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: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
9 0 4 0.25 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
9 0 4 0.25 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
11 0 4 0.22 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures
12 0 4 0.21 0 0
Sudden unexplained death in epilepsy
12 0 4 0.21 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy
19 0 5 0.20 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER
13 0 4 0.20 0 0
Epilepsy of infancy with migrating focal seizures
7 0 3 0.20 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure
8 0 3 0.19 0 0
CUI: C0393676
Disease: Panayiotopoulos Syndrome
Panayiotopoulos Syndrome
2 0 2 0.18 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory
2 0 2 0.18 0 0
SCN8A-related epilepsy with encephalopathy
2 0 2 0.18 0 0
SEIZURES, BENIGN FAMILIAL INFANTILE, 5
2 0 2 0.18 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn
17 0 4 0.17 0 0
CUI: C0270855
Disease: Early myoclonic encephalopathy
Early myoclonic encephalopathy
10 0 3 0.17 0 0
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
17 0 4 0.17 0 0
SEIZURES, BENIGN FAMILIAL INFANTILE, 3
4 0 2 0.15 0 0
CUI: C1843146
Disease: Normal interictal EEG
Normal interictal EEG
4 0 2 0.15 0 0
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis
12 0 3 0.15 0 0
Generalized Epilepsy with Febrile Seizures Plus
13 0 3 0.14 0 0
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
30 0 5 0.14 0 0
CUI: C0392699
Disease: Dysesthesia
Dysesthesia
22 0 4 0.14 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy
6 0 2 0.13 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies
16 0 3 0.12 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1
16 0 3 0.12 0 0