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:99952
Charcot-Marie-Tooth disease type 4F
OrphanetORPHA:99952
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO