SERPING1, serpin family G member 1, 710

N. diseases: 207; N. variants: 43
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: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.150 None 1.000 5 1 1995 2015
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
phenotype Sign or Symptom 17 3 0.010 None 1.000 1 2015 2015
CUI: C4025190
Disease: Abnormal epiglottis morphology
Abnormal epiglottis morphology
phenotype Anatomical Abnormality 2 1 0.100 None 0
CUI: C4021978
Disease: Abnormality of salivation
Abnormality of salivation
phenotype Finding 3 1 0.100 None 0
CUI: C4021777
Disease: Abnormality of the larynx
Abnormality of the larynx
phenotype Anatomical Abnormality 11 1 0.100 None 0
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula
phenotype Anatomical Abnormality 2 2 0.100 None 0
CUI: C2931758
Disease: Acquired angioedema
Acquired angioedema
disease Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.400 None 1.000 16 1989 2019
CUI: C3506079
Disease: Acquired C1 inhibitor deficiency
Acquired C1 inhibitor deficiency
disease Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.080 None 1.000 8 1989 2019
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 41 30 0.010 None 1.000 1 2007 2007
CUI: C0701807
Disease: Acute anterior uveitis
Acute anterior uveitis
disease Eye Diseases Disease or Syndrome 90 30 0.010 None < 0.001 1 2013 2013
CUI: C0333240
Disease: Acute edema
Acute edema
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0.020 None 1.000 2 2010 2010
Acute exacerbation of chronic obstructive airways disease
phenotype Respiratory Tract Diseases Disease or Syndrome 63 1 0.010 None 1.000 1 2018 2018
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 766 118 0.230 None 1.000 3 2016 2018
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
disease Digestive System Diseases Disease or Syndrome 435 51 0.010 None 1.000 1 2019 2019
CUI: C0748355
Disease: Acute respiratory distress
Acute respiratory distress
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 147 6 0.010 None 1.000 1 2017 2017
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
disease Neoplasms Neoplastic Process 2528 98 0.210 None 1.000 2 2017 2019
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 399 27 0.010 None 1.000 1 2016 2016
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1169 66 0.020 None 1.000 2 2001 2019
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 370 39 0.030 None 1.000 3 2017 2019
CUI: C0279550
Disease: Adult Rhabdomyosarcoma
Adult Rhabdomyosarcoma
disease Neoplasms Neoplastic Process 509 12 0.010 None 1.000 1 1996 1996
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
disease Eye Diseases Disease or Syndrome 685 663 0.100 None 0.692 13 3 2008 2015
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction
group Respiratory Tract Diseases Disease or Syndrome 110 5 0.030 None 1.000 3 2010 2013
CUI: C0002020
Disease: Alexithymia
Alexithymia
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 39 12 0.010 None 1.000 1 2018 2018
CUI: C0740903
Disease: allergic symptom
allergic symptom
phenotype Sign or Symptom 37 2 0.010 None 1.000 1 2001 2001
CUI: C0856904
Disease: Allergy to fish
Allergy to fish
phenotype Disease or Syndrome 3 0.010 None 1.000 1 2019 2019