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8A03.16 category

Spinocerebellar ataxia

Definition

Autosomal dominantly inherited ataxias associated with over 37 gene loci that involve progressive degeneration of the cerebellum and spinocerebellar tracts of the spinal cord, presenting with characteristic sensory loss, diminished tendon reflexes, Romberg sign, and positive Babinski sign(s).

Also indexed as

Autosomal dominant cerebellar ataxia type 1Autosomal dominant cerebellar ataxia type 2Autosomal dominant cerebellar ataxia type 3Autosomal dominant cerebellar ataxia type 4Machado-Joseph diseaseMachado-Joseph disease type 1Machado-Joseph disease type 2Machado-Joseph disease type 3Spinocerebellar ataxiaSpinocerebellar ataxia type 1Spinocerebellar ataxia type 10Spinocerebellar ataxia type 11Spinocerebellar ataxia type 12Spinocerebellar ataxia type 13Spinocerebellar ataxia type 14Spinocerebellar ataxia type 15Spinocerebellar ataxia type 15/16Spinocerebellar ataxia type 16Spinocerebellar ataxia type 17Spinocerebellar ataxia type 18Spinocerebellar ataxia type 19Spinocerebellar ataxia type 2Spinocerebellar ataxia type 20Spinocerebellar ataxia type 21Spinocerebellar ataxia type 22Spinocerebellar ataxia type 23Spinocerebellar ataxia type 25Spinocerebellar ataxia type 26Spinocerebellar ataxia type 27Spinocerebellar ataxia type 28Spinocerebellar ataxia type 29Spinocerebellar ataxia type 3Spinocerebellar ataxia type 30Spinocerebellar ataxia type 31Spinocerebellar ataxia type 32Spinocerebellar ataxia type 35Spinocerebellar ataxia type 36Spinocerebellar ataxia type 4Spinocerebellar ataxia type 5Spinocerebellar ataxia type 6Spinocerebellar ataxia type 7Spinocerebellar ataxia type 8

Nearby in Hereditary ataxia