(Q22443082)
English
spinocerebellar ataxia type 2
Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea
- SPINOCEREBELLAR ATAXIA 2
- SPINOCEREBELLAR ATAXIA 2; SCA2
- Spinocerebellar Atrophy 2
- Olivopontocerebellar Atrophy, Holguin Type
- Wadia-Swami Syndrome
- Olivopontocerebellar Atrophy 2
- Spinocerebellar Ataxia type 2
- Spinocerebellar Ataxia, Cuban Type
- Amyotrophic Lateral Sclerosis, Susceptibility To, 13
- Spinocerebellar Degeneration With Slow Eye Movements
- SCA2
- Cerebellar Degeneration With Slow Eye Movements
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C148315
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Wikipedia(1 entry)
- jawiki 脊髄小脳変性症2型