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: C3829514
Disease: Intrapartum fever
Intrapartum fever 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 3 0.010 None < 0.001 1 2019 2019
CUI: C4049279
Disease: Post stroke epilepsy
Post stroke epilepsy 		disease Disease or Syndrome 7 2 0.010 None < 0.001 1 2012 2012
CUI: C4310512
Disease: Sporadic CJD
Sporadic CJD 		disease Infections; Nervous System Diseases; Mental Disorders; Animal Diseases Disease or Syndrome 30 17 0.010 None < 0.001 1 2014 2014
CUI: C4511579
Disease: Peripheral spondyloarthritis
Peripheral spondyloarthritis 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 3 0.010 None < 0.001 1 2020 2020
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
Primary differentiated carcinoma of thyroid gland 		disease Neoplastic Process 167 41 0.010 None < 0.001 1 2018 2018
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis 		disease Digestive System Diseases Disease or Syndrome 252 90 0.030 None 0.333 3 2009 2018
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 577 441 0.340 None 0.500 4 2009 2019
CUI: C0947622
Disease: Cholecystolithiasis
Cholecystolithiasis 		disease Digestive System Diseases Disease or Syndrome 156 62 0.040 None 0.500 4 1996 2018
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 184 32 0.020 None 0.500 2 2015 2018
CUI: C0021841
Disease: Intestinal Neoplasms
Intestinal Neoplasms 		group Digestive System Diseases; Neoplasms Neoplastic Process 182 2 0.020 None 0.500 2 2016 2018
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		group Nervous System Diseases Disease or Syndrome 351 81 0.020 None 0.500 2 2017 2019
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 507 248 0.020 None 0.500 2 2002 2003
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 615 45 0.020 None 0.500 2 2014 2020
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 51 16 0.020 None 0.500 2 2005 2012
CUI: C0282160
Disease: Aplasia Cutis Congenita
Aplasia Cutis Congenita 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 393 14 0.020 None 0.500 2 2014 2020
CUI: C0282687
Disease: Hemorrhagic Fever, Ebola
Hemorrhagic Fever, Ebola 		disease Infections Disease or Syndrome 164 1 0.020 None 0.500 2 1999 2005
CUI: C0349217
Disease: Depressive episode, unspecified
Depressive episode, unspecified 		disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 27 2 0.020 None 0.500 2 2016 2020
CUI: C0426576
Disease: Gastrointestinal symptom
Gastrointestinal symptom 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 69 7 0.020 None 0.500 2 2019 2019
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 72 33 0.020 None 0.500 2 2005 2013
CUI: C0524988
Disease: Schnitzler Syndrome
Schnitzler Syndrome 		disease Immune System Diseases Disease or Syndrome 14 2 0.020 None 0.500 2 2013 2018
CUI: C1841972
Disease: Glucocorticoid Receptor Deficiency
Glucocorticoid Receptor Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 104 12 0.020 None 0.500 2 2018 2019
CUI: C3810365
Disease: Central visual impairment
Central visual impairment 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 158 1 0.020 None 0.500 2 1990 1993
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
Congenital atresia of extrahepatic bile duct 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 172 19 0.020 None 0.500 2 2015 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 1719 297 0.600 None 0.600 108 1 1995 2020
CUI: C0011206
Disease: Delirium
Delirium 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 110 7 0.400 None 0.600 12 1 2009 2020