IL1B, interleukin 1 beta, 3553

N. diseases: 1801; N. variants: 22
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 0.966 58 2001 2020
CUI: C3267073
Disease: Autoinflammatory disease
Autoinflammatory disease
disease Disease or Syndrome 81 10 0.100 None 1.000 42 2007 2020
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 593 24 0.100 None 1.000 29 1999 2018
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.100 None 1.000 18 1990 2019
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.100 None 1.000 14 2004 2019
CUI: C3860213
Disease: Autoinflammatory disorder
Autoinflammatory disorder
disease Disease or Syndrome 60 4 0.100 None 1.000 13 2010 2019
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 467 14 0.100 None 1.000 11 1993 2019
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.100 None 1.000 11 2016 2020
CUI: C2062441
Disease: Influenza A
Influenza A
disease Disease or Syndrome 563 19 0.100 None 1.000 11 2 2003 2020
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
disease Disease or Syndrome 695 94 0.100 None 1.000 11 1 1990 2019
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.080 None 1.000 8 2016 2019
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.080 None 1.000 8 3 1997 2019
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia
phenotype Disease or Syndrome 266 24 0.050 None 1.000 5 2003 2013
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.050 None 1.000 5 2006 2016
CUI: C2363774
Disease: Neutrophilic asthma
Neutrophilic asthma
disease Disease or Syndrome 40 2 0.050 None 1.000 5 2014 2019
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
disease Acquired Abnormality 115 15 0.040 None 1.000 4 2014 2020
CUI: C3160909
Disease: Autoimmune arthritis
Autoimmune arthritis
disease Disease or Syndrome 113 0.040 None 1.000 4 2006 2018
CUI: C4721773
Disease: Postoperative cognitive dysfunction
Postoperative cognitive dysfunction
phenotype Mental or Behavioral Dysfunction 93 0.230 None 1.000 4 2012 2019
CUI: C0238790
Disease: bone destruction
bone destruction
disease Disease or Syndrome 234 3 0.030 None 0.667 3 1996 2018
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.030 None 1.000 3 1995 2019
CUI: C2712871
Disease: Gout attack
Gout attack
disease Disease or Syndrome 4 0.030 None 1.000 3 2017 2020
CUI: C2939094
Disease: Skin sensitisation
Skin sensitisation
disease Disease or Syndrome 34 0.030 None 1.000 3 2000 2019
CUI: C3495798
Disease: Periodontal inflammation
Periodontal inflammation
disease Disease or Syndrome 82 2 0.030 None 1.000 3 1 2017 2020
Neutrophil extracellular trap formation
disease Disease or Syndrome 55 0.030 None 1.000 3 2017 2019
Temporomandibular joint osteoarthritis
disease Disease or Syndrome 32 0.030 None 1.000 3 2016 2018