Source: CURATED ×
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: C1721096
Disease: Brugada ECG Pattern
Brugada ECG Pattern 		4 0 2 0.33 0 0
CUI: C0006384
Disease: Bundle-Branch Block
Bundle-Branch Block 		1 0 1 0.25 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 11 1 0.25 6 0.29
CUI: C1837845
Disease: SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE 		1 10 1 0.25 3 0.13
CUI: C1858672
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 		1 0 1 0.25 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3 		1 153 1 0.25 7 4.3E-02
CUI: C1970298
Disease: Progressive Familial Heart Block, Type Ib
Progressive Familial Heart Block, Type Ib 		1 0 1 0.25 0 0
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		1 0 1 0.25 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5 		1 0 1 0.25 0 0
CUI: C2931401
Disease: Long QT syndrome type 3
Long QT syndrome type 3 		1 0 1 0.25 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 17 1 0.25 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 0.25 0 0
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.25 0 0
CUI: C3280795
Disease: HYPOPLASTIC LEFT HEART SYNDROME 2
HYPOPLASTIC LEFT HEART SYNDROME 2 		1 0 1 0.25 0 0
CUI: C3502353
Disease: Atrial Septal Defect with Atrioventricular Conduction Defects
Atrial Septal Defect with Atrioventricular Conduction Defects 		1 0 1 0.25 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 0 1 0.25 0 0
CUI: C4479236
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		1 0 1 0.25 0 0
CUI: C0266283
Disease: Ectopic thyroid tissue (disorder)
Ectopic thyroid tissue (disorder) 		2 0 1 0.20 0 0
CUI: C0541782
Disease: Atrial standstill
Atrial standstill 		2 0 1 0.20 0 0
CUI: C0685889
Disease: Splenic Hypoplasia
Splenic Hypoplasia 		2 0 1 0.20 0 0
CUI: C2751898
Disease: Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Fibrillation, Paroxysmal Familial, 1 		2 4 1 0.20 3 0.18
CUI: C2931574
Disease: Chromosome 5, monosomy 5q35
Chromosome 5, monosomy 5q35 		2 0 1 0.20 0 0
CUI: C4017668
Disease: VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO 		2 0 1 0.20 0 0
CUI: C4551959
Disease: ATRIAL STANDSTILL 1
ATRIAL STANDSTILL 1 		2 3 1 0.20 1 5.6E-02
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		3 0 1 0.17 0 0