All diseases

OMIM ID
607631
OMIM term:
EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1; EJA1
Alternative terms:

(∗) Location:
6p12.2  
(†) Associated OMIM genes:
EFHC1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/qld0x1iz