inflammatory bowel disease 2

Preferred Label : inflammatory bowel disease 2;

Obsolete resource : true;

Approved symbol HGNC : IBD2;

Chromosome HGNC : 12p13.2-q24.1;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:5332;

UMLS CUI

C1415834;

Automatic exact mappings (from CISMeF team)
- Inflammatory bowel disease 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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