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: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 10 0.13 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 0 8 0.13 0 0
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration 		136 0 20 0.13 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 9 0.12 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 6 0.12 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 9 0.12 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		227 0 29 0.12 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 6 0.12 0 0
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 6 0.12 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 10 0.12 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 5 0.12 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 5 0.12 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 0 7 0.12 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 7 0.12 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 14 0.12 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		16 0 6 0.12 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 6 0.12 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus 		269 0 32 0.11 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 13 0.11 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 9 0.11 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 19 0.11 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 0 6 0.11 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 25 0.11 0 0
CUI: C0271215
Disease: Blindness, Legal
Blindness, Legal 		10 0 5 0.11 0 0
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1 		32 0 7 0.10 0 0