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: C0234512
Disease: Prosopagnosia
Prosopagnosia 		0 2 0 0 2 1.7E-02
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 8.5E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 8.5E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 8.5E-03
CUI: C4546209
Disease: Chronic pain following trauma
Chronic pain following trauma 		0 1 0 0 1 8.5E-03
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 1.9E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 1.9E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 1.9E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 1.9E-03 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		96 0 1 1.9E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		96 0 1 1.9E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 2.0E-03 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		91 0 1 2.0E-03 0 0
CUI: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive 		91 0 1 2.0E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 1 2.0E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 2.0E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 2.0E-03 0 0
CUI: C0431371
Disease: Absence of septum pellucidum
Absence of septum pellucidum 		84 0 1 2.0E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 2.0E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 2.0E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 2.0E-03 0 0
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		77 0 1 2.0E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 1 2.0E-03 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 1 2.0E-03 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 1 2.0E-03 0 0