SERPINF1, serpin family F member 1, 5176

N. diseases: 294; N. variants: 15
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 10 2004 2019
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.040 None 0.750 4 2015 2019
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy
disease Disease or Syndrome 56 67 0.040 None 1.000 4 1 2009 2015
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.040 None 1.000 4 2010 2018
CUI: C1707516
Disease: Corneal Sensitivity
Corneal Sensitivity
phenotype Sign or Symptom 8 0.020 None 1.000 2 2017 2018
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 2 3 2018 2018
CUI: C4049446
Disease: Neointimal hyperplasia
Neointimal hyperplasia
disease Disease or Syndrome 198 0.020 None 1.000 2 2007 2010
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.020 None 1.000 2 2017 2018
Osteogenesis imperfecta type IV (disorder)
disease Disease or Syndrome; Congenital Abnormality 12 65 0.300 None 1.000 1 2015 2015
CUI: C0279068
Disease: Childhood Solid Neoplasm
Childhood Solid Neoplasm
phenotype Neoplastic Process 169 3 0.010 None 1.000 1 2010 2010
CUI: C0280099
Disease: Adult Solid Neoplasm
Adult Solid Neoplasm
group Neoplastic Process 163 3 0.010 None 1.000 1 2010 2010
CUI: C0398620
Disease: Alpha-2-antiplasmin deficiency
Alpha-2-antiplasmin deficiency
disease Disease or Syndrome 2 0.010 None 1.000 1 1982 1982
Metastasis from malignant tumor of prostate
disease Neoplastic Process 342 18 0.010 None 1.000 1 2014 2014
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature
disease Acquired Abnormality 84 0.010 None 1.000 1 2003 2003
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2016 2016
CUI: C1868702
Disease: Diabetic keratopathy
Diabetic keratopathy
disease Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
disease Acquired Abnormality 115 15 0.010 None 1.000 1 2010 2010
CUI: C3495840
Disease: Pancreatic steatosis
Pancreatic steatosis
disease Disease or Syndrome 4 0.010 None 1.000 1 2012 2012
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3
disease Disease or Syndrome 209 20 0.010 None 1.000 1 2014 2014
CUI: C3888523
Disease: Autoimmune uveitis
Autoimmune uveitis
disease Disease or Syndrome 31 0.010 None 1.000 1 2009 2009
Wet age-related macular degeneration
disease Disease or Syndrome 20 2 0.010 None 1.000 1 1 2008 2008
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
disease Disease or Syndrome 138 21 0.010 None 1.000 1 1999 1999
CUI: C4068858
Disease: Avascular retina
Avascular retina
disease Disease or Syndrome 19 0.010 None 1.000 1 2010 2010
Obesity-Associated Insulin Resistance
disease Disease or Syndrome 36 0.010 None 1.000 1 2013 2013
CUI: C0409495
Disease: Protrusio acetabuli
Protrusio acetabuli
disease Anatomical Abnormality 10 2 0.100 None 0