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: C0272241
Disease: Complement abnormality
Complement abnormality
1 0 1 0.33 0 0
Verotoxigenic Escherichia coli gastrointestinal tract infection
1 0 1 0.33 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency
5 0 2 0.33 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis
1 0 1 0.33 0 0
CUI: C0427437
Disease: MCH - low
MCH - low
5 0 2 0.33 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement
1 0 1 0.33 0 0
CUI: C0854084
Disease: Streptococcal necrotizing fasciitis
Streptococcal necrotizing fasciitis
1 0 1 0.33 0 0
Diarrhea-negative hemolytic uremic syndrome
1 0 1 0.33 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria
1 0 1 0.33 0 0
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis
1 0 1 0.33 0 0
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
1 0 1 0.33 0 0
Depletion of components of the alternative complement pathway
1 0 1 0.33 0 0
Matrix Metalloproteinase 8 Measurement
1 0 1 0.33 0 0
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2
1 0 1 0.33 0 0
Familial Atypical Hemolytic Uremic Syndrome
5 0 2 0.33 0 0
Sepsis caused by Pseudomonas aeruginosa
1 0 1 0.33 0 0
Glomerular subendothelial electron-dense deposits
1 0 1 0.33 0 0
Complement Factor I (C3 inactivator) deficiency
6 0 2 0.29 0 0
Membranoproliferative Glomerulonephritis, Type I
7 0 2 0.25 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome
7 0 2 0.25 0 0
CUI: C1142126
Disease: Meningococcal bacteraemia
Meningococcal bacteraemia
2 0 1 0.25 0 0
CUI: C1408247
Disease: Renal disease (acute) NOS
Renal disease (acute) NOS
2 0 1 0.25 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria
8 0 2 0.22 0 0
CUI: C0152966
Disease: Pneumococcal sepsis
Pneumococcal sepsis
3 0 1 0.20 0 0
Amphetamine or related acting sympathomimetic abuse
3 0 1 0.20 0 0