Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
drought environment	EO_0007404	[an environment in plant experiments to understand how plants respond to episodic drought and watering pulse by depriving the plants of water supply]
cyclin-dependent kinase 2:cyclin-A2 complex measurement	EFO_0020295	[The determination of the amount of cyclin-dependent kinase 2:cyclin-A2 complex in a sample]
cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement	EFO_0020296	[The determination of the amount of cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex in a sample]
cyclin-dependent kinase 8:cyclin-c complex measurement	EFO_0020297	[The determination of the amount of cyclin-dependent kinase 8:cyclin-c complex in a sample]
obsolete_2q24 microdeletion syndrome	Orphanet_1617	[2q24 microdeletion syndrome is a chromosomal anomaly consisting of a partial long arm deletion of chromosome 2 and characterized clinically by a wide range of manifestations (depending on the specific region deleted) which can include seizures, microcephaly, dysmorphic features, cleft palate, eye abnormalities (coloboma, cataract and microphthalmia), growth retardation, failure to thrive, heart defects, limb anomalies, developmental delay and autism.]
cyclin-dependent kinase inhibitor 1b measurement	EFO_0020298	[The determination of the amount of cyclin-dependent kinase inhibitor 1b in a sample]
obsolete_tetragametic chimerism	Orphanet_199310
creatine kinase m-type measurement	EFO_0020291	[The determination of the amount of creatine kinase m-type in a sample]
Erythema nodosum	HP_0012219	[An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral.]
Inflammatory abnormality of the skin	HP_0011123	[The presence of inflammation of the skin. That is, an abnormality of the skin resulting from the local accumulation of fluid, plasma proteins, and leukocytes.]
Cyprinus carpio	NCBITaxon_7962
creatine kinase m-type:creatine kinase b-type heterodimer measurement	EFO_0020292	[The determination of the amount of creatine kinase m-type:creatine kinase b-type heterodimer in a sample]
cryptic protein measurement	EFO_0020293	[The determination of the amount of cryptic protein in a sample]
cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex measurement	EFO_0020294	[The determination of the amount of cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex in a sample]
obsolete_familial clubfoot with or without associated lower limb anomalies	Orphanet_199315
creatine kinase b-type measurement	EFO_0020290	[The determination of the amount of creatine kinase b-type in a sample]
15q13.3 microdeletion syndrome	Orphanet_199318	[15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features.]
Abnormality of the urinary system physiology	HP_0011277
O-octanoyl-L-carnitine	CHEBI_18102	[The L-enantiomer of an O-octanoylcarnitine.]
MYH7-related late-onset scapuloperoneal muscular dystrophy	MONDO_0008409