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Results 1 - 10 of 53 for Hemochromatosis type 1
  1. ... worldwide. Mutations in several genes can cause hereditary hemochromatosis. Type 1 hemochromatosis results from mutations in the HFE gene, ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov HEMOCHROMATOSIS, TYPE 1; HFE1 HEMOCHROMATOSIS, TYPE 3; HFE3 HEMOCHROMATOSIS, TYPE 2A; ...
  2. ... 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 ...
  3. Hereditary Hemochromatosis (American Academy of Family Physicians)  
    Hemochromatosis/Start Here ... Hemochromatosis ... American Academy of Family Physicians
  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 ...
  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 ...
  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 ...
  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 ...
  8. ... 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 ...
  9. ... 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 ...
  10. ... adrenal glands, and thyroid glands, as well as type 1 diabetes. In ... Radiation (to the pituitary or hypothalamus) Rapid, significant ...
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