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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
/
Combined oxidative phosphorylation deficiency
Combined oxidative phosphorylation deficiency 48
rare
Identifiers
MONDO:0033566
OMIM:619012
Causal genes
NSUN3
Part of
Combined oxidative phosphorylation deficiency
Also known as
COXPD48
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