Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
embryonic foregut sensory structure	FBbt_00005616	[Any internal compound sense organ (FBbt:00007236) that is part of some embryonic foregut (FBbt:00005606).]
TH-2	EFO_0002804
4470	EFO_0002807
familial anetoderma	MONDO_0016445	[Familial anetoderma is an extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder.]
embryonic proventriculus outer layer	FBbt_00005610	[Outer layer of the proventriculus of the embryo. It corresponds to the visceral mesoderm, containing cells that secrete the peritrophic membrane.]
obsolete_retroperitoneum	EFO_0002806
acquired cutis laxa	MONDO_0016446	[An instance of cutis laxa that is acquired during the lifetime of the individual.]
cell outer membrane	GO_0009279	[ A lipid bilayer that forms the outermost layer of the cell envelope; enriched in polysaccharide and protein; the outer leaflet of the membrane contains specific lipopolysaccharide structures. ]
cell envelope	GO_0030313	[ An envelope that surrounds a bacterial cell and includes the cytoplasmic membrane and everything external, encompassing the periplasmic space, cell wall, and outer membrane if present. ]
4483	EFO_0002809
embryonic esophagus	FBbt_00005612	[Esophagus of the embryo. It invaginates to form part of the proventriculus.]
4475	EFO_0002808
embryonic precursor of adult foregut	FBbt_00005611	[Imaginal cell, set aside during embryonic development, that will give rise to the adult posterior foregut. These cells are found in a ring at the anterior part of the proventriculus, the foregut imaginal ring.]
acquired pseudoxanthoma elasticum	MONDO_0016441	[A nonheritable form of pseudoxanthoma elasticum (PXE), lacking the retinal and vascular stigmata associated with the inherited form of the disorder, but having skin lesions that are clinically, histologically, and ultrastructurally similar to those seen in the inherited type.]
pseudoxanthoma elasticum (inherited or acquired)	MONDO_0024308	[An inherited disorder that causes calcium and other minerals to accumulate in the elastic fibers of the skin, eyes, and blood vessels, and less frequently in other areas such as the digestive tract.]
embryonic maxillary sensory complex	FBbt_00005618	[Sense organ of the embryonic maxillary segment that gives rise to the terminal organ of the larval head. It is posterior and ventral to the embryonic brain by stage 13 and migrates ventrally and anteriorly to establish its final position, ventral to the dorsal organ, by stage 17.]
obsolete_congenital muscular dystrophy due to LMNA mutation	Orphanet_157973
embryonic labial sensory complex	FBbt_00005619
Bacillus cereus	NCBITaxon_1396
Broad hallux phalanx	HP_0010059	[An increase in width in one or more phalanges of the big toe.]