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: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal 		7 0 7 1.00 0 0
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical 		8 0 7 0.88 0 0
CUI: C4552765
Disease: Epilepsy, Minor
Epilepsy, Minor 		8 0 7 0.88 0 0
CUI: C4317339
Disease: Juvenile Absence Epilepsy
Juvenile Absence Epilepsy 		13 0 7 0.54 0 0
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1 		6 0 3 0.30 0 0
CUI: C4023685
Disease: EEG with spike-wave complexes (2.5-3.5 Hz)
EEG with spike-wave complexes (2.5-3.5 Hz) 		6 0 3 0.30 0 0
CUI: C1854686
Disease: Uncontrolled eye movements
Uncontrolled eye movements 		7 0 3 0.27 0 0
CUI: C1963933
Disease: Punding
Punding 		7 0 3 0.27 0 0
CUI: C4551857
Disease: Juvenile Myoclonic Epilepsy of Janz
Juvenile Myoclonic Epilepsy of Janz 		4 0 2 0.22 0 0
CUI: C4552768
Disease: Myoclonic Epilepsy, Adolescent
Myoclonic Epilepsy, Adolescent 		4 0 2 0.22 0 0
CUI: C4553087
Disease: Myoclonic Epilepsy, Juvenile, 1
Myoclonic Epilepsy, Juvenile, 1 		4 0 2 0.22 0 0
CUI: C4553298
Disease: Impulsive Petit Mal Epilepsy
Impulsive Petit Mal Epilepsy 		4 0 2 0.22 0 0
CUI: C0679136
Disease: Low self-esteem
Low self-esteem 		10 0 3 0.21 0 0
CUI: C1855568
Disease: Jerky head movements
Jerky head movements 		10 0 3 0.21 0 0
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy 		33 0 7 0.21 0 0
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 2 0.20 0 0
CUI: C4023701
Disease: Impaired visuospatial constructive cognition
Impaired visuospatial constructive cognition 		15 0 3 0.16 0 0
CUI: C4477055
Disease: Limb myoclonus
Limb myoclonus 		15 0 3 0.16 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 0.14 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.14 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.14 0 0
CUI: C0855389
Disease: Renin decreased
Renin decreased 		1 0 1 0.14 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.14 0 0
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		1 0 1 0.14 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 0.14 0 0