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: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 0 1 1.7E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 1.7E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 1.7E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		160 0 1 1.8E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.8E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 1.8E-03 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 1 1.9E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 1.9E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		123 0 1 1.9E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 1.9E-03 0 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		112 0 1 2.0E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 2.0E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 2.0E-03 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		105 0 1 2.0E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		104 0 1 2.0E-03 0 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		104 0 1 2.0E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 2.0E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 2.0E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 2.0E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 2.0E-03 0 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		96 0 1 2.0E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 2.0E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.0E-03 0 0
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure 		91 0 1 2.0E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 2.0E-03 0 0