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: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 1.00 0 0
CUI: C2751195
Disease: Epilepsy, Benign Neonatal, 1, And-Or Myokymia
Epilepsy, Benign Neonatal, 1, And-Or Myokymia 		1 0 1 1.00 0 0
CUI: C3149074
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 		1 104 1 1.00 20 0.11
CUI: C3149075
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA 		1 2 1 1.00 1 1.1E-02
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 1 0.50 0 0
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome 		3 0 1 0.33 0 0
CUI: C3809278
Disease: EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET 		3 0 1 0.33 0 0
CUI: C4551769
Disease: Convulsions, Benign Familial Infantile, 1
Convulsions, Benign Familial Infantile, 1 		3 0 1 0.33 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		4 0 1 0.25 0 0
CUI: C3806403
Disease: Continuous spike and waves during slow sleep
Continuous spike and waves during slow sleep 		5 0 1 0.20 0 0
CUI: C0239488
Disease: Facial erythema
Facial erythema 		6 0 1 0.17 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		6 0 1 0.17 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 0 1 0.12 0 0
CUI: C1704431
Disease: Disorder of electrolytes
Disorder of electrolytes 		8 0 1 0.12 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 20 1 0.11 4 3.7E-02
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 7 1 0.11 1 1.0E-02
CUI: C0270855
Disease: Early myoclonic encephalopathy
Early myoclonic encephalopathy 		10 0 1 1.0E-01 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology 		10 0 1 1.0E-01 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 1 9.1E-02 0 0
CUI: C4014430
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 		11 76 1 9.1E-02 1 6.0E-03
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis 		12 0 1 8.3E-02 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 1 8.3E-02 0 0
CUI: C3463992
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 		12 0 1 8.3E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 1 7.7E-02 0 0
CUI: C0684219
Disease: Myokymia
Myokymia 		15 0 1 6.7E-02 0 0