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Diseases / Mitochondrial disease/ Inborn mitochondrial metabolism disorder/ Mitochondrial oxidative phosphorylation disorder/ Combined oxidative phosphorylation deficiency/ Mitochondrial proton-transporting ATP synthase complex deficiency

Mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1

rare

Identifiers: MONDO:0027069 OMIM:500015
Part of: Mitochondrial proton-transporting ATP synthase complex deficiency
Also known as: MC5DM1 · mitochondrial complex V (ATP synthase) deficiency, mitochondrial type 1

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