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: C2609046
Disease: Sticky platelet syndrome
Sticky platelet syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 2 0.010 None 1.000 1 2005 2005
CUI: C4317320
Disease: Factor V deficiency
Factor V deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 1999 1999
CUI: C1866423
Disease: Quebec platelet disorder
Quebec platelet disorder 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.050 None 1.000 5 2001 2010
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 7 0.010 None 1.000 1 1999 1999
CUI: C0333205
Disease: Mural thrombus
Mural thrombus 		disease Cardiovascular Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 1 2002 2002
CUI: C1260883
Disease: Mural thrombus of heart
Mural thrombus of heart 		disease Cardiovascular Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 1 2002 2002
CUI: C0524688
Disease: Pneumonic Plague
Pneumonic Plague 		disease Infections Disease or Syndrome 8 0.020 None 1.000 2 2002 2019
CUI: C0162510
Disease: Caroli Disease
Caroli Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome; Congenital Abnormality 8 1 0.010 None 1.000 1 2009 2009
CUI: C0554628
Disease: Group A Streptococcal Infections
Group A Streptococcal Infections 		disease Infections Disease or Syndrome 8 0.010 None 1.000 1 2004 2004
CUI: C0728936
Disease: Disorder of circulatory system
Disorder of circulatory system 		group Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 8 0.010 None 1.000 1 1997 1997
CUI: C1709735
Disease: Prosthetic Valve Thrombosis
Prosthetic Valve Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0266249
Disease: Gallbladder anomaly congenital
Gallbladder anomaly congenital 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 8 0.100 None 0
CUI: C0747556
Disease: Recurrent pharyngitis
Recurrent pharyngitis 		phenotype Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Sign or Symptom 8 0.100 None 0
CUI: C4021818
Disease: Abnormality of the ovary
Abnormality of the ovary 		disease Anatomical Abnormality 8 1 0.100 None 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.700 definitive 0.958 24 1 1988 2019
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion 		phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 9 0.010 None 1.000 1 2017 2017
CUI: C0021099
Disease: Impetigo
Impetigo 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 1999 1999
CUI: C0854248
Disease: Pneumonia due to Gram negative bacteria
Pneumonia due to Gram negative bacteria 		group Infections; Respiratory Tract Diseases Disease or Syndrome 9 0.010 None 1.000 1 2008 2008
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		disease Cardiovascular Diseases Anatomical Abnormality 10 2 0.010 None 1.000 1 2004 2004
CUI: C0596452
Disease: disabling disease
disabling disease 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 10 1 0.010 None 1.000 1 2006 2006
CUI: C0729665
Disease: Arteriovenous graft
Arteriovenous graft 		disease Acquired Abnormality 10 2 0.010 None 1.000 1 2009 2009
CUI: C0016397
Disease: Focal Infection
Focal Infection 		disease Infections Disease or Syndrome 11 0.010 None 1.000 1 1999 1999
CUI: C0031144
Disease: Chronic peritoneal effusion (disorder)
Chronic peritoneal effusion (disorder) 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 11 0.010 None 1.000 1 1986 1986
CUI: C0677501
Disease: Congenital Nephrogenic Diabetes Insipidus
Congenital Nephrogenic Diabetes Insipidus 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 11 8 0.010 None 1.000 1 1991 1991
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 11 3 0.010 None 1.000 1 2008 2008