Gallbladder disease 4

Preferred Label : Gallbladder disease 4;

Symbol : GBD4;

CISMeF acronym : GBD4;

Type : Phenotype, molecular basis known;

Prefixed ID : #611465;

Details

Origin ID

611465;

UMLS CUI

C1969115;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily G member 8 [ORDO Gene]
- ATP binding cassette subfamily G member 8 [HGNC gene]
Currated CISMeF NLP mapping
- gallbladder disease 4 [MeSH concept]
- gallbladder disease 4 [MeSH Supplementary Concept]
DO Cross reference
- gallbladder disease [DO Concept]
Genes related to phenotype
- Atp-binding cassette, subfamily g, member 8 [OMIM gene]
HPO term(s)
- Cholelithiasis [HPO term]
- Polygenic inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- gallbladder disease 4 [MeSH Supplementary Concept]
- gallbladder disease 4 [MeSH concept]

Keyword's position in hierarchy(ies) :

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