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Results 1 - 10 of 55 for Hemochromatosis type 1
  1. Hereditary hemochromatosis 
    ... worldwide. Mutations in several genes can cause hereditary hemochromatosis. Type 1 hemochromatosis results from mutations in the HFE gene, ... type 3 Hemochromatosis type 4 Symptomatic form of hemochromatosis type 1 National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../condition/hereditary-hemochromatosis - Genetics
  2. HFE gene 
    ... 100 mutations in the HFE gene that cause type 1 hemochromatosis, a form of hereditary hemochromatosis that begins during ... particular mutations are responsible for most cases of type 1 hemochromatosis. Each of these mutations changes one of the ...
    https://medlineplus.gov/genetics/gene/hfe - Genetics
  3. Hereditary Hemochromatosis (American Academy of Family Physicians)  
    Hemochromatosis/Start Here ... Hemochromatosis ... American Academy of Family Physicians
    https://familydoctor.org/.../hereditary-hemochromatosis/?adfree=true - External Health Links
  4. Learning about Hereditary Hemochromatosis From the National Institutes of Health (National Human Genome Research Institute)  
    Hemochromatosis/Genetics ... Hemochromatosis ... National Human Genome Research Institute ... From the National Institutes of Health ... Hereditary hemochromatosis is a genetic ...
    https://www.genome.gov/Genetic-Disorders/Hereditary-Hemochromatosis - External Health Links
  5. Hepatic Encephalopathy Video (American Liver Foundation)  
    ... Liver Disease (NAFLD) in Children Glycogen Storage Disease Type 1 Progressive Familial Intrahepatic Cholestasis (PFIC) Reye Syndrome Rare Liver Diseases Acute Hepatic Porphyria (AHP) Gilbert Syndrome Hemochromatosis Lysosomal Acide Lipase Deficiency (LALD) Wilson Disease Treatment ...
    https://liverfoundation.org/.../hepatic-encephalopathy - Videos
  6. Alcohol Associated Liver Disease Video (American Liver Foundation)  
    ... Liver Disease (NAFLD) in Children Glycogen Storage Disease Type 1 Progressive Familial Intrahepatic Cholestasis (PFIC) Reye Syndrome Rare Liver Diseases Acute Hepatic Porphyria (AHP) Gilbert Syndrome Hemochromatosis Lysosomal Acide Lipase Deficiency (LALD) Wilson Disease Treatment ...
    https://liverfoundation.org/.../videos/alcohol-related-liver-disease - Videos
  7. American Liver Foundation (American Liver Foundation)  
    ... Liver Disease (NAFLD) in Children Glycogen Storage Disease Type 1 Progressive Familial Intrahepatic Cholestasis (PFIC) Reye Syndrome Rare Liver Diseases Acute Hepatic Porphyria (AHP) Gilbert Syndrome Hemochromatosis Lysosomal Acide Lipase Deficiency (LALD) Wilson Disease Treatment ...
    https://liverfoundation.org - Other Resources
  8. TFR2 gene 
    ... and other signs and symptoms of type 3 hemochromatosis. More About This Health Condition ... A, Gasparini P. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. Nat Genet. 2000 May;25(1):14-5. doi: 10.1038/75534. Citation on ...
    https://medlineplus.gov/genetics/gene/tfr2 - Genetics
  9. SLC40A1 gene 
    ... 1):44-9. doi: 10.1136/gut.53.1.44. Citation on PubMed or Free article on PubMed ... J, Ou X. Type 4B hereditary hemochromatosis associated with a novel mutation ...
    https://medlineplus.gov/genetics/gene/slc40a1 - Genetics
  10. Alagille Syndrome (American Liver Foundation)  
    Alagille Syndrome is an inherited disorder that closely resembles other forms of liver disease seen in infants and young children. ... Liver Diseases/Children
    https://liverfoundation.org/.../alagille-syndrome - External Health Links
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