PLG, plasminogen, 5340

N. diseases: 586; N. variants: 34
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: C0311343
Disease: Membranous conjunctivitis
Membranous conjunctivitis
disease Infections; Eye Diseases Disease or Syndrome 1 0.020 None 1.000 2 2002 2019
CUI: C0574014
Disease: Axillary vein thrombosis
Axillary vein thrombosis
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 1988 1988
CUI: C1274355
Disease: Streptococcal infection of skin
Streptococcal infection of skin
disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2004 2004
CUI: C4280715
Disease: Decreased level of plasminogen
Decreased level of plasminogen
phenotype Finding 1 0.400 strong 0
CUI: C1274789
Disease: Ligneous conjunctivitis
Ligneous conjunctivitis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 2 1 0.600 None 1.000 16 1 1997 2019
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 2 0.300 None 1.000 1 2018 2018
CUI: C0406097
Disease: Streptococcal impetigo
Streptococcal impetigo
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2002 2002
CUI: C0543673
Disease: Fibrinolytic disorder
Fibrinolytic disorder
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1984 1984
Invasive Group A beta-hemolytic streptococcal disease
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C4024810
Disease: Chronic irritative conjunctivitis
Chronic irritative conjunctivitis
disease Eye Diseases Disease or Syndrome 2 0.100 None 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 3 13 0.800 definitive 1.000 28 12 1982 2019
CUI: C0012602
Disease: Dirofilariasis
Dirofilariasis
disease Infections; Animal Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0032059
Disease: Placentitis (disorder)
Placentitis (disorder)
phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Infections Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C4699511
Disease: Stroke of undetermined etiology
Stroke of undetermined etiology
disease Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4020755
Disease: Abnormality of fontanelles
Abnormality of fontanelles
disease Anatomical Abnormality 3 0.100 None 0
CUI: C0333208
Disease: Fibrin thrombus
Fibrin thrombus
disease Cardiovascular Diseases Acquired Abnormality 4 0.010 None 1.000 1 2018 2018
Hereditary angioedema with normal C1 inhibitor
disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
Pleural effusion associated with pulmonary infection
disease Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C1861141
Disease: Abnormality of the middle ear
Abnormality of the middle ear
phenotype Finding 5 0.100 None 0
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
disease Disease or Syndrome 6 3 0.020 None 1.000 2 2011 2016
CUI: C0035022
Disease: Tick-borne relapsing fever
Tick-borne relapsing fever
disease Infections Disease or Syndrome 6 0.010 None 1.000 1 2008 2008
CUI: C0085642
Disease: Livedo Reticularis
Livedo Reticularis
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 1983 1983
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 8 0.010 None 1.000 1 1988 1988
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: C1956391
Disease: Temporal Arteritis
Temporal Arteritis
disease Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 6 0.100 None 1.000 1 1 2017 2017