Hemochromatosis hereditary type 1 (hot spot mutations - p.Cys282Tyr; p.His63Asp)

Genetic test Export to PDF
Full name:
Hemochromatosis hereditary type 1 (hot spot mutations - p.Cys282Tyr; p.His63Asp)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2015 Hereditary Haemochromatosis EMQN
  • 2016 Hereditary Haemochromatosis EMQN
  • 2017 Hereditary Haemochromatosis EMQN
  • 2018 Hereditary Haemochromatosis EMQN
  • 2019 Hereditary Haemochromatosis EMQN
  • 2020 Hereditary Haemochromatosis EMQN
  • 2021 Hereditary Haemochromatosis EMQN
  • 2022 Hereditary Haemochromatosis EMQN
  • 2023 Hereditary Haemochromatosis EMQN
Accreditation (ISO 15189):
2022-12-22 / 2027-12-21
Turnaround time (maximum):
1 month
Document(s):
Created:
19 Jul 2019 - 12:09
Changed:
19 Jan 2024 - 11:57