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: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 11 0.12 0 0
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 9 9.6E-02 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 29 19 9.5E-02 2 4.0E-02
CUI: C4024799
Disease: Granular macular appearance
Granular macular appearance 		8 0 7 8.9E-02 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 0 7 8.0E-02 0 0
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		30 25 8 8.0E-02 3 6.7E-02
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 29 12 7.9E-02 2 4.0E-02
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		19 0 7 7.8E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 39 14 7.6E-02 3 5.1E-02
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 15 21 7.5E-02 1 2.7E-02
CUI: C4025690
Disease: Prenatal maternal abnormality
Prenatal maternal abnormality 		23 0 7 7.4E-02 0 0
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 10 6 7.3E-02 3 1.0E-01
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 7 7.3E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 7 7.2E-02 0 0
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 46 7 6.9E-02 3 4.5E-02
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 7 6.8E-02 3 5.3E-02
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis 		50 0 8 6.7E-02 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 58 8 6.7E-02 5 6.6E-02
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 6 6.5E-02 0 0
CUI: C0155018
Disease: Color Blindness, Acquired
Color Blindness, Acquired 		5 0 5 6.4E-02 0 0
CUI: C0239777
Disease: Color Blindness, Green
Color Blindness, Green 		5 0 5 6.4E-02 0 0
CUI: C0751042
Disease: Color Blindness, Inherited
Color Blindness, Inherited 		5 0 5 6.4E-02 0 0
CUI: C0751043
Disease: Monochromatopsia
Monochromatopsia 		5 0 5 6.4E-02 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 7 6.2E-02 0 0
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		439 617 30 6.2E-02 2 3.1E-03