All diseases

OMIM ID
607628
OMIM term:
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11; EIG11 EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8, INCLUDED; EJM8, INCLUDED
Alternative terms:

(∗) Location:
3q27.1  
(†) Associated OMIM genes:
CLCN2  
(‡) Associated MGI genes:
Cacna2d2  

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