Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
X-07765 measurement	EFO_0021204	[Quantification of the amount of X-07765 in a sample.]
X-06351 measurement	EFO_0021203	[Quantification of the amount of X-06351 in a sample.]
X-06267 measurement	EFO_0021200	[Quantification of the amount of X-06267 in a sample.]
mental development measurement	EFO_0008230	[quantification of some aspect of mental development, including cognition, expressive language and receptive language]
neurodevelopmental measurement	EFO_0008245	[quantification of some aspect of neurodevelopment, such as language development or fine motor skills development. Neurodevelopment scores can used as an indicator of neurodevelopmental delays.]
Saccharum officinarum	NCBITaxon_4547
monocyte chemotactic protein 3 measurement	EFO_0008235	[quantification of the amount of monocyte chemotactic protein 3 in a sample]
isolated congenital adermatoglyphia	MONDO_0007619	[Isolated congenital adermatoglyphia is a rare, genetic develomental defect during embryogenesis disorder characterized by the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a reduced number of sweat gland openings and reduced transpiration of palms and soles.]
monokine induced by gamma interferon measurement	EFO_0008236	[quantification of the amount of monokine induced by gamma interferon in a sample]
motor development measurement	EFO_0008237	[quantification of some aspect of motor development, including fine and gross motor skills]
myeloid cell surface antigen CD33 measurement	EFO_0008238	[quantification of the amount of myeloid cell surface antigen CD33 in a sample]
Cenchrus americanus	NCBITaxon_4543
N(5)-ethyl-L-glutamine	CHEBI_17394	[A N(5)-alkylglutamine where the alkyl group is ethyl. It has been isolated from green tea.]
congenital fibrosis of extraocular muscles	MONDO_0007614
metalloproteinase inhibitor 3 measurement	EFO_0008231	[quantification of the amount of metalloproteinase inhibitor 3 in a sample]
laurin-Sandrow syndrome	MONDO_0007615	[Laurin-Sandrow syndrome (LSS) is characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported, and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.]
methionine aminopeptidase 2 measurement	EFO_0008232	[quantification of the amount of methionine aminopeptidase 2 in a sample]
gingival fibromatosis-progressive deafness syndrome	MONDO_0007612	[Gingival fibromatosis-progressive deafness syndrome is characterized by gingival fibromatosis associated with progressive sensorineural hearing loss. It has been described in two families (with at least 16 affected members spanning five generations in one of the families, and five affected members spanning three generations in the other family). It is transmitted as an autosomal dominant trait.]
MHC class I polypeptide-related sequence A measurement	EFO_0008233	[quantification of the amount of MHC class I polypeptide-related sequence A in a sample]
MHC class I polypeptide-related sequence B measurement	EFO_0008234	[quantification of the amount of MHC class I polypeptide-related sequence B in a sample]