Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
aortic valve stenosis	DOID_1712	[An aortic valve disease that has_physical_basis_in incomplete opening of the aortic valve.]
discrete subaortic stenosis	DOID_5804
5-hydroxytryptamine 2A receptor inverse agonist	CHEBI_133016
inverse agonist	CHEBI_90847
intracranial aneurysm	DOID_10941
cerebral arterial disease	DOID_3527
tongue disease	DOID_10944
mouth disease	DOID_403	[A gastrointestinal system disease that is located_in the mouth.]
EC 3.5.4.4 (adenosine deaminase) inhibitor	CHEBI_50445
EC 3.5.4.* (non-peptide cyclic amidine C-N hydrolase) inhibitor	CHEBI_76809
adenosine phosphodiesterase inhibitor	CHEBI_50444
nematicide	CHEBI_25491
lymphocyte function-associated antigen-1 antagonist	CHEBI_133024
receptor binding	GO_0005102	[Interacting selectively and non-covalently with one or more specific sites on a receptor molecule, a macromolecule that undergoes combination with a hormone, neurotransmitter, drug or intracellular messenger to initiate a change in cell function.]
protein binding	GO_0005515	[Interacting selectively and non-covalently with any protein or protein complex (a complex of two or more proteins that may include other nonprotein molecules).]
nephritis	DOID_10952	[A kidney disease that is characterized by an inflammation of the kidneys.]
B-cell lymphoma 2 inhibitor	CHEBI_133022
strongyloidiasis	DOID_10955	[A parasitic helminthiasis infectious disease that involves infection of the intestine, lungs, skin and central nervous system with nematode Strongyloides stercoralis.]
platelet glycoprotein-IIb/IIIa receptor antagonist	CHEBI_50433
purine nucleoside phosphorylase deficiency	DOID_5813	[A combined T cell and B cell immunodeficiency that is a rare autosomal recessive metabolic disorder that has material basis in mutation in the PNP gene and characterized mainly by decreased T-cell function.]