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: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 4 0.80 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 4 0.50 0 0
CUI: C2749604
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1 		4 0 3 0.50 0 0
CUI: C0344386
Disease: Schistocytosis
Schistocytosis 		5 0 3 0.43 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 5 0.42 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 0.33 0 0
CUI: C4055342
Disease: C3 Glomerulonephritis
C3 Glomerulonephritis 		7 0 3 0.33 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		16 0 5 0.31 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3 		12 0 4 0.31 0 0
CUI: C0677628
Disease: Macular drusen
Macular drusen 		4 0 2 0.29 0 0
CUI: C4022807
Disease: Foveal hypopigmentation
Foveal hypopigmentation 		4 0 2 0.29 0 0
CUI: C0003460
Disease: Anuria
Anuria 		18 0 5 0.28 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 2 0.25 0 0
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		5 0 2 0.25 0 0
CUI: C1970263
Disease: Recurrent meningococcal disease
Recurrent meningococcal disease 		5 0 2 0.25 0 0
CUI: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		5 0 2 0.25 0 0
CUI: C1864205
Disease: Macular Degeneration, Age-Related, 1
Macular Degeneration, Age-Related, 1 		6 0 2 0.22 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 2 0.22 0 0
CUI: C0017575
Disease: Necrotizing Ulcerative Gingivitis
Necrotizing Ulcerative Gingivitis 		1 0 1 0.20 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 0.20 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 0.20 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.20 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 0.20 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 0.20 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 0.20 0 0