Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.110 GeneticVariation disease BEFREE ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation. 29130122 2018
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.110 Biomarker disease HPO