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| Term | celiac disease | ID (Ontology) | DOID:10608 (Human Disease) |
| 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. | ||
| Also Known As | "celiac sprue" ; "coeliac disease" ; "idiopathic steatorrhea" | ||
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autoimmune disease_______________ gastrointestinal system disease__| autoimmune disease of gastrointestinal tract |__celiac disease |
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| Is a | autoimmune disease of gastrointestinal tract | ||
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EFO:0001060 GARD:11998 ICD10CM:K90.0 ICD9CM:579.0 MESH:D002446 MIM:607202 MIM:609754 MIM:611598 MIM:612005 MIM:612006 MIM:612007 MIM:612008 MIM:612009 MIM:612011 NCI:C26714 ORDO:555 SNOMEDCT_US_2023_03_01:197477005 UMLS_CUI:C0007570 |
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