Coenzyme Q10 deficiency
MONDO:0018151A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency.
Also known as: CoQ10 deficiency, coenzyme Q10 deficiency disease, coenzyme Q10 deficiency, primary, CoQ10 deficiency, primary
21 clinical trials for this condition and its sub-types, 3 tagged with Coenzyme Q10 deficiency itself.
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Sub-types of Coenzyme Q10 deficiency
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Coenzyme Q10 deficiency, primary, 1 0 trials
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Coenzyme Q10 deficiency, primary, 3 0 trials
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Coenzyme q10 deficiency, primary, 9 0 trials
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Primary coenzyme Q10 deficiency 8 0 trials