Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
lateral displacement of eye	DOID_12360
dermoid cyst of skin	DOID_13691	[A dermoid cyst that is located_in the skin.]
arrhythmogenic right ventricular dysplasia 12	DOID_0110083
arrhythmogenic right ventricular cardiomyopathy	DOID_0050431	[An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle.]
acute gonococcal cystitis	DOID_13690	[An acute cystitis that is caused by gonorrhea.]
arrhythmogenic right ventricular dysplasia 13	DOID_0110084	[An arrhythmogenic right ventricular dysplasia that xhas_material_basis_in heterozygous mutation in the CTNNA3 gene on chromosome 10q21.]
arrhythmogenic right ventricular dysplasia 10	DOID_0110081	[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmoglein-2 gene (DSG2) on chromosome 18q12.]
arrhythmogenic right ventricular dysplasia 11	DOID_0110082	[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmocollin-2 gene (DSC2) on chromosome 18q.]
depersonalization disorder	DOID_11038	[A dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization.]
skull	UBERON_0003129
subdivision of skeletal system	UBERON_0000075
prolapse of urethra	DOID_12369	[A prolapse of female genital organ that is characterized by the descent of the urethra from the normal anatomic location toward or through the vaginal opening.]
chronic rapidly progressive glomerulonephritis	DOID_11036
dissociative amnesia	DOID_11037	[A dissociative disorder where he continuity of the patient's memory is disrupted. Patients with dissociative amnesia have recurrent episodes in which they forget important personal information or events, usually connected with trauma or severe stress.]
contact lens corneal edema	DOID_11034
asphyxiating thoracic dystrophy 5	DOID_0110089	[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the WDR19 gene on chromosome 4p14.]
obsolete vesicoureteral reflux with reflux nephropathy	DOID_13696
short-rib thoracic dysplasia 7 with or without polydactyly	DOID_0110090	[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1.]
developmental coordination disorder	DOID_9923	[A specific developmental disorder that involves disordered motor skills where coordinated muscle movement is impaired.]
short-rib thoracic dysplasia 10 with or without polydactyly	DOID_0110091	[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23.]