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: C1832600
Disease: Naxos disease
Naxos disease
4 0 4 0.27 0 0
Ventricular Arrhythmia by ECG Finding
17 0 6 0.23 0 0
CUI: C1883529
Disease: Ventricular Arrhythmia, CTCAE 3.0
Ventricular Arrhythmia, CTCAE 3.0
17 0 6 0.23 0 0
CUI: C4553764
Disease: Ventricular Arrhythmia, CTCAE 5.0
Ventricular Arrhythmia, CTCAE 5.0
17 0 6 0.23 0 0
CUI: C0348617
Disease: Other cardiomyopathies
Other cardiomyopathies
4 0 3 0.19 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
18 0 5 0.18 0 0
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
5 0 3 0.18 0 0
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
5 0 3 0.18 0 0
CUI: C0519097
Disease: Left ventricular aneurysm
Left ventricular aneurysm
6 0 3 0.17 0 0
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
6 0 3 0.17 0 0
Dilatation of the ventricular cavity
6 0 3 0.17 0 0
CUI: C0232216
Disease: Ventricular escape rhythm
Ventricular escape rhythm
7 0 3 0.16 0 0
Paroxysmal familial ventricular fibrillation
18 0 4 0.14 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder)
10 0 3 0.14 0 0
CUI: C0541782
Disease: Atrial standstill
Atrial standstill
2 0 2 0.13 0 0
Epidermolysis bullosa, lethal acantholytic
2 0 2 0.13 0 0
CUI: C0235475
Disease: Wide QRS complex
Wide QRS complex
3 0 2 0.12 0 0
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)
3 0 2 0.12 0 0
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR
3 0 2 0.12 0 0
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
13 0 3 0.12 0 0
CUI: C0340486
Disease: Induced ventricular tachycardia
Induced ventricular tachycardia
4 0 2 0.12 0 0
CUI: C3698186
Disease: Cardiac channelopathy
Cardiac channelopathy
4 0 2 0.12 0 0
Arrhythmogenic Right Ventricular Dysplasia
82 0 10 0.11 0 0
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
5 0 2 0.11 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions
56 0 7 0.11 0 0