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C12orf65-related combined oxidative phosphorylation defect

MedGen UID:
1842928
•Concept ID:
C5680089
•
Disease or Syndrome
Synonyms: C12ORF65-related combined oxidative phosphorylation defect; C12ORF65-related COXPD
 
Orphanet: ORPHA497623

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVC12orf65-related combined oxidative phosphorylation defect

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