Mitochondrial complex V (atp synthase) deficiency, nuclear type 7

Preferred Label : Mitochondrial complex V (atp synthase) deficiency, nuclear type 7;

Symbol : MC5DN7;

Type : Phenotype, molecular basis known;

Prefixed ID : #620359;

Details

Origin ID

620359;

UMLS CUI

C5830482;

Genes related to phenotype
- Atp synthase peripheral stalk, subunit oscp [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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