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: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 8 7 0.24 3 7.0E-02
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 6 0.22 0 0
CUI: C4477077
Disease: Abnormal cardiac exercise stress test
Abnormal cardiac exercise stress test 		16 0 7 0.22 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		31 0 9 0.20 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		38 0 10 0.20 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave 		20 0 7 0.19 0 0
CUI: C1963175
Disease: Sinus Bradycardia, CTCAE
Sinus Bradycardia, CTCAE 		20 0 7 0.19 0 0
CUI: C2108107
Disease: continuous electrocardiogram sinus bradycardia (finding)
continuous electrocardiogram sinus bradycardia (finding) 		20 0 7 0.19 0 0
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		22 0 7 0.18 0 0
CUI: C0085610
Disease: Sinus bradycardia
Sinus bradycardia 		22 0 7 0.18 0 0
CUI: C4025797
Disease: Abnormality of prenatal development or birth
Abnormality of prenatal development or birth 		23 0 7 0.18 0 0
CUI: C0340464
Disease: Premature Cardiac Complex
Premature Cardiac Complex 		4 0 4 0.17 0 0
CUI: C3698186
Disease: Cardiac channelopathy
Cardiac channelopathy 		4 0 4 0.17 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		11 0 5 0.17 0 0
CUI: C0344432
Disease: Ventricular tachycardia, polymorphic
Ventricular tachycardia, polymorphic 		11 11 5 0.17 5 0.11
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change 		18 0 6 0.17 0 0
CUI: C1560305
Disease: Prolonged QTc interval
Prolonged QTc interval 		25 0 7 0.17 0 0
CUI: C1963217
Disease: Prolonged QTc Interval, CTCAE
Prolonged QTc Interval, CTCAE 		25 0 7 0.17 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 4 0.17 0 0
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2 		13 0 5 0.16 0 0
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 4 0.15 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 4 0.14 0 0
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation 		25 0 6 0.14 0 0
CUI: C1560249
Disease: Adverse Event Associated with Cardiac Arrhythmia
Adverse Event Associated with Cardiac Arrhythmia 		42 0 8 0.14 0 0
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 23 7 0.13 3 5.2E-02