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: C4049262
Disease: Febrile infection related epilepsy syndrome
Febrile infection related epilepsy syndrome 		8 0 4 0.33 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 4 0.25 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 2 0.25 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 4 0.25 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 4 0.24 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 3 0.21 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 3 0.21 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		4 46 2 0.20 1 2.2E-02
CUI: C1843146
Disease: Normal interictal EEG
Normal interictal EEG 		4 0 2 0.20 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 3 0.19 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 3 0.19 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 3 0.18 0 0
CUI: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		12 0 3 0.18 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		19 0 4 0.17 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		19 0 4 0.17 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 3 0.17 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		6 0 2 0.17 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 3 0.17 0 0
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 3 0.16 0 0
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		7 0 2 0.15 0 0
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures 		30 0 5 0.15 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies 		16 0 3 0.14 0 0
CUI: C1704431
Disease: Disorder of electrolytes
Disorder of electrolytes 		8 0 2 0.14 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 3 0.14 0 0
CUI: C2129214
Disease: Loose stool
Loose stool 		8 0 2 0.14 0 0