Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1834144
Disease: Sick Sinus Syndrome 2, Autosomal Dominant
Sick Sinus Syndrome 2, Autosomal Dominant 		0.700 Biomarker disease CTD_human
CUI: C1834144
Disease: Sick Sinus Syndrome 2, Autosomal Dominant
Sick Sinus Syndrome 2, Autosomal Dominant 		0.700 CausalMutation disease CLINVAR
CUI: C2751083
Disease: Brugada Syndrome 8
Brugada Syndrome 8 		0.600 Biomarker disease CTD_human
CUI: C4707243
Disease: Familial thoracic aortic aneurysm and aortic dissection
Familial thoracic aortic aneurysm and aortic dissection 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.490 Biomarker disease HPO
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		0.440 GermlineCausalMutation disease ORPHANET
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		0.440 Biomarker disease HPO
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		0.110 Biomarker disease HPO
CUI: C0015967
Disease: Fever
Fever 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		0.100 Biomarker disease HPO
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		0.100 Biomarker disease HPO
CUI: C0039070
Disease: Syncope
Syncope 		0.100 Biomarker phenotype HPO
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia 		0.100 Biomarker disease HPO
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		0.100 Biomarker disease HPO
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0085610
Disease: Sinus bradycardia
Sinus bradycardia 		0.100 Biomarker phenotype HPO
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block 		0.100 Biomarker disease HPO
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		0.100 Biomarker disease HPO
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		0.100 Biomarker disease HPO
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		0.100 Biomarker phenotype HPO
CUI: C1963175
Disease: Sinus Bradycardia, CTCAE
Sinus Bradycardia, CTCAE 		0.100 Biomarker phenotype HPO
CUI: C2108107
Disease: continuous electrocardiogram sinus bradycardia (finding)
continuous electrocardiogram sinus bradycardia (finding) 		0.100 Biomarker phenotype HPO
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		0.100 Biomarker phenotype HPO
CUI: C4310906
Disease: SICK SINUS SYNDROME 2 WITH CARDIAC NONCOMPACTION AND ASCENDING AORTA DILATION
SICK SINUS SYNDROME 2 WITH CARDIAC NONCOMPACTION AND ASCENDING AORTA DILATION 		0.100 CausalMutation disease CLINVAR
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.370 GeneticVariation disease BEFREE In a candidate gene approach, a heterozygous 1-bp deletion (1631delC) in exon 5 of the human HCN4 gene was detected in a patient with idiopathic SND. 12750403 2003