Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Microcephaly - brachydactyly - kyphoscoliosis	Orphanet_3433
round cell liposarcoma	EFO_0003084	[A poorly differentiated liposarcoma, characterized by the presence of solid sheets of primitive round mesenchymal cells and the absence of myxoid stroma.]
pleomorphic liposarcoma	EFO_0003083	[Pleomorphic liposarcoma (PLS), the rarest subtype of liposarcoma (LS), is an aggressive, fast growing tumor located usually in the deep soft tissues of the lower and upper extremities. It is characterized by a variable number of pleomorphic lipoblasts and, in contrast to dedifferentiated liposarcoma, it lacks any association with well-differentiated liposarcoma.]
dedifferentiated liposarcoma	EFO_0003085	[Dedifferentiated liposarcoma (DDLS) is a high-grade subtype of liposarcoma (LS) that progresses from well-differentiated liposarcoma (WDLS), and most often occurs in the retroperitoneum. It is defined as a region of nonlipogenic sarcoma associated with WDLS.]
obsolete_ventricular myocardium	EFO_0003088
obsolete_atrial myocardium	EFO_0003087
obsolete_spinocerebellar ataxia type 1	EFO_0003089
2-hydroxyglutarate(2-)	CHEBI_11596	[A dicarboxylic acid dianion resulting from the removal of a proton from both of the carboxylic acid groups of 2-hydroxyglutaric acid.]
obsolete_von Voss-Cherstvoy syndrome	Orphanet_3439
beta-adrenergic agonist	CHEBI_35522	[An agent that selectively binds to and activates beta-adrenergic receptors.]
obsolete_Vogt-Koyanagi-Harada disease	Orphanet_3437	[A hypersensitivity reaction type II disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.]
hypoglycemic drug	CHEBI_35526	[A drug which lowers the blood glucose level.]
obsolete_MMEP syndrome	Orphanet_3434
cis-ketoconazole	CHEBI_47519
obsolete_sacrum	EFO_0003071
obsolete_buttock	EFO_0003070
asymptomatic myeloma	EFO_0003073	[A plasma cell myeloma lacking clinical manifestations and organ impairment.]
SK-N-SH	EFO_0003072
obsolete_Waardenburg syndrome	Orphanet_3440	[Waardenburg syndrome (WS) is an autosomal dominant disorder characterized by varying degrees of deafness, minor defects in structures arising from neural crest and pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.]
trabecular meshwork	EFO_0003077	[A porelike structure surrounding the entire circumference of the anterior chamber through which aqueous humor circulates to the canal of Schlemm. (MeSH)]