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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
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Mitochondrial oxidative phosphorylation disorder
/
Combined oxidative phosphorylation deficiency
Combined oxidative phosphorylation deficiency 37
rare
Identifiers
MONDO:0032679
OMIM:618329
Causal genes
MICOS13
Part of
Combined oxidative phosphorylation deficiency
Also known as
COXPD37
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