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Disease Spinocerebellar Ataxias

Name Spinocerebellar Ataxias
Synonyms ADCA, TYPE II | ALS13, INCLUDED | Ataxia 1, Spinocerebellar | Ataxia 2, Spinocerebellar | Ataxia 2s, Spinocerebellar | Ataxia 4, Spinocerebellar | Ataxia 4s, Spinocerebellar | Ataxia 5, Spinocerebellar | Ataxia 5s, Spinocerebellar | Ataxia 6, Spinocerebellar | Ataxia 6s, Spinocerebellar | Ataxia 7, Spinocerebellar | Ataxia 7s, Spinocerebellar | Ataxia, Dominantly-Inherited Spinocerebellar | Ataxias, Dominantly-Inherited Spinocerebellar | Ataxia, Spinocerebellar | Ataxias, Spinocerebellar | Atrophies, Spinocerebellar | Atrophy 2, Olivopontocerebellar | Atrophy 2s, Olivopontocerebellar | Atrophy 2, Spinocerebellar | Atrophy 2s, Spinocerebellar | Atrophy III, Olivopontocerebellar | Atrophy II, Olivopontocerebellar | Atrophy IIs, Olivopontocerebellar | Atrophy II, Spinocerebellar | Atrophy IIs, Spinocerebellar | Atrophy I, Olivopontocerebellar | Atrophy I, Spinocerebellar | Atrophy IV, Olivopontocerebellar | Atrophy IVs, Olivopontocerebellar | Atrophy, Spinocerebellar | Autosomal Dominant Cerebellar Ataxia, Type II | Cerebellar Degeneration with Slow Eye Movements | Cerebelloparenchymal Disorder I | Cerebelloparenchymal Disorder Is | CPD1 | Dominantly-Inherited Spinocerebellar Ataxia | Dominantly Inherited Spinocerebellar Ataxias | Dominantly-Inherited Spinocerebellar Ataxias | II, Olivopontocerebellar Atrophy | IIs, Olivopontocerebellar Atrophy | II, Spinocerebellar Atrophy | IIs, Spinocerebellar Atrophy | Menzel Type OPCA | Olivopontocerebellar Atrophy 2 | Olivopontocerebellar Atrophy 2s | Olivopontocerebellar Atrophy, Holguin Type | Olivopontocerebellar Atrophy I | Olivopontocerebellar Atrophy II | Olivopontocerebellar Atrophy III | Olivopontocerebellar Atrophy IIIs | Olivopontocerebellar Atrophy IIs | Olivopontocerebellar Atrophy Is | Olivopontocerebellar Atrophy IV | Olivopontocerebellar Atrophy IVs | OPCA1 | OPCA2 | OPCA3 | OPCA4 | OPCA I | OPCA III | OPCA IV | OPCA, Menzel Type | OPCA, Schut-Haymaker Type | OPCA with Macular Degeneration and External Ophthalmoplegia | OPCA with Retinal Degeneration | SCA1 | SCA1s | SCA2 | SCA32 | SCA4 | SCA5 | SCA6 | SCA7 | SCA9 | Schut Haymaker Type OPCA | Schut-Haymaker Type OPCA | Spinocerebellar Ataxia | Spinocerebellar Ataxia 1 | Spinocerebellar Ataxia-1 | Spinocerebellar Ataxia 1s | Spinocerebellar Ataxia 2 | Spinocerebellar Ataxia-2 | Spinocerebellar Ataxia 2s | SPINOCEREBELLAR ATAXIA 32 | Spinocerebellar Ataxia 4 | Spinocerebellar Ataxia-4 | Spinocerebellar Ataxia 4s | Spinocerebellar Ataxia 5 | Spinocerebellar Ataxia-5 | Spinocerebellar Ataxia 5s | Spinocerebellar Ataxia 6 | Spinocerebellar Ataxia-6 | Spinocerebellar Ataxia 6s | Spinocerebellar Ataxia 7 | Spinocerebellar Ataxia-7 | Spinocerebellar Ataxia 7s | SPINOCEREBELLAR ATAXIA 9 | Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy | Spinocerebellar Ataxia, Cuban Type | Spinocerebellar Ataxia, Dominantly-Inherited | Spinocerebellar Ataxias, Dominantly Inherited | Spinocerebellar Ataxias, Dominantly-Inherited | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 4 | Spinocerebellar Ataxia Type 5 | Spinocerebellar Ataxia Type 6 | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia with Slow Eye Movements | Spinocerebellar Atrophies | Spinocerebellar Atrophy | Spinocerebellar Atrophy 2 | Spinocerebellar Atrophy 2s | Spinocerebellar Atrophy I | Spinocerebellar Atrophy II | Spinocerebellar Atrophy IIs | Spinocerebellar Atrophy Is | Spinocerebellar Degeneration with Slow Eye Movements | SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS;SDSEM AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13, INCLUDED | Swami Syndrome, Wadia | Syndrome, Wadia Swami | Syndrome, Wadia-Swami | Type 1 Spinocerebellar Ataxia | Type 2 Spinocerebellar Ataxia | Type 4 Spinocerebellar Ataxia | Type 5 Spinocerebellar Ataxia | Type 6 Spinocerebellar Ataxia | Type 7 Spinocerebellar Ataxia | Wadia Swami Syndrome | Wadia-Swami Syndrome
Definition 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)
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID D020754
OMIM® IDs 164400 | 164500 | 183086 | 183090 | 600223 | 600224 | 612876 | 613909
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Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Cerebellar Diseases Has associated chemicals Has associated genes Cerebellar Ataxia Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Cerebellar Diseases Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes
3. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Spinal Cord Diseases Has associated chemicals Has associated genes Has associated exposure references Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes
4. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes
5. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurologic Manifestations Has associated chemicals Has associated genes Has associated exposure references Dyskinesias Has associated chemicals Has associated genes Has associated exposure references Ataxia Has associated chemicals Has associated genes Cerebellar Ataxia Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes
6. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar Ataxias Has associated chemicals Has associated genes

Top ↑ Descendants

Spinocerebellar Ataxias Has associated chemicals Has associated genes
  Anemia, sideroblastic spinocerebellar ataxia Has associated chemicals Has associated genes
View node Ataxia Telangiectasia Has associated chemicals Has associated genes
  Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
  Gemignani syndrome
  MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) Has associated chemicals Has associated genes
  Spastic Ataxia
  Spastic ataxia Charlevoix-Saguenay type Has associated chemicals Has associated genes
  Spinocerebellar Ataxia 10 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia 11 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia 12 Has associated chemicals Has associated genes
  Spinocerebellar ataxia 13 Has associated chemicals Has associated genes
  Spinocerebellar ataxia 14 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia 15 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia 17 Has associated chemicals Has associated genes
  Spinocerebellar ataxia 20
  Spinocerebellar ataxia 25
  Spinocerebellar ataxia 26 Has associated chemicals Has associated genes
  Spinocerebellar ataxia 28 Has associated chemicals Has associated genes
  Spinocerebellar ataxia 30
  Spinocerebellar Ataxia 31 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia And Plaque-Like Deposits
  Spinocerebellar ataxia, autosomal recessive 1 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia, Autosomal Recessive 7
  Spinocerebellar Ataxia, Autosomal Recessive 8 Has associated chemicals Has associated genes
View node Spinocerebellar Ataxia, Autosomal Recessive 9 Has associated chemicals Has associated genes
View node Machado-Joseph Disease Has associated chemicals Has associated genes
  Spinocerebellar Ataxia with Dysmorphism
  Spinocerebellar Ataxia with Epilepsy
  Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy
  Spinocerebellar Ataxia, X-Linked 1
  Spinocerebellar Ataxia, X-Linked 5