Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
superficial cervical thymus	UBERON_0018244	[A cervical thymus that is located directly beneath the skin.]
cyclooxygenase 2 inhibitor	CHEBI_50629	[A cyclooxygenase inhibitor with specificity for cyclooxygenase 2.]
obsolete_salivary gland body primordium	EFO_0003381
obsolete_pars intercerebralis primordium	EFO_0003380
atrioventricular ring	UBERON_2005073
cardiac ventricle	UBERON_0002082	[Cardiac chamber through which blood leaves the heart.]
obsolete_midline primordium	EFO_0003383
deep cervical thymus	UBERON_0018245	[A cervical thymus that is located deep in the ventral cervical region, superficial to hyoid, sternomastoid, and depressor neck muscles.]
obsolete_somatic muscle primordium	EFO_0003382
obsolete_stomatogastric nervous system primordium	EFO_0003385
obsolete_ventral epidermis primordium	EFO_0003384
obsolete_ventral midline neuroblast	EFO_0003387
obsolete_central brain primordium	EFO_0003386
Complete duplication of thumb phalanx	HP_0009943	[A complete duplication affecting one or more of the phalanges of the thumb. As opposed to a partial duplication were there is still a variable degree of fusion between the duplicated bones, a complete duplication leads to two separate bones appearing side to side (radio-ulnar axis) as seen on x-rays. A duplication leading to an accesory bone appearing in the proximo-distal axis on x-rays, this is actually a different entity called a Pseudoepiphyses (see according terms) sometimes also referred to as Hyperphalangism.]
trichothiodystrophy 3, photosensitive	MONDO_0014619
photosensitive trichothiodystrophy	MONDO_0002470	[A trichothiodystrophy that is photosensitive, and caused by defects in the NER pathway]
obsolete_embryonic hindgut	EFO_0003389
Partial duplication of thumb phalanx	HP_0009944	[A partial duplication, depending on severity leading to a broad or bifid appearance, affecting one or more of the phalanges of the thumb. As opposed to a complete duplication there is still a variable degree of fusion between the duplicated bones.]
retinitis pigmentosa 71	MONDO_0014618	[Any retinitis pigmentosa in which the cause of the disease is a mutation in the IFT172 gene.]
obsolete_embryonic maxillary sensory complex	EFO_0003388