spinocerebellar ataxia type 5 (Q18553532)
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autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has material basis in mutation in the SPTBN2 gene
- SPINOCEREBELLAR ATAXIA 5; SCA5
- SCA5
- Spinocerebellar Ataxia type 5
- SPINOCEREBELLAR ATAXIA 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | spinocerebellar ataxia type 5 |
autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has material basis in mutation in the SPTBN2 gene |
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