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: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		7 0 7 0.78 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		7 0 7 0.78 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		9 0 5 0.38 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		13 0 4 0.22 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 0.11 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 0 1 0.11 0 0
CUI: C1858672
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 		1 0 1 0.11 0 0
CUI: C1858673
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 		1 0 1 0.11 0 0
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		1 0 1 0.11 0 0
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		1 0 1 0.11 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5 		1 0 1 0.11 0 0
CUI: C3150987
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 		1 0 1 0.11 0 0
CUI: C3554374
Disease: DYSTONIA 24
DYSTONIA 24 		1 0 1 0.11 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 0 1 0.11 0 0
CUI: C4015395
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9 		1 0 1 0.11 0 0
CUI: C4225245
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14 		1 0 1 0.11 0 0
CUI: C4225257
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34 		1 0 1 0.11 0 0
CUI: C4479236
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		1 0 1 0.11 0 0
CUI: C4747891
Disease: GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17 		1 0 1 0.11 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		2 0 1 1.0E-01 0 0
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		2 0 1 1.0E-01 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		3 0 1 9.1E-02 0 0
CUI: C2363129
Disease: Benign Rolandic Epilepsy
Benign Rolandic Epilepsy 		3 0 1 9.1E-02 0 0
CUI: C0393706
Disease: Early infantile epileptic encephalopathy with suppression bursts
Early infantile epileptic encephalopathy with suppression bursts 		16 0 2 8.7E-02 0 0
CUI: C0017332
Disease: Generalized Nonconvulsive Seizure Disorder
Generalized Nonconvulsive Seizure Disorder 		4 0 1 8.3E-02 0 0