- TypeGroup
- Disease group(s)
- Child entries
- Primary coenzyme Q10 deficiency
- Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- Prenyl diphosphate synthase subunit 1 deficiency
- Prenyl diphosphate synthase subunit 2 deficiency
- Coenzyme Q2 polyprenyltranferase deficiency
- Coenzyme Q4 deficiency
- Coenzyme Q5 methyltransferase deficiency
- Coenzyme Q6 monooxygenase deficiency
- Coenzyme Q7 hydroxylase deficiency
- ADCK2 deficiency
- Coenzyme Q8A deficiency
- Coenzyme Q8B deficiency
- Coenzyme 9 deficiency