Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
finger fracture	EFO_0009616	[A traumatic break in one or more of the bones in one of the digits of the hand. [ NCI ]]
upper extremity fracture	EFO_0009514	[A traumatic break in one or more of the bones in the arm, forearm, or hand. [ NCI ]]
knee fracture	EFO_0009617	[A traumatic break in one or more of the bones that compose the knee joint. [ NCI ]]
bacterial thylakoid	GO_0030075	[A thylakoid that is derived from and attached to, but not necessarily continuous with, the plasma membrane, and is not enclosed in a plastid. It bears the photosynthetic pigments in photosynthetic cyanobacteria.]
intracellular non-membrane-bounded organelle	GO_0043232	[ Organized structure of distinctive morphology and function, not bounded by a lipid bilayer membrane and occurring within the cell. Includes ribosomes, the cytoskeleton and chromosomes. ]
Epidermolysis bullosa simplex with mottled pigmentation	Orphanet_79397	[Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a basal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized blistering with mottled or reticulate brown pigmentation.]
Basal epidermolysis bullosa simplex	Orphanet_158665
pro‐interleukin‐16 measurement	EFO_0010629	[quantification of pro‐interleukin 16 in a sample]
Epidermolysis bullosa simplex, Dowling-Meara type	Orphanet_79396	[Epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM) is a basal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by the presence of generalized vesicles and small blisters in grouped or arcuate configuration.]
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type	Orphanet_79399	[Non-Dowling-Meara generalized epidermolysis bullosa simplex, formerly known as epidermolysis bullosa simplex, Köbner type (EBS-K) is a generalized basal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by non-herpetiform blisters and erosions arising in particular at sites of friction.]
pro‐adrenomedullin measurement	EFO_0010627	[quantification of pro‐adrenomedullin in a sample]
natriuretic peptides B measurement	EFO_0010628	[quantification of natriuretic peptides B in a sample]
xaa‐pro aminopeptidase 2 measurement	EFO_0010625	[quantification of xaa‐pro aminopeptidase 2 in a sample]
GM15385	CLO_0026789	[DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION]
placenta growth factor measurement	EFO_0010626	[quantification of placenta growth factor in a sample]
Keratoderma hereditarium mutilans with ichthyosis	Orphanet_79395
Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature	Orphanet_98352
tissue factor measurement	EFO_0010623	[quantification of tissue factor in a sample]
obsolete_congenital non-bullous ichthyosiform erythroderma	Orphanet_79394
tumor necrosis factor receptor superfamily member 1B measurement	EFO_0010624	[quantification of tumor necrosis factor receptor superfamily member 1B in a sample]