Disease: Brugada Syndrome 8 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 Biomarker disease GENOMICS_ENGLAND Genetics of Brugada syndrome. 27761167 2016
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 CausalMutation disease CLINVAR HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy. 26206080 2015
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 CausalMutation disease CLINVAR HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. 25145517 2014
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 CausalMutation disease CLINVAR The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel. 25145518 2014
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 Biomarker disease GENOMICS_ENGLAND Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia. 17646576 2007
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 Biomarker disease GENOMICS_ENGLAND Short QT syndrome. 16301704 2005
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 Biomarker disease CTD_human