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: C0085636
Disease: Photophobia
Photophobia
227 0 65 0.21 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 53 0.20 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 53 0.17 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 44 0.17 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness
87 0 30 0.15 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 30 0.14 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 43 0.13 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 20 0.13 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 39 0.13 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 27 0.13 0 0
Night blindness, congenital stationary
32 0 20 0.13 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 0 26 0.13 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 61 0.13 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central
43 0 21 0.12 0 0
Amaurosis congenita of Leber, type 1
81 0 25 0.12 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 60 0.12 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 24 0.12 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 19 0.11 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding)
25 0 17 0.11 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus
269 0 41 0.11 0 0
CUI: C0456909
Disease: Blindness
Blindness
393 0 53 0.11 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 20 0.11 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 87 0.10 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 87 0.10 0 0
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
136 0 26 0.10 0 0