Source: ALL
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: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 1 24 0.62 1 0.50
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 8 0.17 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 17 0.16 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 12 0.16 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 11 0.16 0 0
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina 		49 0 12 0.16 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 0 8 0.15 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 16 0.15 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 3 16 0.15 1 0.25
CUI: C0311338
Disease: Fundus Albipunctatus
Fundus Albipunctatus 		9 0 6 0.14 0 0
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 0 8 0.14 0 0
CUI: C1301509
Disease: Severe visual impairment
Severe visual impairment 		35 9 9 0.14 1 1.0E-01
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 11 0.14 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 16 0.14 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 10 0.14 0 0
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy 		39 0 9 0.13 0 0
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 6 0.13 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 9 0.12 0 0
CUI: C0423420
Disease: Absent foveal reflex
Absent foveal reflex 		6 0 5 0.12 0 0
CUI: C2748203
Disease: Vitreomacular adhesion
Vitreomacular adhesion 		6 0 5 0.12 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 7 0.12 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 5 0.12 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 10 21 0.12 1 9.1E-02
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 13 0.12 0 0
CUI: C4551633
Disease: Pigmentary retinal dystrophy
Pigmentary retinal dystrophy 		9 0 5 0.12 0 0