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: C0152191
Disease: Scotoma, Central
Scotoma, Central
43 0 7 0.11 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy
25 0 5 0.11 0 0
CUI: C4282180
Disease: Juvenile macular degeneration
Juvenile macular degeneration
5 0 3 0.11 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 0 11 0.11 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia
26 0 5 0.11 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3
6 0 3 0.11 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 7 0.11 0 0
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy
39 0 6 0.10 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss
19 0 4 1.0E-01 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy
52 0 7 1.0E-01 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 6 9.8E-02 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1
20 0 4 9.8E-02 0 0
Amaurosis congenita of Leber, type 1
81 0 9 9.3E-02 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 10 9.2E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 9 9.1E-02 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy
24 0 4 8.9E-02 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 17 8.9E-02 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia
12 0 3 8.8E-02 0 0
Paroxysmal involuntary eye movements
39 0 5 8.5E-02 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome
14 0 3 8.3E-02 0 0
CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2
2 0 2 8.0E-02 0 0
CUI: C4477018
Disease: Sectoral retinitis pigmentosa
Sectoral retinitis pigmentosa
2 0 2 8.0E-02 0 0
CUI: C4551824
Disease: Oguchi Disease 1
Oguchi Disease 1
2 0 2 8.0E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
44 0 5 7.8E-02 0 0
CUI: C1858806
Disease: CONE-ROD DYSTROPHY 3 (disorder)
CONE-ROD DYSTROPHY 3 (disorder)
3 0 2 7.7E-02 0 0