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: C0266539
Disease: Congenital total cataract
Congenital total cataract 		16 0 4 0.14 0 0
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract 		18 0 4 0.13 0 0
CUI: C0235259
Disease: Subcapsular cataract
Subcapsular cataract 		17 0 3 1.0E-01 0 0
CUI: C0029531
Disease: Other cataract
Other cataract 		32 0 4 9.1E-02 0 0
CUI: C1850191
Disease: Posterior polar cataract
Posterior polar cataract 		8 0 2 9.1E-02 0 0
CUI: C2025392
Disease: Polar cataract
Polar cataract 		9 0 2 8.7E-02 0 0
CUI: C1510497
Disease: Lens Opacities
Lens Opacities 		24 0 3 8.1E-02 0 0
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		39 0 4 7.8E-02 0 0
CUI: C1708502
Disease: Induced cataract
Induced cataract 		13 0 2 7.4E-02 0 0
CUI: C0524524
Disease: Pseudoaphakia
Pseudoaphakia 		28 0 3 7.3E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 6.2E-02 0 0
CUI: C0220721
Disease: CATARACT 46, JUVENILE-ONSET
CATARACT 46, JUVENILE-ONSET 		1 1 1 6.2E-02 1 0.33
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 6.2E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 6.2E-02 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 6.2E-02 0 0
CUI: C1834042
Disease: Hypoplasia of facial musculature
Hypoplasia of facial musculature 		1 0 1 6.2E-02 0 0
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		1 0 1 6.2E-02 0 0
CUI: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 6.2E-02 0 0
CUI: C1850039
Disease: Pericardial Effusion, Chronic
Pericardial Effusion, Chronic 		1 0 1 6.2E-02 0 0
CUI: C1861825
Disease: CATARACT, POSTERIOR POLAR, 1
CATARACT, POSTERIOR POLAR, 1 		1 0 1 6.2E-02 0 0
CUI: C1861832
Disease: CATARACT, CRYSTALLINE ACULEIFORM
CATARACT, CRYSTALLINE ACULEIFORM 		1 0 1 6.2E-02 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 6.2E-02 0 0
CUI: C2675204
Disease: Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract 		1 0 1 6.2E-02 0 0
CUI: C2675205
Disease: Distal muscle atrophy due to neurologic disease
Distal muscle atrophy due to neurologic disease 		1 0 1 6.2E-02 0 0
CUI: C2675206
Disease: Normal serum phytanic and pristanic acid
Normal serum phytanic and pristanic acid 		1 0 1 6.2E-02 0 0