Term Name:	spinocerebellar ataxia type 4
Synonyms:	SCA4
Definition:	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy that has_material_basis_in heterozygous trinucleotide repeat expansion (GGCn) in the ZFHX3 gene on chromosome 16q22.
Ontology:	Human Disease [DOID:0050957]   ( DOID:0050957 )