Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis	MONDO_0019655
tenascin measurement	EFO_0008296	[quantification of the amount of tenascin in a sample]
X-11795 measurement	EFO_0021261	[Quantification of the amount of X-11795 in a sample.]
spondin-1 measurement	EFO_0008290	[quantification of the amount of spondin-1 in a sample]
familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation	MONDO_0019652
stem Cell Factor measurement	EFO_0008291	[quantification of the amount of stem Cell Factor in a sample]
stem Cell Growth Factor beta measurement	EFO_0008292	[quantification of the amount of stem Cell Growth Factor beta in a sample]
cystine	CHEBI_17376	[A sulfur-containing amino acid obtained by the oxidation of two cysteine molecules which are then linked via a disulfide bond.]
teratocarcinoma-derived growth factor 1 measurement	EFO_0008297	[quantification of the amount of teratocarcinoma-derived growth factor 1 in a sample]
thioredoxin domain-containing protein 12 measurement	EFO_0008298	[quantification of the amount of thioredoxin domain-containing protein 12 in a sample]
Triticum durum	NCBITaxon_4567
thrombospondin-2 measurement	EFO_0008299	[quantification of the amount of thrombospondin-2 in a sample]
GMS syndrome	MONDO_0007679	[GMS syndrome describes an extremely rare syndrome involving goniodysgenesis, intellectual disability and short stature in addition to microcephaly, short nose, small hands and ears, and that has been seen in one family to date. There have been no further descriptions in the literature since 1992.]
vaginal glandular neoplasm	MONDO_0001704	[A benign or malignant neoplasm that arises from the vagina and is characterized by the presence of neoplastic glandular epithelial cells. Representative examples include adenoma, endometrioid adenocarcinoma, and clear cell adenocarcinoma.]
(S)-3-phenyllactate	CHEBI_32979	[A (2S)-2-hydroxy monocarboxylic acid anion resulting from the removal of a proton from the carboxylic acid group of (S)-3-phenyllactic acid.]
glomuvenous malformation	MONDO_0007672	[Glomuvenous malformations (GVMs) are hereditary vascular malformations characterized by the presence of small, multifocal bluish-purple venous lesions involving the skin.]
obsolete_partial duplication of the short arm of chromosome 4	Orphanet_262716
hypotrichosis-lymphedema-telangiectasia syndrome (grouping)	MONDO_0007670	[Hypotrichosis - lymphedema - telangiectasia is an extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms.]
fibronectin glomerulopathy	MONDO_0007671	[A hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life.]
X-11786--methylcysteine measurement	EFO_0021257	[Quantification of the amount of X-11786--methylcysteine in a sample.]