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: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 0 4 0.25 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 3 0.16 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 5 0.14 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 5 0.14 0 0
CUI: C1857618
Disease: Achromatopsia 2
Achromatopsia 2 		2 0 2 0.14 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 4 0.13 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 3 0.13 0 0
CUI: C1857743
Disease: LEBER CONGENITAL AMAUROSIS 12 (disorder)
LEBER CONGENITAL AMAUROSIS 12 (disorder) 		4 0 2 0.12 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 5 0.12 0 0
CUI: C0234629
Disease: Abnormal color vision
Abnormal color vision 		5 5 2 0.12 1 4.0E-02
CUI: C3275758
Disease: Choriocapillaris atrophy
Choriocapillaris atrophy 		5 0 2 0.12 0 0
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 0 4 0.11 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 9 3 0.11 2 7.1E-02
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		6 0 2 0.11 0 0
CUI: C1854065
Disease: LATE-ONSET RETINAL DEGENERATION (disorder)
LATE-ONSET RETINAL DEGENERATION (disorder) 		17 0 3 0.11 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 2 0.11 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 9 0.10 0 0
CUI: C3540662
Disease: Congenital Amaurosis of Retinal Origin
Congenital Amaurosis of Retinal Origin 		8 0 2 1.0E-01 0 0
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		9 0 2 9.5E-02 0 0
CUI: C0271092
Disease: Progressive cone dystrophy (without rod involvement)
Progressive cone dystrophy (without rod involvement) 		9 0 2 9.5E-02 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 3 9.4E-02 0 0
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary 		10 0 2 9.1E-02 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 3 8.6E-02 0 0
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 3 8.3E-02 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 2 8.3E-02 0 0