| Disease Aliases (39) | Atxn1 autosomal dominant cerebellar ataxia type i Ataxia 1, spinocerebellar Atrophy i, olivopontocerebellar Atrophy i, spinocerebellar Atrophy iv, olivopontocerebellar Atrophy ivs, olivopontocerebellar Cerebelloparenchymal disorder i Cpd1 Cerebelloparenchymal disorder is Cerebelloparenchymal disorder 1 Menzel type opca Olivopontocerebellar atrophy i Olivopontocerebellar atrophy iv Opca 1 Opca 4 Opca i Opca iv Opca, menzel type Opca, schut-haymaker type Opca1 Opca4 Olivopontocerebellar atrophy ivs Olivopontocerebellar atrophy is Olivopontocerebellar atrophy 1 Olivopontocerebellar atrophy 4 Sca1 Sca1s Schut-haymaker type opca Spinocerebellar atrophy i Schut haymaker type opca Spinocerebellar ataxia 1s Spinocerebellar ataxia-1 Spinocerebellar atrophy is Spinocerebellar ataxia 1 Spinocerebellar atrophy 1 Type 1 spinocerebellar ataxia Autosomal dominant cerebellar ataxia type i caused by mutation in atxn1 Spinocerebellar ataxia 1; sca1 |
Associated Genes (1) NCBI-RefSeq: ATXN1 (Ataxin 1) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Spinocerebellar ataxia type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |