IL1RN, interleukin 1 receptor antagonist, 3557

N. diseases: 701; N. variants: 52
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: C0206669
Disease: Hepatocellular Adenoma
Hepatocellular Adenoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 114 7 0.010 None 1.000 1 1999 1999
CUI: C0267055
Disease: Erosive esophagitis
Erosive esophagitis
disease Digestive System Diseases Disease or Syndrome 16 0.010 None 1.000 1 2013 2013
CUI: C0267561
Disease: Perianal fistula
Perianal fistula
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases Anatomical Abnormality 7 2 0.010 None 1.000 1 2001 2001
CUI: C0268074
Disease: Indian childhood cirrhosis
Indian childhood cirrhosis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 67 6 0.010 None 1.000 1 2012 2012
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 20 7 0.010 None 1.000 1 2007 2007
CUI: C0268390
Disease: Muckle-Wells Syndrome
Muckle-Wells Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 34 16 0.010 None 1.000 1 2007 2007
CUI: C0269084
Disease: Vulvar Vestibulitis
Vulvar Vestibulitis
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 11 0.010 None 1.000 1 2000 2000
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
disease Nervous System Diseases Disease or Syndrome 94 24 0.010 None 1.000 1 2020 2020
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 596 81 0.010 None 1.000 1 2018 2018
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.010 None 1.000 1 2009 2009
Thrombocytopenia due to platelet alloimmunization
disease Hemic and Lymphatic Diseases Disease or Syndrome 111 7 0.010 None 1.000 1 2010 2010
CUI: C0275518
Disease: Acute infectious disease
Acute infectious disease
group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 198 5 0.010 None 1.000 1 2018 2018
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis
disease Infections; Cardiovascular Diseases Disease or Syndrome 129 2 0.010 None 1.000 1 2002 2002
CUI: C0276609
Disease: Acute type B viral hepatitis
Acute type B viral hepatitis
disease Digestive System Diseases; Infections Disease or Syndrome 38 0.010 None 1.000 1 2017 2017
CUI: C0264490
Disease: Acute respiratory failure
Acute respiratory failure
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Respiratory Tract Diseases Disease or Syndrome 78 5 0.010 None 1.000 1 2018 2018
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 303 317 0.010 None 1.000 1 1 2007 2007
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 19 2 0.010 None < 0.001 1 2002 2002
CUI: C0206694
Disease: Mucoepidermoid Carcinoma
Mucoepidermoid Carcinoma
disease Neoplasms Neoplastic Process 153 6 0.010 None 1.000 1 1996 1996
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
disease Neoplasms; Eye Diseases Neoplastic Process 376 22 0.010 None 1.000 1 2011 2011
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 41 11 0.010 None 1.000 1 2009 2009
CUI: C0221765
Disease: Chronic schizophrenia
Chronic schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 48 7 0.010 None 1.000 1 2003 2003
CUI: C0233794
Disease: Memory impairment
Memory impairment
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 763 48 0.010 None 1.000 1 2019 2019
CUI: C0234251
Disease: Inflammatory pain
Inflammatory pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 266 1 0.010 None 1.000 1 2019 2019
CUI: C0235820
Disease: Neonatal encephalopathy
Neonatal encephalopathy
disease Nervous System Diseases Disease or Syndrome 26 10 0.010 None 1.000 1 2018 2018
CUI: C0235842
Disease: Decidual endometritis
Decidual endometritis
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 6 0.010 None 1.000 1 2008 2008