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: C0349255
Disease: Nonorganic Insomnia
Nonorganic Insomnia 		4 0 4 1.00 0 0
CUI: C0393759
Disease: Transient Insomnia
Transient Insomnia 		4 0 4 1.00 0 0
CUI: C0751251
Disease: Secondary Insomnia
Secondary Insomnia 		4 0 4 1.00 0 0
CUI: C0751252
Disease: Sleep Initiation Dysfunction
Sleep Initiation Dysfunction 		4 0 4 1.00 0 0
CUI: C0751250
Disease: Psychophysiological Insomnia
Psychophysiological Insomnia 		5 0 4 0.80 0 0
CUI: C0751249
Disease: Chronic Insomnia
Chronic Insomnia 		6 0 4 0.67 0 0
CUI: C0033139
Disease: Primary Insomnia
Primary Insomnia 		7 0 4 0.57 0 0
CUI: C0541798
Disease: Early Awakening
Early Awakening 		10 0 4 0.40 0 0
CUI: C0021603
Disease: Sleep Initiation and Maintenance Disorders
Sleep Initiation and Maintenance Disorders 		15 0 4 0.27 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 0.25 0 0
CUI: C0860602
Disease: Anxious personality
Anxious personality 		1 0 1 0.25 0 0
CUI: C1834383
Disease: Thickening of the lateral border of the scapula
Thickening of the lateral border of the scapula 		1 0 1 0.25 0 0
CUI: C1834392
Disease: Disproportionate prominence of the femoral medial condyle
Disproportionate prominence of the femoral medial condyle 		1 0 1 0.25 0 0
CUI: C1868158
Disease: Absence of pectoralis minor muscle
Absence of pectoralis minor muscle 		1 0 1 0.25 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 0.25 0 0
CUI: C3805764
Disease: Biceps aplasia
Biceps aplasia 		1 0 1 0.25 0 0
CUI: C3805765
Disease: Quadriceps aplasia
Quadriceps aplasia 		1 0 1 0.25 0 0
CUI: C3810484
Disease: Triceps aplasia
Triceps aplasia 		1 0 1 0.25 0 0
CUI: C4024210
Disease: Lester's sign
Lester's sign 		1 0 1 0.25 0 0
CUI: C4025048
Disease: Elongated radius
Elongated radius 		1 0 1 0.25 0 0
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		1 0 1 0.25 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		2 0 1 0.20 0 0
CUI: C1834384
Disease: Glenoid fossa hypoplasia
Glenoid fossa hypoplasia 		2 0 1 0.20 0 0
CUI: C4021695
Disease: Hypoplastic radial head
Hypoplastic radial head 		2 0 1 0.20 0 0
CUI: C1834386
Disease: Hypoplasia of first ribs
Hypoplasia of first ribs 		3 0 1 0.17 0 0