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
