IL17A, interleukin 17A, 3605

N. diseases: 1074; N. variants: 19
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: C0009766
Disease: Allergic Conjunctivitis
Allergic Conjunctivitis 		disease Eye Diseases; Immune System Diseases Disease or Syndrome 38 2 0.010 None < 0.001 1 2008 2008
CUI: C0018824
Disease: Heart valve disease
Heart valve disease 		group Cardiovascular Diseases Disease or Syndrome 79 5 0.010 None < 0.001 1 2019 2019
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		group Infections Disease or Syndrome 51 10 0.010 None < 0.001 1 2019 2019
CUI: C0021818
Disease: Intervertebral Disk Displacement
Intervertebral Disk Displacement 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 35 0.010 None < 0.001 1 2013 2013
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer 		disease Digestive System Diseases Disease or Syndrome 150 25 0.010 None < 0.001 1 1 2018 2018
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 136 55 0.010 None < 0.001 1 2018 2018
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 153 37 0.010 None < 0.001 1 2018 2018
CUI: C0162323
Disease: Polyarthritis
Polyarthritis 		disease Musculoskeletal Diseases Disease or Syndrome 65 9 0.010 None < 0.001 1 2019 2019
CUI: C0242362
Disease: Disk, Herniated
Disk, Herniated 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 31 0.010 None < 0.001 1 2013 2013
CUI: C0333998
Disease: Nodular lymphoid hyperplasia
Nodular lymphoid hyperplasia 		disease Disease or Syndrome 5 0.010 None < 0.001 1 2019 2019
CUI: C4049273
Disease: Systemic immune activation
Systemic immune activation 		disease Disease or Syndrome 23 0.010 None < 0.001 1 2019 2019
CUI: C4505456
Disease: HIV Coinfection
HIV Coinfection 		disease Infections; Immune System Diseases Disease or Syndrome 129 3 0.010 None < 0.001 1 2016 2016
CUI: C4552513
Disease: Temporomandibular joint osteoarthritis
Temporomandibular joint osteoarthritis 		disease Disease or Syndrome 32 0.010 None < 0.001 1 2018 2018
CUI: C4733092
Disease: estrogen receptor-negative breast cancer
estrogen receptor-negative breast cancer 		disease Neoplastic Process 356 40 0.010 None < 0.001 1 2017 2017
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		phenotype Behavior and Behavior Mechanisms Sign or Symptom 421 120 0.030 None 0.333 3 2018 2019
CUI: C0023343
Disease: Leprosy
Leprosy 		disease Infections Disease or Syndrome 190 120 0.020 None 0.500 2 2 2013 2016
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		disease Neoplasms Neoplastic Process 3111 6892 0.020 None 0.500 2 2015 2016
CUI: C0024198
Disease: Lyme Disease
Lyme Disease 		disease Infections Disease or Syndrome 178 4 0.020 None 0.500 2 2011 2017
CUI: C0025202
Disease: melanoma
melanoma 		disease Neoplasms Neoplastic Process 3087 515 0.020 None 0.500 2 2013 2019
CUI: C0039101
Disease: synovial sarcoma
synovial sarcoma 		disease Neoplasms Neoplastic Process 299 4 0.020 None 0.500 2 2014 2017
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome 		disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 132 4 0.020 None 0.500 2 2014 2017
CUI: C0243038
Disease: Carcinoma, Lewis Lung
Carcinoma, Lewis Lung 		disease Neoplasms Neoplastic Process; Experimental Model of Disease 188 0.020 None 0.500 2 2010 2017
CUI: C1701940
Disease: Pneumonia, Ventilator-Associated
Pneumonia, Ventilator-Associated 		disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 56 3 0.020 None 0.500 2 2017 2019
CUI: C1832588
Disease: Chromosome 11p11.2 Deletion Syndrome
Chromosome 11p11.2 Deletion Syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases Disease or Syndrome 65 6 0.020 None 0.500 2 2017 2018
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 209 37 0.020 None 0.500 2 2017 2019