Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
sedation	EFO_0009868	[The process of allaying nervous excitement or the state of being calmed.]
xerostomia	EFO_0009869	[Dryness of the mouth resulting from reduced salivary secretion.]
Ciliophora infectious disease	EFO_0007209	[Infections with protozoa of the phylum ciliophora., An Alveolata infectious disease that involves infection caused by the members of the phylum Ciliophora, which are characterized by the presence of hair-like organelles called cilia.]
Pierre-Robin sequence	HP_0000201	[Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate.]
Bifidobacterium longum	NCBITaxon_216816
Oral cleft	HP_0000202	[The presence of a cleft in the oral cavity, the two main types of which are cleft lip and cleft palate. In cleft lip, there is the congenital failure of the maxillary and median nasal processes to fuse, forming a groove or fissure in the lip. In cleft palate, there is a congenital failure of the palate to fuse properly, forming a grooved depression or fissure in the roof of the mouth. Clefts of the lip and palate can occur individually or together. It is preferable to code each defect separately.]
Cleft upper lip	HP_0000204	[A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development.]
cleft lip	EFO_0003959	[Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.]
Postaxial polydactyly of toes	Orphanet_295008
cefuroxime	CHEBI_3515	[A 3-(carbamoyloxymethyl)cephalosporin compound having a 7-(2Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido side chain.]
Short lingual frenulum	HP_0000200	[The presence of an abnormally short lingual frenulum.]
GM21515	EFO_0010838	[Lymphoblastoid cell line from a Maasai male from Kinyawa, Kenya]
GM21737	EFO_0010839	[Lymphoblastoid cell line from a Maasai male from Kinyawa, Kenya]
GM19025	EFO_0010836	[Lymphoblastoid cell line from a Luhya male from Webuye, Kenya]
GM19043	EFO_0010837	[Lymphoblastoid cell line from a Luhya male from Webuye, Kenya]
obsolete_Kleefstra syndrome due to a point mutation	Orphanet_261652
tumor necrosis factor measurement	EFO_0010834	[The determination of the amount of tumor necrosis factor present in a sample.]
GM19023	EFO_0010835	[Lymphoblastoid cell line from a Luhya female from Webuye, Kenya]
primary central chondrosarcoma	EFO_0010832	[A chondrosarcoma arising from the central portion of bone without a benign precursor.]
bone chondrosarcoma	MONDO_0000515	[A chondrosarcoma (disease) that involves the bone tissue.]