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Search 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:
Mouse
Zebrafish
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