Source: CLINVAR ×
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: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		2 7 1 0.17 4 0.22
CUI: C0426440
Disease: Large nostrils
Large nostrils 		2 0 1 0.17 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		2 0 1 0.17 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC 		2 0 1 0.17 0 0
CUI: C3276241
Disease: LONG QT SYNDROME 3/6, DIGENIC Disorder
LONG QT SYNDROME 3/6, DIGENIC Disorder 		2 0 1 0.17 0 0
CUI: C3277700
Disease: LONG QT SYNDROME 1/2, DIGENIC (disorder)
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		2 0 1 0.17 0 0
CUI: C4021637
Disease: Abnormality of the nares
Abnormality of the nares 		2 0 1 0.17 0 0
CUI: C4021770
Disease: Clinodactyly of toe
Clinodactyly of toe 		2 0 1 0.17 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood 		2 0 1 0.17 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change 		18 0 3 0.15 0 0
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		3 0 1 0.14 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		3 0 1 0.14 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		3 0 1 0.14 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 103 1 0.14 2 1.7E-02
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		3 0 1 0.14 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		3 0 1 0.14 0 0
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2 		3 0 1 0.14 0 0
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		3 0 1 0.14 0 0
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		4 0 1 0.12 0 0
CUI: C4024923
Disease: Diffuse white matter abnormalities
Diffuse white matter abnormalities 		4 0 1 0.12 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		14 0 2 0.12 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		5 0 1 0.11 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		5 0 1 0.11 0 0
CUI: C1398312
Disease: Narrow palate
Narrow palate 		5 0 1 0.11 0 0
CUI: C1836906
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 		5 0 1 0.11 0 0