Mitochondrial complex V (ATP synthase) deficiency, nuclear type 5

MONDO:0020858

Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the ATP5F1D gene.

Also known as: MC5DN5, MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5, Mitochondrial Complex 5 (ATP Synthase) Deficiency, ATP5F1D Type, mitochondrial complex v (atp synthase) deficiency

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex V (ATP synthase) deficiency, nuclear type 5 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Mitochondrial respiratory chain complex deficiency (5)

Including sub-types (13) Tagged with Mitochondrial complex V (ATP synthase) deficiency, nuclear type 5 (0)

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