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- Hemochromatosis
Hemochromatosis(Topical Term)
Used for/see from:
- n: Bronze Diabetes
- n: Bronzed Cirrhosis
- n: Familial Hemochromatosis
- n: Genetic Hemochromatosis
- n: Haemochromatosis
- n: Hemochromatoses
- n: Iron Storage Disorder
- n: Pigmentary Cirrhosis
- n: Primary Hemochromatosis
- n: Troisier-Hanot-Chauffard Syndrome
- n: Von Recklenhausen-Applebaum Disease
- Diabetes, Bronze
- n: Bronzed Cirrhoses
- n: Cirrhoses, Bronzed
- n: Cirrhoses, Pigmentary
- n: Cirrhosis, Bronzed
- n: Cirrhosis, Pigmentary
- n: Disease, Von Recklenhausen-Applebaum
- n: Diseases, Von Recklenhausen-Applebaum
- n: Disorder, Iron Storage
- n: Disorders, Iron Storage
- n: Familial Hemochromatoses
- n: Genetic Hemochromatoses
- n: Haemochromatoses
- n: Hemochromatose
- n: Hemochromatoses, Familial
- n: Hemochromatoses, Genetic
- n: Hemochromatosis, Familial
- n: Hemochromatosis, Genetic
- n: Iron Storage Disorders
- n: Pigmentary Cirrhoses
- n: Recklenhausen-Applebaum Disease, Von
- n: Recklenhausen-Applebaum Diseases, Von
- n: Storage Disorder, Iron
- n: Storage Disorders, Iron
- n: Syndrome, Troisier-Hanot-Chauffard
- n: Syndromes, Troisier-Hanot-Chauffard
- n: Troisier Hanot Chauffard Syndrome
- n: Troisier-Hanot-Chauffard Syndromes
- n: Von Recklenhausen Applebaum Disease
- n: Von Recklenhausen-Applebaum Diseases
See also:
accumulation of hemosiderin in tissue
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)