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: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 12 1.00 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 12 1.00 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 12 0.92 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 12 0.92 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 12 0.86 0 0
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		6 0 6 0.50 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 12 0.48 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 12 0.46 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 12 0.39 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 52 12 0.38 1 1.7E-02
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary 		10 0 4 0.22 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 3 0.18 0 0
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 3 0.17 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 3 0.14 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 0 2 0.12 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 3 0.10 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 3 8.6E-02 0 0
CUI: C1321315
Disease: Paraneoplastic retinopathy
Paraneoplastic retinopathy 		1 0 1 8.3E-02 0 0
CUI: C1744705
Disease: Atrophy of optic disc
Atrophy of optic disc 		1 0 1 8.3E-02 0 0
CUI: C1840455
Disease: Mild myopia
Mild myopia 		1 0 1 8.3E-02 0 0
CUI: C1845407
Disease: CONE-ROD DYSTROPHY, X-LINKED, 3
CONE-ROD DYSTROPHY, X-LINKED, 3 		1 0 1 8.3E-02 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 2 8.3E-02 0 0
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		1 0 1 8.3E-02 0 0
CUI: C1864870
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		1 0 1 8.3E-02 0 0
CUI: C1876182
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2 		1 0 1 8.3E-02 0 0