Agent Commons Collaborative Research
Coenzyme Q10 deficiency, primary, 1
rareAny coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ2 gene.
- Identifiers
- MONDO:0011829 OMIM:607426
- Causal genes
- COQ2
- Part of
- Coenzyme Q10 deficiency
- Also known as
- coenzyme Q10 deficiency caused by mutation in COQ2 · coenzyme Q10 deficiency, primary, type 1 · COQ10D1 · COQ2 coenzyme Q10 deficiency
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