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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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