Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Hemochromatosis
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Iron Metabolism Disorders » Iron Overload » Hemochromatosis
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Hemochromatosis
Description
A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) MeSH
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Phase 3 Indicated Drugs (4)
Phase 2 Indicated Drugs (4)
Phase 1 Indicated Drugs (3)
Other Experimental Indicated Drugs (2)
Organization Involved with Phase 4 Indications (2)
Organization Involved with Phase 3 Indications (7)
Organization Involved with Phase 2 Indications (7)
Organization Involved with Phase 1 Indications (1)
Organization Involved with Other Experimental Indications (2)
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