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: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
559 111 53 8.5E-02 7 4.7E-02
Cardiomyopathy, Hypertrophic, Familial
83 0 15 8.0E-02 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
226 0 25 7.8E-02 0 0
CUI: C0428977
Disease: Bradycardia
Bradycardia
63 0 13 7.7E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction
35 26 11 7.7E-02 1 1.4E-02
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome
23 38 10 7.6E-02 4 5.1E-02
Left ventricular noncompaction cardiomyopathy
39 28 11 7.5E-02 2 2.8E-02
Ventricular tachycardia, polymorphic
11 11 9 7.4E-02 5 9.8E-02
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart
41 0 11 7.4E-02 0 0
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter
13 2 9 7.3E-02 2 4.4E-02
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval
13 0 9 7.3E-02 0 0
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
20 240 9 6.9E-02 9 3.3E-02
Arrhythmogenic Right Ventricular Dysplasia
82 0 13 6.9E-02 0 0
CUI: C0741923
Disease: cardiac event
cardiac event
82 0 13 6.9E-02 0 0
CUI: C0040264
Disease: Tinnitus
Tinnitus
103 14 14 6.7E-02 2 3.5E-02
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
10 0 8 6.6E-02 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation
156 0 17 6.6E-02 0 0
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
140 68 16 6.6E-02 4 3.7E-02
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation
157 0 17 6.6E-02 0 0
CUI: C0392188
Disease: Abnormal rapid eye movement sleep
Abnormal rapid eye movement sleep
11 0 8 6.6E-02 0 0
CUI: C4551761
Disease: Excessive daytime sleepiness
Excessive daytime sleepiness
46 0 10 6.5E-02 0 0
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome
30 0 9 6.4E-02 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 15 6.4E-02 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur
31 0 9 6.4E-02 0 0
Amelogenesis imperfecta nephrocalcinosis
19 0 8 6.2E-02 0 0