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: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 1.0E-01 0 0
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies 		62 0 8 9.9E-02 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 9.7E-02 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 3 9.4E-02 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease 		9 0 3 9.1E-02 0 0
CUI: C0268743
Disease: Membranoproliferative Glomerulonephritis, Type II
Membranoproliferative Glomerulonephritis, Type II 		10 0 3 8.8E-02 0 0
CUI: C2609282
Disease: Reticular pseudodrusen
Reticular pseudodrusen 		10 0 3 8.8E-02 0 0
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease 		11 0 3 8.6E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 3 8.3E-02 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 3 8.1E-02 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		40 0 5 8.1E-02 0 0
CUI: C4477095
Disease: Increased lactate dehydrogenase activity
Increased lactate dehydrogenase activity 		27 0 4 8.0E-02 0 0
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		110 0 10 7.9E-02 0 0
CUI: C0017662
Disease: Glomerulonephritis, Membranoproliferative
Glomerulonephritis, Membranoproliferative 		57 0 6 7.7E-02 0 0
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury 		185 0 15 7.6E-02 0 0
CUI: C0232493
Disease: Epigastric pain
Epigastric pain 		17 0 3 7.3E-02 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile 		17 0 3 7.3E-02 0 0
CUI: C0037011
Disease: Shoulder Pain
Shoulder Pain 		18 0 3 7.1E-02 0 0
CUI: C0238304
Disease: Chronic interstitial nephritis
Chronic interstitial nephritis 		18 0 3 7.1E-02 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 7.1E-02 0 0
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 7.1E-02 0 0
CUI: C0034155
Disease: Purpura, Thrombotic Thrombocytopenic
Purpura, Thrombotic Thrombocytopenic 		80 0 7 7.0E-02 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		19 0 3 7.0E-02 0 0
CUI: C0266239
Disease: Congenital anomaly of bile ducts
Congenital anomaly of bile ducts 		4 0 2 6.9E-02 0 0
CUI: C0677628
Disease: Macular drusen
Macular drusen 		4 0 2 6.9E-02 0 0