Spinocerebellar Ataxia 36, also known as spinocerebellar ataxia type 36, is related to olivopontocerebellar atrophy and lateral sclerosis, and has symptoms including cerebellar ataxia and gait ataxia. An important gene associated with Spinocerebellar Ataxia 36 is NOP56 (NOP56 Ribonucleoprotein). Affiliated tissues include tongue and spinal cord, and related phenotypes are ataxia and dysarthria