Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Epilepsy, Familial Mesial Temporal Lobe DEPDC5 disease C1968848 GeneticVariation 0.01 disgenet
Epilepsy, Familial Mesial Temporal Lobe SCN2A disease C1968848 Biomarker 0.01 disgenet
Epilepsy, Familial Mesial Temporal Lobe CPA6 NA C1968848 NA NA orphanet
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