Term Name:	autosomal recessive spinocerebellar ataxia 2
Synonyms:	SCAR2
Definition:	An autosomal recessive cerebellar ataxia that is characterized by juvenile onset of progressive cerebellar ataxia, axonal sensorimotor peripheral neuropathy, and increased serum alpha-fetoprotein, and has_material_basis_in homozygous or compound heterozygous mutation in the senataxin gene on chromosome 9q34.
Ontology:	Human Disease [DOID:0080061]   ( DOID:0080061 )