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Disease Ontology Browser
celiac disease (DOID:10608)
Alliance: disease page
Synonyms: celiac sprue; coeliac disease; idiopathic steatorrhea
Alt IDs: OMIM:607202, OMIM:609754, OMIM:611598, OMIM:612005, OMIM:612006, OMIM:612007, OMIM:612008, OMIM:612009, OMIM:612011, EFO:0001060, ICD10CM:K90.0, ICD9CM:579.0, MESH:D002446, NCI:C26714, ORDO:555, UMLS_CUI:C0007570
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory