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DYT15

Introduction: DYT15

Description of DYT15

DYT15 (medical condition): A rare genetic movement disorder. The muscles contract involuntarily...more »

See also:

Dystonia 15, myoclonic:
  »Introduction: Dystonia 15, myoclonic
  »Symptoms of Dystonia 15, myoclonic

DYT15: Rare Disease

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

DYT15 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that DYT15, or a subtype of DYT15, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

DYT15 as a Disease

DYT15: Another name for Dystonia 15, myoclonic (or close medical condition association).
  »Introduction: Dystonia 15, myoclonic
  »Symptoms of Dystonia 15, myoclonic

DYT15: Related Diseases

DYT15: DYT15 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of DYT15 (Dystonia 15, myoclonic)

Some of the symptoms of DYT15 incude:

Terms associated with DYT15:

Terms Similar to DYT15:

Source - NIH

Interesting Medical Articles:

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