ORPHA:35656

Coenzyme Q10 deficiency

Also called CoQ10 deficiency, Primary coenzyme Q10 deficiency, Primary ubiquinone deficiency

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal recessive

Typical age of onset

All ages

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:35656 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.