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autosomal dominant striatal neurodegeneration type 1

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Autosomal dominant striatal degeneration is a neurologic disorder characterized by variable movement abnormalities due to dysfunction in the striatal part of the basal ganglia.
Uniprot Description A movement disorder affecting the striatal part of the basal ganglia and characterized by bradykinesia, dysarthria and muscle rigidity. These symptoms resemble idiopathic Parkinson disease, but tremor is not present.
Mondo Term and Equivalent IDs
MONDO:0012205:  autosomal dominant striatal neurodegeneration type 1
SCTID:725392005: