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EPM2 (medical condition): A rare genetic disorder caused by the inclusion of a...more »
EPM2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that EPM2, or a subtype of EPM2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
EPM2: EPM2 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of EPM2 incude:
These medical disease topics may be related to EPM2:
Source - NIH
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