Combined oxidative phosphorylation deficiency 56

Preferred Label : Combined oxidative phosphorylation deficiency 56;

Symbol : COXPD56;

Type : Phenotype, molecular basis known;

Prefixed ID : #620139;

Details

Origin ID

620139;

UMLS CUI

C5774261;

Genes related to phenotype
- Tam41 mitochondrial translocator assembly and maintenance homolog [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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