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: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		56 13 9 8.0E-02 2 9.4E-03
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 7 7.4E-02 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		411 0 33 7.4E-02 0 0
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
Arrhythmogenic Right Ventricular Dysplasia 		82 0 10 7.2E-02 0 0
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		39 0 7 7.1E-02 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		559 111 41 7.0E-02 7 2.3E-02
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		11 0 5 6.9E-02 0 0
CUI: C2751898
Disease: Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Fibrillation, Paroxysmal Familial, 1 		42 8 7 6.9E-02 4 2.0E-02
CUI: C0428977
Disease: Bradycardia
Bradycardia 		63 0 8 6.6E-02 0 0
CUI: C0694539
Disease: Chronic atrial fibrillation
Chronic atrial fibrillation 		31 0 6 6.6E-02 0 0
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy 		15 0 5 6.6E-02 0 0
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE 		64 0 8 6.6E-02 0 0
CUI: C0030252
Disease: Palpitations
Palpitations 		70 0 8 6.2E-02 0 0
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		140 68 12 6.2E-02 7 2.7E-02
CUI: C0340464
Disease: Premature Cardiac Complex
Premature Cardiac Complex 		4 0 4 6.1E-02 0 0
CUI: C1721096
Disease: Brugada ECG Pattern
Brugada ECG Pattern 		4 0 4 6.1E-02 0 0
CUI: C3698186
Disease: Cardiac channelopathy
Cardiac channelopathy 		4 0 4 6.1E-02 0 0
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		75 226 8 6.0E-02 2 4.7E-03
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		41 11 6 5.9E-02 4 1.9E-02
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		226 0 16 5.8E-02 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		7 16 4 5.8E-02 10 4.8E-02
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 6 5.6E-02 0 0
CUI: C0429021
Disease: P wave duration (observable entity)
P wave duration (observable entity) 		10 0 4 5.6E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 5 5.4E-02 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		148 0 11 5.4E-02 0 0