Hemochromatosis
Hemochromatosis
Hereditary hemochromatosis 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.

Product | Code | CE Mark | Description |
---|---|---|---|
Haemochromatosis - C282Y | EER044032 | ![]() | 32 Tests Available for QiaSymphony SP/AS - Ref: EER032032QS |
Haemochromatosis - H63D | EER045032 | ![]() | 32 Tests Available for QiaSymphony SP/AS - Ref: EER33032QS |
Haemochromatosis - S65C | EER046032 | ![]() | 32 Tests Available for QiaSymphony SP/AS - Ref: EER031032QS |
Hemochromatosis mutations Kit RQ (C282Y, H63D, S65C) | HE.01RQ | ![]() | 40 Tests |