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: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 0.100 None 0
CUI: C3550150
Disease: Recurrent thrombophlebitis
Recurrent thrombophlebitis
phenotype Cardiovascular Diseases Finding 5 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: C0151942
Disease: Arterial thrombosis
Arterial thrombosis
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 33 1 0.100 None 0
CUI: C4025286
Disease: Recurrent thromboembolism
Recurrent thromboembolism
phenotype Cardiovascular Diseases Finding 2 0.100 None 0
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis
phenotype Digestive System Diseases; Cardiovascular Diseases Pathologic Function 3 0.100 None 0
CUI: C0264995
Disease: Occlusion of artery (disorder)
Occlusion of artery (disorder)
phenotype 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: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE
phenotype Finding 3 0.100 None 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE
phenotype Finding 7 0.100 None 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis
disease Cardiovascular Diseases Disease or Syndrome 5 0.100 None 0
CUI: C4280702
Disease: Reduced antithrombin antigen
Reduced antithrombin antigen
phenotype Finding 1 0.100 None 0
CUI: C2242682
Disease: Recurrent cerebral infarction
Recurrent cerebral infarction
disease Disease or Syndrome 1 0.010 None < 0.001 1 1993 1993
CUI: C0023234
Disease: Legg-Calve-Perthes Disease
Legg-Calve-Perthes Disease
disease Musculoskeletal Diseases Disease or Syndrome 36 9 0.010 None < 0.001 1 2002 2002
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 72 38 0.010 None < 0.001 1 2006 2006
CUI: C0019880
Disease: Homocystinuria
Homocystinuria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 39 27 0.020 None 0.500 2 1986 1994
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.020 None 0.500 2 1995 1996
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: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 27 52 1.000 strong 0.987 75 44 1984 2019
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: 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: 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