Disease Information | ||||||
---|---|---|---|---|---|---|
Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
Epilepsy, Progressive Myoclonic 2B | NHLRC1 | disease | C1850764 | CausalMutation | 0.1 | disgenet |
Epilepsy, Progressive Myoclonic 2B | EPM2A | disease | C1850764 | Biomarker | 0.01 | disgenet |
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