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: C1744705
Disease: Atrophy of optic disc
Atrophy of optic disc 		1 0 1 0.50 0 0
CUI: C1845407
Disease: CONE-ROD DYSTROPHY, X-LINKED, 3
CONE-ROD DYSTROPHY, X-LINKED, 3 		1 0 1 0.50 0 0
CUI: C4016457
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE 		1 0 1 0.50 0 0
CUI: C4072995
Disease: Difficulty adjusting from light to dark
Difficulty adjusting from light to dark 		1 0 1 0.50 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 0 2 0.33 0 0
CUI: C1858806
Disease: CONE-ROD DYSTROPHY 3 (disorder)
CONE-ROD DYSTROPHY 3 (disorder) 		3 0 1 0.25 0 0
CUI: C4073107
Disease: Incomplete congenital stationary night blindness
Incomplete congenital stationary night blindness 		3 0 1 0.25 0 0
CUI: C4302876
Disease: Oligocone trichromacy
Oligocone trichromacy 		3 0 1 0.25 0 0
CUI: C0155018
Disease: Color Blindness, Acquired
Color Blindness, Acquired 		5 0 1 0.17 0 0
CUI: C0234629
Disease: Abnormal color vision
Abnormal color vision 		5 5 1 0.17 1 2.1E-02
CUI: C0239777
Disease: Color Blindness, Green
Color Blindness, Green 		5 0 1 0.17 0 0
CUI: C0751042
Disease: Color Blindness, Inherited
Color Blindness, Inherited 		5 0 1 0.17 0 0
CUI: C0751043
Disease: Monochromatopsia
Monochromatopsia 		5 0 1 0.17 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 2 0.14 0 0
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		6 0 1 0.14 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 0 1 0.12 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 1 0.12 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 1 0.11 0 0
CUI: C4024799
Disease: Granular macular appearance
Granular macular appearance 		8 0 1 0.11 0 0
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		9 0 1 1.0E-01 0 0
CUI: C0271092
Disease: Progressive cone dystrophy (without rod involvement)
Progressive cone dystrophy (without rod involvement) 		9 0 1 1.0E-01 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 14 2 1.0E-01 4 7.5E-02
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 1 1.0E-01 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 2 8.0E-02 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 1 7.7E-02 0 0