Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Caulobacter vibrioides	NCBITaxon_155892
articulation	UBERON_0004905	[Anatomical cluster that connects two or more adjacent skeletal elements or hardened body parts.]
articular system	UBERON_0004770	[Anatomical system that consists of all the joints of the body.]
hindlimb bone	UBERON_0003464	[A bone that is part of a hindlimb region. Examples: any pes phalanx, femur. Counter-examples: ischium, pubis (they are part of the pelvic girdle).]
GM17173	CLO_0014026	[HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100]
pleura	UBERON_0000977	[The invaginated serous membrane that surrounds the lungs (the visceral portion) and lines the walls of the pleural cavity (parietal portion).]
GM17789	CLO_0016688	[HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100]
humerus	UBERON_0000976	[Paired endochondral long bone that extends between the pectoral girdle and the skeletal parts of the forelimb. [PHENOSCAPE:mah].]
limb bone	UBERON_0002428	[A bone that is part of a limb [Automatically generated definition].]
arm	UBERON_0001460	[The part of the forelimb extending from the shoulder to the autopod[cjm].]
forelimb	UBERON_0002102	[A (free) limb that is connected to a pectoral girdle. The extent of this structure includes autopod, stylopod and zeugopod regions when present, but excludes the pectoral girdle and its parts.]
GM17179	CLO_0014028	[HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100]
GM17178	CLO_0014029	[HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100]
tibia	UBERON_0000979	[The major preaxial endochondral bone in the posterior zeugopod[Phenoscape].]
Rajab interstitial lung disease with brain calcifications 2	MONDO_0100220
IFAP syndrome 2	MONDO_0100221
mitochondrial complex I deficiency, nuclear type	MONDO_0100223
mitochondrial complex I deficiency	MONDO_0100133	[A type of mitochondrial disease charcterized by macrocephaly (large head) with progressive leukodystrophy, encephalopathy, hypertrophic cardiomyopathy, myopathy, liver disease, Leigh syndrome, Leber hereditary optic neuropathy, and some forms of Parkinson disease. The disease is caused by mutations in any of many genes and the inheritance pattern depends on the responsible gene.]
GM17795	CLO_0016682	[HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100]
benzene	CHEBI_16716	[A six-carbon aromatic compound in which each carbon atom donates one of its two 2p electrons into a delocalised pi system. A toxic, flammable liquid byproduct of coal distillation, it is used as an industrial solvent. Benzene is a carcinogen that also damages bone marrow and the central nervous system., The sixth of the seven cervical vertebrae.]