NHS North West Genomics
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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

: North West Genomics Test Code - JSON Representation

Active as of 2026-06-04

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{
  "resourceType" : "CodeSystem",
  "id" : "NWTestCode",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem NWTestCode</b></p><a name=\"NWTestCode\"> </a><a name=\"hcNWTestCode\"> </a><p>This case-sensitive code system <code>https://fhir.nwgenomics.nhs.uk/CodeSystem/NWTestCode</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">HX01<a name=\"NWTestCode-HX01\"> </a></td><td>Genomic testing (Haemato-Oncology) Not in National Genomic Test Directory</td></tr><tr><td style=\"white-space:nowrap\">MX01.1<a name=\"NWTestCode-MX01.461\"> </a></td><td>Genomic testing (Solid Tumour), Not in National Genomic Test Directory</td></tr><tr><td style=\"white-space:nowrap\">MX02.1<a name=\"NWTestCode-MX02.461\"> </a></td><td>BRAF V600E Testing, Lynch syndrome</td></tr><tr><td style=\"white-space:nowrap\">MX04.1<a name=\"NWTestCode-MX04.461\"> </a></td><td>DNA to be stored, Cancer (Other)</td></tr><tr><td style=\"white-space:nowrap\">MX05.1<a name=\"NWTestCode-MX05.461\"> </a></td><td>RNA to be stored, Cancer (Other)</td></tr><tr><td style=\"white-space:nowrap\">MX07.1<a name=\"NWTestCode-MX07.461\"> </a></td><td>FaR-RMS trial, Multi-target NGS Panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">MX07.2<a name=\"NWTestCode-MX07.462\"> </a></td><td>FaR-RMS trial, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">MX08.1<a name=\"NWTestCode-MX08.461\"> </a></td><td>Melanoma, Detection trial, small variant (BRAF, NRAS, TERT)</td></tr><tr><td style=\"white-space:nowrap\">MX10.1<a name=\"NWTestCode-MX10.461\"> </a></td><td>Triple-Negative Myeloproliferative Neoplasm (MPN), MPL non-canonical variant screening</td></tr><tr><td style=\"white-space:nowrap\">MX11.1<a name=\"NWTestCode-MX11.461\"> </a></td><td>Acute Myeloid Leukaemia (AML), FLT3-ITD MRD</td></tr><tr><td style=\"white-space:nowrap\">MX12.1<a name=\"NWTestCode-MX12.461\"> </a></td><td>Large-Cell Neuroendocrine Carcinoma (LCNEC) Project</td></tr><tr><td style=\"white-space:nowrap\">MX13.1<a name=\"NWTestCode-MX13.461\"> </a></td><td>Colorectal Cancer, Multi-target ctDNA NGS panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">MX14.1<a name=\"NWTestCode-MX14.461\"> </a></td><td>Cancer of Unknown Primary, Multi-target ctDNA NGS panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">RX01.1<a name=\"NWTestCode-RX01.461\"> </a></td><td>Genomic testing (Rare Disease) Not in National Genomic Test Directory</td></tr><tr><td style=\"white-space:nowrap\">RX02.1<a name=\"NWTestCode-RX02.461\"> </a></td><td>Genomic testing Research Study</td></tr><tr><td style=\"white-space:nowrap\">RX03.1<a name=\"NWTestCode-RX03.461\"> </a></td><td>Complement Tx i-Gain Clinical Trial</td></tr><tr><td style=\"white-space:nowrap\">RX03.2<a name=\"NWTestCode-RX03.462\"> </a></td><td>Genomic testing Clinical Trial</td></tr><tr><td style=\"white-space:nowrap\">RX04.1<a name=\"NWTestCode-RX04.461\"> </a></td><td>Molecular Pathology of Human Genetic Disease (HumGenDis)</td></tr><tr><td style=\"white-space:nowrap\">RX05.1<a name=\"NWTestCode-RX05.461\"> </a></td><td>LEAP Study</td></tr><tr><td style=\"white-space:nowrap\">RX06.1<a name=\"NWTestCode-RX06.461\"> </a></td><td>Implementing Pharmocogenetics to Improve Prescribing (IPTIP)</td></tr><tr><td style=\"white-space:nowrap\">RX07.1<a name=\"NWTestCode-RX07.461\"> </a></td><td>TPMT (Thiopurine S-methyltransferase) genotyping (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">RX08.1<a name=\"NWTestCode-RX08.461\"> </a></td><td>Factor V Leiden and Prothrombin thrombophilia (FVL and PGV)</td></tr><tr><td style=\"white-space:nowrap\">RX09.1<a name=\"NWTestCode-RX09.461\"> </a></td><td>Genome-wide DNA Methylation Profiling (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">RX11.1<a name=\"NWTestCode-RX11.461\"> </a></td><td>Jewish BRCA Project Germline Screening</td></tr><tr><td style=\"white-space:nowrap\">RX16.1<a name=\"NWTestCode-RX16.461\"> </a></td><td>FOVEA Study</td></tr><tr><td style=\"white-space:nowrap\">RX18.1<a name=\"NWTestCode-RX18.461\"> </a></td><td>Inherited ovarian cancer (without breast cancer) RetroBRCA Project</td></tr><tr><td style=\"white-space:nowrap\">RX18.2<a name=\"NWTestCode-RX18.462\"> </a></td><td>Inherited breast cancer and ovarian cancer RetroBRCA Project</td></tr><tr><td style=\"white-space:nowrap\">RX19.1<a name=\"NWTestCode-RX19.461\"> </a></td><td>PROGRESS Study</td></tr><tr><td style=\"white-space:nowrap\">RX20.1<a name=\"NWTestCode-RX20.461\"> </a></td><td>Renal Tract Abnormalities Study</td></tr><tr><td style=\"white-space:nowrap\">RX21.1<a name=\"NWTestCode-RX21.461\"> </a></td><td>Ashkenazi Jewish and Polish Population Screening (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">XX01.1<a name=\"NWTestCode-XX01.461\"> </a></td><td>Not Processed (No Extraction)</td></tr><tr><td style=\"white-space:nowrap\">XX02.1<a name=\"NWTestCode-XX02.461\"> </a></td><td>Cell line extraction &amp; aliquot for DNA storage (Other)</td></tr></table></div>"
  },
  "url" : "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWTestCode",
  "version" : "2.0.12",
  "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)"
    }
  ]
}