Charcot-Marie-Tooth disease dominant intermediate D

MeSH: C564333ORPHA: 100046

Overview

Charcot-Marie-Tooth disease intermediate type that has material basis in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C564333

Orphanet Code

ORPHA:100046
Charcot-Marie-Tooth disease dominant intermediate D
MeSHC564333
OrphanetORPHA:100046
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO