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: C4025849
Disease: Abnormal foveal morphology
Abnormal foveal morphology 		5 0 5 0.45 0 0
CUI: C4072987
Disease: Yellow/white lesions of the macula
Yellow/white lesions of the macula 		5 0 5 0.45 0 0
CUI: C3549703
Disease: Retinal thinning
Retinal thinning 		11 0 5 0.29 0 0
CUI: C4025836
Disease: Abnormal choroid morphology
Abnormal choroid morphology 		12 0 5 0.28 0 0
CUI: C1863534
Disease: Stargardt disease 4
Stargardt disease 4 		3 0 3 0.27 0 0
CUI: C4282180
Disease: Juvenile macular degeneration
Juvenile macular degeneration 		5 0 3 0.23 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 5 0.23 0 0
CUI: C0271092
Disease: Progressive cone dystrophy (without rod involvement)
Progressive cone dystrophy (without rod involvement) 		9 0 3 0.18 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 0 5 0.17 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 5 0.16 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 5 0.16 0 0
CUI: C1838644
Disease: Stargardt disease 3
Stargardt disease 3 		4 0 2 0.15 0 0
CUI: C4021559
Disease: Retinitis pigmentosa inversa
Retinitis pigmentosa inversa 		4 0 2 0.15 0 0
CUI: C0423414
Disease: Retinal flecking
Retinal flecking 		5 0 2 0.14 0 0
CUI: C4023327
Disease: Central opacification of the cornea
Central opacification of the cornea 		5 0 2 0.14 0 0
CUI: C4073099
Disease: Perifoveal ring of hyperautofluorescence
Perifoveal ring of hyperautofluorescence 		5 0 2 0.14 0 0
CUI: C4477011
Disease: Thinning of Descemet membrane
Thinning of Descemet membrane 		5 0 2 0.14 0 0
CUI: C1828210
Disease: Macular dystrophy, concentric annular
Macular dystrophy, concentric annular 		6 0 2 0.13 0 0
CUI: C0152252
Disease: Anterior synechiae
Anterior synechiae 		7 0 2 0.12 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 2 0.12 0 0
CUI: C3714873
Disease: Axenfeld-Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome, Type 1 		7 0 2 0.12 0 0
CUI: C4310809
Disease: ANTERIOR SEGMENT DYSGENESIS 5
ANTERIOR SEGMENT DYSGENESIS 5 		7 0 2 0.12 0 0
CUI: C4024799
Disease: Granular macular appearance
Granular macular appearance 		8 0 2 0.12 0 0
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		19 0 3 0.11 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 5 0.11 0 0