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

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

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Full name:
Hemochromatosis hereditary type 1 (HFE gene hot spot mutations - p.Cys282Tyr; p.His63Asp)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centrum Medische Genetica - UZ Brussel VUB
RIZIV code:
565316-565320
EQA:
  • 2015 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2016 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2017 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2018 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2019 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2020 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2021 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
  • 2022 Hereditary Haemochromatosis (Molecular genetics 1-set D) DGKL/RfB-Reference Institute for Bioanalytics
Accreditation (ISO 15189):
2021-10-07 / 2026-06-14
Turnaround time (maximum):
1 month
Document(s):
Created:
19 Jul 2019 - 12:09
Changed:
09 Mar 2023 - 15:56
URL:
https://laboguide.uzbrussel.be/laboguide#Analyses:Hemochromatose&&&&&978&COLLEC…