Spinocerebellar ataxia type 4 (Q101101): Difference between revisions
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Revision as of 17:54, 16 August 2026
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1686006145 |
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| English | Spinocerebellar ataxia type 4 |
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy. |
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CID11:ID_1686006145
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