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: C0151878
Disease: Prolonged QT interval
Prolonged QT interval
5 0 3 0.43 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome
2 7 2 0.40 4 0.17
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
2 0 2 0.40 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC
2 0 2 0.40 0 0
LONG QT SYNDROME 1/2, DIGENIC (disorder)
2 0 2 0.40 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
3 103 2 0.33 3 2.5E-02
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
3 70 2 0.33 2 2.2E-02
Jervell And Lange-Nielsen Syndrome 1
3 18 2 0.33 2 5.4E-02
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
16 245 5 0.31 14 5.6E-02
CUI: C0039070
Disease: Syncope
Syncope
8 0 3 0.30 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
5 0 2 0.25 0 0
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
5 15 2 0.25 2 5.9E-02
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
5 73 2 0.25 5 5.6E-02
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia
1 0 1 0.20 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome
1 0 1 0.20 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
1 1 1 0.20 1 4.8E-02
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E
1 0 1 0.20 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3
1 10 1 0.20 1 3.3E-02
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
1 0 1 0.20 0 0
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
1 0 1 0.20 0 0
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
1 0 1 0.20 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3
1 30 1 0.20 1 2.0E-02
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive
1 0 1 0.20 0 0
Cardiac Conduction Defect, Nonprogressive
1 0 1 0.20 0 0
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder)
1 9 1 0.20 1 3.4E-02