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: 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: 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: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		disease Digestive System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C0584983
Disease: Homozygous Factor V Leiden mutation
Homozygous Factor V Leiden mutation 		disease Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C1142442
Disease: Intrahepatic biloma
Intrahepatic biloma 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4021097
Disease: Reduced prothrombin activity
Reduced prothrombin activity 		phenotype Finding 1 1 0.100 None 1.000 1 1 2019 2019
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		disease Finding 1 1 0.400 None 0 1
CUI: C3890031
Disease: prothrombin type 3 phenotype
prothrombin type 3 phenotype 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4016343
Disease: DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II
DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II 		phenotype Finding 1 1 0.100 None 0 1
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: C0272317
Disease: Hereditary factor II deficiency disease
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: C0259744
Disease: dysproteinemia
dysproteinemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1988 1988
CUI: C0749087
Disease: Thrombosis of subclavian vein
Thrombosis of subclavian vein 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2004 2004
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: 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: 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: C0752155
Disease: Central Nervous System Vascular Malformations
Central Nervous System Vascular Malformations 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Anatomical Abnormality 2 0.010 None 1.000 1 2007 2007
CUI: C0919631
Disease: Upper Extremity Deep Vein Thrombosis, Primary
Upper Extremity Deep Vein Thrombosis, Primary 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 1999 1999
CUI: C1739406
Disease: Acute coagulopathy
Acute coagulopathy 		disease Disease or Syndrome 2 0.010 None 1.000 1 2020 2020
CUI: C3852984
Disease: Acute Mesenteric Arterial Embolus
Acute Mesenteric Arterial Embolus 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C3852985
Disease: Occlusive Mesenteric Arterial Ischemia
Occlusive Mesenteric Arterial Ischemia 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C3852987
Disease: Acute Mesenteric Arterial Thrombosis
Acute Mesenteric Arterial Thrombosis 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C1856857
Disease: STROKE, ISCHEMIC, SUSCEPTIBILITY TO
STROKE, ISCHEMIC, SUSCEPTIBILITY TO 		phenotype Finding 2 2 0.100 None 0 1
CUI: C4022610
Disease: Excessive bleeding from superficial cuts
Excessive bleeding from superficial cuts 		phenotype Pathologic Function 2 0.100 None 0
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen 		phenotype Finding 2 0.100 None 0