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: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 6 0.38 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 6 0.38 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia 		7 14 5 0.33 1 4.5E-02
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 6 0.32 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 5 0.24 0 0
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		4 0 3 0.21 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 4 0.20 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 3 0.20 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 4 0.20 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 4 0.19 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 4 0.19 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		19 0 5 0.19 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 4 0.18 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		7 0 3 0.18 0 0
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 4 0.17 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 0 3 0.17 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		17 0 4 0.15 0 0
CUI: C0234241
Disease: Indifference to pain
Indifference to pain 		2 0 2 0.15 0 0
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		2 0 2 0.15 0 0
CUI: C2751756
Disease: Febrile Convulsions, Familial, 3a
Febrile Convulsions, Familial, 3a 		2 0 2 0.15 0 0
CUI: C2751778
Disease: Generalized Epilepsy With Febrile Seizures Plus, 7
Generalized Epilepsy With Febrile Seizures Plus, 7 		2 25 2 0.15 2 6.2E-02
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B 		2 0 2 0.15 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 2 0.15 0 0
CUI: C4012054
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID 		2 0 2 0.15 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 4 0.15 0 0