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: C0155707
Disease: Trifascicular block
Trifascicular block
23 0 9 8.3E-02 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding)
23 0 9 8.3E-02 0 0
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
62 0 12 8.3E-02 0 0
Abnormality of prenatal development or birth
23 0 9 8.3E-02 0 0
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE
64 0 12 8.2E-02 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular
104 0 15 8.2E-02 0 0
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation
25 0 9 8.2E-02 0 0
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block
26 0 9 8.1E-02 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
40 7 10 8.1E-02 1 7.1E-02
AV Block First Degree by ECG Finding
28 0 9 8.0E-02 0 0
CUI: C0030252
Disease: Palpitations
Palpitations
70 0 12 7.9E-02 0 0
CUI: C0039231
Disease: Tachycardia
Tachycardia
73 0 12 7.7E-02 0 0
CUI: C0238358
Disease: Hypokalemic periodic paralysis
Hypokalemic periodic paralysis
19 0 8 7.6E-02 0 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
133 0 16 7.6E-02 0 0
CUI: C0428977
Disease: Bradycardia
Bradycardia
63 0 11 7.5E-02 0 0
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
24 0 8 7.3E-02 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block
39 0 9 7.3E-02 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
10 0 7 7.2E-02 0 0
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
176 0 18 7.1E-02 0 0
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval
13 0 7 7.0E-02 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
63 0 10 6.8E-02 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
18 0 7 6.7E-02 0 0
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
22 0 7 6.4E-02 0 0
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
94 0 11 6.2E-02 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia
148 0 14 6.1E-02 0 0