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: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 253 0.27 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 253 0.27 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 111 0.26 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 255 0.26 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
235 0 128 0.24 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 164 0.20 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 101 0.19 0 0
CUI: C0086543
Disease: Cataract
Cataract
878 0 197 0.18 0 0
Sensorineural Hearing Loss (disorder)
783 0 179 0.17 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 164 0.17 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 85 0.17 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 140 0.16 0 0
CUI: C0085636
Disease: Photophobia
Photophobia
227 0 89 0.16 0 0
CUI: C0033377
Disease: Ptosis
Ptosis
607 0 139 0.16 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 82 0.15 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 127 0.15 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 84 0.15 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 180 0.15 0 0
CUI: C0456909
Disease: Blindness
Blindness
393 0 105 0.15 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 165 0.15 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 147 0.14 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 101 0.14 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 61 0.13 0 0
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
305 0 85 0.13 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 133 0.13 0 0