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: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		6 0 5 0.50 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 5 0.50 0 0
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		6 0 3 0.25 0 0
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		8 0 3 0.21 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 0.20 0 0
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding 		10 0 3 0.19 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: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.17 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 0.16 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.14 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		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: C1832174
Disease: DOYNE HONEYCOMB RETINAL DYSTROPHY
DOYNE HONEYCOMB RETINAL DYSTROPHY 		9 0 2 0.12 0 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		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: 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
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 0.11 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 0.11 0 0
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 0.11 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 0.11 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria 		1 0 1 0.11 0 0