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: C0152200
Disease: Achromatopsia
Achromatopsia 		26 63 20 0.77 14 0.22
CUI: C4024799
Disease: Granular macular appearance
Granular macular appearance 		8 0 6 0.27 0 0
CUI: C0155018
Disease: Color Blindness, Acquired
Color Blindness, Acquired 		5 0 5 0.25 0 0
CUI: C0239777
Disease: Color Blindness, Green
Color Blindness, Green 		5 0 5 0.25 0 0
CUI: C0751042
Disease: Color Blindness, Inherited
Color Blindness, Inherited 		5 0 5 0.25 0 0
CUI: C0751043
Disease: Monochromatopsia
Monochromatopsia 		5 0 5 0.25 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 9 7 0.24 1 4.5E-02
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 8 0.22 0 0
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		9 0 5 0.21 0 0
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 7 0.18 0 0
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		19 0 6 0.18 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 0 4 0.18 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 4 0.17 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 9 0.17 0 0
CUI: C0271092
Disease: Progressive cone dystrophy (without rod involvement)
Progressive cone dystrophy (without rod involvement) 		9 0 4 0.16 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 6 0.16 0 0
CUI: C0155017
Disease: Color Blindness, Blue
Color Blindness, Blue 		25 0 6 0.15 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 6 0.15 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 6 0.15 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 4 0.14 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 8 0.13 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 4 0.13 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 7 0.13 0 0
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 0 5 0.12 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 0.10 0 0