Autosomal dominant striatal degeneration is a neurologic disorder characterized by variable movement abnormalities due to dysfunction in the striatal part of the basal ganglia. The disease is autosomal dominant striatal neurodegeneration type 1 (Monarch Disease Ontology id MONDO_0012205). Also known as: ADSD1, PDE8B striatal degeneration, autosomal dominant, striatal Degeneration, autosomal dominant 1, striatal degeneration, autosomal dominant 1, striatal degeneration, autosomal dominant caused by mutation in PDE8B.