Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
complex partial epilepsy	DOID_12382
obsolete predominant disturbance of consciousness	DOID_12380
neurohypophyseal diabetes insipidus	DOID_12388
obsolete Pasteurella hemorrhagic septicemia	DOID_11056
nephrogenic diabetes insipidus	DOID_12387	[An impaired renal function disease characterized by a complete or partial resistance of the kidneys to vasopressin (ADH).]
obsolete protracted reactive paranoid psychosis	DOID_9900
follicular mucinosis	DOID_9905
meibomian cyst	DOID_9903	[A blepharitis that is characterized as a cyst in the eyelid that is caused by inflammation of a blocked meibomian gland, usually on the upper eyelid.]
cow milk based food product	FOODON_00001771
cattle dairy food product	FOODON_00001118
atopic dermatitis 2	DOID_0110098	[An atopic dermatitis conferred by variation in the FLG gene on chromosome 1q21.]
obsolete entropion and trichiasis of eyelid	DOID_12396
atopic dermatitis 3	DOID_0110099	[An atopic dermatitis associated with variation in the region 20p.]
spastic entropion	DOID_12395
obsolete malignant neoplasm of thoracic esophagus	DOID_9919
short-rib thoracic dysplasia 14 with polydactyly	DOID_0110096	[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the KIAA0586 gene on chromosome 14q23.]
short-rib thoracic dysplasia 9 with or without polydactyly	DOID_0110097	[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13.]
lining cell	CL_0000213
meso-epithelial cell	CL_0002078
short-rib thoracic dysplasia 8 with or without polydactyly	DOID_0110094	[An asphyxiating thoracic dystrophy that has_material_basis_in compound heterozygous mutation in the WDR60 gene on chromosome 7q36.]