Mitochondrial DNA maintenance syndrome

MONDO:0018121

An inherited metabolic disease that is has its basis in the disruption of mitochondrial genome maintenance.

Also known as: inborn error of mitochondrial genome maintenance, inborn mitochondrial genome maintenance disorder, mtDNA maintenance syndrome, rare inborn error of mitochondrial genome maintenance

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial DNA maintenance syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Mitochondrial oxidative phosphorylation disorder (58)

Including sub-types (13) Tagged with Mitochondrial DNA maintenance syndrome (0)

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