hemosiderosis inborn metal metabolism disorder hereditary hemochromatosis https://github.com/monarch-initiative/mondo/issues/3557 https://www.malacards.org/card/hemochromatosis_type_1_2 true hemochromatosis MONDO:0006507 OMIMPS:235200 GARD:0024434 MEDGEN:140272 An inherited metabolic disorder characterized by iron accumulation in the tissues. DOID:2352 UMLS:C0392514 SCTID:399187006 MESH:D006432 SCTID:35400008 ICD10CM:E83.110 NCIT:C84481 hemochromatosis, hereditary haemochromatosis disorder of iron metabolism and transport