Preferred Label : Spinocerebellar ataxia type 26;
ICD-11 definition : Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar
ataxia type 3, described to date in patients from one American family of Norwegian
descent, and characterized by late-onset and slowly progressive gait ataxia, and eye
movement problems.;
Origin ID : 586976339;
UMLS CUI : C1836395;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar
ataxia type 3, described to date in patients from one American family of Norwegian
descent, and characterized by late-onset and slowly progressive gait ataxia, and eye
movement problems.