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: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures
12 0 8 0.19 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status
12 0 8 0.19 0 0
Generalized tonic-clonic seizures with focal onset
23 0 8 0.15 0 0
Complex partial seizure with impairment of consciousness
41 10 10 0.14 1 3.0E-02
CUI: C1844690
Disease: Limited knee extension
Limited knee extension
11 0 5 0.11 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion
12 0 5 0.11 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes
23 0 6 0.11 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple
13 0 5 0.11 0 0
Generalized Epilepsy with Febrile Seizures Plus
13 0 5 0.11 0 0
Generalized cerebral atrophy/hypoplasia
14 0 5 0.10 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes
46 0 8 0.10 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures
5 0 4 1.0E-01 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait
18 0 5 9.6E-02 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex
19 0 5 9.4E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
57 0 8 9.1E-02 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
9 0 4 9.1E-02 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
9 0 4 9.1E-02 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 81 7 9.0E-02 1 9.6E-03
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 8 8.9E-02 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile
11 0 4 8.7E-02 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy
63 0 8 8.5E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER
13 0 4 8.3E-02 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation
98 0 10 7.9E-02 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies
16 0 4 7.8E-02 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure
17 0 4 7.7E-02 0 0