hemochromatosis type 2 (DOID:0111034)
Alliance: disease page
Synonyms: HFE2; JHH; juvenile hemochromatosis
Alt IDs: ICD10CM:E83.1, MESH:C537247, ORDO:79230
Definition: 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.