| Disease Aliases (50) | Als13 Amyotrophic lateral sclerosis, susceptibility to, 13 Atxn2 autosomal dominant cerebellar ataxia type i Ataxia 2, spinocerebellar Ataxia 2s, spinocerebellar Atrophy 2, olivopontocerebellar Atrophy 2, spinocerebellar Atrophy 2s, olivopontocerebellar Atrophy 2s, spinocerebellar Atrophy ii, olivopontocerebellar Atrophy ii, spinocerebellar Atrophy iis, olivopontocerebellar Atrophy iis, spinocerebellar Cerebellar degeneration with slow eye movements Ii, olivopontocerebellar atrophy Ii, spinocerebellar atrophy Iis, olivopontocerebellar atrophy Iis, spinocerebellar atrophy Olivopontocerebellar atrophy ii Olivopontocerebellar atrophy, holguin type Opca2 Olivopontocerebellar atrophy 2s Olivopontocerebellar atrophy iis Olivopontocerebellar atrophy 2 Olivopontocerebellar atrophy holguin type Sca 2 Sca2 Sdsem Spinocerebellar ataxia, cuban type Spinocerebellar atrophy ii Spinocerebellar degeneration with slow eye movements Spinocerebellar ataxia 2s Spinocerebellar ataxia-2 Spinocerebellar atrophy 2s Spinocerebellar atrophy iis Spinocerebellar ataxia 2 Spinocerebellar ataxia cuban type Spinocerebellar ataxia with slow eye movements Spinocerebellar atrophy 2 Swami syndrome, wadia Syndrome, wadia swami Syndrome, wadia-swami Type 2 spinocerebellar ataxia Wadia-swami syndrome Wadia swami syndrome Amyotrophic lateral sclerosis 13 Amyotrophic lateral sclerosis type 13 Autosomal dominant cerebellar ataxia type i caused by mutation in atxn2 Spinocerebellar ataxia 2; sca2 |
Associated Genes (1) NCBI-RefSeq: ATXN2 (Ataxin 2) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Spinocerebellar ataxia type 2 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |