Charcot-Marie-Tooth disease type 4F
ORPHA: 99952
Overview
Charcot-Marie-Tooth disease type 4 that has material basis in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:99952Charcot-Marie-Tooth disease type 4F
| Orphanet | ORPHA:99952 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO