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Key terms:
adrenal
allele
arthropathy
autosomal
body iron stores
cirrhosis
clinical disease
clinical iron
clinically relevant
deposition
diabetes
diagnosis of haemochromatosis
dietary iron
dysfunction
enterocyte
excess iron
ferritin
genotype
haemochromatosis
haemochromatosis type
heart failure
hemochromatosis
hepcidin
hereditary form
hereditary haemochromatosis
hfe
hfe gene
homozygous
increased iron
iron
iron absorption
iron accumulation
iron metabolism
iron overload
iron stores
juvenile haemochromatosis
liver
liver biopsy
liver disease
manifestations
mutation
pancreas
pigmentation
recessive
screening
serum
serum ferritin
transferrin
transferrin saturation
trousseau
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