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: C0600125
Disease: Prolonged PR interval
Prolonged PR interval 		5 0 1 0.20 0 0
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		5 0 1 0.20 0 0
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		12 0 1 8.3E-02 0 0
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		12 0 1 8.3E-02 0 0
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		13 0 1 7.7E-02 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		13 0 1 7.7E-02 0 0
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		13 0 1 7.7E-02 0 0
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		22 0 1 4.5E-02 0 0
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		23 0 1 4.3E-02 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		23 0 1 4.3E-02 0 0
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		24 0 1 4.2E-02 0 0
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block 		26 0 1 3.8E-02 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 1 3.6E-02 0 0
CUI: C0391957
Disease: idiopathic epilepsy
idiopathic epilepsy 		30 0 1 3.3E-02 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 1 2.6E-02 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		40 0 1 2.5E-02 0 0
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia 		50 0 1 2.0E-02 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		51 0 1 2.0E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 1 1.8E-02 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		63 0 1 1.6E-02 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		66 0 1 1.5E-02 0 0
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		96 0 1 1.0E-02 0 0
CUI: C0039070
Disease: Syncope
Syncope 		119 0 1 8.4E-03 0 0
CUI: C0029882
Disease: Otitis Media
Otitis Media 		175 0 1 5.7E-03 0 0
CUI: C0270824
Disease: Visual seizure
Visual seizure 		209 0 1 4.8E-03 0 0