Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Paroxysmal familial ventricular fibrillation
18 0 11 0.15 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
18 0 11 0.15 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 11 0.15 0 0
Abnormality of prenatal development or birth
23 0 11 0.14 0 0
CUI: C1560305
Disease: Prolonged QTc interval
Prolonged QTc interval
25 0 11 0.14 0 0
CUI: C1963217
Disease: Prolonged QTc Interval, CTCAE
Prolonged QTc Interval, CTCAE
25 0 11 0.14 0 0
CUI: C1720983
Disease: Channelopathies
Channelopathies
94 8 18 0.13 2 9.7E-03
Amelogenesis imperfecta nephrocalcinosis
19 17 9 0.12 1 4.6E-03
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
133 0 21 0.12 0 0
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
20 0 9 0.12 0 0
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes
51 14 12 0.11 1 4.7E-03
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
22 0 9 0.11 0 0
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval
13 0 8 0.11 0 0
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome
23 38 9 0.11 1 4.2E-03
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation
25 0 9 0.11 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval
38 0 10 0.11 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia
61 0 12 0.10 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
63 17 12 0.10 1 4.6E-03
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
31 0 9 0.10 0 0
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
176 37 22 1.0E-01 4 1.7E-02
CUI: C0011071
Disease: Sudden death
Sudden death
30 0 8 9.1E-02 0 0
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
7 0 6 9.0E-02 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
10 0 6 8.6E-02 0 0
Ventricular tachycardia, polymorphic
11 11 6 8.5E-02 4 1.9E-02
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
13 0 6 8.2E-02 0 0