Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (50 hot spot mutations)

Genetic test Export to PDF
Full name:
Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (50 hot spot mutations)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2015 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2016 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2017 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2018 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2019 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2020 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
  • 2021 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
  • 2022 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
  • 2023 Cystic Fibrosis (CF) and CFTR-related disorders GenQA (Genomics Quality Assessment)
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
1 month
Document(s):
Created:
18 Jul 2019 - 15:04
Changed:
22 Jan 2024 - 13:40
URL: