Term Name:	autosomal recessive spinocerebellar ataxia 32
Synonyms:	SCAR32
Definition:	An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26.
Ontology:	Human Disease [DOID:0070413]   ( DOID:0070413 )