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Dictionary » Hereditary essential myoclonus
 

Hereditary essential myoclonus

Introduction: Hereditary essential myoclonus

Description of Hereditary essential myoclonus

Hereditary essential myoclonus (medical condition): A very rare inherited syndrome characterized mainly by mild...more »

See also:

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

Hereditary essential myoclonus: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hereditary essential myoclonus:

Hereditary essential myoclonus: Rare Disease

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

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

Hereditary essential myoclonus as a Disease

Hereditary essential myoclonus: Another name for Myoclonic dystonia (or close medical condition association).
  »Introduction: Myoclonic dystonia
  »Symptoms of Myoclonic dystonia

Hereditary essential myoclonus: Related Diseases

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

Symptoms of Hereditary essential myoclonus (Myoclonic dystonia)

Some of the symptoms of Hereditary essential myoclonus incude:

Terms associated with Hereditary essential myoclonus:

Terms Similar to Hereditary essential myoclonus:

Source: Diseases Database

Source - NIH

External links related to: Hereditary essential myoclonus

Source: Diseases Database

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