Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1 		20 0 5 0.13 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 3 0.13 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 3 0.13 0 0
CUI: C1865018
Disease: Short QT Syndrome 3
Short QT Syndrome 3 		3 9 3 0.13 8 0.21
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		3 0 3 0.13 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 3 0.13 0 0
CUI: C4053736
Disease: Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 		3 0 3 0.13 0 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		30 54 6 0.13 3 3.4E-02
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval 		13 0 4 0.12 0 0
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		22 0 5 0.12 0 0
CUI: C1865020
Disease: Short QT Syndrome 1
Short QT Syndrome 1 		4 0 3 0.12 0 0
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes 		51 14 8 0.12 3 6.1E-02
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		61 0 9 0.12 0 0
CUI: C1720983
Disease: Channelopathies
Channelopathies 		94 0 12 0.11 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		66 201 9 0.11 1 4.2E-03
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 3 0.11 0 0
CUI: C0751534
Disease: Syncopal Episode
Syncopal Episode 		7 0 3 0.11 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3 		7 0 3 0.11 0 0
CUI: C3150852
Disease: EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION 		7 0 3 0.11 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		18 10 4 0.11 4 9.1E-02
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		18 0 4 0.11 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		18 11 4 0.11 4 8.9E-02
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		19 0 4 0.11 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		10 0 3 1.0E-01 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		56 13 7 9.7E-02 1 2.0E-02