Dymeclin - CISMeF

Preferred Label : Dymeclin;

Symbol : DYM;

CISMeF acronym : DYM;

Type : Gene;

Ensembl ID : ENSG00000141627;

Prefixed ID : *607461;

Details

Origin ID

607461;

UMLS CUI

C1539322;

Automatic exact mappings (from CISMeF team)
- dymeclin [ORDO Gene]
- dymeclin [HGNC gene]
HGNC gene
- dymeclin [HGNC gene]
NCIt concept(s)
- DYM Gene [NCIt concept]
- DYM wt Allele [NCIt concept]
- Dymeclin [NCIt concept]
ORDO concept(s)
- dymeclin [ORDO Gene]
Phenotypes related
- Dyggve-melchior-clausen disease [OMIM Phenotype]
- Smith-mccort dysplasia 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DYM Gene [NCIt concept]
- dymeclin [HGNC gene]

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