disease has basis in disruption of disease caused by disruption of ubiquinone biosynthetic process metabolic disease mitochondrial oxidative phosphorylation disorder coenzyme Q10 deficiency https://rarediseases.info.nih.gov/diseases/10423/coenzyme-q10-deficiency https://www.malacards.org/card/coenzyme_q10_deficiency_disease GARD:0010423 A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency. CoQ10 deficiency coenzyme Q10 deficiency disease SCTID:724575009 MESH:C564403 coenzyme Q10 deficiency, primary UMLS:C1843920 CoQ10 deficiency, primary Orphanet:35656 NCIT:C142083 DOID:0050730 MEDGEN:334528 MONDO:0018151 OMIMPS:607426 icd11.foundation:1251664337 hereditary peripheral neuropathy