Provides education, information and resources for health care providers, patients, and relatives of people with hereditary hemochromatosis.

Information on hemochromatosis. Covered are the accepted protocols for diagnosis, treatment, maintenance and diet.

Merck Manual looks at this disorder, its signs and symptoms, diagnosis and treatment.

A supplement to the Annals of Internal Medicine with articles about hemochromatosis.

A collection of links to sites, including scientific articles, related to the genetic iron overload disease.

Non-profit National Voluntary Health Agency that provides information about disorders of iron such as hemochromatosis.

This organisation provides information and educates the public about hemochromatosis. They publish a newsletter and have an online support group.

The US Centers for Disease Control and Prevention provide reviewed information on hemochromatosis, including screening, information for patients, FAQ and resources.

Detailed up-to-date scientific information on hemochromatosis.

The website of a family whose members have hemochromatosis, with a description of how they are affected, and links to hemochromatosis sites.

Light hearted and simple terms in explaining the serious disease of haemochromatosis.

Voluntary organisation for patients in England, Wales, Scotland and Northern Ireland.

Multimedia guide where you can learn what it is, what causes it, what it is like to have it, and how it is inherited, diagnosed, and treated.

Irish volunteer organisation to support people with haemochromatosis and promote the disease.

Offers information about the symptoms and treatment of hereditary hemochromatosis.

A laymans non-technical account of living with hemochromatosis by Alan Mannering.

Support group for those affected by hemochromatosis

Resources and information about Idiopathic Pulmonary Hemosiderosis, a very rare lung disorder affecting children and adults.