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 |
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