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Autosomal Recessive Spinocerebellar Ataxia 13

Disease ID: disease_node_16033

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DbxrefMIM:614831
SubclassofDOID_0050950
Data SourceDOID
SynonymsSCAR13
Doid Labelautosomal recessive spinocerebellar ataxia 13
Doid DescriptionAn autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.
Disease Node Iddisease_node_16033
Doid IdDOID_0080062
LabelAutosomal Recessive Spinocerebellar Ataxia 13