Primary Care eLearning Module on Genetic Haemochromatosis

eLearning Module

This module specifically covers type 1 (HFE mutation) genetic haemochromatosis.

This module is available for download and printing (including worksheets for capturing reflections).

Additional resources

The following additional resources provide a "deep dive" into specific topics :

body iron fundamentals
other types of genetic haemochromatosis (types 2,3,4)
UK Biobank studies into genetic haemochromatosis

We have primary-care specific resources available online :

GP's Quick Guide to Genetic Haemochromatosis (booklet)
Clinician's Guide to Genetic Haemochromatosis and Mental Health (booklet)
Pharmacist's Guide to Genetic Haemochromatosis (booklet)
Primary Care Training (video)

Post-module Assessment

Completed the eLearning module? See how much have your learned with the post-module assessment.

Take the post-module assessment (10 minutes)

Feedback

We welcome your feedback on this module.

*This module was previously accredited by RCGP. Following a decision in August 2024, the RCGP decided to no longer process new applications or reaccredit CPD resources already granted the use of the RCGP Accreditation Kitemark, including this eLearning module on Genetic Haemochromatosis. The material remains current and we continue to provide CPD certificates upon successful completion. We recommend using Chrome, Safari or Firefox browsers - please ensure you have accepted cookies to access the course.

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A GH test direct from the charity, a result within two weeks of return and a consultation with our Advanced Nurse Practitioner. Available online now.
What is genetic haemochromatosis?

Genetic haemochromatosis (GH) is a genetic disorder that increases the risk of the body absorbing an excessive amount of iron from the diet.
Breakfast Cereals and their Iron Content

A rough guide to the Iron content in cereals
Treatment & Care

With treatment, many people live full and active lives with genetic haemochromatosis. Here's what to expect.
Clinical Guidelines for Genetic Haemochromatosis

Published in 2025, this patient-centred guideline sets out a framework for high-quality, evidence-based care in primary and secondary care settings for people with genetic haemochromatosis.
HFE (Type 1) Genetic Haemochromatosis

Genetic haemochromatosis is an autosomal recessive condition, meaning that it is inherited. Whether someone inherits the condition, depends upon their parents' genetics.
Employers' guide to haemochromatosis

People with genetic haemochromatosis want to play an active role in society. These guidelines are intended to help employers understand how they can help people with genetic haemochromatosis in the workplace.
Haemochromatosis Carriers

Carrier is the term used when someone has been shown to have inherited a single copy of the HFE gene mutation from one of the parents. This is sometimes called a heterozygous carrier. Carriers might be at risk of iron loading.
H63D carrier (also known as “H63D heterozygous”)

If you are a “H63d carrier” it means that you have inherited a single copy of the H63d variant from one of your parents.
Help lines

Our help lines are available by phone and email. Worried about genetic haemochromatosis? Don't be. Talk to us for friendly, practical help & understanding.

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