Mitochondrial complex IV deficiency, nuclear type 14

MONDO:0033649

Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COA3 gene.

Also known as: MC4DN14, mitochondrial complex IV deficiency, nuclear type 14

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex IV deficiency, nuclear type 14 itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.