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  • Types of GH
  1. Info
  2. All Types of GH

Types of GH

Genetic haemochromatosis comes in several variants, depending upon genetic mutation. Each has its own characteristics.

HFE variants (common)

The most common type, known as HFE (or type 1) genetic haemochromatosis is present in around 1 in 150 people in England & Wales, 1 in 113 people in Scotland and around 1 in 10 people in Northern Ireland. HFE variants are not rare, but rarely diagnosed.:

  • C282y homozygous
  • H63d homozygous
  • S65C homozygous
  • Compound heterozygous (C282y/H63d)
  • Compound heterozygous (C282y/S65C)
  • Compound heterozygous (H63d/S65C)
  • Haemochromatosis Carriers

Non-HFE Variants (rare)

Over the years, other non-HFE causes of iron overload have been isolated. These are known as "non-HFE" variants as they are caused by genetic mutations associated with genes other than the HFE gene. These variants are also known as types 2, 3 and 4. Type 4 is also sometimes called Ferroportin Disease. The prevalence of non-HFE variants is under-studied but thought to be "rare" (affecting 1 in 30,000 people or fewer).

Overall, it is thought that around 160 genetic mutations can cause or contribute to iron overload, to varying degrees. There are also "molecularly undefined" variants, for which the genetic cause is unknown or unexplored, but where iron overload has been demonstrated. These variants are rare.

  • Type 2 (juvenile) haemochromatosis
  • Type 3 (TFR2) haemochromatosis
  • Type 4 haemochromatosis (ferroportin disease)
  • Digenic Inheritance

There may also be other genetic mutations which predispose people to iron overload. As medical research and our understanding of the human genome progress, these may become distinctly identified. In the meantime, our charity works to support anyone affected by genetic haemochromatosis, whatever its cause.

There are several known types of genetic haemochromatosis.

Getting Tested for Genetic Haemochromatosis

In the UK, the NHS typically only tests for HFE (type 1) mutations in C282Y and H63D. This is known as a R95 test. The NHS Genomic Test Directory makes provision for people exhibiting symptoms of iron overload who have been tested for Type 1, to receive further testing for non-HFE causes of haemochromatosis. This is known as a R96 test.

Our charity provides a postal testing service for genetic haemochromatosis, for HFE and non-HFE variants. For further details, read more about genetic testing.

Non-HFE HAMP/HJV (Type 2) Juvenile Haemochromatosis

Non-HFE HAMP/HJV (Type 2) Juvenile Haemochromatosis

Type 2 haemochromatosis is known as a juvenile-onset disorder because symptoms often begin in childhood. Read more

Published: 14th May, 2024

Updated: 25th June, 2024

Author: Neil McClements

Non-HFE TFR2 (Type 3) Genetic Haemochromatosis

Non-HFE TFR2 (Type 3) Genetic Haemochromatosis

This guide explains the rarer form of non-HFE genetic haemochromatosis, also known as type 3 or TFR2-related GH. Read more

Published: 16th April, 2024

Updated: 25th June, 2024

Author: Neil McClements

Non-HFE (Type 4) Genetic Haemochromatosis - Ferroportin Disease

Non-HFE (Type 4) Genetic Haemochromatosis - Ferroportin Disease

This guide explains the rarer form of non-HFE genetic haemochromatosis, called Ferroportin Disease. Read more

Published: 16th March, 2024

Updated: 17th March, 2025

Author: Neil McClements

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    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.

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  • 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

    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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