DEFICIENCY 2
+C4479549	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME
+C4479552	46,XX SEX REVERSAL 4
+C4479566	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
+C4479569	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS
+C4479577	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2
+C4479588	IMMUNODEFICIENCY 52
+C4479599	STANKIEWICZ-ISIDOR SYNDROME
+C4479603	MYOPATHY, CONGENITAL, WITH NEUROPATHY AND DEAFNESS
+C4479608	MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT
+C4479613	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS
+C4479618	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2
+C4479619	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3
+C4479620	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4
+C4479631	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES
+C4479636	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES
+C4479637	RAHMAN SYNDROME
+C4479640	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2
+C4479651	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA
+C4479652	GABRIELE-DE VRIES SYNDROME
+C4479653	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY
+C4479654	COHEN-GIBSON SYNDROME
+C4479655	MEIER-GORLIN SYNDROME 8
+C4479656	PERRAULT SYNDROME 6
+C4479664	ADRENAL INSUFFICIENCY, NR5A1-RELATED
+C4479708	FCD IIA
+C4479709	FCD IIB
+C4505065	Noncommunicable Diseases
+C4505072	Epileptic Syndromes
+C4505222	Sleep Latency
+C4505262	Oncogene Addiction
+C4505291	Xp21 Contiguous Gene Deletion Syndrome
+C4505323	Clinical Deterioration
+C4505353	Diverticular Bleeding
+C4505386	Giardia duodenalis Infection
+C4505387	Giardia intestinalis Infection
+C4505390	Heroin Smoking
+C4505432	XMRV Infection
+C4505436	Generalized Absence Seizures
+C4505439	Moral Injury
+C4505442	Trichophyton mentagrophytes Infection
+C4505456	HIV Coinfection
+C4505467	Raccoon Roundworm Encephalitis
+C4505473	Burkholderia cepacia Sepsis
+C4505492	Chemical and Drug Induced Liver Injury, Chronic
+C4505493	Chemical-Induced Liver Injury, Chronic
+C4509017	Blastic plasmacytoid dendritic cell neoplasm (BPDCN)
+C4509020	Isolated bone marrow mastocytosis
+C4509816	Squamous non-small cell lung cancer
+C4509836	Familial acute necrotizing encephalopathy
+C4509881	Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
+C4509918	Polyvalvular heart disease syndrome
+C4509920	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
+C4509933	Peripheral neuropathy with sensorineural hearing impairment syndrome
+C4510731	Familial primary hypomagnesemia with normocalciuria and normocalcemia
+C4510744	46,XY partial gonadal dysgenesis
+C4510873	Atypical juvenile parkinsonism
+C4511003	Acute myeloid leukemia with t(8;16)(p11;p13) translocation
+C4511056	Centripetalis recessive dystrophic epidermolysis bullosa
+C4511057	Congenital muscular dystrophy Paradas type
+C4511136	Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
+C4511138	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
+C4511230	Bathing suit ichthyosis
+C4511237	Butterfly-shaped pigmentary macular dystrophy
+C4511452	Sporadic Parkinson disease
+C4511595	Methamphetamine intoxication
+C4511620	Autosomal dominant tubulointerstitial kidney disease
+C4517996	Autosomal recessive limb girdle muscular dystrophy type 2S
+C4518087	Acral dystrophic epidermolysis bullosa
+C4518333	Clear cell papillary renal cell carcinoma
+C4518338	Wolfram-like syndrome
+C4518356	MiT family translocation renal cell carcinoma
+C4518436	Anaplastic lymphoma kinase positive anaplastic large cell lymphoma
+C4518548	Non-intestinal type adenocarcinoma
+C4518639	Epilepsy of infancy with migrating focal seizures
+C4518774	Joubert syndrome with Jeune asphyxiating thoracic dystrophy
+C4518785	Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
+C4518839	Combined oxidative phosphorylation defect type 8
+C4520679	Abnormal macular morphology
+C4520732	Stage IV Cutaneous Melanoma AJCC v6 and v7
+C4520840	Erythroleukemia
+C4520843	Pterygium
+C4520847	Immunoglobulin G subclass deficiency (finding)
+C4520892	Otospondylomegaepiphyseal dysplasia
+C4520898	Stage IV Breast Cancer AJCC v6 and v7
+C4520981	Abnormality of the basal ganglia
+C4520983	Congenital atresia of extrahepatic bile duct
+C4521042	Complete Trisomy 21 Syndrome
+C4521075	Childhood Overweight
+C4521132	ACROMEGALY DUE TO PITUITARY ADENOMA 1
+C4521481	Pseudomyotonia (finding)
+C4521563	SPINOCEREBELLAR ATAXIA 44
+C4521678	AUDITORY NEUROPATHY AND OPTIC ATROPHY
+C4522089	Hepatocyte Growth Factor Measurement
+C4522123	Nerve Growth Factor Measurement
+C4522164	HELIX SYNDROME
+C4522181	Brachial Amyotrophic Diplegia
+C4523846	MSI-high
+C4524040	Atherogenic dyslipidaemia
+C4524092	Chronic rhinosinusitis with nasal polyps
+C4524268	Advanced lung cancer
+C4524856	Refractory Classical Hodgkin Lymphoma
+C4528408	Advanced Head and Neck Squamous Cell Carcinoma
+C4528668	Refractory Acute Myeloid Leukemia
+C4528747	Recurrent Atypical Teratoid/Rhabdoid Tumor
+C4529962	Fatty Liver Disease
+C4531012	Dull burning sensation with urination
+C4531017	Missed heartbeat
+C4531018	Absent thymic shadow
+C4531019	Arterial disease of legs
+C4531021	Undergrowth
+C4531022	Breaking out
+C4531023	Brain and/or spinal cord issue
+C4531026	Elevated circulating ribitol concentration
+C4531299	Premature occlusive vascular stenosis
+C4531300	Frequent nosebleeds
+C4538355	PITUITARY ADENOMA 1, MULTIPLE TYPES
+C4538533	SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER
+C4538570	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY
+C4538630	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS
+C4538784	GALLOWAY-MOWAT SYNDROME 2, X-LINKED
+C4538788	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE
+C4538795	MYOPIA 26, X-LINKED, FEMALE-LIMITED
+C4539386	JOUBERT SYNDROME 34
+C4539685	PITUITARY ADENOMA 5, MULTIPLE TYPES
+C4539714	MECKEL SYNDROME 13
+C4539715	JOUBERT SYNDROME 29
+C4539729	OROFACIODIGITAL SYNDROME XVI
+C4539754	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14
+C4539767	EXUDATIVE VITREORETINOPATHY 7
+C4539772	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13
+C4539778	NEPHROTIC SYNDROME 14
+C4539783	SPERMATOGENIC FAILURE 18
+C4539798	CILIARY DYSKINESIA, PRIMARY, 37
+C4539808	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25
+C4539811	IMMUNODEFICIENCY 53
+C4539818	SPERMATOGENIC FAILURE 19
+C4539824	SPERMATOGENIC FAILURE 20
+C4539828	BIRK-LANDAU-PEREZ SYNDROME
+C4539839	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3
+C4539843	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55
+C4539848	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45
+C4539851	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46
+C4539857	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
+C4539873	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES
+C4539881	DEAFNESS, AUTOSOMAL DOMINANT 71
+C4539886	DEAFNESS, AUTOSOMAL DOMINANT 72
+C4539896	NEPHROTIC SYNDROME 15
+C4539903	POLYCYSTIC KIDNEY DISEASE 5
+C4539919	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5
+C4539927	SKRABAN-DEARDORFF SYNDROME
+C4539937	JOUBERT SYNDROME 30
+C4539944	SCHIZOPHRENIA 19
+C4539948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26
+C4539951	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47
+C4539957	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS
+C4539964	DEAFNESS, AUTOSOMAL RECESSIVE 107
+C4539976	POLYDACTYLY, POSTAXIAL, TYPE A7
+C4539985	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES
+C4539991	SPERMATOGENIC FAILURE 21
+C4539997	DEAFNESS, AUTOSOMAL RECESSIVE 108
+C4540004	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1
+C4540014	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2
+C4540029	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32
+C4540034	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56
+C4540036	FRASER SYNDROME 2
+C4540040	FRASER SYNDROME 3
+C4540052	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES
+C4540059	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY
+C4540086	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY
+C4540096	MYOPATHY, MITOCHONDRIAL, AND ATAXIA
+C4540131	PILAROWSKI-BJORNSSON SYNDROME
+C4540135	PITUITARY ADENOMA 3, MULTIPLE TYPES
+C4540141	OVARIAN DYSGENESIS 5
+C4540156	AL KAISSI SYNDROME
+C4540164	PONTOCEREBELLAR HYPOPLASIA, TYPE 11
+C4540171	3-METHYLGLUTACONIC ACIDURIA, TYPE IX
+C4540179	SPERMATOGENIC FAILURE 22
+C4540188	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES
+C4540192	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES
+C4540199	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD
+C4540205	OOCYTE MATURATION DEFECT 3
+C4540209	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33
+C4540232	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE
+C4540251	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7
+C4540265	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX
+C4540266	GALLOWAY-MOWAT SYNDROME 3
+C4540270	GALLOWAY-MOWAT SYNDROME 4
+C4540274	GALLOWAY-MOWAT SYNDROME 5
+C4540277	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION
+C4540284	OOCYTE MATURATION DEFECT 4
+C4540293	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA
+C4540321	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
+C4540327	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES
+C4540331	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5
+C4540342	JOUBERT SYNDROME 32
+C4540355	JOUBERT SYNDROME 31
+C4540358	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET
+C4540367	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES
+C4540389	JOUBERT SYNDROME 33
+C4540395	KLEEFSTRA SYNDROME 2
+C4540400	SPINOCEREBELLAR ATAXIA 45
+C4540404	SPINOCEREBELLAR ATAXIA 46
+C4540411	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57
+C4540434	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA
+C4540439	RETINITIS PIGMENTOSA 80
+C4540470	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50
+C4540493	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY
+C4540496	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE
+C4540499	COFFIN-SIRIS SYNDROME 6
+C4540520	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15
+C4540521	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16
+C4540534	PITUITARY ADENOMA 3, MULTIPLE TYPES, SOMATIC
+C4540535	PITUITARY ADENOMA 3, ACTH-SECRETING, SOMATIC
+C4540536	PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC
+C4540602	PITUITARY ADENOMA 3, GROWTH HORMONE-SECRETING, SOMATIC
+C4543822	Gaming disorder
+C4543926	Narcolepsy type 1
+C4544822	Microsatellite instability-high colorectal cancer
+C4545381	Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement
+C4546023	Congenital Zika Syndrome
+C4551463	Colon adenoma
+C4551472	Hypertrophic obstructive cardiomyopathy
+C4551479	Schwartz-Jampel Syndrome, Type 1
+C4551484	LEOPARD Syndrome, 1
+C4551485	Clinodactyly
+C4551496	Hyperuricemic Nephropathy, Familial Juvenile 1
+C4551500	Amyloid Polyneuropathy, Iowa Type
+C4551509	Jervell And Lange-Nielsen Syndrome 1
+C4551514	Hemophagocytic Lymphohistiocytosis, Familial, 1
+C4551518	Venous stasis
+C4551519	Abducens Nerve Palsy
+C4551520	Intention tremor
+C4551529	Renal dialysis
+C4551557	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1
+C4551558	Fibromatosis, Gingival, Type 1
+C4551560	Truncal obesity
+C4551595	Biliary Cirrhosis, Primary, 1
+C4551602	Noonan Syndrome 1
+C4551627	Granulocytopenia
+C4551628	Opiate Abuse
+C4551630	Ichthyosis Congenita I
+C4551632	Pancreatitis relapsing
+C4551635	Deuteranopia
+C4551647	Romano-Ward Syndrome
+C4551649	Congenital Dysplasia Of The Hip
+C4551650	Esophageal Stricture
+C4551670	Exodeviation
+C4551675	Keratoderma, Palmoplantar
+C4551678	Eye inflammation
+C4551681	Periodontitis, Aggressive, 1
+C4551683	Phaeochromocytoma
+C4551685	Diaphragmatic paralysis
+C4551689	Sleep-Disordered Breathing
+C4551693	Wolfram Syndrome 1
+C4551702	Branchiootorenal Syndrome 1
+C4551720	Primary Ciliary Dyskinesia
+C4551722	Encephalocele
+C4551734	Esodeviation
+C4551761	Excessive Daytime Sleepiness
+C4551767	Protanopia
+C4551769	Seizures, Benign Familial Infantile, 1
+C4551804	Brugada Syndrome 1
+C4551825	Megaloblastic Anemia 1
+C4551826	Deafness-symphalangism syndrome of Herrmann
+C4551829	Median Nerve Entrapment
+C4551851	Cornelia de Lange Syndrome 1
+C4551858	Vesicoureteral Reflux 1
+C4551861	Telangiectasia, Hereditary Hemorrhagic, Type 1
+C4551862	Ophthalmoplegia, Progressive Supranuclear
+C4551863	Supranuclear Palsy, Progressive, 1
+C4551895	Familial Cold Autoinflammatory Syndrome 1
+C4551902	Craniosynostosis, Type 1
+C4551906	Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
+C4551910	Acute Inflammatory Demyelinating Polyneuropathy
+C4551952	Myopathy, Centronuclear, 1
+C4551955	Loeys-Dietz Syndrome, Type 1a
+C4551957	Epilepsy, Familial Temporal Lobe 1
+C4551967	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY
+C4551968	Lissencephaly, X-Linked, 1
+C4551969	Bilateral Periventricular Nodular Heterotopia
+C4551981	Familial Multiple Coagulation Factor Deficiency I
+C4551995	Mitochondrial DNA Depletion Syndrome 1
+C4551998	Porencephaly, Type 1, Autosomal Dominant
+C4552004	Distal Myopathy 1
+C4552048	ABDOMINAL OBESITY-METABOLIC SYNDROME 1
+C4552049	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1
+C4552070	Pulmonary Hypertension, Primary, 1
+C4552078	PSEUDO-TORCH SYNDROME 1
+C4552079	Premature Ovarian Failure 1
+C4552091	Polyarthritis, Juvenile, Rheumatoid Factor Negative
+C4552097	Nevus Sebaceus of Jadassohn
+C4552100	Lynch Syndrome
+C4552103	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM
+C4552765	Epilepsy, Minor
+C4552766	Miscarriage
+C4553297	Cystic Echinocccosis
+C4553478	Infantile Obesity
+C4553705	Absence Seizure Disorder
+C4554007	Uveoretinal Coloboma
+C4554052	Common Peroneal Nerve Entrapment
+C4554120	Leukoencephalopathy with mild cerebellar ataxia and white matter edema
+C4693133	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ibb
+C4704862	Polyarthritis, Juvenile, Rheumatoid Factor Positive
+C4704874	Mammary Carcinoma, Human
+C4704876	Genital Vulvovaginal Candidiasis
+C4704884	Fibrocystic Dysplasia of Bone
+C4704885	Fibrocartilaginous Dysplasia of Bone
+C4704910	Maternal Sepsis
+C4704929	Dysthymia and Chronic Depression
+C4704934	Posterior Interosseous Nerve Syndrome
+C4704935	Femoral Nerve Dysfunction
+C4704955	Infant Overweight
+C4704956	Adolescent Overweight
+C4706555	Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
+C4706563	Intellectual disability, alacrima, achalasia syndrome
+C4721400	Heterophoria
+C4721411	Osteolysis
+C4721414	Mantle cell lymphomas
+C4721421	Breast cancer stage III
+C4721444	Burkitt Leukemia
+C4721453	Peripheral Nervous System Diseases
+C4721505	Sarcoma, Myeloid
+C4721507	Alveolitis, Fibrosing
+C4721509	Usual Interstitial Pneumonia
+C4721532	Lymphoma, Non-Hodgkin, Familial
+C4721549	Autosomal dominant neovascular inflammatory vitreoretinopathy
+C4721555	Autoimmune hepatitis
+C4721579	Colorectal cancer metastatic
+C4721610	Carcinoma, Ovarian Epithelial
+C4721644	Tracheal oedema
+C4721666	Ca bladder stage IV
+C4721698	Metastatic renal cell carcinoma
+C4721769	Citrullinemia Type 1
+C4721779	Ovarian epithelial cancer stage IV
+C4721806	Carcinoma, Basal Cell
+C4721845	Marfan Syndrome, Type I
+C4721916	Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
+C4721952	Familial Idiopathic Pulmonary Fibrosis
+C4722227	Hypoprothrombinemias
+C4722330	Generalized Thyroid Hormone Resistance
+C4746851	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1
+C4746986	ALPORT SYNDROME 1, X-LINKED
+C4747646	LYMPHATIC MALFORMATION 3
+C4747737	RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS
+C4747743	IMMUNODEFICIENCY 15B
+C4747769	LYMPHATIC MALFORMATION 4
+C4749059	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1, DIGENIC
+C4759657	Anal ulcer
+C4759705	Intracapillary glomerulosclerosis due to diabetes mellitus
+C4759706	Diabetic Glomerulosclerosis
+C4759713	Malformation skull
+C4759723	Elephantiasis, Bancroftian
+C4759774	Scapuloperoneal Myopathy, MYH7-Related
+C4759840	Deafness neurosensory
+C4760573	Arthrosis
+C4761103	Muscle-Specific Receptor Tyrosine Kinase Myasthenia Gravis
+C5193002	ARTHROGRYPOSIS, DISTAL, TYPE 2B4
+C5193017	MICROPHTHALMIA, SYNDROMIC 15
+C5193018	CONE-ROD DYSTROPHY AND HEARING LOSS 1
+C5193150	MICROPHTHALMIA AND/OR COLOBOMA WITH DEVELOPMENTAL DELAY
+C5194182	Microcytic anaemia
+C5197731	X-Linked Familial Exudative Vitreoretinopathy
+C5197832	Malayi Filariasis
+C5197838	Pancreatic Parenchymal Edema
+C5197850	Evaporative Dry Eye Disease
+C5197857	Marginal Mandibular Nerve Injury
+C5200782	Pes Anserine Bursitis
+C5200801	Innate Inflammatory Response
+C5200821	Congenital Biliary Dilatation
+C5200822	Sea Fan Neovascularization
+C5200838	Submassive Hepatic Necrosis
+C5200933	Giant Axonal Neuropathy
+C5200989	Mast Cell Activation Disease
+C5200990	Mast Cell Disease
+C5201145	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1
+C5232927	Hyperthermia
+C5234846	Olfactory Impairment
+C5234850	Antley-Bixler Syndrome
+C5234852	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA
+C5234856	Cushingoid
+C5234914	Heat Syncope
+C5234922	Haemorrhagic stroke
+C5234944	Paracoccidioides brasiliensis Infection
+C5235044	Central Nervous System Cysticercosis
+C5235087	Cryptococcosis
+C5235118	Eosinophilic pneumonia acute
+C5235211	Hereditary sensory autonomic neuropathy type IA
+C5241301	Manic Depression
+C5241305	Nicotine Addiction
+C5243468	Conversion Neurosis
+C5243471	Cerebral Coenurosis
+C5243476	Cardiometabolic Syndrome
+C5243499	Fetal Malformations
+C5392184	Respiratory Distress Syndrome, Pediatric
+C5392210	Exertional Heat Illness
+C5392790	Oral Tongue Squamous Cell Carcinoma
+C5392883	Smell Dysfunction
+C5392895	Clostridioides Infections
+C5392905	Coenurus cerebralis Infection
+C5392906	Taenia solium Cysticercosis
+C5392919	Prescription Opioid Misuse
+C5392920	Opioid Misuse
+C5392921	Prescription Opioid Abuse
+C5392947	Sleep Insufficiency
+C5392948	Sleep Debt
+C5392954	Sporothrix brasiliensis Infection
+C5392955	Taenia serialis Infection
+C5392956	Taenia brauni Infection
+C5392957	Taenia multiceps Infection
+C5392958	Taenia glomeratus Infection
+C5392959	Taste Dysfunction
+C5392960	Pityriasis Folliculitis
+C5392971	Idiopathic Ventricular Tachycardia
+C5392973	Callous-Unemotional Traits
+C5393299	INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE
+C5393830	NESCAV SYNDROME
+C5399837	Familial Mediterranean Fever, Autosomal Recessive
+C5436276	RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 1
+C5436279	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 6
+C5436345	MENTAL RETARDATION, AUTOSOMAL DOMINANT 25, FORMERLY
-- 
2.24.1