Dynamin 2 - CISMeF

Preferred Label : Dynamin 2;

Symbol : DNM2;

CISMeF acronym : DNM2;

Type : Gene;

Alternative titles and symbols : DYN2;

Ensembl ID : ENSG00000079805;

Prefixed ID : *602378;

Details

Origin ID

602378;

UMLS CUI

C1414120;

Automatic exact mappings (from CISMeF team)
- DNM2 Gene [NCIt concept]
- DNM2 wt Allele [NCIt concept]
- Dynamin-2 [NCIt concept]
- dynamin 2 [ORDO Gene]
- dynamin 2 [HGNC gene]
- dynamin ii [MeSH Descriptor]
HGNC gene
- dynamin 2 [HGNC gene]
NCIt concept(s)
- DNM2 Gene [NCIt concept]
- DNM2 wt Allele [NCIt concept]
- Dynamin-2 [NCIt concept]
ORDO concept(s)
- dynamin 2 [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth disease, dominant intermediate b [OMIM Phenotype]
- Lethal congenital contracture syndrome 5 [OMIM Phenotype]
- Myopathy, centronuclear, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DNM2 Gene [NCIt concept]
- DNM2 gene [LOINC component]
- dynamin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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