Classic view of this page
Dihydropyrimidine dehydrogenase Deficiency (DPYD)
Clinical Genetic Test
Help
offered by
Amsterdam UMC, Location AMC
View lab's test page
LinkOut
GTR Test Accession: Help GTR000238866.3
INHERITED DISEASEMETABOLIC DISEASEMUSCULOSKELETAL ... View more
Last updated in GTR: 2023-10-05
View version history
Last annual review date for the lab: 2023-10-12 LinkOut
At a Glance
Test purpose: Help
Mutation Confirmation; Risk Assessment; Diagnosis; ...
Conditions (1): Help
Dihydropyrimidine dehydrogenase deficiency
Genes (1): Help
DPYD (1p21.3)
Methods (4): Help
Biochemical Genetics - Analyte: Metabolite analysis; ...
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
Amsterdam UMC, Location AMC
View lab's website
View lab's test page
Test short name: Help
DPD deficiency
Specimen Source: Help
Who can order: Help
  • Health Care Provider
  • Genetic Counselor
Contact Policy: Help
Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
How to Order: Help
Instructions including forms can be found on www.labgmd.nl
Order URL
Test service: Help
Confirmation of research findings
Clinical Testing/Confirmation of Mutations Identified Previously
Custom Sequence Analysis
Custom Deletion/Duplication Testing
Test additional service: Help
Custom mutation-specific/Carrier testing
Custom Prenatal Testing
Informed consent required: Help
No
Pre-test genetic counseling required: Help
No
Post-test genetic counseling required: Help
No
Recommended fields not provided:
Test Order Code, Lab contact for this test, Test strategy, Test development
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 1
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 4
Method Category Help
Test method Help
Instrument *
Analyte
Metabolite analysis
Enzyme assay
Enzyme diagnostics
Deletion/duplication analysis
Multiplex Ligation-dependent Probe Amplification (MLPA)
Sequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis
* Instrument: Not provided
Clinical Information
Test purpose: Help
Mutation Confirmation; Risk Assessment; Diagnosis; Screening
Recommended fields not provided:
Clinical validity, Clinical utility, Target population, What is the protocol for interpreting a variation as a VUS?, Are family members with defined clinical status recruited to assess significance of VUS without charge?, Will the lab re-contact the ordering physician if variant interpretation changes?, Is research allowed on the sample after clinical testing is complete?, Sample negative report, Sample positive report
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Because the method includes sequence analysis of all exons plus flanking intronic sequences and the vast majority of known mutations are located within these regions, we expect that the mutation detection frequency of our method will be similar as for most other molecular tests we offer, i.e. >95%.
Assay limitations: Help
Whole gene testing includes analysis of all coding exons plus flanking intron sequences by Sanger sequencing. In principle, this method will identify all missense and nonsense mutations, small deletions, small duplications and small insertions located in the analysed fragments. The presence of large deletions or duplications, or pathogenic mutations located … View more
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Test Confirmation, Citations to support assay limitations, Description of internal test validation method, Citations for Analytical validity, PT Provider, Description of PT method, Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review: Help
Category: Not Applicable
Additional Information

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.