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SCA3

Introduction: SCA3

Description of SCA3

SCA3 (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

SCA3: Rare Disease

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

SCA3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SCA3, or a subtype of SCA3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SCA3 as a Disease

SCA3: Another name for Spinocerebellar ataxia 3 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 3
  »Symptoms of Spinocerebellar ataxia 3

SCA3: Related Diseases

SCA3: SCA3 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SCA3 (Spinocerebellar ataxia 3)

Some of the symptoms of SCA3 incude:

Terms associated with SCA3:

Terms Similar to SCA3:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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