Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
0.120 GeneticVariation disease BEFREE Lack of association of SCN2A rs17183814 polymorphism with the efficacy of lamotrigine monotherapy in patients with focal epilepsy from Herzegovina area, Bosnia and Herzegovina. 31707316 2019
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
0.120 Biomarker disease LHGDN A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline. 15028761 2004
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
0.120 GeneticVariation disease CLINVAR