myoclonic dystonia 11
ORPHA: 36899
Overview
myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with myoclonic dystonia 11, sourced from HPO and Orphanet clinical annotations.
DystoniaMyoclonusSpinal myoclonusLimb myoclonusTorticollisDepressionCompulsive behaviorsAnxietyWriter's crampPersonality disorderPanic attack
Classification & Codes
Orphanet Code
ORPHA:36899myoclonic dystonia 11
| Orphanet | ORPHA:36899 |
| Treatments | 0 drug(s) |
| Symptoms on record | 11 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO