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: C2216002
Disease: electrocardiogram left posterior hemiblock (finding)
electrocardiogram left posterior hemiblock (finding) 		1 0 1 0.14 0 0
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		1 0 1 0.14 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5 		1 0 1 0.14 0 0
CUI: C2930805
Disease: Sudden unexpected nocturnal death syndrome
Sudden unexpected nocturnal death syndrome 		1 0 1 0.14 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 17 1 0.14 5 0.18
CUI: C3276096
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		1 0 1 0.14 0 0
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.14 0 0
CUI: C3502353
Disease: Atrial Septal Defect with Atrioventricular Conduction Defects
Atrial Septal Defect with Atrioventricular Conduction Defects 		1 0 1 0.14 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 0 1 0.14 0 0
CUI: C3814825
Disease: Sudden Unexplained Infant Death
Sudden Unexplained Infant Death 		1 0 1 0.14 0 0
CUI: C4014393
Disease: CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS
CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS 		1 0 1 0.14 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 1 1 0.14 1 6.2E-02
CUI: C4310708
Disease: EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3
EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3 		1 0 1 0.14 0 0
CUI: C4476543
Disease: Complete heart block with broad QRS complexes
Complete heart block with broad QRS complexes 		1 0 1 0.14 0 0
CUI: C4479236
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		1 0 1 0.14 0 0
CUI: C4703660
Disease: Increased troponin I level in blood
Increased troponin I level in blood 		1 0 1 0.14 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change 		18 0 3 0.14 0 0
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		19 0 3 0.13 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 4 0.13 0 0
CUI: C0155708
Disease: Other specified conduction disorders
Other specified conduction disorders 		2 0 1 0.12 0 0
CUI: C0340850
Disease: Neurally mediated syncope
Neurally mediated syncope 		2 0 1 0.12 0 0
CUI: C0541782
Disease: Atrial standstill
Atrial standstill 		2 0 1 0.12 0 0
CUI: C0740281
Disease: Multiple allergies
Multiple allergies 		2 0 1 0.12 0 0
CUI: C1096378
Disease: Near sudden infant death syndrome
Near sudden infant death syndrome 		2 0 1 0.12 0 0
CUI: C1837845
Disease: SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE 		2 10 1 0.12 3 0.13