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