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: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 3 0.43 0 0
CUI: C1832174
Disease: DOYNE HONEYCOMB RETINAL DYSTROPHY
DOYNE HONEYCOMB RETINAL DYSTROPHY 		9 1 4 0.33 1 1.00
CUI: C0271083
Disease: Nonexudative age-related macular degeneration
Nonexudative age-related macular degeneration 		3 0 2 0.25 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 2 0.22 0 0
CUI: C0398677
Disease: Ocular sarcoidosis
Ocular sarcoidosis 		5 0 2 0.20 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 2 0.20 0 0
CUI: C1533060
Disease: Multifocal choroiditis
Multifocal choroiditis 		5 0 2 0.20 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.20 0 0
CUI: C0029128
Disease: Optic Disk Drusen
Optic Disk Drusen 		6 0 2 0.18 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 2 0.18 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.17 0 0
CUI: C1720251
Disease: Retinal pigment epithelium atrophy
Retinal pigment epithelium atrophy 		7 0 2 0.17 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 2 0.17 0 0
CUI: C4055342
Disease: C3 Glomerulonephritis
C3 Glomerulonephritis 		7 0 2 0.17 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 2 0.15 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 2 0.14 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 0.14 0 0
CUI: C0035312
Disease: Retinal Drusen
Retinal Drusen 		9 0 2 0.14 0 0
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm 		1 0 1 0.14 0 0
CUI: C0154884
Disease: Acute posterior multifocal placoid pigment epitheliopathy
Acute posterior multifocal placoid pigment epitheliopathy 		1 0 1 0.14 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 0.14 0 0
CUI: C0340648
Disease: dissection of coronary artery
dissection of coronary artery 		1 0 1 0.14 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 0.14 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 0.14 0 0
CUI: C0423262
Disease: Corneal endotheliitis
Corneal endotheliitis 		1 0 1 0.14 0 0