Dynamin 1 - CISMeF

Preferred Label : Dynamin 1;

Symbol : DNM1;

CISMeF acronym : DNM1;

Type : Gene;

Ensembl ID : ENSG00000106976;

Prefixed ID : *602377;

Details

Origin ID

602377;

UMLS CUI

C1414118;

Automatic exact mappings (from CISMeF team)
- dynamin 1 [ORDO Gene]
- dynamin 1 [HGNC gene]
- dynamin i [MeSH Descriptor]
HGNC gene
- dynamin 1 [HGNC gene]
NCIt concept(s)
- DNM1 Gene [NCIt concept]
- DNM1 wt Allele [NCIt concept]
- Dynamin-1 [NCIt concept]
ORDO concept(s)
- dynamin 1 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 31a [OMIM Phenotype]
- Developmental and epileptic encephalopathy 31b [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DNM1 Gene [NCIt concept]
- dynamin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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