Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.130 GeneticVariation phenotype BEFREE SCN1B mutations have been associated with Brugada syndrome as well as with other cardiac arrhythmias and familial epilepsy. 25253298 2014
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.130 GeneticVariation phenotype BEFREE Human mutations in SCN1B result in epilepsy and cardiac arrhythmia. 21994374 2011
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.130 Biomarker phenotype BEFREE These findings implicate SCN1B as a disease gene for human arrhythmia susceptibility. 18464934 2008
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.130 Biomarker phenotype HPO