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: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		12 0 6 0.38 0 0
CUI: C1858679
Disease: CATARACT, AUTOSOMAL DOMINANT
CATARACT, AUTOSOMAL DOMINANT 		14 0 6 0.33 0 0
CUI: C4721890
Disease: CATARACT 2, MULTIPLE TYPES
CATARACT 2, MULTIPLE TYPES 		3 0 3 0.30 0 0
CUI: C1852438
Disease: CATARACT, COPPOCK-LIKE
CATARACT, COPPOCK-LIKE 		20 0 6 0.25 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 5 0.24 0 0
CUI: C0344523
Disease: Cataract, congenital, cerulean type 1
Cataract, congenital, cerulean type 1 		6 0 3 0.23 0 0
CUI: C0702108
Disease: Coronary cataract
Coronary cataract 		2 0 2 0.20 0 0
CUI: C1510497
Disease: Lens Opacities
Lens Opacities 		24 0 5 0.17 0 0
CUI: C4023734
Disease: Sutural cataract
Sutural cataract 		5 0 2 0.15 0 0
CUI: C0524524
Disease: Pseudoaphakia
Pseudoaphakia 		28 0 5 0.15 0 0
CUI: C1854021
Disease: Cataract, Central Saccular, With Sutural Opacities
Cataract, Central Saccular, With Sutural Opacities 		6 0 2 0.14 0 0
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		39 0 6 0.14 0 0
CUI: C0266539
Disease: Congenital total cataract
Congenital total cataract 		16 0 3 0.13 0 0
CUI: C0029531
Disease: Other cataract
Other cataract 		32 0 4 0.11 0 0
CUI: C0344525
Disease: Congenital membranous cataract
Congenital membranous cataract 		1 0 1 1.0E-01 0 0
CUI: C0393697
Disease: Epilepsy with grand mal seizures on awakening (disorder)
Epilepsy with grand mal seizures on awakening (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 1.0E-01 0 0
CUI: C1832812
Disease: Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation
Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation 		1 0 1 1.0E-01 0 0
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		1 0 1 1.0E-01 0 0
CUI: C1850039
Disease: Pericardial Effusion, Chronic
Pericardial Effusion, Chronic 		1 0 1 1.0E-01 0 0
CUI: C1857768
Disease: Cataract, Pulverulent, Juvenile-Onset
Cataract, Pulverulent, Juvenile-Onset 		1 0 1 1.0E-01 0 0
CUI: C1861832
Disease: CATARACT, CRYSTALLINE ACULEIFORM
CATARACT, CRYSTALLINE ACULEIFORM 		1 0 1 1.0E-01 0 0
CUI: C1866984
Disease: Sclerocornea, Autosomal Dominant
Sclerocornea, Autosomal Dominant 		1 0 1 1.0E-01 0 0
CUI: C1969062
Disease: Cataract, Congenital Nuclear, Autosomal Recessive 3
Cataract, Congenital Nuclear, Autosomal Recessive 3 		1 0 1 1.0E-01 0 0
CUI: C1970456
Disease: Surfactant Metabolism Dysfunction, Pulmonary, 3
Surfactant Metabolism Dysfunction, Pulmonary, 3 		1 0 1 1.0E-01 0 0