MONDO_0014601 (autosomal recessive spinocerebellar ataxia 20) is any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the SNX14 gene. Also known as: SCAR20, SNX14 autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in SNX14, autosomal recessive spinocerebellar ataxia type 20, intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome, spinocerebellar ataxia, autosomal recessive type 20.