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: C1405458
Disease: Language Problems
Language Problems 		0 2 0 0 1 4.6E-03
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 2.2E-03 0 0
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise 		133 0 1 2.2E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.2E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.2E-03 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 1 2.2E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 2.2E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 2.3E-03 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney 		121 0 1 2.3E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.3E-03 0 0
CUI: C3839280
Disease: High grade serous carcinoma
High grade serous carcinoma 		118 0 1 2.3E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 1 2.3E-03 0 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		112 0 1 2.3E-03 0 0
CUI: C3495676
Disease: Anorectal Malformations
Anorectal Malformations 		112 0 1 2.3E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 2.3E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 2.3E-03 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 1 2.3E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 2.4E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 2.4E-03 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain 		103 0 1 2.4E-03 0 0
CUI: C1849265
Disease: Overgrowth
Overgrowth 		103 0 1 2.4E-03 0 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy 		97 0 1 2.4E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula 		97 0 1 2.4E-03 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		96 0 1 2.4E-03 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 0 1 2.4E-03 0 0