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: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling
16 0 5 9.1E-02 0 0
Attenuation of retinal blood vessels
41 0 7 9.0E-02 0 0
Retinal Pigment Epithelial Detachment
17 0 5 8.9E-02 0 0
CUI: C4282180
Disease: Juvenile macular degeneration
Juvenile macular degeneration
5 0 4 8.9E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 7 8.9E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central
43 2 7 8.7E-02 2 0.12
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 17 8.7E-02 0 0
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia
19 0 5 8.6E-02 0 0
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7
7 0 4 8.5E-02 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese
7 1 4 8.5E-02 1 6.2E-02
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
136 0 14 8.4E-02 0 0
Adult-Onset Vitelliform Macular Dystrophy
8 0 4 8.3E-02 0 0
CUI: C4024799
Disease: Granular macular appearance
Granular macular appearance
8 0 4 8.3E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 0 10 8.3E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 7 8.2E-02 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 15 8.0E-02 0 0
CUI: C0521694
Disease: Atrophic retina
Atrophic retina
24 2 5 7.9E-02 2 0.12
Bone spicule pigmentation of the retina
24 0 5 7.9E-02 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy
24 4 5 7.9E-02 1 5.3E-02
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome
25 0 5 7.8E-02 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 5 7.8E-02 0 0
CUI: C2609315
Disease: Retinal angiomatous proliferation
Retinal angiomatous proliferation
12 4 4 7.7E-02 1 5.3E-02
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 9 7.6E-02 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis
13 0 4 7.5E-02 0 0
Chronic central serous chorioretinopathy
13 0 4 7.5E-02 0 0