Spinocerebellar Ataxia Type 2
| Disease Aliases (6) | Atxn2 autosomal dominant cerebellar ataxia type i Autosomal dominant cerebellar ataxia type i caused by mutation in atxn2 Cerebellar degeneration with slow eye movements Olivopontocerebellar atrophy ii Opca2 Sca2 |
Associated Genes (0) | |||||||
| Cross-references of Spinocerebellar ataxia type 2 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |