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: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
10 5 7 6.5E-02 1 2.8E-03
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE
64 0 10 6.3E-02 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
226 0 19 6.1E-02 0 0
CUI: C0030252
Disease: Palpitations
Palpitations
70 0 10 6.1E-02 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
411 50 29 6.0E-02 11 2.8E-02
Arrhythmogenic Right Ventricular Dysplasia
82 0 10 5.6E-02 0 0
Hypertrophic obstructive cardiomyopathy
233 0 18 5.6E-02 0 0
Cardiomyopathy, Hypertrophic, Familial
83 355 10 5.6E-02 1 1.4E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
560 635 35 5.6E-02 1 1.0E-03
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval
13 0 6 5.4E-02 0 0
CUI: C2732979
Disease: Acquired long QT syndrome
Acquired long QT syndrome
14 8 6 5.3E-02 3 8.5E-03
QT interval feature (observable entity)
75 226 9 5.3E-02 4 7.0E-03
Amelogenesis imperfecta nephrocalcinosis
19 0 6 5.1E-02 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 11 8 4.7E-02 1 2.8E-03
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
7 0 5 4.7E-02 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
9 0 5 4.6E-02 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
9 0 5 4.6E-02 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
80 0 8 4.5E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction
35 0 6 4.5E-02 0 0
CUI: C0741923
Disease: cardiac event
cardiac event
82 18 8 4.5E-02 5 1.4E-02
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
12 0 5 4.5E-02 0 0
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias
12 0 5 4.5E-02 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
83 0 8 4.4E-02 0 0
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm
13 0 5 4.4E-02 0 0
NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME
13 0 5 4.4E-02 0 0