Inflammatory bowel disease 3

Preferred Label : Inflammatory bowel disease 3;

Symbol : IBD3;

CISMeF acronym : IBD3;

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 and ulcerative colitis, see IBD1 (266600).;

Inheritance : Autosomal dominant;

Prefixed ID : %604519;

Details

Origin ID

604519;

UMLS CUI

C1858303;

Currated CISMeF NLP mapping
- inflammatory bowel disease 3 [DO Concept]
- inflammatory bowel disease 3 [MeSH concept]
- inflammatory bowel disease 3 [MeSH Supplementary Concept]
DO Cross reference
- inflammatory bowel disease 3 [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]
See also inter- (CISMeF)
- Crohn disease [ORDO Disease]
- Ulcerative colitis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- inflammatory bowel disease 3 [MeSH Supplementary Concept]
- inflammatory bowel disease 3 [MeSH concept]
- inflammatory bowel disease 3 [DO Concept]

Keyword's position in hierarchy(ies) :

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