Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
obsolete_embryonic central brain surface glia	EFO_0000446
embryonic central nervous system	EFO_0000447
Tetrahymena thermophila	NCBITaxon_5911
46,XX ovotesticular disorder of sex development	MONDO_0016281	[46,XX ovotesticular disorder of sex development (46,XX ovotesticular DSD) is characterized by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype.]
46,XX disorder of gonadal development	MONDO_0017961
environmental stress treatment	EFO_0000470	[Environmental stress is a treatment where some aspect of the environment is perturbed in order to stress the organism or culture, e.g. change in temperature, change in watering regime]
epigenetic factor	EFO_0000472
epigenetic status	EFO_0000473	[Epigenetic status describes the imprinting state of a sample. E.g. Loss of imprinting occurs in some tumour cells]
obsolete_epithelial cell of lung	EFO_0000476
esophageal adenocarcinoma	EFO_0000478	[A malignant tumor with glandular differentiation arising predominantly from Barrett mucosa in the lower third of the esophagus. Rare examples of esophageal adenocarcinoma deriving from ectopic gastric mucosa in the upper esophagus have also been reported. Grossly, esophageal adenocarcinomas are similar to esophageal squamous cell carcinomas. Microscopically, adenocarcinomas arising in the setting of Barrett esophagus are typically papillary and/or tubular. The prognosis is poor.]
kainic acid	CHEBI_31746	[A pyrrolidinemonocarboxylic acid that has formula C10H15NO4.]
essential thrombocythemia	EFO_0000479	[A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage. (WHO, 2008)]
familial thrombocytosis	MONDO_0019111	[Familial thrombocytosis is a type of thrombocytosis, a sustained elevation of platelet numbers, which affects the platelet/megakaryocyte lineage and may create a tendency for thrombosis and hemorrhage but does not cause myeloproliferation.]
obsolete_embryonic ganglion mother cell	EFO_0000459
fluoxetine	CHEBI_5118	["A benzenoid aromatic compound that has formula C17H18F3NO." []]
postlingual non-syndromic genetic hearing loss	MONDO_0016298	[Postlingual non-syndromic genetic deafness is a rare, genetically highly heterogeneous otorhinolaryngologic disease, resulting from inner and/or middle ear or hearing nerve anomalies, typically characterized by progressive, bilateral, moderate to profound hearing loss (mean sensorineural hearing impairment equal to 40 dB or more for 500-, 1,000-, and 2,000-Hz frequency tones in the better ear) which occurs after the onset of speech development and is not associated with visible external ear abnormalities or any other medical problems. Language development is not initially significantly delayed.]
nonsyndromic genetic hearing loss	MONDO_0019497	[A disease characterized by hearing loss that is not part of a larger syndrome.]
Xanthomonas axonopodis pv. citri str. 306	NCBITaxon_190486
Hirschsprung disease-type D brachydactyly syndrome	MONDO_0016294	[Hirschsprung disease-type D brachydactyly syndrome is characterized by Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two maternal uncles). Transmission appears to be X-linked recessive but autosomal dominant inheritance with incomplete penetrance in females can not be ruled out.]
neuronal ceroid lipofuscinosis	MONDO_0016295	[A group of inherited progressive degenerative brain diseases characterized clinically by a decline of mental and other capacities, epilepsy, and vision loss through retinal degeneration, and histopathologically by intracellular accumulation of an autofluorescent material, ceroid lipofuscin, in the neuronal cells in the brain and in the retina.]