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: C0028738
Disease: Nystagmus
Nystagmus 		833 95 90 0.10 2 1.9E-02
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 16 9.9E-02 0 0
CUI: C0042798
Disease: Low Vision
Low Vision 		157 0 27 9.7E-02 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia 		184 0 29 9.6E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 17 9.6E-02 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 15 9.5E-02 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 16 9.4E-02 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 21 9.4E-02 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 31 9.3E-02 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 60 9.2E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 16 9.1E-02 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 16 9.0E-02 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		546 0 57 9.0E-02 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 0 14 8.9E-02 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 15 8.9E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 14 8.8E-02 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 13 8.8E-02 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 31 8.8E-02 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 16 8.7E-02 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 18 8.5E-02 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 30 8.5E-02 0 0
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 13 8.2E-02 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 13 8.2E-02 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 12 8.2E-02 0 0
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 12 8.2E-02 0 0