Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B

MONDO:0014091

Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the ATP5F1A gene.

Also known as: ATP5F1A mitochondrial complex deficiency, MC5DN4B, mitochondrial complex deficiency caused by mutation in ATP5F1A, mitochondrial Complex 5 (ATP synthase) deficiency, ATP5A1 type, mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 4, mitochondrial complex V (ATP synthase) deficiency, nuclear type 4

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B 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 4B (0)

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