TMPRSS2, transmembrane serine protease 2, 7113

N. diseases: 69; N. variants: 3
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: C0272138
Disease: Erythroblastosis
Erythroblastosis
disease Disease or Syndrome 89 0.100 None 1.000 11 2008 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.060 None 1.000 6 2008 2017
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
disease Neoplastic Process 398 7 0.040 None 1.000 4 2013 2016
CUI: C2062441
Disease: Influenza A
Influenza A
disease Disease or Syndrome 563 19 0.040 None 1.000 4 2013 2019
Metastasis from malignant tumor of prostate
disease Neoplastic Process 342 18 0.030 None 1.000 3 2008 2012
Metastatic castration-resistant prostate cancer
disease Neoplastic Process 140 2 0.020 None 1.000 2 2016 2019
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.010 None 1.000 1 2018 2018
androgen independent prostate cancer
disease Neoplastic Process 190 5 0.010 None 1.000 1 2007 2007
Influenza due to Influenza A virus subtype H7N9
disease Disease or Syndrome 6 3 0.010 None 1.000 1 2 2015 2015
CUI: C4727916
Disease: H3N2 influenza
H3N2 influenza
disease Disease or Syndrome 16 0.010 None 1.000 1 2013 2013
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
disease Cardiovascular Diseases Disease or Syndrome 377 8 0.030 None 1.000 3 2012 2018
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 757 47 0.020 None 1.000 2 2007 2007
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 546 541 0.010 None 1.000 1 2016 2016
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 230 24 0.100 None 1.000 10 1 2007 2019
CUI: C1264610
Disease: Infectious peritonitis
Infectious peritonitis
disease Digestive System Diseases; Infections Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 1296 609 0.010 None 1.000 1 2007 2007
Squamous cell carcinoma of esophagus
disease Digestive System Diseases; Neoplasms Neoplastic Process 2053 329 0.010 None 1.000 1 2019 2019
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 2689 322 0.010 None 1.000 1 2019 2019
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 2667 277 0.010 None 1.000 1 2019 2019
CUI: C0206750
Disease: Coronavirus Infections
Coronavirus Infections
group Infections Disease or Syndrome 33 0.020 None 1.000 2 2017 2019
CUI: C3694279
Disease: Middle East Respiratory Syndrome
Middle East Respiratory Syndrome
disease Infections Disease or Syndrome 53 0.020 None 1.000 2 2017 2019
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
group Infections Disease or Syndrome 1471 42 0.010 None 1.000 1 2016 2016
CUI: C0282687
Disease: Hemorrhagic Fever, Ebola
Hemorrhagic Fever, Ebola
disease Infections Disease or Syndrome 164 1 0.010 None < 0.001 1 2012 2012
CUI: C0021400
Disease: Influenza
Influenza
disease Infections; Respiratory Tract Diseases Disease or Syndrome 858 17 0.050 None 1.000 5 2012 2019
CUI: C1175175
Disease: Severe Acute Respiratory Syndrome
Severe Acute Respiratory Syndrome
disease Infections; Respiratory Tract Diseases Disease or Syndrome 117 1 0.040 None 1.000 4 2014 2019