Atpase, cu(2 )-transporting, alpha polypeptide

Preferred Label : Atpase, cu(2 )-transporting, alpha polypeptide;

Symbol : ATP7A;

CISMeF acronym : ATP7A;

Type : Gene;

Ensembl ID : ENSG00000165240;

Prefixed ID : *300011;

Détails

Origin ID

300011;

UMLS CUI

C1412688;

Automatic exact mappings (from CISMeF team)
- ATP7A Gene [NCIt concept]
- ATP7A gene [LOINC component]
- ATPase copper transporting alpha [HGNC gene]
- ATPase copper transporting alpha [ORDO Gene]
- Copper-Transporting ATPase 1 [NCIt concept]
HGNC gene
- ATPase copper transporting alpha [HGNC gene]
NCIt concept(s)
- ATP7A Gene [NCIt concept]
- ATP7A wt Allele [NCIt concept]
- Copper-Transporting ATPase 1 [NCIt concept]
ORDO concept(s)
- ATPase copper transporting alpha [ORDO Gene]
Phenotypes related
- Menkes disease [OMIM Phenotype]
- Neuronopathy, distal hereditary motor, X-linked [OMIM Phenotype]
- Occipital horn syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATP7A Gene [NCIt concept]
- ATP7A gene [LOINC component]
- ATPase copper transporting alpha [HGNC gene]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients