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Coenzyme Q10 deficiency

MONDO:0018151

A 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.

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Sub-types

Autosomal recessive ataxia due to ubiquinone deficiency (0) Coenzyme Q10 deficiency, primary, 1 (0) Coenzyme Q10 deficiency, primary, 3 (0) Coenzyme q10 deficiency, primary, 9 (0) COQ7-related distal hereditary motor neuropathy (0) Deafness-encephaloneuropathy-obesity-valvulopathy syndrome (0) Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome (0) Familial steroid-resistant nephrotic syndrome with sensorineural deafness (0) Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome (0) Primary coenzyme Q10 deficiency 8 (0)

Broader categories

Disease (717) Nervous system disorder (243) Metabolic disease (241) Hereditary disease (188) Peripheral nervous system disorder (119) Neuromuscular disease (110) Peripheral neuropathy (92) Inborn mitochondrial metabolism disorder (59) Inborn errors of metabolism (47) Mitochondrial disease (40)

Trials to join now! 10 Not yet recruiting 1 Not yet finished but already full! 4 Completed 4 Terminated 2