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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
/
Mitochondrial oxidative phosphorylation disorder
/
Mitochondrial DNA depletion syndrome
Mitochondrial DNA depletion syndrome 17
rare
Identifiers
MONDO:0032815
OMIM:618567
Causal genes
MRM2
Part of
Mitochondrial DNA depletion syndrome
Also known as
MTDPS17
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