IL10, interleukin 10, 3586

N. diseases: 1679; N. variants: 21
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: C4553018
Disease: Avascular Necrosis, CTCAE
Avascular Necrosis, CTCAE 		phenotype Finding 41 0.100 None 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0 		phenotype Finding 108 0.100 None 0
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 430 96 0.030 None < 0.001 3 2018 2019
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 177 63 0.020 None < 0.001 2 2008 2011
CUI: C0010201
Disease: Chronic cough
Chronic cough 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 14 1 0.010 None < 0.001 1 2018 2018
CUI: C0015773
Disease: Felty Syndrome
Felty Syndrome 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 13 0.010 None < 0.001 1 1998 1998
CUI: C0015923
Disease: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Chemically-Induced Disorders Disease or Syndrome 89 8 0.010 None < 0.001 1 2001 2001
CUI: C0027092
Disease: Myopia
Myopia 		disease Eye Diseases Disease or Syndrome 490 167 0.010 None < 0.001 1 2006 2006
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 257 11 0.110 None < 0.001 1 2019 2019
CUI: C0033838
Disease: Kimura Disease
Kimura Disease 		disease Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 9 0.010 None < 0.001 1 2013 2013
CUI: C0040264
Disease: Tinnitus
Tinnitus 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 103 14 0.010 None < 0.001 1 2019 2019
CUI: C0149825
Disease: Hypertrophy of adenoids
Hypertrophy of adenoids 		disease Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2018 2018
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 230 93 0.010 None < 0.001 1 2014 2014
CUI: C0263666
Disease: Dermatomyositis, Childhood Type
Dermatomyositis, Childhood Type 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 62 1 0.010 None < 0.001 1 2018 2018
CUI: C0272199
Disease: Familial Hemophagocytic Lymphocytosis
Familial Hemophagocytic Lymphocytosis 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 35 6 0.010 None < 0.001 1 2019 2019
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		group Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 827 60 0.010 None < 0.001 1 1994 1994
CUI: C0400936
Disease: Autoimmune liver disease
Autoimmune liver disease 		disease Digestive System Diseases; Immune System Diseases Disease or Syndrome 26 3 0.010 None < 0.001 1 3 2018 2018
CUI: C0410623
Disease: Prolapsed thoracic intervertebral disc
Prolapsed thoracic intervertebral disc 		phenotype Respiratory Tract Diseases Acquired Abnormality 2 0.010 None < 0.001 1 2018 2018
CUI: C1096155
Disease: Macrophage Activation Syndrome
Macrophage Activation Syndrome 		disease Immune System Diseases Disease or Syndrome 57 6 0.010 None < 0.001 1 2019 2019
CUI: C1304140
Disease: Familial psoriasis
Familial psoriasis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 13 4 0.010 None < 0.001 1 2003 2003
CUI: C1512433
Disease: Cervical high grade squamous intraepithelial lesion
Cervical high grade squamous intraepithelial lesion 		disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 42 0.010 None < 0.001 1 2009 2009
CUI: C2985290
Disease: Fetal Alcohol Spectrum Disorders
Fetal Alcohol Spectrum Disorders 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Chemically-Induced Disorders Disease or Syndrome; Congenital Abnormality 46 2 0.010 None < 0.001 1 2018 2018
CUI: C3887524
Disease: Skin Erosion
Skin Erosion 		disease Skin and Connective Tissue Diseases Disease or Syndrome 225 2 0.010 None < 0.001 1 2005 2005
CUI: C3887639
Disease: Autoimmune gastritis
Autoimmune gastritis 		disease Digestive System Diseases Disease or Syndrome 28 1 0.010 None < 0.001 1 2014 2014
CUI: C4049435
Disease: Chronic hepatitis C genotype 3
Chronic hepatitis C genotype 3 		disease Disease or Syndrome 3 0.010 None < 0.001 1 2005 2005