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Autosomal Recessive Spinocerebellar Ataxia 32

Disease ID: disease_node_16024

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DbxrefMIM:619862
SubclassofDOID_0050950
Data SourceDOID
SynonymsSCAR32
Doid Labelautosomal recessive spinocerebellar ataxia 32
Doid DescriptionAn 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.
Disease Node Iddisease_node_16024
Doid IdDOID_0070413
LabelAutosomal Recessive Spinocerebellar Ataxia 32