Disease: Brugada Syndrome 7 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 Biomarker disease GENOMICS_ENGLAND Genetics of Brugada syndrome. 27761167 2016
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 GeneticVariation disease UNIPROT Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation. 21051419 2011
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 GeneticVariation disease UNIPROT Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population. 20558140 2010
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 Biomarker disease MGD Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties. 19351516 2009
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 GeneticVariation disease UNIPROT A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype. 20031595 2009
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 Biomarker disease CTD_human
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 GeneticVariation disease CLINVAR
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		0.900 CausalMutation disease CLINVAR