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)
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
Term relations
Equivalent to:
Subclass of: