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: C0242301
Disease: furuncle
furuncle 		3 0 1 0.20 0 0
CUI: C0268750
Disease: Necrotizing glomerulonephritis
Necrotizing glomerulonephritis 		3 0 1 0.20 0 0
CUI: C0271083
Disease: Nonexudative age-related macular degeneration
Nonexudative age-related macular degeneration 		3 0 1 0.20 0 0
CUI: C0403518
Disease: Microalbuminuric diabetic nephropathy
Microalbuminuric diabetic nephropathy 		9 0 2 0.20 0 0
CUI: C1397523
Disease: Stapes fixation
Stapes fixation 		3 0 1 0.20 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 1 0.20 0 0
CUI: C0398762
Disease: Properdin deficiency disease
Properdin deficiency disease 		4 0 1 0.17 0 0
CUI: C0523688
Disease: Hemopexin measurement
Hemopexin measurement 		4 0 1 0.17 0 0
CUI: C1504514
Disease: Infection by human herpesvirus 7
Infection by human herpesvirus 7 		4 0 1 0.17 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 1 0.17 0 0
CUI: C2749604
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1 		4 0 1 0.17 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 2 0.15 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 2 0.15 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 2 0.15 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 2 0.15 0 0
CUI: C0344386
Disease: Schistocytosis
Schistocytosis 		5 0 1 0.14 0 0
CUI: C0398677
Disease: Ocular sarcoidosis
Ocular sarcoidosis 		5 0 1 0.14 0 0
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		5 0 1 0.14 0 0
CUI: C1268936
Disease: Diarrhea-associated hemolytic uremic syndrome
Diarrhea-associated hemolytic uremic syndrome 		5 0 1 0.14 0 0
CUI: C1533060
Disease: Multifocal choroiditis
Multifocal choroiditis 		5 0 1 0.14 0 0
CUI: C1956258
Disease: Familial Thrombotic Thrombocytopenic Purpura
Familial Thrombotic Thrombocytopenic Purpura 		5 0 1 0.14 0 0
CUI: C2242539
Disease: Subcutaneous infection
Subcutaneous infection 		5 0 1 0.14 0 0
CUI: C3888104
Disease: Glomerulopathy with fibronectin deposits
Glomerulopathy with fibronectin deposits 		5 0 1 0.14 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 1 0.14 0 0
CUI: C4703391
Disease: Choroidal vascular hyperpermeability
Choroidal vascular hyperpermeability 		5 0 1 0.14 0 0