Coenzyme Q10 Deficiency, Primary, 8, also known as primary coenzyme q10 deficiency 8, is related to neuronopathy, distal hereditary motor, autosomal recessive 9. An important gene associated with Coenzyme Q10 Deficiency, Primary, 8 is COQ7 (Coenzyme Q7, Hydroxylase). Affiliated tissues include lung and kidney, and related phenotypes are hypertension and hypotonia