Term Name:	spinocerebellar ataxia type 1
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22.
Ontology:	Human Disease [DOID:0050954]   ( DOID:0050954 )