Autosomal dominant cerebellar ataxia type 2 (Q85239): Difference between revisions
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13 August 2026
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Latest revision as of 10:36, 15 August 2026
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 |
|---|---|---|---|
| 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. |
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CID11:ID_1803607232
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dki-india-ID_1803607232
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Concluído
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13 August 2026
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