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Dictionary » Spinocerebellar ataxia 8
 

Spinocerebellar ataxia 8

Introduction: Spinocerebellar ataxia 8

Description of Spinocerebellar ataxia 8

Spinocerebellar ataxia 8 (medical condition): A rare genetic disorder (chromosome 13q21 defect) characterized...more »

See also:

Spinocerebellar ataxia 8:
  »Introduction: Spinocerebellar ataxia 8
  »Symptoms of Spinocerebellar ataxia 8

Spinocerebellar ataxia 8: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spinocerebellar ataxia 8:

Spinocerebellar ataxia 8: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Spinocerebellar ataxia 8 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Spinocerebellar ataxia 8, or a subtype of Spinocerebellar ataxia 8, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Spinocerebellar ataxia 8 as a Disease

Spinocerebellar ataxia 8 (medical condition): See Spinocerebellar ataxia 8 (disease information).
  »Introduction: Spinocerebellar ataxia 8
  »Symptoms of Spinocerebellar ataxia 8

Spinocerebellar ataxia 8: Related Diseases

Spinocerebellar ataxia 8: Spinocerebellar ataxia 8 is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Spinocerebellar ataxia 8:

Terms associated with Spinocerebellar ataxia 8:

Terms Similar to Spinocerebellar ataxia 8:

Source - NIH

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