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: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy
39 10 39 0.75 10 0.17
CUI: C1866422
Disease: RETINITIS PIGMENTOSA 19
RETINITIS PIGMENTOSA 19
1 22 1 1.9E-02 6 8.0E-02
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease
45 24 16 0.20 6 7.8E-02
CUI: C1858806
Disease: CONE-ROD DYSTROPHY 3 (disorder)
CONE-ROD DYSTROPHY 3 (disorder)
3 53 1 1.9E-02 8 7.7E-02
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 53 23 0.20 7 6.7E-02
Macular Degeneration, Age-Related, 2
2 27 1 1.9E-02 5 6.2E-02
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina
49 24 17 0.20 4 5.1E-02
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
254 51 23 8.1E-02 5 4.8E-02
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder)
23 317 13 0.21 17 4.7E-02
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
714 56 36 4.9E-02 5 4.5E-02
CUI: C1838647
Disease: RETINITIS PIGMENTOSA 12 (disorder)
RETINITIS PIGMENTOSA 12 (disorder)
3 38 2 3.8E-02 4 4.3E-02
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 227 26 0.11 11 4.0E-02
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 33 24 0.11 3 3.4E-02
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 4 6 4.2E-02 2 3.3E-02
CUI: C0422943
Disease: Visual symptoms
Visual symptoms
17 5 2 3.0E-02 2 3.2E-02
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 5 24 9.9E-02 2 3.2E-02
CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2
2 5 2 3.8E-02 2 3.2E-02
CUI: C3809299
Disease: CONE-ROD DYSTROPHY 18
CONE-ROD DYSTROPHY 18
1 5 1 1.9E-02 2 3.2E-02
CUI: C1865869
Disease: CONE DYSTROPHY 3 (disorder)
CONE DYSTROPHY 3 (disorder)
3 6 1 1.9E-02 2 3.2E-02
CUI: C1867326
Disease: RETINAL CONE DYSTROPHY 1
RETINAL CONE DYSTROPHY 1
6 6 2 3.6E-02 2 3.2E-02
CUI: C3151202
Disease: LEBER CONGENITAL AMAUROSIS 8
LEBER CONGENITAL AMAUROSIS 8
2 42 1 1.9E-02 3 3.1E-02
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 10 22 0.12 2 3.0E-02
CUI: C1857779
Disease: SENIOR-LOKEN SYNDROME 6
SENIOR-LOKEN SYNDROME 6
2 13 1 1.9E-02 2 2.9E-02
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
44 16 12 0.14 2 2.7E-02
CUI: C2673874
Disease: BARDET-BIEDL SYNDROME 14 (disorder)
BARDET-BIEDL SYNDROME 14 (disorder)
2 17 1 1.9E-02 2 2.7E-02