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Summary Literature (0)
MIM:616500 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 9; MC4DN9

Xenbase Genes: coa5

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014667 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
MONDO:0015487 - fatal infantile encephalocardiomyopathy

Disease Ontology (DO):
DOID:0080359 - mitochondrial complex IV deficiency nuclear type 9