About Iron

 

Understanding Hemochromatosis

Hemochromatosis (HH) is a disease that results from excessive amounts of iron in the body (iron overload).

Hereditary (genetic) hemochromatosis (HHC) an inherited disorder of abnormal iron metabolism. Individuals with hereditary hemochromatosis absorb too much dietary iron. Once absorbed, the body does not have an efficient way of excreting iron excesses.  Over time, these excesses build to a condition of iron overload, which is a toxic to cells. Glands and organs, including the liver, heart, pituitary, thyroid, pancreas, synovium (joints) and bone marrow burdened with excess iron cannot function properly.  Symptoms develop and disease progresses.

There are several types of genetic hemochromatosis. These include: Type I or Classic (HHC); Type II a, b or Juvenile (JHC); Type III or Transferrin Receptor Mutation; and Type IV or Ferroportin Mutation.

Iron Tools

Explore life-saving resources

Utilize tools that patients rely on every single day.

Support group

Reading Room

Forms & Charts

Genetics

Videos About Iron

Real Stories. Real Patients. 

Gerry Koenig - The Dangers of Misdiagnosis

Christine O'Leary - A Family Story

Explore all articles

Order Iron Tests

Simple and Secure

This iron blood test panel measures the hemoglobin, ferritin, fasting serum iron, TIBC (total iron binding capacity) and transferrin levels.

Order Now

Copyright 2020. Iron Disorders Institute. All Rights Reserved. Privacy Policy  |  Terms of Use