Disease Diagnosis
Clinical Report (Download a sample report here)
3-6 weeks
For detailed information about the sample requirements, please consult our clinical sample requirements page.
Hereditary Hemochromatosis is an autosomal recessive metabolic disorder characterised by excessive iron absorption from the diet, this is due to mutations in the HFE gene. This results in abnormal iron accumulation in various tissues and organs, leading to potential damage to the liver, heart, pancreas and joints. The test allows the Healthcare Practitioner to determine treatment and monitoring based on the patients HFE gene status.
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