Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Upslanted palpebral fissure	HP_0000582	[The palpebral fissure inclination is more than two standard deviations above the mean for age (objective); or, the inclination of the palpebral fissure is greater than typical for age.]
L2 larva	EFO_0002719	[C. elegans second stage larva. At 25 Centigrade, it ranges 25.5-32.5 hours after fertilization, 11.5-18.5 hours after hatch.]
Caenorhabditis elegans larval stage	EFO_0007694	[Under environmental conditions which are favourable for reproduction, hatched larvae develop through four stages or molts, designated as L1 to L4. When conditions are stressed as in food insufficiency, C. elegans can enter an alternative third larval stage called the dauer state. Dauer is German for permanent. Dauer larvae are stress-resistant; they are thin and their mouths are sealed and cannot take in food, and they can remain in this stage for a few months.[14] Hermaphrodites produce all their sperm in the L4 stage (150 sperm per gonadal arm) and then produce only oocytes. The sperm cells are stored in the same area of the gonad as the oocytes until the first oocyte pushes the sperm into the spermatheca (a chamber wherein the oocytes become fertilized by the sperm).]
maxillary sensory complex primordium	FBbt_00005544
sensory nervous system primordium	FBbt_00005551
hatching long-pec	EFO_0002718
hatching stage	EFO_0001298
labral sensory complex primordium	FBbt_00005546
labial sensory complex primordium	FBbt_00005545
Hartsfield-Bixler-Demyer syndrome	MONDO_0014196
ectrodactyly with and without other manifestations	MONDO_0800090
microcornea-myopic chorioretinal atrophy	MONDO_0014195
Pigmentary retinopathy	HP_0000580	[An abnormality of the retina characterized by pigment deposition. It is typically associated with migration and proliferation of macrophages or retinal pigment epithelial cells into the retina; melanin from these cells causes the pigmentary changes. Pigmentary retinopathy is a common final pathway of many retinal conditions and is often associated with visual loss.]
obsolete_mesoaxial synostotic syndactyly with phalangeal reduction	Orphanet_157801
Blepharophimosis	HP_0000581	[A fixed reduction in the vertical distance between the upper and lower eyelids with short palpebral fissures.]
anti-arrhythmia drug	CHEBI_38070
mitochondrial DNA depletion syndrome 13	MONDO_0014198	[Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the FBXL4 gene.]
combined immunodeficiency due to MALT1 deficiency	MONDO_0014197	[Combined immunodeficiency due to MALT1 deficiency is a rare, genetic form of primary immunodeficiency characterized by growth retardation, early recurrent pulmonary infections leading to bronchiectasis, inflammatory gastrointestinal disease, and other symptoms, such as rash, dermatitis, skin infections.]
obsolete_congenital pseudoarthrosis of the limbs	Orphanet_157808
antimalarial	CHEBI_38068