All diseases

OMIM ID
254770
OMIM term:
EPILEPSY, MYOCLONIC JUVENILE; EJM
Alternative terms:
MYOCLONIC EPILEPSY, JUVENILE; JME
PETIT MAL, IMPULSIVE
JANZ SYNDROME MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1, INCLUDED
(∗) Location:
6p12.2  
(†) Associated OMIM genes:
EFHC1  
(‡) Associated MGI genes:
Efhc1  

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