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Mitochondrial complex IV deficiency, nuclear type 18

MONDO:0033653

Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX6A2 gene.

Also known as: MC4DN18, mitochondrial complex IV deficiency, nuclear type 18

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex IV deficiency, nuclear type 18 itself.

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