Hemochromatosis

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)

Also Known As:

Bronze Diabetes; Hemochromatoses; Bronzed Cirrhosis; Familial Hemochromatosis; Genetic Hemochromatosis; Haemochromatosis; Iron Storage Disorder; Pigmentary Cirrhosis; Primary Hemochromatosis; Troisier-Hanot-Chauffard Syndrome; Von Recklenhausen-Applebaum Disease; Bronzed Cirrhoses; Cirrhoses, Bronzed; Cirrhoses, Pigmentary; Cirrhosis, Bronzed; Cirrhosis, Pigmentary; Disease, Von Recklenhausen-Applebaum; Diseases, Von Recklenhausen-Applebaum; Disorder, Iron Storage; Disorders, Iron Storage; Familial Hemochromatoses; Genetic Hemochromatoses; Haemochromatoses; Hemochromatose; Hemochromatoses, Familial; Hemochromatoses, Genetic; Hemochromatosis, Familial; Hemochromatosis, Genetic; Iron Storage Disorders; Pigmentary Cirrhoses; Recklenhausen-Applebaum Disease, Von; Recklenhausen-Applebaum Diseases, Von; Storage Disorder, Iron; Storage Disorders, Iron; Syndrome, Troisier-Hanot-Chauffard; Syndromes, Troisier-Hanot-Chauffard; Troisier Hanot Chauffard Syndrome; Troisier-Hanot-Chauffard Syndromes; Von Recklenhausen Applebaum Disease; Von Recklenhausen-Applebaum Diseases; Diabetes, Bronze

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Hemochromatosis: 4165
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Hemochromatosis: 4165
  - Iron Metabolism Disorders: 78
    - Iron Overload: 7614
      - Hemochromatosis: 4165

K V Voelkerding Selected Research

K V Voelkerding Research Topics

Disease

Drug/Important Bio-Agent (IBA)