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: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H
4 0 4 0.57 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B
5 0 4 0.50 0 0
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
4 0 3 0.38 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3
12 0 5 0.36 0 0
CUI: C0344386
Disease: Schistocytosis
Schistocytosis
5 0 3 0.33 0 0
CUI: C3150902
Disease: C1q DEFICIENCY
C1q DEFICIENCY
5 0 3 0.33 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased
12 0 4 0.27 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant
3 0 2 0.25 0 0
CUI: C0677628
Disease: Macular drusen
Macular drusen
4 0 2 0.22 0 0
CUI: C4022807
Disease: Foveal hypopigmentation
Foveal hypopigmentation
4 0 2 0.22 0 0
Membranoproliferative Glomerulonephritis, Type II
10 0 3 0.21 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy
16 0 4 0.21 0 0
CUI: C0427437
Disease: MCH - low
MCH - low
5 0 2 0.20 0 0
Familial Atypical Hemolytic Uremic Syndrome
5 0 2 0.20 0 0
CUI: C0003460
Disease: Anuria
Anuria
18 0 4 0.19 0 0
Membranoproliferative Glomerulonephritis, Type III
6 0 2 0.18 0 0
Macular Degeneration, Age-Related, 1
6 0 2 0.18 0 0
Complement Factor I (C3 inactivator) deficiency
6 0 2 0.18 0 0
Membranoproliferative Glomerulonephritis, Type I
7 0 2 0.17 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
42 0 7 0.17 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome
7 0 2 0.17 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese
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: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
31 0 5 0.15 0 0