Disease table of EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI OMIM ID: 604364

Gene-disease associations table

Gene	Associated with EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
DEPDC5	ClinVar, OMIM, HUMSAVAR	HGNC link	22q12.2	1	604364