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Source1

{
  "resourceType": "CodeSystem",
  "id": "NWTestCode",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "url": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWTestCode",
  "version": "2.1.4",
  "name": "NWTestCode",
  "title": "North West Genomics Test Code",
  "status": "active",
  "experimental": false,
  "date": "2026-06-04",
  "publisher": "NHS North West Genomics",
  "contact": [
    {
      "telecom": [
        {
          "system": "url",
          "value": "https://www.nwgenomics.nhs.uk/contact-us"
        }
      ]
    }
  ],
  "description": "HL7 v2 CodeSystem : NWTestCode",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "GB",
          "display": "United Kingdom of Great Britain and Northern Ireland"
        }
      ]
    }
  ],
  "caseSensitive": true,
  "content": "complete",
  "count": 32,
  "concept": [
    {
      "code": "HX01",
      "display": "Genomic testing (Haemato-Oncology) Not in National Genomic Test Directory"
    },
    {
      "code": "MX01.1",
      "display": "Genomic testing (Solid Tumour), Not in National Genomic Test Directory"
    },
    {
      "code": "MX02.1",
      "display": "BRAF V600E Testing, Lynch syndrome"
    },
    {
      "code": "MX04.1",
      "display": "DNA to be stored, Cancer (Other)"
    },
    {
      "code": "MX05.1",
      "display": "RNA to be stored, Cancer (Other)"
    },
    {
      "code": "MX07.1",
      "display": "FaR-RMS trial, Multi-target NGS Panel, small variant"
    },
    {
      "code": "MX07.2",
      "display": "FaR-RMS trial, Multi-target NGS panel, structural variant"
    },
    {
      "code": "MX08.1",
      "display": "Melanoma, Detection trial, small variant (BRAF, NRAS, TERT)"
    },
    {
      "code": "MX10.1",
      "display": "Triple-Negative Myeloproliferative Neoplasm (MPN), MPL non-canonical variant screening"
    },
    {
      "code": "MX11.1",
      "display": "Acute Myeloid Leukaemia (AML), FLT3-ITD MRD"
    },
    {
      "code": "MX12.1",
      "display": "Large-Cell Neuroendocrine Carcinoma (LCNEC) Project"
    },
    {
      "code": "MX13.1",
      "display": "Colorectal Cancer, Multi-target ctDNA NGS panel, small variant"
    },
    {
      "code": "MX14.1",
      "display": "Cancer of Unknown Primary, Multi-target ctDNA NGS panel, small variant"
    },
    {
      "code": "RX01.1",
      "display": "Genomic testing (Rare Disease) Not in National Genomic Test Directory"
    },
    {
      "code": "RX02.1",
      "display": "Genomic testing Research Study"
    },
    {
      "code": "RX03.1",
      "display": "Complement Tx i-Gain Clinical Trial"
    },
    {
      "code": "RX03.2",
      "display": "Genomic testing Clinical Trial"
    },
    {
      "code": "RX04.1",
      "display": "Molecular Pathology of Human Genetic Disease (HumGenDis)"
    },
    {
      "code": "RX05.1",
      "display": "LEAP Study"
    },
    {
      "code": "RX06.1",
      "display": "Implementing Pharmocogenetics to Improve Prescribing (IPTIP)"
    },
    {
      "code": "RX07.1",
      "display": "TPMT (Thiopurine S-methyltransferase) genotyping (Targeted variant testing)"
    },
    {
      "code": "RX08.1",
      "display": "Factor V Leiden and Prothrombin thrombophilia (FVL and PGV)"
    },
    {
      "code": "RX09.1",
      "display": "Genome-wide DNA Methylation Profiling (Methylation testing)"
    },
    {
      "code": "RX11.1",
      "display": "Jewish BRCA Project Germline Screening"
    },
    {
      "code": "RX16.1",
      "display": "FOVEA Study"
    },
    {
      "code": "RX18.1",
      "display": "Inherited ovarian cancer (without breast cancer) RetroBRCA Project"
    },
    {
      "code": "RX18.2",
      "display": "Inherited breast cancer and ovarian cancer RetroBRCA Project"
    },
    {
      "code": "RX19.1",
      "display": "PROGRESS Study"
    },
    {
      "code": "RX20.1",
      "display": "Renal Tract Abnormalities Study"
    },
    {
      "code": "RX21.1",
      "display": "Ashkenazi Jewish and Polish Population Screening (Targeted variant testing)"
    },
    {
      "code": "XX01.1",
      "display": "Not Processed (No Extraction)"
    },
    {
      "code": "XX02.1",
      "display": "Cell line extraction & aliquot for DNA storage (Other)"
    }
  ]
}