Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy
0.400 GermlineCausalMutation disease ORPHANET Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. 23708187 2013
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy
0.400 Biomarker disease HPO