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Results 1 - 9 of 9 for Hemochromatosis type 5
  1. ... 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 PubMed Crownover BK, Covey CJ. Hereditary hemochromatosis. Am Fam Physician. 2013 Feb 1;87(3): ...
  2. ... genotype/phenotype correlations in 7 Italian families with type 4 hereditary ... Pflugers Arch. 2004 Feb;447(5):801-6. doi: 10.1007/s00424-003-1102- ...
  3. ... in hereditary hemochromatosis. More About This Health Condition hemochromatosis type 2 (juvenile) HFE2 HFE2A JH RGM domain family, ... AL, Cox TM, Gasparini P, Camaschella C. Juvenile hemochromatosis locus maps to chromosome 1q. Am J Hum Genet. 1999 May;64(5):1388-93. doi: 10.1086/302379. Citation on ...
  4. ... 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 ...
  5. ... About 50 mutations in the TFR2 gene cause type 3 hemochromatosis, a form of hereditary hemochromatosis that begins in ... organ damage and other signs and symptoms of type 3 hemochromatosis. More About This Health Condition HFE3 TFR2_HUMAN ...
  6. ... of iron from the diet and result in hemochromatosis, which is another type of iron overload disorder. ALAS2 HFE This condition ... iron overload by phlebotomy and coinheritance of hereditary hemochromatosis. Blood. 1999 Mar 1;93(5):1757-69. Citation on PubMed May A, Bishop ...
  7. ... of serum ferritin in African Americans in the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Blood Cells Mol Dis. 2007 May-Jun;38(3):247-52. doi: 10.1016/j.bcmd.2006.12.002. Epub 2007 Feb 5. Citation on PubMed or Free article on PubMed ...
  8. ... gene (which cause an iron overload disorder called hemochromatosis) are also associated with porphyria cutanea tarda. Other, as-yet-unidentified genetic factors may also play a role in this ... UROS Some types of porphyria are inherited in an autosomal dominant ...
  9. ... during fetal development. These include heart problems, congenital hemochromatosis, and a complication that can occur in twin ... renal tubular dysgenesis. Kidney Int. 2010 Mar;77(5):400-6. doi: 10.1038/ki.2009.423. ...