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Up to: Hereditary peripheral neuropathy · Mitochondrial oxidative phosphorylation disorder
Coenzyme Q10 deficiency
A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by 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