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: C4023734
Disease: Sutural cataract
Sutural cataract 		5 0 3 0.38 0 0
CUI: C1858679
Disease: CATARACT, AUTOSOMAL DOMINANT
CATARACT, AUTOSOMAL DOMINANT 		14 0 5 0.33 0 0
CUI: C0344523
Disease: Cataract, congenital, cerulean type 1
Cataract, congenital, cerulean type 1 		6 0 2 0.20 0 0
CUI: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		12 0 3 0.20 0 0
CUI: C0344525
Disease: Congenital membranous cataract
Congenital membranous cataract 		1 0 1 0.17 0 0
CUI: C0393697
Disease: Epilepsy with grand mal seizures on awakening (disorder)
Epilepsy with grand mal seizures on awakening (disorder) 		1 0 1 0.17 0 0
CUI: C1833229
Disease: Cataract, Congenital Zonular, with Sutural Opacities
Cataract, Congenital Zonular, with Sutural Opacities 		1 0 1 0.17 0 0
CUI: C1866984
Disease: Sclerocornea, Autosomal Dominant
Sclerocornea, Autosomal Dominant 		1 0 1 0.17 0 0
CUI: C1969032
Disease: Cataract, Autosomal Dominant, Multiple Types 1
Cataract, Autosomal Dominant, Multiple Types 1 		1 0 1 0.17 0 0
CUI: C3665439
Disease: Mature cataract
Mature cataract 		1 0 1 0.17 0 0
CUI: C3805410
Disease: CATARACT 20, MULTIPLE TYPES
CATARACT 20, MULTIPLE TYPES 		1 0 1 0.17 0 0
CUI: C3809001
Disease: CATARACT 15, MULTIPLE TYPES
CATARACT 15, MULTIPLE TYPES 		1 0 1 0.17 0 0
CUI: C4023735
Disease: Lamellar pulverulent cataract
Lamellar pulverulent cataract 		1 0 1 0.17 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 3 0.16 0 0
CUI: C0266539
Disease: Congenital total cataract
Congenital total cataract 		16 0 3 0.16 0 0
CUI: C0154974
Disease: Cortical, lamellar, or zonular nonsenile cataract
Cortical, lamellar, or zonular nonsenile cataract 		2 0 1 0.14 0 0
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract 		18 0 3 0.14 0 0
CUI: C0271165
Disease: Punctate cataract
Punctate cataract 		2 0 1 0.14 0 0
CUI: C0272160
Disease: Chronic neutrophilia
Chronic neutrophilia 		2 0 1 0.14 0 0
CUI: C0702108
Disease: Coronary cataract
Coronary cataract 		2 0 1 0.14 0 0
CUI: C1832526
Disease: CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT
CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT 		2 0 1 0.14 0 0
CUI: C1852449
Disease: Cataract, Autosomal Dominant Nuclear
Cataract, Autosomal Dominant Nuclear 		2 0 1 0.14 0 0
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		10 0 2 0.14 0 0
CUI: C2675897
Disease: Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 		2 0 1 0.14 0 0
CUI: C3808115
Disease: CATARACT 12, MULTIPLE TYPES
CATARACT 12, MULTIPLE TYPES 		2 0 1 0.14 0 0