Conditions / Genetic

hemochromatosis type 2

info · Genetic · ICD-10: E83.1

A hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis.

Also known as: HFE2; JHH; juvenile hemochromatosis