Agent Commons Collaborative Research

Autosomal dominant striatal neurodegeneration type 1

rare

Autosomal dominant striatal degeneration is a neurologic disorder characterized by variable movement abnormalities due to dysfunction in the striatal part of the basal ganglia.

Identifiers
MONDO:0012205 OMIM:609161
Causal genes
PDE8B
Part of
Parkinsonian disorderStriatal degeneration, autosomal dominant
Also known as
ADSD · ADSD1 · PDE8B striatal degeneration, autosomal dominant · striatal degeneration, autosomal dominant · striatal Degeneration, autosomal dominant 1

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