Term Name: spinocerebellar ataxia type 17
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by chorea, dementia, dystonia, spasiticity and seizure, has_material_basis_in CAG repeat expansion in the TBP gene.
Ontology: Human Disease [DOID:0050967]   ( DOID:0050967 )

Relationships
is a type of: autosomal dominant cerebellar ataxia digenic disease