diff --git a/data/nodes/.ipynb_checkpoints/dis-checkpoint.tsv b/data/nodes/.ipynb_checkpoints/dis-checkpoint.tsv
deleted file mode 100644
index 49a66bd6e0619bb77b2d5546eae9975621cd7a96..0000000000000000000000000000000000000000
--- a/data/nodes/.ipynb_checkpoints/dis-checkpoint.tsv
+++ /dev/null
@@ -1,30732 +0,0 @@
-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