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
49 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal recessive ataxia due to ubiquinone deficiency
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Coenzyme Q10 deficiency, primary, 1
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Coenzyme Q10 deficiency, primary, 3
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Coenzyme q10 deficiency, primary, 9
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COQ7-related distal hereditary motor neuropathy
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Deafness-encephaloneuropathy-obesity-valvulopathy syndrome
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Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
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Familial steroid-resistant nephrotic syndrome with sensorineural deafness
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Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
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Primary coenzyme Q10 deficiency 8
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