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: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 0.33 0 0
CUI: C0344386
Disease: Schistocytosis
Schistocytosis 		5 0 2 0.25 0 0
CUI: C0427437
Disease: MCH - low
MCH - low 		5 0 2 0.25 0 0
CUI: C1956258
Disease: Familial Thrombotic Thrombocytopenic Purpura
Familial Thrombotic Thrombocytopenic Purpura 		5 0 2 0.25 0 0
CUI: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		5 0 2 0.25 0 0
CUI: C4551514
Disease: Hemophagocytic Lymphohistiocytosis, Familial, 1
Hemophagocytic Lymphohistiocytosis, Familial, 1 		5 0 2 0.25 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 2 0.22 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 0.21 0 0
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		7 0 2 0.20 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 0.20 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.20 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 0.20 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 0.20 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 0.20 0 0
CUI: C0854084
Disease: Streptococcal necrotizing fasciitis
Streptococcal necrotizing fasciitis 		1 0 1 0.20 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 0.20 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria 		1 0 1 0.20 0 0
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis 		1 0 1 0.20 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 0.20 0 0
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		1 5 1 0.20 1 7.7E-02
CUI: C1969220
Disease: Depletion of components of the alternative complement pathway
Depletion of components of the alternative complement pathway 		1 0 1 0.20 0 0
CUI: C2584777
Disease: Autoimmune thrombotic thrombocytopenic purpura
Autoimmune thrombotic thrombocytopenic purpura 		1 0 1 0.20 0 0
CUI: C2678015
Disease: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Childhood-Onset 		1 0 1 0.20 0 0
CUI: C2678027
Disease: Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe 		1 0 1 0.20 0 0
CUI: C2678055
Disease: MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)
MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder) 		1 0 1 0.20 0 0