Concept/Terms |
Spinocerebellar Ataxias- Spinocerebellar Ataxias
- 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- 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- 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- 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- 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- 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 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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