|  Help  |  About  |  Contact Us

DO Term : celiac disease [DOID:10608] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • UMLS_CUI:C0007570,
  • OMIM:612009,
  • SNOMEDCT_US_2023_03_01:197477005,
  • 612007,
  • OMIM:609754,
  • OMIM:611598,
  • EFO:0001060,
  • 612008,
  • OMIM:607202,
  • 609754,
  • OMIM:612005,
  • OMIM:612008,
  • 612011,
  • GARD:11998,
  • 611598,
  • NCI:C26714,
  • coeliac disease,
  • 612009,
  • ICD9CM:579.0,
  • ICD10CM:K90.0,
  • OMIM:612007,
  • 612006,
  • 607202,
  • ORDO:555,
  • OMIM:612006,
  • MESH:D002446,
  • idiopathic steatorrhea,
  • celiac sprue,
  • 612005,
  • OMIM:612011
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents