Updated Dec 2025

Bottom line:  Hereditary Hemochromatosis (HH) is a common inherited iron overload disorder. Affected individuals are predisposed to absorb excess iron from their diet due to improper regulation of iron homeostasis.  Over time excess iron can be deposited in organs leading to dysfunction. The most common type of HH is caused by pathogenic variants in the HFE gene. Homozygosity (two copies) of the C282Y variant in this gene is associated with highest risk for iron overload. HFE-related HH is an autosomal recessive condition where one must inherit two pathogenic variants (one from each parent) to be at risk for iron overload. Most individuals with this predisposition never develop clinical disease.  While HH does have the potential to cause morbidity and mortality, with early identification of at-risk individuals, appropriate surveillance of iron indices, and treatment (phlebotomy) when necessary, many complications can be avoided. Genetic testing for HH should be considered for adult individuals with: a positive family history even in the ab­sence of symptoms sustained elevation on multiple occasions of serum transferrin saturation (TS), serum ferritin (SF) levels, or aminotransferase levels (ALT) in the absence of symptoms TS >45% and SF >300ug/L in men and post-menopausal women or >200ug/L in pre-menopausal women ALT can be elevated in up to 14% of the general population. If ALT is elevated, consider ordering SF and TS. If those are also elevated then consider genetic testing. the pres­ence of symptoms, especially two or more, and in particular liver disease or arthritis mean red-cell volume >94 fL

 

 

 Jump to a section

• What is Hereditary Hemochromatosis?
• What do I need to know about the genetics of HH?
• Who should be offered genetic testing?
• What does the genetic test result mean?
• How do I order the genetic test?
• Where do I refer my patient?
• Are there benefits or considerations of genetic testing?
• Surveillance and Management
• References
• Resources for the public

What is Hereditary Hemochromatosis?

Hereditary Hemochromatosis (HH) can be caused by harmful changes (pathogenic variants) in different genes. Pathogenic variants in the HFE gene are the cause of 95% of cases of hemochromatosis.^1,2 This GECKO Deep dive deals EXCLUSIVELY with HFE-associated HH.

Pathogenic variants in the HFE gene alter the regulation of iron absorption through the mucosal lining of the gastrointestinal tract. In some predisposed individuals, excessive iron absorption and subsequent storage in various organs (Table 1) eventually lead to cellular injury. If untreated, over time this can cause irreversible tissue damage and shorten life expectancy. With early identification of at-risk individuals, surveillance of iron indices, and treatment, when necessary, many complications can be avoided.^1,2

While any of these health concerns can be caused by HH, the initial presentation of the condition may be non-specific and can include features such as fatigue and lethargy. The presence of two or more of the features in Table 1 should greatly increase suspicion that the condition is present. 

Table 1. Organs at risk of damage due to excessive iron storage^1,2.

Organ	Damage
Liver	Hepatomegaly, cirrhosis, primary liver cancer (hepatocellular carcinoma, cholangiocarcinoma)
Pancreas	Diabetes mellitus
Heart	Dilated cardiomyopathy, congestive heart failure +/- arrhythmia
Joints	Arthritis, especially metacarpophalangeal joints, hips, knees
Skin	Progressive hyperpigmentation
Testes	Hypogonadism, decreased libido and impotence in males

Additional symptoms of advanced iron overload:¹

• Weakness, chronic fatigue
• Abdominal pain
• Weight loss

What do I need to know about the genetics of HH?

Inherited HH is most commonly caused by pathogenic variants in the HFE gene on chromosome 6.

An individual is at risk for HH when they have inherited two pathogenic variants in the HFE gene (one from each parent). Common variants (C282Y and H63D) are known to be present in individuals who are of northern European ethnicity. Homozygosity for the C282Y variant (having two copies of the C282Y variant, one inherited from each parent) causes 95% of HH.¹ About 1 in 150 individuals of northern European ethnicity are affected by HH.¹

Pattern of inheritance

Autosomal recessive

• An individual who has inherited two pathogenic variants in the HFE gene, one from each parent, has the predisposition to develop iron overload.
• A person with a single pathogenic variant is called a ‘carrier’ and is not at risk of iron overload.

How common is HFE-HH?

About 1 in 3 individuals of northern European ancestry are carriers (heterozygotes) of either the C282Y or H63D pathogenic variants.^1,2 About 1 in 150 individuals have two copies of (are homozygous for) the C282Y pathogenic variant (genotype C282Y/C282Y).¹ The prevalence of HFE-HH in other ethnicities is lower.

Who should be offered genetic testing?

Standard testing performed by molecular genetics laboratories typically involves targeted analysis looking for the two most common HFE pathogenic variants, C282Y and H63D. Some laboratories may also test for a rare HFE gene variant called S65C.³ Multigene panel testing may be considered when an individual is not of northern European ethnicity.²

Genetic testing for HH should be considered for adult individuals with:^1,2

• a positive family history of HH even in the ab­sence of symptoms
• sustained elevation on multiple occasions of serum transferrin saturation (TS), serum ferritin levels (SF), or aminotransferase levels (ALT) in the absence of symptoms
  • TS >45% and SF >300ug/L in men and post-menopausal women or >200ug/L in pre-menopausal women
  • Elevation of ferritin alone is not necessarily due to iron overload.  Ferritin is an acute phase reactant, and secondary causes of increased levels may be infection, chronic liver disease, iron-loading anemia, chronic inflammatory state, or malignancy. 
  • Individuals with HFE-HH occasionally demonstrate a normal TS and an elevated ferritin. If clinical suspicion is high and/or the patient has a family history of HFE-HH, genetic testing is still warranted.
  • ALT can be elevated in up to 14% of the general population. If ALT is elevated, consider ordering SF and TS and, if those are also elevated, consider genetic testing.
• the pres­ence of symptoms, especially two or more, and, in particular, liver disease or arthritis
• mean red-cell volume >94 fL

Symptoms and clinical features of HH:^1,2

• Weakness, chronic fatigue
• Abdominal pain, weight loss
• Arthropathy (especially metacarpophalangeal joints, hips, knees)
• Diabetes
• Hepatomegaly
• Cirrhosis
• Primary liver cancer (hepatocellular carcinoma, cholangiocarcinoma)
• Hypogonadotropic hypogonadism (decreased libido and impotence in males, amenorrhea in females)
• Cardiomyopathy, arrhythmias
• Progressive increase in skin pigmentation

Who should not be offered genetic testing?

Population screening for HFE-HH is not recommended as the disease penetrance is low.^1,2

Children do not require genetic testing for HFE-HH. Please refer to the Canadian Paediatric Society Bioethics Committee policy statement that recommends against genetic testing for genetic conditions that usually manifest in adulthood. Predictive or susceptibility genetic testing should be postponed until a child is capable of making an informed decision about undergoing testing.⁴

What does the genetic test result mean?

If an individual is found to have inherited only one HFE pathogenic variant, they are a carrier and are not expected to develop iron overload. Adult relatives can be offered genetic testing to know if they also carry the HFE pathogenic variant, and possibly a second variant and thus be at risk for HH.

The actual risk to develop iron overload is dependent upon which pathogenic variants are present, in addition to other genetic and non-genetic factors. Individuals who are homozygous for the C282Y variant (C282Y/C282Y) have about a 38-50% risk to develop iron overload and about 10-33% will develop iron overload-related symptoms.² Many individuals never accumulate enough iron to cause disease.² Individuals with a C282Y and a H63D pathogenic variant (C282Y/H63D) have about a 2% chance of developing iron overload. Those who are homozygous for the H63D variant (H63D/H63D) have about a 1% chance of developing iron overload.

If no pathogenic variants are identified:

• If the individual was tested because of a known family variant, they no longer need frequent monitoring of iron indices and are not at increased risk to develop iron overload. The test has ruled out HH.
• If the individual was tested because of a reported positive family history, more information is needed before ruling out HH. Your patient should be encouraged to obtain confirmation of the familial variants and/or diagnosis.
• If the individual was tested because of persistently high iron indices, additional investigations may be considered. Consider consulting a specialist e.g. hematology, internal medicine, or gastroenterology for next steps.

Other considerations:

• Women are less likely to develop iron overload as a result of menstruation and pregnancy^1,2,3
• Iron overload due to HFE pathogenic variants does not occur in childhood¹
• Typically, symptoms of HH present in men aged 40 to 60 and in post-menopausal women; however, onset is variable and can occur much earlier or much later^1,2
• Early symptoms are nonspecific and include weakness, lethargy, joint pain and/or stiffness, and abdominal pain with or without hepatomegaly¹
• Before the onset of symptoms, biochemical evidence of iron overload will be present: >45% transferrin saturation (TS) and >300µg/L serum ferritin (SF) in men and post-menopausal women, or >200µg/L SF in pre-menopausal women ^1,2
• Alcohol consumption can exacerbate iron overload and HH- related liver disease¹

How do I order the genetic test?

Genetic testing for HH is performed in a specialized hospital laboratory (molecular) on a blood sample. The blood sample can be obtained at any community lab. Click here to find your closest molecular genetics laboratory and the requisition to order testing. Some laboratories prefer that you attach their requisition to the Provincial Ministry of Health requisition. This process will expedite and simplify genetic testing when blood is drawn at a community laboratory.

It is important to include the following information on any requisition for the best test interpretation:

• Indication for testing e.g. ‘symptoms of indicated disease’ or ‘abnormal iron indices’ or ‘positive family history’
• Ethnicity e.g. Northern European
• Relevant family history e.g. parent/sibling with HH (include genetic test results of affected individual if known)
• Relevant medical history/investigations, e.g. biochemical iron overload

Where do I refer my patient?

Across Canada, many Genetics clinics will no longer see individuals for the indication of HFE-related HH. Check your local genetics clinic for their referral criteria here.  You may consider referral to a specialist e.g. haematologist or gastroenterologist for evaluation and initiation of treatment

Are there benefits or considerations of genetic testing?

If pathogenic variants are identified

• Appropriate surveillance and management of the risk of iron overload can be initiated

If no pathogenic variants are identified

• If an individual was tested because of a known family variant, they no longer need frequent monitoring of iron indices and are not at increased risk to develop iron overload. The test has ruled out HH.

Targeted analysis

• Typically, only the C282Y and H63D variants are tested, not any HFE gene variant. However, the most common pathogenic variants account for more than 90% of all variants, thus fewer than 10% will be missed using current testing strategies.

Insurance discrimination

• In Canada, the Genetic Non-Discrimination Act (GNA) became law in 2017. This law protects Canadians and their genomic information. Some key points of the law are that GNA prohibits:
  • Discrimination based on genomic characteristics
  • Providers of goods and services (including insurance) from:
    • requesting or requiring a genomic test
    • requesting or requiring the disclosure of genomic test results either past or future

• Federally regulated employers from using genomic test results in decisions about hiring, firing, job assignments, or promotions

Surveillance and Management

Homozygosity for the C282Y pathogenetic variant is associated with complications in up to 40% of men and 13% of women.¹ Symptoms are nonspecific and can be observed among those with and those without HH.¹

Individuals with positive genetic testing and/or family history who are asymptomatic¹

Transferrin saturation (TS) and serum ferritin (SF) levels should be measured in these individuals and, if elevated (i.e. TS (>45%) AND SF are elevated (>300ug/L in men and post-menopausal women; >200ug/L in pre-menopausal women)), further workup should proceed as outlined below. In homozygous individuals (C282Y/C282Y) with a normal SF at diagnosis, ongoing monitoring of TS, SF and liver aminotransferase every 5 years should be considered to detect progression.^1,5

Liver¹

The most frequent clinical manifestations are liver disease (advanced liver fibrosis or cirrhosis and primary liver cancer) and arthritis. Liver fibrosis occurs in about 8% of women and 25% of men with hemochromatosis.¹ Risk factors include heavy alcohol use, the presence of diabetes mellitus or arthritis, SF concentrations above 1000 µg/L, platelet counts below 200 × 10⁹/L, increased aspartate aminotransferase (ALT) levels, hepatic iron concentrations exceeding 200 µmol/g, and total mobilizable iron stores from therapeutic phlebotomy greater than 9.6g. Men who are homozygous for the C282Y variant have a 12-fold increased likelihood of  liver cancer over men who do not. Homozygous women are not known to have an increased risk for liver cancer.

Individuals with advanced liver fibrosis should undergo routine liver ultrasonography cancer sur­veillance at 6-month intervals.

Arthritis¹

HH-related arthritis affects at least 24% of individuals and is a major cause of disability and re­duced quality of life. Arthritis may occur at any point during the natural history of hemochromatosis, even after successful therapeutic phlebotomy. Risk factors for arthritis include older age, advanced liver fibrosis, SF concentrations above 1000 µg/L, and serum transferrin saturation greater than 50% sustained for at least six years.

Treatment

Therapeutic phlebotomy, which is both safe and effective, is the mainstay of treatment for iron overload. With treatment, many complications can be avoided.^1,2 Treatment is usually indicated in the presence of biochemical evidence of iron overload (i.e. TS >45% AND SF are elevated (>300 ug/L in men and post-menopausal women; >200 ug/L in pre-menopausal women) or clinical manifestations e.g. end-organ damage.^1,2  A SF of 1000ug/L or greater significantly increases mor­bidity.¹ A genetic predisposition to iron overload (e.g. C282Y/C282Y genotype) is not, on its own, an indication for treatment in the absence of abnormal iron indices.

After initial treatment, maintenance therapy is performed to keep SF levels within the target range. Hemoglobin is also monitored. In most cases, this involves phlebotomy approximately every three months; however, the frequency varies widely and should be tailored to each patient’s individual needs.¹

Individuals should also be advised to avoid consuming raw seafood to minimize the risk of Vibrio vulnificus infection (a bacteria that thrives on iron), to limit alcohol intake to decrease the likelihood of advanced liver fibrosis, and to avoid cast iron cookware and vitamin C supplements. Dietary iron modification does not significantly alter SF levels and is not a substitute treatment for individuals with iron overload.^1,2 Individuals with two HFE gene pathogenic variants should consider the hepatitis A&B vaccines.²

References

1. Olynyk JK, Ramm GA. Hemochromatosis. N Engl J Med. 2022 Dec 8;387(23):2159-2170
2. Barton JC, Parker CJ. HFE-Related Hemochromatosis. 2000 Apr 3 [Updated 2024 Apr 11]. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2025. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1440/ [Accessed Dec 2025]
3. Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, et al. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y. J Hepatol. 2002. 36(4):474-479.
4. Moore AM, Richer J; Canadian Paediatric Society, Bioethics Committee. Genetic testing and screening in children. Paediatr Child Health 2022 27(4):243–247. https://cps.ca/en/documents/position/genetic-testing [Accessed Dec 2025].
5. Kowdley KV, Brown KE, Ahn J, Sundaram V. ACG Clinical Guideline: Hereditary Hemochromatosis. Am J Gastroenterol. 2019 Aug;114(8):1202-1218. Erratum in: Am J Gastroenterol. 2019 Dec;114(12):1927

Resources for the public

Canadian Hemochromatosis Society.  Established to create awareness about the disorder.  Additionally provides information and support.  www.toomuchiron.ca  [Accessed Dec 2025].

Authors: S Morrison MS CGC, JE Allanson MD FRCPC, S Walji MD CCFP and JC Carroll MD CCFP

 

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