HFE, homeostatic iron regulator, 3077

N. diseases: 415; N. variants: 59
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Prevalence and characteristics of anti-HCV positivity and chronic hepatitis C virus infection in HFE p.C282Y homozygotes. 31056361 2020
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Liver steatosis correlates with iron overload but not with HFE gene mutations in chronic hepatitis C. 23924495 2013
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Clinical impact of HFE mutations in Japanese patients with chronic hepatitis C. 22098610 2012
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE The role of iron overload and HFE gene mutations in the era of pegylated interferon and ribavirin treatment of chronic hepatitis C. 20190684 2010
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE To further examine this question, 45 liver explants with alpha-1-antitrypsin deficiency and 33 control livers with chronic hepatitis C were examined for histological iron accumulation, graded on a scale of 0 to 4+, and HFE mutations. 20208481 2010
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE To evaluate the role of HFE mutations in the severity of liver disease and in the response to therapy in chronic hepatitis C. 20555268 2010
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE We studied the status of hepatic iron deposition and its relationship with blood iron indices, liver histology, and HFE gene mutations in Korean patients with chronic hepatitis C (CH-C). 19602897 2009
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 Biomarker disease LHGDN HFE gene in primary and secondary hepatic iron overload. 17729389 2007
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE The aim of this work was to assess the influence of HFE mutations and serum and hepatic measures of iron status on baseline features and response to lead-in therapy in subjects with advanced chronic hepatitis C enrolled in the Hepatitis C Anti-viral Long-term Treatment to prevent Cirrhosis (HALT-C) Trial. 17101320 2006
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan. 15991291 2005
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease LHGDN The relationship of H63D HFE gene mutations with chronic hepatitis C and the possible influence of HCV infection on iron metabolism needs further analysis. 16273299 2005
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE The relationship of H63D HFE gene mutations with chronic hepatitis C and the possible influence of HCV infection on iron metabolism needs further analysis. 16273299 2005
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE The aim of the present study was to describe the histopathologic features of hepatic iron accumulation in patients with chronic hepatitis C (CH-C) infection, the relation between HFE mutations and hepatic iron location and among iron distribution, HFE, and hepatic damage. 16416733 2005
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease LHGDN Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan. 15991291 2005
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease LHGDN Our findings support a role of HFE mutations as primary risk factors for fibrogenesis and disease progression in chronic hepatitis C. 15287851 2004
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Histological activity and virological response to antiviral therapy (n = 146) were analysed in 273 immunocompetent and nonalcoholic patients with chronic hepatitis C, in terms of serum iron load, intrahepatic iron load (n = 110) and HFE mutations. 14996353 2004
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Our findings support a role of HFE mutations as primary risk factors for fibrogenesis and disease progression in chronic hepatitis C. 15287851 2004
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE HFE mutations must therefore be considered as important comorbidity factors in chronic hepatitis C infection. 15464655 2004
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease LHGDN The presence of HFE mutations is independently associated with iron loading and advanced fibrosis in patients with compensated liver disease from chronic hepatitis C, especially after controlling for duration of disease. 12557137 2003
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE The presence of HFE mutations is independently associated with iron loading and advanced fibrosis in patients with compensated liver disease from chronic hepatitis C, especially after controlling for duration of disease. 12557137 2003
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE HFE mutations and chronic hepatitis C: H63D and C282Y heterozygosity are independent risk factors for liver fibrosis and cirrhosis. 12586300 2003
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE To investigate the relations between hemochromatosis gene (HFE) mutations and PCT in the south of France and their links with chronic hepatitis C virus (HCV) infection. 12673077 2003
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Heterozygosity for the C282Y mutation in HFE contributes to iron accumulation and fibrosis progression in chronic hepatitis C. 14557859 2003
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C. 12445428 2002
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.100 GeneticVariation disease BEFREE HFE mutations were seen in 47% of patients with chronic hepatitis C and in 28% of control subjects; they were related to stage and the His63Asp mutation to portal HDI. 10761457 2000