F2RL1, F2R like trypsin receptor 1, 2150

N. diseases: 256; N. variants: 4
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 22 2003 2019
CUI: C3495798
Disease: Periodontal inflammation
Periodontal inflammation
disease Disease or Syndrome 82 2 0.040 None 1.000 4 2010 2017
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.040 None 1.000 4 2014 2020
CUI: C0747479
Disease: Periodontal infection
Periodontal infection
disease Disease or Syndrome 17 0.020 None 1.000 2 2013 2017
CUI: C0876991
Disease: Histiocytosis haematophagic
Histiocytosis haematophagic
disease Disease or Syndrome 36 2 0.020 None 1.000 2 2013 2015
Diarrhoea predominant irritable bowel syndrome
disease Disease or Syndrome 57 8 0.020 None 1.000 2 2010 2015
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
disease Disease or Syndrome 297 3 0.020 None 1.000 2 2013 2019
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 563 1418 0.100 None 1.000 1 1 2012 2012
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
disease Neoplastic Process 573 14 0.010 None 1.000 1 2011 2011
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 593 24 0.010 None 1.000 1 2007 2007
High density lipoprotein measurement
phenotype Laboratory Procedure 545 1440 0.100 None 1.000 1 1 2012 2012
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
phenotype Laboratory Procedure 283 679 0.100 None 1.000 1 1 2012 2012
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2017 2017
CUI: C0856687
Disease: Infection caused by Trichinella
Infection caused by Trichinella
disease Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1262048
Disease: Glial scar
Glial scar
phenotype Acquired Abnormality 51 0.010 None 1.000 1 2019 2019
CUI: C1334177
Disease: Infiltrating Cervical Carcinoma
Infiltrating Cervical Carcinoma
disease Neoplastic Process 76 13 0.010 None 1.000 1 2008 2008
CUI: C1510885
Disease: Angiogenic Switch
Angiogenic Switch
disease Neoplastic Process 96 3 0.010 None 1.000 1 2008 2008
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.010 None 1.000 1 2017 2017
CUI: C1855038
Disease: Hepatocellular necrosis
Hepatocellular necrosis
phenotype Disease or Syndrome 41 0.010 None 1.000 1 2016 2016
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.010 None 1.000 1 2010 2010
CUI: C2062441
Disease: Influenza A
Influenza A
disease Disease or Syndrome 563 19 0.010 None 1.000 1 2016 2016
CUI: C3544205
Disease: Ovarian clear cell carcinoma
Ovarian clear cell carcinoma
disease Neoplastic Process 103 0.010 None 1.000 1 2017 2017
CUI: C4020969
Disease: Inflammatory abnormality of the eye
Inflammatory abnormality of the eye
disease Disease or Syndrome 88 1 0.010 None 1.000 1 2006 2006
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.010 None 1.000 1 2020 2020
Heart failure with preserved ejection fraction [HFpEF]
disease Disease or Syndrome 89 4 0.010 None 1.000 1 2019 2019