disease caused by disruption of disease has basis in disruption of ubiquinone biosynthetic process metabolic disease mitochondrial disease with epilepsy mitochondrial disease with peripheral neuropathy mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies coenzyme Q10 deficiency A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency. CoQ10 deficiency CoQ10 deficiency, primary DOID:0050730 GARD:0010423 MESH:C564403 MONDO:0018151 NCIT:C142083 OMIMPS:607426 Orphanet:35656 SCTID:724575009 UMLS:C1843920 UMLS:CN229570 coenzyme Q10 deficiency disease coenzyme Q10 deficiency, primary https://rarediseases.info.nih.gov/diseases/10423/coenzyme-q10-deficiency neurometabolic disease