Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
behavioural inhibitory control measurement	EFO_0008467	[Some quantification of the ability to inhibit maladaptive or inappropriate behavior.]
midregional pro atrial natriuretic peptide measurement	EFO_0008468	[Quantification of the levels of midregional pro atrial natriuretic peptide.]
B-type natriuretic peptide to N-terminal pro B-type natriuretic peptide ratio	EFO_0008469	[Quantification of the ratio of B-type natriuretic levels to N-terminal pro B-type natriuretic peptide levels.]
pregnancy induced alloimmunization	EFO_0008462	[An immune response to foreign (donor) antigens due to fetomaternal hemorrhage (ie, transplacental passage of fetal erythrocytes) associated with delivery, trauma, spontaneous or induced abortion, ectopic pregnancy, or invasive obstetric procedures.]
alloimmunization	EFO_0006804	[An immune response to foreign (donor) antigens.]
glucagon measurement	EFO_0008463	[The quantification of glucagon, a hormone involved in glucose homeostasis.]
glucose-dependent insulinotropic peptide measurement	EFO_0008464	[The quantification of glucose-dependent insulinotropic peptide, an incretin hormone secreted in response to nutrient stimulation that acts to increase insulin secretion.]
glucagon-like peptide-1 measurement	EFO_0008465	[The quantification of glucagon-like peptide 1, an incretin hormone secreted in response to nutrient stimulation that acts to increase insulin secretion.]
obsolete_congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency	Orphanet_95699
N-acetylarginine measurement	EFO_0021429	[Quantification of N-acetylarginine levels in a sample.]
L-arginine measurement	EFO_0006524	[quantification of the amount of L-arginine in a sample, eg in blood]
Persistent Müllerian duct syndrome	Orphanet_2856
Rare genetic disorder with obstructive azoospermia	Orphanet_400003
Bronchospasm	HP_0025428	[A spasm (sudden, involuntary constriction) of the bronchioles.]
Partial duplication of the long arm of chromosome 11	Orphanet_262923
obsolete_Perrault syndrome	Orphanet_2855
obsolete_Fuhrmann syndrome	Orphanet_2854
humanized mouse	EFO_0021426	[The mice carry the human CYP1A1 and CYP1A2 genes in the absence of functional mouse Cyp1a1 and Cyp1a2 orthologs and mimic the human poor-affinity aryl hydrocarbon receptor (AHR) by carrying the poor-affinity Ahrd allele derived from DBA/2J mice. These may be useful in drug or carcinogen metabolism research; specifically as a model for human risk assessment studies involving drug or environmental toxicants that may be substrates for the aryl hydrocarbon receptor (AHR) or cytochrome P450 family 1 members.]
pigmentary glaucoma	EFO_0021425	[Pigmentary glaucoma is a type of secondary open-angle glaucoma characterized by heavy homogenous pigmentation of the trabecular meshwork, iris transillumination defects, and pigment along the corneal endothelium (Krukenberg spindle).]
N6-succinyladenosine measurement	EFO_0021428	[Quantification of the N6-succinyladenosine levels in a sample.]