DO_rare_slim NCIthesaurus has symptom has major susceptibility factor autoimmune disease of gastrointestinal tract celiac disease UMLS_CUI:C0007570 DOID:10608 ORDO:555 MESH:D002446 disease_ontology ICD9CM:579.0 SNOMEDCT_US_2025_09_01:197477005 NCI:C26714 MIM:612011 MIM:607202 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. MIM:612009 MIM:612008 GARD:11998 EFO:0001060 MIM:609754 MIM:612005 MIM:611598 ICD10CM:K90.0 MIM:612007 MIM:612006 Xref MGI. OMIM mapping confirmed by DO. [SN]. celiac sprue coeliac disease idiopathic steatorrhea susceptibility to celiac disease 1 susceptibility to celiac disease 5 susceptibility to celiac disease 4 susceptibility to celiac disease 2 susceptibility to celiac disease 3 susceptibility to celiac disease 6 susceptibility to celiac disease 7 susceptibility to celiac disease 8 susceptibility to celiac disease 9 susceptibility to celiac disease 10 susceptibility to celiac disease 11 susceptibility to celiac disease 12 susceptibility to celiac disease 13 abdominal pain nausea diarrhea vomiting constipation