Haemochromatosis

Hereditary haemochromatosis is an inherited disorder of iron metabolism potentially resulting in injury and organ failure. The disease is a consequence of different mutations in the HFE gene, which is involved in intracellular iron transport, that in turn causes disorders such as: cirrhosis, hepatoma, heart failure, arhythmia, infectious diseases and diabetes.

Haemochromatosis
ProductCodeCE MarkDescription
Haemochromatosis - C282YEER044032EER044032

32 Tests 

Available for QiaSymphony SP/AS - Ref: EER032032QS

Haemochromatosis - H63DEER045032EER045032

32 Tests 

Available for QiaSymphony SP/AS - Ref: EER33032QS

Haemochromatosis - S65CEER046032EER046032

32 Tests 

Available for QiaSymphony SP/AS - Ref: EER031032QS