DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive spinocerebellar ataxia 13

Autosomal recessive spinocerebellar ataxia 13 [DOID:0080062]

An 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.

Synonyms:  autosomal recessive spinocerebellar ataxia 13,  DOID:0080062