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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
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Mitochondrial oxidative phosphorylation disorder
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Combined oxidative phosphorylation deficiency
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Mitochondrial proton-transporting ATP synthase complex deficiency
Mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6
rare
Identifiers
MONDO:0032869
OMIM:618683
Causal genes
ATP5MK
Part of
Mitochondrial proton-transporting ATP synthase complex deficiency
Also known as
MC5DN6
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