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SCA8

Introduction: SCA8

Description of SCA8

SCA8 (medical condition): A rare genetic disorder (chromosome 13q21 defect) characterized by...more »

See also:

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

SCA8: Rare Disease

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

SCA8 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SCA8, or a subtype of SCA8, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SCA8 as a Disease

SCA8: Another name for Spinocerebellar ataxia 8 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 8
  »Symptoms of Spinocerebellar ataxia 8

SCA8: Related Diseases

SCA8: SCA8 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SCA8 (Spinocerebellar ataxia 8)

Some of the symptoms of SCA8 incude:

Terms associated with SCA8:

Terms Similar to SCA8:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

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  • Broncho-aortic constriction
  • Bronchoalveolar
  • Bronchoalveolar carcinoma
  • Bronchoalveolar fluid
  • Bronchoalveolar lavage
  • Bronchoalveolar lavage (BAL)
  • Bronchoalveolar Lavage Fluid
  • Bronchobiliary fistula
  • Bronchocavernous
  • Bronchocavitary fistula
  • Bronchoconstriction
  • Bronchoconstrictor
  • Bronchoconstrictor Agents

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