Disease Term Disease ID Gene Symbol Classification References Source
BENIGN FAMILIAL INFANTILE EPILEPSY SCN2A Causal GWAS catalog
CHRNA2 Unknown ClinGen
KCNQ2 Unknown GenCC
KCNQ3 Unknown ClinGen
PRRT2 Unknown CTD
SCN8A Unknown GWAS catalog
BENIGN FAMILIAL INFANTILE SEIZURES CHRNA2 Unknown Disgenet
KCNQ2 Unknown Disgenet
KCNQ3 Unknown Disgenet
PRRT2 Unknown Disgenet
SCN2A Unknown Disgenet
SCN8A Unknown Disgenet