Coiled-coil-helix-coiled-coil-helix domain-containing protein 2

Preferred Label : Coiled-coil-helix-coiled-coil-helix domain-containing protein 2;

Symbol : CHCHD2;

CISMeF acronym : CHCHD2;

Type : Gene;

Ensembl ID : ENSG00000106153;

Prefixed ID : *616244;

Details

Origin ID

616244;

UMLS CUI

C1427670;

Automatic exact mappings (from CISMeF team)
- coiled-coil-helix-coiled-coil-helix domain containing 2 [HGNC gene]
HGNC gene
- coiled-coil-helix-coiled-coil-helix domain containing 2 [HGNC gene]
NCIt concept(s)
- CHCHD2 Gene [NCIt concept]
- CHCHD2 wt Allele [NCIt concept]
- Coiled-Coil-Helix-Coiled-Coil-Helix Domain-Containing Protein 2 [NCIt concept]
Phenotypes related
- Parkinson disease 22, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- coiled-coil-helix-coiled-coil-helix domain containing 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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