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: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 21 0.23 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 12 0.22 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 11 0.20 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 21 0.20 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 15 0.16 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 11 0.16 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 6 0.15 0 0
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 4 0.14 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 23 0.14 0 0
CUI: C1301509
Disease: Severe visual impairment
Severe visual impairment 		35 0 7 0.13 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 0 5 0.13 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 21 0.13 0 0
CUI: C4021570
Disease: Undetectable light- and dark-adapted electroretinogram
Undetectable light- and dark-adapted electroretinogram 		11 0 4 0.13 0 0
CUI: C1833245
Disease: Retinitis Pigmentosa 17
Retinitis Pigmentosa 17 		3 0 3 0.12 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 23 0.12 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 5 0.11 0 0
CUI: C1828210
Disease: Macular dystrophy, concentric annular
Macular dystrophy, concentric annular 		6 0 3 0.11 0 0
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7 		7 0 3 0.11 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 23 0.11 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 0 5 0.10 0 0
CUI: C3540662
Disease: Congenital Amaurosis of Retinal Origin
Congenital Amaurosis of Retinal Origin 		8 0 3 0.10 0 0
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1 		32 0 5 9.8E-02 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 21 9.6E-02 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		227 0 21 9.1E-02 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 9 9.0E-02 0 0