IL6, interleukin 6, 3569

N. diseases: 2367; 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: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
disease Skin and Connective Tissue Diseases Disease or Syndrome 64 11 0.010 None 1.000 1 2019 2019
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 209 21 0.010 None 1.000 1 2018 2018
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 24 0.010 None 1.000 1 2008 2008
Acute vascular insufficiency of intestine (disorder)
disease Digestive System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0001403
Disease: Addison Disease
Addison Disease
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 111 13 0.010 None 1.000 1 2018 2018
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 43 1 0.010 None 1.000 1 2007 2007
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex
disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 4 0.010 None 1.000 1 1996 1996
CUI: C0001857
Disease: AIDS related complex
AIDS related complex
disease Infections; Immune System Diseases Disease or Syndrome 100 43 0.010 None 1.000 1 1994 1994
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 52 4 0.010 None 1.000 1 2019 2019
CUI: C0002020
Disease: Alexithymia
Alexithymia
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 39 12 0.010 None 1.000 1 2019 2019
CUI: C0002170
Disease: Alopecia
Alopecia
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 491 375 0.010 None 1.000 1 2017 2017
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis
group Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 65 2 0.010 None 1.000 1 2009 2009
CUI: C0002793
Disease: Anaplasia
Anaplasia
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 538 7 0.010 None 1.000 1 2017 2017
CUI: C0002880
Disease: Autoimmune hemolytic anemia
Autoimmune hemolytic anemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 81 0.010 None 1.000 1 2012 2012
CUI: C0002940
Disease: Aneurysm
Aneurysm
disease Cardiovascular Diseases Pathologic Function 22 36 0.010 None 1.000 1 2002 2002
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 108 206 0.010 None 1.000 1 2008 2008
CUI: C0003130
Disease: Anoxia
Anoxia
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 287 0.010 None 1.000 1 2007 2007
CUI: C0003164
Disease: Anthracosilicosis
Anthracosilicosis
disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 1 2018 2018
CUI: C0003460
Disease: Anuria
Anuria
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis
disease Cardiovascular Diseases Disease or Syndrome 234 19 0.010 None 1.000 1 2018 2018
CUI: C0003578
Disease: Apnea
Apnea
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 262 11 0.010 None 1.000 1 2009 2009
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 206 2356 0.010 None 1.000 1 2006 2006
CUI: C0004030
Disease: Aspergillosis
Aspergillosis
disease Infections Disease or Syndrome 47 2 0.010 None 1.000 1 2017 2017
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 45 5 0.010 None 1.000 1 2018 2018
CUI: C0004941
Disease: Behavioral Symptoms
Behavioral Symptoms
group Behavior and Behavior Mechanisms Sign or Symptom 45 9 0.010 None 1.000 1 2019 2019