Autosomal recessive spinocerebellar ataxia 10

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene.

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, adult-onset autosomal recessive cerebellar ataxia, spinocerebellar ataxia, autosomal recessive 10

18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spinocerebellar ataxia 10 itself.