Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
17-Hydroxypregnenolone sulfate	CHEBI_89454	[A steroid sulfate that is 17-hydroxypregnenolone in which the hydroxy hydrogen at position 3 has been replaced by a sulfo group.]
breast adenoma	MONDO_0002058	[A benign, well circumscribed neoplasm that arises from the breast. Representative examples include apocrine adenoma, tubular adenoma, and pleomorphic adenoma.]
breast benign neoplasm	MONDO_0000620	[A non-metastasizing neoplasm arising from the breast parenchyma.]
Synechocystis sp. PCC 6803	NCBITaxon_1148
obsolete_congenital muscular dystrophy with hyperlaxity	Orphanet_371007
mood disorder	EFO_0004247	[Those disorders that have a disturbance in mood as their predominant feature., A cognitive disorder a disturbance in which the person's mood is hypothesized to be the main underlying feature.]
obsolete_short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome	Orphanet_397623
narrow occludable anterior chamber angle	EFO_0600087	[A narrow or occludable angle is when the angle of the eye is narrow or closed by the iris. Occludable anterior chamber angle is considered as a primary risk factor for primary angle closure glaucoma (PACG).]
anterior chamber depth measurement	EFO_0005668	[quantification of the depth of the anterior chamber of the eye as an indicator for eye disease such as primary angle closure glaucoma]
appendectomy	EFO_0600086	[Procedure to remove the appendix.]
peritoneal solute transfer rate	EFO_0600089	[Quantification of the rate at which small molecules cross the peritoneal membrane typically measured as the ratio of the concentration of creatinine in the dialysate at 4 hours of a dwell of dialysate solution to that in the plasma (4-hr D/P creatinine).]
dysmorphism-conductive hearing loss-heart defect syndrome	MONDO_0014044	[A syndrome characterized by distinctive facial features, cleft palate, conductive hearing loss, and mild developmental delay. The craniofacial dysmorphism included low frontal hairline, ptosis, prominent eyes, flat midface, Cupid's bow configuration of the upper lip, and low-set, posteriorly rotated small ears.]
Synechococcus elongatus PCC 7942	NCBITaxon_1140
lymphocyte:monocyte ratio	EFO_0600088	[Quantification of the ratio between absolute lymphocyte count and absolute monocyte count.]
microcephalic primordial dwarfism due to ZNF335 deficiency	MONDO_0014043	[Microcephalic primordial dwarfism due to ZNF335 deficiency is characterized by severe antenatal microencephaly, simplified gyration, agenesis of the corpus callosum, absence of basal ganglia (very rare), pontocerebellar atrophy and involvement of the white matter with secondary cerebral atrophy. Congenital cataract, choanal atresia, multiple arthrogryposis and spastic tetraparesis can occur.]
family history of prostate cancer	EFO_0600083	[A reported family history of prostate cancer in one or more family members.]
prostate cancer	MONDO_0008315	[A primary or metastatic malignant tumor involving the prostate gland. The vast majority are carcinomas.]
insulin use measurement	EFO_0600082	[Quantification of some aspect of the use of insulin.]
insulin	CHEBI_5931
PP interval	EFO_0600085	[An interval measured from the onset of the P wave in one PQRST wave complex to the onset of the P wave in the following PQRST wave complex.]