Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
Cricetulus griseus	NCBITaxon_10029
localization assay	BAO_0002196
hypermethioninemia	DOID_0050544	[An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body.]
congenital adrenal insufficiency	DOID_0050546
T-25	BAO_0002199
visceral heterotaxy	DOID_0050545	[A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen.]
familial medullary thyroid carcinoma	DOID_0050547	[A thyroid medullary carcinoma that has_material_basis_in autosomal dominant inheritance.]
thyroid medullary carcinoma	DOID_3973	[A follicular thyroid carcinoma that has_material_basis_in parafollicular cells.]
acrodermatitis	DOID_2722	[A dermatitis that selectively affects the hands and feet.]
endpoint modifier	BAO_0002170
2-hydroxyglutaric aciduria	DOID_0050573	[An amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage.]
ln	BAO_0002171	[Natural log (log base e)]
cone-rod dystrophy	DOID_0050572	[A retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells.]
log	BAO_0002172	[Log base 10]
D-2-hydroxyglutaric aciduria	DOID_0050575	[An 2-hydroxyglutaric aciduria that involves developmental delay, seizures, weak muscle tone (hypotonia), and abnormalities in the largest part of the brain (the cerebrum), which controls many important functions such as muscle movement, speech, vision, thinking, emotion, and memory.]
mean	BAO_0002173
L-2-hydroxyglutaric aciduria	DOID_0050574	[An 2-hydroxyglutaric aciduria that involves damage to cerebellum affecting movement coordination resulting in problems with balance and muscle coordination (ataxia).]
choledocholithiasis	DOID_11755
common bile duct disease	DOID_4137
hypochromic anemia	DOID_11759