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: 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
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis 		1 0 1 0.11 0 0
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		1 0 1 0.11 0 0
CUI: C1859970
Disease: Hypodysfibrinogenemia, Congenital
Hypodysfibrinogenemia, Congenital 		1 0 1 0.11 0 0
CUI: C1969220
Disease: Depletion of components of the alternative complement pathway
Depletion of components of the alternative complement pathway 		1 0 1 0.11 0 0
CUI: C2608083
Disease: Cholestasis, benign recurrent intrahepatic 2
Cholestasis, benign recurrent intrahepatic 2 		1 0 1 0.11 0 0
CUI: C2698027
Disease: Matrix Metalloproteinase 8 Measurement
Matrix Metalloproteinase 8 Measurement 		1 0 1 0.11 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 0.11 0 0
CUI: C2752039
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3 		1 0 1 0.11 0 0
CUI: C3809523
Disease: MACULAR DEGENERATION, AGE-RELATED, 13
MACULAR DEGENERATION, AGE-RELATED, 13 		1 0 1 0.11 0 0
CUI: C4016070
Disease: Fibrinogen dusart phenotype
Fibrinogen dusart phenotype 		1 0 1 0.11 0 0
CUI: C4016097
Disease: FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE 		1 0 1 0.11 0 0
CUI: C4016436
Disease: MACULAR DEGENERATION, AGE-RELATED, 13, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, 13, SUSCEPTIBILITY TO 		1 0 1 0.11 0 0
CUI: C4303270
Disease: Sepsis caused by Pseudomonas aeruginosa
Sepsis caused by Pseudomonas aeruginosa 		1 0 1 0.11 0 0
CUI: C4476539
Disease: Glomerular subendothelial electron-dense deposits
Glomerular subendothelial electron-dense deposits 		1 0 1 0.11 0 0
CUI: C0008352
Disease: Cholemia
Cholemia 		2 0 1 1.0E-01 0 0
CUI: C0013533
Disease: Echovirus Infections
Echovirus Infections 		2 0 1 1.0E-01 0 0
CUI: C0340704
Disease: Superior mesenteric vein thrombosis
Superior mesenteric vein thrombosis 		2 0 1 1.0E-01 0 0