| Disease Aliases (30) | Adca type 2 Adca, type ii Atxn7 autosomal dominant cerebellar ataxia type ii Autosomal dominant cerebellar ataxia, type ii Adca, type 2 Ataxia 7, spinocerebellar Ataxia 7s, spinocerebellar Ataxia with pigmentary retinopathy Atrophy iii, olivopontocerebellar Autosomal dominant cerebellar ataxia type 2 Cerebellar syndrome - pigmentary maculopathy Cerebellar syndrome pigmentary maculopathy Cerebellar syndrome-pigmentary maculopathy syndrome Olivopontocerebellar atrophy iii Opca 3 Opca iii Opca with macular degeneration and external ophthalmoplegia Opca with retinal degeneration Opca3 Olivopontocerebellar atrophy iiis Olivopontocerebellar atrophy 3 Sca7 Spinocerebellar ataxia 7s Spinocerebellar ataxia-7 Spinocerebellar ataxia 7 Type 7 spinocerebellar ataxia Autosomal dominant cerebellar ataxia type ii caused by mutation in atxn7 Autosomal dominant cerebellar ataxia, type 2 Spinocerebellar ataxia 7; sca7 |
Associated Genes (1) NCBI-RefSeq: ATXN7 (Ataxin 7) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Spinocerebellar ataxia type 7 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |