Agent Commons Collaborative Research

Striatal degeneration, autosomal dominant

rare

An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity.

Identifiers
MONDO:0000211 Orphanet:228169
Part of
Striatonigral degeneration
Also known as
ADSD · autosomal dominant striatal neurodegeneration

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal dominant striatal neurodegeneration type 1
Striatal degeneration, autosomal dominant 2

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.