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: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 1.00 0 0
CUI: C0270541
Disease: Rebound Insomnia
Rebound Insomnia 		4 0 1 0.25 0 0
CUI: C0349255
Disease: Nonorganic Insomnia
Nonorganic Insomnia 		4 0 1 0.25 0 0
CUI: C0393759
Disease: Transient Insomnia
Transient Insomnia 		4 0 1 0.25 0 0
CUI: C0751251
Disease: Secondary Insomnia
Secondary Insomnia 		4 0 1 0.25 0 0
CUI: C0751252
Disease: Sleep Initiation Dysfunction
Sleep Initiation Dysfunction 		4 0 1 0.25 0 0
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 1 0.20 0 0
CUI: C0751250
Disease: Psychophysiological Insomnia
Psychophysiological Insomnia 		5 0 1 0.20 0 0
CUI: C0751249
Disease: Chronic Insomnia
Chronic Insomnia 		6 0 1 0.17 0 0
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1 		6 0 1 0.17 0 0
CUI: C4023479
Disease: EEG with focal sharp slow waves
EEG with focal sharp slow waves 		6 0 1 0.17 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 1 0.17 0 0
CUI: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal 		7 0 1 0.14 0 0
CUI: C0033139
Disease: Primary Insomnia
Primary Insomnia 		7 0 1 0.14 0 0
CUI: C1854686
Disease: Uncontrolled eye movements
Uncontrolled eye movements 		7 0 1 0.14 0 0
CUI: C1963933
Disease: Punding
Punding 		7 0 1 0.14 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 1 0.14 0 0
CUI: C4553705
Disease: Absence Seizure Disorder
Absence Seizure Disorder 		7 0 1 0.14 0 0
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical 		8 0 1 0.12 0 0
CUI: C4552765
Disease: Epilepsy, Minor
Epilepsy, Minor 		8 0 1 0.12 0 0
CUI: C0541798
Disease: Early Awakening
Early Awakening 		10 0 1 1.0E-01 0 0
CUI: C0679136
Disease: Low self-esteem
Low self-esteem 		10 0 1 1.0E-01 0 0
CUI: C1855568
Disease: Jerky head movements
Jerky head movements 		10 0 1 1.0E-01 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 1 9.1E-02 0 0
CUI: C0795875
Disease: Chromosome 21 monosomy
Chromosome 21 monosomy 		13 0 1 7.7E-02 0 0