IL17A, interleukin 17A, 3605

N. diseases: 1074; N. variants: 19
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 0.971 35 1 2006 2019
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.100 None 0.958 24 2 2013 2019
CUI: C0238790
Disease: bone destruction
bone destruction
disease Disease or Syndrome 234 3 0.100 None 1.000 16 2003 2019
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.100 None 0.909 11 2007 2020
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 593 24 0.090 None 1.000 9 2008 2019
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 467 14 0.070 None 1.000 7 2011 2019
CUI: C2062441
Disease: Influenza A
Influenza A
disease Disease or Syndrome 563 19 0.070 None 1.000 7 1 2017 2019
CUI: C3160909
Disease: Autoimmune arthritis
Autoimmune arthritis
disease Disease or Syndrome 113 0.060 None 1.000 6 2007 2017
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.040 None 1.000 4 2014 2019
CUI: C2363774
Disease: Neutrophilic asthma
Neutrophilic asthma
disease Disease or Syndrome 40 2 0.040 None 1.000 4 2015 2019
Chronic rhinosinusitis with nasal polyps
disease Neoplastic Process 168 1 0.040 None 1.000 4 2014 2018
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.040 None 1.000 4 2011 2019
CUI: C0853662
Disease: Oestrogen deficiency
Oestrogen deficiency
disease Disease or Syndrome 85 1 0.030 None 1.000 3 2017 2018
CUI: C3267073
Disease: Autoinflammatory disease
Autoinflammatory disease
disease Disease or Syndrome 81 10 0.030 None 1.000 3 2017 2019
CUI: C3544347
Disease: Intestinal fibrosis
Intestinal fibrosis
phenotype Anatomical Abnormality 65 0.030 None 1.000 3 2018 2019
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
disease Disease or Syndrome 133 54 0.030 None 1.000 3 2018 2019
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.030 None 1.000 3 2016 2018
CUI: C0018129
Disease: Graft Rejection
Graft Rejection
phenotype Organ or Tissue Function 47 0.200 None 1.000 2 2010 2013
CUI: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.020 None 1.000 2 2008 2020
CUI: C0848771
Disease: neurological disability
neurological disability
phenotype Sign or Symptom 18 6 0.020 None 1.000 2 2013 2014
CUI: C0863129
Disease: AGEP
AGEP
disease Disease or Syndrome 9 0.020 None 1.000 2 2014 2016
CUI: C0919747
Disease: Cytokine storm
Cytokine storm
disease Disease or Syndrome 97 0.020 None 1.000 2 2017 2019
CUI: C0920235
Disease: Psoriatic plaque
Psoriatic plaque
disease Disease or Syndrome 12 0.020 None 1.000 2 2009 2017
CUI: C1262091
Disease: Lymphocytic infiltration
Lymphocytic infiltration
disease Disease or Syndrome 84 2 0.020 None 1.000 2 2009 2014
Hepatitis B Virus-Related Hepatocellular Carcinoma
disease Neoplastic Process 76 8 0.020 None 1.000 2 2015 2017