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Dictionary » Myoclonus, hereditary essential
 

Myoclonus, hereditary essential

Introduction: Myoclonus, hereditary essential

Description of Myoclonus, hereditary essential

Myoclonus, hereditary essential (medical condition): A very rare inherited syndrome characterized mainly by mild dystonia and...more »

See also:

Myoclonic dystonia:
  »Introduction: Myoclonic dystonia
  »Symptoms of Myoclonic dystonia

Myoclonus, hereditary essential: Related Topics

These medical condition or symptom topics may be relevant to medical information for Myoclonus, hereditary essential:

Myoclonus, hereditary essential: Rare Disease

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

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

Myoclonus, hereditary essential as a Disease

Myoclonus, hereditary essential: Another name for Myoclonic dystonia (or close medical condition association).
  »Introduction: Myoclonic dystonia
  »Symptoms of Myoclonic dystonia

Myoclonus, hereditary essential: Related Diseases

Myoclonus, hereditary essential: Myoclonus, hereditary essential is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Myoclonus, hereditary essential (Myoclonic dystonia)

Some of the symptoms of Myoclonus, hereditary essential incude:

Terms associated with Myoclonus, hereditary essential:

Terms Similar to Myoclonus, hereditary essential:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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