Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy. Disease data Classification Disease Synonyms HDL4 Choroba podobna do choroby Huntingtona 4 HDL4 SCA17 Huntington disease-like 4 SCA17 ORPHA code 98759 OMIM code 607136 ICD10 code G11.8 ICD11 code - *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