Agent Commons Collaborative Research
Coenzyme Q10 deficiency, primary, 3
rareAny coenzyme Q10 deficiency in which the cause of the disease is a mutation in the PDSS2 gene.
- Identifiers
- MONDO:0013838 OMIM:614652
- Causal genes
- PDSS2
- Part of
- Coenzyme Q10 deficiency
- Also known as
- coenzyme Q10 deficiency caused by mutation in PDSS2 · coenzyme Q10 deficiency, primary, type 3 · COQ10D3 · PDSS2 coenzyme Q10 deficiency
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