TNF, tumor necrosis factor, 7124

N. diseases: 2475; N. variants: 28
Source: BEFREE ×
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: C0205204
Disease: Scab
Scab
disease Acquired Abnormality 24 0.010 None 1.000 1 2018 2018
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
disease Acquired Abnormality 115 15 0.010 None 1.000 1 2012 2012
CUI: C2939127
Disease: Indolent ulcer
Indolent ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 3 0.010 None 1.000 1 2013 2013
Surgical incision wound (morphologic abnormality)
disease Wounds and Injuries Acquired Abnormality 10 0.010 None 1.000 1 2018 2018
CUI: C0016169
Disease: pathologic fistula
pathologic fistula
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 69 8 0.080 None 1.000 8 2012 2020
CUI: C0019270
Disease: Hernia
Hernia
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 107 9 0.050 None 1.000 5 2002 2018
CUI: C0031094
Disease: Periodontal Pocket
Periodontal Pocket
disease Stomatognathic Diseases Anatomical Abnormality 28 0.040 None 0.750 4 2010 2019
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 379 18 0.030 None 1.000 3 2011 2018
CUI: C1510420
Disease: Cavitation
Cavitation
disease Anatomical Abnormality 47 0.020 None 0.500 2 2005 2017
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula
phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 83 8 0.010 None 1.000 1 2014 2014
CUI: C0009917
Disease: Contracture
Contracture
disease Musculoskeletal Diseases Anatomical Abnormality 102 12 0.010 None 1.000 1 2007 2007
CUI: C0018536
Disease: Hallux Valgus
Hallux Valgus
disease Musculoskeletal Diseases Anatomical Abnormality 14 0.010 None 1.000 1 2019 2019
CUI: C0021846
Disease: Intestinal Polyps
Intestinal Polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 45 0.010 None 1.000 1 2017 2017
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 2018 2018
CUI: C0575157
Disease: Deformity of spine
Deformity of spine
disease Anatomical Abnormality 38 0.010 None 1.000 1 2006 2006
CUI: C0679403
Disease: Vascular stenosis
Vascular stenosis
disease Pathological Conditions, Signs and Symptoms Anatomical Abnormality 15 3 0.010 None 1.000 1 2017 2017
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis
disease Musculoskeletal Diseases Anatomical Abnormality 25 0.010 None 1.000 1 2018 2018
CUI: C1387925
Disease: Abnormality of limbs
Abnormality of limbs
phenotype Anatomical Abnormality 5 0.010 None 1.000 1 2006 2006
CUI: C2717759
Disease: Degenerative Intervertebral Discs
Degenerative Intervertebral Discs
disease Musculoskeletal Diseases Anatomical Abnormality 22 0.010 None 1.000 1 2015 2015
CUI: C2919945
Disease: Cavernous Hemangioma of Brain
Cavernous Hemangioma of Brain
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Anatomical Abnormality 127 10 0.010 None 1.000 1 2013 2013
CUI: C3495890
Disease: Osteochondral defects
Osteochondral defects
phenotype Anatomical Abnormality 17 0.010 None 1.000 1 2019 2019
CUI: C3544347
Disease: Intestinal fibrosis
Intestinal fibrosis
phenotype Anatomical Abnormality 65 0.010 None 1.000 1 2019 2019
Congenital contractural arachnodactyly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 557 20 0.060 None 1.000 6 2011 2019
Congenital arteriovenous malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 127 23 0.050 None 1.000 5 1 1999 2018
CUI: C0037221
Disease: Situs Inversus
Situs Inversus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 121 3 0.050 None 1.000 5 1999 2018