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: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 8 0.30 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 8 0.30 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 13 0.25 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure 		17 0 8 0.25 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 5 0.22 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 5 0.17 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 10 0.17 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes 		46 0 10 0.17 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 5 0.17 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 5 0.16 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 5 0.16 0 0
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 5 0.16 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes 		23 0 6 0.15 0 0
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		39 0 8 0.15 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies 		16 0 5 0.15 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 4 0.14 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 4 0.14 0 0
CUI: C4049830
Disease: Focal seizures, afebril
Focal seizures, afebril 		25 0 6 0.14 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 5 0.14 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		19 0 5 0.14 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		63 0 10 0.13 0 0
CUI: C1838063
Disease: Focal sensory auditory seizure
Focal sensory auditory seizure 		3 0 3 0.13 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 9 0.13 0 0
CUI: C0234974
Disease: Simple Partial Seizures
Simple Partial Seizures 		4 0 3 0.12 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 4 0.12 0 0