GenoType HH (haemochromatosis) PCR CE/IVD

Our GenoType HH test system allows you to have a definite and rapid diagnosis of hereditary haemochromatosis by the detection of these important mutations.

Your benefits with GenoType HH
- Unambiguous diagnosis: With the detection of certain genotypes, the suspicion of the presence of hereditary haemochromatosis can be confirmed.
- More information: Along with the two most common mutations (C282Y and H63D), rare genotypes such as S65C and E168X are also detected. This allows a comprehensive diagnosis of the disease.
- Definite result: If the test is not processed under optimal conditions, this will be indicated by an internal control.

Molecular genetic assay for analysis of the HFE gene mutations C282Y, H65D, S65C and E168X

Starting material:
EDTA/Citrate blood

DNA Isolation:
GENO•CARD or
GenoType DNA Isolation Kit or
GXT Blood Extraction Kit (with GenoXtract®)