Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
obsolete_basal plate midbrain region	EFO_0003567	[Portion of tissue that is dorsolateral to the floor plate and part of the midbrain.]
obsolete_somite 3	EFO_0003566
obsolete_floor plate rhombomere 5	EFO_0003569	[Floor plate that is part of the rhombomere 5.]
obsolete_floor plate rhombomere 2	EFO_0003568	[Floor plate that is part of the rhombomere 2.]
obsolete_1p21.3 microdeletion syndrome	Orphanet_293948	[1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder(see this term).]
Clostridium baratii	NCBITaxon_1561
obsolete_descending octaval nucleus	EFO_0003550
obsolete_ectopterygoid	EFO_0003552
obsolete_dorsal fin musculature	EFO_0003551
obsolete_gill filament	EFO_0003554	[Portion of tissue that projects outward from the gill and is a thread-like, soft, red respiratory and excretory structure.]
obsolete_entopterygoid	EFO_0003553
obsolete_hyomandibula	EFO_0003556
obsolete_horizontal myoseptum	EFO_0003555	[A connective tissue partition developing at the apex of the chevron-shaped myotome and separating dorsal (epaxial) and ventral (hypaxial) body wall muscle masses.]
obsolete_segmental intercostal artery	EFO_0003558
obsolete_interopercle	EFO_0003557
obsolete_hair cell anterior macula	EFO_0003559
Miscarriage	HP_0005268	[A pregnancy that ends at a stage in which the fetus is incapable of surviving on its own, defined as the spontaneous loss of a fetus before the 22th week of pregnancy.]
Progressive supranuclear palsy - corticobasal syndrome	Orphanet_240103	[PSP-corticobasal syndrome (PSP-CBS) is an atypical variant of progressive supranuclear palsy (PSP; see this term), a rare late-onset neurodegenerative disease.]
Immunodeficiency with natural-killer cell deficiency and adrenal insufficiency	Orphanet_75391
obsolete_focal facial dermal dysplasia type II	Orphanet_398173