Hereditary haemochromatosis is the most frequent autosomal recessive disorder of metabolism and is based on an increased iron absorption in the upper small intestine. It may cause irreversible damage with risk of cardiomyopathy, arthropathy, and liver and pancreas carcinoma. Two mutations in the HFE gene (C282Y and H63D) may lead to a loss or a reduction of the physiological function of the Hfe protein.
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|768||EUROArray||EUROArray Hemochromatosis (4 SNP+)|
|769||EUROArray||EUROArray Hemochromatosis (2 SNP+)|