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Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency

MedGen UID:
346817
•Concept ID:
C1858424
•
Disease or Syndrome
Synonym: Cytochrome C Oxidase Deficiency, Fatal Infantile, with Cardioencephalomyopathy
 
OMIM®: 604377

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