Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
spinocerebellar ataxia type 6

Also known as: CACNA1A autosomal dominant cerebellar ataxia type III, SCA6, autosomal dominant cerebellar ataxia type III caused by mutation in CACNA1A, spinocerebellar ataxia 6, spinocerebellar ataxia type 6

spinocerebellar ataxia, autosomal recessive 22

Also known as: SCAR22, VWA3B autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in VWA3B, spinocerebellar ataxia, autosomal recessive 22, spinocerebellar ataxia, autosomal recessive 22; SCAR22, spinocerebellar ataxia, autosomal recessive type 22

spinocerebellar ataxia, autosomal recessive 23

Also known as: SCAR23, autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency, spinocerebellar ataxia autosomal recessive type 23, spinocerebellar ataxia, autosomal recessive 23, spinocerebellar ataxia, autosomal recessive type 23

spinocerebellar ataxia, autosomal recessive 24

Also known as: SCAR24, UBA5 autosomal dominant cerebellar ataxia, autosomal dominant cerebellar ataxia caused by mutation in UBA5, spinocerebellar ataxia, autosomal recessive 24, spinocerebellar ataxia, autosomal recessive 24; SCAR24, spinocerebellar ataxia, autosomal recessive type 24

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