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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
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Combined oxidative phosphorylation deficiency
Combined oxidative phosphorylation deficiency 39
rare
Identifiers
MONDO:0032726
OMIM:618397
Orphanet:565624
Causal genes
GFM2
Part of
Combined oxidative phosphorylation deficiency
Also known as
COXPD39
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