Inflammatory bowel disease 21

Preferred Label : Inflammatory bowel disease 21;

Symbol : IBD21;

CISMeF acronym : IBD21;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general description and a discussion of genetic heterogeneity of inflammatory bowel disease (IBD), including Crohn disease (CD) and ulcerative colitis (UC), see IBD1 (266600).;

Inheritance : Autosomal dominant;

Prefixed ID : %612354;

Details

Origin ID

612354;

UMLS CUI

C2676507;

Automatic exact mappings (from CISMeF team)
- Crohn disease [ORDO Disease]
- Ulcerative colitis [ORDO Disease]
Currated CISMeF NLP mapping
- inflammatory bowel disease 21 [DO Concept]
- inflammatory bowel disease 21 [MeSH concept]
- inflammatory bowel disease 21 [MeSH Supplementary Concept]
DO Cross reference
- inflammatory bowel disease 21 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Ulcerative colitis [HPO term]
ORDO concept(s)
- Crohn disease [ORDO Disease]
- Ulcerative colitis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- inflammatory bowel disease 21 [MeSH Supplementary Concept]
- inflammatory bowel disease 21 [MeSH concept]
- inflammatory bowel disease 21 [DO Concept]

Keyword's position in hierarchy(ies) :

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