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: C4024817
Disease: Vitelliform-like macular lesions
Vitelliform-like macular lesions
4 0 4 1.00 0 0
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment
7 0 4 0.57 0 0
Adult-Onset Vitelliform Macular Dystrophy
8 0 4 0.50 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma
1 0 1 0.25 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma
1 0 1 0.25 0 0
CUI: C1720732
Disease: Subretinal fluid (finding)
Subretinal fluid (finding)
1 0 1 0.25 0 0
CUI: C2678493
Disease: BESTROPHINOPATHY
BESTROPHINOPATHY
1 0 1 0.25 0 0
RETINITIS PIGMENTOSA, CONCENTRIC (disorder)
1 0 1 0.25 0 0
CUI: C2937228
Disease: Tunnel visual field constriction
Tunnel visual field constriction
1 0 1 0.25 0 0
CUI: C3150819
Disease: RETINITIS PIGMENTOSA 56
RETINITIS PIGMENTOSA 56
1 0 1 0.25 0 0
CUI: C4013102
Disease: LEBER CONGENITAL AMAUROSIS 18
LEBER CONGENITAL AMAUROSIS 18
1 0 1 0.25 0 0
CUI: C4015342
Disease: MACULAR DYSTROPHY, VITELLIFORM, 4
MACULAR DYSTROPHY, VITELLIFORM, 4
1 0 1 0.25 0 0
CUI: C4015343
Disease: MACULAR DYSTROPHY, VITELLIFORM, 5
MACULAR DYSTROPHY, VITELLIFORM, 5
1 0 1 0.25 0 0
CUI: C4024761
Disease: Retinal arteriolar occlusion
Retinal arteriolar occlusion
1 0 1 0.25 0 0
CUI: C4024776
Disease: Reticular retinal dystrophy
Reticular retinal dystrophy
1 0 1 0.25 0 0
Abnormality of chorioretinal pigmentation
1 0 1 0.25 0 0
CUI: C4551999
Disease: MACULAR DYSTROPHY, PATTERNED, 1
MACULAR DYSTROPHY, PATTERNED, 1
1 0 1 0.25 0 0
CUI: C0271004
Disease: Absent anterior chamber of eye
Absent anterior chamber of eye
2 0 1 0.20 0 0
CUI: C0730366
Disease: Rod dystrophy
Rod dystrophy
2 0 1 0.20 0 0
CUI: C0948825
Disease: Systremma
Systremma
2 0 1 0.20 0 0
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma
2 0 1 0.20 0 0
BEST VITELLIFORM MACULAR DYSTROPHY, MULTIFOCAL (disorder)
2 0 1 0.20 0 0
CUI: C2675552
Disease: Retinitis Pigmentosa 7, Digenic
Retinitis Pigmentosa 7, Digenic
2 0 1 0.20 0 0
CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2
2 0 1 0.20 0 0
CUI: C4288779
Disease: Major Congenital Anomaly
Major Congenital Anomaly
2 0 1 0.20 0 0