Genetic Disorders


The AusDiagnostics Haemochromatosis panel includes sequence variants that account for 80% of hereditary haemochromatosis cases. In addition to automated results interpretation and diagnosis, the results software provides the Heterozygous or homozygous mutation status. A further diagnostic benefit is the ability to estimate the risk of iron overload based on the variant and prevalence, allowing for better informed treatments. The AusDiagnostics Haemochromatosis 8-well panel allows for the simultaneous detection of wildtype and mutant variations at 3 amino acid positions in the HFE gene that are responsible for iron overload, with a sensitivity and specificity above 95%.
Haemochromatosis 8-well (REF 23156)
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  • HFE gene – amino acid position 63 (wt and H63D mutant)
  • HFE gene – amino acid position 65 (wt and S65C mutant)
  • HFE gene – amino acid position 282 (wt and C282Y mutant)

Ordering Information

Pack size
​Haemochromatosis 8-well Step 1 Tubes
12 x 8 well Strips
Haemochromatosis 8-well Step 2 Plates
​Box of 12 Plates
Demi DNA Reagent Cassettes
Box of 10
Synthetic Positive Controls for Haemochromatosis
Box of 10

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TandemPlex® panels are intended for in vitro diagnostics use by authorised clinical testing laboratories in Australia, New Zealand, and the European Economic Area and is included on the Australian Register of Therapeutic Goods (ARTG), and compliant with the European IVD Directive 98/79/EC. Research use only in USA.