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: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		7 1 4 0.33 1 1.00
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 3 0.33 0 0
CUI: C1850938
Disease: FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY 		16 0 5 0.25 0 0
CUI: C1720251
Disease: Retinal pigment epithelium atrophy
Retinal pigment epithelium atrophy 		7 0 3 0.23 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 2 0.18 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 2 0.17 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 3 0.17 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.17 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 3 0.17 0 0
CUI: C0029128
Disease: Optic Disk Drusen
Optic Disk Drusen 		6 0 2 0.15 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 2 0.15 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.14 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 2 0.14 0 0
CUI: C4055342
Disease: C3 Glomerulonephritis
C3 Glomerulonephritis 		7 0 2 0.14 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 2 0.13 0 0
CUI: C1854065
Disease: LATE-ONSET RETINAL DEGENERATION (disorder)
LATE-ONSET RETINAL DEGENERATION (disorder) 		17 0 3 0.13 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 16 6 0.13 1 6.2E-02
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 2 0.12 0 0
CUI: C0035312
Disease: Retinal Drusen
Retinal Drusen 		9 0 2 0.12 0 0
CUI: C2609282
Disease: Reticular pseudodrusen
Reticular pseudodrusen 		10 0 2 0.12 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 0.11 0 0
CUI: C0220761
Disease: Dizygotic twins (disorder)
Dizygotic twins (disorder) 		1 0 1 0.11 0 0
CUI: C0233200
Disease: Cullen's sign
Cullen's sign 		1 0 1 0.11 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 0.11 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 0.11 0 0