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Dictionary » Spinocerebellar ataxia 13
 

Spinocerebellar ataxia 13

Introduction: Spinocerebellar ataxia 13

Description of Spinocerebellar ataxia 13

Spinocerebellar ataxia 13 (medical condition): A rare genetic disorder (chromosome 19 defect) characterized by...more »

See also:

Spinocerebellar ataxia 13:
  »Introduction: Spinocerebellar ataxia 13
  »Symptoms of Spinocerebellar ataxia 13

Spinocerebellar ataxia 13: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spinocerebellar ataxia 13:

Spinocerebellar ataxia 13: Rare Disease

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

Spinocerebellar ataxia 13 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 13, or a subtype of Spinocerebellar ataxia 13, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Spinocerebellar ataxia 13 as a Disease

Spinocerebellar ataxia 13 (medical condition): See Spinocerebellar ataxia 13 (disease information).
  »Introduction: Spinocerebellar ataxia 13
  »Symptoms of Spinocerebellar ataxia 13

Spinocerebellar ataxia 13: Related Diseases

Spinocerebellar ataxia 13: Spinocerebellar ataxia 13 is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Spinocerebellar ataxia 13:

Spinocerebellar ataxia 13: Related Disease Topics

These medical disease topics may be related to Spinocerebellar ataxia 13:

Terms associated with Spinocerebellar ataxia 13:

Terms Similar to Spinocerebellar ataxia 13:

Source - NIH

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