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: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 9 0.27 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 9 0.26 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 9 0.26 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 9 0.26 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 10 0.26 0 0
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 9 0.25 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes 		23 0 9 0.20 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 6 0.16 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 9 0.14 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 4 11 0.14 1 0.17
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 5 0.13 0 0
CUI: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		5 0 4 0.12 0 0
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		5 0 4 0.12 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		19 0 5 0.11 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 4 0.11 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 4 0.11 0 0
CUI: C0877017
Disease: Generalized tonic-clonic seizures with focal onset
Generalized tonic-clonic seizures with focal onset 		23 0 5 0.10 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 4 1.0E-01 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes 		46 0 7 1.0E-01 0 0
CUI: C3887527
Disease: Fused cervical vertebrae
Fused cervical vertebrae 		15 0 4 9.5E-02 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 14 9.3E-02 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 3 9.1E-02 0 0
CUI: C4085238
Disease: MYOCLONIC-ATONIC EPILEPSY
MYOCLONIC-ATONIC EPILEPSY 		6 0 3 8.8E-02 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 3 8.6E-02 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 6 8.5E-02 0 0