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: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction
35 26 20 0.37 2 3.8E-02
CUI: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy
9 0 6 0.14 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
83 0 15 0.14 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly
10 0 5 0.11 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur
31 0 7 0.11 0 0
CUI: C4551854
Disease: HYPOPLASTIC LEFT HEART SYNDROME 1
HYPOPLASTIC LEFT HEART SYNDROME 1
37 0 7 0.10 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome
48 0 8 0.10 0 0
CUI: C1839832
Disease: Noncompaction cardiomyopathy
Noncompaction cardiomyopathy
17 0 5 9.8E-02 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality
74 0 10 9.7E-02 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
18 27 5 9.6E-02 2 3.8E-02
CUI: C0011071
Disease: Sudden death
Sudden death
30 0 6 9.5E-02 0 0
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex
8 0 4 9.3E-02 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S
9 53 4 9.1E-02 1 1.3E-02
Arrhythmogenic Right Ventricular Dysplasia
82 0 10 9.0E-02 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy
10 0 4 8.9E-02 0 0
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter
13 2 4 8.3E-02 2 7.1E-02
CUI: C1280433
Disease: Lipoatrophy
Lipoatrophy
106 0 11 8.2E-02 0 0
NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1
3 2 3 7.7E-02 1 3.4E-02
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
176 0 15 7.5E-02 0 0
CUI: C0340486
Disease: Induced ventricular tachycardia
Induced ventricular tachycardia
4 0 3 7.5E-02 0 0
CUI: C0039070
Disease: Syncope
Syncope
119 45 11 7.5E-02 2 2.8E-02
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11
5 0 3 7.3E-02 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
66 0 7 7.1E-02 0 0
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
6 0 3 7.1E-02 0 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 0 4 7.1E-02 0 0