TF, transferrin, 7018

N. diseases: 168; N. variants: 74
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.
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
phenotype Finding 1 0.200 None 1.000 1 1987 1987
CUI: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C4225610
Disease: TRANSFERRIN VARIANT D(CHI)
TRANSFERRIN VARIANT D(CHI)
phenotype Finding 1 1 0.100 None 0 1
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 4 0.910 strong 1.000 9 4 1987 2007
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement
phenotype Laboratory Procedure 6 10 0.100 None 1.000 3 3 2011 2015
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement
phenotype Laboratory Procedure 6 10 0.100 None 1.000 3 3 2011 2015
Acute and subacute liver necrosis (disorder)
disease Digestive System Diseases Disease or Syndrome 6 0.200 None 1.000 1 2006 2006
HFE-Associated Hereditary Hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 3 0.100 None 1.000 1 1 2015 2015
CUI: C0337439
Disease: Iron measurement
Iron measurement
phenotype Laboratory Procedure 12 16 0.100 None 1.000 1 1 2011 2011
CUI: C0428578
Disease: Iron level result
Iron level result
phenotype Laboratory or Test Result 12 16 0.100 None 1.000 1 1 2011 2011
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas
disease Anatomical Abnormality 13 1 0.100 None 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
group Nutritional and Metabolic Diseases Disease or Syndrome 15 3 0.100 None 1.000 1 1 2015 2015
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 16 0.100 None 0
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
phenotype Laboratory Procedure 17 25 0.100 None 1.000 2 2 2014 2015
Total iron binding capacity function
phenotype Clinical Attribute 20 35 0.100 None 1.000 3 5 2011 2017
Iron binding capacity total measurement
phenotype Laboratory Procedure 20 35 0.100 None 1.000 3 5 2011 2017
CUI: C0013502
Disease: Echinococcosis
Echinococcosis
disease Infections Disease or Syndrome 21 1 0.300 None 1.000 1 2014 2014
CUI: C0268070
Disease: Hypocupremia
Hypocupremia
disease Disease or Syndrome 23 2 0.010 None 1.000 1 2017 2017
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 24 0.200 None 1.000 1 2007 2007
Microcytic hypochromic anemia (disorder)
disease Hemic and Lymphatic Diseases Disease or Syndrome 25 3 0.300 None 1.000 1 2000 2000
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
phenotype Laboratory Procedure 26 36 0.100 None 1.000 2 3 2014 2017
CUI: C4553297
Disease: Cystic Echinocccosis
Cystic Echinocccosis
disease Infections Disease or Syndrome 26 1 0.300 None 1.000 1 2014 2014
Human anaplasmosis due to Anaplasma phagocytophilum
disease Infections; Animal Diseases Disease or Syndrome 29 0.010 None 1.000 1 1999 1999