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: C0153261
Disease: Histoplasma capsulatum Infection
Histoplasma capsulatum Infection 		group Infections Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0154565
Disease: Non-organic sleep disorder
Non-organic sleep disorder 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2019 2019
CUI: C0267448
Disease: Eosinophilic colitis
Eosinophilic colitis 		disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 1997 1997
CUI: C0553548
Disease: Necrotizing Arteritis
Necrotizing Arteritis 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2007 2007
CUI: C0851882
Disease: Infection caused by Francisella
Infection caused by Francisella 		disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
CUI: C0858727
Disease: Joint swelling inflammatory
Joint swelling inflammatory 		disease Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
CUI: C1541844
Disease: PRESENILE AND SENILE DEMENTIA
PRESENILE AND SENILE DEMENTIA 		disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 1 0.200 None 1.000 1 2012 2012
CUI: C1867047
Disease: Systemic granulomatous disease
Systemic granulomatous disease 		disease Disease or Syndrome 1 0.010 None 1.000 1 1995 1995
CUI: C2608043
Disease: Folliculitis decalvans
Folliculitis decalvans 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C2721730
Disease: Burkholderia cenocepacia infection
Burkholderia cenocepacia infection 		disease Disease or Syndrome 1 0.010 None 1.000 1 2013 2013
CUI: C4510851
Disease: Duodenal ulcer caused by Helicobacter pylori
Duodenal ulcer caused by Helicobacter pylori 		disease Disease or Syndrome 1 0.010 None 1.000 1 2006 2006
CUI: C4016230
Disease: GASTRIC CANCER SUSCEPTIBILITY AFTER H. PYLORI INFECTION
GASTRIC CANCER SUSCEPTIBILITY AFTER H. PYLORI INFECTION 		phenotype Finding 1 1 0.100 None 0 1
CUI: C0232492
Disease: Upper abdominal pain
Upper abdominal pain 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Sign or Symptom 2 0.010 None 1.000 1 2015 2015
CUI: C0266025
Disease: Ectopic tooth
Ectopic tooth 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 2 0.010 None 1.000 1 2018 2018
CUI: C0276832
Disease: Congenital malaria
Congenital malaria 		disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0343387
Disease: Enterocolitis, Neutropenic
Enterocolitis, Neutropenic 		disease Digestive System Diseases Disease or Syndrome 2 0.200 None 1.000 1 2013 2013
CUI: C0679424
Disease: iron loading anemia
iron loading anemia 		disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1992 1992
CUI: C3666010
Disease: Breakthrough infection
Breakthrough infection 		disease Disease or Syndrome 2 1 0.010 None 1.000 1 2017 2017
CUI: C3854422
Disease: Root canal infection
Root canal infection 		disease Disease or Syndrome 2 0.010 None 1.000 1 2010 2010
CUI: C4510988
Disease: Monogenic autoinflammatory syndrome
Monogenic autoinflammatory syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 2 0.010 None 1.000 1 2011 2011
CUI: C4544985
Disease: Fibropolycystic disease of liver
Fibropolycystic disease of liver 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C4707790
Disease: Idiopathic recurrent pericarditis
Idiopathic recurrent pericarditis 		disease Cardiovascular Diseases Disease or Syndrome 3 0.040 None 1.000 4 2018 2019
CUI: C2748507
Disease: INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 3 2 0.020 None 1.000 2 2011 2013
CUI: C0024799
Disease: Marginal ulcer
Marginal ulcer 		disease Digestive System Diseases Disease or Syndrome 3 0.300 None 1.000 1 2009 2009
CUI: C0263949
Disease: Proliferative synovitis
Proliferative synovitis 		disease Musculoskeletal Diseases Disease or Syndrome 3 0.010 None 1.000 1 1991 1991