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Coenzyme Q10 deficiency, primary, 1

MONDO:0011829

Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ2 gene.

Also known as: COQ2 coenzyme Q10 deficiency, coenzyme Q10 deficiency caused by mutation in COQ2, coenzyme Q10 deficiency, primary, 1, coenzyme Q10 deficiency, primary, type 1, COQ10D1, CoQ deficiency 1, Coq10 deficiency, primary, 1, coenzyme Q deficiency 1

19 clinical trials for this condition and its sub-types, 0 tagged with Coenzyme Q10 deficiency, primary, 1 itself.

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