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: C1858672
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 		1 5 1 1.00 2 0.33
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 3 1 1.00 2 0.50
CUI: C4479236
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		1 4 1 1.00 2 0.40
CUI: C0232310
Disease: P mitrale (finding)
P mitrale (finding) 		3 0 1 0.33 0 0
CUI: C0238705
Disease: Left atrial hypertrophy
Left atrial hypertrophy 		3 0 1 0.33 0 0
CUI: C2721586
Disease: Sudden arrhythmic death syndrome
Sudden arrhythmic death syndrome 		3 0 1 0.33 0 0
CUI: C1721096
Disease: Brugada ECG Pattern
Brugada ECG Pattern 		4 0 1 0.25 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 1 0.20 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		7 0 1 0.14 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 0.11 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 0.11 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 1 9.1E-02 0 0
CUI: C0006384
Disease: Bundle-Branch Block
Bundle-Branch Block 		12 0 1 8.3E-02 0 0
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		12 0 1 8.3E-02 0 0
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		12 0 1 8.3E-02 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 1 8.3E-02 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 1 8.3E-02 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 1 8.3E-02 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 1 7.7E-02 0 0
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		13 0 1 7.7E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 1 7.7E-02 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		13 0 1 7.7E-02 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 13 1 7.7E-02 1 6.7E-02
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		13 0 1 7.7E-02 0 0
CUI: C1848980
Disease: Developmental stagnation
Developmental stagnation 		14 0 1 7.1E-02 0 0