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Dictionary » Epilepsy progressive myoclonic 2
 

Epilepsy progressive myoclonic 2

Introduction: Epilepsy progressive myoclonic 2

Description of Epilepsy progressive myoclonic 2

Epilepsy progressive myoclonic 2 (medical condition): A rare genetic disorder caused by the inclusion of...more »

See also:

Lafora disease:
  »Introduction: Lafora disease
  »Symptoms of Lafora disease

Epilepsy progressive myoclonic 2: Related Topics

These medical condition or symptom topics may be relevant to medical information for Epilepsy progressive myoclonic 2:

Epilepsy progressive myoclonic 2: Rare Disease

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

Epilepsy progressive myoclonic 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Epilepsy progressive myoclonic 2, or a subtype of Epilepsy progressive myoclonic 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Epilepsy progressive myoclonic 2 as a Disease

Epilepsy progressive myoclonic 2: Another name for Lafora disease (or close medical condition association).
  »Introduction: Lafora disease
  »Symptoms of Lafora disease

Epilepsy progressive myoclonic 2: Related Diseases

Epilepsy progressive myoclonic 2: Epilepsy progressive myoclonic 2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Epilepsy progressive myoclonic 2 (Lafora disease)

Some of the symptoms of Epilepsy progressive myoclonic 2 incude:

Epilepsy progressive myoclonic 2: Related Disease Topics

These medical disease topics may be related to Epilepsy progressive myoclonic 2:

Terms associated with Epilepsy progressive myoclonic 2:

Terms Similar to Epilepsy progressive myoclonic 2:

Source - NIH

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