primary coenzyme Q10 deficiency 6
ORPHA: 280406
Overview
primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ6 on chromosome 14q24.3
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:280406primary coenzyme Q10 deficiency 6
| Orphanet | ORPHA:280406 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO