Fibroblast growth factor 13

Preferred Label : Fibroblast growth factor 13;

Symbol : FGF13;

CISMeF acronym : FGF13;

Type : Gene;

Alternative titles and symbols : Fibroblast growth factor homologous factor 2; FHF2;

Ensembl ID : ENSG00000129682;

Prefixed ID : *300070;

Details

Origin ID

300070;

UMLS CUI

C1414598;

Automatic exact mappings (from CISMeF team)
- FGF13 Gene [NCIt concept]
- FGF13 wt Allele [NCIt concept]
- Fibroblast Growth Factor 13 [NCIt concept]
- fibroblast growth factor 13 [MeSH Supplementary Concept]
- fibroblast growth factor 13 [HGNC gene]
- fibroblast growth factor 13 [MeSH concept]
- fibroblast growth factor 17 [ORDO Gene]
HGNC gene
- fibroblast growth factor 13 [HGNC gene]
NCIt concept(s)
- FGF13 Gene [NCIt concept]
- FGF13 wt Allele [NCIt concept]
- Fibroblast Growth Factor 13 [NCIt concept]
ORDO concept(s)
- fibroblast growth factor 13 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 90 [OMIM Phenotype]
- Intellectual developmental disorder, X-linked 110 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FGF13 Gene [NCIt concept]
- fibroblast growth factor 13 [HGNC gene]

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