Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Huntington disease-like syndrome due to C9ORF72 expansions is a rare, genetic neurodegenerative disease characterized by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioral problems. Disease data Klasyfikacja Disease Synonimy C9ORF72-related Huntington disease phenocopy Fenokopia choroby Huntingtona z powodu ekspansji C9ORF72 Fenokopia choroby Huntingtona związana z C9ORF72 Zespół podobny do choroby Huntingtona związany z C9ORF72 C9ORF72-related Huntington disease-like syndrome Huntington disease phenocopy due to C9ORF72 expansions Kod ORPHA 401901 Kod OMIM - Kod ICD10 G10 Kod ICD11 - *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