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: C1832174
Disease: DOYNE HONEYCOMB RETINAL DYSTROPHY
DOYNE HONEYCOMB RETINAL DYSTROPHY 		9 1 5 8.2E-02 1 5.6E-02
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 0 6 8.1E-02 0 0
CUI: C1536451
Disease: Central areolar choroidal sclerosis
Central areolar choroidal sclerosis 		10 0 5 8.1E-02 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 5 7.8E-02 0 0
CUI: C0154822
Disease: Serous retinal detachment
Serous retinal detachment 		12 2 5 7.8E-02 1 5.3E-02
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 5 7.7E-02 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body 		14 0 5 7.6E-02 0 0
CUI: C0730321
Disease: Punctate inner choroidopathy
Punctate inner choroidopathy 		14 0 5 7.6E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 24 7 7.4E-02 2 5.0E-02
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies 		62 8 8 7.2E-02 1 4.0E-02
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome 		94 0 10 7.1E-02 0 0
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		685 663 49 7.1E-02 12 1.8E-02
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 4 7.0E-02 0 0
CUI: C0085635
Disease: Photopsia
Photopsia 		35 0 6 7.0E-02 0 0
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		5 5 4 6.9E-02 2 9.5E-02
CUI: C0155733
Disease: Atherosclerosis of aorta
Atherosclerosis of aorta 		37 0 6 6.8E-02 0 0
CUI: C2748203
Disease: Vitreomacular adhesion
Vitreomacular adhesion 		6 0 4 6.8E-02 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 4 6.7E-02 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 4 6.7E-02 0 0
CUI: C0751587
Disease: CADASIL Syndrome
CADASIL Syndrome 		40 0 6 6.6E-02 0 0
CUI: C1695782
Disease: Cerebral hypoperfusion
Cerebral hypoperfusion 		40 0 6 6.6E-02 0 0
CUI: C0017662
Disease: Glomerulonephritis, Membranoproliferative
Glomerulonephritis, Membranoproliferative 		57 3 7 6.5E-02 1 5.0E-02
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 0 5 6.5E-02 0 0
CUI: C0333641
Disease: Atrophic
Atrophic 		58 0 7 6.5E-02 0 0
CUI: C0021775
Disease: Intermittent Claudication
Intermittent Claudication 		60 0 7 6.4E-02 0 0