SERPINC1, serpin family C member 1, 462

N. diseases: 184; N. variants: 46
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.050 None 1.000 5 1981 1988
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		phenotype Laboratory Procedure 483 1142 0.100 None 1.000 1 1 2012 2012
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C0341426
Disease: Small intestinal infarction
Small intestinal infarction 		disease Disease or Syndrome 2 0.010 None 1.000 1 1997 1997
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		phenotype Laboratory Procedure 269 555 0.100 None 1.000 1 1 2012 2012
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		disease Disease or Syndrome 60 14 0.010 None 1.000 1 1988 1988
CUI: C0747194
Disease: Biliary acute pancreatitis
Biliary acute pancreatitis 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		disease Neoplastic Process 860 154 0.010 None 1.000 1 2017 2017
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2020 2020
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature 		disease Acquired Abnormality 84 0.010 None 1.000 1 2008 2008
CUI: C1868938
Disease: End stage cardiac failure
End stage cardiac failure 		disease Disease or Syndrome 76 2 0.010 None 1.000 1 2017 2017
CUI: C1959635
Disease: Parvovirus B19 (disease)
Parvovirus B19 (disease) 		disease Disease or Syndrome 59 0.010 None 1.000 1 2001 2001
CUI: C2242682
Disease: Recurrent cerebral infarction
Recurrent cerebral infarction 		disease Disease or Syndrome 1 0.010 None < 0.001 1 1993 1993
CUI: C2363955
Disease: Venous reflux
Venous reflux 		disease Disease or Syndrome 6 0.010 None 1.000 1 1992 1992
CUI: C3805038
Disease: Acquired antithrombin III deficiency
Acquired antithrombin III deficiency 		disease Disease or Syndrome 1 0.010 None 1.000 1 1993 1993
CUI: C4055183
Disease: Contrast - Induced Nephropathy
Contrast - Induced Nephropathy 		disease Disease or Syndrome 19 0.010 None 1.000 1 2017 2017
CUI: C4225412
Disease: Spondylo-ocular syndrome
Spondylo-ocular syndrome 		disease Disease or Syndrome 24 5 0.010 None 1.000 1 2020 2020
CUI: C0264995
Disease: Occlusion of artery (disorder)
Occlusion of artery (disorder) 		phenotype Pathologic Function 3 0.100 None 0
CUI: C4280702
Disease: Reduced antithrombin antigen
Reduced antithrombin antigen 		phenotype Finding 1 0.100 None 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE 		phenotype Finding 7 0.100 None 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		phenotype Finding 3 0.100 None 0
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 230 93 0.500 None 1.000 15 4 1976 2019
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.400 None 1.000 13 1 1979 2019
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		phenotype Cardiovascular Diseases Pathologic Function 117 218 0.340 None 1.000 7 1976 2007
CUI: C0040053
Disease: Thrombosis
Thrombosis 		phenotype Cardiovascular Diseases Pathologic Function 98 0.510 None 1.000 6 1983 2007