Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
12 0 12 0.92 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
12 0 12 0.92 0 0
Night blindness, congenital stationary, type 1
12 0 12 0.92 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb
13 0 12 0.86 0 0
Cone-rod synaptic disorder, congenital nonprogressive
14 0 12 0.80 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
26 0 13 0.50 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 12 0.46 0 0
Complete congenital stationary night blindness
6 0 6 0.46 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc
31 0 12 0.38 0 0
Night blindness, congenital stationary
32 0 12 0.36 0 0
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary
10 0 4 0.21 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease
8 0 3 0.17 0 0
Abnormal light- and dark-adapted electroretinogram
9 0 3 0.16 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1
20 0 4 0.14 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia
12 0 3 0.14 0 0
CUI: C0029128
Disease: Optic Disk Drusen
Optic Disk Drusen
6 0 2 0.12 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3
6 0 2 0.12 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia
26 0 4 0.11 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease
45 0 5 9.4E-02 0 0
CUI: C0268425
Disease: Alstrom Syndrome
Alstrom Syndrome
12 0 2 8.7E-02 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 12 8.1E-02 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome
14 0 2 8.0E-02 0 0
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm
1 0 1 7.7E-02 0 0
Acute posterior multifocal placoid pigment epitheliopathy
1 0 1 7.7E-02 0 0
CUI: C0340648
Disease: dissection of coronary artery
dissection of coronary artery
1 0 1 7.7E-02 0 0