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

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:
Targeted variant analysis
Method technique:
Real-time PCR
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565316-565320
EQA:
  • 2016 Hereditary Haemochromatosis EMQN
  • 2019 Hereditary Haemochromatosis EMQN
  • 2022 Hereditary Haemochromatosis EMQN
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
2 - 4 weeks
Document(s):
Created:
19 Jul 2019 - 12:09
Changed:
01 Mar 2023 - 15:09
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/12331