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: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 5 0.50 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 3 0.38 0 0
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		6 0 3 0.33 0 0
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		6 10 3 0.33 2 1.0E-01
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 0.30 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 0.29 0 0
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 0.29 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 3 0.27 0 0
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		8 0 3 0.27 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 2 0.25 0 0
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding 		10 0 3 0.23 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency 		5 0 2 0.22 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.22 0 0
CUI: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		5 0 2 0.22 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 3 0.20 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 0.20 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 3 0.20 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 3 0.20 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 0.19 0 0
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		7 0 2 0.18 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		7 0 2 0.18 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 2 0.18 0 0
CUI: C4055342
Disease: C3 Glomerulonephritis
C3 Glomerulonephritis 		7 0 2 0.18 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 2 1 0.17 2 0.17
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 0.17 0 0