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: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy 		94 0 11 0.11 0 0
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis 		12 0 3 0.11 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 3 0.11 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 3 0.11 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 2 0.11 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 2 0.11 0 0
CUI: C4310728
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 5
SEIZURES, BENIGN FAMILIAL INFANTILE, 5 		2 0 2 0.11 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple 		13 0 3 0.10 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 3 0.10 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness 		35 0 5 0.10 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 7 0.10 0 0
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome 		3 0 2 1.0E-01 0 0
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 3 1.0E-01 0 0
CUI: C4551769
Disease: Convulsions, Benign Familial Infantile, 1
Convulsions, Benign Familial Infantile, 1 		3 0 2 1.0E-01 0 0
CUI: C0017332
Disease: Generalized Nonconvulsive Seizure Disorder
Generalized Nonconvulsive Seizure Disorder 		4 0 2 9.5E-02 0 0
CUI: C0086236
Disease: Epilepsy, Atonic
Epilepsy, Atonic 		4 0 2 9.5E-02 0 0
CUI: C0086241
Disease: Epilepsy, Tonic
Epilepsy, Tonic 		4 0 2 9.5E-02 0 0
CUI: C0347869
Disease: Epilepsy, Akinetic
Epilepsy, Akinetic 		4 0 2 9.5E-02 0 0
CUI: C1843140
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		4 0 2 9.5E-02 0 0
CUI: C1865926
Disease: Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) 		4 0 2 9.5E-02 0 0
CUI: C2675462
Disease: Convulsions, Benign Familial Infantile, 4
Convulsions, Benign Familial Infantile, 4 		4 0 2 9.5E-02 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia 		63 0 7 9.3E-02 0 0
CUI: C0004310
Disease: Auditory Perceptual Disorders
Auditory Perceptual Disorders 		5 0 2 9.1E-02 0 0
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 2 9.1E-02 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 2 9.1E-02 0 0