Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
non-receptor tyrosine-protein kinase TYK2 measurement	EFO_0008251	[quantification of the amount of non-receptor tyrosine-protein kinase TYK2 in a sample]
TSH-secreting pituitary adenoma	MONDO_0019611	[A rare adenoma of the anterior lobe of the pituitary gland that produces thyrotropin. It is usually associated with goiter and hyperthyroidism.]
TSH producing pituitary tumor	MONDO_0003837	[An adenoma or carcinoma of the anterior lobe of the pituitary gland that produces thyrotropin.]
OCIA domain-containing protein 1 measurement	EFO_0008252	[quantification of the amount of OCIA domain-containing protein 1 in a sample]
peptidyl-prolyl cis-trans isomerase E measurement	EFO_0008257	[quantification of the amount of peptidyl-prolyl cis-trans isomerase E in a sample]
persulfide dioxygenase ETHE1, mitochondrial measurement	EFO_0008258	[quantification of the amount of persulfide dioxygenase ETHE1, mitochondrial in a sample]
fruit development stage	PO_0001002	[A multi-tissue plant structure development stage (PO:0025571) that has as primary participant a single fruit (PO:0009001).]
phospholipase A2, membrane associated measurement	EFO_0008259	[quantification of the amount of phospholipase A2, membrane associated in a sample]
frontorhiny	MONDO_0007636	[Frontorhiny is a distinct syndromic type of frontonasal malformation characterized by hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. An autosomal recessive inheritance has been proposed.]
OX-2 membrane glycoprotein measurement	EFO_0008253	[quantification of the amount of OX-2 membrane glycoprotein in a sample]
P-Selectin measurement	EFO_0008254	[quantification of the amount of P-Selectin in a sample]
particulate matter air pollution measurement	EFO_0008255	[quantification of some aspect of particulate matter air pollution, such as daily levels of exposure]
Lolium perenne	NCBITaxon_4522
Frasier syndrome	MONDO_0007635	[Frasier syndrome is characterised by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma.]
peptidyl-prolyl cis-trans isomerase D measurement	EFO_0008256	[quantification of the amount of peptidyl-prolyl cis-trans isomerase D in a sample]
North Carolina macular dystrophy	MONDO_0007630	[North Carolina macular dystrophy (NCMD) is a non-progressive autosomal dominant macular disorder of congenital or infantile onset characterized by loss of central vision, the accumulation of drusen in the macula and atrophy of photoreceptor cells with a variable phenotype at macular examination.]
chromosome 16p12.1 deletion syndrome, 520kb	MONDO_0007631	[A condition caused by a 520 kb deletion at 16p12.1. It is characterized by developmental delay, craniofacial dysmorphology and congenital heart defects.]
Oryza rufipogon	NCBITaxon_4529
X-10510 measurement	EFO_0021217	[Quantification of the amount of X-10510 in a sample.]
dioxygen(2+)	CHEBI_29371