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Dictionary » Spinopontine atrophy
 

Spinopontine atrophy

Introduction: Spinopontine atrophy

Description of Spinopontine atrophy

Spinopontine atrophy (medical condition): A rare genetic disorder (chromosome 14q32.1defect) characterized by . Gait...more »

See also:

Spinocerebellar ataxia 3:
  »Introduction: Spinocerebellar ataxia 3
  »Symptoms of Spinocerebellar ataxia 3

Spinopontine atrophy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spinopontine atrophy:

Spinopontine atrophy: Rare Disease

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

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

Spinopontine atrophy as a Disease

Spinopontine atrophy: Another name for Spinocerebellar ataxia 3 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 3
  »Symptoms of Spinocerebellar ataxia 3

Spinopontine atrophy: Related Diseases

Spinopontine atrophy: Spinopontine atrophy is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Spinopontine atrophy (Spinocerebellar ataxia 3)

Some of the symptoms of Spinopontine atrophy incude:

Terms associated with Spinopontine atrophy:

Terms Similar to Spinopontine atrophy:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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