Any inflammatory bowel disease in which the cause of the disease is a mutation in the NOD2 gene. [ MONDO : patterns/disease_series_by_gene ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:266600 (MONDO:equivalentTo)
  • GARD:0009857 (MONDO:equivalentTo)
  • UMLS:C0009324 (OMIM:266600)
  • SCTID:34000006 (MONDO:equivalentTo)
  • DOID:0110892 (MONDO:equivalentTo)
  • ICD9:555.9 (MONDO:i2s)
abbreviation
IBD1 [ https://omim.org/entry/266600 DOID : 0110892 MONDO : Lexical ]
conformsTo
  • http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml
definition
  • Any inflammatory bowel disease in which the cause of the disease is a mutation in the NOD2 gene.
exactMatch
  • https://omim.org/entry/266600
  • http://identifiers.org/snomedct/34000006
  • http://purl.obolibrary.org/obo/DOID_0110892
has exact synonym
  • inflammatory bowel disease 1
  • inflammatory bowel disease caused by mutation in NOD2
  • NOD2 inflammatory bowel disease
  • inflammatory bowel disease 1, Crohn disease
  • IBD1
  • inflammatory bowel disease type 1
  • crohn disease-associated growth failure
has related synonym
  • ulcerative colitis
  • pediatric ulcerative colitis
  • inflammatory bowel disease (Crohn disease) 1
  • ulcerative colitis, pediatric
  • regional enteritis
  • Crohn disease
  • Crohn disease-associated Growth failure, susceptibility to
id
  • MONDO:0009960
term tracker item
  • https://github.com/monarch-initiative/mondo/issues/4521