Summary Literature (0)

DOID:10608 - celiac disease

Disease Ontology Definition:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite.

Synonyms: celiac sprue, coeliac disease, idiopathic steatorrhea

Xenbase Genes : sh2b3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0005130 - metanephric loop of Henle

MIM:

MIM:607202 - CELIAC DISEASE, SUSCEPTIBILITY TO, 5; CELIAC5

MIM:609754 - CELIAC DISEASE, SUSCEPTIBILITY TO, 2; CELIAC2

MIM:611598 - CELIAC DISEASE, SUSCEPTIBILITY TO, 6; CELIAC6

MIM:612005 - CELIAC DISEASE, SUSCEPTIBILITY TO, 7; CELIAC7

MIM:612006 - CELIAC DISEASE, SUSCEPTIBILITY TO, 8; CELIAC8

MIM:612007 - CELIAC DISEASE, SUSCEPTIBILITY TO, 9; CELIAC9

MIM:612008 - CELIAC DISEASE, SUSCEPTIBILITY TO, 10; CELIAC10

MIM:612009 - CELIAC DISEASE, SUSCEPTIBILITY TO, 11; CELIAC11

MIM:612011 - CELIAC DISEASE, SUSCEPTIBILITY TO, 13; CELIAC13

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee