Preferred Label : Spinocerebellar ataxia type 36;
ICD-11 definition : Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia
type 1 characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle
fasiculations, tongue atrophy and hyperreflexia.;
Origin ID : 1544814018;
UMLS CUI : C3472711;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)
Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia
type 1 characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle
fasiculations, tongue atrophy and hyperreflexia.