autosomal recessive spinocerebellar ataxia 32 (DOID:0070413)
Alliance: disease page
Synonyms: SCAR32
Alt IDs: OMIM:619862
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.