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Metadata
ID	DOID:0070413
Name	autosomal recessive spinocerebellar ataxia 32
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. https://pubmed.ncbi.nlm.nih.gov/33889951/
Xrefs	MIM:619862
Synonyms	SCAR32 [EXACT]
Parent Relationships	is_a autosomal recessive cerebellar ataxia