Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
peripheral nervous system disease	EFO_0009387	[A disease involving the peripheral nervous system.]
sum of basophil and neutrophil counts	EFO_0009388	[Sum of quantification of basophil and neutrophil in the blood.]
granulocyte count	EFO_0007987	[The number of granulocytes (polymorphonuclear leukocytes) in a specified volume of blood, usually 1 cubic millimeter.]
blood component	EFO_0001941
phosphatidylcholine 32:1 measurement	EFO_0010373	[The quantification of phosphatidylcholine 32:1 levels in a sample.]
sum of eosinophil and basophil counts	EFO_0009389	[Sum of quantification of eosinophil and basophil in the blood.]
phosphatidylcholine 32:2 measurement	EFO_0010374	[The quantification of phosphatidylcholine 32:2 levels in a sample.]
lysophosphatidylethanolamine 22:6 measurement	EFO_0010371	[The quantification of lysophosphatidylethanolamine 22:6 levels in a sample.]
lysophosphatidylethanolamine measurement	EFO_0010225	[A quantification of lysophosphatidylethanolamines.]
median fin fold	UBERON_2000040	[Surface structure that will develop into one of the median fins. Extends from dorsal surface of fish, caudal to the 8th somite, to the ventral surface ending at the caudal side of the vent.]
zebrafish component	EFO_0003331
phosphatidylcholine 32:0 measurement	EFO_0010372	[The quantification of phosphatidylcholine 32:0 levels in a sample.]
obsolete nonepidermolytic palmoplantar keratoderma	MONDO_0006588
lysophosphatidylethanolamine 20:4 measurement	EFO_0010370	[The quantification of lysophosphatidylethanolamine 20:4 levels in a sample.]
obsolete_faciocardiorenal syndrome	Orphanet_1973
Autosomal recessive facio-digito-genital syndrome	Orphanet_1974	[Autosomal recessive facio-digito-genital syndrome is a very rare syndrome including short stature, facial dysmorphism, hand abnormalities and shawl scrotum.]
Genetic malformation syndrome with short stature	Orphanet_183570
Genetic urogenital tract malformation	Orphanet_156622
obsolete_lethal faciocardiomelic dysplasia	Orphanet_1972
Akinesia	HP_0002304	[Inability to initiate changes in activity or movement and to perform ordinary volitional movements rapidly and easily.]