Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant LGI1 disease C1838062 GeneticVariation 0.8 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant LGI1 disease C1838062 Biomarker 0.8 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant LGI1 disease C1838062 GermlineCausalMutation 0.8 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant RELN disease C1838062 GermlineCausalMutation 0.31 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant RELN disease C1838062 GeneticVariation 0.31 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant DEPDC5 disease C1838062 GermlineCausalMutation 0.3 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant ADGRV1 disease C1838062 GeneticVariation 0.02 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant ADAM22 disease C1838062 Biomarker 0.02 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant ADAM22 disease C1838062 GeneticVariation 0.02 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant CRISPLD2 disease C1838062 GeneticVariation 0.01 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant LLGL1 disease C1838062 GeneticVariation 0.01 disgenet
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant LGI4 disease C1838062 GeneticVariation 0.01 disgenet
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