Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hereditary factor I deficiency disease
1 0 1 0.25 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality
1 0 1 0.25 0 0
Verotoxigenic Escherichia coli gastrointestinal tract infection
1 0 1 0.25 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis
1 0 1 0.25 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement
1 0 1 0.25 0 0
Diarrhea-negative hemolytic uremic syndrome
1 0 1 0.25 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria
1 0 1 0.25 0 0
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis
1 0 1 0.25 0 0
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
1 0 1 0.25 0 0
Depletion of components of the alternative complement pathway
1 0 1 0.25 0 0
Matrix Metalloproteinase 8 Measurement
1 0 1 0.25 0 0
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
1 0 1 0.25 0 0
MACULAR DEGENERATION, AGE-RELATED, 13
1 0 1 0.25 0 0
MACULAR DEGENERATION, AGE-RELATED, 13, SUSCEPTIBILITY TO
1 0 1 0.25 0 0
Sepsis caused by Pseudomonas aeruginosa
1 0 1 0.25 0 0
Glomerular subendothelial electron-dense deposits
1 0 1 0.25 0 0
CUI: C1142126
Disease: Meningococcal bacteraemia
Meningococcal bacteraemia
2 0 1 0.20 0 0
CUI: C1408247
Disease: Renal disease (acute) NOS
Renal disease (acute) NOS
2 0 1 0.20 0 0
CUI: C3553720
Disease: CFHR5 DEFICIENCY
CFHR5 DEFICIENCY
2 0 1 0.20 0 0
CUI: C0152966
Disease: Pneumococcal sepsis
Pneumococcal sepsis
3 0 1 0.17 0 0
Amphetamine or related acting sympathomimetic abuse
3 0 1 0.17 0 0
CUI: C0242301
Disease: furuncle
furuncle
3 0 1 0.17 0 0
CUI: C0268750
Disease: Necrotizing glomerulonephritis
Necrotizing glomerulonephritis
3 0 1 0.17 0 0
Nonexudative age-related macular degeneration
3 0 1 0.17 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant
3 0 2 0.40 0 0