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: C2609315
Disease: Retinal angiomatous proliferation
Retinal angiomatous proliferation 		12 4 5 0.29 1 0.12
CUI: C1719777
Disease: Hard drusen
Hard drusen 		4 0 3 0.27 0 0
CUI: C0035312
Disease: Retinal Drusen
Retinal Drusen 		9 0 4 0.27 0 0
CUI: C2748203
Disease: Vitreomacular adhesion
Vitreomacular adhesion 		6 0 3 0.23 0 0
CUI: C1720251
Disease: Retinal pigment epithelium atrophy
Retinal pigment epithelium atrophy 		7 0 3 0.21 0 0
CUI: C3888896
Disease: Wet age-related macular degeneration
Wet age-related macular degeneration 		20 2 5 0.20 1 0.17
CUI: C0271083
Disease: Nonexudative age-related macular degeneration
Nonexudative age-related macular degeneration 		3 0 2 0.18 0 0
CUI: C2609282
Disease: Reticular pseudodrusen
Reticular pseudodrusen 		10 10 3 0.18 1 7.1E-02
CUI: C2748502
Disease: CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS
CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS 		4 0 2 0.17 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 2 0.15 0 0
CUI: C0271214
Disease: Central blindness
Central blindness 		5 0 2 0.15 0 0
CUI: C0398677
Disease: Ocular sarcoidosis
Ocular sarcoidosis 		5 1 2 0.15 1 0.20
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		5 5 2 0.15 1 0.11
CUI: C1533060
Disease: Multifocal choroiditis
Multifocal choroiditis 		5 1 2 0.15 1 0.20
CUI: C4703391
Disease: Choroidal vascular hyperpermeability
Choroidal vascular hyperpermeability 		5 0 2 0.15 0 0
CUI: C0730314
Disease: Chronic central serous chorioretinopathy
Chronic central serous chorioretinopathy 		13 0 3 0.15 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 0 4 0.14 0 0
CUI: C1260959
Disease: Drusen
Drusen 		57 18 8 0.14 5 0.28
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		7 0 2 0.13 0 0
CUI: C0339546
Disease: Retinal Pigment Epithelial Detachment
Retinal Pigment Epithelial Detachment 		17 0 3 0.12 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 2 0.12 0 0
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous 		9 0 2 0.12 0 0
CUI: C0340291
Disease: Silent myocardial ischemia
Silent myocardial ischemia 		9 0 2 0.12 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		9 0 2 0.12 0 0
CUI: C0240805
Disease: Prodrome
Prodrome 		10 0 2 0.11 0 0