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Searched for "Spinocerebellar Ataxias".

46 results found on Genetics Home Reference.

Showing results 1 to 20.
  • spinocerebellar ataxia type 6 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • spinocerebellar ataxia type 1 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • infantile-onset spinocerebellar ataxia condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • spinocerebellar ataxia type 3 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • spinocerebellar ataxia type 2 condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • Friedreich ataxia condition summary
    Found in name or synonym: Friedreich spinocerebellar ataxia
    Related genes:
  • myoclonic epilepsy myopathy sensory ataxia condition summary
    Found in name or synonym: spinocerebellar ataxia with epilepsy
    Related genes:
  • ataxia with oculomotor apraxia condition summary
    Found in name or synonym: spinocerebellar ataxia with axonal neuropathy type 2
    Related genes:
  • autosomal recessive cerebellar ataxia type 1 condition summary
    Found in name or synonym: autosomal recessive spinocerebellar ataxia 8
    Related genes:
  • ATXN2 gene summary
    Official name: ataxin 2
    Found: Spinocerebellar ataxia type 2 (SCA2) is a condition characterized...
  • ATXN1 gene summary
    Official name: ataxin 1
    Found: Spinocerebellar ataxia type 1 (SCA1) is a condition characterized...
  • CACNA1A gene summary
    Official name: calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
    Found: Spinocerebellar ataxia type 6 (SCA6) is another disorder...
  • ATXN3 gene summary
    Official name: ataxin 3
    Found: Spinocerebellar ataxia type 3 (SCA3) is a condition characterized...
  • C10orf2 gene summary
    Official name: chromosome 10 open reading frame 2
    Found: ...found to cause infantile-onset spinocerebellar ataxia (IOSCA). The most common mutation...
  • Huntington disease-like syndrome condition summary
    Found: ...for HDL4 (also known as spinocerebellar ataxia type 17). The genetic cause of...
    Related genes:
  • TBP gene summary
    Official name: TATA box binding protein
    Found: ...disease-like 4 (HDL4) or spinocerebellar ataxia type 17 (SCA17). The features of...
  • ataxia-telangiectasia condition summary
    Related classification: Spinocerebellar Ataxias
    Related genes:
  • Marinesco-Sjögren syndrome condition summary
    Related classification: Spinocerebellar Degenerations
    Related genes:
  • ATXN7 gene information
    Official name: ataxin 7
    Found: Spinocerebellar ataxia 7 (SCA7): Spinocerebellar ataxia...
  • ATXN10 gene information
    Official name: ataxin 10
    Found: Spinocerebellar ataxia 10 (SCA10): Spinocerebellar ataxia...
 
Published: July 7, 2014