Spinocerebellar Ataxia, Autosomal Recessive 10 (SCAR10)

Spinocerebellar Ataxia, Autosomal Recessive 10, also known as autosomal recessive spinocerebellar ataxia 10, is related to spastic ataxia and spinocerebellar ataxia 10, and has symptoms including muscular fasciculation, ataxia, truncal and gait ataxia. An important gene associated with Spinocerebellar Ataxia, Autosomal Recessive 10 is ANO10 (Anoctamin 10), and among its related pathways/superpathways are Infectious disease and Transport of inorganic cations/anions and amino acids/oligopeptides. Affiliated tissues include spinal cord and cerebellum, and related phenotypes are progressive cerebellar ataxia and abnormal circulating enzyme concentration or activity