Hemochromatosis
"Hemochromatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron. Acquired hemochromatosis may be the result of blood transfusions, excessive dietary iron, or secondary to other disease. Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the A locus of the HLA complex on chromosome 6. (From Dorland, 27th ed)
Descriptor ID |
D006432
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MeSH Number(s) |
C16.320.565.618.337 C18.452.565.500.480 C18.452.648.618.337
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Concept/Terms |
Hemochromatosis- Hemochromatosis
- Hemochromatoses
- Diabetes, Bronze
- Bronze Diabetes
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Below are MeSH descriptors whose meaning is more general than "Hemochromatosis".
Below are MeSH descriptors whose meaning is more specific than "Hemochromatosis".
This graph shows the total number of publications written about "Hemochromatosis" by people in UAMS Profiles by year, and whether "Hemochromatosis" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2017 | 0 | 1 | 1 | 2009 | 0 | 1 | 1 | 2001 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemochromatosis" by people in Profiles over the past ten years.
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Preziosi ME, Singh S, Valore EV, Jung G, Popovic B, Poddar M, Nagarajan S, Ganz T, Monga SP. Mice lacking liver-specific ?-catenin develop steatohepatitis and fibrosis after iron overload. J Hepatol. 2017 08; 67(2):360-369.
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People People who have written about this concept. _
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