Mitochondrial complex III deficiency nuclear type 5

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRC2 gene.

Also known as: UQCRC2 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in UQCRC2, MC3DN5, mitochondrial Complex 3 deficiency, nuclear type 5, mitochondrial complex III deficiency, nuclear type 5

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 5 itself.