Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
human herpesvirus 8 seropositivity	EFO_0007039	[human herpesvirus 8 seropositivity is the result of a measurement of circulating human herpesvirus 8 specific antibodies ]
human herpesvirus 8 infection	EFO_0002612	[A gammaherpesvirus that contributes to the development of Kaposi sarcoma., An infectious process caused by the human herpesvirus 8. This infection is associated with Kaposi sarcoma.]
malunion fracture	EFO_0010684	[A malunion fracture is a fracture which has healed in such a position that it can cause malalignment or deformity.]
Influenza A seropositivity	EFO_0007038	[Influenza A seropositivity is the result of a measurement of circulating Influenza A specific antibodies ]
household income	EFO_0009695	[A demographic parameter indicating the amount of earning made by a family.]
cytomegalovirus seropositivity	EFO_0007037	[cytomegalovirus seropositivity is the result of a measurement of circulating cytomegalovirus specific antibodies ]
social deprivation	EFO_0009696	[Absence of social environment which is necessary for the social development of the individual.]
ileostomy	EFO_0010681	[An ileostomy is an operation where a temporary or permanent surgical opening is created in the abdominal wall. The small bowel is brought through the opening in order to evacuate the stool via the small bowel instead of the anus.]
digestive system surgery	EFO_0020979	[Surgery performed on any part of the digestive system.]
pathological complete response	EFO_0009697	[The disappearance of all signs of cancer, supported by pathological examination.]
liver transplant	EFO_0010682	[A liver transplant is an operation in which a donor liver is implanted into a recipient.]
herpes virus seropositivity	EFO_0007036	[herpes virus seropositivity is the result of a measurement of circulating herpes virus specific antibodies ]
obsolete_otospondylomegaepiphyseal dysplasia	Orphanet_1427
Familial chondromalacia patellae	Orphanet_1428	[Familial chondromalacia patellae is an inherited bone disorder described in 5 families in 1963 and is characterized by localized patellar pain and male-to-male transmission.]
humerus trochlea aplasia	MONDO_0008611	[Humerus trochlea aplasia is an extremely rare familial bone deformity described only in Japanese patients to date. The deformity is bilateral in nearly half of patients (with bilateral involvement, the condition is symmetrical) and sometimes causes ulnar nerve palsy or cubitus varus.]
hematoma	EFO_0010680	[A hematoma is a collection of blood from a vascular structure into an extravascular space.]
Desbuquois syndrome	Orphanet_1425	[Desbuquois syndrome (DBQD) is an osteochondrodysplasia characterized by severe micromelic dwarfism, facial dysmorphism, joint laxity, multiple dislocations, vertebral and metaphyseal abnormalities and advanced carpotarsal ossification. Two forms have been distinguished on the basis of the presence (type 1) or the absence (type 2) of characteristic hand anomalies.]
Malformation syndrome with connective tissue involvement	Orphanet_139030
blue color blindness	MONDO_0008610	[Tritanopia is an extremely rare form of colour blindness characterised by a selective deficiency of blue vision.]
color vision disorder	MONDO_0001703	[The absence of or defect in the perception of colors.]