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Summary Literature (0)
MIM:615119 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 6; MC4DN6

Xenbase Genes: cox15

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014051 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
MONDO:0015487 - fatal infantile encephalocardiomyopathy

Disease Ontology (DO):
DOID:0080358 - mitochondrial complex IV deficiency nuclear type 6