myoclonic dystonia 15
MeSH: C538002ORPHA: 210566
Overview
myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C538002Orphanet Code
ORPHA:210566myoclonic dystonia 15
| MeSH | C538002 |
| Orphanet | ORPHA:210566 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO