Coenzyme Q10 deficiency, primary, 3
MONDO:0013838Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the PDSS2 gene.
Also known as: PDSS2 coenzyme Q10 deficiency, coenzyme Q10 deficiency caused by mutation in PDSS2, coenzyme Q10 deficiency, primary, 3, coenzyme Q10 deficiency, primary, type 3, COQ10D3
47 clinical trials for this condition and its sub-types.
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