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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 - celiac disease


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autoimmune disease of gastrointestinal tract (is_a)