CPB2, carboxypeptidase B2, 1361

N. diseases: 148; N. variants: 11
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: C2937359
Disease: Old thrombus
Old thrombus 		disease Cardiovascular Diseases Anatomical Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0014371
Disease: Enterotoxemia
Enterotoxemia 		disease Infections; Animal Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1867596
Disease: Hyperprothrombinemia
Hyperprothrombinemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2004 2004
CUI: C0032796
Disease: Postpartum Amenorrhea
Postpartum Amenorrhea 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 1 2005 2005
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		disease Disease or Syndrome 10 1 0.010 None 1.000 1 2007 2007
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 11 0.010 None 1.000 1 2018 2018
CUI: C0264766
Disease: Rheumatic mitral stenosis
Rheumatic mitral stenosis 		disease Cardiovascular Diseases Disease or Syndrome 12 0.010 None 1.000 1 2018 2018
CUI: C0267454
Disease: Necrotic enteritis
Necrotic enteritis 		disease Digestive System Diseases Disease or Syndrome 13 0.010 None < 0.001 1 2018 2018
CUI: C0578159
Disease: Antibiotic-associated diarrhea
Antibiotic-associated diarrhea 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 14 0.030 None 1.000 3 2005 2019
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2007 2007
CUI: C0043407
Disease: Yersinia infections
Yersinia infections 		group Infections Disease or Syndrome 17 0.010 None 1.000 1 2011 2011
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 7 0.010 None 1.000 1 2009 2009
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		disease Hemic and Lymphatic Diseases Disease or Syndrome 17 9 0.010 None 1.000 1 2009 2009
CUI: C0025306
Disease: Meningococcemia
Meningococcemia 		disease Infections Disease or Syndrome 20 0.020 None 1.000 2 2004 2008
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 20 9 0.010 None 1.000 1 2004 2004
CUI: C2609253
Disease: Macrovascular disease
Macrovascular disease 		disease Disease or Syndrome 23 1 0.010 None 1.000 1 2015 2015
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 24 0.010 None 1.000 1 2007 2007
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.200 None 1.000 1 2009 2009
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		group Hemic and Lymphatic Diseases Disease or Syndrome 30 3 0.010 None 1.000 1 2002 2002
CUI: C0524702
Disease: Pulmonary Thromboembolisms
Pulmonary Thromboembolisms 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 33 6 0.010 None 1.000 1 2002 2002
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease 		group Cardiovascular Diseases Disease or Syndrome 34 4 0.010 None 1.000 1 1997 1997
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 11 0.030 None 1.000 3 2013 2018
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		phenotype Pathological Conditions, Signs and Symptoms Finding 37 2 0.300 None 1.000 1 2005 2005
CUI: C0036983
Disease: Septic Shock
Septic Shock 		phenotype Pathological Conditions, Signs and Symptoms; Infections Pathologic Function 37 1 0.010 None 1.000 1 2008 2008
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 37 15 0.010 None 1.000 1 2020 2020