Spinocerebellar Ataxia 35 (SCA35)

Spinocerebellar Ataxia 35, also known as spinocerebellar ataxia type 35, is related to early myoclonic encephalopathy and autosomal dominant cerebellar ataxia, and has symptoms including abnormal pyramidal signs and action tremor. An important gene associated with Spinocerebellar Ataxia 35 is TGM6 (Transglutaminase 6), and among its related pathways/superpathways is Ciliopathies. Affiliated tissues include spinal cord and cerebellum, and related phenotypes are progressive cerebellar ataxia and hyperreflexia