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Spinocerebellar Ataxias

A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)

Year introduced: 2000

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Subheadings:

Tree Number(s): C10.228.140.252.190.530, C10.228.140.252.700.700, C10.228.854.787.875, C10.574.500.825.700, C10.597.350.090.500.530, C16.320.400.780.875

MeSH Unique ID: D020754

Entry Terms:

  • Ataxia, Spinocerebellar
  • Ataxias, Spinocerebellar
  • Spinocerebellar Ataxia
  • Dominantly-Inherited Spinocerebellar Ataxias
  • Ataxia, Dominantly-Inherited Spinocerebellar
  • Ataxias, Dominantly-Inherited Spinocerebellar
  • Dominantly Inherited Spinocerebellar Ataxias
  • Dominantly-Inherited Spinocerebellar Ataxia
  • Spinocerebellar Ataxia, Dominantly-Inherited
  • Spinocerebellar Ataxias, Dominantly-Inherited
  • Spinocerebellar Ataxias, Dominantly Inherited
  • Spinocerebellar Atrophies
  • Atrophies, Spinocerebellar
  • Atrophy, Spinocerebellar
  • Spinocerebellar Atrophy
  • Spinocerebellar Ataxia Type 2
  • Type 2 Spinocerebellar Ataxia
  • Spinocerebellar Ataxia 2
  • Ataxia 2, Spinocerebellar
  • Ataxia 2s, Spinocerebellar
  • Spinocerebellar Ataxia 2s
  • Wadia-Swami Syndrome
  • Syndrome, Wadia-Swami
  • Cerebellar Degeneration with Slow Eye Movements
  • Olivopontocerebellar Atrophy II
  • Atrophy II, Olivopontocerebellar
  • Atrophy IIs, Olivopontocerebellar
  • II, Olivopontocerebellar Atrophy
  • IIs, Olivopontocerebellar Atrophy
  • Olivopontocerebellar Atrophy IIs
  • Spinocerebellar Atrophy II
  • Atrophy II, Spinocerebellar
  • Atrophy IIs, Spinocerebellar
  • II, Spinocerebellar Atrophy
  • IIs, Spinocerebellar Atrophy
  • Spinocerebellar Atrophy IIs
  • Olivopontocerebellar Atrophy 2
  • Atrophy 2, Olivopontocerebellar
  • Atrophy 2s, Olivopontocerebellar
  • Olivopontocerebellar Atrophy 2s
  • Spinocerebellar Ataxia with Slow Eye Movements
  • Spinocerebellar Ataxia, Cuban Type
  • Spinocerebellar Atrophy 2
  • Atrophy 2, Spinocerebellar
  • Atrophy 2s, Spinocerebellar
  • Spinocerebellar Atrophy 2s
  • Spinocerebellar Degeneration with Slow Eye Movements
  • Wadia Swami Syndrome
  • Swami Syndrome, Wadia
  • Syndrome, Wadia Swami
  • Olivopontocerebellar Atrophy, Holguin Type
  • Spinocerebellar Ataxia-2
  • Spinocerebellar Ataxia Type 7
  • Type 7 Spinocerebellar Ataxia
  • OPCA with Retinal Degeneration
  • Olivopontocerebellar Atrophy III
  • Atrophy III, Olivopontocerebellar
  • Olivopontocerebellar Atrophy IIIs
  • Autosomal Dominant Cerebellar Ataxia, Type II
  • OPCA with Macular Degeneration and External Ophthalmoplegia
  • Spinocerebellar Ataxia-7
  • Spinocerebellar Ataxia 7
  • Ataxia 7, Spinocerebellar
  • Ataxia 7s, Spinocerebellar
  • Spinocerebellar Ataxia 7s
  • Spinocerebellar Ataxia Type 5
  • Type 5 Spinocerebellar Ataxia
  • Spinocerebellar Ataxia 5
  • Ataxia 5, Spinocerebellar
  • Ataxia 5s, Spinocerebellar
  • Spinocerebellar Ataxia 5s
  • Spinocerebellar Ataxia-5
  • Spinocerebellar Ataxia Type 6
  • Type 6 Spinocerebellar Ataxia
  • Spinocerebellar Ataxia 6
  • Ataxia 6, Spinocerebellar
  • Ataxia 6s, Spinocerebellar
  • Spinocerebellar Ataxia 6s
  • Spinocerebellar Ataxia-6
  • Spinocerebellar Ataxia Type 1
  • Type 1 Spinocerebellar Ataxia
  • Spinocerebellar Ataxia 1
  • Ataxia 1, Spinocerebellar
  • Spinocerebellar Ataxia 1s
  • Spinocerebellar Atrophy I
  • Atrophy I, Spinocerebellar
  • Spinocerebellar Atrophy Is
  • SCA1
  • SCA1s
  • Cerebelloparenchymal Disorder I
  • Cerebelloparenchymal Disorder Is
  • Menzel Type OPCA
  • OPCA, Menzel Type
  • Schut-Haymaker Type OPCA
  • OPCA, Schut-Haymaker Type
  • Schut Haymaker Type OPCA
  • Olivopontocerebellar Atrophy IV
  • Atrophy IV, Olivopontocerebellar
  • Atrophy IVs, Olivopontocerebellar
  • Olivopontocerebellar Atrophy IVs
  • Spinocerebellar Ataxia-1
  • Olivopontocerebellar Atrophy I
  • Atrophy I, Olivopontocerebellar
  • Olivopontocerebellar Atrophy Is
  • Spinocerebellar Ataxia Type 4
  • Spinocerebellar Ataxia 4
  • Ataxia 4, Spinocerebellar
  • Ataxia 4s, Spinocerebellar
  • Spinocerebellar Ataxia 4s
  • Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
  • Spinocerebellar Ataxia-4
  • Type 4 Spinocerebellar Ataxia

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