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: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy 		39 10 39 0.75 10 0.17
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 317 13 0.21 17 4.7E-02
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 4 13 0.20 1 1.6E-02
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina 		49 24 17 0.20 4 5.1E-02
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 23 0.20 7 6.7E-02
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 24 16 0.20 6 7.8E-02
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 31 16 0.19 2 2.3E-02
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 12 0.15 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 12 0.14 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 16 12 0.14 2 2.7E-02
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 17 0.14 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 11 0.14 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 18 26 0.13 2 2.7E-02
CUI: C1842914
Disease: Adult-Onset Vitelliform Macular Dystrophy
Adult-Onset Vitelliform Macular Dystrophy 		8 16 7 0.13 1 1.4E-02
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 15 0.12 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 10 0.12 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 10 22 0.12 2 3.0E-02
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 14 0.12 0 0
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 2 8 0.12 1 1.7E-02
CUI: C1301509
Disease: Severe visual impairment
Severe visual impairment 		35 0 9 0.12 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 7 0.11 0 0
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		19 0 7 0.11 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 15 0.11 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 33 24 0.11 3 3.4E-02
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 227 26 0.11 11 4.0E-02