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: 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: C0398623
Disease: Thrombophilia
Thrombophilia
disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.600 None 0.956 114 6 1992 2019
Disseminated Intravascular Coagulation
disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.600 None 0.941 17 1991 2019
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: C0040053
Disease: Thrombosis
Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 98 0.580 None 1.000 14 1992 2013
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 117 218 0.570 None 1.000 11 1999 2013
CUI: C0028754
Disease: Obesity
Obesity
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2821 1111 0.540 None 1.000 6 1 2007 2015
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.500 None 0.937 143 10 1997 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: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.500 None 0.946 37 4 1995 2020
Hereditary factor II deficiency disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 14 0.500 None 1.000 11 13 1978 2014
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 47 0.500 None 1.000 3 1994 2013
CUI: C0027720
Disease: Nephrosis
Nephrosis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 68 0.500 None 1.000 1 2008 2008
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
phenotype Cardiovascular Diseases Pathologic Function 25 3 0.420 None 1.000 3 2003 2004
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: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 267 31 0.400 None 0.960 50 2 1975 2020
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: 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: 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
THROMBOPHILIA DUE TO THROMBIN DEFECT
phenotype Finding 4 2 0.400 strong 1.000 14 2 1986 2013
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2872 2897 0.400 None 1.000 2 1 2015 2017
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
disease Finding 1 1 0.400 None 0 1
CUI: C0085605
Disease: Liver Failure
Liver Failure
disease Digestive System Diseases Disease or Syndrome 293 20 0.360 None 1.000 7 2004 2019
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1179 64 0.350 None 1.000 6 1999 2019
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 687 123 0.350 None 1.000 5 2 1999 2009