TF, transferrin, 7018

N. diseases: 47; N. variants: 70
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease UNIPROT Molecular characterization of a third case of human atransferrinemia. 15466165 2004
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease CTD_human Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia. 12111369 2002
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND The effect of transferrin polymorphisms on iron metabolism. 10660486 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease UNIPROT Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease CTD_human Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND Congenital atransferrinemia. A case report and review of the literature. 1862777 1991
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GermlineCausalMutation disease ORPHANET
CUI: C0028754
Disease: Obesity
Obesity
0.500 Biomarker disease CTD_human Orchestrated downregulation of genes involved in oxidative metabolic pathways in obese vs. lean high-fat young male consumers. 20882379 2011
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 Biomarker disease CTD_human Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. 17192785 2007
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 Biomarker disease CTD_human Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. 15060098 2004
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.340 Biomarker disease PSYGENET The aim of this study was to investigate the possible influence of hemochromatosis gene mutations (HFE-C282Y and H63D) and transferrin gene C2 variant (TF-C2) on susceptibility to schizophrenia and schizoaffective disorder and/or age at first hospital admission. 21643746 2012
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.340 Biomarker disease PSYGENET Polymorphisms of Transferrin gene are associated with schizophrenia in Chinese Han population. 18045615 2008
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.340 Biomarker disease PSYGENET The present results suggest that the transferrin gene is not related to the development of schizophrenia in the Japanese population. 17496814 2007
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse
0.310 Biomarker disease CTD_human Different binding affinities of Pb2+ and Cu2+ to glycosylation variants of human serum transferrin interfere with the detection of carbohydrate-deficient transferrin. 21792595 2011
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.310 Biomarker disease CTD_human Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. 17192785 2007
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.310 Biomarker disease CTD_human Considering the causes of RLS. 16930377 2006
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.310 Biomarker disease CTD_human Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. 15060098 2004
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse
0.310 Biomarker disease CTD_human The validity of self-reported drug use in non-treatment seeking individuals with cocaine dependence: correlation with biochemical assays. 11000917 2000
CUI: C0013221
Disease: Drug toxicity
Drug toxicity
0.300 Biomarker group CTD_human A Multiplatform Approach for the Discovery of Novel Drug-Induced Kidney Injury Biomarkers. 28885000 2017
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
0.300 Biomarker disease CTD_human A Multiplatform Approach for the Discovery of Novel Drug-Induced Kidney Injury Biomarkers. 28885000 2017
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug
0.300 Biomarker group CTD_human A Multiplatform Approach for the Discovery of Novel Drug-Induced Kidney Injury Biomarkers. 28885000 2017
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency
0.300 Biomarker disease CTD_human A Multiplatform Approach for the Discovery of Novel Drug-Induced Kidney Injury Biomarkers. 28885000 2017
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
0.300 Biomarker disease CTD_human A Multiplatform Approach for the Discovery of Novel Drug-Induced Kidney Injury Biomarkers. 28885000 2017
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma
0.300 Biomarker disease CTD_human Iron signature in asbestos-induced malignant pleural mesothelioma: A population-based autopsy study. 26818092 2016