Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition An autosomal dominant cerebellar ataxia type III that is characterized by the late-onset of ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties. Disease data Classification Disease Synonyms SCA31 SCA31 ORPHA code 217012 OMIM code 117210 ICD10 code G11.8 ICD11 code 8A03.16 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl