Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Benign Neonatal Epilepsies KCNQ2 disease C0270851 GeneticVariation 0.59 disgenet
Benign Neonatal Epilepsies KCNQ2 disease C0270851 Biomarker 0.59 disgenet
Benign Neonatal Epilepsies KCNQ3 disease C0270851 GeneticVariation 0.22 disgenet
Benign Neonatal Epilepsies KCNQ3 disease C0270851 Biomarker 0.22 disgenet
Benign Neonatal Epilepsies MC3R disease C0270851 GeneticVariation 0.01 disgenet
Benign Neonatal Epilepsies KCNQ5 disease C0270851 Biomarker 0.01 disgenet
Benign Neonatal Epilepsies PRRT2 disease C0270851 Biomarker 0.01 disgenet
Benign Neonatal Epilepsies KCNA1 disease C0270851 GeneticVariation 0.01 disgenet
click here to return to the previous page