Inflammatory bowel disease 13

Preferred Label : Inflammatory bowel disease 13;

Symbol : IBD13;

CISMeF acronym : IBD13;

Type : Phenotype, molecular basis known;

Prefixed ID : #612244;

Details

Origin ID

612244;

UMLS CUI

C2677101;

Currated CISMeF NLP mapping
- inflammatory bowel disease 13 [DO Concept]
- inflammatory bowel disease 13 [MeSH concept]
- inflammatory bowel disease 13 [MeSH Supplementary Concept]
DO Cross reference
- inflammatory bowel disease 13 [DO Concept]
Genes related to phenotype
- Atp-binding cassette, subfamily b, member 1 [OMIM gene]
HPO term(s)
- Inflammation of the large intestine [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 13 [MeSH Supplementary Concept]
- inflammatory bowel disease 13 [MeSH concept]
- inflammatory bowel disease 13 [DO Concept]
Validated automatic mappings to NTBT
- Crohn disease [ORDO Disease]
- Ulcerative colitis [ORDO Disease]

Keyword's position in hierarchy(ies) :

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