Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
LysoPC 20:1 measurement	EFO_0021644	[Quantification of the amount of LysoPC 20:1 in a sample.]
LysoPC 20:0 measurement	EFO_0021643	[Quantification of the amount of LysoPC 20:0 in a sample.]
LysoPC 16:1 measurement	EFO_0021640	[Quantification of the amount of LysoPC 16:1 in a sample.]
choroid plexus	UBERON_0001886	[A network formed by blood vessels and the tela choroidea which secretes CSF into the ventricular spaces.]
caMAB-seq	EFO_0008670	[5caC methylase-assisted bisulfite sequencing (caMAB-seq)]
bed nucleus of stria terminalis	UBERON_0001880	[A brain structure in the forebrain wrapped around the stria terminalis. It's largest extent can be found around the crossing of the anterior commissure[INCF].]
Capsicum annuum	NCBITaxon_4072
obsolete_neurofibromatosis-Noonan syndrome	Orphanet_638
obsolete_neurofibromatosis type 2	Orphanet_637
ventral striatum	UBERON_0005403	[A composite structure of the telencephalon that is defined in the striatopallidal system by connectivity and neurochemical staining. It includes the nucleus accumbens, the most ventral portions of the caudate nucleus and the putamen, the rostrolateral portion of the anterior perforated substance, the islands of Calleja and a rostral subcommissural portion of substantia innominata. The boundary between the ventral striatum and dorsal striatum is indistinct in sections stained for Nissl substance (Heimer-1995; adapted from Brain Info).]
obsolete_neurofibromatosis type 1	Orphanet_636
CaptureSeq	EFO_0008675	[RNA capture sequencing (CaptureSeq)]
obsolete_sitosterolemia	Orphanet_2882
CAST-ChIP	EFO_0008676	[Chromatin affinity purification from specific cell types by chromatin immunoprecipitation (CAST-ChIP)]
obsolete_glycerol kinase deficiency, infantile form	Orphanet_284408
N-acetyl-L-glutamate(2-)	CHEBI_44337	[An N-acyl-L-alpha-amino acid anion resulting from deprotonation of both carboxy groups of N-acetyl-L-glutamic acid.]
obsolete_Netherton syndrome	Orphanet_634
CATCH-IT	EFO_0008677	[Covalent attachment of tags to capture histones (CATCH‑IT)]
obsolete_phosphoenolpyruvate carboxykinase deficiency	Orphanet_2880
obsolete_Laron syndrome	Orphanet_633	[Laron syndrome is a congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration.]