Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
anterior endoderm anlage in statu nascendi	EFO_0000260
anterior endoderm primordium	EFO_0000261
obsolete_anterior midgut primordium	EFO_0000262
anterior spiracle specific anlage	EFO_0000263
antibody	EFO_0000264	[An antibody function (or antigen binding function) is an infection-fighting protein molecule in blood or secretory fluids that tags, neutralizes, and helps destroy pathogenic microorganisms such as bacteria, viruses and toxins.]
molecular function	GO_0003674	[Elemental activities, such as catalysis or binding, describing the actions of a gene product at the molecular level. A given gene product may exhibit one or more molecular functions.]
obsolete_aorta	EFO_0000265	[Principal unpaired, median artery of the trunk, leading from the paired roots (radices) of the dorsal aorta to the caudal artery., The main trunk of the systemic arteries., The major arterial trunk that carries oxygenated blood from the left ventricle into the ascending aorta behind the heart, the aortic arch, through the thorax as the descending aorta and through the abdomen as the abdominal aorta; it bifurcates into the left and right common iliac arteries., The great arterial trunk that carries blood from the heart to be distributed by branch arteries through the body., Principal unpaired, median artery of the trunk, leading from the paired roots (radices) of the dorsal aorta to the caudal artery. Kimmel et al, 1995.]
obsolete_apical meristem	EFO_0000267	[A group of cells at the tip of the stem and root that give rise by cell division to the primary tissues and are ultimately responsible for the structural organization of the entire primary plant body.]
obsolete_apoptotic amnioserosa	EFO_0000268
array design	EFO_0000269	[An instrument design which describes the design of the array.]
instrument design	EFO_0001451	[An instrument design is information in the form of a specification that describes the setup and design of an instrument.]
obsolete_non-syndromic developmental defect of the eye	Orphanet_108985
obsolete_Goldmann-Favre syndrome	Orphanet_53540	[Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis).]
fructose	CHEBI_28757	[A ketohexose that is an isomer of glucose.]
obsolete_bladder	EFO_0000290	[Organ with organ cavity which is continuous proximally with the right and left ureters and distally with the urethra. Examples: There is only one urinary bladder., A membranous sac in animals that serves as the receptacle of a liquid or contains gas., The distensible sac-like organ that functions as a reservoir of urine, collecting from the kidneys and eliminating via the urethra.]
obsolete_bladder MMHCC	EFO_0000291
obsolete_bladder carcinoma	EFO_0000292	[A carcinoma that arises from epithelial cells of the urinary bladder]
obsolete_bladder mucosa	EFO_0000293
mitochondrial complex II deficiency, nuclear type 1	MONDO_0100294	[Complex II deficiency is a mitochondrial disease. Mitochondria are specialized compartments in cells that create more than 90% of the energy needed by the body. In mitochondrial diseases, the mitochondria don't work correctly resulting in less energy in the cell, cell injury and cell death. The signs and symptoms of mitochondrial complex II deficiency can vary greatly from severe life-threatening symptoms in infancy to muscle disease beginning in adulthood. Complex II deficiency can be caused by mutations in the SDHA, SDHB, SDHD, or SDHAF1 genes. In many cases the underlying gene mutations cannot be identified. Complex II deficiency is inherited in an autosomal recessive fashion. Complex II deficiency gene mutation carriers may be at an increased risk for certain cancers.]
isolated oxidative phosphorylation complex disorder	MONDO_0016805