An autosomal recessive cerebellar ataxia that is characterized by severely delayed psychomotor development with poor or absent speech, wide-based or absent gait, coarse facies, and cerebellar atrophy and that has_material_basis_in homozygous mutation in the SNX14 gene on chromosome 6q14. (DO)
autosomal recessive spinocerebellar ataxia 21
autosomal recessive spinocerebellar ataxia 22
autosomal recessive spinocerebellar ataxia 23
autosomal recessive spinocerebellar ataxia 24
autosomal recessive spinocerebellar ataxia 25
autosomal recessive spinocerebellar ataxia 26
autosomal recessive spinocerebellar ataxia 27
autosomal recessive spinocerebellar ataxia 28
autosomal recessive spinocerebellar ataxia 29
autosomal recessive spinocerebellar ataxia 3
autosomal recessive spinocerebellar ataxia 30
autosomal recessive spinocerebellar ataxia 31
autosomal recessive spinocerebellar ataxia 32
autosomal recessive spinocerebellar ataxia 33
autosomal recessive spinocerebellar ataxia 4
autosomal recessive spinocerebellar ataxia 6
autosomal recessive spinocerebellar ataxia 7
autosomal recessive spinocerebellar ataxia 8
Autosomal Recessive Spinocerebellar Ataxia with Axonal Neuropathy +
Cayman type cerebellar ataxia
cerebellar ataxia, mental retardation and dysequlibrium syndrome +