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
C564333Orphanet Code
ORPHA:100046Charcot-Marie-Tooth disease dominant intermediate D
| MeSH | C564333 |
| Orphanet | ORPHA:100046 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO