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: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 13 0.50 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 13 0.50 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 13 0.48 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 12 0.46 0 0
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 12 0.46 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 12 0.46 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 13 0.34 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 52 14 0.32 3 5.2E-02
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 13 0.30 0 0
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		6 0 6 0.23 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 9 0.21 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 5 0.15 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 6 0.15 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 7 0.15 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 5 0.14 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 0 4 0.14 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 3 4 0.14 1 9.1E-02
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 8 0.13 0 0
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary 		10 0 4 0.12 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 21 0.12 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis 		13 0 4 0.11 0 0
CUI: C0268542
Disease: Ornithine carbamoyltransferase deficiency
Ornithine carbamoyltransferase deficiency 		17 0 4 0.10 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 7 3 9.7E-02 1 6.7E-02
CUI: C1845667
Disease: RETINITIS PIGMENTOSA 3
RETINITIS PIGMENTOSA 3 		8 0 3 9.7E-02 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 15 9.5E-02 0 0