Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3

MONDO:0013547

Any mitochondrial proton-transporting ATP synthase complex deficiency in which the cause of the disease is a mutation in the ATP5F1E gene.

Also known as: ATP5F1E mitochondrial proton-transporting ATP synthase complex deficiency, MC5DN3, mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATP5F1E, mitochondrial Complex 5 (ATP synthase) deficiency, Atp5E type

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 itself.

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↑ Mitochondrial respiratory chain complex deficiency (5) ↑ Mitochondrial proton-transporting ATP synthase complex deficiency (0)

Including sub-types (13) Tagged with Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 (0)

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