F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
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: 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 0.100 None 0.954 174 6 1996 2019
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.600 None 0.956 114 6 1992 2019
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 230 93 0.500 None 0.969 65 7 1997 2020
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.400 None 1.000 56 1987 2019
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.400 None 0.892 37 4 1997 2019
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1159 704 0.200 None 0.938 32 5 1998 2019
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1182 189 0.400 None 0.966 29 1 1999 2019
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 29 3 1996 2016
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 13 0.800 strong 0.964 28 11 1983 2019
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 143 295 0.100 None 0.952 21 2 1989 2019
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		disease Immune System Diseases Disease or Syndrome 99 17 0.100 None 0.952 21 1 1998 2019
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		disease Hemic and Lymphatic Diseases Disease or Syndrome 19 14 0.100 None 0.944 18 4 1992 2016
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.600 None 0.941 17 1991 2019
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		disease Digestive System Diseases; Infections Disease or Syndrome 1449 519 0.100 None 0.941 17 1 2005 2019
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 246 45 0.300 None 1.000 17 2 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 0.100 None 1.000 16 2 2000 2019
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		disease Cardiovascular Diseases Disease or Syndrome 1708 1577 0.100 None 0.812 16 2 1997 2012
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 4 0.400 None 0.938 16 1 1983 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		disease Cardiovascular Diseases Disease or Syndrome 1576 1178 0.100 None 0.867 15 2 1997 2019
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 43 14 0.100 None 1.000 15 3 1998 2019
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 82 8 0.100 None 1.000 14 1989 2019
CUI: C4552766
Disease: Miscarriage
Miscarriage 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 426 56 0.100 None 0.786 14 2 2000 2016
CUI: C4722227
Disease: Hypoprothrombinemias
Hypoprothrombinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 5 0.600 strong 0.929 14 2 1983 2019
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 11 0.200 None 1.000 13 2 1998 2018
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 59 8 0.100 None 0.846 13 2 2000 2019