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: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 13 0.39 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 16 0.39 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 8 12 0.38 1 1.7E-02
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 12 0.38 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 12 0.38 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 12 0.36 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 12 0.36 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 9 14 0.32 3 5.2E-02
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 15 0.31 0 0
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary 		10 0 8 0.24 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 7 7 0.21 3 5.4E-02
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		6 0 6 0.19 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 10 0.15 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 18 23 0.13 2 2.9E-02
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 9 0.13 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 20 0.13 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 5 0.12 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 5 0.12 0 0
CUI: C0311338
Disease: Fundus Albipunctatus
Fundus Albipunctatus 		9 0 4 0.11 0 0
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 4 0.11 0 0
CUI: C4551633
Disease: Pigmentary retinal dystrophy
Pigmentary retinal dystrophy 		9 0 4 0.11 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 7 0.10 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 4 1.0E-01 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 5 9.4E-02 0 0
CUI: C4073107
Disease: Incomplete congenital stationary night blindness
Incomplete congenital stationary night blindness 		3 0 3 9.4E-02 0 0