You are using an outdated browser. Please upgrade your browser to improve your experience.

striatal degeneration, autosomal dominant

Disease Summary
Associated Targets (2)
Tclin

2


Mondo Description An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity.
Mondo Term and Equivalent IDs
MONDO:0000211:  striatal degeneration, autosomal dominant
DC:0000722: 
MESH:C563783: 
OMIMPS:609161: 
Orphanet:228169: 
UMLS:C1836694: