Coenzyme Q10 Deficiency, Primary, 3 (COQ10D3)

Coenzyme Q10 Deficiency, Primary, 3, also known as coq10d3, is related to cardiofaciocutaneous syndrome 1 and intellectual developmental disorder, x-linked, syndromic, billuart type, and has symptoms including edema An important gene associated with Coenzyme Q10 Deficiency, Primary, 3 is PDSS2 (Decaprenyl Diphosphate Synthase Subunit 2), and among its related pathways/superpathways are Metabolism of water-soluble vitamins and cofactors and Nephrotic syndrome. Affiliated tissues include skeletal muscle and bone marrow, and related phenotypes are neonatal hypotonia and proteinuria