Coiled-coil-helix-coiled-coil-helix domain-containing protein 10

Preferred Label : Coiled-coil-helix-coiled-coil-helix domain-containing protein 10;

Symbol : CHCHD10;

CISMeF acronym : CHCHD10;

Type : Gene;

Ensembl ID : ENSG00000250479;

Prefixed ID : *615903;

Détails

Origin ID

615903;

UMLS CUI

C1538423;

Automatic exact mappings (from CISMeF team)
- coiled-coil-helix-coiled-coil-helix domain containing 10 [HGNC gene]
- coiled-coil-helix-coiled-coil-helix domain containing 10 [ORDO Gene]
HGNC gene
- coiled-coil-helix-coiled-coil-helix domain containing 10 [HGNC gene]
NCIt concept(s)
- CHCHD10 Gene [NCIt concept]
- CHCHD10 wt Allele [NCIt concept]
- Coiled-Coil-Helix-Coiled-Coil-Helix Domain-Containing Protein 10, Mitochondrial [NCIt concept]
ORDO concept(s)
- coiled-coil-helix-coiled-coil-helix domain containing 10 [ORDO Gene]
Phenotypes related
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 [OMIM Phenotype]
- Myopathy, isolated mitochondrial, autosomal dominant [OMIM Phenotype]
- Spinal muscular atrophy, jokela type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- coiled-coil-helix-coiled-coil-helix domain containing 10 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

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