TNF, tumor necrosis factor, 7124

N. diseases: 2724; N. variants: 31
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.
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
phenotype Finding 20 19 0.300 None 0
CUI: C0079485
Disease: Heart Valve Prolapse
Heart Valve Prolapse
disease Cardiovascular Diseases Disease or Syndrome 3 0.200 None 0
CUI: C0152417
Disease: Congenital stenosis of aortic valve
Congenital stenosis of aortic valve
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 5 0.200 None 0
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis
disease Infections; Cardiovascular Diseases Disease or Syndrome 7 5 0.200 None 0
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.100 None 0
CUI: C0085636
Disease: Photophobia
Photophobia
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Sign or Symptom 227 7 0.100 None 0
CUI: C0751466
Disease: Phonophobia
Phonophobia
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Mental or Behavioral Dysfunction 18 1 0.100 None 0
CUI: C4016415
Disease: TNF RECEPTOR BINDING, ALTERED
TNF RECEPTOR BINDING, ALTERED
phenotype Finding 1 1 0.100 None 0 1
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia
phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 78 3 0.500 None 1.000 1 1999 1999
CUI: C0027497
Disease: Nausea
Nausea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 161 14 0.400 None 1.000 1 1999 1999
CUI: C0948480
Disease: Coronary Restenosis
Coronary Restenosis
disease Cardiovascular Diseases Disease or Syndrome 16 2 0.310 None 1.000 1 2005 2005
CUI: C0001925
Disease: Albuminuria
Albuminuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 76 59 0.300 None 1.000 1 2006 2006
CUI: C0003875
Disease: Arthritis, Viral
Arthritis, Viral
disease Infections; Musculoskeletal Diseases Disease or Syndrome 3 0.300 None 1.000 1 2009 2009
CUI: C0003949
Disease: Asbestosis
Asbestosis
disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 47 2 0.300 None 1.000 1 2010 2010
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic
disease Digestive System Diseases Disease or Syndrome 87 0.300 None 1.000 1 2017 2017
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema
phenotype Nervous System Diseases Pathologic Function 26 0.300 None 1.000 1 2011 2011
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections
group Infections Disease or Syndrome 48 1 0.300 None 1.000 1 2014 2014
CUI: C0013604
Disease: Edema
Edema
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 126 1 0.300 None 1.000 1 2010 2010
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 125 0.300 None 1.000 1 2017 2017
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 131 27 0.300 None 1.000 1 1999 1999
CUI: C0020542
Disease: Pulmonary Hypertension
Pulmonary Hypertension
phenotype Respiratory Tract Diseases Pathologic Function 156 0.300 None 1.000 1 1989 1989
CUI: C0020672
Disease: Hypothermia, natural
Hypothermia, natural
phenotype Pathological Conditions, Signs and Symptoms Finding 52 3 0.300 None 1.000 1 2006 2006
CUI: C0023904
Disease: Liver Neoplasms, Experimental
Liver Neoplasms, Experimental
phenotype Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 152 0.300 None 1.000 1 2017 2017
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome
disease Nutritional and Metabolic Diseases Disease or Syndrome 13 0.300 None 1.000 1 1999 1999
CUI: C0026846
Disease: Muscular Atrophy
Muscular Atrophy
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Pathologic Function 49 0.300 None 1.000 1 2014 2014