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: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 4.1E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula 		97 0 1 4.2E-03 0 0
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis 		96 0 1 4.2E-03 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		96 0 1 4.2E-03 0 0
CUI: C0026946
Disease: Mycoses
Mycoses 		94 0 1 4.2E-03 0 0
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome 		94 0 1 4.2E-03 0 0
CUI: C1720983
Disease: Channelopathies
Channelopathies 		94 0 1 4.2E-03 0 0
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
Aspirin exacerbated respiratory disease 		94 0 1 4.2E-03 0 0
CUI: C0438696
Disease: Suicidal
Suicidal 		93 0 1 4.2E-03 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism 		92 0 1 4.3E-03 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		91 0 1 4.3E-03 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 0 1 4.3E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 4.3E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 1 4.3E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 1 4.3E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 1 4.3E-03 0 0
CUI: C0019572
Disease: Hirsutism
Hirsutism 		88 0 1 4.3E-03 0 0
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		87 0 1 4.3E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 4.3E-03 0 0
CUI: C4553962
Disease: Hyperkeratosis, CTCAE
Hyperkeratosis, CTCAE 		87 0 1 4.3E-03 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 1 4.4E-03 0 0
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		86 0 1 4.4E-03 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		86 0 1 4.4E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 4.4E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 4.4E-03 0 0