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: idiopathic steatorrhea coeliac disease celiac sprue
Term information
- OMIM:612005
- OMIM:607202
- OMIM:612007
- GARD:11998
- ORDO:555
- ICD9CM:579.0
- OMIM:612009
- MESH:D002446
- NCI:C26714
- EFO:0001060
- OMIM:609754
- OMIM:611598
- OMIM:612006
- OMIM:612008
- UMLS_CUI:C0007570
- ICD10CM:K90.0
- OMIM:612011
- SNOMEDCT_US_2022_09_01:197477005
DO_rare_slim, NCIthesaurus
GARD:11998
MESH:D002446
NCI:C26714
OMIM:612011
ORDO:555
UMLS_CUI:C0007570
OMIM:612006
ICD9CM:579.0
EFO:0001060
OMIM:611598
OMIM:612005
OMIM:612008
SNOMEDCT_US_2022_09_01:197477005
OMIM:612007
OMIM:609754
OMIM:607202
OMIM:612009
ICD10CM:K90.0