All diseases

OMIM ID
117100
OMIM term:
CENTRALOPATHIC EPILEPSY
Alternative terms:
CENTROTEMPORAL EPILEPSY; ECT
TEMPORAL-CENTRAL FOCAL EPILEPSY
BENIGN ROLANDIC EPILEPSY
BENIGN EPILEPSY OF CHILDHOOD WITH CENTROTEMPORAL SPIKES; BECTS
(∗) Location:
11p13  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/342rr279