Terminology Service < Semantic Lookup Platform

Label	Id	Description
slate pneumoconiosis	DOID_10330
flaccid muscle tone	SYMP_0000707
kaolin pneumoconiosis	DOID_10331
blue color blindness	DOID_11661	[A color blindness that is characterised by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.]
color blindness	DOID_13399	[A blindness that is characterized by the inability or decreased ability to see color, or perceive color differences, under normal lighting conditions.]
childhood embryonal testis carcinoma	DOID_6162	[An embryonal testis carcinoma that occurs in children.]
familial renal papillary carcinoma	DOID_6163
renal system	UBERON_0001008
Aplasia/hypoplasia involving the skeleton	HP_0009115	[Absence (due to failure to form) or underdevelopment of one or more components of the skeleton.]
obsolete subchronic schizophrenia	DOID_10338
prostatic urethra urothelial carcinoma	DOID_6166
prostatic urethral cancer	DOID_6167
Aplasia/Hypoplasia involving bones of the skull	HP_0009116
Aplasia/hypoplasia affecting bones of the axial skeleton	HP_0009122	[Absence (due to failure to form) or underdevelopment of bones of the axial skeleton.]
obsolete schizophrenia simplex	DOID_10339
hypertrichosis of eyelid	DOID_11669
hypertrichosis	DOID_420	[A hair disease characterized by hair growth that is abnormal in quantity or location.]
parametrium	UBERON_0010391
mesometrium	UBERON_0003885
male urethral cancer	DOID_736