Huntington disease-like syndrome due to C9ORF72 expansions

Orpha code: 401901OMIM code:

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
-

No additional description.

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