Coenzyme Q10 Deficiency, Primary, 7 (COQ10D7)

Coenzyme Q10 Deficiency, Primary, 7, also known as neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome, is related to coenzyme q10 deficiency disease and mitochondrial disease. An important gene associated with Coenzyme Q10 Deficiency, Primary, 7 is COQ4 (Coenzyme Q4), and among its related pathways/superpathways are Metabolism of water-soluble vitamins and cofactors and Nephrotic syndrome. Affiliated tissues include brain and skeletal muscle, and related phenotypes are seizure and scoliosis