Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene. The disease is autosomal recessive spinocerebellar ataxia 10 (Monarch Disease Ontology id MONDO_0013392). Also known as: ANO10 autosomal recessive cerebellar ataxia, SCAR10, autosomal recessive cerebellar ataxia caused by mutation in ANO10, autosomal recessive spinocerebellar ataxia type 10, spinocerebellar ataxia, autosomal recessive type 10.