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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
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:609161
SCTID:725392005
MONDO:0012205
High level summary of knowledge for a disease, including descriptions and datasource references.