Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		1.000 Biomarker disease CTD_human
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		0.720 Biomarker disease GENOMICS_ENGLAND
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		0.720 GeneticVariation disease CLINVAR
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		0.720 CausalMutation disease CLINVAR
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		0.720 Biomarker disease CTD_human
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 CausalMutation disease CLINVAR
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 GeneticVariation disease CLINVAR
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker disease CTD_human
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		0.700 Biomarker disease CTD_human
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		0.700 GeneticVariation disease CLINVAR
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		0.520 Biomarker disease GENOMICS_ENGLAND
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		0.500 Biomarker disease CTD_human
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		0.500 CausalMutation disease CLINVAR
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		0.500 GeneticVariation disease CLINVAR
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		0.390 Biomarker disease GENOMICS_ENGLAND
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		0.300 SusceptibilityMutation disease CLINVAR
CUI: C3277700
Disease: LONG QT SYNDROME 1/2, DIGENIC (disorder)
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		0.300 CausalMutation disease CLINVAR
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.200 CausalMutation phenotype CLINVAR
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.200 Biomarker disease HPO
CUI: C0039070
Disease: Syncope
Syncope 		0.200 Biomarker phenotype HPO
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		0.200 GeneticVariation disease CLINVAR
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2 		0.200 CausalMutation disease CLINVAR