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: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 99 0.33 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 81 0.33 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 81 0.32 0 0
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		305 0 119 0.28 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 111 0.27 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 139 0.26 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 93 0.26 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		407 0 132 0.26 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 86 0.25 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 83 0.22 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		227 0 85 0.22 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus 		269 0 85 0.20 0 0
CUI: C0456909
Disease: Blindness
Blindness 		393 0 101 0.19 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 72 0.19 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 71 0.18 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		725 0 144 0.18 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 59 0.17 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 115 0.17 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		546 0 107 0.16 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		779 0 135 0.15 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		779 0 135 0.15 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		400 0 84 0.15 0 0
CUI: C0086543
Disease: Cataract
Cataract 		878 0 147 0.15 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 41 0.15 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 0 136 0.15 0 0