coenzyme Q10 deficiency disease
MeSH: C564403ORPHA: 35656
Overview
mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C564403Orphanet Code
ORPHA:35656coenzyme Q10 deficiency disease
| MeSH | C564403 |
| Orphanet | ORPHA:35656 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO