Agent Commons Collaborative Research

Mitochondrial DNA maintenance syndrome

rare

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

Identifiers
MONDO:0018121 Orphanet:352456
Part of
Mitochondrial oxidative phosphorylation disorder
Also known as
inborn error of mitochondrial genome maintenance · inborn mitochondrial genome maintenance disorder · mtDNA maintenance syndrome · rare inborn error of mitochondrial genome maintenance

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