NHS North West Genomics
2.0.12 - ci-build United Kingdom flag

NHS North West Genomics - Local Development build (v2.0.12) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

CodeSystem: North West Genomics Test Code

Official URL: https://fhir.nwgenomics.nhs.uk/CodeSystem/NWTestCode Version: 2.0.12
Active as of 2026-06-04 Computable Name: NWTestCode

HL7 v2 CodeSystem : NWTestCode

This Code system is referenced in the content logical definition of the following value sets:

This case-sensitive code system https://fhir.nwgenomics.nhs.uk/CodeSystem/NWTestCode defines the following codes:

CodeDisplay
HX01 Genomic testing (Haemato-Oncology) Not in National Genomic Test Directory
MX01.1 Genomic testing (Solid Tumour), Not in National Genomic Test Directory
MX02.1 BRAF V600E Testing, Lynch syndrome
MX04.1 DNA to be stored, Cancer (Other)
MX05.1 RNA to be stored, Cancer (Other)
MX07.1 FaR-RMS trial, Multi-target NGS Panel, small variant
MX07.2 FaR-RMS trial, Multi-target NGS panel, structural variant
MX08.1 Melanoma, Detection trial, small variant (BRAF, NRAS, TERT)
MX10.1 Triple-Negative Myeloproliferative Neoplasm (MPN), MPL non-canonical variant screening
MX11.1 Acute Myeloid Leukaemia (AML), FLT3-ITD MRD
MX12.1 Large-Cell Neuroendocrine Carcinoma (LCNEC) Project
MX13.1 Colorectal Cancer, Multi-target ctDNA NGS panel, small variant
MX14.1 Cancer of Unknown Primary, Multi-target ctDNA NGS panel, small variant
RX01.1 Genomic testing (Rare Disease) Not in National Genomic Test Directory
RX02.1 Genomic testing Research Study
RX03.1 Complement Tx i-Gain Clinical Trial
RX03.2 Genomic testing Clinical Trial
RX04.1 Molecular Pathology of Human Genetic Disease (HumGenDis)
RX05.1 LEAP Study
RX06.1 Implementing Pharmocogenetics to Improve Prescribing (IPTIP)
RX07.1 TPMT (Thiopurine S-methyltransferase) genotyping (Targeted variant testing)
RX08.1 Factor V Leiden and Prothrombin thrombophilia (FVL and PGV)
RX09.1 Genome-wide DNA Methylation Profiling (Methylation testing)
RX11.1 Jewish BRCA Project Germline Screening
RX16.1 FOVEA Study
RX18.1 Inherited ovarian cancer (without breast cancer) RetroBRCA Project
RX18.2 Inherited breast cancer and ovarian cancer RetroBRCA Project
RX19.1 PROGRESS Study
RX20.1 Renal Tract Abnormalities Study
RX21.1 Ashkenazi Jewish and Polish Population Screening (Targeted variant testing)
XX01.1 Not Processed (No Extraction)
XX02.1 Cell line extraction & aliquot for DNA storage (Other)