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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
/
Inborn mitochondrial metabolism disorder
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Mitochondrial oxidative phosphorylation disorder
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Coenzyme Q10 deficiency
Coenzyme q10 deficiency, primary, 9
rare
Identifiers
MONDO:0033615
OMIM:619028
Causal genes
COQ5
Part of
Coenzyme Q10 deficiency
Also known as
COQ10D9
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