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: C2675462
Disease: Convulsions, Benign Familial Infantile, 4
Convulsions, Benign Familial Infantile, 4 		4 0 3 0.60 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 2 0.50 0 0
CUI: C1853995
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 2
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 		3 0 2 0.40 0 0
CUI: C4551769
Disease: Convulsions, Benign Familial Infantile, 1
Convulsions, Benign Familial Infantile, 1 		3 0 2 0.40 0 0
CUI: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 0.25 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 0.25 0 0
CUI: C2751195
Disease: Epilepsy, Benign Neonatal, 1, And-Or Myokymia
Epilepsy, Benign Neonatal, 1, And-Or Myokymia 		1 0 1 0.25 0 0
CUI: C3149074
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 		1 0 1 0.25 0 0
CUI: C3149075
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA 		1 0 1 0.25 0 0
CUI: C3150986
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 		1 0 1 0.25 0 0
CUI: C3150987
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 		1 65 1 0.25 33 0.42
CUI: C3494899
Disease: Early infantile epileptic encephalopathy, refractory
Early infantile epileptic encephalopathy, refractory 		1 0 1 0.25 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 1 2 0.20 1 2.2E-02
CUI: C1968848
Disease: Epilepsy, Familial Mesial Temporal Lobe
Epilepsy, Familial Mesial Temporal Lobe 		2 0 1 0.20 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 2 0.18 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 2 0.18 0 0
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome 		3 0 1 0.17 0 0
CUI: C3809278
Disease: EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET 		3 0 1 0.17 0 0
CUI: C4225398
Disease: CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY 		3 0 1 0.17 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 2 0.15 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 2 0.14 0 0
CUI: C0857345
Disease: Late onset epilepsy
Late onset epilepsy 		4 0 1 0.14 0 0
CUI: C1843146
Disease: Normal interictal EEG
Normal interictal EEG 		4 0 1 0.14 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 2 0.13 0 0
CUI: C2674512
Disease: Truncal titubation
Truncal titubation 		5 2 1 0.12 1 2.1E-02