Mitochondrial complex III deficiency nuclear type 2

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the TTC19 gene.

Also known as: MC3DN2, TTC19 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in TTC19, mitochondrial complex III deficiency nuclear type 2, mitochondrial Complex 3 deficiency, nuclear type 2, mitochondrial complex III deficiency, nuclear type 2

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 2 itself.