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: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 5 0.38 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 8 0.24 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 4 0.22 0 0
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 4 0.22 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 4 0.22 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 4 0.21 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 4 0.21 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 4 0.20 0 0
CUI: C4551824
Disease: Oguchi Disease 1
Oguchi Disease 1 		2 0 2 0.20 0 0
CUI: C0311338
Disease: Fundus Albipunctatus
Fundus Albipunctatus 		9 0 3 0.19 0 0
CUI: C3151111
Disease: Abnormal light- and dark-adapted electroretinogram
Abnormal light- and dark-adapted electroretinogram 		9 0 3 0.19 0 0
CUI: C4551633
Disease: Pigmentary retinal dystrophy
Pigmentary retinal dystrophy 		9 0 3 0.19 0 0
CUI: C1857743
Disease: LEBER CONGENITAL AMAUROSIS 12 (disorder)
LEBER CONGENITAL AMAUROSIS 12 (disorder) 		4 0 2 0.17 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 5 0.17 0 0
CUI: C4072991
Disease: Yellow/white lesions of the retina
Yellow/white lesions of the retina 		4 0 2 0.17 0 0
CUI: C0239119
Disease: Lenticonus
Lenticonus 		6 0 2 0.14 0 0
CUI: C0423420
Disease: Absent foveal reflex
Absent foveal reflex 		6 0 2 0.14 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 5 0.14 0 0
CUI: C4024760
Disease: Progressive visual field defects
Progressive visual field defects 		7 0 2 0.13 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 4 0.12 0 0
CUI: C0015398
Disease: Eye Diseases, Hereditary
Eye Diseases, Hereditary 		9 0 2 0.12 0 0
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		10 0 2 0.11 0 0
CUI: C0268072
Disease: Hypercupremia
Hypercupremia 		1 0 1 1.0E-01 0 0
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		1 0 1 1.0E-01 0 0
CUI: C1864870
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		1 0 1 1.0E-01 0 0