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Iron Overload and Hemochromatosis: For More Information

Downloadable Patient Resources

Resources developed by the CDC and its partners:

Additional Hemochromatosis Information

Genetic Information

Patient Group Information

Iron Disorders Institute* (IDI)
A national voluntary health agency that provides patient services, books, and literature about hemochromatosis and other disorders of iron such as non-HFE related iron overload, iron loading anemia, anemia of chronic disease, and iron deficiency anemia.

Phlebotomy Information

Family Health History

Health Care Professional Online Training Site

In addition to this Web site, the CDC and its partners have developed a training site for health care professionals, Hemochromatosis: What Every Clinician and Health Care Professional Needs to Know, an online training course for primary care providers describing the pathophysiology, epidemiology, diagnosis, treatment, and management of patients with adult onset hemochromatosis.

The course also provides FREE Continuing Education Credits for physicians, nurses, and other professionals; please visit the site for more detail.

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*Links to non-Federal organizations are provided solely as a service to our users. Links do not constitute an endorsement of any organization by CDC or the Federal Government, and none should be inferred. The CDC is not responsible for the content of the individual organization Web pages found at this link.

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Hemochromatosis: What Every Clinician and Health Care Professional Needs to Know
Hemochromatosis: What Every Clinician and
Health Care Professional Needs to Know

Cover of Iron Overload and Hemocromatosis Brochure:  Information for Patients and Their Families
Iron overload and Hemochromatosis
Information for Patients and Family

 
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Contact Info

Thank you for visiting the CDC-NCBDDD Web site. Click here to contact the National Center on Birth Defects and Developmental Disabilities

We are not able to answer personal medical questions. Please see your health care provider concerning appropriate care, treatment, or other medical advice.
 

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Date last reviewed: 11/01/2007
Content source: Division of Hereditary Blood Disorders, National Center on Birth Defects and Developmental Disabilities
  
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