Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
Barth syndrome	DOID_0050476	[A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.]
Weill-Marchesani syndrome	DOID_0050475	[An autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.]
Mikulicz disease	DOID_12900
bromodomain-containing protein 4 inhibitor	CHEBI_137114
uterus	UBERON_0000995	[the female muscular organ of gestation in which the developing embryo or fetus is nourished until birth]
ovary	UBERON_0000992	[the gonad of a female organism which contains germ cells]
mucocele of salivary gland	DOID_12904
necrotizing sialometaplasia	DOID_12901
Liddle syndrome	DOID_0050477
Luminex	BAO_0002021
cytokine	BAO_0002023	[The role played by a protein in modulating immune cell function via cell signaling, subsequent to binding to its cognate cell surface receptor.]
follicular thyroid carcinoma	DOID_3962	[A thyroid carcinoma that has_material_basis_in follicular cells.]
growth factor	BAO_0002024	[The role played by a protein in initiating cell division via cell signaling, subsequent to binding to its cognate cell surface receptor.]
Merkel cell carcinoma	DOID_3965
cystadenoma	DOID_2634	[An adenoma that is a cystic.]
parachordoma	DOID_2647
cardiomyopathy	DOID_0050700	[A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.]
sebaceous adenoma	DOID_2648
aspartylglucosaminuria	DOID_0050461
chondroblastoma	DOID_2649