Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
acyl-CoA:cholesterol acyltransferase 2 inhibitor	CHEBI_64697
EC 2.3.1.26 (sterol O-acyltransferase) inhibitor	CHEBI_64696
neuromuscular agent	CHEBI_51372
Crimean-Congo hemorrhagic fever	DOID_12287	[A viral infectious disease that is a hemorrhagic fever, has_material_basis_in Crimean-Congo hemorrhagic fever virus, which is transmitted_by Hyalomma ticks. The infection has_symptom headache, has_symptom high fever, has_symptom back pain, has_symptom joint pain, has_symptom stomach pain, has_symptom vomiting, has_symptom red eyes, has_symptom flushed face, has_symptom red throat, has_symptom petechiae (red spots) on the palate, has_symptom jaundice, has_symptom nosebleeds, and has_symptom blood in the feces and urine.]
GABA agent	CHEBI_51374
testicular leukemia	DOID_12286
muscle relaxant	CHEBI_51371
chronic lymphocytic leukemia	DOID_1040	[A lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood.]
hereditary elliptocytosis	DOID_2373	[A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present.]
multiple sclerosis	DOID_2377	[A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.]
sterol demethylation inhibitor	CHEBI_83734
Vogt-Koyanagi-Harada disease	DOID_12297	[A hypersensitivity reaction type II disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.]
intellectual disability	DOID_1059	[A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills.]
oculocerebrorenal syndrome	DOID_1056
EC 1.8.1.9 (thioredoxin reductase) inhibitor	CHEBI_64670
EC 1.8.1.* (oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor) inhibitor	CHEBI_76869
kernicterus	DOID_2382	[A brain disease that is characterized by hyperbilirubinemia-induced brain dysfunction.]
neonatal jaundice	DOID_2383	[A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant.]
Wernicke encephalopathy	DOID_2384	[A brain disease that is characterised by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1).]
renal artery disease	DOID_2388