Source: ALL
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: C3279791
Disease: SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO
SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO 		1 0 1 0.14 0 0
CUI: C3665332
Disease: Primary hypertrophic cardiomyopathy
Primary hypertrophic cardiomyopathy 		1 0 1 0.14 0 0
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		1 0 1 0.14 0 0
CUI: C3808145
Disease: LEFT VENTRICULAR NONCOMPACTION 9
LEFT VENTRICULAR NONCOMPACTION 9 		1 0 1 0.14 0 0
CUI: C3809346
Disease: CARDIOMYOPATHY, DILATED, 1MM
CARDIOMYOPATHY, DILATED, 1MM 		1 0 1 0.14 0 0
CUI: C4016270
Disease: CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC 		1 0 1 0.14 0 0
CUI: C4023127
Disease: Toe extensor amyotrophy
Toe extensor amyotrophy 		1 0 1 0.14 0 0
CUI: C4023292
Disease: Imperforate tricuspid valve
Imperforate tricuspid valve 		1 0 1 0.14 0 0
CUI: C4025298
Disease: Effort-induced polymorphic ventricular tachycardias
Effort-induced polymorphic ventricular tachycardias 		1 0 1 0.14 0 0
CUI: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy 		9 0 2 0.14 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		10 0 2 0.13 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 0.12 0 0
CUI: C0751172
Disease: Adult Glycogen Storage Disease Type II
Adult Glycogen Storage Disease Type II 		2 0 1 0.12 0 0
CUI: C0751174
Disease: Glycogen Storage Disease Type II, Juvenile
Glycogen Storage Disease Type II, Juvenile 		2 0 1 0.12 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy 		2 0 1 0.12 0 0
CUI: C1839030
Disease: Weakness of orbicularis oculi muscle
Weakness of orbicularis oculi muscle 		2 0 1 0.12 0 0
CUI: C1841658
Disease: Progressive Familial Heart Block, Type II
Progressive Familial Heart Block, Type II 		2 0 1 0.12 0 0
CUI: C1868705
Disease: Shone complex
Shone complex 		2 0 1 0.12 0 0
CUI: C1963282
Disease: Wolff-Parkinson-White Syndrome, CTCAE
Wolff-Parkinson-White Syndrome, CTCAE 		2 0 1 0.12 0 0
CUI: C4023800
Disease: Limitation of movement at ankles
Limitation of movement at ankles 		2 0 1 0.12 0 0
CUI: C4024604
Disease: Amyotrophy of ankle musculature
Amyotrophy of ankle musculature 		2 0 1 0.12 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 4 0.12 0 0
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		31 0 4 0.12 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 0 5 0.12 0 0
CUI: C0031192
Disease: Persistent Ostium Primum
Persistent Ostium Primum 		3 0 1 0.11 0 0