SERPINE1, serpin family E member 1, 5054

N. diseases: 770; N. variants: 23
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.
Plasminogen Activator Inhibitor-1 Deficiency
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 2 0.700 strong 1.000 3 2 1992 2011
CUI: C1851184
Disease: Fibrinolytic Defect
Fibrinolytic Defect
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.020 None 1.000 2 2003 2004
Subendocardial myocardial infarction
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2002 2002
CUI: C0332561
Disease: Fibrous nodule
Fibrous nodule
disease Pathological Conditions, Signs and Symptoms Anatomical Abnormality 1 0.010 None 1.000 1 2006 2006
CUI: C1262200
Disease: Cerebrovascular infarction
Cerebrovascular infarction
disease Disease or Syndrome 1 0.010 None 1.000 1 2003 2003
TRANSCRIPTION OF PLASMINOGEN ACTIVATOR INHIBITOR, MODULATOR OF
phenotype Finding 1 1 0.300 strong 0 1
Peritoneal adhesions (postoperative) (postinfection)
disease Disease or Syndrome 2 0.200 None 1.000 2 2015 2016
CUI: C0022682
Disease: Kienbock Disease
Kienbock Disease
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0342940
Disease: Android obesity
Android obesity
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1999 1999
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
disease Eye Diseases; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 2 1 0.010 None 1.000 1 2017 2017
CUI: C2584611
Disease: Hereditary protein S deficiency
Hereditary protein S deficiency
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1998 1998
Chronic hyperplastic eosinophilic sinusitis
disease Disease or Syndrome 2 0.010 None 1.000 1 2007 2007
CUI: C4728231
Disease: Chronic gastroduodenitis
Chronic gastroduodenitis
disease Disease or Syndrome 2 0.010 None 1.000 1 2012 2012
CUI: C4054127
Disease: Radiation Nephropathy
Radiation Nephropathy
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 3 0.210 None 1.000 2 1997 2010
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein
disease Cardiovascular Diseases Disease or Syndrome 4 0.020 None 1.000 2 1994 2010
CUI: C0155860
Disease: Pneumonia due to Pseudomonas
Pneumonia due to Pseudomonas
disease Infections; Respiratory Tract Diseases Disease or Syndrome 4 0.010 None 1.000 1 2011 2011
Pleural effusion associated with pulmonary infection
disease Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0265010
Disease: Ruptured thoracic aortic aneurysm
Ruptured thoracic aortic aneurysm
disease Respiratory Tract Diseases; Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 5 0.200 None 1.000 1 1998 1998
CUI: C0265012
Disease: Ruptured abdominal aortic aneurysm
Ruptured abdominal aortic aneurysm
disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 5 0.200 None 1.000 1 1998 1998
Thoracoabdominal aortic aneurysm, ruptured
disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 5 0.200 None 1.000 1 1998 1998
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
disease Disease or Syndrome 6 3 0.100 None 0.778 27 1 1995 2019
CUI: C0264683
Disease: Coronary artery atheroma
Coronary artery atheroma
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 1997 1997
Atherosclerotic renal artery stenosis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 6 4 0.010 None 1.000 1 2006 2006
CUI: C0409983
Disease: Secondary antiphospholipid syndrome
Secondary antiphospholipid syndrome
disease Immune System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2013 2013
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
disease Digestive System Diseases Acquired Abnormality 6 0.010 None 1.000 1 2007 2007