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.
GASTRIC CANCER SUSCEPTIBILITY AFTER H. PYLORI INFECTION
phenotype Finding 1 1 0.100 None 0 1
CUI: C0001430
Disease: Adenoma
Adenoma
group Neoplasms Neoplastic Process 1183 103 0.010 None < 0.001 1 2011 2011
CUI: C0002792
Disease: anaphylaxis
anaphylaxis
phenotype Immune System Diseases Disease or Syndrome 180 4 0.010 None < 0.001 1 2019 2019
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 1112 395 0.010 None < 0.001 1 2017 2017
CUI: C0010043
Disease: Corneal Ulcer
Corneal Ulcer
disease Infections; Eye Diseases Disease or Syndrome 33 1 0.010 None < 0.001 1 2013 2013
CUI: C0010418
Disease: Cryptosporidiosis
Cryptosporidiosis
disease Digestive System Diseases; Infections; Animal Diseases Disease or Syndrome 40 0.010 None < 0.001 1 2001 2001
CUI: C0015674
Disease: Chronic Fatigue Syndrome
Chronic Fatigue Syndrome
disease Infections; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 118 14 0.010 None < 0.001 1 2017 2017
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
disease Eye Diseases Disease or Syndrome 94 56 0.010 None < 0.001 1 2007 2007
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
disease Eye Diseases Disease or Syndrome 87 55 0.010 None < 0.001 1 2007 2007
Lupus Erythematosus, Subacute Cutaneous
disease Skin and Connective Tissue Diseases Disease or Syndrome 39 1 0.010 None < 0.001 1 2001 2001
CUI: C0032051
Disease: Placental Insufficiency
Placental Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 45 0.010 None < 0.001 1 2019 2019
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 51 7 0.010 None < 0.001 1 2001 2001
Septicaemia due to gram-negative organism, unspecified
group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 33 2 0.010 None < 0.001 1 2007 2007
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 247 176 0.010 None < 0.001 1 2017 2017
CUI: C0154575
Disease: Rumination Disorders
Rumination Disorders
group Mental Disorders Mental or Behavioral Dysfunction 33 13 0.010 None < 0.001 1 2017 2017
CUI: C0221268
Disease: Colloid goiter
Colloid goiter
disease Endocrine System Diseases Disease or Syndrome 7 0.010 None < 0.001 1 2019 2019
CUI: C0242723
Disease: Parasitemia
Parasitemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 140 3 0.010 None < 0.001 1 2019 2019
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 237 21 0.010 None < 0.001 1 2020 2020
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 67 18 0.010 None < 0.001 1 2020 2020
CUI: C0268405
Disease: Hemodialysis-associated amyloidosis
Hemodialysis-associated amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None < 0.001 1 1994 1994
CUI: C0270736
Disease: Essential Tremor
Essential Tremor
disease Nervous System Diseases Disease or Syndrome 122 79 0.010 None < 0.001 1 1 2019 2019
CUI: C0282312
Disease: Bubonic Plague
Bubonic Plague
disease Infections Disease or Syndrome 3 0.010 None < 0.001 1 2012 2012
CUI: C0396060
Disease: Congenital laryngeal adductor palsy
Congenital laryngeal adductor palsy
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 17 0.010 None < 0.001 1 2013 2013
CUI: C0438696
Disease: Suicidal
Suicidal
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 93 29 0.010 None < 0.001 1 2008 2008
CUI: C0521170
Disease: Osteoporotic Fractures
Osteoporotic Fractures
group Wounds and Injuries Disease or Syndrome 108 40 0.010 None < 0.001 1 2000 2000