Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
BENIGN NEONATAL EPILEPSY	C0270851	SCN2A	Causal	—	Disgenet
		ATP1A2	Unknown	—	Disgenet
		KCNQ2	Unknown	—	Disgenet
		KCNQ3	Unknown	—	Disgenet
BENIGN NEONATAL SEIZURES	MONDO:0016027	KCNQ3	Causal	24851285 24375629	GWAS catalog
BENIGN NEONATAL SEIZURES	MONDO:0016027	KCNQ2	Unknown	20437616 24375629	GWAS catalog
EPILEPSY, BENIGN NEONATAL	MESH:D020936	KCNQ2	Unknown	19380078 26910900	CTD
EPILEPSY, BENIGN NEONATAL, 2	C1852581	KCNQ2	Unknown	—	Disgenet
EPILEPSY, BENIGN NEONATAL, 2	C1852581	KCNQ3	Unknown	—	Disgenet
EPILEPSY, BENIGN NEONATAL, 3	MESH:C564274	SCN2A	Unknown	—	CTD
FAMILIAL BENIGN NEONATAL EPILEPSY	C0220669	KCNQ2	Unknown	—	Disgenet
FAMILIAL BENIGN NEONATAL EPILEPSY	C0220669	KCNQ3	Unknown	—	Disgenet

Benign neonatal epilepsy