Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®
 
 
Your Search

Search Results

Searched for "Spinocerebellar Ataxias".

41 results found on Genetics Home Reference.

Showing results 1 to 20.
  1. spinocerebellar ataxia type 6 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  2. spinocerebellar ataxia type 1 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  3. infantile-onset spinocerebellar ataxia condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  4. spinocerebellar ataxia type 3 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  5. spinocerebellar ataxia type 2 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  6. Friedreich ataxia condition summary
    Found in name or synonym: Friedreich spinocerebellar ataxia
    Related genes:
  7. myoclonic epilepsy myopathy sensory ataxia condition summary
    Found in name or synonym: spinocerebellar ataxia with epilepsy
    Related genes:
  8. ataxia with oculomotor apraxia condition summary
    Found in name or synonym: spinocerebellar ataxia, recessive, non-Friedreich type...
    Related genes:
  9. autosomal recessive cerebellar ataxia type 1 condition summary
    Found in name or synonym: autosomal recessive spinocerebellar ataxia 8
    Related genes:
  10. ATXN2 gene summary
    Official name: ataxin 2
    Found: Spinocerebellar ataxia type 2 (SCA2) is a condition characterized...
  11. ATXN1 gene summary
    Official name: ataxin 1
    Found: Spinocerebellar ataxia type 1 (SCA1) is a condition characterized...
  12. CACNA1A gene summary
    Official name: calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
    Found: Spinocerebellar ataxia type 6 (SCA6) is another disorder...
  13. ATXN3 gene summary
    Official name: ataxin 3
    Found: Spinocerebellar ataxia type 3 (SCA3) is a condition characterized...
  14. C10orf2 gene summary
    Official name: chromosome 10 open reading frame 2
    Found: ...found to cause infantile-onset spinocerebellar ataxia (IOSCA). The most common mutation...
  15. Huntington disease-like syndrome condition summary
    Found: ...for HDL4 (also known as spinocerebellar ataxia type 17). The genetic cause of...
    Related genes:
  16. TBP gene summary
    Official name: TATA box binding protein
    Found: ...disease-like 4 (HDL4) or spinocerebellar ataxia type 17 (SCA17). The features of...
  17. ataxia-telangiectasia condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  18. Marinesco-Sjögren syndrome condition summary
    Related classification: Spinocerebellar Degenerations
    Related genes:
  19. ATXN7 gene information
    Official name: ataxin 7
    Found: Spinocerebellar ataxia 7 (SCA7) [MIM:164500]: Spinocerebellar...
  20. ATXN10 gene information
    Official name: ataxin 10
    Found: Spinocerebellar ataxia 10 (SCA10) [MIM:603516]: Spinocerebellar...
 
Published: May 20, 2013