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: C0685108
Disease: Lenegre's disease
Lenegre's disease
1 0 1 0.50 0 0
CUI: C0748694
Disease: sick sinus
sick sinus
1 0 1 0.50 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E
1 11 1 0.50 1 7.7E-02
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
1 0 1 0.50 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive
1 0 1 0.50 0 0
Cardiac Conduction Defect, Nonprogressive
1 0 1 0.50 0 0
CUI: C2114320
Disease: preterm contractions
preterm contractions
1 0 1 0.50 0 0
electrocardiogram left posterior hemiblock (finding)
1 0 1 0.50 0 0
Sudden unexpected nocturnal death syndrome
1 0 1 0.50 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10
1 17 1 0.50 1 5.3E-02
CUI: C3279693
Disease: ATRIAL FIBRILLATION, FAMILIAL, 11
ATRIAL FIBRILLATION, FAMILIAL, 11
1 0 1 0.50 0 0
CUI: C3814825
Disease: Sudden Unexplained Infant Death
Sudden Unexplained Infant Death
1 0 1 0.50 0 0
CUI: C4015977
Disease: ATRIAL FIBRILLATION, SOMATIC
ATRIAL FIBRILLATION, SOMATIC
1 1 1 0.50 1 0.33
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC
1 1 1 0.50 1 0.33
Complete heart block with broad QRS complexes
1 0 1 0.50 0 0
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
5 0 2 0.40 0 0
Other specified conduction disorders
2 0 1 0.33 0 0
CUI: C0340850
Disease: Neurally mediated syncope
Neurally mediated syncope
2 0 1 0.33 0 0
CUI: C0541782
Disease: Atrial standstill
Atrial standstill
2 0 1 0.33 0 0
CUI: C0683382
Disease: renin-dependent hypertension
renin-dependent hypertension
2 1 1 0.33 1 0.33
CUI: C1096378
Disease: Near sudden infant death syndrome
Near sudden infant death syndrome
2 0 1 0.33 0 0
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
2 0 1 0.33 0 0
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
2 0 1 0.33 0 0
CUI: C2931401
Disease: Long QT syndrome type 3
Long QT syndrome type 3
2 0 1 0.33 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC
2 0 1 0.33 0 0