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hereditary hemochromatosis
Used for:
diabetes bronze
Broader Terms:
inborn metal metabolism disorder
Related Terms:
autosomal recessive trait
Scope Note:
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; an autosomal recessive disorder of metabolism associated with a gene tightly linked to the A locus of the HLA complex on chromosome 6.
Term Number:
1849-4292
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