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: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 12 1.00 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 4 0.31 0 0
CUI: C0151603
Disease: Anasarca
Anasarca 		41 0 12 0.29 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 4 0.25 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 4 0.20 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 0.20 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 0.19 0 0
CUI: C1832174
Disease: DOYNE HONEYCOMB RETINAL DYSTROPHY
DOYNE HONEYCOMB RETINAL DYSTROPHY 		9 0 3 0.17 0 0
CUI: C4022830
Disease: Heavy proteinuria
Heavy proteinuria 		2 0 2 0.17 0 0
CUI: C0232493
Disease: Epigastric pain
Epigastric pain 		17 0 4 0.16 0 0
CUI: C0037011
Disease: Shoulder Pain
Shoulder Pain 		18 0 4 0.15 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 0.15 0 0
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 0.15 0 0
CUI: C0034063
Disease: Pulmonary Edema
Pulmonary Edema 		26 0 5 0.15 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		19 0 4 0.15 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 0.14 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 2 0.14 0 0
CUI: C4023481
Disease: EEG with focal spikes
EEG with focal spikes 		4 0 2 0.14 0 0
CUI: C0151872
Disease: Prothrombin time increased
Prothrombin time increased 		30 0 5 0.14 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency 		5 0 2 0.13 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.13 0 0
CUI: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		5 0 2 0.13 0 0
CUI: C1850069
Disease: Undetectable visual evoked potentials
Undetectable visual evoked potentials 		6 0 2 0.12 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		16 0 3 0.12 0 0
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		7 0 2 0.12 0 0