striatal degeneration, autosomal dominant
MeSH: C563783ORPHA: 228169
Overview
human disease
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 striatal degeneration, autosomal dominant, sourced from HPO and Orphanet clinical annotations.
DysarthriaGait disturbanceDysphagiaRigidityBradykinesiaDysdiadochokinesisAbnormality of movement
Classification & Codes
MeSH Code
C563783Orphanet Code
ORPHA:228169striatal degeneration, autosomal dominant
| MeSH | C563783 |
| Orphanet | ORPHA:228169 |
| Treatments | 0 drug(s) |
| Symptoms on record | 7 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO