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: C1843146
Disease: Normal interictal EEG
Normal interictal EEG 		4 0 3 0.23 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 4 0.21 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 0 3 0.18 0 0
CUI: C0393676
Disease: Panayiotopoulos Syndrome
Panayiotopoulos Syndrome 		2 0 2 0.17 0 0
CUI: C1968848
Disease: Epilepsy, Familial Mesial Temporal Lobe
Epilepsy, Familial Mesial Temporal Lobe 		2 0 2 0.17 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 2 0.17 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		19 0 4 0.15 0 0
CUI: C1865926
Disease: Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) 		4 0 2 0.14 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 3 0.14 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 3 0.14 0 0
CUI: C1851936
Disease: Paroxysmal choreoathetosis
Paroxysmal choreoathetosis 		5 0 2 0.13 0 0
CUI: C0752210
Disease: Dyskinesias, Paroxysmal
Dyskinesias, Paroxysmal 		15 0 3 0.12 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 2 0.12 0 0
CUI: C3696898
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 		17 0 3 0.12 0 0
CUI: C0349251
Disease: Behavioral syndrome associated with physiological disturbance and physical factors
Behavioral syndrome associated with physiological disturbance and physical factors 		8 0 2 0.11 0 0
CUI: C4049262
Disease: Febrile infection related epilepsy syndrome
Febrile infection related epilepsy syndrome 		8 0 2 0.11 0 0
CUI: C4707658
Disease: Acute encephalopathy with biphasic seizures and late reduced diffusion
Acute encephalopathy with biphasic seizures and late reduced diffusion 		8 0 2 0.11 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 2 0.11 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 2 0.11 0 0
CUI: C0085541
Disease: Epilepsy, Frontal Lobe
Epilepsy, Frontal Lobe 		10 0 2 1.0E-01 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 2 1.0E-01 0 0
CUI: C1869117
Disease: Paroxysmal nonkinesigenic dyskinesia
Paroxysmal nonkinesigenic dyskinesia 		10 0 2 1.0E-01 0 0
CUI: C0392699
Disease: Dysesthesia
Dysesthesia 		22 0 3 9.7E-02 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 2 9.5E-02 0 0
CUI: C4014430
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 		11 0 2 9.5E-02 0 0