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: C0017332
Disease: Generalized Nonconvulsive Seizure Disorder
Generalized Nonconvulsive Seizure Disorder 		4 0 4 1.00 0 0
CUI: C0086241
Disease: Epilepsy, Tonic
Epilepsy, Tonic 		4 0 4 1.00 0 0
CUI: C0347869
Disease: Epilepsy, Akinetic
Epilepsy, Akinetic 		4 0 4 1.00 0 0
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 4 0.80 0 0
CUI: C0311334
Disease: Generalized convulsive epilepsy
Generalized convulsive epilepsy 		6 0 4 0.67 0 0
CUI: C4551857
Disease: Juvenile Myoclonic Epilepsy of Janz
Juvenile Myoclonic Epilepsy of Janz 		4 0 2 0.33 0 0
CUI: C4552768
Disease: Myoclonic Epilepsy, Adolescent
Myoclonic Epilepsy, Adolescent 		4 0 2 0.33 0 0
CUI: C4553087
Disease: Myoclonic Epilepsy, Juvenile, 1
Myoclonic Epilepsy, Juvenile, 1 		4 0 2 0.33 0 0
CUI: C4553298
Disease: Impulsive Petit Mal Epilepsy
Impulsive Petit Mal Epilepsy 		4 0 2 0.33 0 0
CUI: C1839565
Disease: Optic Atrophy Spastic Paraplegia Syndrome
Optic Atrophy Spastic Paraplegia Syndrome 		1 0 1 0.25 0 0
CUI: C1866039
Disease: EPISODIC ATAXIA, TYPE 5
EPISODIC ATAXIA, TYPE 5 		1 0 1 0.25 0 0
CUI: C2750887
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9 		1 0 1 0.25 0 0
CUI: C2750888
Disease: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6 		1 0 1 0.25 0 0
CUI: C2751729
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7 		1 0 1 0.25 0 0
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 0.25 0 0
CUI: C3827273
Disease: Sudden Unexplained Death in Childhood
Sudden Unexplained Death in Childhood 		1 0 1 0.25 0 0
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		7 0 2 0.22 0 0
CUI: C0393676
Disease: Panayiotopoulos Syndrome
Panayiotopoulos Syndrome 		2 0 1 0.20 0 0
CUI: C0750942
Disease: Auditory Inattention
Auditory Inattention 		2 0 1 0.20 0 0
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		2 0 1 0.20 0 0
CUI: C2751756
Disease: Febrile Convulsions, Familial, 3a
Febrile Convulsions, Familial, 3a 		2 0 1 0.20 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 1 0.20 0 0
CUI: C3698357
Disease: Refractory myoclonic epilepsy
Refractory myoclonic epilepsy 		2 0 1 0.20 0 0
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		2 0 1 0.20 0 0
CUI: C0270857
Disease: Epilepsy, Reflex
Epilepsy, Reflex 		3 0 1 0.17 0 0