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  2. Hemochromatosis hereditary type 1 (hot spot mutations - p.Cys282Tyr; p.His63Asp in HFE gene)

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

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Full name:
Hemochromatosis hereditary type 1 (hot spot mutations - p.Cys282Tyr; p.His63Asp in HFE gene)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Targeted variant analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Gent
RIZIV code:
565316-565320
EQA:
  • 2017 Hereditary Haemochromatosis EMQN
  • 2019 Hereditary Haemochromatosis EMQN
  • 2022 Hereditary Haemochromatosis EMQN
Accreditation (ISO 15189):
2021-09-11 / 2026-09-10
Turnaround time (maximum):
3 - weeks
Document(s):
Created:
19 Jul 2019 - 12:09
Changed:
31 Jan 2023 - 14:17