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: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 5 0.12 0 0
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7 		7 0 4 0.11 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 7 0.11 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 7 0.10 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 11 0.10 0 0
CUI: C1836926
Disease: Bone spicule pigmentation of the retina
Bone spicule pigmentation of the retina 		24 0 5 9.8E-02 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 65 10 9.3E-02 2 2.4E-02
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 11 9.0E-02 0 0
CUI: C0521691
Disease: Generalized progressive retinal atrophy
Generalized progressive retinal atrophy 		5 0 3 8.8E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 7 8.5E-02 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 0 4 8.5E-02 0 0
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 3 7.9E-02 0 0
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		10 0 3 7.7E-02 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 8 7.5E-02 0 0
CUI: C4021570
Disease: Undetectable light- and dark-adapted electroretinogram
Undetectable light- and dark-adapted electroretinogram 		11 0 3 7.5E-02 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 4 6.7E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 12 6.4E-02 0 0
CUI: C0002136
Disease: Allogenic disease
Allogenic disease 		2 0 2 6.2E-02 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 11 6.1E-02 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 13 6.1E-02 0 0
CUI: C1320640
Disease: Peripheral retinal degeneration
Peripheral retinal degeneration 		4 0 2 5.9E-02 0 0
CUI: C4024762
Disease: Pattern dystrophy of the retina
Pattern dystrophy of the retina 		4 0 2 5.9E-02 0 0
CUI: C4072991
Disease: Yellow/white lesions of the retina
Yellow/white lesions of the retina 		4 0 2 5.9E-02 0 0
CUI: C4073101
Disease: Hyperautofluorescent macular lesion
Hyperautofluorescent macular lesion 		4 0 2 5.9E-02 0 0
CUI: C4073099
Disease: Perifoveal ring of hyperautofluorescence
Perifoveal ring of hyperautofluorescence 		5 0 2 5.7E-02 0 0