| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Epilepsy, Myoclonic, Benign Adult Familial, Type 1 | SAMD12 | disease | C1832841 | Biomarker | 0.5 | disgenet |
| Epilepsy, Myoclonic, Benign Adult Familial, Type 1 | SAMD12 | disease | C1832841 | GermlineCausalMutation | 0.5 | disgenet |
| Epilepsy, Myoclonic, Benign Adult Familial, Type 1 | CTNND2 | disease | C1832841 | GermlineCausalMutation | 0.3 | disgenet |
| Epilepsy, Myoclonic, Benign Adult Familial, Type 1 | ADRA2B | disease | C1832841 | GermlineCausalMutation | 0.3 | disgenet |
| Epilepsy, Myoclonic, Benign Adult Familial, Type 1 | CNTN2 | disease | C1832841 | GermlineCausalMutation | 0.3 | disgenet |
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