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Hemochromatosis type 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; ...
- ... 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 ...
- Hereditary Hemochromatosis (American Academy of Family Physicians)Hemochromatosis/Start Here ... Hemochromatosis ... American Academy of Family Physicians
- Learning about Hereditary Hemochromatosis (National Human Genome Research Institute)Hemochromatosis/Genetics ... Hemochromatosis ... National Human Genome Research Institute ... From the National Institutes of Health ... Hereditary hemochromatosis is a genetic ...
- Hepatic Encephalopathy (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 ...
- Alcohol Associated Liver Disease (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 ...
- 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 ...
- ... 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 ...
- ... 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 ...
- ... adrenal glands, and thyroid glands, as well as type 1 diabetes. In ... Radiation (to the pituitary or hypothalamus) Rapid, significant ...