Term Name:	spinocerebellar ataxia type 37
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene.
Ontology:	Human Disease [DOID:0050984]   ( DOID:0050984 )