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: C1959635
Disease: Parvovirus B19 (disease)
Parvovirus B19 (disease) 		disease Disease or Syndrome 59 0.010 None 1.000 1 2002 2002
CUI: C0023223
Disease: Leg Ulcer
Leg Ulcer 		disease Skin and Connective Tissue Diseases Disease or Syndrome 40 0.010 None 1.000 1 2002 2002
CUI: C0751502
Disease: Petrous Sinus Thrombosis
Petrous Sinus Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2002 2002
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6385 327 0.010 None 1.000 1 2002 2002
CUI: C0013922
Disease: Embolism
Embolism 		phenotype Cardiovascular Diseases Pathologic Function 3 0.010 None 1.000 1 2002 2002
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 424 28 0.010 None 1.000 1 2002 2002
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 35 2 0.010 None 1.000 1 2002 2002
CUI: C0243038
Disease: Carcinoma, Lewis Lung
Carcinoma, Lewis Lung 		disease Neoplasms Neoplastic Process; Experimental Model of Disease 188 0.010 None 1.000 1 2002 2002
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 36 0.010 None 1.000 1 2002 2002
CUI: C0751500
Disease: Petrous Sinus Thrombophlebitis
Petrous Sinus Thrombophlebitis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2002 2002
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis 		disease Respiratory Tract Diseases Disease or Syndrome 924 25 0.010 None 1.000 1 2002 2002
CUI: C0751501
Disease: Intracranial Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2002 2002
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		group Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2492 85 0.010 None 1.000 1 2002 2002
CUI: C0085650
Disease: Purpura Fulminans
Purpura Fulminans 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.020 None 1.000 2 2000 2003
CUI: C0013537
Disease: Eclampsia
Eclampsia 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 241 38 0.020 None 1.000 2 2000 2003
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		disease Disease or Syndrome 6 0.020 None 1.000 2 2000 2003
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 9 1 0.020 None 0.500 2 2002 2003
CUI: C0745497
Disease: Thrombosis of internal jugular vein
Thrombosis of internal jugular vein 		disease Cardiovascular Diseases Disease or Syndrome 3 0.020 None 1.000 2 2001 2003
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2003 2003
CUI: C0432474
Disease: Klinefelter's syndrome - male with more than two X chromosomes
Klinefelter's syndrome - male with more than two X chromosomes 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 90 5 0.010 None 1.000 1 2003 2003
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 150 18 0.010 None 1.000 1 2003 2003
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		phenotype Cardiovascular Diseases Pathologic Function 25 3 0.420 None 1.000 3 2003 2004
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 23 5 0.030 None 1.000 3 2 2000 2004
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.310 None 1.000 2 1998 2004
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 440 139 0.020 None 1.000 2 1 2002 2004