All diseases

OMIM ID
611726
OMIM term:
EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS; EPM3
Alternative terms:

(∗) Location:
7q11.21  
(†) Associated OMIM genes:
KCTD7  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/83r94bh3