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: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 1.00 0 0
CUI: C3494899
Disease: Early infantile epileptic encephalopathy, refractory
Early infantile epileptic encephalopathy, refractory 		1 0 1 1.00 0 0
CUI: C1968848
Disease: Epilepsy, Familial Mesial Temporal Lobe
Epilepsy, Familial Mesial Temporal Lobe 		2 0 1 0.50 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 1 0.50 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 0.33 0 0
CUI: C0857345
Disease: Late onset epilepsy
Late onset epilepsy 		4 0 1 0.25 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		4 46 1 0.25 33 0.42
CUI: C1843146
Disease: Normal interictal EEG
Normal interictal EEG 		4 0 1 0.25 0 0
CUI: C2675462
Disease: Convulsions, Benign Familial Infantile, 4
Convulsions, Benign Familial Infantile, 4 		4 0 1 0.25 0 0
CUI: C2674512
Disease: Truncal titubation
Truncal titubation 		5 2 1 0.20 1 1.5E-02
CUI: C3539063
Disease: Bart's Hemoglobinopathy
Bart's Hemoglobinopathy 		5 0 1 0.20 0 0
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		7 0 1 0.14 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 1 0.14 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 0 1 0.12 0 0
CUI: C4049262
Disease: Febrile infection related epilepsy syndrome
Febrile infection related epilepsy syndrome 		8 0 1 0.12 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 1 0.12 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 0.11 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 0.11 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 1 9.1E-02 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 1 9.1E-02 0 0
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section 		11 15 1 9.1E-02 1 1.3E-02
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		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: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		12 0 1 8.3E-02 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 1 8.3E-02 0 0