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.
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
group Mental or Behavioral Dysfunction 360 56 0.010 None < 0.001 1 2019 2019
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1348 204 0.010 None 1.000 1 2011 2011
CUI: C0240912
Disease: Vertical Talus
Vertical Talus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 69 20 0.010 None 1.000 1 2012 2012
CUI: C0241868
Disease: acute aortic dissection
acute aortic dissection
disease Cardiovascular Diseases Disease or Syndrome 63 0.010 None 1.000 1 2019 2019
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 16 2 0.010 None 1.000 1 1 2011 2011
CUI: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy
disease Eye Diseases Disease or Syndrome 142 14 0.010 None 1.000 1 2003 2003
Subendocardial myocardial infarction
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2002 2002
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 303 317 0.010 None < 0.001 1 2015 2015
CUI: C0264545
Disease: Thickening of pleura
Thickening of pleura
disease Respiratory Tract Diseases Disease or Syndrome 25 0.010 None 1.000 1 2013 2013
CUI: C0279988
Disease: Childhood Angiosarcoma
Childhood Angiosarcoma
disease Neoplasms Neoplastic Process 101 1 0.010 None 1.000 1 2013 2013
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 518 138 0.010 None 1.000 1 2012 2012
CUI: C0342649
Disease: Vascular calcification
Vascular calcification
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 257 3 0.010 None 1.000 1 2016 2016
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 59 123 0.010 None 1.000 1 2001 2001
Familial hypercholesterolemia - heterozygous
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 42 34 0.010 None 1.000 1 2001 2001
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: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome
disease Disease or Syndrome 17 6 0.010 None 1.000 1 2010 2010
CUI: C0344505
Disease: Alacrima
Alacrima
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2020 2020
Malignant neoplasm of cardioesophageal junction of stomach
disease Digestive System Diseases; Neoplasms Neoplastic Process 26 0.010 None 1.000 1 2017 2017
CUI: C0347950
Disease: Asthma attack
Asthma attack
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 32 1 0.010 None 1.000 1 2000 2000
CUI: C0349782
Disease: Ischemic cardiomyopathy
Ischemic cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 110 5 0.010 None 1.000 1 2010 2010
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 467 14 0.010 None 1.000 1 2016 2016
Hantavirus infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 21 1 0.010 None 1.000 1 2012 2012
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
group Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 827 60 0.010 None 1.000 1 2018 2018
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 2019 2019
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 43 14 0.010 None 1.000 1 1999 1999