Autosomal dominant cerebellar ataxia type 2 (Q85239)
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Spinocerebellar ataxia 2 is associated with ataxia, hypotonia, neuropathy, dystonia, and slow eye movements with symptom onset during mid-adulthood. Associated with an exonic CAG repeat expansion in the ATXN2 gene coding for ataxin-2.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1803607232 |
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| English | Autosomal dominant cerebellar ataxia type 2 |
Spinocerebellar ataxia 2 is associated with ataxia, hypotonia, neuropathy, dystonia, and slow eye movements with symptom onset during mid-adulthood. Associated with an exonic CAG repeat expansion in the ATXN2 gene coding for ataxin-2. |
