Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
spinocerebellar ataxia type 1

Also known as: ATXN1 autosomal dominant cerebellar ataxia type I, Menzel type OPCA, OPCA 1, OPCA 4, OPCA1, OPCA4, SCA1, Sca1, Schut-haymaker type OPCA, autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1, cerebelloparenchymal disorder 1, olivopontocerebellar atrophy 1, olivopontocerebellar atrophy 4, spinocerebellar ataxia 1, spinocerebellar ataxia type 1, spinocerebellar atrophy 1

spinocerebellar ataxia type 13

Also known as: SCA13, autosomal dominant cerebellar ataxia with intellectual disability, autosomal dominant cerebellar ataxia with mental retardation, cerebellar ataxia, autosomal dominant with intellectual disability, cerebellar ataxia, autosomal dominant with mental retardation, spinocerebellar ataxia 13, spinocerebellar ataxia type 13

spinocerebellar ataxia type 15/16

Also known as: SCA15, SCA15/16, SCA16 (formerly), SCAR16, spinocerebellar ataxia 15, spinocerebellar ataxia 16, spinocerebellar ataxia 16 (formerly), spinocerebellar ataxia 16, formerly, spinocerebellar ataxia type 15, spinocerebellar ataxia type 15/16, spinocerebellar ataxia type 16

spinocerebellar ataxia type 17

Also known as: CPD, late-onset recessive type, CPD2, HDL4, Huntington disease-like 4, OPCA V, OPCA with dementia and extrapyramidal signs, SCA 17, SCA17, cerebelloparenchymal disorder II, olivopontocerebellar atrophy 5, olivopontocerebellar atrophy V, olivopontocerebellar atrophy type 5, spinocerebellar ataxia 17, spinocerebellar ataxia type 17

spinocerebellar ataxia type 18

Also known as: SCA18, SMNA, sensorimotor neuropathy with ataxia autosomal dominant, sensorimotor neuropathy with ataxia, autosomal dominant, spinocerebellar ataxia 18

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