Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Autosomal recessive retinitis pigmentosa
82 31 13 0.11 1 1.6E-02
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 13 0.11 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 26 0.11 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder)
23 317 7 0.11 3 8.7E-03
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 227 26 0.11 4 1.6E-02
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 7 0.11 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 33 23 0.11 3 4.9E-02
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina
49 24 9 0.10 1 1.9E-02
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 17 9.6E-02 0 0
Retinitis punctata albescens (disorder)
10 0 5 9.4E-02 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green
24 0 6 9.1E-02 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change
24 0 6 9.1E-02 0 0
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
254 51 25 9.0E-02 3 3.8E-02
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding)
25 0 6 9.0E-02 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness
87 0 11 8.9E-02 0 0
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation
14 0 5 8.8E-02 0 0
Amaurosis congenita of Leber, type 1
81 0 10 8.4E-02 0 0
CUI: C1320640
Disease: Peripheral retinal degeneration
Peripheral retinal degeneration
4 0 4 8.3E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 8 8.2E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
44 0 7 8.2E-02 0 0
CUI: C0155018
Disease: Color Blindness, Acquired
Color Blindness, Acquired
5 0 4 8.2E-02 0 0
CUI: C0239777
Disease: Color Blindness, Green
Color Blindness, Green
5 0 4 8.2E-02 0 0
CUI: C0751042
Disease: Color Blindness, Inherited
Color Blindness, Inherited
5 0 4 8.2E-02 0 0
CUI: C0751043
Disease: Monochromatopsia
Monochromatopsia
5 0 4 8.2E-02 0 0
CUI: C0339530
Disease: Progressive cone-rod dystrophy
Progressive cone-rod dystrophy
6 0 4 8.0E-02 0 0