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: C1299247
Disease: Primary malignant neoplasm of ovary and other uterine adnexa
Primary malignant neoplasm of ovary and other uterine adnexa 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 6 0.200 None 1.000 1 2012 2012
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 472 83 0.200 None 1.000 1 2007 2007
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 11 0.110 None 1.000 1 1980 1980
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 59 8 0.110 None 1.000 1 2018 2018
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 23 4 0.110 None 1.000 1 2001 2001
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.100 None 1.000 13 1992 2017
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 41 30 0.100 None 1.000 12 1996 2015
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: 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: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		phenotype Digestive System Diseases; Cardiovascular Diseases Pathologic Function 3 0.100 None 0
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 76 15 0.100 None 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		disease Cardiovascular Diseases Disease or Syndrome 5 0.100 None 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 0.100 None 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 33 1 0.100 None 0
CUI: C0264995
Disease: Occlusion of artery (disorder)
Occlusion of artery (disorder) 		phenotype Pathologic Function 3 0.100 None 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		phenotype Finding 3 0.100 None 0
CUI: C4280702
Disease: Reduced antithrombin antigen
Reduced antithrombin antigen 		phenotype Finding 1 0.100 None 0
CUI: C3279439
Disease: Recurrent spontaneous abortion
Recurrent spontaneous abortion 		phenotype Female Urogenital Diseases and Pregnancy Complications Finding 7 0.100 None 0
CUI: C4025286
Disease: Recurrent thromboembolism
Recurrent thromboembolism 		phenotype Cardiovascular Diseases Finding 2 0.100 None 0
CUI: C3550150
Disease: Recurrent thrombophlebitis
Recurrent thrombophlebitis 		phenotype Cardiovascular Diseases Finding 5 0.100 None 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE 		phenotype Finding 7 0.100 None 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 46 0.090 None 0.889 9 1997 2016
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 66 14 0.090 None 1.000 9 1994 2012
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		disease Hemic and Lymphatic Diseases Disease or Syndrome 19 14 0.070 None 1.000 7 1988 2012
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 826 32 0.050 None 1.000 5 2015 2019