spinocerebellar ataxia type 36 (MONDO_0013594, a Monarch Disease Ontology term) (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia. Also known as: Asidan, SCA36.