Cofilin 2 - CISMeF

Preferred Label : Cofilin 2;

Symbol : CFL2;

CISMeF acronym : CFL2;

Type : Gene;

Alternative titles and symbols : Cofilin, muscle; Cofilin, M-type;

Ensembl ID : ENSG00000165410;

Prefixed ID : *601443;

Details

Origin ID

601443;

UMLS CUI

C1413356;

Automatic exact mappings (from CISMeF team)
- cofilin 2 [ORDO Gene]
- cofilin 2 [MeSH Descriptor]
- cofilin 2 [HGNC gene]
- cofilin 2 [MeSH concept]
HGNC gene
- cofilin 2 [HGNC gene]
ORDO concept(s)
- cofilin 2 [ORDO Gene]
Phenotypes related
- Nemaline myopathy 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- cofilin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients