Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
prolapse of female genital organ	DOID_1284
cytoplasm	GO_0005737	[All of the contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.]
mitochondrion	GO_0005739	[A semiautonomous, self replicating organelle that occurs in varying numbers, shapes, and sizes in the cytoplasm of virtually all eukaryotic cells. It is notably the site of tissue respiration.]
phytosiderophore	CHEBI_38155
sphingosine-1-phosphate receptor agonist	CHEBI_63114
antispasmodic drug	CHEBI_53784
iron(2+) chelator	CHEBI_38162
shortened	PATO_0002364	[A quality inhering in a bearer by virtue of the bearer's length being notably lower than its width.]
plant growth stimulator	CHEBI_26157
parametritis	DOID_1260
EC 1.13.11.52 (indoleamine 2,3-dioxygenase) inhibitor	CHEBI_72854
Rattus norvegicus	NCBITaxon_10116
glottis cancer	DOID_2595
glottis carcinoma	DOID_2599
tolosa-hunt syndrome	DOID_1278
lysosome	GO_0005764	[A small lytic vacuole that has cell cycle-independent morphology and is found in most animal cells and that contains a variety of hydrolases, most of which have their maximal activities in the pH range 5-6. The contained enzymes display latency if properly isolated. About 40 different lysosomal hydrolases are known and lysosomes have a great variety of morphologies and functions.]
respiratory syncytial virus infectious disease	DOID_1273	[A viral infectious disease that results_in infection located_in upper respiratory tract or located_in lower respiratory tract, has_material_basis_in Human respiratory syncytial virus, which is transmitted_by droplet spread of nasal secretions from an infected person while coughing or sneezing, or transmitted_by contaminated fomites. The infection has_symptom runny nose, has_symptom fever, has_symptom cough, has_symptom wheezing, and has_symptom respiratory distress.]
EC 1.3.1.43 (arogenate dehydrogenase) inhibitor	CHEBI_64416
telangiectasis	DOID_1272
hereditary hemorrhagic telangiectasia	DOID_1270	[An autosomal dominant disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.]