Disease #00641

Official abbreviation 615119
Name Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
OMIM ID 615119
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COX15
Associated tissues -
Disease features -
Remarks -

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