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: C0270541
Disease: Rebound Insomnia
Rebound Insomnia 		4 0 4 0.27 0 0
CUI: C0349255
Disease: Nonorganic Insomnia
Nonorganic Insomnia 		4 0 4 0.27 0 0
CUI: C0393759
Disease: Transient Insomnia
Transient Insomnia 		4 0 4 0.27 0 0
CUI: C0751251
Disease: Secondary Insomnia
Secondary Insomnia 		4 0 4 0.27 0 0
CUI: C0751252
Disease: Sleep Initiation Dysfunction
Sleep Initiation Dysfunction 		4 0 4 0.27 0 0
CUI: C0751250
Disease: Psychophysiological Insomnia
Psychophysiological Insomnia 		5 0 4 0.25 0 0
CUI: C0751249
Disease: Chronic Insomnia
Chronic Insomnia 		6 3 4 0.24 1 3.6E-02
CUI: C0033139
Disease: Primary Insomnia
Primary Insomnia 		7 0 4 0.22 0 0
CUI: C0541798
Disease: Early Awakening
Early Awakening 		10 0 4 0.19 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 6.7E-02 0 0
CUI: C0860602
Disease: Anxious personality
Anxious personality 		1 0 1 6.7E-02 0 0
CUI: C1561993
Disease: Valvular sclerosis
Valvular sclerosis 		1 0 1 6.7E-02 0 0
CUI: C1834383
Disease: Thickening of the lateral border of the scapula
Thickening of the lateral border of the scapula 		1 0 1 6.7E-02 0 0
CUI: C1834392
Disease: Disproportionate prominence of the femoral medial condyle
Disproportionate prominence of the femoral medial condyle 		1 0 1 6.7E-02 0 0
CUI: C1868158
Disease: Absence of pectoralis minor muscle
Absence of pectoralis minor muscle 		1 0 1 6.7E-02 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 6.7E-02 0 0
CUI: C2677325
Disease: RETINITIS PIGMENTOSA 29 (disorder)
RETINITIS PIGMENTOSA 29 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C3554018
Disease: SINOATRIAL NODE DYSFUNCTION AND DEAFNESS
SINOATRIAL NODE DYSFUNCTION AND DEAFNESS 		1 0 1 6.7E-02 0 0
CUI: C3805764
Disease: Biceps aplasia
Biceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C3805765
Disease: Quadriceps aplasia
Quadriceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C3809609
Disease: PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES
PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C3810484
Disease: Triceps aplasia
Triceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C4014833
Disease: IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C4016698
Disease: IMMUNODEFICIENCY 26 WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C4024210
Disease: Lester's sign
Lester's sign 		1 0 1 6.7E-02 0 0