NHS England Genomic Test Code - XML Representation - NHS North West Genomics v2.0.12

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
: NHS England Genomic Test Code - XML Representation

Active as of 2026-06-04
Raw xml | Download

<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="GenomicTestCode"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: CodeSystem GenomicTestCode</b></p><a name="GenomicTestCode"> </a><a name="hcGenomicTestCode"> </a><p>This case-sensitive code system <code>https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory</code> provides <b>a fragment</b> that includes 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">M1.1<a name="GenomicTestCode-M1.461"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF)</td></tr><tr><td style="white-space:nowrap">M1.2<a name="GenomicTestCode-M1.462"> </a></td><td>Colorectal Carcinoma, KRAS hotspot</td></tr><tr><td style="white-space:nowrap">M1.3<a name="GenomicTestCode-M1.463"> </a></td><td>Colorectal Carcinoma, NRAS hotspot</td></tr><tr><td style="white-space:nowrap">M1.4<a name="GenomicTestCode-M1.464"> </a></td><td>Colorectal Carcinoma, MSI Testing</td></tr><tr><td style="white-space:nowrap">M1.5<a name="GenomicTestCode-M1.465"> </a></td><td>Colorectal Carcinoma, MLH1 promoter hypermethylation</td></tr><tr><td style="white-space:nowrap">M1.6<a name="GenomicTestCode-M1.466"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M1.7<a name="GenomicTestCode-M1.467"> </a></td><td>Colorectal Carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M1.9<a name="GenomicTestCode-M1.469"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2, POLE, POLD1)</td></tr><tr><td style="white-space:nowrap">M10.1<a name="GenomicTestCode-M10.461"> </a></td><td>Thyroid Follicular Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, HRAS)</td></tr><tr><td style="white-space:nowrap">M10.2<a name="GenomicTestCode-M10.462"> </a></td><td>Thyroid Follicular Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET)</td></tr><tr><td style="white-space:nowrap">M100.1<a name="GenomicTestCode-M100.461"> </a></td><td>Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M100.2<a name="GenomicTestCode-M100.462"> </a></td><td>Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 Copy number FISH</td></tr><tr><td style="white-space:nowrap">M100.3<a name="GenomicTestCode-M100.463"> </a></td><td>Primary Mediastinal B Cell Lymphoma, REL copy number FISH</td></tr><tr><td style="white-space:nowrap">M100.4<a name="GenomicTestCode-M100.464"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M100.5<a name="GenomicTestCode-M100.465"> </a></td><td>Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, copy number variant (CD274, PDCD1LG2, REL)</td></tr><tr><td style="white-space:nowrap">M100.6<a name="GenomicTestCode-M100.466"> </a></td><td>Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, rearrangement (CD274, PDCD1LG2)</td></tr><tr><td style="white-space:nowrap">M100.7<a name="GenomicTestCode-M100.467"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M100.8<a name="GenomicTestCode-M100.468"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M101.1<a name="GenomicTestCode-M101.461"> </a></td><td>ALK Positive Large B Cell Lymphoma, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M101.2<a name="GenomicTestCode-M101.462"> </a></td><td>ALK Positive Large B Cell Lymphoma, t(2;17)(p23;q23) CLTC-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M101.3<a name="GenomicTestCode-M101.463"> </a></td><td>ALK Positive Large B Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M101.4<a name="GenomicTestCode-M101.464"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M101.5<a name="GenomicTestCode-M101.465"> </a></td><td>ALK Positive Large B Cell Lymphoma, Multi-target NGS panel, structural variant (CLTC-ALK, ALK-NPM1, other ALK rearrangements)</td></tr><tr><td style="white-space:nowrap">M101.6<a name="GenomicTestCode-M101.466"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M101.7<a name="GenomicTestCode-M101.467"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M102.1<a name="GenomicTestCode-M102.461"> </a></td><td>Mantle Cell Lymphoma, t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M102.2<a name="GenomicTestCode-M102.462"> </a></td><td>Mantle Cell Lymphoma, CCND1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M102.3<a name="GenomicTestCode-M102.463"> </a></td><td>Mantle Cell Lymphoma, CCND2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M102.4<a name="GenomicTestCode-M102.464"> </a></td><td>Mantle Cell Lymphoma, Multi-target NGS panel, structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)</td></tr><tr><td style="white-space:nowrap">M102.5<a name="GenomicTestCode-M102.465"> </a></td><td>Mantle Cell Lymphoma, Multi-target NGS panel, small variant (TP53)</td></tr><tr><td style="white-space:nowrap">M103.1<a name="GenomicTestCode-M103.461"> </a></td><td>Follicular Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M103.2<a name="GenomicTestCode-M103.462"> </a></td><td>Follicular Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M103.3<a name="GenomicTestCode-M103.463"> </a></td><td>Follicular Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M103.4<a name="GenomicTestCode-M103.464"> </a></td><td>Follicular Lymphoma, Multi-target NGS panel, small variant (CARD11, CREBBP, EZH2, ARID1A, EP300, MEF2B, FOXO1)</td></tr><tr><td style="white-space:nowrap">M103.5<a name="GenomicTestCode-M103.465"> </a></td><td>Follicular Lymphoma, Multi-target NGS panel, structural variant (IGH-BCL2, BCL2, BCL6)</td></tr><tr><td style="white-space:nowrap">M104.1<a name="GenomicTestCode-M104.461"> </a></td><td>Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, Multi-target NGS panel, small variant (MYD88, CXCR4)</td></tr><tr><td style="white-space:nowrap">M104.2<a name="GenomicTestCode-M104.462"> </a></td><td>Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, MYD88 hotspot</td></tr><tr><td style="white-space:nowrap">M105.1<a name="GenomicTestCode-M105.461"> </a></td><td>Igm Monoclonal Gammopathy of Uncertain Significance, Multi-target NGS panel, small variant (MYD88, CXCR4)</td></tr><tr><td style="white-space:nowrap">M105.2<a name="GenomicTestCode-M105.462"> </a></td><td>Igm Monoclonal Gammopathy of Uncertain Significance, MYD88 hotspot</td></tr><tr><td style="white-space:nowrap">M106.1<a name="GenomicTestCode-M106.461"> </a></td><td>Intra-Ocular Lymphoma, MYD88 hotspot</td></tr><tr><td style="white-space:nowrap">M107.1<a name="GenomicTestCode-M107.461"> </a></td><td>Malt-Lymphoma, t(11;18)(q21;q21) BIRC3-MALT1  FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M107.10<a name="GenomicTestCode-M107.4610"> </a></td><td>Malt-Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M107.2<a name="GenomicTestCode-M107.462"> </a></td><td>Malt-Lymphoma, t(1;14)(p22;q32) IGH-BCL10 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M107.3<a name="GenomicTestCode-M107.463"> </a></td><td>Malt-Lymphoma, t(14;18)(q32;q21) IGH-MALT1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M107.4<a name="GenomicTestCode-M107.464"> </a></td><td>Malt-Lymphoma, MALT1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M107.5<a name="GenomicTestCode-M107.465"> </a></td><td>Malt-Lymphoma, BCL10 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M107.6<a name="GenomicTestCode-M107.466"> </a></td><td>Malt-Lymphoma, FOXP1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M107.7<a name="GenomicTestCode-M107.467"> </a></td><td>Malt-Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M107.8<a name="GenomicTestCode-M107.468"> </a></td><td>Malt-Lymphoma, Multi-target NGS panel, structural variant (BIRC3-MALT1, IGH-BCL10, IGH-MALT1, other MALT rearrangements, other BCL10 rearrangements, FOXP1)</td></tr><tr><td style="white-space:nowrap">M107.9<a name="GenomicTestCode-M107.469"> </a></td><td>Malt-Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M108.1<a name="GenomicTestCode-M108.461"> </a></td><td>Hairy Cell Leukaemia, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style="white-space:nowrap">M108.2<a name="GenomicTestCode-M108.462"> </a></td><td>Hairy Cell Leukaemia, BRAF V600 hotspot</td></tr><tr><td style="white-space:nowrap">M108.5<a name="GenomicTestCode-M108.465"> </a></td><td>Hairy Cell Leukaemia, Ig gene hypermutation detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M108.6<a name="GenomicTestCode-M108.466"> </a></td><td>Hairy Cell Leukaemia, Ig gene hypermutation detection NGS</td></tr><tr><td style="white-space:nowrap">M109.1<a name="GenomicTestCode-M109.461"> </a></td><td>Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M109.2<a name="GenomicTestCode-M109.462"> </a></td><td>Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection NGS</td></tr><tr><td style="white-space:nowrap">M11.1<a name="GenomicTestCode-M11.461"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, small variant (TP53, BRAF)</td></tr><tr><td style="white-space:nowrap">M11.2<a name="GenomicTestCode-M11.462"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, copy number variant (TP53)</td></tr><tr><td style="white-space:nowrap">M11.3<a name="GenomicTestCode-M11.463"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M11.4<a name="GenomicTestCode-M11.464"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET, ALK)</td></tr><tr><td style="white-space:nowrap">M110.1,<a name="GenomicTestCode-M110.461.44"> </a></td><td>Paediatric Type Follicular Lymphoma, Multi-target NGS panel, small variant (MAP2K1)</td></tr><tr><td style="white-space:nowrap">M110.2,<a name="GenomicTestCode-M110.462.44"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M110.3,<a name="GenomicTestCode-M110.463.44"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M110.4,<a name="GenomicTestCode-M110.464.44"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M111.1<a name="GenomicTestCode-M111.461"> </a></td><td>T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (RHOA, DNMT3A, IDH2, TET2)</td></tr><tr><td style="white-space:nowrap">M111.2<a name="GenomicTestCode-M111.462"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M111.3<a name="GenomicTestCode-M111.463"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection NGS</td></tr><tr><td style="white-space:nowrap">M111.4<a name="GenomicTestCode-M111.464"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M111.5<a name="GenomicTestCode-M111.465"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M111.6<a name="GenomicTestCode-M111.466"> </a></td><td>T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (TCR rearrangement)</td></tr><tr><td style="white-space:nowrap">M111.7<a name="GenomicTestCode-M111.467"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M111.8<a name="GenomicTestCode-M111.468"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M112.3<a name="GenomicTestCode-M112.463"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), IRF4/DUSP22 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M112.4<a name="GenomicTestCode-M112.464"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), TP63 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M112.5<a name="GenomicTestCode-M112.465"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M112.6<a name="GenomicTestCode-M112.466"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), Multi-target NGS panel, structural variant (IRF4/DUSP22, TP63)</td></tr><tr><td style="white-space:nowrap">M112.7<a name="GenomicTestCode-M112.467"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M112.8<a name="GenomicTestCode-M112.468"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M113.1<a name="GenomicTestCode-M113.461"> </a></td><td>T Prolymphocytic Leukaemia, TCL1A rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M113.2<a name="GenomicTestCode-M113.462"> </a></td><td>T Prolymphocytic Leukaemia, Chr8 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M113.3<a name="GenomicTestCode-M113.463"> </a></td><td>T Prolymphocytic Leukaemia, Multi-target NGS panel, structural variant (TCL1A, Chr8)</td></tr><tr><td style="white-space:nowrap">M113.6<a name="GenomicTestCode-M113.466"> </a></td><td>T Prolymphocytic Leukaemia, Karyotype (to include TCL1 rearrangements t(X;14))</td></tr><tr><td style="white-space:nowrap">M114.1<a name="GenomicTestCode-M114.461"> </a></td><td>Large Granular Lymphocyte Leukaemia, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style="white-space:nowrap">M115.1<a name="GenomicTestCode-M115.461"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style="white-space:nowrap">M115.2<a name="GenomicTestCode-M115.462"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M115.3<a name="GenomicTestCode-M115.463"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M115.4<a name="GenomicTestCode-M115.464"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M116.1<a name="GenomicTestCode-M116.461"> </a></td><td>Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style="white-space:nowrap">M116.2<a name="GenomicTestCode-M116.462"> </a></td><td>Hepatosplenic T Cell Lymphoma, i7q rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M116.3<a name="GenomicTestCode-M116.463"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M116.4<a name="GenomicTestCode-M116.464"> </a></td><td>Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, structural variant (i17q)</td></tr><tr><td style="white-space:nowrap">M116.5<a name="GenomicTestCode-M116.465"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M116.6<a name="GenomicTestCode-M116.466"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M117.1<a name="GenomicTestCode-M117.461"> </a></td><td>Histiocytosis, Multi-target NGS panel, small variant (BRAF, MAP2K1, NRAS, KRAS, HRAS, ERBB3, ARAF, MAP3K1, PIK3CA, PIK3CD)</td></tr><tr><td style="white-space:nowrap">M117.12<a name="GenomicTestCode-M117.4612"> </a></td><td>Histiocytosis, NTRK1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M117.16<a name="GenomicTestCode-M117.4616"> </a></td><td>Histiocytosis, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M117.17<a name="GenomicTestCode-M117.4617"> </a></td><td>Histiocytosis, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M117.18<a name="GenomicTestCode-M117.4618"> </a></td><td>Histiocytosis, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M117.19<a name="GenomicTestCode-M117.4619"> </a></td><td>Histiocytosis, High Sensitivity BRAF</td></tr><tr><td style="white-space:nowrap">M117.2<a name="GenomicTestCode-M117.462"> </a></td><td>Histiocytosis, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M117.3<a name="GenomicTestCode-M117.463"> </a></td><td>Histiocytosis, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M117.7<a name="GenomicTestCode-M117.467"> </a></td><td>Histiocytosis, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M118.1<a name="GenomicTestCode-M118.461"> </a></td><td>Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, STR Testing</td></tr><tr><td style="white-space:nowrap">M118.2<a name="GenomicTestCode-M118.462"> </a></td><td>Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, Sex chromosome FISH</td></tr><tr><td style="white-space:nowrap">M119.1,<a name="GenomicTestCode-M119.461.44"> </a></td><td>Paediatric Tumours, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M119.2,<a name="GenomicTestCode-M119.462.44"> </a></td><td>Paediatric Tumours, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M119.4,<a name="GenomicTestCode-M119.464.44"> </a></td><td>Paediatric Tumours, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M119.5,<a name="GenomicTestCode-M119.465.44"> </a></td><td>Paediatric Tumours, Multi-target NGS-small variant</td></tr><tr><td style="white-space:nowrap">M12.1<a name="GenomicTestCode-M12.461"> </a></td><td>Thyroid Medullary Carcinoma, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style="white-space:nowrap">M12.2<a name="GenomicTestCode-M12.462"> </a></td><td>Thyroid Medullary Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M120.1<a name="GenomicTestCode-M120.461"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1)</td></tr><tr><td style="white-space:nowrap">M120.10<a name="GenomicTestCode-M120.4610"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.11<a name="GenomicTestCode-M120.4611"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.12<a name="GenomicTestCode-M120.4612"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.13<a name="GenomicTestCode-M120.4613"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.14<a name="GenomicTestCode-M120.4614"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.15<a name="GenomicTestCode-M120.4615"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M120.16<a name="GenomicTestCode-M120.4616"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M120.17<a name="GenomicTestCode-M120.4617"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, SMARCB1)</td></tr><tr><td style="white-space:nowrap">M120.18<a name="GenomicTestCode-M120.4618"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M120.2<a name="GenomicTestCode-M120.462"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 seq</td></tr><tr><td style="white-space:nowrap">M120.3<a name="GenomicTestCode-M120.463"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 seq</td></tr><tr><td style="white-space:nowrap">M120.4<a name="GenomicTestCode-M120.464"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M120.5<a name="GenomicTestCode-M120.465"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M120.6<a name="GenomicTestCode-M120.466"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M120.7<a name="GenomicTestCode-M120.467"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.8<a name="GenomicTestCode-M120.468"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M120.9<a name="GenomicTestCode-M120.469"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M124.1<a name="GenomicTestCode-M124.461"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, small variant (BCOR)</td></tr><tr><td style="white-space:nowrap">M124.10<a name="GenomicTestCode-M124.4610"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, structural variant (BCOR, NUTM2B-YWHAE, NUTM2E-YWHAE, NUTM1-YWHAE, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M124.11<a name="GenomicTestCode-M124.4611"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, copy number variant (BCOR, YWHAE)</td></tr><tr><td style="white-space:nowrap">M124.2<a name="GenomicTestCode-M124.462"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR seq</td></tr><tr><td style="white-space:nowrap">M124.3<a name="GenomicTestCode-M124.463"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR copy number FISH</td></tr><tr><td style="white-space:nowrap">M124.4<a name="GenomicTestCode-M124.464"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M124.5<a name="GenomicTestCode-M124.465"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM2B-YWHAE FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M124.6<a name="GenomicTestCode-M124.466"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM2E-YWHAE FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M124.7<a name="GenomicTestCode-M124.467"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM1-YWHAE FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M124.8<a name="GenomicTestCode-M124.468"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, YWHAE copy number FISH</td></tr><tr><td style="white-space:nowrap">M124.9<a name="GenomicTestCode-M124.469"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M126.1<a name="GenomicTestCode-M126.461"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, MN1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M126.2<a name="GenomicTestCode-M126.462"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M126.3<a name="GenomicTestCode-M126.463"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, Multi-target NGS panel, structural variant (MN1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M126.4<a name="GenomicTestCode-M126.464"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M127.1<a name="GenomicTestCode-M127.461"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, NTRK3-ETV6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M127.3<a name="GenomicTestCode-M127.463"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M127.4<a name="GenomicTestCode-M127.464"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK3-ETV6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M13.1<a name="GenomicTestCode-M13.461"> </a></td><td>Phaeochromocytoma, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style="white-space:nowrap">M13.2<a name="GenomicTestCode-M13.462"> </a></td><td>Phaeochromocytoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M130.1<a name="GenomicTestCode-M130.461"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCB1)</td></tr><tr><td style="white-space:nowrap">M130.2<a name="GenomicTestCode-M130.462"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 seq</td></tr><tr><td style="white-space:nowrap">M130.3<a name="GenomicTestCode-M130.463"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M130.4<a name="GenomicTestCode-M130.464"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M130.5<a name="GenomicTestCode-M130.465"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M130.6<a name="GenomicTestCode-M130.466"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)</td></tr><tr><td style="white-space:nowrap">M130.7<a name="GenomicTestCode-M130.467"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M131.1<a name="GenomicTestCode-M131.461"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M131.2<a name="GenomicTestCode-M131.462"> </a></td><td>Cystic Nephroma, Paediatric, DICER1 seq</td></tr><tr><td style="white-space:nowrap">M131.3<a name="GenomicTestCode-M131.463"> </a></td><td>Cystic Nephroma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M131.4<a name="GenomicTestCode-M131.464"> </a></td><td>Cystic Nephroma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M131.5<a name="GenomicTestCode-M131.465"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M131.6<a name="GenomicTestCode-M131.466"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M132.1<a name="GenomicTestCode-M132.461"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style="white-space:nowrap">M132.10<a name="GenomicTestCode-M132.4610"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.11<a name="GenomicTestCode-M132.4611"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M132.12<a name="GenomicTestCode-M132.4612"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M132.13<a name="GenomicTestCode-M132.4613"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M132.2<a name="GenomicTestCode-M132.462"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M132.3<a name="GenomicTestCode-M132.463"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.4<a name="GenomicTestCode-M132.464"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.5<a name="GenomicTestCode-M132.465"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.6<a name="GenomicTestCode-M132.466"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.7<a name="GenomicTestCode-M132.467"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.8<a name="GenomicTestCode-M132.468"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M132.9<a name="GenomicTestCode-M132.469"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M133.1<a name="GenomicTestCode-M133.461"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SUFU)</td></tr><tr><td style="white-space:nowrap">M133.2<a name="GenomicTestCode-M133.462"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, SUFU seq</td></tr><tr><td style="white-space:nowrap">M133.3<a name="GenomicTestCode-M133.463"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M133.4<a name="GenomicTestCode-M133.464"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M133.5<a name="GenomicTestCode-M133.465"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M136.1<a name="GenomicTestCode-M136.461"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, DNAJB1-PRKACA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M136.2<a name="GenomicTestCode-M136.462"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M136.3<a name="GenomicTestCode-M136.463"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, Multi-target NGS panel, structural variant (DNAJB1-PRKACA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M136.5<a name="GenomicTestCode-M136.465"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M137.1<a name="GenomicTestCode-M137.461"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style="white-space:nowrap">M137.10<a name="GenomicTestCode-M137.4610"> </a></td><td>Ganglioglioma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.11<a name="GenomicTestCode-M137.4611"> </a></td><td>Ganglioglioma, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style="white-space:nowrap">M137.12<a name="GenomicTestCode-M137.4612"> </a></td><td>Ganglioglioma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M137.13<a name="GenomicTestCode-M137.4613"> </a></td><td>Ganglioglioma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M137.14<a name="GenomicTestCode-M137.4614"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)</td></tr><tr><td style="white-space:nowrap">M137.15<a name="GenomicTestCode-M137.4615"> </a></td><td>Ganglioglioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M137.2<a name="GenomicTestCode-M137.462"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M137.3<a name="GenomicTestCode-M137.463"> </a></td><td>Ganglioglioma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.4<a name="GenomicTestCode-M137.464"> </a></td><td>Ganglioglioma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.5<a name="GenomicTestCode-M137.465"> </a></td><td>Ganglioglioma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.6<a name="GenomicTestCode-M137.466"> </a></td><td>Ganglioglioma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.7<a name="GenomicTestCode-M137.467"> </a></td><td>Ganglioglioma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.8<a name="GenomicTestCode-M137.468"> </a></td><td>Ganglioglioma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M137.9<a name="GenomicTestCode-M137.469"> </a></td><td>Ganglioglioma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M138.1<a name="GenomicTestCode-M138.461"> </a></td><td>Glial Tumours, Paediatric, Multi-target NGS panel, small variant (ATRX)</td></tr><tr><td style="white-space:nowrap">M138.2<a name="GenomicTestCode-M138.462"> </a></td><td>Glial Tumours, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M138.3<a name="GenomicTestCode-M138.463"> </a></td><td>Glial Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M138.4<a name="GenomicTestCode-M138.464"> </a></td><td>Glial Tumours, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M139.1<a name="GenomicTestCode-M139.461"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, small variant (BRAF, CDKN2A, FGFR4)</td></tr><tr><td style="white-space:nowrap">M139.10<a name="GenomicTestCode-M139.4610"> </a></td><td>Glioblastoma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.12<a name="GenomicTestCode-M139.4612"> </a></td><td>Glioblastoma, Paediatric, CDKN2A seq</td></tr><tr><td style="white-space:nowrap">M139.13<a name="GenomicTestCode-M139.4613"> </a></td><td>Glioblastoma, Paediatric, FGFR4 seq</td></tr><tr><td style="white-space:nowrap">M139.14<a name="GenomicTestCode-M139.4614"> </a></td><td>Glioblastoma, Paediatric, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M139.15<a name="GenomicTestCode-M139.4615"> </a></td><td>Glioblastoma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M139.16<a name="GenomicTestCode-M139.4616"> </a></td><td>Glioblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M139.17<a name="GenomicTestCode-M139.4617"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, copy number variant (CDKN2A)</td></tr><tr><td style="white-space:nowrap">M139.18<a name="GenomicTestCode-M139.4618"> </a></td><td>Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M139.2<a name="GenomicTestCode-M139.462"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B,  BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M139.3<a name="GenomicTestCode-M139.463"> </a></td><td>Glioblastoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.4<a name="GenomicTestCode-M139.464"> </a></td><td>Glioblastoma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.5<a name="GenomicTestCode-M139.465"> </a></td><td>Glioblastoma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.6<a name="GenomicTestCode-M139.466"> </a></td><td>Glioblastoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.7<a name="GenomicTestCode-M139.467"> </a></td><td>Glioblastoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.8<a name="GenomicTestCode-M139.468"> </a></td><td>Glioblastoma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M139.9<a name="GenomicTestCode-M139.469"> </a></td><td>Glioblastoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M14.1<a name="GenomicTestCode-M14.461"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, small variant (TP53)</td></tr><tr><td style="white-space:nowrap">M14.2<a name="GenomicTestCode-M14.462"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, copy number variant (TP53)</td></tr><tr><td style="white-space:nowrap">M14.3<a name="GenomicTestCode-M14.463"> </a></td><td>Adrenal Cortical Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M14.4<a name="GenomicTestCode-M14.464"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M14.5<a name="GenomicTestCode-M14.465"> </a></td><td>Adrenal Cortical Carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M143.1<a name="GenomicTestCode-M143.461"> </a></td><td>Lung, Paediatric, Multi-target NGS panel, small variant (H3-3A, H3-3B)</td></tr><tr><td style="white-space:nowrap">M143.2<a name="GenomicTestCode-M143.462"> </a></td><td>Lung, Paediatric, H3-3A seq</td></tr><tr><td style="white-space:nowrap">M143.3<a name="GenomicTestCode-M143.463"> </a></td><td>Lung, Paediatric, H3-3B seq</td></tr><tr><td style="white-space:nowrap">M143.4<a name="GenomicTestCode-M143.464"> </a></td><td>Lung, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M143.5<a name="GenomicTestCode-M143.465"> </a></td><td>Lung, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M145.1<a name="GenomicTestCode-M145.461"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, BCOR, PTCH1, PTCH2, PTEN, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M145.10<a name="GenomicTestCode-M145.4610"> </a></td><td>Medulloblastoma, Paediatric, BCOR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M145.11<a name="GenomicTestCode-M145.4611"> </a></td><td>Medulloblastoma, Paediatric, C19MC copy number FISH</td></tr><tr><td style="white-space:nowrap">M145.12<a name="GenomicTestCode-M145.4612"> </a></td><td>Medulloblastoma, Paediatric, PTEN copy number FISH</td></tr><tr><td style="white-space:nowrap">M145.13<a name="GenomicTestCode-M145.4613"> </a></td><td>Medulloblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M145.14<a name="GenomicTestCode-M145.4614"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (ALK, BCOR, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M145.15<a name="GenomicTestCode-M145.4615"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (ALK, BCOR, C19MC, PTEN)</td></tr><tr><td style="white-space:nowrap">M145.16<a name="GenomicTestCode-M145.4616"> </a></td><td>Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M145.2<a name="GenomicTestCode-M145.462"> </a></td><td>Medulloblastoma, Paediatric, ALK seq</td></tr><tr><td style="white-space:nowrap">M145.3<a name="GenomicTestCode-M145.463"> </a></td><td>Medulloblastoma, Paediatric, BCOR seq</td></tr><tr><td style="white-space:nowrap">M145.4<a name="GenomicTestCode-M145.464"> </a></td><td>Medulloblastoma, Paediatric, PTCH1 seq</td></tr><tr><td style="white-space:nowrap">M145.5<a name="GenomicTestCode-M145.465"> </a></td><td>Medulloblastoma, Paediatric, PTCH2 seq</td></tr><tr><td style="white-space:nowrap">M145.6<a name="GenomicTestCode-M145.466"> </a></td><td>Medulloblastoma, Paediatric, TERT promoter seq</td></tr><tr><td style="white-space:nowrap">M145.7<a name="GenomicTestCode-M145.467"> </a></td><td>Medulloblastoma, Paediatric, ALK copy number FISH</td></tr><tr><td style="white-space:nowrap">M145.8<a name="GenomicTestCode-M145.468"> </a></td><td>Medulloblastoma, Paediatric, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M145.9<a name="GenomicTestCode-M145.469"> </a></td><td>Medulloblastoma, Paediatric, BCOR copy number FISH</td></tr><tr><td style="white-space:nowrap">M146.1<a name="GenomicTestCode-M146.461"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, small variant (SMARCA4, DDX3X)</td></tr><tr><td style="white-space:nowrap">M146.2<a name="GenomicTestCode-M146.462"> </a></td><td>Medulloblastoma Group 3, Paediatric, SMARCA4 seq</td></tr><tr><td style="white-space:nowrap">M146.3<a name="GenomicTestCode-M146.463"> </a></td><td>Medulloblastoma Group 3, Paediatric, DDX3X seq</td></tr><tr><td style="white-space:nowrap">M146.4<a name="GenomicTestCode-M146.464"> </a></td><td>Medulloblastoma Group 3, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M146.5<a name="GenomicTestCode-M146.465"> </a></td><td>Medulloblastoma Group 3, Paediatric, PVT1-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M146.6<a name="GenomicTestCode-M146.466"> </a></td><td>Medulloblastoma Group 3, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M146.7<a name="GenomicTestCode-M146.467"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, structural variant (PVT1-MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M146.8<a name="GenomicTestCode-M146.468"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4)</td></tr><tr><td style="white-space:nowrap">M146.9<a name="GenomicTestCode-M146.469"> </a></td><td>Medulloblastoma Group 3, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M147.1<a name="GenomicTestCode-M147.461"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, small variant (MYCN, EZH2)</td></tr><tr><td style="white-space:nowrap">M147.10<a name="GenomicTestCode-M147.4610"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M147.2<a name="GenomicTestCode-M147.462"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYCN seq</td></tr><tr><td style="white-space:nowrap">M147.3<a name="GenomicTestCode-M147.463"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, EZH2 seq</td></tr><tr><td style="white-space:nowrap">M147.4<a name="GenomicTestCode-M147.464"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M147.5<a name="GenomicTestCode-M147.465"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M147.6<a name="GenomicTestCode-M147.466"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M147.7<a name="GenomicTestCode-M147.467"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M147.8<a name="GenomicTestCode-M147.468"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M147.9<a name="GenomicTestCode-M147.469"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, copy number variant (MYCN, MYC)</td></tr><tr><td style="white-space:nowrap">M148.1<a name="GenomicTestCode-M148.461"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, small variant (YAP1, PTCH1)</td></tr><tr><td style="white-space:nowrap">M148.10<a name="GenomicTestCode-M148.4610"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (YAP1, PTCH1)</td></tr><tr><td style="white-space:nowrap">M148.11<a name="GenomicTestCode-M148.4611"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M148.2<a name="GenomicTestCode-M148.462"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1 seq</td></tr><tr><td style="white-space:nowrap">M148.3<a name="GenomicTestCode-M148.463"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, PTCH1 seq</td></tr><tr><td style="white-space:nowrap">M148.4<a name="GenomicTestCode-M148.464"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M148.5<a name="GenomicTestCode-M148.465"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M148.6<a name="GenomicTestCode-M148.466"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M148.7<a name="GenomicTestCode-M148.467"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, PTCH1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M148.8<a name="GenomicTestCode-M148.468"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M148.9<a name="GenomicTestCode-M148.469"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, structural variant (YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M149.1<a name="GenomicTestCode-M149.461"> </a></td><td>Melanotic Tumours, Paediatric, Multi-target NGS panel, small variant (NRAS)</td></tr><tr><td style="white-space:nowrap">M149.2<a name="GenomicTestCode-M149.462"> </a></td><td>Melanotic Tumours, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M149.3<a name="GenomicTestCode-M149.463"> </a></td><td>Melanotic Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M15.1<a name="GenomicTestCode-M15.461"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, small variant (CDKN2A, EGFR, TP53)</td></tr><tr><td style="white-space:nowrap">M15.2<a name="GenomicTestCode-M15.462"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M15.3<a name="GenomicTestCode-M15.463"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, copy number variant (CDKN2A, TP53)</td></tr><tr><td style="white-space:nowrap">M15.4<a name="GenomicTestCode-M15.464"> </a></td><td>Head and Neck Squamous Cell Carcinoma, RET rearrangement FISH/RT-PC</td></tr><tr><td style="white-space:nowrap">M15.5<a name="GenomicTestCode-M15.465"> </a></td><td>Head and Neck Squamous Cell Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M15.6<a name="GenomicTestCode-M15.466"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M15.7<a name="GenomicTestCode-M15.467"> </a></td><td>Head and Neck Squamous Cell Carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M150.1<a name="GenomicTestCode-M150.461"> </a></td><td>Meningioma, Paediatric, Multi-target NGS panel, small variant (SMARCE1, AKT1, NF2, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M150.2<a name="GenomicTestCode-M150.462"> </a></td><td>Meningioma, Paediatric, SMARCE1 seq</td></tr><tr><td style="white-space:nowrap">M150.3<a name="GenomicTestCode-M150.463"> </a></td><td>Meningioma, Paediatric, AKT1 seq</td></tr><tr><td style="white-space:nowrap">M150.4<a name="GenomicTestCode-M150.464"> </a></td><td>Meningioma, Paediatric, NF2 seq</td></tr><tr><td style="white-space:nowrap">M150.5<a name="GenomicTestCode-M150.465"> </a></td><td>Meningioma, Paediatric, TERT promoter seq</td></tr><tr><td style="white-space:nowrap">M150.6<a name="GenomicTestCode-M150.466"> </a></td><td>Meningioma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M150.7<a name="GenomicTestCode-M150.467"> </a></td><td>Meningioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M150.8<a name="GenomicTestCode-M150.468"> </a></td><td>Meningioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M151.1<a name="GenomicTestCode-M151.461"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD2 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M151.2<a name="GenomicTestCode-M151.462"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M151.3<a name="GenomicTestCode-M151.463"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD4 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M151.4<a name="GenomicTestCode-M151.464"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-CIC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M151.5<a name="GenomicTestCode-M151.465"> </a></td><td>Midline Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M151.6<a name="GenomicTestCode-M151.466"> </a></td><td>Midline Carcinoma, Paediatric, Multi-target NGS panel, structural variant (NUTM1-BRD2, NUTM1-BRD3, NUTM1-BRD4, NUTM1-CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M152.1<a name="GenomicTestCode-M152.461"> </a></td><td>Neuroblastoma, Paediatric, SNP Array</td></tr><tr><td style="white-space:nowrap">M152.10<a name="GenomicTestCode-M152.4610"> </a></td><td>Neuroblastoma, Paediatric, 17q rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M152.11<a name="GenomicTestCode-M152.4611"> </a></td><td>Neuroblastoma, Paediatric, 11q copy number FISH</td></tr><tr><td style="white-space:nowrap">M152.12<a name="GenomicTestCode-M152.4612"> </a></td><td>Neuroblastoma, Paediatric, 1p36 copy number FISH</td></tr><tr><td style="white-space:nowrap">M152.13<a name="GenomicTestCode-M152.4613"> </a></td><td>Neuroblastoma, Paediatric, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M152.14<a name="GenomicTestCode-M152.4614"> </a></td><td>Neuroblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M152.15<a name="GenomicTestCode-M152.4615"> </a></td><td>Neuroblastoma, Paediatric, MYCN seq</td></tr><tr><td style="white-space:nowrap">M152.16<a name="GenomicTestCode-M152.4616"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, structural variant (17q, ALK, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M152.17<a name="GenomicTestCode-M152.4617"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, copy number variant (MYCN, ALK, 17q, 11q, 1p36)</td></tr><tr><td style="white-space:nowrap">M152.18<a name="GenomicTestCode-M152.4618"> </a></td><td>Neuroblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M152.19<a name="GenomicTestCode-M152.4619"> </a></td><td>Neuroblastoma, Paediatric, TERT promoter rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M152.2<a name="GenomicTestCode-M152.462"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, ATRX, FGFR1, MYCN, NRAS, PHOX2B, TP53)</td></tr><tr><td style="white-space:nowrap">M152.3<a name="GenomicTestCode-M152.463"> </a></td><td>Neuroblastoma, Paediatric, ALK seq</td></tr><tr><td style="white-space:nowrap">M152.4<a name="GenomicTestCode-M152.464"> </a></td><td>Neuroblastoma, Paediatric, FGFR1 seq</td></tr><tr><td style="white-space:nowrap">M152.5<a name="GenomicTestCode-M152.465"> </a></td><td>Neuroblastoma, Paediatric, PHOX2B seq</td></tr><tr><td style="white-space:nowrap">M152.6<a name="GenomicTestCode-M152.466"> </a></td><td>Neuroblastoma, Paediatric, TP53 seq</td></tr><tr><td style="white-space:nowrap">M152.7<a name="GenomicTestCode-M152.467"> </a></td><td>Neuroblastoma, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M152.8<a name="GenomicTestCode-M152.468"> </a></td><td>Neuroblastoma, Paediatric, ALK copy number FISH</td></tr><tr><td style="white-space:nowrap">M152.9<a name="GenomicTestCode-M152.469"> </a></td><td>Neuroblastoma, Paediatric, 17q copy number FISH</td></tr><tr><td style="white-space:nowrap">M153.1<a name="GenomicTestCode-M153.461"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, small variant (SMO)</td></tr><tr><td style="white-space:nowrap">M153.2<a name="GenomicTestCode-M153.462"> </a></td><td>Nodular Brain Tumour, Paediatric, SMO seq</td></tr><tr><td style="white-space:nowrap">M153.3<a name="GenomicTestCode-M153.463"> </a></td><td>Nodular Brain Tumour, Paediatric, SMO copy number FISH</td></tr><tr><td style="white-space:nowrap">M153.4<a name="GenomicTestCode-M153.464"> </a></td><td>Nodular Brain Tumour, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M153.5<a name="GenomicTestCode-M153.465"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M153.6<a name="GenomicTestCode-M153.466"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMO)</td></tr><tr><td style="white-space:nowrap">M153.7<a name="GenomicTestCode-M153.467"> </a></td><td>Nodular Brain Tumour, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M155.1<a name="GenomicTestCode-M155.461"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, small variant (KIT)</td></tr><tr><td style="white-space:nowrap">M155.2<a name="GenomicTestCode-M155.462"> </a></td><td>Oligoastrocytoma, Paediatric, KIT copy number FISH</td></tr><tr><td style="white-space:nowrap">M155.3<a name="GenomicTestCode-M155.463"> </a></td><td>Oligoastrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M155.4<a name="GenomicTestCode-M155.464"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M155.5<a name="GenomicTestCode-M155.465"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIT)</td></tr><tr><td style="white-space:nowrap">M155.6<a name="GenomicTestCode-M155.466"> </a></td><td>Oligoastrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M156.1<a name="GenomicTestCode-M156.461"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, small variant (RB1, ATRX)</td></tr><tr><td style="white-space:nowrap">M156.10<a name="GenomicTestCode-M156.4610"> </a></td><td>Oligodendroglioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M156.2<a name="GenomicTestCode-M156.462"> </a></td><td>Oligodendroglioma, Paediatric, ATRX seq</td></tr><tr><td style="white-space:nowrap">M156.3<a name="GenomicTestCode-M156.463"> </a></td><td>Oligodendroglioma, Paediatric, RB1 seq</td></tr><tr><td style="white-space:nowrap">M156.4<a name="GenomicTestCode-M156.464"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, copy number variant (1p19q, RB1, ATRX)</td></tr><tr><td style="white-space:nowrap">M156.5<a name="GenomicTestCode-M156.465"> </a></td><td>Oligodendroglioma, Paediatric, 1p19q codel FISH</td></tr><tr><td style="white-space:nowrap">M156.6<a name="GenomicTestCode-M156.466"> </a></td><td>Oligodendroglioma, Paediatric, RB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M156.7<a name="GenomicTestCode-M156.467"> </a></td><td>Oligodendroglioma, Paediatric, ATRX copy number FISH</td></tr><tr><td style="white-space:nowrap">M156.8<a name="GenomicTestCode-M156.468"> </a></td><td>Oligodendroglioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M156.9<a name="GenomicTestCode-M156.469"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M157.1<a name="GenomicTestCode-M157.461"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style="white-space:nowrap">M157.2<a name="GenomicTestCode-M157.462"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, RET seq</td></tr><tr><td style="white-space:nowrap">M157.3<a name="GenomicTestCode-M157.463"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M157.4<a name="GenomicTestCode-M157.464"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, RET rearrangement FISH/RT-PC</td></tr><tr><td style="white-space:nowrap">M157.5<a name="GenomicTestCode-M157.465"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M158.1<a name="GenomicTestCode-M158.461"> </a></td><td>Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (RAF1)</td></tr><tr><td style="white-space:nowrap">M158.2<a name="GenomicTestCode-M158.462"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1 seq</td></tr><tr><td style="white-space:nowrap">M158.3<a name="GenomicTestCode-M158.463"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1-SRGAP3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M158.4<a name="GenomicTestCode-M158.464"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1-NF1A FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M158.5<a name="GenomicTestCode-M158.465"> </a></td><td>Pilocytic Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M158.6<a name="GenomicTestCode-M158.466"> </a></td><td>Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant (RAF1-SRGAP3, RAF1-NF1A, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M158.7<a name="GenomicTestCode-M158.467"> </a></td><td>Pilocytic Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M159.1<a name="GenomicTestCode-M159.461"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M159.2<a name="GenomicTestCode-M159.462"> </a></td><td>Pituitary Blastoma, Paediatric, DICER1 seq</td></tr><tr><td style="white-space:nowrap">M159.3<a name="GenomicTestCode-M159.463"> </a></td><td>Pituitary Blastoma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M159.4<a name="GenomicTestCode-M159.464"> </a></td><td>Pituitary Blastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M159.5<a name="GenomicTestCode-M159.465"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M159.6<a name="GenomicTestCode-M159.466"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M159.7<a name="GenomicTestCode-M159.467"> </a></td><td>Pituitary Blastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M16.1<a name="GenomicTestCode-M16.461"> </a></td><td>Adenoid Cystic Carcinoma, MYB-NFIB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M16.2<a name="GenomicTestCode-M16.462"> </a></td><td>Adenoid Cystic Carcinoma, Multi-target NGS panel, structural variant (MYB-NFIB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M16.4<a name="GenomicTestCode-M16.464"> </a></td><td>Adenoid Cystic Carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M160.1<a name="GenomicTestCode-M160.461"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF, H3-3A)</td></tr><tr><td style="white-space:nowrap">M160.10<a name="GenomicTestCode-M160.4610"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.11<a name="GenomicTestCode-M160.4611"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, H3-3A seq</td></tr><tr><td style="white-space:nowrap">M160.12<a name="GenomicTestCode-M160.4612"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style="white-space:nowrap">M160.13<a name="GenomicTestCode-M160.4613"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M160.14<a name="GenomicTestCode-M160.4614"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style="white-space:nowrap">M160.15<a name="GenomicTestCode-M160.4615"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)</td></tr><tr><td style="white-space:nowrap">M160.16<a name="GenomicTestCode-M160.4616"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M160.2<a name="GenomicTestCode-M160.462"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M160.3<a name="GenomicTestCode-M160.463"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.4<a name="GenomicTestCode-M160.464"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.5<a name="GenomicTestCode-M160.465"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.6<a name="GenomicTestCode-M160.466"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.7<a name="GenomicTestCode-M160.467"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.8<a name="GenomicTestCode-M160.468"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M160.9<a name="GenomicTestCode-M160.469"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M161.1<a name="GenomicTestCode-M161.461"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M161.2<a name="GenomicTestCode-M161.462"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, DICER1 seq</td></tr><tr><td style="white-space:nowrap">M161.3<a name="GenomicTestCode-M161.463"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M161.4<a name="GenomicTestCode-M161.464"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M161.5<a name="GenomicTestCode-M161.465"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M161.6<a name="GenomicTestCode-M161.466"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M162.1<a name="GenomicTestCode-M162.461"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, small variant (MSH6, PMS2, PTEN)</td></tr><tr><td style="white-space:nowrap">M162.10<a name="GenomicTestCode-M162.4610"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, copy number variant (MYC, MSH6, PTEN)</td></tr><tr><td style="white-space:nowrap">M162.11<a name="GenomicTestCode-M162.4611"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M162.2<a name="GenomicTestCode-M162.462"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MSH6 seq</td></tr><tr><td style="white-space:nowrap">M162.3<a name="GenomicTestCode-M162.463"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, PMS2 seq</td></tr><tr><td style="white-space:nowrap">M162.4<a name="GenomicTestCode-M162.464"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M162.5<a name="GenomicTestCode-M162.465"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M162.6<a name="GenomicTestCode-M162.466"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MSH6 copy number FISH</td></tr><tr><td style="white-space:nowrap">M162.7<a name="GenomicTestCode-M162.467"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, PTEN copy number FISH</td></tr><tr><td style="white-space:nowrap">M162.8<a name="GenomicTestCode-M162.468"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M162.9<a name="GenomicTestCode-M162.469"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M165.1<a name="GenomicTestCode-M165.461"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX)</td></tr><tr><td style="white-space:nowrap">M165.2<a name="GenomicTestCode-M165.462"> </a></td><td>Renal Tumours, Paediatric, ATRX seq</td></tr><tr><td style="white-space:nowrap">M165.3<a name="GenomicTestCode-M165.463"> </a></td><td>Renal Tumours, Paediatric, CTNNB1 seq</td></tr><tr><td style="white-space:nowrap">M165.4<a name="GenomicTestCode-M165.464"> </a></td><td>Renal Tumours, Paediatric, DAXX seq</td></tr><tr><td style="white-space:nowrap">M165.5<a name="GenomicTestCode-M165.465"> </a></td><td>Renal Tumours, Paediatric, ATRX copy number FISH</td></tr><tr><td style="white-space:nowrap">M165.6<a name="GenomicTestCode-M165.466"> </a></td><td>Renal Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M165.7<a name="GenomicTestCode-M165.467"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M165.8<a name="GenomicTestCode-M165.468"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, copy number variant (ATRX)</td></tr><tr><td style="white-space:nowrap">M166.1<a name="GenomicTestCode-M166.461"> </a></td><td>Retinoblastoma, Paediatric, Multi-target NGS panel, small variant (RB1)</td></tr><tr><td style="white-space:nowrap">M166.2<a name="GenomicTestCode-M166.462"> </a></td><td>Retinoblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M166.3<a name="GenomicTestCode-M166.463"> </a></td><td>Retinoblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M166.4<a name="GenomicTestCode-M166.464"> </a></td><td>Retinoblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M167.1<a name="GenomicTestCode-M167.461"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, small variant (SMARCB1)</td></tr><tr><td style="white-space:nowrap">M167.2<a name="GenomicTestCode-M167.462"> </a></td><td>Rhabdoid Tumours, Paediatric, SMARCB1 seq</td></tr><tr><td style="white-space:nowrap">M167.3<a name="GenomicTestCode-M167.463"> </a></td><td>Rhabdoid Tumours, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M167.4<a name="GenomicTestCode-M167.464"> </a></td><td>Rhabdoid Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M167.5<a name="GenomicTestCode-M167.465"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M167.6<a name="GenomicTestCode-M167.466"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)</td></tr><tr><td style="white-space:nowrap">M168.1<a name="GenomicTestCode-M168.461"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, small variant (PIK3CA, FGFR1)</td></tr><tr><td style="white-space:nowrap">M168.2<a name="GenomicTestCode-M168.462"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 seq</td></tr><tr><td style="white-space:nowrap">M168.3<a name="GenomicTestCode-M168.463"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M168.4<a name="GenomicTestCode-M168.464"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 ITD FISH</td></tr><tr><td style="white-space:nowrap">M168.5<a name="GenomicTestCode-M168.465"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M168.6<a name="GenomicTestCode-M168.466"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, structural variant (FGFR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M168.7<a name="GenomicTestCode-M168.467"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, copy number variant (FGFR1 ITD)</td></tr><tr><td style="white-space:nowrap">M168.8<a name="GenomicTestCode-M168.468"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M169.1<a name="GenomicTestCode-M169.461"> </a></td><td>Secondary Glioblastoma, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2)</td></tr><tr><td style="white-space:nowrap">M169.2<a name="GenomicTestCode-M169.462"> </a></td><td>Secondary Glioblastoma, Paediatric, IDH1 seq</td></tr><tr><td style="white-space:nowrap">M169.3<a name="GenomicTestCode-M169.463"> </a></td><td>Secondary Glioblastoma, Paediatric, IDH2 seq</td></tr><tr><td style="white-space:nowrap">M169.4<a name="GenomicTestCode-M169.464"> </a></td><td>Secondary Glioblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M169.5<a name="GenomicTestCode-M169.465"> </a></td><td>Secondary Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M169.6<a name="GenomicTestCode-M169.466"> </a></td><td>Secondary Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M17.1<a name="GenomicTestCode-M17.461"> </a></td><td>Secretory Carcinoma (Salivary Gland), ETV6-NTRK3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M17.2<a name="GenomicTestCode-M17.462"> </a></td><td>Secretory Carcinoma (Salivary Gland), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M17.4<a name="GenomicTestCode-M17.464"> </a></td><td>Secretory Carcinoma (Salivary Gland), DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M170.1<a name="GenomicTestCode-M170.461"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SMO, DDX3X)</td></tr><tr><td style="white-space:nowrap">M170.2<a name="GenomicTestCode-M170.462"> </a></td><td>SHH Medulloblastoma, Paediatric, SMO seq</td></tr><tr><td style="white-space:nowrap">M170.3<a name="GenomicTestCode-M170.463"> </a></td><td>SHH Medulloblastoma, Paediatric, DDX3X seq</td></tr><tr><td style="white-space:nowrap">M170.4<a name="GenomicTestCode-M170.464"> </a></td><td>SHH Medulloblastoma, Paediatric, SMO copy number FISH</td></tr><tr><td style="white-space:nowrap">M170.5<a name="GenomicTestCode-M170.465"> </a></td><td>SHH Medulloblastoma, Paediatric, DDX3X copy number FISH</td></tr><tr><td style="white-space:nowrap">M170.6<a name="GenomicTestCode-M170.466"> </a></td><td>SHH Medulloblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M170.7<a name="GenomicTestCode-M170.467"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M170.8<a name="GenomicTestCode-M170.468"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMO, DDX3X)</td></tr><tr><td style="white-space:nowrap">M170.9<a name="GenomicTestCode-M170.469"> </a></td><td>SHH Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M171.1<a name="GenomicTestCode-M171.461"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, small variant (SUFU, TERT promoter, PTCH1)</td></tr><tr><td style="white-space:nowrap">M171.10<a name="GenomicTestCode-M171.4610"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M171.2<a name="GenomicTestCode-M171.462"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 seq</td></tr><tr><td style="white-space:nowrap">M171.3<a name="GenomicTestCode-M171.463"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, SUFU seq</td></tr><tr><td style="white-space:nowrap">M171.4<a name="GenomicTestCode-M171.464"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, TERT promoter seq</td></tr><tr><td style="white-space:nowrap">M171.5<a name="GenomicTestCode-M171.465"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M171.6<a name="GenomicTestCode-M171.466"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, TERT copy number FISH</td></tr><tr><td style="white-space:nowrap">M171.7<a name="GenomicTestCode-M171.467"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M171.8<a name="GenomicTestCode-M171.468"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M171.9<a name="GenomicTestCode-M171.469"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (PTCH1, TERT)</td></tr><tr><td style="white-space:nowrap">M172.1<a name="GenomicTestCode-M172.461"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, small variant (TP53, MYCN)</td></tr><tr><td style="white-space:nowrap">M172.2<a name="GenomicTestCode-M172.462"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, TP53 seq</td></tr><tr><td style="white-space:nowrap">M172.3<a name="GenomicTestCode-M172.463"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN seq</td></tr><tr><td style="white-space:nowrap">M172.4<a name="GenomicTestCode-M172.464"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M172.5<a name="GenomicTestCode-M172.465"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M172.6<a name="GenomicTestCode-M172.466"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M172.7<a name="GenomicTestCode-M172.467"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M172.8<a name="GenomicTestCode-M172.468"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, copy number variant (TP53, MYCN)</td></tr><tr><td style="white-space:nowrap">M172.9<a name="GenomicTestCode-M172.469"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M173.1<a name="GenomicTestCode-M173.461"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, TFEB-MALAT1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M173.2<a name="GenomicTestCode-M173.462"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M173.3<a name="GenomicTestCode-M173.463"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M174.1<a name="GenomicTestCode-M174.461"> </a></td><td>Testicular, Paediatric, Multi-target NGS panel, small variant (PRKAR1A)</td></tr><tr><td style="white-space:nowrap">M174.2<a name="GenomicTestCode-M174.462"> </a></td><td>Testicular, Paediatric, PRKAR1A seq</td></tr><tr><td style="white-space:nowrap">M174.3<a name="GenomicTestCode-M174.463"> </a></td><td>Testicular, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M174.4<a name="GenomicTestCode-M174.464"> </a></td><td>Testicular, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M178.1<a name="GenomicTestCode-M178.461"> </a></td><td>Wilms Tumours, Paediatric, Multi-target NGS panel, small variant (DROSHA)</td></tr><tr><td style="white-space:nowrap">M178.2<a name="GenomicTestCode-M178.462"> </a></td><td>Wilms Tumours, Paediatric, DROSHA seq</td></tr><tr><td style="white-space:nowrap">M178.3<a name="GenomicTestCode-M178.463"> </a></td><td>Wilms Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M178.4<a name="GenomicTestCode-M178.464"> </a></td><td>Wilms Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M179.1<a name="GenomicTestCode-M179.461"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (DDX3X, CTNNB1, SMARCA4, TP53)</td></tr><tr><td style="white-space:nowrap">M179.10<a name="GenomicTestCode-M179.4610"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, TP53)</td></tr><tr><td style="white-space:nowrap">M179.11<a name="GenomicTestCode-M179.4611"> </a></td><td>WNT Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M179.2<a name="GenomicTestCode-M179.462"> </a></td><td>WNT Medulloblastoma, Paediatric, DDX3X seq</td></tr><tr><td style="white-space:nowrap">M179.3<a name="GenomicTestCode-M179.463"> </a></td><td>WNT Medulloblastoma, Paediatric, CTNNB1 seq</td></tr><tr><td style="white-space:nowrap">M179.4<a name="GenomicTestCode-M179.464"> </a></td><td>WNT Medulloblastoma, Paediatric, SMARCA4 seq</td></tr><tr><td style="white-space:nowrap">M179.5<a name="GenomicTestCode-M179.465"> </a></td><td>WNT Medulloblastoma, Paediatric, TP53 seq</td></tr><tr><td style="white-space:nowrap">M179.6<a name="GenomicTestCode-M179.466"> </a></td><td>WNT Medulloblastoma, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M179.7<a name="GenomicTestCode-M179.467"> </a></td><td>WNT Medulloblastoma, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M179.8<a name="GenomicTestCode-M179.468"> </a></td><td>WNT Medulloblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M179.9<a name="GenomicTestCode-M179.469"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M18.1<a name="GenomicTestCode-M18.461"> </a></td><td>Renal Cell Carcinoma, Adult, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M18.2<a name="GenomicTestCode-M18.462"> </a></td><td>Renal Cell Carcinoma,Adult, Multi-target NGS panel small variant (FH, SDHA, SDHB, SDHC, SDHD, VHL, ELOC (TCEB-1), TSC1/2, MET, BRAF)</td></tr><tr><td style="white-space:nowrap">M18.3<a name="GenomicTestCode-M18.463"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 3 FISH</td></tr><tr><td style="white-space:nowrap">M18.4<a name="GenomicTestCode-M18.464"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 8 FISH</td></tr><tr><td style="white-space:nowrap">M18.5<a name="GenomicTestCode-M18.465"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 7 &amp; 17 FISH</td></tr><tr><td style="white-space:nowrap">M18.6<a name="GenomicTestCode-M18.466"> </a></td><td>Renal Cell Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, TFE3, TFEB)</td></tr><tr><td style="white-space:nowrap">M18.7<a name="GenomicTestCode-M18.467"> </a></td><td>Renal Cell Carcinoma, Adult, TFEB rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M180.1<a name="GenomicTestCode-M180.461"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, small variant (TFE3)</td></tr><tr><td style="white-space:nowrap">M180.2<a name="GenomicTestCode-M180.462"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3 seq</td></tr><tr><td style="white-space:nowrap">M180.3<a name="GenomicTestCode-M180.463"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M180.4<a name="GenomicTestCode-M180.464"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-MITF FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M180.5<a name="GenomicTestCode-M180.465"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-PRCC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M180.6<a name="GenomicTestCode-M180.466"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M180.7<a name="GenomicTestCode-M180.467"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFE3-ASPSCR1, TFE3-MITF,  TFE3-PRCC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M181.1<a name="GenomicTestCode-M181.461"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Multi-target NGS panel, small variant (MAP2K1)</td></tr><tr><td style="white-space:nowrap">M181.4<a name="GenomicTestCode-M181.464"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M181.5<a name="GenomicTestCode-M181.465"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection NGS</td></tr><tr><td style="white-space:nowrap">M182.1<a name="GenomicTestCode-M182.461"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M182.2<a name="GenomicTestCode-M182.462"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M182.3<a name="GenomicTestCode-M182.463"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M182.4<a name="GenomicTestCode-M182.464"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, Multi-target NGS panel, structural variant (ALK-NPM1, other ALK rearrangements)</td></tr><tr><td style="white-space:nowrap">M182.5<a name="GenomicTestCode-M182.465"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M182.6<a name="GenomicTestCode-M182.466"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M183.1<a name="GenomicTestCode-M183.461"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3A, NF1, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M183.2<a name="GenomicTestCode-M183.462"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M183.3<a name="GenomicTestCode-M183.463"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M183.4<a name="GenomicTestCode-M183.464"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M183.5<a name="GenomicTestCode-M183.465"> </a></td><td>Diffuse Midline Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M183.6<a name="GenomicTestCode-M183.466"> </a></td><td>Diffuse Midline Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M183.7<a name="GenomicTestCode-M183.467"> </a></td><td>Diffuse Midline Glioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M183.8<a name="GenomicTestCode-M183.468"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, MYC, MYCN)</td></tr><tr><td style="white-space:nowrap">M183.9<a name="GenomicTestCode-M183.469"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M184.1<a name="GenomicTestCode-M184.461"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3B, H3C2, H3C3, H3C14, IDH1, IDH2, TP53, VHL)</td></tr><tr><td style="white-space:nowrap">M184.2<a name="GenomicTestCode-M184.462"> </a></td><td>Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M184.3<a name="GenomicTestCode-M184.463"> </a></td><td>Glioma, Paediatric, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M184.4<a name="GenomicTestCode-M184.464"> </a></td><td>Glioma, Paediatric, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M184.5<a name="GenomicTestCode-M184.465"> </a></td><td>Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M184.6<a name="GenomicTestCode-M184.466"> </a></td><td>Glioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M184.7<a name="GenomicTestCode-M184.467"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M184.8<a name="GenomicTestCode-M184.468"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M185.1<a name="GenomicTestCode-M185.461"> </a></td><td>High Grade Glioma, Paediatric, Multi-target NGS panel, small variant (CDKN2B)</td></tr><tr><td style="white-space:nowrap">M185.2<a name="GenomicTestCode-M185.462"> </a></td><td>High Grade Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M185.3<a name="GenomicTestCode-M185.463"> </a></td><td>High Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M185.4<a name="GenomicTestCode-M185.464"> </a></td><td>High Grade Glioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M185.5<a name="GenomicTestCode-M185.465"> </a></td><td>High Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M186.1<a name="GenomicTestCode-M186.461"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, small variant (TSC1, TSC2, IDH1, IDH2, FGFR1)</td></tr><tr><td style="white-space:nowrap">M186.2<a name="GenomicTestCode-M186.462"> </a></td><td>Low Grade Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M186.3<a name="GenomicTestCode-M186.463"> </a></td><td>Low Grade Glioma, Paediatric, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M186.4<a name="GenomicTestCode-M186.464"> </a></td><td>Low Grade Glioma, Paediatric, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M186.5<a name="GenomicTestCode-M186.465"> </a></td><td>Low Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M186.6<a name="GenomicTestCode-M186.466"> </a></td><td>Low Grade Glioma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M186.7<a name="GenomicTestCode-M186.467"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M186.8<a name="GenomicTestCode-M186.468"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M187.1<a name="GenomicTestCode-M187.461"> </a></td><td>Uveal melanoma, 1p, 3, 6, 8 MLPA</td></tr><tr><td style="white-space:nowrap">M187.2<a name="GenomicTestCode-M187.462"> </a></td><td>Uveal melanoma, BRAF hotspot</td></tr><tr><td style="white-space:nowrap">M187.3<a name="GenomicTestCode-M187.463"> </a></td><td>Uveal melanoma, Multi-target NGS panel, small variant (BRAF, NRAS, NF1)</td></tr><tr><td style="white-space:nowrap">M187.4<a name="GenomicTestCode-M187.464"> </a></td><td>Uveal melanoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M189.1<a name="GenomicTestCode-M189.461"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2, BRAF, H3C2, H3C3, H3C14, H3-3A, H3-3B, TERT promoter, TP53, VHL, YAP1, SMARCA4, SMARCB1, DDX3X, CTNNB1)</td></tr><tr><td style="white-space:nowrap">M189.10<a name="GenomicTestCode-M189.4610"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M189.11<a name="GenomicTestCode-M189.4611"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SNP Array</td></tr><tr><td style="white-space:nowrap">M189.12<a name="GenomicTestCode-M189.4612"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, C19MC copy number FISH</td></tr><tr><td style="white-space:nowrap">M189.13<a name="GenomicTestCode-M189.4613"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M189.14<a name="GenomicTestCode-M189.4614"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M189.15<a name="GenomicTestCode-M189.4615"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M189.16<a name="GenomicTestCode-M189.4616"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M189.17<a name="GenomicTestCode-M189.4617"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M189.18<a name="GenomicTestCode-M189.4618"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M189.19<a name="GenomicTestCode-M189.4619"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M189.2<a name="GenomicTestCode-M189.462"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, structural variant (CIC, BCOR, BCOR-CCNB3, C11orf95-RELA, YAP1-C11orf95, YAP1-TFE3, EWSR1, MN1, RELA, YAP1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M189.20<a name="GenomicTestCode-M189.4620"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M189.21<a name="GenomicTestCode-M189.4621"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, copy number variant  (C19MC, SMARCA4, SMARCB1, YAP1)</td></tr><tr><td style="white-space:nowrap">M189.3<a name="GenomicTestCode-M189.463"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M189.4<a name="GenomicTestCode-M189.464"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M189.5<a name="GenomicTestCode-M189.465"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M189.6<a name="GenomicTestCode-M189.466"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M189.7<a name="GenomicTestCode-M189.467"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, EWSR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M189.8<a name="GenomicTestCode-M189.468"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, MN1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M189.9<a name="GenomicTestCode-M189.469"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.1<a name="GenomicTestCode-M190.461"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, small variant (CDKN2A, DICER1, RB1, YAP1, SMARCA4, SMARCB1, MSH6, PMS2, PTEN, ATRX)</td></tr><tr><td style="white-space:nowrap">M190.10<a name="GenomicTestCode-M190.4610"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.11<a name="GenomicTestCode-M190.4611"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.12<a name="GenomicTestCode-M190.4612"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M190.13<a name="GenomicTestCode-M190.4613"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.14<a name="GenomicTestCode-M190.4614"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.15<a name="GenomicTestCode-M190.4615"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, TTYH1-C19MC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.16<a name="GenomicTestCode-M190.4616"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.17<a name="GenomicTestCode-M190.4617"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.18<a name="GenomicTestCode-M190.4618"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.19<a name="GenomicTestCode-M190.4619"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M190.2<a name="GenomicTestCode-M190.462"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M190.20<a name="GenomicTestCode-M190.4620"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MN1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M190.21<a name="GenomicTestCode-M190.4621"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SNP Array</td></tr><tr><td style="white-space:nowrap">M190.22<a name="GenomicTestCode-M190.4622"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, C19MC copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.23<a name="GenomicTestCode-M190.4623"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, DICER1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.24<a name="GenomicTestCode-M190.4624"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MSH6 copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.25<a name="GenomicTestCode-M190.4625"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.26<a name="GenomicTestCode-M190.4626"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.27<a name="GenomicTestCode-M190.4627"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.28<a name="GenomicTestCode-M190.4628"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M190.3<a name="GenomicTestCode-M190.463"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.30<a name="GenomicTestCode-M190.4630"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M190.31<a name="GenomicTestCode-M190.4631"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M190.32<a name="GenomicTestCode-M190.4632"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, copy number variant  (C19MC, DICER1, MSH6, MYC, PTEN, SMARCA4, SMARCB1)</td></tr><tr><td style="white-space:nowrap">M190.4<a name="GenomicTestCode-M190.464"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.5<a name="GenomicTestCode-M190.465"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.6<a name="GenomicTestCode-M190.466"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.7<a name="GenomicTestCode-M190.467"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.8<a name="GenomicTestCode-M190.468"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-FRX1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M190.9<a name="GenomicTestCode-M190.469"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.1<a name="GenomicTestCode-M191.461"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style="white-space:nowrap">M191.10<a name="GenomicTestCode-M191.4610"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M191.11<a name="GenomicTestCode-M191.4611"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style="white-space:nowrap">M191.12<a name="GenomicTestCode-M191.4612"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.13<a name="GenomicTestCode-M191.4613"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M191.14<a name="GenomicTestCode-M191.4614"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M191.15<a name="GenomicTestCode-M191.4615"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.16<a name="GenomicTestCode-M191.4616"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.17<a name="GenomicTestCode-M191.4617"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M191.18<a name="GenomicTestCode-M191.4618"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M191.19<a name="GenomicTestCode-M191.4619"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M191.2<a name="GenomicTestCode-M191.462"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.20<a name="GenomicTestCode-M191.4620"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M191.21<a name="GenomicTestCode-M191.4621"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M191.22<a name="GenomicTestCode-M191.4622"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M191.3<a name="GenomicTestCode-M191.463"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.4<a name="GenomicTestCode-M191.464"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.5<a name="GenomicTestCode-M191.465"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.6<a name="GenomicTestCode-M191.466"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.7<a name="GenomicTestCode-M191.467"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.8<a name="GenomicTestCode-M191.468"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M191.9<a name="GenomicTestCode-M191.469"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.1<a name="GenomicTestCode-M192.461"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX,  H3-3A, H3-3B, H3C2, H3C3,  H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style="white-space:nowrap">M192.10<a name="GenomicTestCode-M192.4610"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M192.11<a name="GenomicTestCode-M192.4611"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style="white-space:nowrap">M192.12<a name="GenomicTestCode-M192.4612"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.13<a name="GenomicTestCode-M192.4613"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M192.14<a name="GenomicTestCode-M192.4614"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M192.15<a name="GenomicTestCode-M192.4615"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.16<a name="GenomicTestCode-M192.4616"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.17<a name="GenomicTestCode-M192.4617"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M192.18<a name="GenomicTestCode-M192.4618"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M192.19<a name="GenomicTestCode-M192.4619"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M192.2<a name="GenomicTestCode-M192.462"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.20<a name="GenomicTestCode-M192.4620"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M192.21<a name="GenomicTestCode-M192.4621"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M192.22<a name="GenomicTestCode-M192.4622"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style="white-space:nowrap">M192.23<a name="GenomicTestCode-M192.4623"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M192.3<a name="GenomicTestCode-M192.463"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.4<a name="GenomicTestCode-M192.464"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.5<a name="GenomicTestCode-M192.465"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.6<a name="GenomicTestCode-M192.466"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.7<a name="GenomicTestCode-M192.467"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.8<a name="GenomicTestCode-M192.468"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M192.9<a name="GenomicTestCode-M192.469"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.1<a name="GenomicTestCode-M193.461"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style="white-space:nowrap">M193.10<a name="GenomicTestCode-M193.4610"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M193.11<a name="GenomicTestCode-M193.4611"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style="white-space:nowrap">M193.12<a name="GenomicTestCode-M193.4612"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.13<a name="GenomicTestCode-M193.4613"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M193.14<a name="GenomicTestCode-M193.4614"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M193.15<a name="GenomicTestCode-M193.4615"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.16<a name="GenomicTestCode-M193.4616"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.17<a name="GenomicTestCode-M193.4617"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M193.18<a name="GenomicTestCode-M193.4618"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M193.19<a name="GenomicTestCode-M193.4619"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M193.2<a name="GenomicTestCode-M193.462"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.20<a name="GenomicTestCode-M193.4620"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M193.21<a name="GenomicTestCode-M193.4621"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M193.22<a name="GenomicTestCode-M193.4622"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style="white-space:nowrap">M193.23<a name="GenomicTestCode-M193.4623"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M193.3<a name="GenomicTestCode-M193.463"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.4<a name="GenomicTestCode-M193.464"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.5<a name="GenomicTestCode-M193.465"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.6<a name="GenomicTestCode-M193.466"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.7<a name="GenomicTestCode-M193.467"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.8<a name="GenomicTestCode-M193.468"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M193.9<a name="GenomicTestCode-M193.469"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M194.1<a name="GenomicTestCode-M194.461"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, small variant (ALK, BCOR, CTNNB1, DDX3X, DDX3X, EZH2, MYCN,  PTCH1, PTCH2, PTEN, SMARCA4, SMO, SUFU, TERT promoter, TP53,  YAP1)</td></tr><tr><td style="white-space:nowrap">M194.10<a name="GenomicTestCode-M194.4610"> </a></td><td>Medulloblastoma all Subtypes, BCOR copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.11<a name="GenomicTestCode-M194.4611"> </a></td><td>Medulloblastoma all Subtypes, C19MC copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.12<a name="GenomicTestCode-M194.4612"> </a></td><td>Medulloblastoma all Subtypes, DDX3X copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.13<a name="GenomicTestCode-M194.4613"> </a></td><td>Medulloblastoma all Subtypes, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.14<a name="GenomicTestCode-M194.4614"> </a></td><td>Medulloblastoma all Subtypes, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.15<a name="GenomicTestCode-M194.4615"> </a></td><td>Medulloblastoma all Subtypes, PTCH1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.16<a name="GenomicTestCode-M194.4616"> </a></td><td>Medulloblastoma all Subtypes, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M194.17<a name="GenomicTestCode-M194.4617"> </a></td><td>Medulloblastoma all Subtypes, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.18<a name="GenomicTestCode-M194.4618"> </a></td><td>Medulloblastoma all Subtypes, SMO copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.19<a name="GenomicTestCode-M194.4619"> </a></td><td>Medulloblastoma all Subtypes, TERT copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.2<a name="GenomicTestCode-M194.462"> </a></td><td>Medulloblastoma all Subtypes, ALK rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M194.20<a name="GenomicTestCode-M194.4620"> </a></td><td>Medulloblastoma all Subtypes, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.21<a name="GenomicTestCode-M194.4621"> </a></td><td>Medulloblastoma all Subtypes, YAP1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M194.22<a name="GenomicTestCode-M194.4622"> </a></td><td>Medulloblastoma all Subtypes, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M194.23<a name="GenomicTestCode-M194.4623"> </a></td><td>Medulloblastoma all Subtypes, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M194.24<a name="GenomicTestCode-M194.4624"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, structural variant (ALK, BCOR, MYC, PVT1-MYC, YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M194.25<a name="GenomicTestCode-M194.4625"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, copy number variant  (ALK, BCOR, C19MC, DDX3X, MYC, MYCN, PTCH1, PTEN, SMARCA4, SMO, TERT, TP53, YAP1)</td></tr><tr><td style="white-space:nowrap">M194.3<a name="GenomicTestCode-M194.463"> </a></td><td>Medulloblastoma all Subtypes, BCOR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M194.4<a name="GenomicTestCode-M194.464"> </a></td><td>Medulloblastoma all Subtypes, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M194.5<a name="GenomicTestCode-M194.465"> </a></td><td>Medulloblastoma all Subtypes, PVT1-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M194.6<a name="GenomicTestCode-M194.466"> </a></td><td>Medulloblastoma all Subtypes, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M194.7<a name="GenomicTestCode-M194.467"> </a></td><td>Medulloblastoma all Subtypes, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M194.8<a name="GenomicTestCode-M194.468"> </a></td><td>Medulloblastoma all Subtypes, SNP Array</td></tr><tr><td style="white-space:nowrap">M194.9<a name="GenomicTestCode-M194.469"> </a></td><td>Medulloblastoma all Subtypes, ALK copy number FISH</td></tr><tr><td style="white-space:nowrap">M195.1<a name="GenomicTestCode-M195.461"> </a></td><td>Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, small variant (BRAF, CTNNB1)</td></tr><tr><td style="white-space:nowrap">M195.2<a name="GenomicTestCode-M195.462"> </a></td><td>Craniopharyngioma, Adult and Paediatric, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M195.3<a name="GenomicTestCode-M195.463"> </a></td><td>Craniopharyngioma, Adult and Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M195.4<a name="GenomicTestCode-M195.464"> </a></td><td>Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M195.5<a name="GenomicTestCode-M195.465"> </a></td><td>Craniopharyngioma, Adult and Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M196.1<a name="GenomicTestCode-M196.461"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M196.2<a name="GenomicTestCode-M196.462"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M196.3<a name="GenomicTestCode-M196.463"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M196.4<a name="GenomicTestCode-M196.464"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M196.5<a name="GenomicTestCode-M196.465"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M197.1<a name="GenomicTestCode-M197.461"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, Multi-target NGS panel, structural variant (BCOR, CIC, DDIT3, EWSR1, FOXO1, WT1, BCOR-CCNB3, HEY1-NCOA2, PAX3-FOXO1, PAX7-FOXO1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M197.10<a name="GenomicTestCode-M197.4610"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M197.2<a name="GenomicTestCode-M197.462"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.3<a name="GenomicTestCode-M197.463"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.4<a name="GenomicTestCode-M197.464"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.5<a name="GenomicTestCode-M197.465"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.6<a name="GenomicTestCode-M197.466"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.7<a name="GenomicTestCode-M197.467"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.8<a name="GenomicTestCode-M197.468"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, PAX3-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M197.9<a name="GenomicTestCode-M197.469"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, PAX7-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M198.1<a name="GenomicTestCode-M198.461"> </a></td><td>Vascular Soft Tissue Tumour Differential, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M198.2<a name="GenomicTestCode-M198.462"> </a></td><td>Vascular Soft Tissue Tumour Differential, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M198.3<a name="GenomicTestCode-M198.463"> </a></td><td>Vascular Soft Tissue Tumour Differential, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M198.4<a name="GenomicTestCode-M198.464"> </a></td><td>Vascular Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M198.5<a name="GenomicTestCode-M198.465"> </a></td><td>Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M198.6<a name="GenomicTestCode-M198.466"> </a></td><td>Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style="white-space:nowrap">M199.1<a name="GenomicTestCode-M199.461"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, small variant (APC, CTNNB1)</td></tr><tr><td style="white-space:nowrap">M199.10<a name="GenomicTestCode-M199.4610"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, TPM4-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M199.11<a name="GenomicTestCode-M199.4611"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, ETV6-NTRK3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M199.12<a name="GenomicTestCode-M199.4612"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M199.13<a name="GenomicTestCode-M199.4613"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M199.2<a name="GenomicTestCode-M199.462"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, SS18, USP6, COL1A1-PDGFB, TPM3-ALK, TPM4-ALK, ETV6-NTRK3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M199.3<a name="GenomicTestCode-M199.463"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M199.4<a name="GenomicTestCode-M199.464"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, FUS rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M199.5<a name="GenomicTestCode-M199.465"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M199.6<a name="GenomicTestCode-M199.466"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M199.7<a name="GenomicTestCode-M199.467"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M199.8<a name="GenomicTestCode-M199.468"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, COL1A1-PDGFB rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M199.9<a name="GenomicTestCode-M199.469"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, TPM3-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M2.1<a name="GenomicTestCode-M2.461"> </a></td><td>Ovarian Carcinoma, Multi-target NGS panel, small variant (BRCA1, BRCA2, SMARCA4)</td></tr><tr><td style="white-space:nowrap">M2.3<a name="GenomicTestCode-M2.463"> </a></td><td>Ovarian Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M2.5<a name="GenomicTestCode-M2.465"> </a></td><td>Ovarian Carcinoma, HRD status (either positive for BRCA 1 and/or 2, or HRD positive)</td></tr><tr><td style="white-space:nowrap">M20.1<a name="GenomicTestCode-M20.461"> </a></td><td>Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style="white-space:nowrap">M20.2<a name="GenomicTestCode-M20.462"> </a></td><td>Anaplastic Astrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M20.3<a name="GenomicTestCode-M20.463"> </a></td><td>Anaplastic Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M20.4<a name="GenomicTestCode-M20.464"> </a></td><td>Anaplastic Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M20.5<a name="GenomicTestCode-M20.465"> </a></td><td>Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M200.1<a name="GenomicTestCode-M200.461"> </a></td><td>Myxoid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (BCOR, DDIT3, FUS, NR4A3, TGFBR3-OGA, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M200.2<a name="GenomicTestCode-M200.462"> </a></td><td>Myxoid Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M200.3<a name="GenomicTestCode-M200.463"> </a></td><td>Myxoid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M200.4<a name="GenomicTestCode-M200.464"> </a></td><td>Myxoid Soft Tissue Tumour Differential, NR4A3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M200.5<a name="GenomicTestCode-M200.465"> </a></td><td>Myxoid Soft Tissue Tumour Differential, TGFBR3-OGA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M200.6<a name="GenomicTestCode-M200.466"> </a></td><td>Myxoid Soft Tissue Tumour Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M200.7<a name="GenomicTestCode-M200.467"> </a></td><td>Myxoid Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M201.1<a name="GenomicTestCode-M201.461"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M201.2<a name="GenomicTestCode-M201.462"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M201.3<a name="GenomicTestCode-M201.463"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M201.4<a name="GenomicTestCode-M201.464"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M201.5<a name="GenomicTestCode-M201.465"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M202.1<a name="GenomicTestCode-M202.461"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M202.2<a name="GenomicTestCode-M202.462"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M202.3<a name="GenomicTestCode-M202.463"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M202.4<a name="GenomicTestCode-M202.464"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M202.5<a name="GenomicTestCode-M202.465"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, WWTR1-CAMTA1  RT-PCR</td></tr><tr><td style="white-space:nowrap">M202.6<a name="GenomicTestCode-M202.466"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M202.7<a name="GenomicTestCode-M202.467"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (EWSR1, FUS, SS18, TFE3, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M203.1<a name="GenomicTestCode-M203.461"> </a></td><td>Uterine Sarcomas (Inc Endometrial), EPC1-PHF1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M203.2<a name="GenomicTestCode-M203.462"> </a></td><td>Uterine Sarcomas (Inc Endometrial), JAZF1-PHF1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M203.3<a name="GenomicTestCode-M203.463"> </a></td><td>Uterine Sarcomas (Inc Endometrial), JAZF1-SUZ12 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M203.4<a name="GenomicTestCode-M203.464"> </a></td><td>Uterine Sarcomas (Inc Endometrial), NUTM2B-YWHAE FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M203.5<a name="GenomicTestCode-M203.465"> </a></td><td>Uterine Sarcomas (Inc Endometrial), WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M203.6<a name="GenomicTestCode-M203.466"> </a></td><td>Uterine Sarcomas (Inc Endometrial), Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NUTM2B-YWHAE, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M204.1<a name="GenomicTestCode-M204.461"> </a></td><td>Undifferentiated tumour, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M204.2<a name="GenomicTestCode-M204.462"> </a></td><td>Undifferentiated tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M205.1<a name="GenomicTestCode-M205.461"> </a></td><td>Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B, IDH1, IDH2)</td></tr><tr><td style="white-space:nowrap">M205.2<a name="GenomicTestCode-M205.462"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style="white-space:nowrap">M205.3<a name="GenomicTestCode-M205.463"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3A seq</td></tr><tr><td style="white-space:nowrap">M205.4<a name="GenomicTestCode-M205.464"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3B seq</td></tr><tr><td style="white-space:nowrap">M205.5<a name="GenomicTestCode-M205.465"> </a></td><td>Cartilage Forming Bone Tumour Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M205.6<a name="GenomicTestCode-M205.466"> </a></td><td>Cartilage Forming Bone Tumour Differential, SNP Array</td></tr><tr><td style="white-space:nowrap">M205.7<a name="GenomicTestCode-M205.467"> </a></td><td>Cartilage Forming Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M205.8<a name="GenomicTestCode-M205.468"> </a></td><td>Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M206.1<a name="GenomicTestCode-M206.461"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B)</td></tr><tr><td style="white-space:nowrap">M206.2<a name="GenomicTestCode-M206.462"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style="white-space:nowrap">M206.3<a name="GenomicTestCode-M206.463"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3A seq</td></tr><tr><td style="white-space:nowrap">M206.4<a name="GenomicTestCode-M206.464"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3B seq</td></tr><tr><td style="white-space:nowrap">M206.5<a name="GenomicTestCode-M206.465"> </a></td><td>Bone Forming Bone Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M206.6<a name="GenomicTestCode-M206.466"> </a></td><td>Bone Forming Bone Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M206.7<a name="GenomicTestCode-M206.467"> </a></td><td>Bone Forming Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M206.8<a name="GenomicTestCode-M206.468"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M206.9<a name="GenomicTestCode-M206.469"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M207.1<a name="GenomicTestCode-M207.461"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3B)</td></tr><tr><td style="white-space:nowrap">M207.2<a name="GenomicTestCode-M207.462"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, H3-3B seq</td></tr><tr><td style="white-space:nowrap">M207.3<a name="GenomicTestCode-M207.463"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style="white-space:nowrap">M207.4<a name="GenomicTestCode-M207.464"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M207.5<a name="GenomicTestCode-M207.465"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M207.6<a name="GenomicTestCode-M207.466"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M207.7<a name="GenomicTestCode-M207.467"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M207.8<a name="GenomicTestCode-M207.468"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M208.1<a name="GenomicTestCode-M208.461"> </a></td><td>Round Cell Sarcoma of Bone Differential, Multi-target NGS panel, structural variant (BCOR, CIC, EWSR1, WT1, BCOR-CCNB3, HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M208.2<a name="GenomicTestCode-M208.462"> </a></td><td>Round Cell Sarcoma of Bone Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M208.3<a name="GenomicTestCode-M208.463"> </a></td><td>Round Cell Sarcoma of Bone Differential, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M208.4<a name="GenomicTestCode-M208.464"> </a></td><td>Round Cell Sarcoma of Bone Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M208.5<a name="GenomicTestCode-M208.465"> </a></td><td>Round Cell Sarcoma of Bone Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M208.6<a name="GenomicTestCode-M208.466"> </a></td><td>Round Cell Sarcoma of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M209.1<a name="GenomicTestCode-M209.461"> </a></td><td>Vascular Tumour of Bone Differential, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M209.2<a name="GenomicTestCode-M209.462"> </a></td><td>Vascular Tumour of Bone Differential, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M209.3<a name="GenomicTestCode-M209.463"> </a></td><td>Vascular Tumour of Bone Differential, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M209.4<a name="GenomicTestCode-M209.464"> </a></td><td>Vascular Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M209.5<a name="GenomicTestCode-M209.465"> </a></td><td>Vascular Tumour of Bone Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M209.6<a name="GenomicTestCode-M209.466"> </a></td><td>Vascular Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style="white-space:nowrap">M21.1<a name="GenomicTestCode-M21.461"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A,H3C2, BRAF, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M21.2<a name="GenomicTestCode-M21.462"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, copy number variant (EGFR, CDKN2A, CDKN2B)</td></tr><tr><td style="white-space:nowrap">M21.20<a name="GenomicTestCode-M21.4620"> </a></td><td>Astrocytoma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M21.21<a name="GenomicTestCode-M21.4621"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M21.22<a name="GenomicTestCode-M21.4622"> </a></td><td>Astrocytoma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M21.23<a name="GenomicTestCode-M21.4623"> </a></td><td>Astrocytoma, Adult, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M21.24<a name="GenomicTestCode-M21.4624"> </a></td><td>Astrocytoma, Adult, CDKN2B copy number FISH</td></tr><tr><td style="white-space:nowrap">M21.3<a name="GenomicTestCode-M21.463"> </a></td><td>Astrocytoma, Adult, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M21.5<a name="GenomicTestCode-M21.465"> </a></td><td>Astrocytoma, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M21.6<a name="GenomicTestCode-M21.466"> </a></td><td>Astrocytoma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M21.8<a name="GenomicTestCode-M21.468"> </a></td><td>Astrocytoma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M21.9<a name="GenomicTestCode-M21.469"> </a></td><td>Astrocytoma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M210.1<a name="GenomicTestCode-M210.461"> </a></td><td>Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M210.2<a name="GenomicTestCode-M210.462"> </a></td><td>Spindle Cell Tumour of Bone Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M210.3<a name="GenomicTestCode-M210.463"> </a></td><td>Spindle Cell Tumour of Bone Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M210.4<a name="GenomicTestCode-M210.464"> </a></td><td>Spindle Cell Tumour of Bone Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M210.5<a name="GenomicTestCode-M210.465"> </a></td><td>Spindle Cell Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M210.6<a name="GenomicTestCode-M210.466"> </a></td><td>Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M211.1<a name="GenomicTestCode-M211.461"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, small variant (GNAS)</td></tr><tr><td style="white-space:nowrap">M211.2<a name="GenomicTestCode-M211.462"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M211.3<a name="GenomicTestCode-M211.463"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M211.4<a name="GenomicTestCode-M211.464"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M211.5<a name="GenomicTestCode-M211.465"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M212.1<a name="GenomicTestCode-M212.461"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX, TP53, TFE3)</td></tr><tr><td style="white-space:nowrap">M212.10<a name="GenomicTestCode-M212.4610"> </a></td><td>Renal Tumour Differential, Paediatric, TFEB-MALAT1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M212.11<a name="GenomicTestCode-M212.4611"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M212.12<a name="GenomicTestCode-M212.4612"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-MITF FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M212.13<a name="GenomicTestCode-M212.4613"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-PRCC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M212.14<a name="GenomicTestCode-M212.4614"> </a></td><td>Renal Tumour Differential, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M212.15<a name="GenomicTestCode-M212.4615"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, TFE3-ASPSCR1, TFE3-MITF, TFE3-PRCC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M212.16<a name="GenomicTestCode-M212.4616"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (ATRX, TP53, WT1)</td></tr><tr><td style="white-space:nowrap">M212.2<a name="GenomicTestCode-M212.462"> </a></td><td>Renal Tumour Differential, Paediatric, ATRX seq</td></tr><tr><td style="white-space:nowrap">M212.3<a name="GenomicTestCode-M212.463"> </a></td><td>Renal Tumour Differential, Paediatric, CTNNB1 seq</td></tr><tr><td style="white-space:nowrap">M212.4<a name="GenomicTestCode-M212.464"> </a></td><td>Renal Tumour Differential, Paediatric, DAXX seq</td></tr><tr><td style="white-space:nowrap">M212.5<a name="GenomicTestCode-M212.465"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3 seq</td></tr><tr><td style="white-space:nowrap">M212.6<a name="GenomicTestCode-M212.466"> </a></td><td>Renal Tumour Differential, Paediatric, TP53 seq</td></tr><tr><td style="white-space:nowrap">M212.7<a name="GenomicTestCode-M212.467"> </a></td><td>Renal Tumour Differential, Paediatric, ATRX copy number FISH</td></tr><tr><td style="white-space:nowrap">M212.8<a name="GenomicTestCode-M212.468"> </a></td><td>Renal Tumour Differential, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M212.9<a name="GenomicTestCode-M212.469"> </a></td><td>Renal Tumour Differential, Paediatric, WT1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.1<a name="GenomicTestCode-M213.461"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1, DDX3X, CTNNB1, CDKN2A, TP53, RAF1, PIK3CA, FGFR1, FGFR4, KIT,  BRAF, H3-3A, ALK, ATRX, NRAS, PHOX2B)</td></tr><tr><td style="white-space:nowrap">M213.10<a name="GenomicTestCode-M213.4610"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.11<a name="GenomicTestCode-M213.4611"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.12<a name="GenomicTestCode-M213.4612"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, ALK-NPM1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M213.13<a name="GenomicTestCode-M213.4613"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.14<a name="GenomicTestCode-M213.4614"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EWSR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M213.15<a name="GenomicTestCode-M213.4615"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M213.16<a name="GenomicTestCode-M213.4616"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-NF1A FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.17<a name="GenomicTestCode-M213.4617"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-SRGAP3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.18<a name="GenomicTestCode-M213.4618"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.19<a name="GenomicTestCode-M213.4619"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.2<a name="GenomicTestCode-M213.462"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, ALK, C1</td></tr><tr><td style="white-space:nowrap">M213.20<a name="GenomicTestCode-M213.4620"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.21<a name="GenomicTestCode-M213.4621"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.22<a name="GenomicTestCode-M213.4622"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, EGFR, ALK, C19MC, CDKN2A,  FGFR1, KIAA1549, KIT, MYCN, PDGFRA, SMARCA4, SMARCB1, YAP1)</td></tr><tr><td style="white-space:nowrap">M213.23<a name="GenomicTestCode-M213.4623"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.24<a name="GenomicTestCode-M213.4624"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, ALK copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.25<a name="GenomicTestCode-M213.4625"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, C19MC copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.26<a name="GenomicTestCode-M213.4626"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.27<a name="GenomicTestCode-M213.4627"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.28<a name="GenomicTestCode-M213.4628"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 ITD FISH</td></tr><tr><td style="white-space:nowrap">M213.29<a name="GenomicTestCode-M213.4629"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.3<a name="GenomicTestCode-M213.463"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M213.30<a name="GenomicTestCode-M213.4630"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, KIT copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.31<a name="GenomicTestCode-M213.4631"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.32<a name="GenomicTestCode-M213.4632"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, PDGFRA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.33<a name="GenomicTestCode-M213.4633"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.34<a name="GenomicTestCode-M213.4634"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.35<a name="GenomicTestCode-M213.4635"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M213.36<a name="GenomicTestCode-M213.4636"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.37<a name="GenomicTestCode-M213.4637"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M213.38<a name="GenomicTestCode-M213.4638"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M213.4<a name="GenomicTestCode-M213.464"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.5<a name="GenomicTestCode-M213.465"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.6<a name="GenomicTestCode-M213.466"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.7<a name="GenomicTestCode-M213.467"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.8<a name="GenomicTestCode-M213.468"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FRX1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M213.9<a name="GenomicTestCode-M213.469"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M215.1<a name="GenomicTestCode-M215.461"> </a></td><td>Endometrial Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M215.2<a name="GenomicTestCode-M215.462"> </a></td><td>Endometrial Cancer, MLH1 promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M215.4<a name="GenomicTestCode-M215.464"> </a></td><td>Endometrial Cancer, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2)</td></tr><tr><td style="white-space:nowrap">M215.5<a name="GenomicTestCode-M215.465"> </a></td><td>Endometrial Cancer, Multi-target NGS panel-small variant detection POLE</td></tr><tr><td style="white-space:nowrap">M217.1<a name="GenomicTestCode-M217.461"> </a></td><td>Urothelial Cancer, Multi-target NGS panel, small variant (FGFR3, FGFR2)</td></tr><tr><td style="white-space:nowrap">M217.2<a name="GenomicTestCode-M217.462"> </a></td><td>Bladder Cancer, Multi-target NGS panel, copy number variant (FGFR3, FGFR2)</td></tr><tr><td style="white-space:nowrap">M217.3<a name="GenomicTestCode-M217.463"> </a></td><td>Bladder Cancer, Multi-target NGS panel, structural variant (FGFR3, FGFR2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M218.1<a name="GenomicTestCode-M218.461"> </a></td><td>Prostate Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2, ATM, CDK12)</td></tr><tr><td style="white-space:nowrap">M218.2<a name="GenomicTestCode-M218.462"> </a></td><td>Prostate Cancer, Multi-target NGS panel, structural variant (TMPRSS2-ERG, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M218.3<a name="GenomicTestCode-M218.463"> </a></td><td>Prostate Cancer, TMPRSS2-ERG FISH</td></tr><tr><td style="white-space:nowrap">M219.1<a name="GenomicTestCode-M219.461"> </a></td><td>Pancreatic Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2)</td></tr><tr><td style="white-space:nowrap">M219.2<a name="GenomicTestCode-M219.462"> </a></td><td>Pancreatic Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M219.3<a name="GenomicTestCode-M219.463"> </a></td><td>Pancreatic Cancer, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M219.5<a name="GenomicTestCode-M219.465"> </a></td><td>Pancreatic Cancer, MSI Testing</td></tr><tr><td style="white-space:nowrap">M22.1<a name="GenomicTestCode-M22.461"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, small variant (H3C2, H3C14, IDH1, IDH2)</td></tr><tr><td style="white-space:nowrap">M22.10<a name="GenomicTestCode-M22.4610"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYB rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M22.11<a name="GenomicTestCode-M22.4611"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYBL1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M22.12<a name="GenomicTestCode-M22.4612"> </a></td><td>Diffuse Astrocytoma, Paediatric, MN1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M22.2<a name="GenomicTestCode-M22.462"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M22.3<a name="GenomicTestCode-M22.463"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M22.4<a name="GenomicTestCode-M22.464"> </a></td><td>Diffuse Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M22.5<a name="GenomicTestCode-M22.465"> </a></td><td>Diffuse Astrocytoma, Paediatric, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M22.6<a name="GenomicTestCode-M22.466"> </a></td><td>Diffuse Astrocytoma, Paediatric, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M22.7<a name="GenomicTestCode-M22.467"> </a></td><td>Diffuse Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M22.8<a name="GenomicTestCode-M22.468"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style="white-space:nowrap">M22.9<a name="GenomicTestCode-M22.469"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M220.1<a name="GenomicTestCode-M220.461"> </a></td><td>Cholangiocarcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, FGFR2)</td></tr><tr><td style="white-space:nowrap">M220.3<a name="GenomicTestCode-M220.463"> </a></td><td>Cholangiocarcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M220.5<a name="GenomicTestCode-M220.465"> </a></td><td>Cholangiocarcinoma, MSI Testing</td></tr><tr><td style="white-space:nowrap">M220.6<a name="GenomicTestCode-M220.466"> </a></td><td>Cholangiocarcinoma, Multi-target NGS panel -small variant (IDH1)</td></tr><tr><td style="white-space:nowrap">M220.7<a name="GenomicTestCode-M220.467"> </a></td><td>Cholangiocarcinoma, FGFR2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M221.1<a name="GenomicTestCode-M221.461"> </a></td><td>Spitzoid tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M222.2<a name="GenomicTestCode-M222.462"> </a></td><td>Hepatocellular carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M222.4<a name="GenomicTestCode-M222.464"> </a></td><td>Hepatocellular carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M224.1<a name="GenomicTestCode-M224.461"> </a></td><td>MDS/MPN, Multi-target NGS panel, small variant</td></tr><tr><td style="white-space:nowrap">M224.10<a name="GenomicTestCode-M224.4610"> </a></td><td>MDS/MPN, BCR-ABL1 multiplex</td></tr><tr><td style="white-space:nowrap">M224.11<a name="GenomicTestCode-M224.4611"> </a></td><td>MDS/MPN, Other RT-PCR</td></tr><tr><td style="white-space:nowrap">M224.13<a name="GenomicTestCode-M224.4613"> </a></td><td>MDS/MPN, JAK2 V617F hotspot</td></tr><tr><td style="white-space:nowrap">M224.14<a name="GenomicTestCode-M224.4614"> </a></td><td>MDS/MPN, JAK2 exon 12 hotspot</td></tr><tr><td style="white-space:nowrap">M224.15<a name="GenomicTestCode-M224.4615"> </a></td><td>MDS/MPN, CALR exon 9 hotspot</td></tr><tr><td style="white-space:nowrap">M224.16<a name="GenomicTestCode-M224.4616"> </a></td><td>MDS/MPN, MPL exon 10 hotspot</td></tr><tr><td style="white-space:nowrap">M224.18<a name="GenomicTestCode-M224.4618"> </a></td><td>MDS/MPN, Chr8 copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.19<a name="GenomicTestCode-M224.4619"> </a></td><td>MDS/MPN, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.2<a name="GenomicTestCode-M224.462"> </a></td><td>MDS/MPN, Karyotype (To include detection of complex karyotype)</td></tr><tr><td style="white-space:nowrap">M224.20<a name="GenomicTestCode-M224.4620"> </a></td><td>MDS/MPN, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.21<a name="GenomicTestCode-M224.4621"> </a></td><td>MDS/MPN, i(17q)/t(17p) FISH</td></tr><tr><td style="white-space:nowrap">M224.22<a name="GenomicTestCode-M224.4622"> </a></td><td>MDS/MPN, Chr12p copy number FISH, t(12p) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M224.23<a name="GenomicTestCode-M224.4623"> </a></td><td>MDS/MPN, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M224.24<a name="GenomicTestCode-M224.4624"> </a></td><td>MDS/MPN, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)</td></tr><tr><td style="white-space:nowrap">M224.25<a name="GenomicTestCode-M224.4625"> </a></td><td>MDS/MPN, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)</td></tr><tr><td style="white-space:nowrap">M224.26<a name="GenomicTestCode-M224.4626"> </a></td><td>MDS/MPN, FGFR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M224.27<a name="GenomicTestCode-M224.4627"> </a></td><td>MDS/MPN, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)</td></tr><tr><td style="white-space:nowrap">M224.28<a name="GenomicTestCode-M224.4628"> </a></td><td>MDS/MPN, inv(3)/t(3;3) FISH</td></tr><tr><td style="white-space:nowrap">M224.29<a name="GenomicTestCode-M224.4629"> </a></td><td>MDS/MPN, 11q23 (KMT2A) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M224.3<a name="GenomicTestCode-M224.463"> </a></td><td>MDS/MPN, FISH copy number and rearrangement Other: See tests M224. -M224. for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M224.30<a name="GenomicTestCode-M224.4630"> </a></td><td>MDS/MPN, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)</td></tr><tr><td style="white-space:nowrap">M224.31<a name="GenomicTestCode-M224.4631"> </a></td><td>MDS/MPN, FLT3 rearragement FISH</td></tr><tr><td style="white-space:nowrap">M224.32<a name="GenomicTestCode-M224.4632"> </a></td><td>MDS/MPN, RET rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M224.33<a name="GenomicTestCode-M224.4633"> </a></td><td>MDS/MPN, NTRK3 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M224.34<a name="GenomicTestCode-M224.4634"> </a></td><td>MDS/MPN, Chr13/Chr13q copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.35<a name="GenomicTestCode-M224.4635"> </a></td><td>MDS/MPN, Chr11q copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.36<a name="GenomicTestCode-M224.4636"> </a></td><td>MDS/MPN, Chr9q copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.37<a name="GenomicTestCode-M224.4637"> </a></td><td>MDS/MPN, Chr17/Chr17p copy number FISH</td></tr><tr><td style="white-space:nowrap">M224.38<a name="GenomicTestCode-M224.4638"> </a></td><td>MDS/MPN, idic(X)(q13) FISH</td></tr><tr><td style="white-space:nowrap">M224.39<a name="GenomicTestCode-M224.4639"> </a></td><td>MDS/MPN, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p/i(17q) &amp; idic(X)(q13), cryptic deletion of 4q12, trisomy 8)</td></tr><tr><td style="white-space:nowrap">M224.4<a name="GenomicTestCode-M224.464"> </a></td><td>MDS/MPN, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M224.40<a name="GenomicTestCode-M224.4640"> </a></td><td>MDS/MPN, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M224.41<a name="GenomicTestCode-M224.4641"> </a></td><td>MDS/MPN, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M224.42<a name="GenomicTestCode-M224.4642"> </a></td><td>MDS/MPN, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M224.5<a name="GenomicTestCode-M224.465"> </a></td><td>MDS/MPN, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)</td></tr><tr><td style="white-space:nowrap">M224.6<a name="GenomicTestCode-M224.466"> </a></td><td>MDS/MPN, FIP1L1-PDGFRA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M224.7<a name="GenomicTestCode-M224.467"> </a></td><td>MDS/MPN, FIP1L1-PDGFRA RT-qPCR</td></tr><tr><td style="white-space:nowrap">M224.8<a name="GenomicTestCode-M224.468"> </a></td><td>MDS/MPN, ETV6-PDGFRB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M224.9<a name="GenomicTestCode-M224.469"> </a></td><td>MDS/MPN, PCM1-JAK2 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M225.1<a name="GenomicTestCode-M225.461"> </a></td><td>Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M225.2<a name="GenomicTestCode-M225.462"> </a></td><td>Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection NGS</td></tr><tr><td style="white-space:nowrap">M225.3<a name="GenomicTestCode-M225.463"> </a></td><td>Suspected Lymphoma, TCR gene rearrangement detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M225.4<a name="GenomicTestCode-M225.464"> </a></td><td>Suspected Lymphoma, TCR gene rearrangement detection NGS</td></tr><tr><td style="white-space:nowrap">M225.5<a name="GenomicTestCode-M225.465"> </a></td><td>Suspected Lymphoma, Karyotype</td></tr><tr><td style="white-space:nowrap">M226.1<a name="GenomicTestCode-M226.461"> </a></td><td>Cancer of Unknown Primary, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M226.3<a name="GenomicTestCode-M226.463"> </a></td><td>Cancer of Unknown Primary, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M226.4<a name="GenomicTestCode-M226.464"> </a></td><td>Cancer of Unknown Primary, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M227.1<a name="GenomicTestCode-M227.461"> </a></td><td>Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M227.3<a name="GenomicTestCode-M227.463"> </a></td><td>Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M23.1<a name="GenomicTestCode-M23.461"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter,  H3-3A)</td></tr><tr><td style="white-space:nowrap">M23.10<a name="GenomicTestCode-M23.4610"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M23.11<a name="GenomicTestCode-M23.4611"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M23.12<a name="GenomicTestCode-M23.4612"> </a></td><td>Diffuse Midline Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M23.6<a name="GenomicTestCode-M23.466"> </a></td><td>Diffuse Midline Glioma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M23.7<a name="GenomicTestCode-M23.467"> </a></td><td>Diffuse Midline Glioma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M23.8<a name="GenomicTestCode-M23.468"> </a></td><td>Diffuse Midline Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M23.9<a name="GenomicTestCode-M23.469"> </a></td><td>Diffuse Midline Glioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M231.1,<a name="GenomicTestCode-M231.461.44"> </a></td><td>small cell lung cancer, Multi-target NGS panel, copy number variant (RB1)</td></tr><tr><td style="white-space:nowrap">M231.2,<a name="GenomicTestCode-M231.462.44"> </a></td><td>small cell lung cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M232.1<a name="GenomicTestCode-M232.461"> </a></td><td>Solid Tumour Exhausted all Standards of Care Testing and Treatment- Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M233.1<a name="GenomicTestCode-M233.461"> </a></td><td>High Grade Serous Ovarian Carcinoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M234.1<a name="GenomicTestCode-M234.461"> </a></td><td>Triple Negative Breast Cancer, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M235.1<a name="GenomicTestCode-M235.461"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M235.2<a name="GenomicTestCode-M235.462"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M235.3<a name="GenomicTestCode-M235.463"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M236.1<a name="GenomicTestCode-M236.461"> </a></td><td>Oesophageal Cancer, MSI Testing</td></tr><tr><td style="white-space:nowrap">M236.2<a name="GenomicTestCode-M236.462"> </a></td><td>Oesophageal Cancer, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M237.1<a name="GenomicTestCode-M237.461"> </a></td><td>Gastric Cancer, MSI Testing</td></tr><tr><td style="white-space:nowrap">M237.2<a name="GenomicTestCode-M237.462"> </a></td><td>Gastric Cancer, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M238.1,<a name="GenomicTestCode-M238.461.44"> </a></td><td>small Bowel Cancer, MSI Testing</td></tr><tr><td style="white-space:nowrap">M238.2,<a name="GenomicTestCode-M238.462.44"> </a></td><td>small Bowel Cancer, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M239.1<a name="GenomicTestCode-M239.461"> </a></td><td>Thyroid Hurtle Cell Carcinoma, Multi-target NGS panel, structural variant (RET)</td></tr><tr><td style="white-space:nowrap">M24.1<a name="GenomicTestCode-M24.461"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, C19MC copy number  FISH</td></tr><tr><td style="white-space:nowrap">M24.2<a name="GenomicTestCode-M24.462"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, TTYH1-C19MC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M24.3<a name="GenomicTestCode-M24.463"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M24.4<a name="GenomicTestCode-M24.464"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M24.5<a name="GenomicTestCode-M24.465"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, copy number variant (C19MC)</td></tr><tr><td style="white-space:nowrap">M24.6<a name="GenomicTestCode-M24.466"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, structural variant  (TTYH1-C19MC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M240.1<a name="GenomicTestCode-M240.461"> </a></td><td>Non-invasive follicular thyroid neoplasm with papillary like nuclei, Multi-target NGS panel, small variant (BRAF,HRAS,NRAS,KRAS)</td></tr><tr><td style="white-space:nowrap">M241.1<a name="GenomicTestCode-M241.461"> </a></td><td>Conjunctival melanoma, MYB &amp; 6cen (FISH)</td></tr><tr><td style="white-space:nowrap">M241.2<a name="GenomicTestCode-M241.462"> </a></td><td>Conjunctival melanoma, RREB1 (6p25) (FISH)</td></tr><tr><td style="white-space:nowrap">M241.3<a name="GenomicTestCode-M241.463"> </a></td><td>Conjunctival melanoma, CCND1 (11q13) (FISH)</td></tr><tr><td style="white-space:nowrap">M241.4<a name="GenomicTestCode-M241.464"> </a></td><td>Conjunctival melanoma, MYC &amp; 8cen (FISH)</td></tr><tr><td style="white-space:nowrap">M241.5<a name="GenomicTestCode-M241.465"> </a></td><td>Conjunctival melanoma, CDKN2A &amp; 9cen (FISH)</td></tr><tr><td style="white-space:nowrap">M242.1<a name="GenomicTestCode-M242.461"> </a></td><td>Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), STR Testing</td></tr><tr><td style="white-space:nowrap">M242.2<a name="GenomicTestCode-M242.462"> </a></td><td>Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), Sex chromosome FISH</td></tr><tr><td style="white-space:nowrap">M243.1<a name="GenomicTestCode-M243.461"> </a></td><td>Thymic Carcinoma, Multi-target NGS panel (KIT)</td></tr><tr><td style="white-space:nowrap">M244.1<a name="GenomicTestCode-M244.461"> </a></td><td>In all tumours elligible for NTRK1/2/3 testing, FISH</td></tr><tr><td style="white-space:nowrap">M245.1<a name="GenomicTestCode-M245.461"> </a></td><td>Ovarian sex cord stromal tumuors, Multi-target NGS panel-small variant (FOXL2, CTNNB1, APC, DICER1)</td></tr><tr><td style="white-space:nowrap">M25.1<a name="GenomicTestCode-M25.461"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, small variant (YAP1)</td></tr><tr><td style="white-space:nowrap">M25.10<a name="GenomicTestCode-M25.4610"> </a></td><td>Ependymoma, Paediatric, MYCN copy number FISH</td></tr><tr><td style="white-space:nowrap">M25.11<a name="GenomicTestCode-M25.4611"> </a></td><td>Ependymoma, Paediatric, ZFTA rearrangements (several fusion partners)</td></tr><tr><td style="white-space:nowrap">M25.2<a name="GenomicTestCode-M25.462"> </a></td><td>Ependymoma, Paediatric, YAP1 copy number FISH</td></tr><tr><td style="white-space:nowrap">M25.3<a name="GenomicTestCode-M25.463"> </a></td><td>Ependymoma, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M25.4<a name="GenomicTestCode-M25.464"> </a></td><td>Ependymoma, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M25.5<a name="GenomicTestCode-M25.465"> </a></td><td>Ependymoma, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M25.6<a name="GenomicTestCode-M25.466"> </a></td><td>Ependymoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M25.7<a name="GenomicTestCode-M25.467"> </a></td><td>Ependymoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M25.8<a name="GenomicTestCode-M25.468"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, copy number variant (YAP1, MYCN)</td></tr><tr><td style="white-space:nowrap">M25.9<a name="GenomicTestCode-M25.469"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, structural variant  (YAP1-C11orf95, YAP1-TFE3, C11orf95-RELA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M26.1<a name="GenomicTestCode-M26.461"> </a></td><td>Ependymoma Supratentorial, Adult, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M26.2<a name="GenomicTestCode-M26.462"> </a></td><td>Ependymoma, Adult, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M26.3<a name="GenomicTestCode-M26.463"> </a></td><td>Ependymoma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M26.4<a name="GenomicTestCode-M26.464"> </a></td><td>Ependymoma, Adult, Multi-target NGS panel, structural variant  (YAP1, RELA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M26.5<a name="GenomicTestCode-M26.465"> </a></td><td>Ependymoma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M26.6<a name="GenomicTestCode-M26.466"> </a></td><td>Ependymoma, Adult, ZFTA rearrangements (several fusion partners)</td></tr><tr><td style="white-space:nowrap">M27.1<a name="GenomicTestCode-M27.461"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M27.10<a name="GenomicTestCode-M27.4610"> </a></td><td>Glioblastoma, Adult, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M27.11<a name="GenomicTestCode-M27.4611"> </a></td><td>Glioblastoma, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M27.12<a name="GenomicTestCode-M27.4612"> </a></td><td>Glioblastoma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M27.13<a name="GenomicTestCode-M27.4613"> </a></td><td>Glioblastoma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M27.14<a name="GenomicTestCode-M27.4614"> </a></td><td>Glioblastoma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M27.15<a name="GenomicTestCode-M27.4615"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M27.16<a name="GenomicTestCode-M27.4616"> </a></td><td>Glioblastoma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M27.2<a name="GenomicTestCode-M27.462"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, copy number variant (EGFR, PDGFRA, MYC, PTEN, 1p, 19q)</td></tr><tr><td style="white-space:nowrap">M27.3<a name="GenomicTestCode-M27.463"> </a></td><td>Glioblastoma, Adult, EGFRvIII RT-PCR</td></tr><tr><td style="white-space:nowrap">M27.5<a name="GenomicTestCode-M27.465"> </a></td><td>Glioblastoma, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M27.6<a name="GenomicTestCode-M27.466"> </a></td><td>Glioblastoma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M27.7<a name="GenomicTestCode-M27.467"> </a></td><td>Glioblastoma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M27.9<a name="GenomicTestCode-M27.469"> </a></td><td>Glioblastoma, Adult, PDGFRA copy number FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M28.1<a name="GenomicTestCode-M28.461"> </a></td><td>Glioma, Adult, Multi-target NGS panel, small variant (H3C2, H3C3, H3C14, H3-3A, H3-3B, IDH1, IDH2, TP53, VHL, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M28.2<a name="GenomicTestCode-M28.462"> </a></td><td>Glioma, Adult, Multi-target NGS panel, copy number variant (EGFR, 1p, 19q)</td></tr><tr><td style="white-space:nowrap">M28.3<a name="GenomicTestCode-M28.463"> </a></td><td>Glioma, Adult, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M28.4<a name="GenomicTestCode-M28.464"> </a></td><td>Glioma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M28.5<a name="GenomicTestCode-M28.465"> </a></td><td>Glioma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M28.6<a name="GenomicTestCode-M28.466"> </a></td><td>Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M28.7<a name="GenomicTestCode-M28.467"> </a></td><td>Glioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M28.8<a name="GenomicTestCode-M28.468"> </a></td><td>Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M28.9<a name="GenomicTestCode-M28.469"> </a></td><td>Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M29.1<a name="GenomicTestCode-M29.461"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style="white-space:nowrap">M29.2<a name="GenomicTestCode-M29.462"> </a></td><td>High Grade Glioma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M29.3<a name="GenomicTestCode-M29.463"> </a></td><td>High Grade Glioma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M29.4<a name="GenomicTestCode-M29.464"> </a></td><td>High Grade Glioma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M29.5<a name="GenomicTestCode-M29.465"> </a></td><td>High Grade Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M29.6<a name="GenomicTestCode-M29.466"> </a></td><td>High Grade Glioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M29.7<a name="GenomicTestCode-M29.467"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M29.8<a name="GenomicTestCode-M29.468"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M29.9<a name="GenomicTestCode-M29.469"> </a></td><td>High Grade Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M3.12<a name="GenomicTestCode-M3.4612"> </a></td><td>Breast Cancer, Tumour profiling tests to guide adjuvant chemotherapy decisions in early breast cancer</td></tr><tr><td style="white-space:nowrap">M3.13<a name="GenomicTestCode-M3.4613"> </a></td><td>Breast Cancer, Multi-target ctDNA NGS panel, small variant (ESR1)</td></tr><tr><td style="white-space:nowrap">M3.5<a name="GenomicTestCode-M3.465"> </a></td><td>Breast Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M3.6<a name="GenomicTestCode-M3.466"> </a></td><td>Breast Cancer, Multi-target NGS panel, small variant (PIK3CA)</td></tr><tr><td style="white-space:nowrap">M3.7<a name="GenomicTestCode-M3.467"> </a></td><td>Breast Cancer, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M3.9<a name="GenomicTestCode-M3.469"> </a></td><td>Breast Cancer, ETV6-NTRK3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M30.1<a name="GenomicTestCode-M30.461"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, small variant (RB1, NF1)</td></tr><tr><td style="white-space:nowrap">M30.2<a name="GenomicTestCode-M30.462"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M30.3<a name="GenomicTestCode-M30.463"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M30.4<a name="GenomicTestCode-M30.464"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M31.1<a name="GenomicTestCode-M31.461"> </a></td><td>Low Grade Glioma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M31.2<a name="GenomicTestCode-M31.462"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style="white-space:nowrap">M31.3<a name="GenomicTestCode-M31.463"> </a></td><td>Low Grade Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M31.4<a name="GenomicTestCode-M31.464"> </a></td><td>Low Grade Glioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M31.5<a name="GenomicTestCode-M31.465"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M31.6<a name="GenomicTestCode-M31.466"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M31.7<a name="GenomicTestCode-M31.467"> </a></td><td>Low Grade Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M32.1<a name="GenomicTestCode-M32.461"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, small variant (BRAF, IDH1, IDH2, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style="white-space:nowrap">M32.2<a name="GenomicTestCode-M32.462"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M32.3<a name="GenomicTestCode-M32.463"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M32.4<a name="GenomicTestCode-M32.464"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M32.5<a name="GenomicTestCode-M32.465"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M32.6<a name="GenomicTestCode-M32.466"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M33.3<a name="GenomicTestCode-M33.463"> </a></td><td>Meningioma, Adult, Multi-target NGS panel, small variant (TERT promoter)</td></tr><tr><td style="white-space:nowrap">M33.4<a name="GenomicTestCode-M33.464"> </a></td><td>Meningioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M33.5<a name="GenomicTestCode-M33.465"> </a></td><td>Meningioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M34.1<a name="GenomicTestCode-M34.461"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style="white-space:nowrap">M34.2<a name="GenomicTestCode-M34.462"> </a></td><td>Non-Midline Glioma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M34.3<a name="GenomicTestCode-M34.463"> </a></td><td>Non-Midline Glioma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M34.4<a name="GenomicTestCode-M34.464"> </a></td><td>Non-Midline Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M34.5<a name="GenomicTestCode-M34.465"> </a></td><td>Non-Midline Glioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M34.6<a name="GenomicTestCode-M34.466"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M34.7<a name="GenomicTestCode-M34.467"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M34.8<a name="GenomicTestCode-M34.468"> </a></td><td>Non-Midline Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M35.1<a name="GenomicTestCode-M35.461"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M35.2<a name="GenomicTestCode-M35.462"> </a></td><td>OligodendroGlioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M35.4<a name="GenomicTestCode-M35.464"> </a></td><td>OligodendroGlioma, Adult, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M35.5<a name="GenomicTestCode-M35.465"> </a></td><td>OligodendroGlioma, Adult, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M35.6<a name="GenomicTestCode-M35.466"> </a></td><td>OligodendroGlioma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M35.7<a name="GenomicTestCode-M35.467"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style="white-space:nowrap">M35.8<a name="GenomicTestCode-M35.468"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M35.9<a name="GenomicTestCode-M35.469"> </a></td><td>OligodendroGlioma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M36.1<a name="GenomicTestCode-M36.461"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.10<a name="GenomicTestCode-M36.4610"> </a></td><td>Pilocytic Astrocytoma, Adult, KIAA1549 copy number FISH</td></tr><tr><td style="white-space:nowrap">M36.11<a name="GenomicTestCode-M36.4611"> </a></td><td>Pilocytic Astrocytoma, Adult, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M36.12<a name="GenomicTestCode-M36.4612"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, small variant (BRAF, CDKN2A)</td></tr><tr><td style="white-space:nowrap">M36.13<a name="GenomicTestCode-M36.4613"> </a></td><td>Pilocytic Astrocytoma, Adult, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M36.14<a name="GenomicTestCode-M36.4614"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M36.15<a name="GenomicTestCode-M36.4615"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, copy number variant (KIAA1549, CDKN2A)</td></tr><tr><td style="white-space:nowrap">M36.16<a name="GenomicTestCode-M36.4616"> </a></td><td>Pilocytic Astrocytoma, Adult, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M36.2<a name="GenomicTestCode-M36.462"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.3<a name="GenomicTestCode-M36.463"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.4<a name="GenomicTestCode-M36.464"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.5<a name="GenomicTestCode-M36.465"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.6<a name="GenomicTestCode-M36.466"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.7<a name="GenomicTestCode-M36.467"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.8<a name="GenomicTestCode-M36.468"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M36.9<a name="GenomicTestCode-M36.469"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M37.1<a name="GenomicTestCode-M37.461"> </a></td><td>Pineoblastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style="white-space:nowrap">M37.2<a name="GenomicTestCode-M37.462"> </a></td><td>Pineoblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M37.3<a name="GenomicTestCode-M37.463"> </a></td><td>Pineoblastoma, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M37.4<a name="GenomicTestCode-M37.464"> </a></td><td>Pineoblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M38.1<a name="GenomicTestCode-M38.461"> </a></td><td>Pituitary Tumours, MGMT promoter hyperMethylation</td></tr><tr><td style="white-space:nowrap">M38.2<a name="GenomicTestCode-M38.462"> </a></td><td>Pituitary Tumours, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style="white-space:nowrap">M38.3<a name="GenomicTestCode-M38.463"> </a></td><td>Pituitary Tumours, EGFR copy number FISH</td></tr><tr><td style="white-space:nowrap">M38.4<a name="GenomicTestCode-M38.464"> </a></td><td>Pituitary Tumours, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M38.5<a name="GenomicTestCode-M38.465"> </a></td><td>Pituitary Tumours, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M38.6<a name="GenomicTestCode-M38.466"> </a></td><td>Pituitary Tumours, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M39.1<a name="GenomicTestCode-M39.461"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, small variant (CDKN2A)</td></tr><tr><td style="white-space:nowrap">M39.2<a name="GenomicTestCode-M39.462"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M39.3<a name="GenomicTestCode-M39.463"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, DNA Methylation</td></tr><tr><td style="white-space:nowrap">M39.4<a name="GenomicTestCode-M39.464"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M4.1<a name="GenomicTestCode-M4.461"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET)</td></tr><tr><td style="white-space:nowrap">M4.10<a name="GenomicTestCode-M4.4610"> </a></td><td>Non-Small Cell Lung Cancer, EML4-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M4.11<a name="GenomicTestCode-M4.4611"> </a></td><td>Non-Small Cell Lung Cancer, ALK hotspot cDNA</td></tr><tr><td style="white-space:nowrap">M4.13<a name="GenomicTestCode-M4.4613"> </a></td><td>Non-Small Cell Lung Cancer, Combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping, ERBB2*) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon 14 skipping)</td></tr><tr><td style="white-space:nowrap">M4.14<a name="GenomicTestCode-M4.4614"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target ctDNA combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping and copy number variations) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon</td></tr><tr><td style="white-space:nowrap">M4.2<a name="GenomicTestCode-M4.462"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, structural variant (ROS1, RET, EML4-ALK, NTRK1, NTRK1, NTRK3, MET)</td></tr><tr><td style="white-space:nowrap">M4.3<a name="GenomicTestCode-M4.463"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, copy number variant (MET)</td></tr><tr><td style="white-space:nowrap">M4.4<a name="GenomicTestCode-M4.464"> </a></td><td>Non-Small Cell Lung Cancer, EGFR hotspot Tumor</td></tr><tr><td style="white-space:nowrap">M4.5<a name="GenomicTestCode-M4.465"> </a></td><td>Non-Small Cell Lung Cancer, EGFR hotspot ctDNA</td></tr><tr><td style="white-space:nowrap">M4.6<a name="GenomicTestCode-M4.466"> </a></td><td>Non-Small Cell Lung Cancer, ROS1 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M4.7<a name="GenomicTestCode-M4.467"> </a></td><td>Non-Small Cell Lung Cancer, RET rearrangement FISH/RT-PC</td></tr><tr><td style="white-space:nowrap">M4.8<a name="GenomicTestCode-M4.468"> </a></td><td>Non-Small Cell Lung Cancer, MET copy number FISH</td></tr><tr><td style="white-space:nowrap">M42.1<a name="GenomicTestCode-M42.461"> </a></td><td>Alveolar Rhabdomyosarcoma, FOXO1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M42.2<a name="GenomicTestCode-M42.462"> </a></td><td>Alveolar Rhabdomyosarcoma, PAX3-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M42.3<a name="GenomicTestCode-M42.463"> </a></td><td>Alveolar Rhabdomyosarcoma, PAX7-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M42.4<a name="GenomicTestCode-M42.464"> </a></td><td>Alveolar Rhabdomyosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M42.5<a name="GenomicTestCode-M42.465"> </a></td><td>Alveolar Rhabdomyosarcoma, Multi-target NGS panel, structural variant (FOXO1, PAX3-FOXO1, PAX7-FOXO1  NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M43.1<a name="GenomicTestCode-M43.461"> </a></td><td>Alveolar Soft Part Sarcoma, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M43.2<a name="GenomicTestCode-M43.462"> </a></td><td>Alveolar Soft Part Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M43.3<a name="GenomicTestCode-M43.463"> </a></td><td>Alveolar Soft Part Sarcoma, Multi-target NGS panel, structural variant (TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M44.1<a name="GenomicTestCode-M44.461"> </a></td><td>Aneurysmal Bone Cyst, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M44.2<a name="GenomicTestCode-M44.462"> </a></td><td>Aneurysmal Bone Cyst, Multi-target NGS panel, structural variant (USP6)</td></tr><tr><td style="white-space:nowrap">M45.1<a name="GenomicTestCode-M45.461"> </a></td><td>Angiomatoid Fibrous Histiocytoma, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M45.2<a name="GenomicTestCode-M45.462"> </a></td><td>Angiomatoid Fibrous Histiocytoma, FUS rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M45.3<a name="GenomicTestCode-M45.463"> </a></td><td>Angiomatoid Fibrous Histiocytoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M45.4<a name="GenomicTestCode-M45.464"> </a></td><td>Angiomatoid Fibrous Histiocytoma, Multi-target NGS panel, structural variant (EWSR1, FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M46.1<a name="GenomicTestCode-M46.461"> </a></td><td>Chondrosarcoma Conventional Central, Multi-target NGS panel, small variant (IDH1, IDH2)</td></tr><tr><td style="white-space:nowrap">M46.2<a name="GenomicTestCode-M46.462"> </a></td><td>Chondrosarcoma Conventional Central, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M46.3<a name="GenomicTestCode-M46.463"> </a></td><td>Chondrosarcoma Conventional Central, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M47.1<a name="GenomicTestCode-M47.461"> </a></td><td>Chondroblastoma, SNP Array</td></tr><tr><td style="white-space:nowrap">M47.2<a name="GenomicTestCode-M47.462"> </a></td><td>Chondroblastoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M47.3<a name="GenomicTestCode-M47.463"> </a></td><td>Chondroblastoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M48.1<a name="GenomicTestCode-M48.461"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M48.2<a name="GenomicTestCode-M48.462"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M48.3<a name="GenomicTestCode-M48.463"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M49.1<a name="GenomicTestCode-M49.461"> </a></td><td>CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M49.2<a name="GenomicTestCode-M49.462"> </a></td><td>CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M5.1<a name="GenomicTestCode-M5.461"> </a></td><td>Mesothelioma, CDKN2A copy number FISH</td></tr><tr><td style="white-space:nowrap">M5.2<a name="GenomicTestCode-M5.462"> </a></td><td>Mesothelioma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M5.3<a name="GenomicTestCode-M5.463"> </a></td><td>Mesothelioma, Multi-target NGS panel, copy number variant (CDKN2A)</td></tr><tr><td style="white-space:nowrap">M50.1<a name="GenomicTestCode-M50.461"> </a></td><td>Dermatofibrosarcoma Protuberans, COL1A1-PDGFB rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M50.2<a name="GenomicTestCode-M50.462"> </a></td><td>Dermatofibrosarcoma Protuberans, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M50.3<a name="GenomicTestCode-M50.463"> </a></td><td>Dermatofibrosarcoma Protuberans, Multi-target NGS panel, structural variant (COL1A1-PDGFB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M51.1<a name="GenomicTestCode-M51.461"> </a></td><td>Desmoid-Type Fibromatosis, Multi-target NGS panel, small variant (APC, CTNNB1)</td></tr><tr><td style="white-space:nowrap">M52.1<a name="GenomicTestCode-M52.461"> </a></td><td>Desmoplastic Small Round Cell Tumour, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M52.2<a name="GenomicTestCode-M52.462"> </a></td><td>Desmoplastic Small Round Cell Tumour, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M52.3<a name="GenomicTestCode-M52.463"> </a></td><td>Desmoplastic Small Round Cell Tumour, Multi-target NGS panel, structural variant (WT1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M53.1<a name="GenomicTestCode-M53.461"> </a></td><td>Endometrial Stromal Sarcoma, EPC1-PHF1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M53.2<a name="GenomicTestCode-M53.462"> </a></td><td>Endometrial Stromal Sarcoma, JAZF1-PHF1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M53.3<a name="GenomicTestCode-M53.463"> </a></td><td>Endometrial Stromal Sarcoma, JAZF1-SUZ12 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M53.4<a name="GenomicTestCode-M53.464"> </a></td><td>Endometrial Stromal Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M53.5<a name="GenomicTestCode-M53.465"> </a></td><td>Endometrial Stromal Sarcoma, Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NTRK1, NTRK2, NTRK3, ZC3H7B-BCOR)</td></tr><tr><td style="white-space:nowrap">M53.7<a name="GenomicTestCode-M53.467"> </a></td><td>Endometrial Stromal Sarcoma, ZC3H7B-BCOR rearrangment FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M54.1<a name="GenomicTestCode-M54.461"> </a></td><td>Epithelioid Haemangioendothelioma, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M54.2<a name="GenomicTestCode-M54.462"> </a></td><td>Epithelioid Haemangioendothelioma, Multi-target NGS panel, structural variant (WWTR1-CAMTA1)</td></tr><tr><td style="white-space:nowrap">M55.1<a name="GenomicTestCode-M55.461"> </a></td><td>Ewing Like Sarcoma/PNET, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M55.2<a name="GenomicTestCode-M55.462"> </a></td><td>Ewing Like Sarcoma/PNET, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M55.3<a name="GenomicTestCode-M55.463"> </a></td><td>Ewing Like Sarcoma/PNET, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M56.1<a name="GenomicTestCode-M56.461"> </a></td><td>Ewing Sarcoma of Bone, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M56.2<a name="GenomicTestCode-M56.462"> </a></td><td>Ewing Sarcoma of Bone, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M56.3<a name="GenomicTestCode-M56.463"> </a></td><td>Ewing Sarcoma of Bone, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M57.1<a name="GenomicTestCode-M57.461"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M57.2<a name="GenomicTestCode-M57.462"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M57.3<a name="GenomicTestCode-M57.463"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M58.1<a name="GenomicTestCode-M58.461"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, NR4A3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M58.2<a name="GenomicTestCode-M58.462"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M58.3<a name="GenomicTestCode-M58.463"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, Multi-target NGS panel, structural variant (NR4A3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M59.1<a name="GenomicTestCode-M59.461"> </a></td><td>Fibrous Dysplasia/Myxomas (Mazabraud Syndrome), Multi-target NGS panel, small variant (GNAS)</td></tr><tr><td style="white-space:nowrap">M6.1<a name="GenomicTestCode-M6.461"> </a></td><td>Mucoepidermoid Carcinoma, MAML2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M6.2<a name="GenomicTestCode-M6.462"> </a></td><td>Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M6.3<a name="GenomicTestCode-M6.463"> </a></td><td>Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2)</td></tr><tr><td style="white-space:nowrap">M6.5<a name="GenomicTestCode-M6.465"> </a></td><td>Mucoepidermoid Carcinoma, DPYD hotspot</td></tr><tr><td style="white-space:nowrap">M60.1<a name="GenomicTestCode-M60.461"> </a></td><td>Giant Cell Tumour of Bone, H3-3B hotspot</td></tr><tr><td style="white-space:nowrap">M60.2<a name="GenomicTestCode-M60.462"> </a></td><td>Giant Cell Tumour of Bone, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M60.3<a name="GenomicTestCode-M60.463"> </a></td><td>Giant Cell Tumour of Bone, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M61.1<a name="GenomicTestCode-M61.461"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M61.2<a name="GenomicTestCode-M61.462"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M61.3<a name="GenomicTestCode-M61.463"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M62.1<a name="GenomicTestCode-M62.461"> </a></td><td>Infantile Fibrosarcoma, ETV6-NTRK3 RT-PCR or FISH</td></tr><tr><td style="white-space:nowrap">M62.2<a name="GenomicTestCode-M62.462"> </a></td><td>Infantile Fibrosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M62.3<a name="GenomicTestCode-M62.463"> </a></td><td>Infantile Fibrosarcoma, Multi-target NGS panel, structural variant (ETV6-NTRK3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M63.1<a name="GenomicTestCode-M63.461"> </a></td><td>Inflammatory Myofibroblastic Tumour, TPM4-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M63.2<a name="GenomicTestCode-M63.462"> </a></td><td>Inflammatory Myofibroblastic Tumour, TPM3-ALK FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M63.3<a name="GenomicTestCode-M63.463"> </a></td><td>Inflammatory Myofibroblastic Tumour, Multi-target NGS panel, structural variant (ALK, TPM4-ALK, TPM3-ALK, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M63.4<a name="GenomicTestCode-M63.464"> </a></td><td>Inflammatory Myofibroblastic Tumour, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M64.1<a name="GenomicTestCode-M64.461"> </a></td><td>Low Grade Fibromyxoid Sarcoma, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M64.2<a name="GenomicTestCode-M64.462"> </a></td><td>Low Grade Fibromyxoid Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M64.3<a name="GenomicTestCode-M64.463"> </a></td><td>Low Grade Fibromyxoid Sarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M65.1<a name="GenomicTestCode-M65.461"> </a></td><td>Mesenchymal Chondrosarcoma, HEY1-NCOA2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M65.2<a name="GenomicTestCode-M65.462"> </a></td><td>Mesenchymal Chondrosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M65.3<a name="GenomicTestCode-M65.463"> </a></td><td>Mesenchymal Chondrosarcoma, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M66.1<a name="GenomicTestCode-M66.461"> </a></td><td>Myoepithelial Tumours of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M66.2<a name="GenomicTestCode-M66.462"> </a></td><td>Myoepithelial Tumours of Soft Tissue, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M66.3<a name="GenomicTestCode-M66.463"> </a></td><td>Myoepithelial Tumours of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M67.1<a name="GenomicTestCode-M67.461"> </a></td><td>Myxoid/Round Cell Liposarcoma, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M67.2<a name="GenomicTestCode-M67.462"> </a></td><td>Myxoid/Round Cell Liposarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M67.3<a name="GenomicTestCode-M67.463"> </a></td><td>Myxoid/Round Cell Liposarcoma, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M67.4<a name="GenomicTestCode-M67.464"> </a></td><td>Myxoid/Round Cell Lipsarcoma, MDM2 amplification FISH</td></tr><tr><td style="white-space:nowrap">M68.1<a name="GenomicTestCode-M68.461"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, TGFBR3-OGA FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M68.2<a name="GenomicTestCode-M68.462"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M68.3<a name="GenomicTestCode-M68.463"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M68.4<a name="GenomicTestCode-M68.464"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, structural variant (TGFBR3-OGA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M68.5<a name="GenomicTestCode-M68.465"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M69.1<a name="GenomicTestCode-M69.461"> </a></td><td>Nodular Fasciitis, USP6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M69.2<a name="GenomicTestCode-M69.462"> </a></td><td>Nodular Fasciitis, Multi-target NGS panel, structural variant (USP6)</td></tr><tr><td style="white-space:nowrap">M7.1<a name="GenomicTestCode-M7.461"> </a></td><td>Melanoma, Adult, Multi-target NGS panel, small variant (BRAF, KIT, NRAS)</td></tr><tr><td style="white-space:nowrap">M7.10<a name="GenomicTestCode-M7.4610"> </a></td><td>Melanoma, Adult, Copy number variant detection to genomewide resolution</td></tr><tr><td style="white-space:nowrap">M7.2<a name="GenomicTestCode-M7.462"> </a></td><td>Melanoma, Adult, BRAF hotspot</td></tr><tr><td style="white-space:nowrap">M7.3<a name="GenomicTestCode-M7.463"> </a></td><td>Melanoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M7.5<a name="GenomicTestCode-M7.465"> </a></td><td>Melanoma, Adult, MYB &amp; 6cen (FISH)</td></tr><tr><td style="white-space:nowrap">M7.6<a name="GenomicTestCode-M7.466"> </a></td><td>Melanoma, Adult, RREB1 (6p25)</td></tr><tr><td style="white-space:nowrap">M7.7<a name="GenomicTestCode-M7.467"> </a></td><td>Melanoma, Adult, CCND1 (11q13)</td></tr><tr><td style="white-space:nowrap">M7.8<a name="GenomicTestCode-M7.468"> </a></td><td>Melanoma, Adult, MYC &amp; 8cen</td></tr><tr><td style="white-space:nowrap">M7.9<a name="GenomicTestCode-M7.469"> </a></td><td>Melanoma, Adult, CDKN2A &amp; 9cen</td></tr><tr><td style="white-space:nowrap">M70.1<a name="GenomicTestCode-M70.461"> </a></td><td>Osteosarcoma, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M70.2<a name="GenomicTestCode-M70.462"> </a></td><td>Osteosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M70.3<a name="GenomicTestCode-M70.463"> </a></td><td>Osteosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M70.4<a name="GenomicTestCode-M70.464"> </a></td><td>Osteosarcoma, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style="white-space:nowrap">M71.1<a name="GenomicTestCode-M71.461"> </a></td><td>Phosphaturic Mesenchymal Tumour, FN1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M71.2<a name="GenomicTestCode-M71.462"> </a></td><td>Phosphaturic Mesenchymal Tumour, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M71.3<a name="GenomicTestCode-M71.463"> </a></td><td>Phosphaturic Mesenchymal Tumour, Multi-target NGS panel, structural variant (FN1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M72.1<a name="GenomicTestCode-M72.461"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M72.2<a name="GenomicTestCode-M72.462"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M72.3<a name="GenomicTestCode-M72.463"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M73.1<a name="GenomicTestCode-M73.461"> </a></td><td>Pseudomyogenic Haemangioendothelioma, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M73.2<a name="GenomicTestCode-M73.462"> </a></td><td>Pseudomyogenic Haemangioendothelioma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M73.3<a name="GenomicTestCode-M73.463"> </a></td><td>Pseudomyogenic Haemangioendothelioma, Multi-target NGS panel, structural variant (SERPINE1-FOSB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M74.1<a name="GenomicTestCode-M74.461"> </a></td><td>Radiation Induced Angiosarcoma, MYC copy number FISH</td></tr><tr><td style="white-space:nowrap">M74.2<a name="GenomicTestCode-M74.462"> </a></td><td>Radiation Induced Angiosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M74.3<a name="GenomicTestCode-M74.463"> </a></td><td>Radiation Induced Angiosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M74.4<a name="GenomicTestCode-M74.464"> </a></td><td>Radiation Induced Angiosarcoma, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style="white-space:nowrap">M75.1<a name="GenomicTestCode-M75.461"> </a></td><td>Round Cell Sarcoma Nos, Multi-target NGS panel, structural variant (BCOR, CIC, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M75.2<a name="GenomicTestCode-M75.462"> </a></td><td>Round Cell Sarcoma Nos, BCOR-CCNB3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M75.3<a name="GenomicTestCode-M75.463"> </a></td><td>Round Cell Sarcoma Nos, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M76.1<a name="GenomicTestCode-M76.461"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M76.2<a name="GenomicTestCode-M76.462"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M76.3<a name="GenomicTestCode-M76.463"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M77.1<a name="GenomicTestCode-M77.461"> </a></td><td>Synovial Sarcoma, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style="white-space:nowrap">M77.2<a name="GenomicTestCode-M77.462"> </a></td><td>Synovial Sarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M77.3<a name="GenomicTestCode-M77.463"> </a></td><td>Synovial Sarcoma, Multi-target NGS panel, structural variant (SS18, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M78.1<a name="GenomicTestCode-M78.461"> </a></td><td>Undifferentiated Round Cell Sarcoma of Infancy, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M78.2<a name="GenomicTestCode-M78.462"> </a></td><td>Undifferentiated Round Cell Sarcoma of Infancy, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M79.1<a name="GenomicTestCode-M79.461"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, MDM2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M79.2<a name="GenomicTestCode-M79.462"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M79.3<a name="GenomicTestCode-M79.463"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M79.4<a name="GenomicTestCode-M79.464"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, copy number variant (MDM2, DDIT3)</td></tr><tr><td style="white-space:nowrap">M79.6<a name="GenomicTestCode-M79.466"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number FISH</td></tr><tr><td style="white-space:nowrap">M79.7<a name="GenomicTestCode-M79.467"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number RT-PCR/ddPCR</td></tr><tr><td style="white-space:nowrap">M8.1<a name="GenomicTestCode-M8.461"> </a></td><td>Gastrointestinal Stromal Tumour, Multi-target NGS panel, small variant (KIT, PDGFRA)</td></tr><tr><td style="white-space:nowrap">M8.2<a name="GenomicTestCode-M8.462"> </a></td><td>Gastrointestinal Stromal Tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M80.1<a name="GenomicTestCode-M80.461"> </a></td><td>Acute Myeloid Leukaemia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M80.10<a name="GenomicTestCode-M80.4610"> </a></td><td>Acute Myeloid Leukaemia, MRD PML-RARA RT-qPCR</td></tr><tr><td style="white-space:nowrap">M80.11<a name="GenomicTestCode-M80.4611"> </a></td><td>Acute Myeloid Leukaemia, MRD RUNX1-RUNX1T1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M80.12<a name="GenomicTestCode-M80.4612"> </a></td><td>Acute Myeloid Leukaemia, MRD CBFB-MYH11 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M80.13<a name="GenomicTestCode-M80.4613"> </a></td><td>Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M80.14<a name="GenomicTestCode-M80.4614"> </a></td><td>Acute Myeloid Leukaemia, MRD other QF-PCR</td></tr><tr><td style="white-space:nowrap">M80.15<a name="GenomicTestCode-M80.4615"> </a></td><td>Acute Myeloid Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style="white-space:nowrap">M80.18<a name="GenomicTestCode-M80.4618"> </a></td><td>Acute Myeloid Leukaemia, FLT3 ITD</td></tr><tr><td style="white-space:nowrap">M80.19<a name="GenomicTestCode-M80.4619"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (GATA1)</td></tr><tr><td style="white-space:nowrap">M80.2<a name="GenomicTestCode-M80.462"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD), PPM1D, DDX41, PHF6, CUX1</td></tr><tr><td style="white-space:nowrap">M80.21<a name="GenomicTestCode-M80.4621"> </a></td><td>Acute Myeloid Leukaemia, FLT3 TKD hotspot</td></tr><tr><td style="white-space:nowrap">M80.22<a name="GenomicTestCode-M80.4622"> </a></td><td>Acute Myeloid Leukaemia, NPM1 exon 12 hotspot</td></tr><tr><td style="white-space:nowrap">M80.23<a name="GenomicTestCode-M80.4623"> </a></td><td>Acute Myeloid Leukaemia, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M80.24<a name="GenomicTestCode-M80.4624"> </a></td><td>Acute Myeloid Leukaemia, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M80.25<a name="GenomicTestCode-M80.4625"> </a></td><td>Acute Myeloid Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M80.26<a name="GenomicTestCode-M80.4626"> </a></td><td>Acute Myeloid Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M80.27<a name="GenomicTestCode-M80.4627"> </a></td><td>Acute Myeloid Leukaemia, Chr17/Chr17p copy number FISH</td></tr><tr><td style="white-space:nowrap">M80.28<a name="GenomicTestCode-M80.4628"> </a></td><td>Acute Myeloid Leukaemia, Chr12/Chr12p copy number FISH</td></tr><tr><td style="white-space:nowrap">M80.29<a name="GenomicTestCode-M80.4629"> </a></td><td>Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA FISH</td></tr><tr><td style="white-space:nowrap">M80.3<a name="GenomicTestCode-M80.463"> </a></td><td>Acute Myeloid Leukaemia, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)</td></tr><tr><td style="white-space:nowrap">M80.30<a name="GenomicTestCode-M80.4630"> </a></td><td>Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH</td></tr><tr><td style="white-space:nowrap">M80.31<a name="GenomicTestCode-M80.4631"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 FISH</td></tr><tr><td style="white-space:nowrap">M80.32<a name="GenomicTestCode-M80.4632"> </a></td><td>Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH</td></tr><tr><td style="white-space:nowrap">M80.33<a name="GenomicTestCode-M80.4633"> </a></td><td>Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 FISH</td></tr><tr><td style="white-space:nowrap">M80.34<a name="GenomicTestCode-M80.4634"> </a></td><td>Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM FISH</td></tr><tr><td style="white-space:nowrap">M80.35<a name="GenomicTestCode-M80.4635"> </a></td><td>Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA FISH</td></tr><tr><td style="white-space:nowrap">M80.36<a name="GenomicTestCode-M80.4636"> </a></td><td>Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M80.37<a name="GenomicTestCode-M80.4637"> </a></td><td>Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 FISH</td></tr><tr><td style="white-space:nowrap">M80.38<a name="GenomicTestCode-M80.4638"> </a></td><td>Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 FISH</td></tr><tr><td style="white-space:nowrap">M80.39<a name="GenomicTestCode-M80.4639"> </a></td><td>Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 FISH</td></tr><tr><td style="white-space:nowrap">M80.40<a name="GenomicTestCode-M80.4640"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH</td></tr><tr><td style="white-space:nowrap">M80.41<a name="GenomicTestCode-M80.4641"> </a></td><td>Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.42<a name="GenomicTestCode-M80.4642"> </a></td><td>Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.43<a name="GenomicTestCode-M80.4643"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.44<a name="GenomicTestCode-M80.4644"> </a></td><td>Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.45<a name="GenomicTestCode-M80.4645"> </a></td><td>Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.46<a name="GenomicTestCode-M80.4646"> </a></td><td>Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.47<a name="GenomicTestCode-M80.4647"> </a></td><td>Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.48<a name="GenomicTestCode-M80.4648"> </a></td><td>Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.49<a name="GenomicTestCode-M80.4649"> </a></td><td>Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.5<a name="GenomicTestCode-M80.465"> </a></td><td>Acute Myeloid Leukaemia, Other: See tests M80.25-M80.40 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M80.50<a name="GenomicTestCode-M80.4650"> </a></td><td>Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.51<a name="GenomicTestCode-M80.4651"> </a></td><td>Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.52<a name="GenomicTestCode-M80.4652"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M80.53<a name="GenomicTestCode-M80.4653"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, copy number variant (Monosomal karyotype, del5/del5q, del7/del7q, del17/del17p, del12/del12p)</td></tr><tr><td style="white-space:nowrap">M80.54<a name="GenomicTestCode-M80.4654"> </a></td><td>Acute Myeloid Leukaemia, NUP98 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M80.55<a name="GenomicTestCode-M80.4655"> </a></td><td>Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M80.56<a name="GenomicTestCode-M80.4656"> </a></td><td>Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M80.57<a name="GenomicTestCode-M80.4657"> </a></td><td>Acute Myeloid Leukaemia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M80.58<a name="GenomicTestCode-M80.4658"> </a></td><td>Acute Myeloid Leukaemia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M80.7<a name="GenomicTestCode-M80.467"> </a></td><td>Acute Myeloid Leukaemia, Other RT-PCR: See tests M80.41-80.52 for individual specified RT-PCR targets.</td></tr><tr><td style="white-space:nowrap">M80.8<a name="GenomicTestCode-M80.468"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of  Complex karyotype)</td></tr><tr><td style="white-space:nowrap">M80.9<a name="GenomicTestCode-M80.469"> </a></td><td>Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M81.1<a name="GenomicTestCode-M81.461"> </a></td><td>Transient Abnormal Myelopoiesis, Multi-target NGS panel, small variant (GATA1)</td></tr><tr><td style="white-space:nowrap">M82.1<a name="GenomicTestCode-M82.461"> </a></td><td>Myelodysplasia, Multi-target NGS panel, small variant (TP53, SF3B1, IDH1, IDH2, NRAS, KRAS, TET2, SRSF2, ASXL1, DNMT3A, RUNX1, U2AF1, EZH2, BCOR, PTPN11, JAK2, SETBP1, PPM1D, DDX41, PHF6, CUX1, UBA1)</td></tr><tr><td style="white-space:nowrap">M82.10<a name="GenomicTestCode-M82.4610"> </a></td><td>Myelodysplasia, Chr13/Chr13q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.11<a name="GenomicTestCode-M82.4611"> </a></td><td>Myelodysplasia, Chr11q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.12<a name="GenomicTestCode-M82.4612"> </a></td><td>Myelodysplasia, Chr12p copy number FISH, t(12p) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M82.13<a name="GenomicTestCode-M82.4613"> </a></td><td>Myelodysplasia, Chr9q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.14<a name="GenomicTestCode-M82.4614"> </a></td><td>Myelodysplasia, Chr17/Chr17p copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.15<a name="GenomicTestCode-M82.4615"> </a></td><td>Myelodysplasia, idic(X)(q13) FISH</td></tr><tr><td style="white-space:nowrap">M82.16<a name="GenomicTestCode-M82.4616"> </a></td><td>Myelodysplasia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p &amp; idic(X)(q13);-Y; del 20q; +8; +19,del(3q)</td></tr><tr><td style="white-space:nowrap">M82.17<a name="GenomicTestCode-M82.4617"> </a></td><td>Myelodysplasia, Multi-target NGS panel, structural variant (t(12p), t(17p);inv(3)/t(3q)/del(3q)</td></tr><tr><td style="white-space:nowrap">M82.18<a name="GenomicTestCode-M82.4618"> </a></td><td>Myelodysplasia, ChrY copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.19<a name="GenomicTestCode-M82.4619"> </a></td><td>Myelodysplasia, Chr20/20q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.2<a name="GenomicTestCode-M82.462"> </a></td><td>Myelodysplasia, Karyotype (To include detection of complex karyotype, -7/del7q, -5/del5q, i(17q)/t(17p), -13/del13q, del11q, del12p/t(12p), del9q, del17/del17p &amp; idic(X)(q13)); -Y; del 20q; +8; +19,(inv(3)/t(3q)/del(3q))</td></tr><tr><td style="white-space:nowrap">M82.20<a name="GenomicTestCode-M82.4620"> </a></td><td>Myelodysplasia, Chr8 copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.21<a name="GenomicTestCode-M82.4621"> </a></td><td>Myelodysplasia, Chr19 copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.22<a name="GenomicTestCode-M82.4622"> </a></td><td>Myelodysplasia, inv(3)/t(3q)/del(3q)</td></tr><tr><td style="white-space:nowrap">M82.23<a name="GenomicTestCode-M82.4623"> </a></td><td>Myelodysplasia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M82.24<a name="GenomicTestCode-M82.4624"> </a></td><td>Myelodysplasia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M82.4<a name="GenomicTestCode-M82.464"> </a></td><td>Myelodysplasia, FISH copy number and rearrangement Other: See tests M82.7 -M82.22 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M82.6<a name="GenomicTestCode-M82.466"> </a></td><td>Myelodysplasia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M82.7<a name="GenomicTestCode-M82.467"> </a></td><td>Myelodysplasia, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.8<a name="GenomicTestCode-M82.468"> </a></td><td>Myelodysplasia, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M82.9<a name="GenomicTestCode-M82.469"> </a></td><td>Myelodysplasia, i(17q)/t(17p) FISH</td></tr><tr><td style="white-space:nowrap">M83.1<a name="GenomicTestCode-M83.461"> </a></td><td>Aplastic Anaemia, Karyotype (Genomewide)</td></tr><tr><td style="white-space:nowrap">M83.3<a name="GenomicTestCode-M83.463"> </a></td><td>Aplastic Anaemia, FISH copy number and rearrangement</td></tr><tr><td style="white-space:nowrap">M83.4<a name="GenomicTestCode-M83.464"> </a></td><td>Aplastic Anaemia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M83.5<a name="GenomicTestCode-M83.465"> </a></td><td>Aplastic Anaemia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M83.6<a name="GenomicTestCode-M83.466"> </a></td><td>Aplastic Anaemia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M84.1<a name="GenomicTestCode-M84.461"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 multiplex</td></tr><tr><td style="white-space:nowrap">M84.11<a name="GenomicTestCode-M84.4611"> </a></td><td>Chronic Myeloid Leukaemia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M84.12<a name="GenomicTestCode-M84.4612"> </a></td><td>Chronic Myeloid Leukaemia, Chr8 copy number FISH</td></tr><tr><td style="white-space:nowrap">M84.13<a name="GenomicTestCode-M84.4613"> </a></td><td>Chronic Myeloid Leukaemia, Chr19 copy number FISH</td></tr><tr><td style="white-space:nowrap">M84.14<a name="GenomicTestCode-M84.4614"> </a></td><td>Chronic Myeloid Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M84.15<a name="GenomicTestCode-M84.4615"> </a></td><td>Chronic Myeloid Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M84.16<a name="GenomicTestCode-M84.4616"> </a></td><td>Chronic Myeloid Leukaemia, i(17q) FISH</td></tr><tr><td style="white-space:nowrap">M84.17<a name="GenomicTestCode-M84.4617"> </a></td><td>Chronic Myeloid Leukaemia, Chr12p copy number FISH</td></tr><tr><td style="white-space:nowrap">M84.18<a name="GenomicTestCode-M84.4618"> </a></td><td>Chronic Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH and related abnormalities i.e. 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11)</td></tr><tr><td style="white-space:nowrap">M84.19<a name="GenomicTestCode-M84.4619"> </a></td><td>Chronic Myeloid Leukaemia, Inv(3) MECOM FISH</td></tr><tr><td style="white-space:nowrap">M84.2<a name="GenomicTestCode-M84.462"> </a></td><td>Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M84.20<a name="GenomicTestCode-M84.4620"> </a></td><td>Chronic Myeloid Leukaemia, 11q23 (KMT2A) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M84.21<a name="GenomicTestCode-M84.4621"> </a></td><td>Chronic Myeloid Leukaemia, Multi-target NGS panel, copy number variant (trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-)</td></tr><tr><td style="white-space:nowrap">M84.22<a name="GenomicTestCode-M84.4622"> </a></td><td>Chronic Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)</td></tr><tr><td style="white-space:nowrap">M84.23<a name="GenomicTestCode-M84.4623"> </a></td><td>Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M84.24<a name="GenomicTestCode-M84.4624"> </a></td><td>Chronic Myeloid Leukaemia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M84.25<a name="GenomicTestCode-M84.4625"> </a></td><td>Chronic Myeloid Leukaemia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M84.3<a name="GenomicTestCode-M84.463"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M84.4<a name="GenomicTestCode-M84.464"> </a></td><td>Chronic Myeloid Leukaemia, Karyotype (To include detection of trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-&amp; t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)</td></tr><tr><td style="white-space:nowrap">M84.6<a name="GenomicTestCode-M84.466"> </a></td><td>Chronic Myeloid Leukaemia, FISH copy number and rearrangement Other: See tests M84.12 M84.20 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M84.8<a name="GenomicTestCode-M84.468"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style="white-space:nowrap">M85.1<a name="GenomicTestCode-M85.461"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)</td></tr><tr><td style="white-space:nowrap">M85.10<a name="GenomicTestCode-M85.4610"> </a></td><td>Myeloproliferative Neoplasm, PCM1-JAK2 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M85.11<a name="GenomicTestCode-M85.4611"> </a></td><td>Myeloproliferative Neoplasm, BCR-ABL1 multiplex</td></tr><tr><td style="white-space:nowrap">M85.12<a name="GenomicTestCode-M85.4612"> </a></td><td>Myeloproliferative Neoplasm, Other RT-PCR</td></tr><tr><td style="white-space:nowrap">M85.13<a name="GenomicTestCode-M85.4613"> </a></td><td>Myeloproliferative Neoplasm, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M85.14<a name="GenomicTestCode-M85.4614"> </a></td><td>Myeloproliferative Neoplasm, JAK2 V617F hotspot</td></tr><tr><td style="white-space:nowrap">M85.15<a name="GenomicTestCode-M85.4615"> </a></td><td>Myeloproliferative Neoplasm, JAK2  exon 12 hotspot</td></tr><tr><td style="white-space:nowrap">M85.16<a name="GenomicTestCode-M85.4616"> </a></td><td>Myeloproliferative Neoplasm, CALR exon 9 hotspot</td></tr><tr><td style="white-space:nowrap">M85.17<a name="GenomicTestCode-M85.4617"> </a></td><td>Myeloproliferative Neoplasm, MPL exon 10 hotspot</td></tr><tr><td style="white-space:nowrap">M85.19<a name="GenomicTestCode-M85.4619"> </a></td><td>Myeloproliferative Neoplasm, Chr8 copy number FISH</td></tr><tr><td style="white-space:nowrap">M85.2<a name="GenomicTestCode-M85.462"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, small variant</td></tr><tr><td style="white-space:nowrap">M85.20<a name="GenomicTestCode-M85.4620"> </a></td><td>Myeloproliferative Neoplasm, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M85.21<a name="GenomicTestCode-M85.4621"> </a></td><td>Myeloproliferative Neoplasm, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M85.22<a name="GenomicTestCode-M85.4622"> </a></td><td>Myeloproliferative Neoplasm, i(17q) FISH</td></tr><tr><td style="white-space:nowrap">M85.23<a name="GenomicTestCode-M85.4623"> </a></td><td>Myeloproliferative Neoplasm, Chr12p copy number FISH</td></tr><tr><td style="white-space:nowrap">M85.24<a name="GenomicTestCode-M85.4624"> </a></td><td>Myeloproliferative Neoplasm, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M85.25<a name="GenomicTestCode-M85.4625"> </a></td><td>Myeloproliferative Neoplasm, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)</td></tr><tr><td style="white-space:nowrap">M85.26<a name="GenomicTestCode-M85.4626"> </a></td><td>Myeloproliferative Neoplasm, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)</td></tr><tr><td style="white-space:nowrap">M85.27<a name="GenomicTestCode-M85.4627"> </a></td><td>Myeloproliferative Neoplasm, FGFR1 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M85.28<a name="GenomicTestCode-M85.4628"> </a></td><td>Myeloproliferative Neoplasm, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)</td></tr><tr><td style="white-space:nowrap">M85.29<a name="GenomicTestCode-M85.4629"> </a></td><td>Myeloproliferative Neoplasm, inv(3)/t(3;3) FISH</td></tr><tr><td style="white-space:nowrap">M85.3<a name="GenomicTestCode-M85.463"> </a></td><td>Myeloproliferative Neoplasm, Karyotype (To include detection of complex karyotype)</td></tr><tr><td style="white-space:nowrap">M85.30<a name="GenomicTestCode-M85.4630"> </a></td><td>Myeloproliferative Neoplasm, 11q23 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M85.31<a name="GenomicTestCode-M85.4631"> </a></td><td>Myeloproliferative Neoplasm, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)</td></tr><tr><td style="white-space:nowrap">M85.32<a name="GenomicTestCode-M85.4632"> </a></td><td>Myeloproliferative Neoplasm, FLT3 rearragement FISH</td></tr><tr><td style="white-space:nowrap">M85.33<a name="GenomicTestCode-M85.4633"> </a></td><td>Myeloproliferative Neoplasm, RET rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M85.34<a name="GenomicTestCode-M85.4634"> </a></td><td>Myeloproliferative Neoplasm, NTRK3 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M85.35<a name="GenomicTestCode-M85.4635"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M85.36<a name="GenomicTestCode-M85.4636"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)</td></tr><tr><td style="white-space:nowrap">M85.37<a name="GenomicTestCode-M85.4637"> </a></td><td>Myeloproliferative Neoplasm, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M85.38<a name="GenomicTestCode-M85.4638"> </a></td><td>Myeloproliferative Neoplasm, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M85.5<a name="GenomicTestCode-M85.465"> </a></td><td>Myeloproliferative Neoplasm, FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M85.7<a name="GenomicTestCode-M85.467"> </a></td><td>Myeloproliferative Neoplasm, FIP1L1-PDGFRA (4q12) FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M85.8<a name="GenomicTestCode-M85.468"> </a></td><td>Myeloproliferative Neoplasm, FIP1L1-PDGFRA RT-qPCR</td></tr><tr><td style="white-space:nowrap">M85.9<a name="GenomicTestCode-M85.469"> </a></td><td>Myeloproliferative Neoplasm, ETV6-PDGFRB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M86.1<a name="GenomicTestCode-M86.461"> </a></td><td>Systemic Mastocytosis, Multi-target NGS panel, small variant (KIT)</td></tr><tr><td style="white-space:nowrap">M86.2<a name="GenomicTestCode-M86.462"> </a></td><td>Systemic Mastocytosis, KIT D816 QF-PCR</td></tr><tr><td style="white-space:nowrap">M86.3<a name="GenomicTestCode-M86.463"> </a></td><td>Systemic Mastocytosis, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M86.4<a name="GenomicTestCode-M86.464"> </a></td><td>Systemic Mastocytosis, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M86.5<a name="GenomicTestCode-M86.465"> </a></td><td>Systemic Mastocytosis, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M87.1<a name="GenomicTestCode-M87.461"> </a></td><td>Chronic Neutrophilic Leukaemia, Multi-target NGS panel, small variant (CSF3R)</td></tr><tr><td style="white-space:nowrap">M88.1<a name="GenomicTestCode-M88.461"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant (PTPN11, KRAS, NRAS, NF1, CBL)</td></tr><tr><td style="white-space:nowrap">M88.10<a name="GenomicTestCode-M88.4610"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, trisomy 8)</td></tr><tr><td style="white-space:nowrap">M88.11<a name="GenomicTestCode-M88.4611"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M88.12<a name="GenomicTestCode-M88.4612"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M88.2<a name="GenomicTestCode-M88.462"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M88.3<a name="GenomicTestCode-M88.463"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant</td></tr><tr><td style="white-space:nowrap">M88.4<a name="GenomicTestCode-M88.464"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Karyotype</td></tr><tr><td style="white-space:nowrap">M88.5<a name="GenomicTestCode-M88.465"> </a></td><td>Juvenile Myelomonocytic Leukaemia, FISH copy number and rearrangement Other: See tests M88.7-M88.9 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M88.7<a name="GenomicTestCode-M88.467"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr8 copy number FISH</td></tr><tr><td style="white-space:nowrap">M88.8<a name="GenomicTestCode-M88.468"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M88.9<a name="GenomicTestCode-M88.469"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M89.1<a name="GenomicTestCode-M89.461"> </a></td><td>Acute Leukaemia Other, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M89.10<a name="GenomicTestCode-M89.4610"> </a></td><td>Acute Leukaemia Other, MRD PML-RARA RT-qPCR</td></tr><tr><td style="white-space:nowrap">M89.100<a name="GenomicTestCode-M89.46100"> </a></td><td>Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.101<a name="GenomicTestCode-M89.46101"> </a></td><td>Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.102<a name="GenomicTestCode-M89.46102"> </a></td><td>Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.103<a name="GenomicTestCode-M89.46103"> </a></td><td>Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.104<a name="GenomicTestCode-M89.46104"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, copy number variant</td></tr><tr><td style="white-space:nowrap">M89.105<a name="GenomicTestCode-M89.46105"> </a></td><td>Acute Leukaemia Other, NUP98 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.106<a name="GenomicTestCode-M89.46106"> </a></td><td>Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M89.107<a name="GenomicTestCode-M89.46107"> </a></td><td>Acute Leukaemia Other, MRD NPM1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M89.108<a name="GenomicTestCode-M89.46108"> </a></td><td>Acute Leukaemia Other, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M89.109<a name="GenomicTestCode-M89.46109"> </a></td><td>Acute Leukaemia Other, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M89.11<a name="GenomicTestCode-M89.4611"> </a></td><td>Acute Leukaemia Other, MRD RUNX1-RUNX1T1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M89.12<a name="GenomicTestCode-M89.4612"> </a></td><td>Acute Leukaemia Other, MRD CBFB-MYH11 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M89.13<a name="GenomicTestCode-M89.4613"> </a></td><td>Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M89.14<a name="GenomicTestCode-M89.4614"> </a></td><td>Acute Leukaemia Other, MRD other QF-PCR</td></tr><tr><td style="white-space:nowrap">M89.15<a name="GenomicTestCode-M89.4615"> </a></td><td>Acute Leukaemia Other, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)</td></tr><tr><td style="white-space:nowrap">M89.16<a name="GenomicTestCode-M89.4616"> </a></td><td>Acute Leukaemia Other, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR )</td></tr><tr><td style="white-space:nowrap">M89.17<a name="GenomicTestCode-M89.4617"> </a></td><td>Acute Leukaemia Other, BCR-ABL1 TKD NGS</td></tr><tr><td style="white-space:nowrap">M89.2<a name="GenomicTestCode-M89.462"> </a></td><td>Acute Leukaemia Other, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)</td></tr><tr><td style="white-space:nowrap">M89.20<a name="GenomicTestCode-M89.4620"> </a></td><td>Acute Leukaemia Other, FLT3 TKD hotspot</td></tr><tr><td style="white-space:nowrap">M89.21<a name="GenomicTestCode-M89.4621"> </a></td><td>Acute Leukaemia Other, NPM1 exon 12 hotspot</td></tr><tr><td style="white-space:nowrap">M89.22<a name="GenomicTestCode-M89.4622"> </a></td><td>Acute Leukaemia Other, IDH1 hotspot</td></tr><tr><td style="white-space:nowrap">M89.23<a name="GenomicTestCode-M89.4623"> </a></td><td>Acute Leukaemia Other, IDH2 hotspot</td></tr><tr><td style="white-space:nowrap">M89.24<a name="GenomicTestCode-M89.4624"> </a></td><td>Acute Leukaemia Other, Chr5/Chr5q copy number FISH</td></tr><tr><td style="white-space:nowrap">M89.25<a name="GenomicTestCode-M89.4625"> </a></td><td>Acute Leukaemia Other, Chr7/Chr7q copy number FISH</td></tr><tr><td style="white-space:nowrap">M89.26<a name="GenomicTestCode-M89.4626"> </a></td><td>Acute Leukaemia Other, Chr17/Chr17p copy number FISH</td></tr><tr><td style="white-space:nowrap">M89.27<a name="GenomicTestCode-M89.4627"> </a></td><td>Acute Leukaemia Other, Chr12/Chr12p copy number FISH</td></tr><tr><td style="white-space:nowrap">M89.28<a name="GenomicTestCode-M89.4628"> </a></td><td>Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA FISH</td></tr><tr><td style="white-space:nowrap">M89.29<a name="GenomicTestCode-M89.4629"> </a></td><td>Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH</td></tr><tr><td style="white-space:nowrap">M89.3<a name="GenomicTestCode-M89.463"> </a></td><td>Acute Leukaemia Other, FISH copy number and rearrangement other</td></tr><tr><td style="white-space:nowrap">M89.30<a name="GenomicTestCode-M89.4630"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 FISH</td></tr><tr><td style="white-space:nowrap">M89.31<a name="GenomicTestCode-M89.4631"> </a></td><td>Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH</td></tr><tr><td style="white-space:nowrap">M89.32<a name="GenomicTestCode-M89.4632"> </a></td><td>Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 FISH</td></tr><tr><td style="white-space:nowrap">M89.33<a name="GenomicTestCode-M89.4633"> </a></td><td>Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM FISH</td></tr><tr><td style="white-space:nowrap">M89.34<a name="GenomicTestCode-M89.4634"> </a></td><td>Acute Leukaemia Other, t(1;22)(p13;q13) RBM15-MRTFA FISH</td></tr><tr><td style="white-space:nowrap">M89.35<a name="GenomicTestCode-M89.4635"> </a></td><td>Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M89.36<a name="GenomicTestCode-M89.4636"> </a></td><td>Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 FISH</td></tr><tr><td style="white-space:nowrap">M89.37<a name="GenomicTestCode-M89.4637"> </a></td><td>Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 FISH</td></tr><tr><td style="white-space:nowrap">M89.38<a name="GenomicTestCode-M89.4638"> </a></td><td>Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 FISH</td></tr><tr><td style="white-space:nowrap">M89.39<a name="GenomicTestCode-M89.4639"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH</td></tr><tr><td style="white-space:nowrap">M89.4<a name="GenomicTestCode-M89.464"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD, PPM1D, ETV6, NOTCH1, FBXW7, PTEN,  HRAS)</td></tr><tr><td style="white-space:nowrap">M89.40<a name="GenomicTestCode-M89.4640"> </a></td><td>Acute Leukaemia Other, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)</td></tr><tr><td style="white-space:nowrap">M89.41<a name="GenomicTestCode-M89.4641"> </a></td><td>Acute Leukaemia Other, del(1)(p33p33) FISH</td></tr><tr><td style="white-space:nowrap">M89.42<a name="GenomicTestCode-M89.4642"> </a></td><td>Acute Leukaemia Other, iAMP21 FISH</td></tr><tr><td style="white-space:nowrap">M89.5<a name="GenomicTestCode-M89.465"> </a></td><td>Acute Leukaemia Other, FLT3 ITD</td></tr><tr><td style="white-space:nowrap">M89.52<a name="GenomicTestCode-M89.4652"> </a></td><td>Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 FISH</td></tr><tr><td style="white-space:nowrap">M89.53<a name="GenomicTestCode-M89.4653"> </a></td><td>Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 FISH</td></tr><tr><td style="white-space:nowrap">M89.54<a name="GenomicTestCode-M89.4654"> </a></td><td>Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF FISH</td></tr><tr><td style="white-space:nowrap">M89.55<a name="GenomicTestCode-M89.4655"> </a></td><td>Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 FISH</td></tr><tr><td style="white-space:nowrap">M89.56<a name="GenomicTestCode-M89.4656"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH</td></tr><tr><td style="white-space:nowrap">M89.57<a name="GenomicTestCode-M89.4657"> </a></td><td>Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN FISH</td></tr><tr><td style="white-space:nowrap">M89.58<a name="GenomicTestCode-M89.4658"> </a></td><td>Acute Leukaemia Other,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH</td></tr><tr><td style="white-space:nowrap">M89.59<a name="GenomicTestCode-M89.4659"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL FISH</td></tr><tr><td style="white-space:nowrap">M89.6<a name="GenomicTestCode-M89.466"> </a></td><td>Acute Leukaemia Other, Other RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.60<a name="GenomicTestCode-M89.4660"> </a></td><td>Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 FISH</td></tr><tr><td style="white-space:nowrap">M89.61<a name="GenomicTestCode-M89.4661"> </a></td><td>Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 FISH</td></tr><tr><td style="white-space:nowrap">M89.62<a name="GenomicTestCode-M89.4662"> </a></td><td>Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 FISH</td></tr><tr><td style="white-space:nowrap">M89.63<a name="GenomicTestCode-M89.4663"> </a></td><td>Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD FISH</td></tr><tr><td style="white-space:nowrap">M89.64<a name="GenomicTestCode-M89.4664"> </a></td><td>Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 FISH</td></tr><tr><td style="white-space:nowrap">M89.65<a name="GenomicTestCode-M89.4665"> </a></td><td>Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH</td></tr><tr><td style="white-space:nowrap">M89.66<a name="GenomicTestCode-M89.4666"> </a></td><td>Acute Leukaemia Other, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)</td></tr><tr><td style="white-space:nowrap">M89.67<a name="GenomicTestCode-M89.4667"> </a></td><td>Acute Leukaemia Other, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)</td></tr><tr><td style="white-space:nowrap">M89.68<a name="GenomicTestCode-M89.4668"> </a></td><td>Acute Leukaemia Other, PDGFRA rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.69<a name="GenomicTestCode-M89.4669"> </a></td><td>Acute Leukaemia Other, PDGFRB rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.7<a name="GenomicTestCode-M89.467"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M89.70<a name="GenomicTestCode-M89.4670"> </a></td><td>Acute Leukaemia Other, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)</td></tr><tr><td style="white-space:nowrap">M89.71<a name="GenomicTestCode-M89.4671"> </a></td><td>Acute Leukaemia Other, JAK2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.72<a name="GenomicTestCode-M89.4672"> </a></td><td>Acute Leukaemia Other, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)</td></tr><tr><td style="white-space:nowrap">M89.73<a name="GenomicTestCode-M89.4673"> </a></td><td>Acute Leukaemia Other, ABL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.74<a name="GenomicTestCode-M89.4674"> </a></td><td>Acute Leukaemia Other, CSF1R rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.75<a name="GenomicTestCode-M89.4675"> </a></td><td>Acute Leukaemia Other, 14q32 (IGH) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.76<a name="GenomicTestCode-M89.4676"> </a></td><td>Acute Leukaemia Other, CRLF2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.77<a name="GenomicTestCode-M89.4677"> </a></td><td>Acute Leukaemia Other, EPOR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M89.78<a name="GenomicTestCode-M89.4678"> </a></td><td>Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.79<a name="GenomicTestCode-M89.4679"> </a></td><td>Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.8<a name="GenomicTestCode-M89.468"> </a></td><td>Acute Leukaemia Other, BCR-ABL1 multiplex</td></tr><tr><td style="white-space:nowrap">M89.80<a name="GenomicTestCode-M89.4680"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.81<a name="GenomicTestCode-M89.4681"> </a></td><td>Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.82<a name="GenomicTestCode-M89.4682"> </a></td><td>Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.83<a name="GenomicTestCode-M89.4683"> </a></td><td>Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.84<a name="GenomicTestCode-M89.4684"> </a></td><td>Acute Leukaemia Other, t(1;22)(p13;q13)  RBM15-MRTFA RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.85<a name="GenomicTestCode-M89.4685"> </a></td><td>Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.86<a name="GenomicTestCode-M89.4686"> </a></td><td>Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.87<a name="GenomicTestCode-M89.4687"> </a></td><td>Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.88<a name="GenomicTestCode-M89.4688"> </a></td><td>Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.89<a name="GenomicTestCode-M89.4689"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.9<a name="GenomicTestCode-M89.469"> </a></td><td>Acute Leukaemia Other, MRD NPM1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M89.90<a name="GenomicTestCode-M89.4690"> </a></td><td>Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.91<a name="GenomicTestCode-M89.4691"> </a></td><td>Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.92<a name="GenomicTestCode-M89.4692"> </a></td><td>Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.93<a name="GenomicTestCode-M89.4693"> </a></td><td>Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.94<a name="GenomicTestCode-M89.4694"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.95<a name="GenomicTestCode-M89.4695"> </a></td><td>Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.96<a name="GenomicTestCode-M89.4696"> </a></td><td>Acute Leukaemia Other, t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.97<a name="GenomicTestCode-M89.4697"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.98<a name="GenomicTestCode-M89.4698"> </a></td><td>Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M89.99<a name="GenomicTestCode-M89.4699"> </a></td><td>Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M9.1<a name="GenomicTestCode-M9.461"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, small variant (BRAF, KRAS, NRAS, HRAS, TERT promoter)</td></tr><tr><td style="white-space:nowrap">M9.2<a name="GenomicTestCode-M9.462"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M9.3<a name="GenomicTestCode-M9.463"> </a></td><td>Thyroid Papillary Carcinoma, Adult, RET rearrangement FISH/RT-PC</td></tr><tr><td style="white-space:nowrap">M9.4<a name="GenomicTestCode-M9.464"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style="white-space:nowrap">M9.6<a name="GenomicTestCode-M9.466"> </a></td><td>Thyroid Papillary Carcinoma, Adult, TERT promoter hotspot</td></tr><tr><td style="white-space:nowrap">M90.1<a name="GenomicTestCode-M90.461"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M90.2<a name="GenomicTestCode-M90.462"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, Karyotype (Genomewide)</td></tr><tr><td style="white-space:nowrap">M90.3<a name="GenomicTestCode-M90.463"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, FISH copy number and rearrangement</td></tr><tr><td style="white-space:nowrap">M90.4<a name="GenomicTestCode-M90.464"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD)</td></tr><tr><td style="white-space:nowrap">M90.5<a name="GenomicTestCode-M90.465"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, FLT3 ITD</td></tr><tr><td style="white-space:nowrap">M90.6<a name="GenomicTestCode-M90.466"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M90.7<a name="GenomicTestCode-M90.467"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M91.1<a name="GenomicTestCode-M91.461"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M91.10<a name="GenomicTestCode-M91.4610"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 FISH</td></tr><tr><td style="white-space:nowrap">M91.11<a name="GenomicTestCode-M91.4611"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style="white-space:nowrap">M91.14<a name="GenomicTestCode-M91.4614"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD ALL RT-qPCR</td></tr><tr><td style="white-space:nowrap">M91.15<a name="GenomicTestCode-M91.4615"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, small variant (ETV6, NOTCH1, FBXW7, TP53, PTEN, KRAS, NRAS, HRAS)</td></tr><tr><td style="white-space:nowrap">M91.2<a name="GenomicTestCode-M91.462"> </a></td><td>Acute Lymphoblastic Leukaemia, Karyotype (To include detection of complex karyotype, hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc)</td></tr><tr><td style="white-space:nowrap">M91.22<a name="GenomicTestCode-M91.4622"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)</td></tr><tr><td style="white-space:nowrap">M91.23<a name="GenomicTestCode-M91.4623"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR)</td></tr><tr><td style="white-space:nowrap">M91.24<a name="GenomicTestCode-M91.4624"> </a></td><td>Acute Lymphoblastic Leukaemia, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)</td></tr><tr><td style="white-space:nowrap">M91.25<a name="GenomicTestCode-M91.4625"> </a></td><td>Acute Lymphoblastic Leukaemia, del(1)(p33p33) FISH</td></tr><tr><td style="white-space:nowrap">M91.26<a name="GenomicTestCode-M91.4626"> </a></td><td>Acute Lymphoblastic Leukaemia, iAMP21 FISH</td></tr><tr><td style="white-space:nowrap">M91.36<a name="GenomicTestCode-M91.4636"> </a></td><td>Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 FISH</td></tr><tr><td style="white-space:nowrap">M91.37<a name="GenomicTestCode-M91.4637"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(1;19)(q23;p13) TCF3-PBX1 FISH</td></tr><tr><td style="white-space:nowrap">M91.38<a name="GenomicTestCode-M91.4638"> </a></td><td>Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF FISH</td></tr><tr><td style="white-space:nowrap">M91.39<a name="GenomicTestCode-M91.4639"> </a></td><td>Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 FISH</td></tr><tr><td style="white-space:nowrap">M91.4<a name="GenomicTestCode-M91.464"> </a></td><td>Acute Lymphoblastic Leukaemia, FISH copy number and rearrangement other: See tests M91.24-M91.62 for individual specified FISH targets.</td></tr><tr><td style="white-space:nowrap">M91.40<a name="GenomicTestCode-M91.4640"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH</td></tr><tr><td style="white-space:nowrap">M91.41<a name="GenomicTestCode-M91.4641"> </a></td><td>Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN FISH</td></tr><tr><td style="white-space:nowrap">M91.42<a name="GenomicTestCode-M91.4642"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(9;11)(p21;q23) KMT2A-MLLT3 FISH</td></tr><tr><td style="white-space:nowrap">M91.43<a name="GenomicTestCode-M91.4643"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH</td></tr><tr><td style="white-space:nowrap">M91.44<a name="GenomicTestCode-M91.4644"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL FISH</td></tr><tr><td style="white-space:nowrap">M91.45<a name="GenomicTestCode-M91.4645"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 FISH</td></tr><tr><td style="white-space:nowrap">M91.46<a name="GenomicTestCode-M91.4646"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 FISH</td></tr><tr><td style="white-space:nowrap">M91.47<a name="GenomicTestCode-M91.4647"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 FISH</td></tr><tr><td style="white-space:nowrap">M91.48<a name="GenomicTestCode-M91.4648"> </a></td><td>Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD FISH</td></tr><tr><td style="white-space:nowrap">M91.49<a name="GenomicTestCode-M91.4649"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;10)(q34;q24) TRB-TLX1 FISH</td></tr><tr><td style="white-space:nowrap">M91.50<a name="GenomicTestCode-M91.4650"> </a></td><td>Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH</td></tr><tr><td style="white-space:nowrap">M91.51<a name="GenomicTestCode-M91.4651"> </a></td><td>Acute Lymphoblastic Leukaemia, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)</td></tr><tr><td style="white-space:nowrap">M91.52<a name="GenomicTestCode-M91.4652"> </a></td><td>Acute Lymphoblastic Leukaemia, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)</td></tr><tr><td style="white-space:nowrap">M91.53<a name="GenomicTestCode-M91.4653"> </a></td><td>Acute Lymphoblastic Leukaemia, PDGFRA rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.54<a name="GenomicTestCode-M91.4654"> </a></td><td>Acute Lymphoblastic Leukaemia, PDGFRB rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.55<a name="GenomicTestCode-M91.4655"> </a></td><td>Acute Lymphoblastic Leukaemia, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)</td></tr><tr><td style="white-space:nowrap">M91.56<a name="GenomicTestCode-M91.4656"> </a></td><td>Acute Lymphoblastic Leukaemia, JAK2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.57<a name="GenomicTestCode-M91.4657"> </a></td><td>Acute Lymphoblastic Leukaemia, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)</td></tr><tr><td style="white-space:nowrap">M91.58<a name="GenomicTestCode-M91.4658"> </a></td><td>Acute Lymphoblastic Leukaemia, ABL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.59<a name="GenomicTestCode-M91.4659"> </a></td><td>Acute Lymphoblastic Leukaemia, CSF1R rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.6<a name="GenomicTestCode-M91.466"> </a></td><td>Acute Lymphoblastic Leukaemia, Other RT-PCR: See tests M91-63-M91.77 for individual specified RT-PCR targets</td></tr><tr><td style="white-space:nowrap">M91.60<a name="GenomicTestCode-M91.4660"> </a></td><td>Acute Lymphoblastic Leukaemia, 14q32(IGH) rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.61<a name="GenomicTestCode-M91.4661"> </a></td><td>Acute Lymphoblastic Leukaemia, CRLF2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.62<a name="GenomicTestCode-M91.4662"> </a></td><td>Acute Lymphoblastic Leukaemia, EPOR rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.63<a name="GenomicTestCode-M91.4663"> </a></td><td>Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.64<a name="GenomicTestCode-M91.4664"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;19)(q23;p13) TCF3-PBX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.65<a name="GenomicTestCode-M91.4665"> </a></td><td>Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.66<a name="GenomicTestCode-M91.4666"> </a></td><td>Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.67<a name="GenomicTestCode-M91.4667"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.68<a name="GenomicTestCode-M91.4668"> </a></td><td>Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.69<a name="GenomicTestCode-M91.4669"> </a></td><td>Acute Lymphoblastic Leukaemia, t(9;11)(p21;q23) KMT2A-MLLT3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.7<a name="GenomicTestCode-M91.467"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, structural variant</td></tr><tr><td style="white-space:nowrap">M91.70<a name="GenomicTestCode-M91.4670"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.71<a name="GenomicTestCode-M91.4671"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.72<a name="GenomicTestCode-M91.4672"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.73<a name="GenomicTestCode-M91.4673"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.74<a name="GenomicTestCode-M91.4674"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.75<a name="GenomicTestCode-M91.4675"> </a></td><td>Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.76<a name="GenomicTestCode-M91.4676"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;10)q34;q24) TRB-TLX1 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.77<a name="GenomicTestCode-M91.4677"> </a></td><td>Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR</td></tr><tr><td style="white-space:nowrap">M91.78<a name="GenomicTestCode-M91.4678"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, copy number variant (to include hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc.)</td></tr><tr><td style="white-space:nowrap">M91.79<a name="GenomicTestCode-M91.4679"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style="white-space:nowrap">M91.8<a name="GenomicTestCode-M91.468"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 multiplex</td></tr><tr><td style="white-space:nowrap">M91.80<a name="GenomicTestCode-M91.4680"> </a></td><td>Acute Lymphoblastic Leukaemia, TPMT</td></tr><tr><td style="white-space:nowrap">M91.81<a name="GenomicTestCode-M91.4681"> </a></td><td>Acute Lymphoblastic Leukaemia, NUDT15</td></tr><tr><td style="white-space:nowrap">M91.82<a name="GenomicTestCode-M91.4682"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M91.83<a name="GenomicTestCode-M91.4683"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M91.84<a name="GenomicTestCode-M91.4684"> </a></td><td>Acute Lymphoblastic Leukaemia, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.85<a name="GenomicTestCode-M91.4685"> </a></td><td>Acute Lymphoblastic Leukaemia, t(8;14)(q34;q32) IGH-MYC FISH</td></tr><tr><td style="white-space:nowrap">M91.86<a name="GenomicTestCode-M91.4686"> </a></td><td>Acute Lymphoblastic Leukaemia, t(2;8)(p12;q24) IGK-MYC FISH</td></tr><tr><td style="white-space:nowrap">M91.87<a name="GenomicTestCode-M91.4687"> </a></td><td>Acute Lymphoblastic Leukaemia, t(8;22)(q24;q11) IGL-MYC FISH</td></tr><tr><td style="white-space:nowrap">M91.88<a name="GenomicTestCode-M91.4688"> </a></td><td>Acute Lymphoblastic Leukaemia, BCL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.89<a name="GenomicTestCode-M91.4689"> </a></td><td>Acute Lymphoblastic Leukaemia, BCL6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M91.9<a name="GenomicTestCode-M91.469"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style="white-space:nowrap">M92.1<a name="GenomicTestCode-M92.461"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF, TP53, DIS3, TENT5C, IRF4)</td></tr><tr><td style="white-space:nowrap">M92.10<a name="GenomicTestCode-M92.4610"> </a></td><td>Plasma Cell Dyscrasia, del(1p) copy number FISH</td></tr><tr><td style="white-space:nowrap">M92.11<a name="GenomicTestCode-M92.4611"> </a></td><td>Plasma Cell Dyscrasia, gain(1q) copy number FISH</td></tr><tr><td style="white-space:nowrap">M92.12<a name="GenomicTestCode-M92.4612"> </a></td><td>Plasma Cell Dyscrasia, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M92.13<a name="GenomicTestCode-M92.4613"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel (To include hyperdiploidy, del(1p), gain(1q), del17p)</td></tr><tr><td style="white-space:nowrap">M92.14<a name="GenomicTestCode-M92.4614"> </a></td><td>Plasma Cell Dyscrasia, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M92.2<a name="GenomicTestCode-M92.462"> </a></td><td>Plasma Cell Dyscrasia, t(4;14) IGH-FGFR3FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M92.3<a name="GenomicTestCode-M92.463"> </a></td><td>Plasma Cell Dyscrasia, t(6;14)  IGH-CCND3 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M92.4<a name="GenomicTestCode-M92.464"> </a></td><td>Plasma Cell Dyscrasia, t(11;14)(q13;q32)  IGH-CCND1 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M92.5<a name="GenomicTestCode-M92.465"> </a></td><td>Plasma Cell Dyscrasia, t(14;16) IGH-MAF FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M92.6<a name="GenomicTestCode-M92.466"> </a></td><td>Plasma Cell Dyscrasia, t(14;20)  IGH-MAFB FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M92.7<a name="GenomicTestCode-M92.467"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel, structural variant (To include IGH-FGFR3, IGH-CCND3, IGH-CCND1, IGH-MAF, IGH-MAFB, MYC rearrangements)</td></tr><tr><td style="white-space:nowrap">M92.8<a name="GenomicTestCode-M92.468"> </a></td><td>Plasma Cell Dyscrasia, IGH rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M92.9<a name="GenomicTestCode-M92.469"> </a></td><td>Plasma Cell Dyscrasia, Hyperdiploidy copy number FISH</td></tr><tr><td style="white-space:nowrap">M93.3<a name="GenomicTestCode-M93.463"> </a></td><td>Lymphoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M93.4<a name="GenomicTestCode-M93.464"> </a></td><td>Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M93.5<a name="GenomicTestCode-M93.465"> </a></td><td>Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M93.6<a name="GenomicTestCode-M93.466"> </a></td><td>Lymphoma, Multi-target NGS panel-small variant (BTK, PLCG2, RAS, MAP2K1, BCL2)</td></tr><tr><td style="white-space:nowrap">M94.1<a name="GenomicTestCode-M94.461"> </a></td><td>Chronic Lymphocytic Leukaemia, Multi-target NGS panel, small variant (TP53,BTK, PLCG2, BCL2)</td></tr><tr><td style="white-space:nowrap">M94.10<a name="GenomicTestCode-M94.4610"> </a></td><td>Chronic Lymphocytic Leukaemia, chromosome 12 copy number FISH</td></tr><tr><td style="white-space:nowrap">M94.2<a name="GenomicTestCode-M94.462"> </a></td><td>Chronic Lymphocytic Leukaemia, Multi-target NGS panel, copy number variant (TP53,ATM, DLEU2/7, RB1, trisomy 12)</td></tr><tr><td style="white-space:nowrap">M94.4<a name="GenomicTestCode-M94.464"> </a></td><td>Chronic Lymphocytic Leukaemia, del(17p) TP53 copy number FISH</td></tr><tr><td style="white-space:nowrap">M94.5<a name="GenomicTestCode-M94.465"> </a></td><td>Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M94.6<a name="GenomicTestCode-M94.466"> </a></td><td>Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS</td></tr><tr><td style="white-space:nowrap">M94.7<a name="GenomicTestCode-M94.467"> </a></td><td>Chronic Lymphocytic Leukaemia, TP53 seq</td></tr><tr><td style="white-space:nowrap">M94.8<a name="GenomicTestCode-M94.468"> </a></td><td>Chronic Lymphocytic Leukaemia, 11q copy number FISH</td></tr><tr><td style="white-space:nowrap">M94.9<a name="GenomicTestCode-M94.469"> </a></td><td>Chronic Lymphocytic Leukaemia, 13q copy number FISH</td></tr><tr><td style="white-space:nowrap">M95.1<a name="GenomicTestCode-M95.461"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq</td></tr><tr><td style="white-space:nowrap">M95.10<a name="GenomicTestCode-M95.4610"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M95.11<a name="GenomicTestCode-M95.4611"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M95.12<a name="GenomicTestCode-M95.4612"> </a></td><td>B cell Non-Hodgkin Lymphoma, MYD88 (L265P) hotspot</td></tr><tr><td style="white-space:nowrap">M95.2<a name="GenomicTestCode-M95.462"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS</td></tr><tr><td style="white-space:nowrap">M95.3<a name="GenomicTestCode-M95.463"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M95.4<a name="GenomicTestCode-M95.464"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (EZH2)</td></tr><tr><td style="white-space:nowrap">M95.5<a name="GenomicTestCode-M95.465"> </a></td><td>B Cell Non-Hodgkin Lymphoma, EZH2 copy number FISH</td></tr><tr><td style="white-space:nowrap">M95.6<a name="GenomicTestCode-M95.466"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (BTK, PLCG2)</td></tr><tr><td style="white-space:nowrap">M95.7<a name="GenomicTestCode-M95.467"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M95.8<a name="GenomicTestCode-M95.468"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (Ig)</td></tr><tr><td style="white-space:nowrap">M95.9<a name="GenomicTestCode-M95.469"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Mutli-target NGS panel, copy number (EZH2)</td></tr><tr><td style="white-space:nowrap">M96.1<a name="GenomicTestCode-M96.461"> </a></td><td>Burkitt Lymphoma, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M96.10<a name="GenomicTestCode-M96.4610"> </a></td><td>Burkitt Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M96.2<a name="GenomicTestCode-M96.462"> </a></td><td>Burkitt Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M96.3<a name="GenomicTestCode-M96.463"> </a></td><td>Burkitt Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M96.4<a name="GenomicTestCode-M96.464"> </a></td><td>Burkitt Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M96.5<a name="GenomicTestCode-M96.465"> </a></td><td>Burkitt Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M96.6<a name="GenomicTestCode-M96.466"> </a></td><td>Burkitt Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M96.7<a name="GenomicTestCode-M96.467"> </a></td><td>Burkitt Lymphoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M96.8<a name="GenomicTestCode-M96.468"> </a></td><td>Burkitt Lymphoma, Multi-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, other rearrangements of MYC,  BCL2, BCL6)</td></tr><tr><td style="white-space:nowrap">M96.9<a name="GenomicTestCode-M96.469"> </a></td><td>Burkitt Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M97.1<a name="GenomicTestCode-M97.461"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, 11q copy number FISH</td></tr><tr><td style="white-space:nowrap">M97.2<a name="GenomicTestCode-M97.462"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M97.3<a name="GenomicTestCode-M97.463"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, Multi-target NGS panel, copy number variant (11q)</td></tr><tr><td style="white-space:nowrap">M97.4<a name="GenomicTestCode-M97.464"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M97.5<a name="GenomicTestCode-M97.465"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M98.1<a name="GenomicTestCode-M98.461"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, IRF4 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M98.2<a name="GenomicTestCode-M98.462"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M98.3<a name="GenomicTestCode-M98.463"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, Multi-target NGS panel, structural variant (IRF4)</td></tr><tr><td style="white-space:nowrap">M98.4<a name="GenomicTestCode-M98.464"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M98.5<a name="GenomicTestCode-M98.465"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M99.1<a name="GenomicTestCode-M99.461"> </a></td><td>High Grade Lymphoma, MYC rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M99.10<a name="GenomicTestCode-M99.4610"> </a></td><td>High Grade Lymphoma, WGS Tumour First</td></tr><tr><td style="white-space:nowrap">M99.11<a name="GenomicTestCode-M99.4611"> </a></td><td>High Grade Lymphoma, WGS Follow-up Germline</td></tr><tr><td style="white-space:nowrap">M99.2<a name="GenomicTestCode-M99.462"> </a></td><td>High Grade Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M99.3<a name="GenomicTestCode-M99.463"> </a></td><td>High Grade Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M99.4<a name="GenomicTestCode-M99.464"> </a></td><td>High Grade Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M99.5<a name="GenomicTestCode-M99.465"> </a></td><td>High Grade Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M99.6<a name="GenomicTestCode-M99.466"> </a></td><td>High Grade Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR</td></tr><tr><td style="white-space:nowrap">M99.7<a name="GenomicTestCode-M99.467"> </a></td><td>High Grade Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style="white-space:nowrap">M99.8<a name="GenomicTestCode-M99.468"> </a></td><td>High Grade Lymphoma, WGS Germline and Tumor</td></tr><tr><td style="white-space:nowrap">M99.9<a name="GenomicTestCode-M99.469"> </a></td><td>High Grade Lymphoma, Mutli-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, IGH-BCL2, other rearrangements of MYC, BCL2, BCL6)</td></tr><tr><td style="white-space:nowrap">R100.3<a name="GenomicTestCode-R100.463"> </a></td><td>Rare syndromic craniosynostosis or isolated multisuture synostosis (WGS)</td></tr><tr><td style="white-space:nowrap">R101.1<a name="GenomicTestCode-R101.461"> </a></td><td>Ehlers Danlos syndrome with a likely monogenic cause (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R102.1<a name="GenomicTestCode-R102.461"> </a></td><td>Osteogenesis imperfecta (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R104.3<a name="GenomicTestCode-R104.463"> </a></td><td>Skeletal dysplasia (WGS)</td></tr><tr><td style="white-space:nowrap">R104.4<a name="GenomicTestCode-R104.464"> </a></td><td>Skeletal dysplasia (Small Panel)</td></tr><tr><td style="white-space:nowrap">R105.1<a name="GenomicTestCode-R105.461"> </a></td><td>MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ common variant newborn screening follow up (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R106.1<a name="GenomicTestCode-R106.461"> </a></td><td>Alstrom syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R107.1<a name="GenomicTestCode-R107.461"> </a></td><td>Bardet-Biedl syndrome (WES or Large Panel)</td></tr><tr><td style="white-space:nowrap">R109.3<a name="GenomicTestCode-R109.463"> </a></td><td>Childhood onset leukodystrophy (WGS)</td></tr><tr><td style="white-space:nowrap">R110.1<a name="GenomicTestCode-R110.461"> </a></td><td>Segmental overgrowth disorders Deep sequencing (Small panel)</td></tr><tr><td style="white-space:nowrap">R111.1<a name="GenomicTestCode-R111.461"> </a></td><td>X-inactivation testing (X-inactivation testing)</td></tr><tr><td style="white-space:nowrap">R112.1<a name="GenomicTestCode-R112.461"> </a></td><td>Factor II deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R115.1<a name="GenomicTestCode-R115.461"> </a></td><td>Factor V deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R115.2<a name="GenomicTestCode-R115.462"> </a></td><td>Factor V deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R116.1<a name="GenomicTestCode-R116.461"> </a></td><td>Factor VII deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R116.2<a name="GenomicTestCode-R116.462"> </a></td><td>Factor VII deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R117.1<a name="GenomicTestCode-R117.461"> </a></td><td>Factor VIII deficiency (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R117.2<a name="GenomicTestCode-R117.462"> </a></td><td>Factor VIII deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R117.3<a name="GenomicTestCode-R117.463"> </a></td><td>Factor VIII deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R118.1<a name="GenomicTestCode-R118.461"> </a></td><td>Factor IX deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R118.2<a name="GenomicTestCode-R118.462"> </a></td><td>Factor IX deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R119.1<a name="GenomicTestCode-R119.461"> </a></td><td>Factor X deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R119.2<a name="GenomicTestCode-R119.462"> </a></td><td>Factor X deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R120.1<a name="GenomicTestCode-R120.461"> </a></td><td>Factor XI deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R120.2<a name="GenomicTestCode-R120.462"> </a></td><td>Factor XI deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R121.1<a name="GenomicTestCode-R121.461"> </a></td><td>von Willebrand disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R121.2<a name="GenomicTestCode-R121.462"> </a></td><td>von Willebrand disease (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R122.1<a name="GenomicTestCode-R122.461"> </a></td><td>Factor XIII deficiency (Small panel)</td></tr><tr><td style="white-space:nowrap">R123.1<a name="GenomicTestCode-R123.461"> </a></td><td>Combined vitamin K-dependent clotting factor deficiency (Small panel)</td></tr><tr><td style="white-space:nowrap">R124.1<a name="GenomicTestCode-R124.461"> </a></td><td>Combined factor V and VIII deficiency (Small panel)</td></tr><tr><td style="white-space:nowrap">R125.1<a name="GenomicTestCode-R125.461"> </a></td><td>Thoracic aortic aneurysm or dissection (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R127.1<a name="GenomicTestCode-R127.461"> </a></td><td>Long QT syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R128.1<a name="GenomicTestCode-R128.461"> </a></td><td>Brugada syndrome and cardiac sodium channel disease (Small panel)</td></tr><tr><td style="white-space:nowrap">R129.1<a name="GenomicTestCode-R129.461"> </a></td><td>Catecholaminergic polymorphic VT (Small panel)</td></tr><tr><td style="white-space:nowrap">R130.1<a name="GenomicTestCode-R130.461"> </a></td><td>Short QT syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R131.1<a name="GenomicTestCode-R131.461"> </a></td><td>Hypertrophic cardiomyopathy (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R132.1<a name="GenomicTestCode-R132.461"> </a></td><td>Dilated and Arrhythmogenic cardiomyopathy (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R133.1<a name="GenomicTestCode-R133.461"> </a></td><td>Arrhythmogenic right ventricular cardiomyopathy (Small panel)</td></tr><tr><td style="white-space:nowrap">R134.1<a name="GenomicTestCode-R134.461"> </a></td><td>Familial hypercholesterolaemia (Small panel)</td></tr><tr><td style="white-space:nowrap">R135.2<a name="GenomicTestCode-R135.462"> </a></td><td>Paediatric or syndromic cardiomyopathy (WGS)</td></tr><tr><td style="white-space:nowrap">R135.3<a name="GenomicTestCode-R135.463"> </a></td><td>Paediatric or syndromic cardiomyopathy (WES)</td></tr><tr><td style="white-space:nowrap">R136.1<a name="GenomicTestCode-R136.461"> </a></td><td>Primary lymphoedema (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R137.1<a name="GenomicTestCode-R137.461"> </a></td><td>Congenital heart disease microarray (Microarray)</td></tr><tr><td style="white-space:nowrap">R138.1<a name="GenomicTestCode-R138.461"> </a></td><td>Sudden unexplained death or survivors of a cardiac event (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R139.1<a name="GenomicTestCode-R139.461"> </a></td><td>Laterality disorders and isomerism (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R14.1<a name="GenomicTestCode-R14.461"> </a></td><td>Acutely unwell children with a likely monogenic disorder (WGS)</td></tr><tr><td style="white-space:nowrap">R140.1<a name="GenomicTestCode-R140.461"> </a></td><td>Elastin-related phenotypes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R141.1<a name="GenomicTestCode-R141.461"> </a></td><td>Monogenic diabetes (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R142.1<a name="GenomicTestCode-R142.461"> </a></td><td>Glucokinase-related fasting hyperglycaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R143.1<a name="GenomicTestCode-R143.461"> </a></td><td>Neonatal diabetes (Small panel)</td></tr><tr><td style="white-space:nowrap">R143.3<a name="GenomicTestCode-R143.463"> </a></td><td>Neonatal diabetes (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R143.4<a name="GenomicTestCode-R143.464"> </a></td><td>Neonatal diabetes (WGS)</td></tr><tr><td style="white-space:nowrap">R144.1<a name="GenomicTestCode-R144.461"> </a></td><td>Congenital hyperinsulinism (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R144.2<a name="GenomicTestCode-R144.462"> </a></td><td>Congenital hyperinsulinism (Small panel)</td></tr><tr><td style="white-space:nowrap">R145.1<a name="GenomicTestCode-R145.461"> </a></td><td>Congenital hypothyroidism (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R146.1<a name="GenomicTestCode-R146.461"> </a></td><td>Differences in sex development (Microarray)</td></tr><tr><td style="white-space:nowrap">R146.2<a name="GenomicTestCode-R146.462"> </a></td><td>Differences of sex development (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R148.1<a name="GenomicTestCode-R148.461"> </a></td><td>Hypogonadotropic hypogonadism (Small panel)</td></tr><tr><td style="white-space:nowrap">R149.1<a name="GenomicTestCode-R149.461"> </a></td><td>Severe early-onset obesity (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R15.4<a name="GenomicTestCode-R15.464"> </a></td><td>Primary immunodeficiency or monogenic inflammatory bowel disease (WGS)</td></tr><tr><td style="white-space:nowrap">R15.5<a name="GenomicTestCode-R15.465"> </a></td><td>Primary immunodeficiency or monogenic inflammatory bowel disease (WES)</td></tr><tr><td style="white-space:nowrap">R150.1<a name="GenomicTestCode-R150.461"> </a></td><td>Congenital adrenal hypoplasia (Small panel)</td></tr><tr><td style="white-space:nowrap">R151.1<a name="GenomicTestCode-R151.461"> </a></td><td>Familial hyperparathyroidism or Hypocalciuric hypercalcaemia (Small panel)</td></tr><tr><td style="white-space:nowrap">R153.1<a name="GenomicTestCode-R153.461"> </a></td><td>Familial hypoparathyroidism (Small panel)</td></tr><tr><td style="white-space:nowrap">R154.1<a name="GenomicTestCode-R154.461"> </a></td><td>Hypophosphataemia or rickets (Small panel)</td></tr><tr><td style="white-space:nowrap">R155.1<a name="GenomicTestCode-R155.461"> </a></td><td>Autoimmune Polyendocrine Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R156.1<a name="GenomicTestCode-R156.461"> </a></td><td>Carney complex (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R157.1<a name="GenomicTestCode-R157.461"> </a></td><td>IPEX Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R158.1<a name="GenomicTestCode-R158.461"> </a></td><td>Severe insulin resistance and lipodystrophy syndromes (Small panel)</td></tr><tr><td style="white-space:nowrap">R159.1<a name="GenomicTestCode-R159.461"> </a></td><td>Pituitary hormone deficiency (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R16.1<a name="GenomicTestCode-R16.461"> </a></td><td>Severe combined immunodeficiency with adenosine deaminase deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R160.1<a name="GenomicTestCode-R160.461"> </a></td><td>Primary pigmented nodular adrenocortical disease (Small panel)</td></tr><tr><td style="white-space:nowrap">R162.1<a name="GenomicTestCode-R162.461"> </a></td><td>Familial tumoral calcinosis (Small panel)</td></tr><tr><td style="white-space:nowrap">R163.1<a name="GenomicTestCode-R163.461"> </a></td><td>Ectodermal dysplasia (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R164.1<a name="GenomicTestCode-R164.461"> </a></td><td>Epidermolysis bullosa and congenital skin fragility (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R165.1<a name="GenomicTestCode-R165.461"> </a></td><td>Ichthyosis and erythrokeratoderma (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R166.1<a name="GenomicTestCode-R166.461"> </a></td><td>Palmoplantar keratodermas (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R167.1<a name="GenomicTestCode-R167.461"> </a></td><td>Autosomal recessive primary hypertrophic osteoarthropathy (Small panel)</td></tr><tr><td style="white-space:nowrap">R168.1<a name="GenomicTestCode-R168.461"> </a></td><td>Non-acute porphyrias (Small panel)</td></tr><tr><td style="white-space:nowrap">R169.1<a name="GenomicTestCode-R169.461"> </a></td><td>Acute intermittent porphyria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R17.1<a name="GenomicTestCode-R17.461"> </a></td><td>Lymphoproliferative syndrome with absent SAP expression (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R170.1<a name="GenomicTestCode-R170.461"> </a></td><td>Variegate porphyria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R171.1<a name="GenomicTestCode-R171.461"> </a></td><td>Cholestasis (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R172.1<a name="GenomicTestCode-R172.461"> </a></td><td>Wilson disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R173.1<a name="GenomicTestCode-R173.461"> </a></td><td>Polycystic liver disease (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R175.1<a name="GenomicTestCode-R175.461"> </a></td><td>Pancreatitis (Small panel)</td></tr><tr><td style="white-space:nowrap">R176.1<a name="GenomicTestCode-R176.461"> </a></td><td>Gilbert syndrome (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R18.1<a name="GenomicTestCode-R18.461"> </a></td><td>Haemophagocytic syndrome with absent XIAP expression (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R180.1<a name="GenomicTestCode-R180.461"> </a></td><td>Congenital adrenal hyperplasia diagnostic test (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R180.2<a name="GenomicTestCode-R180.462"> </a></td><td>Congenital adrenal hyperplasia diagnostic test (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R181.1<a name="GenomicTestCode-R181.461"> </a></td><td>Congenital adrenal hyperplasia carrier testing (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R181.2<a name="GenomicTestCode-R181.462"> </a></td><td>Congenital adrenal hyperplasia carrier testing (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R182.1<a name="GenomicTestCode-R182.461"> </a></td><td>Hyperthyroidism (Small panel)</td></tr><tr><td style="white-space:nowrap">R183.1<a name="GenomicTestCode-R183.461"> </a></td><td>Glucocorticoid-remediable aldosteronism (GRA) (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R184.1<a name="GenomicTestCode-R184.461"> </a></td><td>Cystic fibrosis diagnostic test (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R184.2<a name="GenomicTestCode-R184.462"> </a></td><td>Cystic fibrosis diagnostic test (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R184.3<a name="GenomicTestCode-R184.463"> </a></td><td>Cystic fibrosis diagnostic test (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R185.1<a name="GenomicTestCode-R185.461"> </a></td><td>Cystic fibrosis carrier testing (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R186.1<a name="GenomicTestCode-R186.461"> </a></td><td>Hereditary haemorrhagic telangiectasia (Small panel)</td></tr><tr><td style="white-space:nowrap">R188.1<a name="GenomicTestCode-R188.461"> </a></td><td>Pulmonary arterial hypertension (Small panel)</td></tr><tr><td style="white-space:nowrap">R189.1<a name="GenomicTestCode-R189.461"> </a></td><td>Respiratory ciliopathies including non-CF bronchiectasis (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R19.1<a name="GenomicTestCode-R19.461"> </a></td><td>Autoimmune lymphoproliferative syndrome with defective apoptosis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R190.1<a name="GenomicTestCode-R190.461"> </a></td><td>Pneumothorax familial (Small panel)</td></tr><tr><td style="white-space:nowrap">R191.1<a name="GenomicTestCode-R191.461"> </a></td><td>Alpha-1-antitrypsin deficiency (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R193.4<a name="GenomicTestCode-R193.464"> </a></td><td>Cystic renal disease (WGS)</td></tr><tr><td style="white-space:nowrap">R194.1<a name="GenomicTestCode-R194.461"> </a></td><td>Haematuria (Small panel)</td></tr><tr><td style="white-space:nowrap">R195.3<a name="GenomicTestCode-R195.463"> </a></td><td>Proteinuric renal disease (WGS)</td></tr><tr><td style="white-space:nowrap">R196.1<a name="GenomicTestCode-R196.461"> </a></td><td>CFHR5 nephropathy (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R197.1<a name="GenomicTestCode-R197.461"> </a></td><td>Membranoproliferative glomerulonephritis including C3 glomerulopathy (Small panel)</td></tr><tr><td style="white-space:nowrap">R197.2<a name="GenomicTestCode-R197.462"> </a></td><td>Membranoproliferative glomerulonephritis including C3 glomerulopathy (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R198.1<a name="GenomicTestCode-R198.461"> </a></td><td>Renal tubulopathies (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R199.1<a name="GenomicTestCode-R199.461"> </a></td><td>Congenital anomalies of the kidney and urinary tract familial (Microarray)</td></tr><tr><td style="white-space:nowrap">R20.1<a name="GenomicTestCode-R20.461"> </a></td><td>Wiskott-Aldrich syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R201.1<a name="GenomicTestCode-R201.461"> </a></td><td>Atypical haemolytic uraemic syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R202.1<a name="GenomicTestCode-R202.461"> </a></td><td>Tubulointerstitial kidney disease (Small panel)</td></tr><tr><td style="white-space:nowrap">R204.1<a name="GenomicTestCode-R204.461"> </a></td><td>Hereditary Systemic Amyloidosis  (Small panel)</td></tr><tr><td style="white-space:nowrap">R207.1<a name="GenomicTestCode-R207.461"> </a></td><td>Inherited ovarian cancer (without breast cancer) (Small panel)</td></tr><tr><td style="white-space:nowrap">R208.1<a name="GenomicTestCode-R208.461"> </a></td><td>Inherited breast cancer and ovarian cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R21.1<a name="GenomicTestCode-R21.461"> </a></td><td>Fetal anomalies with a likely genetic cause (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R21.2<a name="GenomicTestCode-R21.462"> </a></td><td>Fetal anomalies with a likely genetic cause (WES or Large Panel)</td></tr><tr><td style="white-space:nowrap">R21.3<a name="GenomicTestCode-R21.463"> </a></td><td>Fetal anomalies with a likely genetic cause (Microarray)</td></tr><tr><td style="white-space:nowrap">R210.2<a name="GenomicTestCode-R210.462"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (Small panel)</td></tr><tr><td style="white-space:nowrap">R210.4<a name="GenomicTestCode-R210.464"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R210.6<a name="GenomicTestCode-R210.466"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R211.1<a name="GenomicTestCode-R211.461"> </a></td><td>Inherited polyposis and early onset colorectal cancer germline testing (Small panel)</td></tr><tr><td style="white-space:nowrap">R211.3<a name="GenomicTestCode-R211.463"> </a></td><td>Inherited polyposis and early onset colorectal cancer germline testing (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R212.1<a name="GenomicTestCode-R212.461"> </a></td><td>Peutz Jeghers Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R213.1<a name="GenomicTestCode-R213.461"> </a></td><td>PTEN Hamartoma Tumor Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R214.1<a name="GenomicTestCode-R214.461"> </a></td><td>Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R215.1<a name="GenomicTestCode-R215.461"> </a></td><td>Hereditary diffuse gastric cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R216.1<a name="GenomicTestCode-R216.461"> </a></td><td>Li Fraumeni Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R217.1<a name="GenomicTestCode-R217.461"> </a></td><td>Endocrine neoplasia (Small panel)</td></tr><tr><td style="white-space:nowrap">R218.1<a name="GenomicTestCode-R218.461"> </a></td><td>Multiple endocrine neoplasia type 2 (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R219.1<a name="GenomicTestCode-R219.461"> </a></td><td>Retinoblastoma (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R219.2<a name="GenomicTestCode-R219.462"> </a></td><td>Retinoblastoma (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R22.1<a name="GenomicTestCode-R22.461"> </a></td><td>Fetus with a likely chromosomal abnormality (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R22.2<a name="GenomicTestCode-R22.462"> </a></td><td>Fetus with a likely chromosomal abnormality (Microarray)</td></tr><tr><td style="white-space:nowrap">R221.1<a name="GenomicTestCode-R221.461"> </a></td><td>Familial tumours of the nervous system (Small panel)</td></tr><tr><td style="white-space:nowrap">R221.2<a name="GenomicTestCode-R221.462"> </a></td><td>Familial tumours of the nervous system (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R222.1<a name="GenomicTestCode-R222.461"> </a></td><td>Neurofibromatosis type 1 (Small panel)</td></tr><tr><td style="white-space:nowrap">R222.2<a name="GenomicTestCode-R222.462"> </a></td><td>Neurofibromatosis type 1 (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R223.1<a name="GenomicTestCode-R223.461"> </a></td><td>Inherited phaeochromocytoma and paraganglioma excluding NF1 (Small panel)</td></tr><tr><td style="white-space:nowrap">R224.1<a name="GenomicTestCode-R224.461"> </a></td><td>Inherited renal cancer (Small panel)</td></tr><tr><td style="white-space:nowrap">R225.1<a name="GenomicTestCode-R225.461"> </a></td><td>Von Hippel Lindau syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R226.1<a name="GenomicTestCode-R226.461"> </a></td><td>Inherited parathyroid cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R227.1<a name="GenomicTestCode-R227.461"> </a></td><td>Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R227.2<a name="GenomicTestCode-R227.462"> </a></td><td>Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (DNA repair defect testing)</td></tr><tr><td style="white-space:nowrap">R228.1<a name="GenomicTestCode-R228.461"> </a></td><td>Tuberous sclerosis (Small panel)</td></tr><tr><td style="white-space:nowrap">R228.2<a name="GenomicTestCode-R228.462"> </a></td><td>Tuberous sclerosis (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R228.3<a name="GenomicTestCode-R228.463"> </a></td><td>Tuberous sclerosis (Small panel deep sequencing)</td></tr><tr><td style="white-space:nowrap">R229.1<a name="GenomicTestCode-R229.461"> </a></td><td>Confirmed Fanconi anaemia or Bloom syndrome variant testing (Small panel)</td></tr><tr><td style="white-space:nowrap">R23.1<a name="GenomicTestCode-R23.461"> </a></td><td>Apert syndrome (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R230.1<a name="GenomicTestCode-R230.461"> </a></td><td>Multiple monogenic benign skin tumours (Small panel)</td></tr><tr><td style="white-space:nowrap">R231.2<a name="GenomicTestCode-R231.462"> </a></td><td>Neuronal ceroid lipofuscinosis (Small panel)</td></tr><tr><td style="white-space:nowrap">R232.1<a name="GenomicTestCode-R232.461"> </a></td><td>Haemophagocytic syndrome with absent perforin expression (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R233.1<a name="GenomicTestCode-R233.461"> </a></td><td>Agammaglobulinaemia with absent BTK expression (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R234.1<a name="GenomicTestCode-R234.461"> </a></td><td>Severe combined immunodeficiency with PNP deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R235.1<a name="GenomicTestCode-R235.461"> </a></td><td>SCID with features of gamma chain deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R236.1<a name="GenomicTestCode-R236.461"> </a></td><td>Pigmentary skin disorders (WES or Large panel)</td></tr><tr><td style="white-space:nowrap">R236.2<a name="GenomicTestCode-R236.462"> </a></td><td>Pigmentary skin disorders (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R237.1<a name="GenomicTestCode-R237.461"> </a></td><td>Cutaneous photosensitivity with a likely genetic cause (Small panel)</td></tr><tr><td style="white-space:nowrap">R239.1<a name="GenomicTestCode-R239.461"> </a></td><td>Incontinentia pigmenti (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R239.2<a name="GenomicTestCode-R239.462"> </a></td><td>Incontinentia pigmenti (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R24.1<a name="GenomicTestCode-R24.461"> </a></td><td>Achondroplasia (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R240.1<a name="GenomicTestCode-R240.461"> </a></td><td>Diagnostic testing for known variant(s) (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R242.1<a name="GenomicTestCode-R242.461"> </a></td><td>Predictive testing for known familial variant(s) (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R244.1<a name="GenomicTestCode-R244.461"> </a></td><td>Carrier testing for known familial variant(s) (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R246.1<a name="GenomicTestCode-R246.461"> </a></td><td>Carrier testing at population risk for partners of known carriers of nationally agreed autosomal recessive disorders (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R249.1<a name="GenomicTestCode-R249.461"> </a></td><td>NIPD using paternal exclusion testing for very rare conditions where familial variant is known (NIPD)</td></tr><tr><td style="white-space:nowrap">R25.1<a name="GenomicTestCode-R25.461"> </a></td><td>Thanatophoric dysplasia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R250.1<a name="GenomicTestCode-R250.461"> </a></td><td>NIPD for congenital adrenal hyperplasia CYP21A2 haplotype testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R251.1<a name="GenomicTestCode-R251.461"> </a></td><td>Non-invasive prenatal sexing (NIPD)</td></tr><tr><td style="white-space:nowrap">R252.1<a name="GenomicTestCode-R252.461"> </a></td><td>SMA carrier testing at population risk for partners of known carriers (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R253.1<a name="GenomicTestCode-R253.461"> </a></td><td>Cystic fibrosis newborn screening follow-up (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R254.1<a name="GenomicTestCode-R254.461"> </a></td><td>Familial melanoma (Small panel)</td></tr><tr><td style="white-space:nowrap">R255.1<a name="GenomicTestCode-R255.461"> </a></td><td>Epidermodysplasia verruciformis (Small panel)</td></tr><tr><td style="white-space:nowrap">R256.1<a name="GenomicTestCode-R256.461"> </a></td><td>Nephrocalcinosis or nephrolithiasis (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R257.2<a name="GenomicTestCode-R257.462"> </a></td><td>Unexplained young onset end-stage renal disease (WGS)</td></tr><tr><td style="white-space:nowrap">R257.3<a name="GenomicTestCode-R257.463"> </a></td><td>Unexplained young onset end-stage renal disease (WES)</td></tr><tr><td style="white-space:nowrap">R258.1<a name="GenomicTestCode-R258.461"> </a></td><td>Cytopenia Fanconi breakage testing indicated (DNA repair defect testing)</td></tr><tr><td style="white-space:nowrap">R258.2<a name="GenomicTestCode-R258.462"> </a></td><td>Cytopenia Fanconi breakage testing indicated (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R259.1<a name="GenomicTestCode-R259.461"> </a></td><td>Nijmegen breakage syndrome (DNA repair defect testing)</td></tr><tr><td style="white-space:nowrap">R259.2<a name="GenomicTestCode-R259.462"> </a></td><td>Nijmegen breakage syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R26.1<a name="GenomicTestCode-R26.461"> </a></td><td>Likely common aneuploidy (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R260.1<a name="GenomicTestCode-R260.461"> </a></td><td>Fanconi anaemia or Bloom syndrome chromosome breakage testing (DNA repair defect testing)</td></tr><tr><td style="white-space:nowrap">R262.1<a name="GenomicTestCode-R262.461"> </a></td><td>Corneal dystrophy (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R263.1<a name="GenomicTestCode-R263.461"> </a></td><td>Confirmation of uniparental disomy (UPD testing)</td></tr><tr><td style="white-space:nowrap">R264.1<a name="GenomicTestCode-R264.461"> </a></td><td>Identity testing (Identity testing)</td></tr><tr><td style="white-space:nowrap">R265.1<a name="GenomicTestCode-R265.461"> </a></td><td>Chromosomal mosaicism â€“ karyotype / Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style="white-space:nowrap">R268.1<a name="GenomicTestCode-R268.461"> </a></td><td>Kagami-Ogata syndrome paternal uniparental disomy 14 (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R27.3,<a name="GenomicTestCode-R27.463.44"> </a></td><td>Paediatric disorders (WGS)</td></tr><tr><td style="white-space:nowrap">R270.1<a name="GenomicTestCode-R270.461"> </a></td><td>Smith-Lemli-Opitz syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R270.2<a name="GenomicTestCode-R270.462"> </a></td><td>Smith-Lemli-Opitz syndrome (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R271.1<a name="GenomicTestCode-R271.461"> </a></td><td>Neuronal ceroid lipofuscinosis type 2 (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R272.1<a name="GenomicTestCode-R272.461"> </a></td><td>Gaucher disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R273.1<a name="GenomicTestCode-R273.461"> </a></td><td>Glycogen storage disease V (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R274.1<a name="GenomicTestCode-R274.461"> </a></td><td>Glycogen storage disease (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R275.1<a name="GenomicTestCode-R275.461"> </a></td><td>Glutaric acidaemia I newborn screening follow up (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R276.1<a name="GenomicTestCode-R276.461"> </a></td><td>Lysosomal storage disorder (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R277.1<a name="GenomicTestCode-R277.461"> </a></td><td>Mucopolysaccharidosis type IH/S (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R278.1<a name="GenomicTestCode-R278.461"> </a></td><td>Mucopolysaccharidosis type II (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R278.2<a name="GenomicTestCode-R278.462"> </a></td><td>Mucopolysaccharidosis type II (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R279.1<a name="GenomicTestCode-R279.461"> </a></td><td>Isovaleric acidaemia newborn screening follow up (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R28.1<a name="GenomicTestCode-R28.461"> </a></td><td>Congenital malformation and dysmorphism syndromes â€“ microarray only (Microarray)</td></tr><tr><td style="white-space:nowrap">R280.1<a name="GenomicTestCode-R280.461"> </a></td><td>Krabbe disease â€“ GALC deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R280.2<a name="GenomicTestCode-R280.462"> </a></td><td>Krabbe disease â€“ GALC deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R281.1<a name="GenomicTestCode-R281.461"> </a></td><td>Krabbe disease Saposin A deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R282.1<a name="GenomicTestCode-R282.461"> </a></td><td>Niemann-Pick disease type A or B (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R283.1<a name="GenomicTestCode-R283.461"> </a></td><td>Phenylketonuria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R285.1<a name="GenomicTestCode-R285.461"> </a></td><td>Sandhoff disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R286.1<a name="GenomicTestCode-R286.461"> </a></td><td>Tay-Sachs disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R287.1<a name="GenomicTestCode-R287.461"> </a></td><td>Mucopolysaccharidosis type IVA (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R288.1<a name="GenomicTestCode-R288.461"> </a></td><td>GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R289.1<a name="GenomicTestCode-R289.461"> </a></td><td>Mucolipidosis II and III Alpha/Beta (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R290.1<a name="GenomicTestCode-R290.461"> </a></td><td>Mucopolysaccharidosis type VI (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R291.1<a name="GenomicTestCode-R291.461"> </a></td><td>Mucopolysaccharidosis type IIIA (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R292.1<a name="GenomicTestCode-R292.461"> </a></td><td>Mucopolysaccharidosis type IIIB (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R293.1<a name="GenomicTestCode-R293.461"> </a></td><td>Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Small Panel)</td></tr><tr><td style="white-space:nowrap">R293.2<a name="GenomicTestCode-R293.462"> </a></td><td>Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R294.1<a name="GenomicTestCode-R294.461"> </a></td><td>Ataxia telangiectasia DNA repair testing (DNA repair defect testing)</td></tr><tr><td style="white-space:nowrap">R295.1<a name="GenomicTestCode-R295.461"> </a></td><td>Ataxia telangiectasia variant testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R296.1<a name="GenomicTestCode-R296.461"> </a></td><td>RNA analysis of variants (Other)</td></tr><tr><td style="white-space:nowrap">R298.1<a name="GenomicTestCode-R298.461"> </a></td><td>Possible structural or mosaic chromosomal abnormality FISH (FISH)</td></tr><tr><td style="white-space:nowrap">R299.1<a name="GenomicTestCode-R299.461"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Other)</td></tr><tr><td style="white-space:nowrap">R299.2<a name="GenomicTestCode-R299.462"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Heteroplasmy assessment mitochondrial genome)</td></tr><tr><td style="white-space:nowrap">R299.3<a name="GenomicTestCode-R299.463"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Breakpoint mapping mitochondrial genome)</td></tr><tr><td style="white-space:nowrap">R300.1<a name="GenomicTestCode-R300.461"> </a></td><td>Possible mitochondrial disorder whole mitochondrial genome sequencing (Other)</td></tr><tr><td style="white-space:nowrap">R301.1<a name="GenomicTestCode-R301.461"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA depletion testing (Other)</td></tr><tr><td style="white-space:nowrap">R304.1<a name="GenomicTestCode-R304.461"> </a></td><td>NIPD for cystic fibrosis haplotype testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R305.1<a name="GenomicTestCode-R305.461"> </a></td><td>NIPD for cystic fibrosis variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R306.1<a name="GenomicTestCode-R306.461"> </a></td><td>NIPD for Apert syndrome variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R307.1<a name="GenomicTestCode-R307.461"> </a></td><td>NIPD for Crouzon syndrome with acanthosis nigricans variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R308.1<a name="GenomicTestCode-R308.461"> </a></td><td>NIPD for FGFR2-related craniosynostosis syndromes variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R309.1<a name="GenomicTestCode-R309.461"> </a></td><td>NIPD for FGFR3-related skeletal dysplasias variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R31.3<a name="GenomicTestCode-R31.463"> </a></td><td>Bilateral congenital or childhood onset cataracts (WGS)</td></tr><tr><td style="white-space:nowrap">R310.1<a name="GenomicTestCode-R310.461"> </a></td><td>NIPD for Duchenne and Becker muscular dystrophy haplotype testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R311.1<a name="GenomicTestCode-R311.461"> </a></td><td>NIPD for spinal muscular atrophy variant testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R312.1<a name="GenomicTestCode-R312.461"> </a></td><td>Parental sequencing for lethal autosomal recessive disorders (WES or Large penel)</td></tr><tr><td style="white-space:nowrap">R313.1<a name="GenomicTestCode-R313.461"> </a></td><td>Neutropaenia consistent with ELANE variants (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R314.1<a name="GenomicTestCode-R314.461"> </a></td><td>Ambiguous genitalia (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R314.2<a name="GenomicTestCode-R314.462"> </a></td><td>Ambiguous genitalia (Karyotype)</td></tr><tr><td style="white-space:nowrap">R315.1<a name="GenomicTestCode-R315.461"> </a></td><td>POLG-related disorder (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R315.2<a name="GenomicTestCode-R315.462"> </a></td><td>POLG-related disorder (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R316.1<a name="GenomicTestCode-R316.461"> </a></td><td>Pyruvate dehydrogenase (PDH) deficiency (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R317.1<a name="GenomicTestCode-R317.461"> </a></td><td>Mitochondrial liver disease, including transient infantile liver failure (Small panel)</td></tr><tr><td style="white-space:nowrap">R318.1<a name="GenomicTestCode-R318.461"> </a></td><td>Recurrent miscarriage with products of conception available for testing (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R318.2<a name="GenomicTestCode-R318.462"> </a></td><td>Recurrent miscarriage with products of conception available for testing (Microarray)</td></tr><tr><td style="white-space:nowrap">R319.1<a name="GenomicTestCode-R319.461"> </a></td><td>Calcium-sensing receptor phenotypes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R32.2<a name="GenomicTestCode-R32.462"> </a></td><td>Retinal disorders (WGS)</td></tr><tr><td style="white-space:nowrap">R320.1<a name="GenomicTestCode-R320.461"> </a></td><td>Invasive prenatal diagnosis requiring fetal sexing (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R321.1<a name="GenomicTestCode-R321.461"> </a></td><td>Maternal cell contamination testing (Identity testing)</td></tr><tr><td style="white-space:nowrap">R322.1<a name="GenomicTestCode-R322.461"> </a></td><td>Skin fibroblasts to be cultured and stored (Other)</td></tr><tr><td style="white-space:nowrap">R323.1<a name="GenomicTestCode-R323.461"> </a></td><td>Sitosterolaemia (Small panel)</td></tr><tr><td style="white-space:nowrap">R324.1<a name="GenomicTestCode-R324.461"> </a></td><td>Familial Chylomicronaemia Syndrome (FCS) (Small panel)</td></tr><tr><td style="white-space:nowrap">R325.1<a name="GenomicTestCode-R325.461"> </a></td><td>Lysosomal acid lipase deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R326.1<a name="GenomicTestCode-R326.461"> </a></td><td>Vascular skin disorders (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R327.1<a name="GenomicTestCode-R327.461"> </a></td><td>Mosaic skin disorders deep sequencing (Medium panel)</td></tr><tr><td style="white-space:nowrap">R328.1<a name="GenomicTestCode-R328.461"> </a></td><td>Progressive cardiac conduction disease (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R329.1<a name="GenomicTestCode-R329.461"> </a></td><td>Familial dysalbuminaemic hyperthyroxinaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R33.1<a name="GenomicTestCode-R33.461"> </a></td><td>Possible X-linked retinitis pigmentosa (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R330.1<a name="GenomicTestCode-R330.461"> </a></td><td>Alveolar capillary dysplasia with misalignment of pulmonary veins (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R331.1<a name="GenomicTestCode-R331.461"> </a></td><td>Intestinal failure or congenital diarrhoea (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R332.1<a name="GenomicTestCode-R332.461"> </a></td><td>Rare genetic inflammatory skin disorders (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R333.1<a name="GenomicTestCode-R333.461"> </a></td><td>Central congenital hypoventilation (STR testing)</td></tr><tr><td style="white-space:nowrap">R333.2<a name="GenomicTestCode-R333.462"> </a></td><td>Central congenital hypoventilation (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R334.1<a name="GenomicTestCode-R334.461"> </a></td><td>Cystinosis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R335.1<a name="GenomicTestCode-R335.461"> </a></td><td>Fabry disease (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R335.2<a name="GenomicTestCode-R335.462"> </a></td><td>Fabry disease (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R336.1<a name="GenomicTestCode-R336.461"> </a></td><td>Cerebral vascular malformations (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R337.1<a name="GenomicTestCode-R337.461"> </a></td><td>CADASIL (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R338.1<a name="GenomicTestCode-R338.461"> </a></td><td>Monitoring for G(M)CSF escape variants (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R340.1<a name="GenomicTestCode-R340.461"> </a></td><td>Amelogenesis imperfecta (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R341.1<a name="GenomicTestCode-R341.461"> </a></td><td>Hereditary angioedema types I and II (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R343.1<a name="GenomicTestCode-R343.461"> </a></td><td>Chromosomal mosaicism microarray (Microarray)</td></tr><tr><td style="white-space:nowrap">R344.1<a name="GenomicTestCode-R344.461"> </a></td><td>Primary hyperaldosteronism KCNJ5 (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R345.1<a name="GenomicTestCode-R345.461"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R345.2<a name="GenomicTestCode-R345.462"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R345.3<a name="GenomicTestCode-R345.463"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Other)</td></tr><tr><td style="white-space:nowrap">R346.1<a name="GenomicTestCode-R346.461"> </a></td><td>DNA to be stored (Other)</td></tr><tr><td style="white-space:nowrap">R347.1<a name="GenomicTestCode-R347.461"> </a></td><td>Inherited predisposition to acute myeloid leukaemia (AML) (Small panel)</td></tr><tr><td style="white-space:nowrap">R350.1<a name="GenomicTestCode-R350.461"> </a></td><td>MERRF syndrome (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R351.1<a name="GenomicTestCode-R351.461"> </a></td><td>NARP syndrome or maternally inherited Leigh syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R351.2<a name="GenomicTestCode-R351.462"> </a></td><td>NARP syndrome or maternally inherited Leigh syndrome (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R352.1<a name="GenomicTestCode-R352.461"> </a></td><td>Mitochondrial DNA maintenance disorder (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R353.1<a name="GenomicTestCode-R353.461"> </a></td><td>Mitochondrial disorder with complex I deficiency (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R354.1<a name="GenomicTestCode-R354.461"> </a></td><td>Mitochondrial disorder with complex II deficiency (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R355.1<a name="GenomicTestCode-R355.461"> </a></td><td>Mitochondrial disorder with complex III deficiency (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R356.1<a name="GenomicTestCode-R356.461"> </a></td><td>Mitochondrial disorder with complex IV deficiency (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R357.1<a name="GenomicTestCode-R357.461"> </a></td><td>Mitochondrial disorder with complex V deficiency (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R36.2,<a name="GenomicTestCode-R36.462.44"> </a></td><td>structural eye disease (WGS)</td></tr><tr><td style="white-space:nowrap">R361.1<a name="GenomicTestCode-R361.461"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (Small panel)</td></tr><tr><td style="white-space:nowrap">R361.2<a name="GenomicTestCode-R361.462"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R363.1<a name="GenomicTestCode-R363.461"> </a></td><td>Inherited predisposition to GIST (Small panel)</td></tr><tr><td style="white-space:nowrap">R364.1<a name="GenomicTestCode-R364.461"> </a></td><td>DICER1-related cancer predisposition (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R365.1<a name="GenomicTestCode-R365.461"> </a></td><td>Fumarate hydratase-related tumour syndromes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R366.1<a name="GenomicTestCode-R366.461"> </a></td><td>Inherited susceptibility to acute lymphoblastoid leukaemia (ALL) (Small panel)</td></tr><tr><td style="white-space:nowrap">R367.1<a name="GenomicTestCode-R367.461"> </a></td><td>Inherited pancreatic cancer (Small panel)</td></tr><tr><td style="white-space:nowrap">R368.1<a name="GenomicTestCode-R368.461"> </a></td><td>Hereditary angioedema type III (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R370.1<a name="GenomicTestCode-R370.461"> </a></td><td>Validation of unaccredited findings (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R371.1<a name="GenomicTestCode-R371.461"> </a></td><td>Malignant hyperthermia (small panel)</td></tr><tr><td style="white-space:nowrap">R372.1<a name="GenomicTestCode-R372.461"> </a></td><td>Newborn screening for sickle cell disease in a transfused baby (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R373.1<a name="GenomicTestCode-R373.461"> </a></td><td>RNA to be stored (Other)</td></tr><tr><td style="white-space:nowrap">R374.1<a name="GenomicTestCode-R374.461"> </a></td><td>Other sample to be stored (Other)</td></tr><tr><td style="white-space:nowrap">R375.1<a name="GenomicTestCode-R375.461"> </a></td><td>Family follow-up testing to aid variant interpretation (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R376.1<a name="GenomicTestCode-R376.461"> </a></td><td>Segmental or atypical neurofibromatosis type 1 testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R376.2<a name="GenomicTestCode-R376.462"> </a></td><td>Segmental or atypical neurofibromatosis type 1 testing (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R38.2<a name="GenomicTestCode-R38.462"> </a></td><td>Sporadic aniridia (Small panel)</td></tr><tr><td style="white-space:nowrap">R380.1<a name="GenomicTestCode-R380.461"> </a></td><td>Niemann Pick disease type C (Small panel)</td></tr><tr><td style="white-space:nowrap">R380.2<a name="GenomicTestCode-R380.462"> </a></td><td>Niemann Pick disease type C (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R381.2<a name="GenomicTestCode-R381.462"> </a></td><td>Other rare neuromuscular disorders (WGS)</td></tr><tr><td style="white-space:nowrap">R382.1<a name="GenomicTestCode-R382.461"> </a></td><td>Hypochondroplasia (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R383.1<a name="GenomicTestCode-R383.461"> </a></td><td>Linkage testing for Huntington disease (Other)</td></tr><tr><td style="white-space:nowrap">R384.1<a name="GenomicTestCode-R384.461"> </a></td><td>Generalised arterial calcification in infancy (Small panel)</td></tr><tr><td style="white-space:nowrap">R387.1<a name="GenomicTestCode-R387.461"> </a></td><td>Reanalysis of existing data (Other)</td></tr><tr><td style="white-space:nowrap">R389.1<a name="GenomicTestCode-R389.461"> </a></td><td>NIPD pre-pregnancy test work-up (NIPD)</td></tr><tr><td style="white-space:nowrap">R39.1<a name="GenomicTestCode-R39.461"> </a></td><td>Albinism or congenital nystagmus (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R390.1<a name="GenomicTestCode-R390.461"> </a></td><td>Multiple exostoses (Small panel)</td></tr><tr><td style="white-space:nowrap">R390.2<a name="GenomicTestCode-R390.462"> </a></td><td>Multiple exostoses (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R391.1<a name="GenomicTestCode-R391.461"> </a></td><td>Barth syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R394.1<a name="GenomicTestCode-R394.461"> </a></td><td>Mitochondrial neurogastrointestinal encephalopathy (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R395.1<a name="GenomicTestCode-R395.461"> </a></td><td>Thiamine metabolism dysfunction syndrome 2 (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R396.1<a name="GenomicTestCode-R396.461"> </a></td><td>Mitochondrial Complex V deficiency, TMEM70 type (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R397.1<a name="GenomicTestCode-R397.461"> </a></td><td>Maternally inherited cardiomyopathy (Targeted mutation testing)</td></tr><tr><td style="white-space:nowrap">R401.1<a name="GenomicTestCode-R401.461"> </a></td><td>Common aneuploidy testing prenatal (Common aneuploidy testing)</td></tr><tr><td style="white-space:nowrap">R402.1<a name="GenomicTestCode-R402.461"> </a></td><td>Premature ovarian insufficiency (Karyotype or equivalent)</td></tr><tr><td style="white-space:nowrap">R402.2<a name="GenomicTestCode-R402.462"> </a></td><td>Premature ovarian insufficiency (STR testing)</td></tr><tr><td style="white-space:nowrap">R403.1<a name="GenomicTestCode-R403.461"> </a></td><td>MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing newborn screening follow up (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R404.1<a name="GenomicTestCode-R404.461"> </a></td><td>Testing of unaffected individuals for inherited cancer predisposition syndromes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R404.3<a name="GenomicTestCode-R404.463"> </a></td><td>Testing of unaffected individuals for inherited cancer predisposition syndromes (Small panel)</td></tr><tr><td style="white-space:nowrap">R405.1<a name="GenomicTestCode-R405.461"> </a></td><td>Hereditary Erythrocytosis (Small panel)</td></tr><tr><td style="white-space:nowrap">R406.1<a name="GenomicTestCode-R406.461"> </a></td><td>Thrombocythaemia (Small panel)</td></tr><tr><td style="white-space:nowrap">R409.1<a name="GenomicTestCode-R409.461"> </a></td><td>Linkage testing for recognisable Mendelian disorders (Other)</td></tr><tr><td style="white-space:nowrap">R41.1<a name="GenomicTestCode-R41.461"> </a></td><td>Optic neuropathy (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R41.3<a name="GenomicTestCode-R41.463"> </a></td><td>Optic neuropathy (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R410.1<a name="GenomicTestCode-R410.461"> </a></td><td>Myotonic dystrophy type 2 (DM2) (STR testing)</td></tr><tr><td style="white-space:nowrap">R411.1<a name="GenomicTestCode-R411.461"> </a></td><td>Y chromosome microdeletion (Targeted mutation testing or equivalent)</td></tr><tr><td style="white-space:nowrap">R412.1<a name="GenomicTestCode-R412.461"> </a></td><td>Fetal anomalies with a likely genetic cause non urgent (WES or Large Panel)</td></tr><tr><td style="white-space:nowrap">R413.1<a name="GenomicTestCode-R413.461"> </a></td><td>Autoinflammatory Disorders (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R414.1<a name="GenomicTestCode-R414.461"> </a></td><td>APC associated Polyposis  (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R416.1<a name="GenomicTestCode-R416.461"> </a></td><td>Syndromic and non syndromic craniosynostosis involving midline sutures only (metopic, sagittal, metopic &amp; sagittal)  (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R417.1<a name="GenomicTestCode-R417.461"> </a></td><td>Multi Locus Imprinting Disorder (MLPA)</td></tr><tr><td style="white-space:nowrap">R417.2<a name="GenomicTestCode-R417.462"> </a></td><td>Multi Locus Imprinting Disorder (Small Panel)</td></tr><tr><td style="white-space:nowrap">R419.1<a name="GenomicTestCode-R419.461"> </a></td><td>Acute Rhabdomyolysis (Medium Panel)</td></tr><tr><td style="white-space:nowrap">R42.1<a name="GenomicTestCode-R42.461"> </a></td><td>Leber hereditary optic neuropathy (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R42.2<a name="GenomicTestCode-R42.462"> </a></td><td>Leber hereditary optic neuropathy (Other)</td></tr><tr><td style="white-space:nowrap">R420.1<a name="GenomicTestCode-R420.461"> </a></td><td>Pseudoxanthoma elasticum (Small Panel)</td></tr><tr><td style="white-space:nowrap">R421.1<a name="GenomicTestCode-R421.461"> </a></td><td>Pulmonary Fibrosis, Familial (Medium panel)</td></tr><tr><td style="white-space:nowrap">R422.1<a name="GenomicTestCode-R422.461"> </a></td><td>BAP1 associated tumour predisposition syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R423.1<a name="GenomicTestCode-R423.461"> </a></td><td>NIPD for Retinoblastoma haplotype testing (NIPD)</td></tr><tr><td style="white-space:nowrap">R424.1<a name="GenomicTestCode-R424.461"> </a></td><td>Subcutaneous panniculitis T-cell lymphoma (Single gene sequencing &lt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R426.1<a name="GenomicTestCode-R426.461"> </a></td><td>Pulmonary alveolar microlithiasis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R428.1<a name="GenomicTestCode-R428.461"> </a></td><td>Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (STR testing)</td></tr><tr><td style="white-space:nowrap">R428.2<a name="GenomicTestCode-R428.462"> </a></td><td>Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (FISH)</td></tr><tr><td style="white-space:nowrap">R43.1<a name="GenomicTestCode-R43.461"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R43.2<a name="GenomicTestCode-R43.462"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R43.3<a name="GenomicTestCode-R43.463"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (STR testing)</td></tr><tr><td style="white-space:nowrap">R430.1<a name="GenomicTestCode-R430.461"> </a></td><td>Inherited prostate cancer (Small panel)</td></tr><tr><td style="white-space:nowrap">R431.1<a name="GenomicTestCode-R431.461"> </a></td><td>Genome-wide DNA Methylation Profiling to Aid Variant Interpretation (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R433.1<a name="GenomicTestCode-R433.461"> </a></td><td>Monogenic diabetes, subtype glucokinase NIPT (NIPT)</td></tr><tr><td style="white-space:nowrap">R436.1<a name="GenomicTestCode-R436.461"> </a></td><td>Hereditary alpha tryptasaemia (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R438.1,<a name="GenomicTestCode-R438.461.44"> </a></td><td>Paediatric pseudo-obstruction syndrome (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R440.1<a name="GenomicTestCode-R440.461"> </a></td><td>Hereditary isolated diabetes insipidus (Small panel)</td></tr><tr><td style="white-space:nowrap">R441.1<a name="GenomicTestCode-R441.461"> </a></td><td>Unexplained death in infancy and sudden unexplained death in childhood (WGS)</td></tr><tr><td style="white-space:nowrap">R442.1<a name="GenomicTestCode-R442.461"> </a></td><td>Variant Re-interpretation (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R443.1<a name="GenomicTestCode-R443.461"> </a></td><td>Confirmation test (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R444.1<a name="GenomicTestCode-R444.461"> </a></td><td>NICE approved PARP inhibitor treatment (Small panel)</td></tr><tr><td style="white-space:nowrap">R444.2<a name="GenomicTestCode-R444.462"> </a></td><td>NICE approved PARP inhibitor treatment (Small panel)</td></tr><tr><td style="white-space:nowrap">R445.1<a name="GenomicTestCode-R445.461"> </a></td><td>T21, T18 and T13 aneuploidy testing NIPT (previous history) (NIPT)</td></tr><tr><td style="white-space:nowrap">R446.1<a name="GenomicTestCode-R446.461"> </a></td><td>APOL1 kidney donor testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R447.1<a name="GenomicTestCode-R447.461"> </a></td><td>Validation of WGS Diagnostic discovery (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R448.1<a name="GenomicTestCode-R448.461"> </a></td><td>Prenatal testing (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R449.1<a name="GenomicTestCode-R449.461"> </a></td><td>Diagnostic testing for Glutaric acidaemia I (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R45.1<a name="GenomicTestCode-R45.461"> </a></td><td>Stickler syndrome (Small panel)</td></tr><tr><td style="white-space:nowrap">R450.1<a name="GenomicTestCode-R450.461"> </a></td><td>Diagnostic testing for Isovaleric acidaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R451.1<a name="GenomicTestCode-R451.461"> </a></td><td>Diagnostic testing for MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R452.1<a name="GenomicTestCode-R452.461"> </a></td><td>Silver russell syndrome and Temple Syndrome (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R453.1<a name="GenomicTestCode-R453.461"> </a></td><td>Monogenic short stature (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R454.1<a name="GenomicTestCode-R454.461"> </a></td><td>Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R456.1<a name="GenomicTestCode-R456.461"> </a></td><td>Embryonal tumour of possible germline origin (WES or Medium panel)</td></tr><tr><td style="white-space:nowrap">R456.2<a name="GenomicTestCode-R456.462"> </a></td><td>Embryonal tumour of possible germline origin (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R457.1<a name="GenomicTestCode-R457.461"> </a></td><td>Sarcoma of possible germline origin (Small panel)</td></tr><tr><td style="white-space:nowrap">R458.1<a name="GenomicTestCode-R458.461"> </a></td><td>Young onset or familial dementia (WGS)</td></tr><tr><td style="white-space:nowrap">R459.1<a name="GenomicTestCode-R459.461"> </a></td><td>Young onset or complex Parkinson disease (WGS)</td></tr><tr><td style="white-space:nowrap">R46.1<a name="GenomicTestCode-R46.461"> </a></td><td>Congenital fibrosis of the extraocular muscles (Small panel)</td></tr><tr><td style="white-space:nowrap">R460.1<a name="GenomicTestCode-R460.461"> </a></td><td>Amyotrophic lateral sclerosis / Motor Neurone Disease (WGS)</td></tr><tr><td style="white-space:nowrap">R461.1<a name="GenomicTestCode-R461.461"> </a></td><td>Cerebral amyloid angiopathy (WGS)</td></tr><tr><td style="white-space:nowrap">R462.1<a name="GenomicTestCode-R462.461"> </a></td><td>Childhood interstitial lung disease (Medium panel)</td></tr><tr><td style="white-space:nowrap">R463.1<a name="GenomicTestCode-R463.461"> </a></td><td>Cytogenetic characterisation of a genomic abnormality â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style="white-space:nowrap">R464.1<a name="GenomicTestCode-R464.461"> </a></td><td>Recurrent miscarriage where products of conception are not available for testing parental karyotype (Karyotype)</td></tr><tr><td style="white-space:nowrap">R465.1<a name="GenomicTestCode-R465.461"> </a></td><td>Familial cytogenetic rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style="white-space:nowrap">R466.1<a name="GenomicTestCode-R466.461"> </a></td><td>Unexplained infertility (Karyotype)</td></tr><tr><td style="white-space:nowrap">R467.1<a name="GenomicTestCode-R467.461"> </a></td><td>Gamete donors (Karyotype)</td></tr><tr><td style="white-space:nowrap">R468.1<a name="GenomicTestCode-R468.461"> </a></td><td>Possible sex chromosome aneuploidy or structural rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style="white-space:nowrap">R47.1<a name="GenomicTestCode-R47.461"> </a></td><td>Angelman syndrome (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R471.1<a name="GenomicTestCode-R471.461"> </a></td><td>Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing C9orf72 haplotype (Linkage analysis)</td></tr><tr><td style="white-space:nowrap">R471.2<a name="GenomicTestCode-R471.462"> </a></td><td>Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing SOD1 haplotype (Linkage analysis)</td></tr><tr><td style="white-space:nowrap">R471.3<a name="GenomicTestCode-R471.463"> </a></td><td>Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing MAPT haplotype (Linkage analysis)</td></tr><tr><td style="white-space:nowrap">R471.4<a name="GenomicTestCode-R471.464"> </a></td><td>Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing PSEN1 haplotype (Linkage analysis)</td></tr><tr><td style="white-space:nowrap">R48.1<a name="GenomicTestCode-R48.461"> </a></td><td>Prader-Willi syndrome (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R49.1<a name="GenomicTestCode-R49.461"> </a></td><td>Beckwith-Wiedemann syndrome (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R49.3<a name="GenomicTestCode-R49.463"> </a></td><td>Beckwith-Wiedemann syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R50.1<a name="GenomicTestCode-R50.461"> </a></td><td>Isolated hemihypertrophy or macroglossia (Methylation testing)</td></tr><tr><td style="white-space:nowrap">R52.1<a name="GenomicTestCode-R52.461"> </a></td><td>Short stature SHOX deficiency (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R52.2<a name="GenomicTestCode-R52.462"> </a></td><td>Short stature SHOX deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style="white-space:nowrap">R54.3<a name="GenomicTestCode-R54.463"> </a></td><td>Hereditary ataxia with onset in adulthood (WGS)</td></tr><tr><td style="white-space:nowrap">R54.4<a name="GenomicTestCode-R54.464"> </a></td><td>Hereditary ataxia with onset in adulthood (RFC1 STR testing)</td></tr><tr><td style="white-space:nowrap">R55.4<a name="GenomicTestCode-R55.464"> </a></td><td>Hereditary ataxia with onset in childhood (WGS)</td></tr><tr><td style="white-space:nowrap">R56.3<a name="GenomicTestCode-R56.463"> </a></td><td>Adult onset dystonia, chorea or related movement disorder (WGS)</td></tr><tr><td style="white-space:nowrap">R57.5<a name="GenomicTestCode-R57.465"> </a></td><td>Childhood onset dystonia, chorea or related movement disorder (WGS)</td></tr><tr><td style="white-space:nowrap">R60.3<a name="GenomicTestCode-R60.463"> </a></td><td>Adult onset hereditary spastic paraplegia (WGS)</td></tr><tr><td style="white-space:nowrap">R61.4<a name="GenomicTestCode-R61.464"> </a></td><td>Childhood onset hereditary spastic paraplegia (WGS)</td></tr><tr><td style="white-space:nowrap">R62.2<a name="GenomicTestCode-R62.462"> </a></td><td>Adult onset leukodystrophy (WGS)</td></tr><tr><td style="white-space:nowrap">R63.1<a name="GenomicTestCode-R63.461"> </a></td><td>Possible mitochondrial disorder nuclear genes (WES or Large Panel)</td></tr><tr><td style="white-space:nowrap">R64.1<a name="GenomicTestCode-R64.461"> </a></td><td>MELAS or MIDD (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R65.1<a name="GenomicTestCode-R65.461"> </a></td><td>Aminoglycoside exposure posing risk to hearing (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R66.1<a name="GenomicTestCode-R66.461"> </a></td><td>Paroxysmal central nervous system disorders (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R67.1<a name="GenomicTestCode-R67.461"> </a></td><td>Monogenic hearing loss (WES or Large Panel)</td></tr><tr><td style="white-space:nowrap">R68.1<a name="GenomicTestCode-R68.461"> </a></td><td>Huntington disease (STR testing)</td></tr><tr><td style="white-space:nowrap">R69.5<a name="GenomicTestCode-R69.465"> </a></td><td>Hypotonic infant  (WGS)</td></tr><tr><td style="white-space:nowrap">R70.1<a name="GenomicTestCode-R70.461"> </a></td><td>Spinal muscular atrophy type 1 diagnostic test (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R71.1<a name="GenomicTestCode-R71.461"> </a></td><td>Spinal muscular atrophy type 1 rare variant testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R72.1<a name="GenomicTestCode-R72.461"> </a></td><td>Myotonic dystrophy type 1 (STR testing)</td></tr><tr><td style="white-space:nowrap">R73.1<a name="GenomicTestCode-R73.461"> </a></td><td>Duchenne or Becker muscular dystrophy (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style="white-space:nowrap">R73.2<a name="GenomicTestCode-R73.462"> </a></td><td>Duchenne or Becker muscular dystrophy (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R74.1<a name="GenomicTestCode-R74.461"> </a></td><td>Facioscapulohumeral muscular dystrophy (Other)</td></tr><tr><td style="white-space:nowrap">R75.1<a name="GenomicTestCode-R75.461"> </a></td><td>Oculopharyngeal muscular dystrophy (STR testing)</td></tr><tr><td style="white-space:nowrap">R76.1<a name="GenomicTestCode-R76.461"> </a></td><td>Skeletal muscle channelopathy (Small panel)</td></tr><tr><td style="white-space:nowrap">R77.1<a name="GenomicTestCode-R77.461"> </a></td><td>Hereditary neuropathy PMP22 copy number (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R78.4<a name="GenomicTestCode-R78.464"> </a></td><td>Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (WGS)</td></tr><tr><td style="white-space:nowrap">R78.5<a name="GenomicTestCode-R78.465"> </a></td><td>Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (RFC1 STR testing)</td></tr><tr><td style="white-space:nowrap">R79.1<a name="GenomicTestCode-R79.461"> </a></td><td>Congenital muscular dystrophy (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R80.1<a name="GenomicTestCode-R80.461"> </a></td><td>Congenital myaesthenic syndrome (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R81.1<a name="GenomicTestCode-R81.461"> </a></td><td>Congenital myopathy (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R82.1<a name="GenomicTestCode-R82.461"> </a></td><td>Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R83.3<a name="GenomicTestCode-R83.463"> </a></td><td>Arthrogryposis (WGS)</td></tr><tr><td style="white-space:nowrap">R84.4<a name="GenomicTestCode-R84.464"> </a></td><td>Cerebellar anomalies (WGS)</td></tr><tr><td style="white-space:nowrap">R85.2<a name="GenomicTestCode-R85.462"> </a></td><td>Holoprosencephaly (WGS)</td></tr><tr><td style="white-space:nowrap">R86.3<a name="GenomicTestCode-R86.463"> </a></td><td>Hydrocephalus (WGS)</td></tr><tr><td style="white-space:nowrap">R87.3<a name="GenomicTestCode-R87.463"> </a></td><td>Cerebral malformation (WGS)</td></tr><tr><td style="white-space:nowrap">R88.3<a name="GenomicTestCode-R88.463"> </a></td><td>Severe microcephaly (WGS)</td></tr><tr><td style="white-space:nowrap">R89.3<a name="GenomicTestCode-R89.463"> </a></td><td>Ultra-rare and atypical monogenic disorders (WGS)</td></tr><tr><td style="white-space:nowrap">R90.1<a name="GenomicTestCode-R90.461"> </a></td><td>Bleeding and platelet disorders (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R91.1<a name="GenomicTestCode-R91.461"> </a></td><td>Cytopenia NOT Fanconi anaemia (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R91.2<a name="GenomicTestCode-R91.462"> </a></td><td>Cytopenia NOT Fanconi anaemia (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R92.1<a name="GenomicTestCode-R92.461"> </a></td><td>Rare anaemia (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R92.2<a name="GenomicTestCode-R92.462"> </a></td><td>Rare anaemia (Small panel)</td></tr><tr><td style="white-space:nowrap">R92.3<a name="GenomicTestCode-R92.463"> </a></td><td>Rare anaemia (WES or Medium Panel)</td></tr><tr><td style="white-space:nowrap">R93.1<a name="GenomicTestCode-R93.461"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies (MLPA or equivalent)</td></tr><tr><td style="white-space:nowrap">R93.2<a name="GenomicTestCode-R93.462"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies (Small panel)</td></tr><tr><td style="white-space:nowrap">R95.1<a name="GenomicTestCode-R95.461"> </a></td><td>Iron overload hereditary haemochromatosis testing (Targeted variant testing)</td></tr><tr><td style="white-space:nowrap">R96.1<a name="GenomicTestCode-R96.461"> </a></td><td>Iron metabolism disorders NOT common HFE variants (Small panel)</td></tr><tr><td style="white-space:nowrap">R97.1<a name="GenomicTestCode-R97.461"> </a></td><td>Thrombophilia with a likely monogenic cause (WES or Small Panel)</td></tr><tr><td style="white-space:nowrap">R98.2<a name="GenomicTestCode-R98.462"> </a></td><td>Likely inborn error of metabolism (WGS)</td></tr><tr><td style="white-space:nowrap">R98.3<a name="GenomicTestCode-R98.463"> </a></td><td>Likely inborn error of metabolism (WES)</td></tr><tr><td style="white-space:nowrap">R99.1<a name="GenomicTestCode-R99.461"> </a></td><td>Common craniosynostosis syndromes (Small panel)</td></tr><tr><td style="white-space:nowrap">R99.2<a name="GenomicTestCode-R99.462"> </a></td><td>Common craniosynostosis syndromes (Exon level CNV detection by MLPA or equivalent)</td></tr></table></div>
  </text>
  <url value="https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory"/>
  <version value="2.0.12"/>
  <name value="GenomicTestCode"/>
  <title value="NHS England Genomic Test Code"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2026-06-04"/>
  <publisher value="NHS North West Genomics"/>
  <contact>
    <telecom>
      <system value="url"/>
      <value value="https://www.nwgenomics.nhs.uk/contact-us"/>
    </telecom>
  </contact>
  <description
               value="- [Genomic Test Directory](https://www.england.nhs.uk/publication/national-genomic-test-directories)&quot;

HL7 v2 CodeSystem : England-GenomicTestDirectory"/>
  <jurisdiction>
    <coding>
      <system value="urn:iso:std:iso:3166"/>
      <code value="GB"/>
      <display value="United Kingdom of Great Britain and Northern Ireland"/>
    </coding>
  </jurisdiction>
  <caseSensitive value="true"/>
  <content value="fragment"/>
  <concept>
    <code value="M1.1"/>
    <display
             value="Colorectal Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF)"/>
  </concept>
  <concept>
    <code value="M1.2"/>
    <display value="Colorectal Carcinoma, KRAS hotspot"/>
  </concept>
  <concept>
    <code value="M1.3"/>
    <display value="Colorectal Carcinoma, NRAS hotspot"/>
  </concept>
  <concept>
    <code value="M1.4"/>
    <display value="Colorectal Carcinoma, MSI Testing"/>
  </concept>
  <concept>
    <code value="M1.5"/>
    <display value="Colorectal Carcinoma, MLH1 promoter hypermethylation"/>
  </concept>
  <concept>
    <code value="M1.6"/>
    <display
             value="Colorectal Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M1.7"/>
    <display value="Colorectal Carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M1.9"/>
    <display
             value="Colorectal Carcinoma, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2, POLE, POLD1)"/>
  </concept>
  <concept>
    <code value="M10.1"/>
    <display
             value="Thyroid Follicular Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, HRAS)"/>
  </concept>
  <concept>
    <code value="M10.2"/>
    <display
             value="Thyroid Follicular Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET)"/>
  </concept>
  <concept>
    <code value="M100.1"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M100.2"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 Copy number FISH"/>
  </concept>
  <concept>
    <code value="M100.3"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, REL copy number FISH"/>
  </concept>
  <concept>
    <code value="M100.4"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M100.5"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, copy number variant (CD274, PDCD1LG2, REL)"/>
  </concept>
  <concept>
    <code value="M100.6"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, rearrangement (CD274, PDCD1LG2)"/>
  </concept>
  <concept>
    <code value="M100.7"/>
    <display value="Primary Mediastinal B Cell Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M100.8"/>
    <display
             value="Primary Mediastinal B Cell Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M101.1"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M101.2"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, t(2;17)(p23;q23) CLTC-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M101.3"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M101.4"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M101.5"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, Multi-target NGS panel, structural variant (CLTC-ALK, ALK-NPM1, other ALK rearrangements)"/>
  </concept>
  <concept>
    <code value="M101.6"/>
    <display value="ALK Positive Large B Cell Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M101.7"/>
    <display
             value="ALK Positive Large B Cell Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M102.1"/>
    <display
             value="Mantle Cell Lymphoma, t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M102.2"/>
    <display value="Mantle Cell Lymphoma, CCND1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M102.3"/>
    <display value="Mantle Cell Lymphoma, CCND2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M102.4"/>
    <display
             value="Mantle Cell Lymphoma, Multi-target NGS panel, structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)"/>
  </concept>
  <concept>
    <code value="M102.5"/>
    <display
             value="Mantle Cell Lymphoma, Multi-target NGS panel, small variant (TP53)"/>
  </concept>
  <concept>
    <code value="M103.1"/>
    <display
             value="Follicular Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M103.2"/>
    <display value="Follicular Lymphoma, BCL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M103.3"/>
    <display value="Follicular Lymphoma, BCL6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M103.4"/>
    <display
             value="Follicular Lymphoma, Multi-target NGS panel, small variant (CARD11, CREBBP, EZH2, ARID1A, EP300, MEF2B, FOXO1)"/>
  </concept>
  <concept>
    <code value="M103.5"/>
    <display
             value="Follicular Lymphoma, Multi-target NGS panel, structural variant (IGH-BCL2, BCL2, BCL6)"/>
  </concept>
  <concept>
    <code value="M104.1"/>
    <display
             value="Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, Multi-target NGS panel, small variant (MYD88, CXCR4)"/>
  </concept>
  <concept>
    <code value="M104.2"/>
    <display
             value="Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, MYD88 hotspot"/>
  </concept>
  <concept>
    <code value="M105.1"/>
    <display
             value="Igm Monoclonal Gammopathy of Uncertain Significance, Multi-target NGS panel, small variant (MYD88, CXCR4)"/>
  </concept>
  <concept>
    <code value="M105.2"/>
    <display
             value="Igm Monoclonal Gammopathy of Uncertain Significance, MYD88 hotspot"/>
  </concept>
  <concept>
    <code value="M106.1"/>
    <display value="Intra-Ocular Lymphoma, MYD88 hotspot"/>
  </concept>
  <concept>
    <code value="M107.1"/>
    <display
             value="Malt-Lymphoma, t(11;18)(q21;q21) BIRC3-MALT1  FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M107.10"/>
    <display value="Malt-Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M107.2"/>
    <display value="Malt-Lymphoma, t(1;14)(p22;q32) IGH-BCL10 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M107.3"/>
    <display value="Malt-Lymphoma, t(14;18)(q32;q21) IGH-MALT1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M107.4"/>
    <display value="Malt-Lymphoma, MALT1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M107.5"/>
    <display value="Malt-Lymphoma, BCL10 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M107.6"/>
    <display value="Malt-Lymphoma, FOXP1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M107.7"/>
    <display value="Malt-Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M107.8"/>
    <display
             value="Malt-Lymphoma, Multi-target NGS panel, structural variant (BIRC3-MALT1, IGH-BCL10, IGH-MALT1, other MALT rearrangements, other BCL10 rearrangements, FOXP1)"/>
  </concept>
  <concept>
    <code value="M107.9"/>
    <display value="Malt-Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M108.1"/>
    <display
             value="Hairy Cell Leukaemia, Multi-target NGS panel, small variant (BRAF)"/>
  </concept>
  <concept>
    <code value="M108.2"/>
    <display value="Hairy Cell Leukaemia, BRAF V600 hotspot"/>
  </concept>
  <concept>
    <code value="M108.5"/>
    <display
             value="Hairy Cell Leukaemia, Ig gene hypermutation detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M108.6"/>
    <display
             value="Hairy Cell Leukaemia, Ig gene hypermutation detection NGS"/>
  </concept>
  <concept>
    <code value="M109.1"/>
    <display
             value="Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M109.2"/>
    <display
             value="Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection NGS"/>
  </concept>
  <concept>
    <code value="M11.1"/>
    <display
             value="Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, small variant (TP53, BRAF)"/>
  </concept>
  <concept>
    <code value="M11.2"/>
    <display
             value="Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, copy number variant (TP53)"/>
  </concept>
  <concept>
    <code value="M11.3"/>
    <display
             value="Poorly Differentiated Anaplastic Thyroid Carcinoma, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M11.4"/>
    <display
             value="Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET, ALK)"/>
  </concept>
  <concept>
    <code value="M110.1,"/>
    <display
             value="Paediatric Type Follicular Lymphoma, Multi-target NGS panel, small variant (MAP2K1)"/>
  </concept>
  <concept>
    <code value="M110.2,"/>
    <display
             value="Paediatric Type Follicular Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M110.3,"/>
    <display value="Paediatric Type Follicular Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M110.4,"/>
    <display
             value="Paediatric Type Follicular Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M111.1"/>
    <display
             value="T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (RHOA, DNMT3A, IDH2, TET2)"/>
  </concept>
  <concept>
    <code value="M111.2"/>
    <display
             value="T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M111.3"/>
    <display
             value="T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection NGS"/>
  </concept>
  <concept>
    <code value="M111.4"/>
    <display value="T Cell Non-Hodgkin Lymphoma, TCR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M111.5"/>
    <display value="T Cell Non-Hodgkin Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M111.6"/>
    <display
             value="T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (TCR rearrangement)"/>
  </concept>
  <concept>
    <code value="M111.7"/>
    <display value="T Cell Non-Hodgkin Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M111.8"/>
    <display value="T Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M112.3"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), IRF4/DUSP22 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M112.4"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), TP63 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M112.5"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M112.6"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), Multi-target NGS panel, structural variant (IRF4/DUSP22, TP63)"/>
  </concept>
  <concept>
    <code value="M112.7"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M112.8"/>
    <display
             value="ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M113.1"/>
    <display value="T Prolymphocytic Leukaemia, TCL1A rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M113.2"/>
    <display value="T Prolymphocytic Leukaemia, Chr8 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M113.3"/>
    <display
             value="T Prolymphocytic Leukaemia, Multi-target NGS panel, structural variant (TCL1A, Chr8)"/>
  </concept>
  <concept>
    <code value="M113.6"/>
    <display
             value="T Prolymphocytic Leukaemia, Karyotype (to include TCL1 rearrangements t(X;14))"/>
  </concept>
  <concept>
    <code value="M114.1"/>
    <display
             value="Large Granular Lymphocyte Leukaemia, Multi-target NGS panel, small variant (STAT3, STAT5B)"/>
  </concept>
  <concept>
    <code value="M115.1"/>
    <display
             value="NK Cell/Gamma-Delta T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)"/>
  </concept>
  <concept>
    <code value="M115.2"/>
    <display
             value="NK Cell/Gamma-Delta T Cell Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M115.3"/>
    <display value="NK Cell/Gamma-Delta T Cell Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M115.4"/>
    <display
             value="NK Cell/Gamma-Delta T Cell Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M116.1"/>
    <display
             value="Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)"/>
  </concept>
  <concept>
    <code value="M116.2"/>
    <display value="Hepatosplenic T Cell Lymphoma, i7q rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M116.3"/>
    <display value="Hepatosplenic T Cell Lymphoma, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M116.4"/>
    <display
             value="Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, structural variant (i17q)"/>
  </concept>
  <concept>
    <code value="M116.5"/>
    <display value="Hepatosplenic T Cell Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M116.6"/>
    <display value="Hepatosplenic T Cell Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M117.1"/>
    <display
             value="Histiocytosis, Multi-target NGS panel, small variant (BRAF, MAP2K1, NRAS, KRAS, HRAS, ERBB3, ARAF, MAP3K1, PIK3CA, PIK3CD)"/>
  </concept>
  <concept>
    <code value="M117.12"/>
    <display value="Histiocytosis, NTRK1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M117.16"/>
    <display value="Histiocytosis, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M117.17"/>
    <display value="Histiocytosis, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M117.18"/>
    <display value="Histiocytosis, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M117.19"/>
    <display value="Histiocytosis, High Sensitivity BRAF"/>
  </concept>
  <concept>
    <code value="M117.2"/>
    <display
             value="Histiocytosis, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M117.3"/>
    <display value="Histiocytosis, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M117.7"/>
    <display value="Histiocytosis, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M118.1"/>
    <display
             value="Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, STR Testing"/>
  </concept>
  <concept>
    <code value="M118.2"/>
    <display
             value="Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, Sex chromosome FISH"/>
  </concept>
  <concept>
    <code value="M119.1,"/>
    <display value="Paediatric Tumours, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M119.2,"/>
    <display
             value="Paediatric Tumours, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M119.4,"/>
    <display value="Paediatric Tumours, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M119.5,"/>
    <display value="Paediatric Tumours, Multi-target NGS-small variant"/>
  </concept>
  <concept>
    <code value="M12.1"/>
    <display
             value="Thyroid Medullary Carcinoma, Multi-target NGS panel, small variant (RET)"/>
  </concept>
  <concept>
    <code value="M12.2"/>
    <display
             value="Thyroid Medullary Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M120.1"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1)"/>
  </concept>
  <concept>
    <code value="M120.10"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.11"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.12"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.13"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.14"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.15"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M120.16"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M120.17"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, SMARCB1)"/>
  </concept>
  <concept>
    <code value="M120.18"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M120.2"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 seq"/>
  </concept>
  <concept>
    <code value="M120.3"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 seq"/>
  </concept>
  <concept>
    <code value="M120.4"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M120.5"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M120.6"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M120.7"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.8"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M120.9"/>
    <display
             value="Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M124.1"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, small variant (BCOR)"/>
  </concept>
  <concept>
    <code value="M124.10"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, structural variant (BCOR, NUTM2B-YWHAE, NUTM2E-YWHAE, NUTM1-YWHAE, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M124.11"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, copy number variant (BCOR, YWHAE)"/>
  </concept>
  <concept>
    <code value="M124.2"/>
    <display value="Clear Cell Kidney Sarcoma, Paediatric, BCOR seq"/>
  </concept>
  <concept>
    <code value="M124.3"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, BCOR copy number FISH"/>
  </concept>
  <concept>
    <code value="M124.4"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, BCOR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M124.5"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, NUTM2B-YWHAE FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M124.6"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, NUTM2E-YWHAE FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M124.7"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, NUTM1-YWHAE FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M124.8"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, YWHAE copy number FISH"/>
  </concept>
  <concept>
    <code value="M124.9"/>
    <display
             value="Clear Cell Kidney Sarcoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M126.1"/>
    <display
             value="CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, MN1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M126.2"/>
    <display
             value="CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M126.3"/>
    <display
             value="CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, Multi-target NGS panel, structural variant (MN1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M126.4"/>
    <display
             value="CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M127.1"/>
    <display
             value="Congenital Mesoblastic Nephroma, Paediatric, NTRK3-ETV6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M127.3"/>
    <display
             value="Congenital Mesoblastic Nephroma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M127.4"/>
    <display
             value="Congenital Mesoblastic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK3-ETV6, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M13.1"/>
    <display
             value="Phaeochromocytoma, Multi-target NGS panel, small variant (RET)"/>
  </concept>
  <concept>
    <code value="M13.2"/>
    <display
             value="Phaeochromocytoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M130.1"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCB1)"/>
  </concept>
  <concept>
    <code value="M130.2"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 seq"/>
  </concept>
  <concept>
    <code value="M130.3"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M130.4"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M130.5"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M130.6"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)"/>
  </concept>
  <concept>
    <code value="M130.7"/>
    <display
             value="Cribriform Neuroepithelial Tumour, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M131.1"/>
    <display
             value="Cystic Nephroma, Paediatric, Multi-target NGS panel, small variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M131.2"/>
    <display value="Cystic Nephroma, Paediatric, DICER1 seq"/>
  </concept>
  <concept>
    <code value="M131.3"/>
    <display value="Cystic Nephroma, Paediatric, DICER1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M131.4"/>
    <display value="Cystic Nephroma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M131.5"/>
    <display
             value="Cystic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M131.6"/>
    <display
             value="Cystic Nephroma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M132.1"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, small variant (BRAF)"/>
  </concept>
  <concept>
    <code value="M132.10"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.11"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M132.12"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M132.13"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M132.2"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M132.3"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.4"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.5"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.6"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.7"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.8"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M132.9"/>
    <display
             value="Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M133.1"/>
    <display
             value="Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SUFU)"/>
  </concept>
  <concept>
    <code value="M133.2"/>
    <display value="Desmoplastic Medulloblastoma, Paediatric, SUFU seq"/>
  </concept>
  <concept>
    <code value="M133.3"/>
    <display
             value="Desmoplastic Medulloblastoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M133.4"/>
    <display
             value="Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M133.5"/>
    <display
             value="Desmoplastic Medulloblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M136.1"/>
    <display
             value="Fibrolamellar Hepatocellular Carcinoma, Paediatric, DNAJB1-PRKACA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M136.2"/>
    <display
             value="Fibrolamellar Hepatocellular Carcinoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M136.3"/>
    <display
             value="Fibrolamellar Hepatocellular Carcinoma, Paediatric, Multi-target NGS panel, structural variant (DNAJB1-PRKACA, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M136.5"/>
    <display
             value="Fibrolamellar Hepatocellular Carcinoma, Paediatric, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M137.1"/>
    <display
             value="Ganglioglioma, Paediatric, Multi-target NGS panel, small variant (BRAF)"/>
  </concept>
  <concept>
    <code value="M137.10"/>
    <display value="Ganglioglioma, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.11"/>
    <display value="Ganglioglioma, Paediatric, KIAA1549 copy number FISH"/>
  </concept>
  <concept>
    <code value="M137.12"/>
    <display value="Ganglioglioma, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M137.13"/>
    <display value="Ganglioglioma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M137.14"/>
    <display
             value="Ganglioglioma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)"/>
  </concept>
  <concept>
    <code value="M137.15"/>
    <display value="Ganglioglioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M137.2"/>
    <display
             value="Ganglioglioma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M137.3"/>
    <display value="Ganglioglioma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.4"/>
    <display value="Ganglioglioma, Paediatric, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.5"/>
    <display value="Ganglioglioma, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.6"/>
    <display value="Ganglioglioma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.7"/>
    <display value="Ganglioglioma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.8"/>
    <display value="Ganglioglioma, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M137.9"/>
    <display value="Ganglioglioma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M138.1"/>
    <display
             value="Glial Tumours, Paediatric, Multi-target NGS panel, small variant (ATRX)"/>
  </concept>
  <concept>
    <code value="M138.2"/>
    <display value="Glial Tumours, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M138.3"/>
    <display
             value="Glial Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M138.4"/>
    <display value="Glial Tumours, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M139.1"/>
    <display
             value="Glioblastoma, Paediatric, Multi-target NGS panel, small variant (BRAF, CDKN2A, FGFR4)"/>
  </concept>
  <concept>
    <code value="M139.10"/>
    <display value="Glioblastoma, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.12"/>
    <display value="Glioblastoma, Paediatric, CDKN2A seq"/>
  </concept>
  <concept>
    <code value="M139.13"/>
    <display value="Glioblastoma, Paediatric, FGFR4 seq"/>
  </concept>
  <concept>
    <code value="M139.14"/>
    <display value="Glioblastoma, Paediatric, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M139.15"/>
    <display value="Glioblastoma, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M139.16"/>
    <display value="Glioblastoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M139.17"/>
    <display
             value="Glioblastoma, Paediatric, Multi-target NGS panel, copy number variant (CDKN2A)"/>
  </concept>
  <concept>
    <code value="M139.18"/>
    <display value="Glioblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M139.2"/>
    <display
             value="Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B,  BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M139.3"/>
    <display value="Glioblastoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.4"/>
    <display value="Glioblastoma, Paediatric, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.5"/>
    <display value="Glioblastoma, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.6"/>
    <display value="Glioblastoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.7"/>
    <display value="Glioblastoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.8"/>
    <display value="Glioblastoma, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M139.9"/>
    <display value="Glioblastoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M14.1"/>
    <display
             value="Adrenal Cortical Carcinoma, Multi-target NGS panel, small variant (TP53)"/>
  </concept>
  <concept>
    <code value="M14.2"/>
    <display
             value="Adrenal Cortical Carcinoma, Multi-target NGS panel, copy number variant (TP53)"/>
  </concept>
  <concept>
    <code value="M14.3"/>
    <display
             value="Adrenal Cortical Carcinoma, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M14.4"/>
    <display
             value="Adrenal Cortical Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M14.5"/>
    <display value="Adrenal Cortical Carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M143.1"/>
    <display
             value="Lung, Paediatric, Multi-target NGS panel, small variant (H3-3A, H3-3B)"/>
  </concept>
  <concept>
    <code value="M143.2"/>
    <display value="Lung, Paediatric, H3-3A seq"/>
  </concept>
  <concept>
    <code value="M143.3"/>
    <display value="Lung, Paediatric, H3-3B seq"/>
  </concept>
  <concept>
    <code value="M143.4"/>
    <display value="Lung, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M143.5"/>
    <display
             value="Lung, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M145.1"/>
    <display
             value="Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, BCOR, PTCH1, PTCH2, PTEN, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M145.10"/>
    <display value="Medulloblastoma, Paediatric, BCOR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M145.11"/>
    <display value="Medulloblastoma, Paediatric, C19MC copy number FISH"/>
  </concept>
  <concept>
    <code value="M145.12"/>
    <display value="Medulloblastoma, Paediatric, PTEN copy number FISH"/>
  </concept>
  <concept>
    <code value="M145.13"/>
    <display value="Medulloblastoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M145.14"/>
    <display
             value="Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (ALK, BCOR, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M145.15"/>
    <display
             value="Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (ALK, BCOR, C19MC, PTEN)"/>
  </concept>
  <concept>
    <code value="M145.16"/>
    <display value="Medulloblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M145.2"/>
    <display value="Medulloblastoma, Paediatric, ALK seq"/>
  </concept>
  <concept>
    <code value="M145.3"/>
    <display value="Medulloblastoma, Paediatric, BCOR seq"/>
  </concept>
  <concept>
    <code value="M145.4"/>
    <display value="Medulloblastoma, Paediatric, PTCH1 seq"/>
  </concept>
  <concept>
    <code value="M145.5"/>
    <display value="Medulloblastoma, Paediatric, PTCH2 seq"/>
  </concept>
  <concept>
    <code value="M145.6"/>
    <display value="Medulloblastoma, Paediatric, TERT promoter seq"/>
  </concept>
  <concept>
    <code value="M145.7"/>
    <display value="Medulloblastoma, Paediatric, ALK copy number FISH"/>
  </concept>
  <concept>
    <code value="M145.8"/>
    <display value="Medulloblastoma, Paediatric, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M145.9"/>
    <display value="Medulloblastoma, Paediatric, BCOR copy number FISH"/>
  </concept>
  <concept>
    <code value="M146.1"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, small variant (SMARCA4, DDX3X)"/>
  </concept>
  <concept>
    <code value="M146.2"/>
    <display value="Medulloblastoma Group 3, Paediatric, SMARCA4 seq"/>
  </concept>
  <concept>
    <code value="M146.3"/>
    <display value="Medulloblastoma Group 3, Paediatric, DDX3X seq"/>
  </concept>
  <concept>
    <code value="M146.4"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M146.5"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, PVT1-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M146.6"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M146.7"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, structural variant (PVT1-MYC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M146.8"/>
    <display
             value="Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4)"/>
  </concept>
  <concept>
    <code value="M146.9"/>
    <display value="Medulloblastoma Group 3, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M147.1"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, small variant (MYCN, EZH2)"/>
  </concept>
  <concept>
    <code value="M147.10"/>
    <display value="Medulloblastoma Group 3/4, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M147.2"/>
    <display value="Medulloblastoma Group 3/4, Paediatric, MYCN seq"/>
  </concept>
  <concept>
    <code value="M147.3"/>
    <display value="Medulloblastoma Group 3/4, Paediatric, EZH2 seq"/>
  </concept>
  <concept>
    <code value="M147.4"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M147.5"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M147.6"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M147.7"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M147.8"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M147.9"/>
    <display
             value="Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, copy number variant (MYCN, MYC)"/>
  </concept>
  <concept>
    <code value="M148.1"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, small variant (YAP1, PTCH1)"/>
  </concept>
  <concept>
    <code value="M148.10"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (YAP1, PTCH1)"/>
  </concept>
  <concept>
    <code value="M148.11"/>
    <display value="Medulloblastoma TP53 WT, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M148.2"/>
    <display value="Medulloblastoma TP53 WT, Paediatric, YAP1 seq"/>
  </concept>
  <concept>
    <code value="M148.3"/>
    <display value="Medulloblastoma TP53 WT, Paediatric, PTCH1 seq"/>
  </concept>
  <concept>
    <code value="M148.4"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M148.5"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M148.6"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, YAP1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M148.7"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, PTCH1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M148.8"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M148.9"/>
    <display
             value="Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, structural variant (YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M149.1"/>
    <display
             value="Melanotic Tumours, Paediatric, Multi-target NGS panel, small variant (NRAS)"/>
  </concept>
  <concept>
    <code value="M149.2"/>
    <display value="Melanotic Tumours, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M149.3"/>
    <display
             value="Melanotic Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M15.1"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, small variant (CDKN2A, EGFR, TP53)"/>
  </concept>
  <concept>
    <code value="M15.2"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M15.3"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, copy number variant (CDKN2A, TP53)"/>
  </concept>
  <concept>
    <code value="M15.4"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, RET rearrangement FISH/RT-PC"/>
  </concept>
  <concept>
    <code value="M15.5"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M15.6"/>
    <display
             value="Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M15.7"/>
    <display value="Head and Neck Squamous Cell Carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M150.1"/>
    <display
             value="Meningioma, Paediatric, Multi-target NGS panel, small variant (SMARCE1, AKT1, NF2, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M150.2"/>
    <display value="Meningioma, Paediatric, SMARCE1 seq"/>
  </concept>
  <concept>
    <code value="M150.3"/>
    <display value="Meningioma, Paediatric, AKT1 seq"/>
  </concept>
  <concept>
    <code value="M150.4"/>
    <display value="Meningioma, Paediatric, NF2 seq"/>
  </concept>
  <concept>
    <code value="M150.5"/>
    <display value="Meningioma, Paediatric, TERT promoter seq"/>
  </concept>
  <concept>
    <code value="M150.6"/>
    <display value="Meningioma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M150.7"/>
    <display value="Meningioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M150.8"/>
    <display
             value="Meningioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M151.1"/>
    <display value="Midline Carcinoma, Paediatric, NUTM1-BRD2 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M151.2"/>
    <display value="Midline Carcinoma, Paediatric, NUTM1-BRD3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M151.3"/>
    <display value="Midline Carcinoma, Paediatric, NUTM1-BRD4 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M151.4"/>
    <display value="Midline Carcinoma, Paediatric, NUTM1-CIC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M151.5"/>
    <display value="Midline Carcinoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M151.6"/>
    <display
             value="Midline Carcinoma, Paediatric, Multi-target NGS panel, structural variant (NUTM1-BRD2, NUTM1-BRD3, NUTM1-BRD4, NUTM1-CIC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M152.1"/>
    <display value="Neuroblastoma, Paediatric, SNP Array"/>
  </concept>
  <concept>
    <code value="M152.10"/>
    <display value="Neuroblastoma, Paediatric, 17q rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M152.11"/>
    <display value="Neuroblastoma, Paediatric, 11q copy number FISH"/>
  </concept>
  <concept>
    <code value="M152.12"/>
    <display value="Neuroblastoma, Paediatric, 1p36 copy number FISH"/>
  </concept>
  <concept>
    <code value="M152.13"/>
    <display value="Neuroblastoma, Paediatric, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M152.14"/>
    <display value="Neuroblastoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M152.15"/>
    <display value="Neuroblastoma, Paediatric, MYCN seq"/>
  </concept>
  <concept>
    <code value="M152.16"/>
    <display
             value="Neuroblastoma, Paediatric, Multi-target NGS panel, structural variant (17q, ALK, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M152.17"/>
    <display
             value="Neuroblastoma, Paediatric, Multi-target NGS panel, copy number variant (MYCN, ALK, 17q, 11q, 1p36)"/>
  </concept>
  <concept>
    <code value="M152.18"/>
    <display value="Neuroblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M152.19"/>
    <display
             value="Neuroblastoma, Paediatric, TERT promoter rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M152.2"/>
    <display
             value="Neuroblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, ATRX, FGFR1, MYCN, NRAS, PHOX2B, TP53)"/>
  </concept>
  <concept>
    <code value="M152.3"/>
    <display value="Neuroblastoma, Paediatric, ALK seq"/>
  </concept>
  <concept>
    <code value="M152.4"/>
    <display value="Neuroblastoma, Paediatric, FGFR1 seq"/>
  </concept>
  <concept>
    <code value="M152.5"/>
    <display value="Neuroblastoma, Paediatric, PHOX2B seq"/>
  </concept>
  <concept>
    <code value="M152.6"/>
    <display value="Neuroblastoma, Paediatric, TP53 seq"/>
  </concept>
  <concept>
    <code value="M152.7"/>
    <display value="Neuroblastoma, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M152.8"/>
    <display value="Neuroblastoma, Paediatric, ALK copy number FISH"/>
  </concept>
  <concept>
    <code value="M152.9"/>
    <display value="Neuroblastoma, Paediatric, 17q copy number FISH"/>
  </concept>
  <concept>
    <code value="M153.1"/>
    <display
             value="Nodular Brain Tumour, Paediatric, Multi-target NGS panel, small variant (SMO)"/>
  </concept>
  <concept>
    <code value="M153.2"/>
    <display value="Nodular Brain Tumour, Paediatric, SMO seq"/>
  </concept>
  <concept>
    <code value="M153.3"/>
    <display value="Nodular Brain Tumour, Paediatric, SMO copy number FISH"/>
  </concept>
  <concept>
    <code value="M153.4"/>
    <display
             value="Nodular Brain Tumour, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M153.5"/>
    <display
             value="Nodular Brain Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M153.6"/>
    <display
             value="Nodular Brain Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMO)"/>
  </concept>
  <concept>
    <code value="M153.7"/>
    <display value="Nodular Brain Tumour, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M155.1"/>
    <display
             value="Oligoastrocytoma, Paediatric, Multi-target NGS panel, small variant (KIT)"/>
  </concept>
  <concept>
    <code value="M155.2"/>
    <display value="Oligoastrocytoma, Paediatric, KIT copy number FISH"/>
  </concept>
  <concept>
    <code value="M155.3"/>
    <display value="Oligoastrocytoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M155.4"/>
    <display
             value="Oligoastrocytoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M155.5"/>
    <display
             value="Oligoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIT)"/>
  </concept>
  <concept>
    <code value="M155.6"/>
    <display value="Oligoastrocytoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M156.1"/>
    <display
             value="Oligodendroglioma, Paediatric, Multi-target NGS panel, small variant (RB1, ATRX)"/>
  </concept>
  <concept>
    <code value="M156.10"/>
    <display value="Oligodendroglioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M156.2"/>
    <display value="Oligodendroglioma, Paediatric, ATRX seq"/>
  </concept>
  <concept>
    <code value="M156.3"/>
    <display value="Oligodendroglioma, Paediatric, RB1 seq"/>
  </concept>
  <concept>
    <code value="M156.4"/>
    <display
             value="Oligodendroglioma, Paediatric, Multi-target NGS panel, copy number variant (1p19q, RB1, ATRX)"/>
  </concept>
  <concept>
    <code value="M156.5"/>
    <display value="Oligodendroglioma, Paediatric, 1p19q codel FISH"/>
  </concept>
  <concept>
    <code value="M156.6"/>
    <display value="Oligodendroglioma, Paediatric, RB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M156.7"/>
    <display value="Oligodendroglioma, Paediatric, ATRX copy number FISH"/>
  </concept>
  <concept>
    <code value="M156.8"/>
    <display value="Oligodendroglioma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M156.9"/>
    <display
             value="Oligodendroglioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M157.1"/>
    <display
             value="Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, small variant (RET)"/>
  </concept>
  <concept>
    <code value="M157.2"/>
    <display value="Thyroid Papillary Carcinoma, Paediatric, RET seq"/>
  </concept>
  <concept>
    <code value="M157.3"/>
    <display
             value="Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M157.4"/>
    <display
             value="Thyroid Papillary Carcinoma, Paediatric, RET rearrangement FISH/RT-PC"/>
  </concept>
  <concept>
    <code value="M157.5"/>
    <display
             value="Thyroid Papillary Carcinoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M158.1"/>
    <display
             value="Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (RAF1)"/>
  </concept>
  <concept>
    <code value="M158.2"/>
    <display value="Pilocytic Astrocytoma, Paediatric, RAF1 seq"/>
  </concept>
  <concept>
    <code value="M158.3"/>
    <display
             value="Pilocytic Astrocytoma, Paediatric, RAF1-SRGAP3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M158.4"/>
    <display
             value="Pilocytic Astrocytoma, Paediatric, RAF1-NF1A FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M158.5"/>
    <display
             value="Pilocytic Astrocytoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M158.6"/>
    <display
             value="Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant (RAF1-SRGAP3, RAF1-NF1A, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M158.7"/>
    <display value="Pilocytic Astrocytoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M159.1"/>
    <display
             value="Pituitary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M159.2"/>
    <display value="Pituitary Blastoma, Paediatric, DICER1 seq"/>
  </concept>
  <concept>
    <code value="M159.3"/>
    <display value="Pituitary Blastoma, Paediatric, DICER1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M159.4"/>
    <display value="Pituitary Blastoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M159.5"/>
    <display
             value="Pituitary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M159.6"/>
    <display
             value="Pituitary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M159.7"/>
    <display value="Pituitary Blastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M16.1"/>
    <display value="Adenoid Cystic Carcinoma, MYB-NFIB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M16.2"/>
    <display
             value="Adenoid Cystic Carcinoma, Multi-target NGS panel, structural variant (MYB-NFIB, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M16.4"/>
    <display value="Adenoid Cystic Carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M160.1"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF, H3-3A)"/>
  </concept>
  <concept>
    <code value="M160.10"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.11"/>
    <display value="Pleomorphic Xanthoastrocytoma, Paediatric, H3-3A seq"/>
  </concept>
  <concept>
    <code value="M160.12"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, KIAA1549 copy number FISH"/>
  </concept>
  <concept>
    <code value="M160.13"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M160.14"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, WGS Germline and Tumour"/>
  </concept>
  <concept>
    <code value="M160.15"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)"/>
  </concept>
  <concept>
    <code value="M160.16"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M160.2"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M160.3"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.4"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.5"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.6"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.7"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.8"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M160.9"/>
    <display
             value="Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M161.1"/>
    <display
             value="Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M161.2"/>
    <display value="Pleuropulmonary Blastoma, Paediatric, DICER1 seq"/>
  </concept>
  <concept>
    <code value="M161.3"/>
    <display
             value="Pleuropulmonary Blastoma, Paediatric, DICER1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M161.4"/>
    <display
             value="Pleuropulmonary Blastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M161.5"/>
    <display
             value="Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M161.6"/>
    <display
             value="Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M162.1"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, small variant (MSH6, PMS2, PTEN)"/>
  </concept>
  <concept>
    <code value="M162.10"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, copy number variant (MYC, MSH6, PTEN)"/>
  </concept>
  <concept>
    <code value="M162.11"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M162.2"/>
    <display value="Primitive Neuroectodermal Tumours, Paediatric, MSH6 seq"/>
  </concept>
  <concept>
    <code value="M162.3"/>
    <display value="Primitive Neuroectodermal Tumours, Paediatric, PMS2 seq"/>
  </concept>
  <concept>
    <code value="M162.4"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M162.5"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M162.6"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, MSH6 copy number FISH"/>
  </concept>
  <concept>
    <code value="M162.7"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, PTEN copy number FISH"/>
  </concept>
  <concept>
    <code value="M162.8"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M162.9"/>
    <display
             value="Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M165.1"/>
    <display
             value="Renal Tumours, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX)"/>
  </concept>
  <concept>
    <code value="M165.2"/>
    <display value="Renal Tumours, Paediatric, ATRX seq"/>
  </concept>
  <concept>
    <code value="M165.3"/>
    <display value="Renal Tumours, Paediatric, CTNNB1 seq"/>
  </concept>
  <concept>
    <code value="M165.4"/>
    <display value="Renal Tumours, Paediatric, DAXX seq"/>
  </concept>
  <concept>
    <code value="M165.5"/>
    <display value="Renal Tumours, Paediatric, ATRX copy number FISH"/>
  </concept>
  <concept>
    <code value="M165.6"/>
    <display value="Renal Tumours, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M165.7"/>
    <display
             value="Renal Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M165.8"/>
    <display
             value="Renal Tumours, Paediatric, Multi-target NGS panel, copy number variant (ATRX)"/>
  </concept>
  <concept>
    <code value="M166.1"/>
    <display
             value="Retinoblastoma, Paediatric, Multi-target NGS panel, small variant (RB1)"/>
  </concept>
  <concept>
    <code value="M166.2"/>
    <display value="Retinoblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M166.3"/>
    <display
             value="Retinoblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M166.4"/>
    <display value="Retinoblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M167.1"/>
    <display
             value="Rhabdoid Tumours, Paediatric, Multi-target NGS panel, small variant (SMARCB1)"/>
  </concept>
  <concept>
    <code value="M167.2"/>
    <display value="Rhabdoid Tumours, Paediatric, SMARCB1 seq"/>
  </concept>
  <concept>
    <code value="M167.3"/>
    <display value="Rhabdoid Tumours, Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M167.4"/>
    <display value="Rhabdoid Tumours, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M167.5"/>
    <display
             value="Rhabdoid Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M167.6"/>
    <display
             value="Rhabdoid Tumours, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)"/>
  </concept>
  <concept>
    <code value="M168.1"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, small variant (PIK3CA, FGFR1)"/>
  </concept>
  <concept>
    <code value="M168.2"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 seq"/>
  </concept>
  <concept>
    <code value="M168.3"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M168.4"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 ITD FISH"/>
  </concept>
  <concept>
    <code value="M168.5"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M168.6"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, structural variant (FGFR1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M168.7"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, copy number variant (FGFR1 ITD)"/>
  </concept>
  <concept>
    <code value="M168.8"/>
    <display
             value="Rosette-Forming Glioneuronal Tumour, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M169.1"/>
    <display
             value="Secondary Glioblastoma, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2)"/>
  </concept>
  <concept>
    <code value="M169.2"/>
    <display value="Secondary Glioblastoma, Paediatric, IDH1 seq"/>
  </concept>
  <concept>
    <code value="M169.3"/>
    <display value="Secondary Glioblastoma, Paediatric, IDH2 seq"/>
  </concept>
  <concept>
    <code value="M169.4"/>
    <display
             value="Secondary Glioblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M169.5"/>
    <display
             value="Secondary Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M169.6"/>
    <display value="Secondary Glioblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M17.1"/>
    <display
             value="Secretory Carcinoma (Salivary Gland), ETV6-NTRK3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M17.2"/>
    <display
             value="Secretory Carcinoma (Salivary Gland), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M17.4"/>
    <display value="Secretory Carcinoma (Salivary Gland), DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M170.1"/>
    <display
             value="SHH Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SMO, DDX3X)"/>
  </concept>
  <concept>
    <code value="M170.2"/>
    <display value="SHH Medulloblastoma, Paediatric, SMO seq"/>
  </concept>
  <concept>
    <code value="M170.3"/>
    <display value="SHH Medulloblastoma, Paediatric, DDX3X seq"/>
  </concept>
  <concept>
    <code value="M170.4"/>
    <display value="SHH Medulloblastoma, Paediatric, SMO copy number FISH"/>
  </concept>
  <concept>
    <code value="M170.5"/>
    <display value="SHH Medulloblastoma, Paediatric, DDX3X copy number FISH"/>
  </concept>
  <concept>
    <code value="M170.6"/>
    <display value="SHH Medulloblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M170.7"/>
    <display
             value="SHH Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M170.8"/>
    <display
             value="SHH Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMO, DDX3X)"/>
  </concept>
  <concept>
    <code value="M170.9"/>
    <display value="SHH Medulloblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M171.1"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, small variant (SUFU, TERT promoter, PTCH1)"/>
  </concept>
  <concept>
    <code value="M171.10"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M171.2"/>
    <display value="SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 seq"/>
  </concept>
  <concept>
    <code value="M171.3"/>
    <display value="SHH Medulloblastoma, TP53 WT, Paediatric, SUFU seq"/>
  </concept>
  <concept>
    <code value="M171.4"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, TERT promoter seq"/>
  </concept>
  <concept>
    <code value="M171.5"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M171.6"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, TERT copy number FISH"/>
  </concept>
  <concept>
    <code value="M171.7"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M171.8"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M171.9"/>
    <display
             value="SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (PTCH1, TERT)"/>
  </concept>
  <concept>
    <code value="M172.1"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, small variant (TP53, MYCN)"/>
  </concept>
  <concept>
    <code value="M172.2"/>
    <display value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, TP53 seq"/>
  </concept>
  <concept>
    <code value="M172.3"/>
    <display value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN seq"/>
  </concept>
  <concept>
    <code value="M172.4"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M172.5"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M172.6"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M172.7"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M172.8"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, copy number variant (TP53, MYCN)"/>
  </concept>
  <concept>
    <code value="M172.9"/>
    <display
             value="SHH Medulloblastoma, TP53 MUTANT, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M173.1"/>
    <display
             value="t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, TFEB-MALAT1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M173.2"/>
    <display
             value="t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M173.3"/>
    <display
             value="t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M174.1"/>
    <display
             value="Testicular, Paediatric, Multi-target NGS panel, small variant (PRKAR1A)"/>
  </concept>
  <concept>
    <code value="M174.2"/>
    <display value="Testicular, Paediatric, PRKAR1A seq"/>
  </concept>
  <concept>
    <code value="M174.3"/>
    <display value="Testicular, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M174.4"/>
    <display
             value="Testicular, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M178.1"/>
    <display
             value="Wilms Tumours, Paediatric, Multi-target NGS panel, small variant (DROSHA)"/>
  </concept>
  <concept>
    <code value="M178.2"/>
    <display value="Wilms Tumours, Paediatric, DROSHA seq"/>
  </concept>
  <concept>
    <code value="M178.3"/>
    <display value="Wilms Tumours, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M178.4"/>
    <display
             value="Wilms Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M179.1"/>
    <display
             value="WNT Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (DDX3X, CTNNB1, SMARCA4, TP53)"/>
  </concept>
  <concept>
    <code value="M179.10"/>
    <display
             value="WNT Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, TP53)"/>
  </concept>
  <concept>
    <code value="M179.11"/>
    <display value="WNT Medulloblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M179.2"/>
    <display value="WNT Medulloblastoma, Paediatric, DDX3X seq"/>
  </concept>
  <concept>
    <code value="M179.3"/>
    <display value="WNT Medulloblastoma, Paediatric, CTNNB1 seq"/>
  </concept>
  <concept>
    <code value="M179.4"/>
    <display value="WNT Medulloblastoma, Paediatric, SMARCA4 seq"/>
  </concept>
  <concept>
    <code value="M179.5"/>
    <display value="WNT Medulloblastoma, Paediatric, TP53 seq"/>
  </concept>
  <concept>
    <code value="M179.6"/>
    <display
             value="WNT Medulloblastoma, Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M179.7"/>
    <display
             value="WNT Medulloblastoma, Paediatric, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M179.8"/>
    <display value="WNT Medulloblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M179.9"/>
    <display
             value="WNT Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M18.1"/>
    <display
             value="Renal Cell Carcinoma, Adult, TFE3 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M18.2"/>
    <display
             value="Renal Cell Carcinoma,Adult, Multi-target NGS panel small variant (FH, SDHA, SDHB, SDHC, SDHD, VHL, ELOC (TCEB-1), TSC1/2, MET, BRAF)"/>
  </concept>
  <concept>
    <code value="M18.3"/>
    <display value="Renal Cell Carcinoma, Adult, Chromosome 3 FISH"/>
  </concept>
  <concept>
    <code value="M18.4"/>
    <display value="Renal Cell Carcinoma, Adult, Chromosome 8 FISH"/>
  </concept>
  <concept>
    <code value="M18.5"/>
    <display value="Renal Cell Carcinoma, Adult, Chromosome 7 &amp; 17 FISH"/>
  </concept>
  <concept>
    <code value="M18.6"/>
    <display
             value="Renal Cell Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, TFE3, TFEB)"/>
  </concept>
  <concept>
    <code value="M18.7"/>
    <display
             value="Renal Cell Carcinoma, Adult, TFEB rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M180.1"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, small variant (TFE3)"/>
  </concept>
  <concept>
    <code value="M180.2"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3 seq"/>
  </concept>
  <concept>
    <code value="M180.3"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M180.4"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-MITF FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M180.5"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-PRCC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M180.6"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M180.7"/>
    <display
             value="Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFE3-ASPSCR1, TFE3-MITF,  TFE3-PRCC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M181.1"/>
    <display
             value="Hairy Cell Leukaemia, Non-Classical Variant, Multi-target NGS panel, small variant (MAP2K1)"/>
  </concept>
  <concept>
    <code value="M181.4"/>
    <display
             value="Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M181.5"/>
    <display
             value="Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection NGS"/>
  </concept>
  <concept>
    <code value="M182.1"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M182.2"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M182.3"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M182.4"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, Multi-target NGS panel, structural variant (ALK-NPM1, other ALK rearrangements)"/>
  </concept>
  <concept>
    <code value="M182.5"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M182.6"/>
    <display
             value="ALK Positive Anaplastic Large Cell Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M183.1"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3A, NF1, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M183.2"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M183.3"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M183.4"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M183.5"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M183.6"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M183.7"/>
    <display value="Diffuse Midline Glioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M183.8"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, MYC, MYCN)"/>
  </concept>
  <concept>
    <code value="M183.9"/>
    <display
             value="Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M184.1"/>
    <display
             value="Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3B, H3C2, H3C3, H3C14, IDH1, IDH2, TP53, VHL)"/>
  </concept>
  <concept>
    <code value="M184.2"/>
    <display value="Glioma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M184.3"/>
    <display value="Glioma, Paediatric, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M184.4"/>
    <display value="Glioma, Paediatric, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M184.5"/>
    <display value="Glioma, Paediatric, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M184.6"/>
    <display value="Glioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M184.7"/>
    <display
             value="Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M184.8"/>
    <display
             value="Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M185.1"/>
    <display
             value="High Grade Glioma, Paediatric, Multi-target NGS panel, small variant (CDKN2B)"/>
  </concept>
  <concept>
    <code value="M185.2"/>
    <display value="High Grade Glioma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M185.3"/>
    <display value="High Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M185.4"/>
    <display value="High Grade Glioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M185.5"/>
    <display
             value="High Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M186.1"/>
    <display
             value="Low Grade Glioma, Paediatric, Multi-target NGS panel, small variant (TSC1, TSC2, IDH1, IDH2, FGFR1)"/>
  </concept>
  <concept>
    <code value="M186.2"/>
    <display value="Low Grade Glioma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M186.3"/>
    <display value="Low Grade Glioma, Paediatric, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M186.4"/>
    <display value="Low Grade Glioma, Paediatric, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M186.5"/>
    <display value="Low Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M186.6"/>
    <display value="Low Grade Glioma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M186.7"/>
    <display
             value="Low Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M186.8"/>
    <display
             value="Low Grade Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M187.1"/>
    <display value="Uveal melanoma, 1p, 3, 6, 8 MLPA"/>
  </concept>
  <concept>
    <code value="M187.2"/>
    <display value="Uveal melanoma, BRAF hotspot"/>
  </concept>
  <concept>
    <code value="M187.3"/>
    <display
             value="Uveal melanoma, Multi-target NGS panel, small variant (BRAF, NRAS, NF1)"/>
  </concept>
  <concept>
    <code value="M187.4"/>
    <display
             value="Uveal melanoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M189.1"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2, BRAF, H3C2, H3C3, H3C14, H3-3A, H3-3B, TERT promoter, TP53, VHL, YAP1, SMARCA4, SMARCB1, DDX3X, CTNNB1)"/>
  </concept>
  <concept>
    <code value="M189.10"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M189.11"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, SNP Array"/>
  </concept>
  <concept>
    <code value="M189.12"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, C19MC copy number FISH"/>
  </concept>
  <concept>
    <code value="M189.13"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M189.14"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M189.15"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M189.16"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M189.17"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M189.18"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M189.19"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M189.2"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, structural variant (CIC, BCOR, BCOR-CCNB3, C11orf95-RELA, YAP1-C11orf95, YAP1-TFE3, EWSR1, MN1, RELA, YAP1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M189.20"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M189.21"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, copy number variant  (C19MC, SMARCA4, SMARCB1, YAP1)"/>
  </concept>
  <concept>
    <code value="M189.3"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M189.4"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, C11orf95-RELA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M189.5"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M189.6"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M189.7"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, EWSR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M189.8"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, MN1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M189.9"/>
    <display
             value="Brain Tumour, No Further Morphological Classification, Paediatric, RELA rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.1"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, small variant (CDKN2A, DICER1, RB1, YAP1, SMARCA4, SMARCB1, MSH6, PMS2, PTEN, ATRX)"/>
  </concept>
  <concept>
    <code value="M190.10"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.11"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.12"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M190.13"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, C11orf95-RELA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.14"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, RELA rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.15"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, TTYH1-C19MC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.16"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, YAP1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.17"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.18"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.19"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M190.2"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M190.20"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, MN1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M190.21"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, SNP Array"/>
  </concept>
  <concept>
    <code value="M190.22"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, C19MC copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.23"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, DICER1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.24"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, MSH6 copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.25"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.26"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.27"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.28"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M190.3"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.30"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M190.31"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M190.32"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, copy number variant  (C19MC, DICER1, MSH6, MYC, PTEN, SMARCA4, SMARCB1)"/>
  </concept>
  <concept>
    <code value="M190.4"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.5"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.6"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.7"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.8"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-FRX1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M190.9"/>
    <display
             value="Embryonal Tumour Differential, Adult and Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.1"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)"/>
  </concept>
  <concept>
    <code value="M191.10"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M191.11"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"/>
  </concept>
  <concept>
    <code value="M191.12"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.13"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M191.14"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M191.15"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.16"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.17"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M191.18"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M191.19"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M191.2"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.20"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M191.21"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M191.22"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M191.3"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.4"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.5"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.6"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.7"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.8"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M191.9"/>
    <display
             value="Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.1"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX,  H3-3A, H3-3B, H3C2, H3C3,  H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)"/>
  </concept>
  <concept>
    <code value="M192.10"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M192.11"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant (EGFR)"/>
  </concept>
  <concept>
    <code value="M192.12"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.13"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M192.14"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M192.15"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.16"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.17"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M192.18"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M192.19"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M192.2"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.20"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M192.21"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M192.22"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"/>
  </concept>
  <concept>
    <code value="M192.23"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M192.3"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.4"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.5"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.6"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.7"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.8"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M192.9"/>
    <display
             value="High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.1"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)"/>
  </concept>
  <concept>
    <code value="M193.10"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M193.11"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant (EGFR)"/>
  </concept>
  <concept>
    <code value="M193.12"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.13"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M193.14"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M193.15"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.16"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.17"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M193.18"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M193.19"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M193.2"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.20"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M193.21"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M193.22"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"/>
  </concept>
  <concept>
    <code value="M193.23"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M193.3"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.4"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.5"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.6"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.7"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.8"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M193.9"/>
    <display
             value="Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M194.1"/>
    <display
             value="Medulloblastoma all Subtypes, Multi-target NGS panel, small variant (ALK, BCOR, CTNNB1, DDX3X, DDX3X, EZH2, MYCN,  PTCH1, PTCH2, PTEN, SMARCA4, SMO, SUFU, TERT promoter, TP53,  YAP1)"/>
  </concept>
  <concept>
    <code value="M194.10"/>
    <display value="Medulloblastoma all Subtypes, BCOR copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.11"/>
    <display value="Medulloblastoma all Subtypes, C19MC copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.12"/>
    <display value="Medulloblastoma all Subtypes, DDX3X copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.13"/>
    <display value="Medulloblastoma all Subtypes, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.14"/>
    <display value="Medulloblastoma all Subtypes, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.15"/>
    <display value="Medulloblastoma all Subtypes, PTCH1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.16"/>
    <display
             value="Medulloblastoma all Subtypes, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M194.17"/>
    <display value="Medulloblastoma all Subtypes, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.18"/>
    <display value="Medulloblastoma all Subtypes, SMO copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.19"/>
    <display value="Medulloblastoma all Subtypes, TERT copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.2"/>
    <display value="Medulloblastoma all Subtypes, ALK rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M194.20"/>
    <display
             value="Medulloblastoma all Subtypes, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.21"/>
    <display value="Medulloblastoma all Subtypes, YAP1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M194.22"/>
    <display value="Medulloblastoma all Subtypes, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M194.23"/>
    <display value="Medulloblastoma all Subtypes, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M194.24"/>
    <display
             value="Medulloblastoma all Subtypes, Multi-target NGS panel, structural variant (ALK, BCOR, MYC, PVT1-MYC, YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M194.25"/>
    <display
             value="Medulloblastoma all Subtypes, Multi-target NGS panel, copy number variant  (ALK, BCOR, C19MC, DDX3X, MYC, MYCN, PTCH1, PTEN, SMARCA4, SMO, TERT, TP53, YAP1)"/>
  </concept>
  <concept>
    <code value="M194.3"/>
    <display value="Medulloblastoma all Subtypes, BCOR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M194.4"/>
    <display value="Medulloblastoma all Subtypes, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M194.5"/>
    <display value="Medulloblastoma all Subtypes, PVT1-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M194.6"/>
    <display value="Medulloblastoma all Subtypes, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M194.7"/>
    <display value="Medulloblastoma all Subtypes, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M194.8"/>
    <display value="Medulloblastoma all Subtypes, SNP Array"/>
  </concept>
  <concept>
    <code value="M194.9"/>
    <display value="Medulloblastoma all Subtypes, ALK copy number FISH"/>
  </concept>
  <concept>
    <code value="M195.1"/>
    <display
             value="Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, small variant (BRAF, CTNNB1)"/>
  </concept>
  <concept>
    <code value="M195.2"/>
    <display
             value="Craniopharyngioma, Adult and Paediatric, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M195.3"/>
    <display
             value="Craniopharyngioma, Adult and Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M195.4"/>
    <display
             value="Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M195.5"/>
    <display
             value="Craniopharyngioma, Adult and Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M196.1"/>
    <display
             value="Bone Forming Soft Tissue Tumour Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M196.2"/>
    <display
             value="Bone Forming Soft Tissue Tumour Differential, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M196.3"/>
    <display
             value="Bone Forming Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M196.4"/>
    <display
             value="Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M196.5"/>
    <display
             value="Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M197.1"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, Multi-target NGS panel, structural variant (BCOR, CIC, DDIT3, EWSR1, FOXO1, WT1, BCOR-CCNB3, HEY1-NCOA2, PAX3-FOXO1, PAX7-FOXO1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M197.10"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M197.2"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, DDIT3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.3"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.4"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, FOXO1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.5"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, WT1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.6"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.7"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, HEY1-NCOA2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.8"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, PAX3-FOXO1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M197.9"/>
    <display
             value="Round Cell Sarcoma of Soft Tissue Differential, PAX7-FOXO1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M198.1"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M198.2"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, SERPINE1-FOSB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M198.3"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, WWTR1-CAMTA1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M198.4"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M198.5"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M198.6"/>
    <display
             value="Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MYC)"/>
  </concept>
  <concept>
    <code value="M199.1"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, small variant (APC, CTNNB1)"/>
  </concept>
  <concept>
    <code value="M199.10"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, TPM4-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M199.11"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, ETV6-NTRK3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M199.12"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M199.13"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M199.2"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, SS18, USP6, COL1A1-PDGFB, TPM3-ALK, TPM4-ALK, ETV6-NTRK3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M199.3"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M199.4"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, FUS rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M199.5"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M199.6"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M199.7"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M199.8"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, COL1A1-PDGFB rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M199.9"/>
    <display
             value="Spindle Cell Soft Tissue Tumour Differential, TPM3-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M2.1"/>
    <display
             value="Ovarian Carcinoma, Multi-target NGS panel, small variant (BRCA1, BRCA2, SMARCA4)"/>
  </concept>
  <concept>
    <code value="M2.3"/>
    <display
             value="Ovarian Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M2.5"/>
    <display
             value="Ovarian Carcinoma, HRD status (either positive for BRCA 1 and/or 2, or HRD positive)"/>
  </concept>
  <concept>
    <code value="M20.1"/>
    <display
             value="Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF)"/>
  </concept>
  <concept>
    <code value="M20.2"/>
    <display
             value="Anaplastic Astrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M20.3"/>
    <display
             value="Anaplastic Astrocytoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M20.4"/>
    <display value="Anaplastic Astrocytoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M20.5"/>
    <display
             value="Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M200.1"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (BCOR, DDIT3, FUS, NR4A3, TGFBR3-OGA, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M200.2"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M200.3"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M200.4"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, NR4A3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M200.5"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, TGFBR3-OGA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M200.6"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M200.7"/>
    <display
             value="Myxoid Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M201.1"/>
    <display
             value="Adipocytic Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M201.2"/>
    <display
             value="Adipocytic Soft Tissue Tumour Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M201.3"/>
    <display
             value="Adipocytic Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M201.4"/>
    <display
             value="Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M201.5"/>
    <display
             value="Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M202.1"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M202.2"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M202.3"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M202.4"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, TFE3 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M202.5"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, WWTR1-CAMTA1  RT-PCR"/>
  </concept>
  <concept>
    <code value="M202.6"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M202.7"/>
    <display
             value="Epithelioid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (EWSR1, FUS, SS18, TFE3, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M203.1"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), EPC1-PHF1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M203.2"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), JAZF1-PHF1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M203.3"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), JAZF1-SUZ12 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M203.4"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), NUTM2B-YWHAE FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M203.5"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M203.6"/>
    <display
             value="Uterine Sarcomas (Inc Endometrial), Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NUTM2B-YWHAE, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M204.1"/>
    <display value="Undifferentiated tumour, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M204.2"/>
    <display
             value="Undifferentiated tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M205.1"/>
    <display
             value="Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B, IDH1, IDH2)"/>
  </concept>
  <concept>
    <code value="M205.2"/>
    <display
             value="Cartilage Forming Bone Tumour Differential, H3-3B hotspot"/>
  </concept>
  <concept>
    <code value="M205.3"/>
    <display value="Cartilage Forming Bone Tumour Differential, H3-3A seq"/>
  </concept>
  <concept>
    <code value="M205.4"/>
    <display value="Cartilage Forming Bone Tumour Differential, H3-3B seq"/>
  </concept>
  <concept>
    <code value="M205.5"/>
    <display
             value="Cartilage Forming Bone Tumour Differential, HEY1-NCOA2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M205.6"/>
    <display value="Cartilage Forming Bone Tumour Differential, SNP Array"/>
  </concept>
  <concept>
    <code value="M205.7"/>
    <display
             value="Cartilage Forming Bone Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M205.8"/>
    <display
             value="Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M206.1"/>
    <display
             value="Bone Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B)"/>
  </concept>
  <concept>
    <code value="M206.2"/>
    <display value="Bone Forming Bone Tumour Differential, H3-3B hotspot"/>
  </concept>
  <concept>
    <code value="M206.3"/>
    <display value="Bone Forming Bone Tumour Differential, H3-3A seq"/>
  </concept>
  <concept>
    <code value="M206.4"/>
    <display value="Bone Forming Bone Tumour Differential, H3-3B seq"/>
  </concept>
  <concept>
    <code value="M206.5"/>
    <display
             value="Bone Forming Bone Tumour Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M206.6"/>
    <display
             value="Bone Forming Bone Tumour Differential, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M206.7"/>
    <display
             value="Bone Forming Bone Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M206.8"/>
    <display
             value="Bone Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M206.9"/>
    <display
             value="Bone Forming Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M207.1"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3B)"/>
  </concept>
  <concept>
    <code value="M207.2"/>
    <display value="Osteoclast-Rich Bone Tumour Differential, H3-3B seq"/>
  </concept>
  <concept>
    <code value="M207.3"/>
    <display value="Osteoclast-Rich Bone Tumour Differential, H3-3B hotspot"/>
  </concept>
  <concept>
    <code value="M207.4"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M207.5"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M207.6"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M207.7"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M207.8"/>
    <display
             value="Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M208.1"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, Multi-target NGS panel, structural variant (BCOR, CIC, EWSR1, WT1, BCOR-CCNB3, HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M208.2"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M208.3"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, WT1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M208.4"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M208.5"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, HEY1-NCOA2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M208.6"/>
    <display
             value="Round Cell Sarcoma of Bone Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M209.1"/>
    <display
             value="Vascular Tumour of Bone Differential, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M209.2"/>
    <display
             value="Vascular Tumour of Bone Differential, SERPINE1-FOSB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M209.3"/>
    <display
             value="Vascular Tumour of Bone Differential, WWTR1-CAMTA1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M209.4"/>
    <display
             value="Vascular Tumour of Bone Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M209.5"/>
    <display
             value="Vascular Tumour of Bone Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M209.6"/>
    <display
             value="Vascular Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MYC)"/>
  </concept>
  <concept>
    <code value="M21.1"/>
    <display
             value="Astrocytoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A,H3C2, BRAF, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M21.2"/>
    <display
             value="Astrocytoma, Adult, Multi-target NGS panel, copy number variant (EGFR, CDKN2A, CDKN2B)"/>
  </concept>
  <concept>
    <code value="M21.20"/>
    <display value="Astrocytoma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M21.21"/>
    <display
             value="Astrocytoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M21.22"/>
    <display value="Astrocytoma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M21.23"/>
    <display value="Astrocytoma, Adult, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M21.24"/>
    <display value="Astrocytoma, Adult, CDKN2B copy number FISH"/>
  </concept>
  <concept>
    <code value="M21.3"/>
    <display value="Astrocytoma, Adult, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M21.5"/>
    <display value="Astrocytoma, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M21.6"/>
    <display value="Astrocytoma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M21.8"/>
    <display value="Astrocytoma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M21.9"/>
    <display value="Astrocytoma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M210.1"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M210.2"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M210.3"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, FUS rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M210.4"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M210.5"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M210.6"/>
    <display
             value="Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M211.1"/>
    <display
             value="Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, small variant (GNAS)"/>
  </concept>
  <concept>
    <code value="M211.2"/>
    <display
             value="Fibro-Osseous Tumour of Bone Differential, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M211.3"/>
    <display
             value="Fibro-Osseous Tumour of Bone Differential, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M211.4"/>
    <display
             value="Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M211.5"/>
    <display
             value="Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M212.1"/>
    <display
             value="Renal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX, TP53, TFE3)"/>
  </concept>
  <concept>
    <code value="M212.10"/>
    <display
             value="Renal Tumour Differential, Paediatric, TFEB-MALAT1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M212.11"/>
    <display
             value="Renal Tumour Differential, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M212.12"/>
    <display
             value="Renal Tumour Differential, Paediatric, TFE3-MITF FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M212.13"/>
    <display
             value="Renal Tumour Differential, Paediatric, TFE3-PRCC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M212.14"/>
    <display
             value="Renal Tumour Differential, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M212.15"/>
    <display
             value="Renal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, TFE3-ASPSCR1, TFE3-MITF, TFE3-PRCC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M212.16"/>
    <display
             value="Renal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (ATRX, TP53, WT1)"/>
  </concept>
  <concept>
    <code value="M212.2"/>
    <display value="Renal Tumour Differential, Paediatric, ATRX seq"/>
  </concept>
  <concept>
    <code value="M212.3"/>
    <display value="Renal Tumour Differential, Paediatric, CTNNB1 seq"/>
  </concept>
  <concept>
    <code value="M212.4"/>
    <display value="Renal Tumour Differential, Paediatric, DAXX seq"/>
  </concept>
  <concept>
    <code value="M212.5"/>
    <display value="Renal Tumour Differential, Paediatric, TFE3 seq"/>
  </concept>
  <concept>
    <code value="M212.6"/>
    <display value="Renal Tumour Differential, Paediatric, TP53 seq"/>
  </concept>
  <concept>
    <code value="M212.7"/>
    <display
             value="Renal Tumour Differential, Paediatric, ATRX copy number FISH"/>
  </concept>
  <concept>
    <code value="M212.8"/>
    <display
             value="Renal Tumour Differential, Paediatric, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M212.9"/>
    <display
             value="Renal Tumour Differential, Paediatric, WT1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.1"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1, DDX3X, CTNNB1, CDKN2A, TP53, RAF1, PIK3CA, FGFR1, FGFR4, KIT,  BRAF, H3-3A, ALK, ATRX, NRAS, PHOX2B)"/>
  </concept>
  <concept>
    <code value="M213.10"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.11"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.12"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, ALK-NPM1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M213.13"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, C11orf95-RELA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.14"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, EWSR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M213.15"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M213.16"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-NF1A FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.17"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-SRGAP3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.18"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, RELA rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.19"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.2"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, ALK, C1"/>
  </concept>
  <concept>
    <code value="M213.20"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.21"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.22"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, EGFR, ALK, C19MC, CDKN2A,  FGFR1, KIAA1549, KIT, MYCN, PDGFRA, SMARCA4, SMARCB1, YAP1)"/>
  </concept>
  <concept>
    <code value="M213.23"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.24"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, ALK copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.25"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, C19MC copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.26"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.27"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.28"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 ITD FISH"/>
  </concept>
  <concept>
    <code value="M213.29"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, KIAA1549 copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.3"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M213.30"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, KIT copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.31"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.32"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, PDGFRA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.33"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, SMARCA4 copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.34"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, SMARCB1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.35"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M213.36"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.37"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M213.38"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M213.4"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.5"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.6"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.7"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.8"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FRX1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M213.9"/>
    <display
             value="Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M215.1"/>
    <display
             value="Endometrial Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M215.2"/>
    <display value="Endometrial Cancer, MLH1 promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M215.4"/>
    <display
             value="Endometrial Cancer, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2)"/>
  </concept>
  <concept>
    <code value="M215.5"/>
    <display
             value="Endometrial Cancer, Multi-target NGS panel-small variant detection POLE"/>
  </concept>
  <concept>
    <code value="M217.1"/>
    <display
             value="Urothelial Cancer, Multi-target NGS panel, small variant (FGFR3, FGFR2)"/>
  </concept>
  <concept>
    <code value="M217.2"/>
    <display
             value="Bladder Cancer, Multi-target NGS panel, copy number variant (FGFR3, FGFR2)"/>
  </concept>
  <concept>
    <code value="M217.3"/>
    <display
             value="Bladder Cancer, Multi-target NGS panel, structural variant (FGFR3, FGFR2, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M218.1"/>
    <display
             value="Prostate Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2, ATM, CDK12)"/>
  </concept>
  <concept>
    <code value="M218.2"/>
    <display
             value="Prostate Cancer, Multi-target NGS panel, structural variant (TMPRSS2-ERG, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M218.3"/>
    <display value="Prostate Cancer, TMPRSS2-ERG FISH"/>
  </concept>
  <concept>
    <code value="M219.1"/>
    <display
             value="Pancreatic Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2)"/>
  </concept>
  <concept>
    <code value="M219.2"/>
    <display
             value="Pancreatic Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M219.3"/>
    <display value="Pancreatic Cancer, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M219.5"/>
    <display value="Pancreatic Cancer, MSI Testing"/>
  </concept>
  <concept>
    <code value="M22.1"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, small variant (H3C2, H3C14, IDH1, IDH2)"/>
  </concept>
  <concept>
    <code value="M22.10"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, MYB rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M22.11"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, MYBL1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M22.12"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, MN1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M22.2"/>
    <display value="Diffuse Astrocytoma, Paediatric, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M22.3"/>
    <display value="Diffuse Astrocytoma, Paediatric, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M22.4"/>
    <display value="Diffuse Astrocytoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M22.5"/>
    <display value="Diffuse Astrocytoma, Paediatric, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M22.6"/>
    <display value="Diffuse Astrocytoma, Paediatric, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M22.7"/>
    <display value="Diffuse Astrocytoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M22.8"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, copy number variant (MYC)"/>
  </concept>
  <concept>
    <code value="M22.9"/>
    <display
             value="Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (MYC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M220.1"/>
    <display
             value="Cholangiocarcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, FGFR2)"/>
  </concept>
  <concept>
    <code value="M220.3"/>
    <display value="Cholangiocarcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M220.5"/>
    <display value="Cholangiocarcinoma, MSI Testing"/>
  </concept>
  <concept>
    <code value="M220.6"/>
    <display
             value="Cholangiocarcinoma, Multi-target NGS panel -small variant (IDH1)"/>
  </concept>
  <concept>
    <code value="M220.7"/>
    <display value="Cholangiocarcinoma, FGFR2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M221.1"/>
    <display
             value="Spitzoid tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M222.2"/>
    <display
             value="Hepatocellular carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M222.4"/>
    <display value="Hepatocellular carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M224.1"/>
    <display value="MDS/MPN, Multi-target NGS panel, small variant"/>
  </concept>
  <concept>
    <code value="M224.10"/>
    <display value="MDS/MPN, BCR-ABL1 multiplex"/>
  </concept>
  <concept>
    <code value="M224.11"/>
    <display value="MDS/MPN, Other RT-PCR"/>
  </concept>
  <concept>
    <code value="M224.13"/>
    <display value="MDS/MPN, JAK2 V617F hotspot"/>
  </concept>
  <concept>
    <code value="M224.14"/>
    <display value="MDS/MPN, JAK2 exon 12 hotspot"/>
  </concept>
  <concept>
    <code value="M224.15"/>
    <display value="MDS/MPN, CALR exon 9 hotspot"/>
  </concept>
  <concept>
    <code value="M224.16"/>
    <display value="MDS/MPN, MPL exon 10 hotspot"/>
  </concept>
  <concept>
    <code value="M224.18"/>
    <display value="MDS/MPN, Chr8 copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.19"/>
    <display value="MDS/MPN, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.2"/>
    <display
             value="MDS/MPN, Karyotype (To include detection of complex karyotype)"/>
  </concept>
  <concept>
    <code value="M224.20"/>
    <display value="MDS/MPN, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.21"/>
    <display value="MDS/MPN, i(17q)/t(17p) FISH"/>
  </concept>
  <concept>
    <code value="M224.22"/>
    <display
             value="MDS/MPN, Chr12p copy number FISH, t(12p) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M224.23"/>
    <display value="MDS/MPN, t(9;22)(q34;q11) BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M224.24"/>
    <display
             value="MDS/MPN, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)"/>
  </concept>
  <concept>
    <code value="M224.25"/>
    <display
             value="MDS/MPN, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)"/>
  </concept>
  <concept>
    <code value="M224.26"/>
    <display value="MDS/MPN, FGFR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M224.27"/>
    <display
             value="MDS/MPN, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)"/>
  </concept>
  <concept>
    <code value="M224.28"/>
    <display value="MDS/MPN, inv(3)/t(3;3) FISH"/>
  </concept>
  <concept>
    <code value="M224.29"/>
    <display value="MDS/MPN, 11q23 (KMT2A) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M224.3"/>
    <display
             value="MDS/MPN, FISH copy number and rearrangement Other: See tests M224. -M224. for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M224.30"/>
    <display
             value="MDS/MPN, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)"/>
  </concept>
  <concept>
    <code value="M224.31"/>
    <display value="MDS/MPN, FLT3 rearragement FISH"/>
  </concept>
  <concept>
    <code value="M224.32"/>
    <display value="MDS/MPN, RET rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M224.33"/>
    <display value="MDS/MPN, NTRK3 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M224.34"/>
    <display value="MDS/MPN, Chr13/Chr13q copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.35"/>
    <display value="MDS/MPN, Chr11q copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.36"/>
    <display value="MDS/MPN, Chr9q copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.37"/>
    <display value="MDS/MPN, Chr17/Chr17p copy number FISH"/>
  </concept>
  <concept>
    <code value="M224.38"/>
    <display value="MDS/MPN, idic(X)(q13) FISH"/>
  </concept>
  <concept>
    <code value="M224.39"/>
    <display
             value="MDS/MPN, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p/i(17q) &amp; idic(X)(q13), cryptic deletion of 4q12, trisomy 8)"/>
  </concept>
  <concept>
    <code value="M224.4"/>
    <display value="MDS/MPN, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M224.40"/>
    <display value="MDS/MPN, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M224.41"/>
    <display value="MDS/MPN, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M224.42"/>
    <display value="MDS/MPN, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M224.5"/>
    <display
             value="MDS/MPN, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)"/>
  </concept>
  <concept>
    <code value="M224.6"/>
    <display value="MDS/MPN, FIP1L1-PDGFRA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M224.7"/>
    <display value="MDS/MPN, FIP1L1-PDGFRA RT-qPCR"/>
  </concept>
  <concept>
    <code value="M224.8"/>
    <display value="MDS/MPN, ETV6-PDGFRB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M224.9"/>
    <display value="MDS/MPN, PCM1-JAK2 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M225.1"/>
    <display
             value="Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M225.2"/>
    <display
             value="Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection NGS"/>
  </concept>
  <concept>
    <code value="M225.3"/>
    <display
             value="Suspected Lymphoma, TCR gene rearrangement detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M225.4"/>
    <display
             value="Suspected Lymphoma, TCR gene rearrangement detection NGS"/>
  </concept>
  <concept>
    <code value="M225.5"/>
    <display value="Suspected Lymphoma, Karyotype"/>
  </concept>
  <concept>
    <code value="M226.1"/>
    <display
             value="Cancer of Unknown Primary, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M226.3"/>
    <display value="Cancer of Unknown Primary, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M226.4"/>
    <display value="Cancer of Unknown Primary, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M227.1"/>
    <display
             value="Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M227.3"/>
    <display
             value="Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M23.1"/>
    <display
             value="Diffuse Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter,  H3-3A)"/>
  </concept>
  <concept>
    <code value="M23.10"/>
    <display
             value="Diffuse Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M23.11"/>
    <display
             value="Diffuse Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M23.12"/>
    <display value="Diffuse Midline Glioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M23.6"/>
    <display value="Diffuse Midline Glioma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M23.7"/>
    <display value="Diffuse Midline Glioma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M23.8"/>
    <display value="Diffuse Midline Glioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M23.9"/>
    <display value="Diffuse Midline Glioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M231.1,"/>
    <display
             value="small cell lung cancer, Multi-target NGS panel, copy number variant (RB1)"/>
  </concept>
  <concept>
    <code value="M231.2,"/>
    <display
             value="small cell lung cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M232.1"/>
    <display
             value="Solid Tumour Exhausted all Standards of Care Testing and Treatment- Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M233.1"/>
    <display
             value="High Grade Serous Ovarian Carcinoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M234.1"/>
    <display value="Triple Negative Breast Cancer, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M235.1"/>
    <display
             value="Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M235.2"/>
    <display
             value="Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M235.3"/>
    <display
             value="Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M236.1"/>
    <display value="Oesophageal Cancer, MSI Testing"/>
  </concept>
  <concept>
    <code value="M236.2"/>
    <display value="Oesophageal Cancer, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M237.1"/>
    <display value="Gastric Cancer, MSI Testing"/>
  </concept>
  <concept>
    <code value="M237.2"/>
    <display value="Gastric Cancer, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M238.1,"/>
    <display value="small Bowel Cancer, MSI Testing"/>
  </concept>
  <concept>
    <code value="M238.2,"/>
    <display value="small Bowel Cancer, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M239.1"/>
    <display
             value="Thyroid Hurtle Cell Carcinoma, Multi-target NGS panel, structural variant (RET)"/>
  </concept>
  <concept>
    <code value="M24.1"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, C19MC copy number  FISH"/>
  </concept>
  <concept>
    <code value="M24.2"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, TTYH1-C19MC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M24.3"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M24.4"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M24.5"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, copy number variant (C19MC)"/>
  </concept>
  <concept>
    <code value="M24.6"/>
    <display
             value="Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, structural variant  (TTYH1-C19MC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M240.1"/>
    <display
             value="Non-invasive follicular thyroid neoplasm with papillary like nuclei, Multi-target NGS panel, small variant (BRAF,HRAS,NRAS,KRAS)"/>
  </concept>
  <concept>
    <code value="M241.1"/>
    <display value="Conjunctival melanoma, MYB &amp; 6cen (FISH)"/>
  </concept>
  <concept>
    <code value="M241.2"/>
    <display value="Conjunctival melanoma, RREB1 (6p25) (FISH)"/>
  </concept>
  <concept>
    <code value="M241.3"/>
    <display value="Conjunctival melanoma, CCND1 (11q13) (FISH)"/>
  </concept>
  <concept>
    <code value="M241.4"/>
    <display value="Conjunctival melanoma, MYC &amp; 8cen (FISH)"/>
  </concept>
  <concept>
    <code value="M241.5"/>
    <display value="Conjunctival melanoma, CDKN2A &amp; 9cen (FISH)"/>
  </concept>
  <concept>
    <code value="M242.1"/>
    <display
             value="Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), STR Testing"/>
  </concept>
  <concept>
    <code value="M242.2"/>
    <display
             value="Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), Sex chromosome FISH"/>
  </concept>
  <concept>
    <code value="M243.1"/>
    <display value="Thymic Carcinoma, Multi-target NGS panel (KIT)"/>
  </concept>
  <concept>
    <code value="M244.1"/>
    <display value="In all tumours elligible for NTRK1/2/3 testing, FISH"/>
  </concept>
  <concept>
    <code value="M245.1"/>
    <display
             value="Ovarian sex cord stromal tumuors, Multi-target NGS panel-small variant (FOXL2, CTNNB1, APC, DICER1)"/>
  </concept>
  <concept>
    <code value="M25.1"/>
    <display
             value="Ependymoma, Paediatric, Multi-target NGS panel, small variant (YAP1)"/>
  </concept>
  <concept>
    <code value="M25.10"/>
    <display value="Ependymoma, Paediatric, MYCN copy number FISH"/>
  </concept>
  <concept>
    <code value="M25.11"/>
    <display
             value="Ependymoma, Paediatric, ZFTA rearrangements (several fusion partners)"/>
  </concept>
  <concept>
    <code value="M25.2"/>
    <display value="Ependymoma, Paediatric, YAP1 copy number FISH"/>
  </concept>
  <concept>
    <code value="M25.3"/>
    <display value="Ependymoma, Paediatric, YAP1-C11orf95 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M25.4"/>
    <display value="Ependymoma, Paediatric, YAP1-TFE3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M25.5"/>
    <display value="Ependymoma, Paediatric, C11orf95-RELA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M25.6"/>
    <display value="Ependymoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M25.7"/>
    <display value="Ependymoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M25.8"/>
    <display
             value="Ependymoma, Paediatric, Multi-target NGS panel, copy number variant (YAP1, MYCN)"/>
  </concept>
  <concept>
    <code value="M25.9"/>
    <display
             value="Ependymoma, Paediatric, Multi-target NGS panel, structural variant  (YAP1-C11orf95, YAP1-TFE3, C11orf95-RELA, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M26.1"/>
    <display
             value="Ependymoma Supratentorial, Adult, YAP1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M26.2"/>
    <display value="Ependymoma, Adult, RELA rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M26.3"/>
    <display value="Ependymoma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M26.4"/>
    <display
             value="Ependymoma, Adult, Multi-target NGS panel, structural variant  (YAP1, RELA, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M26.5"/>
    <display value="Ependymoma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M26.6"/>
    <display
             value="Ependymoma, Adult, ZFTA rearrangements (several fusion partners)"/>
  </concept>
  <concept>
    <code value="M27.1"/>
    <display
             value="Glioblastoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M27.10"/>
    <display value="Glioblastoma, Adult, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M27.11"/>
    <display
             value="Glioblastoma, Adult, PTEN (10q23) copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M27.12"/>
    <display value="Glioblastoma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M27.13"/>
    <display value="Glioblastoma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M27.14"/>
    <display value="Glioblastoma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M27.15"/>
    <display
             value="Glioblastoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M27.16"/>
    <display value="Glioblastoma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M27.2"/>
    <display
             value="Glioblastoma, Adult, Multi-target NGS panel, copy number variant (EGFR, PDGFRA, MYC, PTEN, 1p, 19q)"/>
  </concept>
  <concept>
    <code value="M27.3"/>
    <display value="Glioblastoma, Adult, EGFRvIII RT-PCR"/>
  </concept>
  <concept>
    <code value="M27.5"/>
    <display value="Glioblastoma, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M27.6"/>
    <display value="Glioblastoma, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M27.7"/>
    <display value="Glioblastoma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M27.9"/>
    <display value="Glioblastoma, Adult, PDGFRA copy number FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M28.1"/>
    <display
             value="Glioma, Adult, Multi-target NGS panel, small variant (H3C2, H3C3, H3C14, H3-3A, H3-3B, IDH1, IDH2, TP53, VHL, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M28.2"/>
    <display
             value="Glioma, Adult, Multi-target NGS panel, copy number variant (EGFR, 1p, 19q)"/>
  </concept>
  <concept>
    <code value="M28.3"/>
    <display value="Glioma, Adult, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M28.4"/>
    <display value="Glioma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M28.5"/>
    <display value="Glioma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M28.6"/>
    <display value="Glioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M28.7"/>
    <display value="Glioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M28.8"/>
    <display
             value="Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M28.9"/>
    <display value="Glioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M29.1"/>
    <display
             value="High Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)"/>
  </concept>
  <concept>
    <code value="M29.2"/>
    <display
             value="High Grade Glioma, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M29.3"/>
    <display value="High Grade Glioma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M29.4"/>
    <display value="High Grade Glioma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M29.5"/>
    <display value="High Grade Glioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M29.6"/>
    <display value="High Grade Glioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M29.7"/>
    <display
             value="High Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M29.8"/>
    <display
             value="High Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M29.9"/>
    <display value="High Grade Glioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M3.12"/>
    <display
             value="Breast Cancer, Tumour profiling tests to guide adjuvant chemotherapy decisions in early breast cancer"/>
  </concept>
  <concept>
    <code value="M3.13"/>
    <display
             value="Breast Cancer, Multi-target ctDNA NGS panel, small variant (ESR1)"/>
  </concept>
  <concept>
    <code value="M3.5"/>
    <display
             value="Breast Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M3.6"/>
    <display
             value="Breast Cancer, Multi-target NGS panel, small variant (PIK3CA)"/>
  </concept>
  <concept>
    <code value="M3.7"/>
    <display value="Breast Cancer, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M3.9"/>
    <display value="Breast Cancer, ETV6-NTRK3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M30.1"/>
    <display
             value="IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, small variant (RB1, NF1)"/>
  </concept>
  <concept>
    <code value="M30.2"/>
    <display
             value="IDH-Wildtype Glioblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M30.3"/>
    <display value="IDH-Wildtype Glioblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M30.4"/>
    <display
             value="IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M31.1"/>
    <display value="Low Grade Glioma, Adult, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M31.2"/>
    <display
             value="Low Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, TERT promoter, H3-3A, H3C2)"/>
  </concept>
  <concept>
    <code value="M31.3"/>
    <display value="Low Grade Glioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M31.4"/>
    <display value="Low Grade Glioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M31.5"/>
    <display
             value="Low Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M31.6"/>
    <display
             value="Low Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M31.7"/>
    <display value="Low Grade Glioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M32.1"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, small variant (BRAF, IDH1, IDH2, TERT promoter, H3-3A, H3C2)"/>
  </concept>
  <concept>
    <code value="M32.2"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M32.3"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M32.4"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M32.5"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M32.6"/>
    <display
             value="Low Grade Glioma/Glioneuronal Tumours, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M33.3"/>
    <display
             value="Meningioma, Adult, Multi-target NGS panel, small variant (TERT promoter)"/>
  </concept>
  <concept>
    <code value="M33.4"/>
    <display value="Meningioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M33.5"/>
    <display value="Meningioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M34.1"/>
    <display
             value="Non-Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)"/>
  </concept>
  <concept>
    <code value="M34.2"/>
    <display value="Non-Midline Glioma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M34.3"/>
    <display value="Non-Midline Glioma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M34.4"/>
    <display value="Non-Midline Glioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M34.5"/>
    <display value="Non-Midline Glioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M34.6"/>
    <display
             value="Non-Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M34.7"/>
    <display
             value="Non-Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M34.8"/>
    <display value="Non-Midline Glioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M35.1"/>
    <display
             value="OligodendroGlioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M35.2"/>
    <display value="OligodendroGlioma, Adult, 1p19q codel FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M35.4"/>
    <display value="OligodendroGlioma, Adult, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M35.5"/>
    <display value="OligodendroGlioma, Adult, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M35.6"/>
    <display value="OligodendroGlioma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M35.7"/>
    <display
             value="OligodendroGlioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"/>
  </concept>
  <concept>
    <code value="M35.8"/>
    <display
             value="OligodendroGlioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M35.9"/>
    <display value="OligodendroGlioma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M36.1"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-KIAA1549 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.10"/>
    <display value="Pilocytic Astrocytoma, Adult, KIAA1549 copy number FISH"/>
  </concept>
  <concept>
    <code value="M36.11"/>
    <display value="Pilocytic Astrocytoma, Adult, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M36.12"/>
    <display
             value="Pilocytic Astrocytoma, Adult, Multi-target NGS panel, small variant (BRAF, CDKN2A)"/>
  </concept>
  <concept>
    <code value="M36.13"/>
    <display value="Pilocytic Astrocytoma, Adult, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M36.14"/>
    <display
             value="Pilocytic Astrocytoma, Adult, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M36.15"/>
    <display
             value="Pilocytic Astrocytoma, Adult, Multi-target NGS panel, copy number variant (KIAA1549, CDKN2A)"/>
  </concept>
  <concept>
    <code value="M36.16"/>
    <display value="Pilocytic Astrocytoma, Adult, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M36.2"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-AGK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.3"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-AKAP9 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.4"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-CCDC6 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.5"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-FAM118B FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.6"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-FXR1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.7"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-GNAI1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.8"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF-MACF1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M36.9"/>
    <display value="Pilocytic Astrocytoma, Adult, BRAF rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M37.1"/>
    <display
             value="Pineoblastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"/>
  </concept>
  <concept>
    <code value="M37.2"/>
    <display value="Pineoblastoma, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M37.3"/>
    <display value="Pineoblastoma, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M37.4"/>
    <display
             value="Pineoblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M38.1"/>
    <display value="Pituitary Tumours, MGMT promoter hyperMethylation"/>
  </concept>
  <concept>
    <code value="M38.2"/>
    <display
             value="Pituitary Tumours, Multi-target NGS panel, copy number variant (EGFR)"/>
  </concept>
  <concept>
    <code value="M38.3"/>
    <display value="Pituitary Tumours, EGFR copy number FISH"/>
  </concept>
  <concept>
    <code value="M38.4"/>
    <display value="Pituitary Tumours, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M38.5"/>
    <display
             value="Pituitary Tumours, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M38.6"/>
    <display value="Pituitary Tumours, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M39.1"/>
    <display
             value="Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, small variant (CDKN2A)"/>
  </concept>
  <concept>
    <code value="M39.2"/>
    <display
             value="Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M39.3"/>
    <display
             value="Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, DNA Methylation"/>
  </concept>
  <concept>
    <code value="M39.4"/>
    <display
             value="Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M4.1"/>
    <display
             value="Non-Small Cell Lung Cancer, Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET)"/>
  </concept>
  <concept>
    <code value="M4.10"/>
    <display value="Non-Small Cell Lung Cancer, EML4-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M4.11"/>
    <display value="Non-Small Cell Lung Cancer, ALK hotspot cDNA"/>
  </concept>
  <concept>
    <code value="M4.13"/>
    <display
             value="Non-Small Cell Lung Cancer, Combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping, ERBB2*) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon 14 skipping)"/>
  </concept>
  <concept>
    <code value="M4.14"/>
    <display
             value="Non-Small Cell Lung Cancer, Multi-target ctDNA combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping and copy number variations) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon"/>
  </concept>
  <concept>
    <code value="M4.2"/>
    <display
             value="Non-Small Cell Lung Cancer, Multi-target NGS panel, structural variant (ROS1, RET, EML4-ALK, NTRK1, NTRK1, NTRK3, MET)"/>
  </concept>
  <concept>
    <code value="M4.3"/>
    <display
             value="Non-Small Cell Lung Cancer, Multi-target NGS panel, copy number variant (MET)"/>
  </concept>
  <concept>
    <code value="M4.4"/>
    <display value="Non-Small Cell Lung Cancer, EGFR hotspot Tumor"/>
  </concept>
  <concept>
    <code value="M4.5"/>
    <display value="Non-Small Cell Lung Cancer, EGFR hotspot ctDNA"/>
  </concept>
  <concept>
    <code value="M4.6"/>
    <display
             value="Non-Small Cell Lung Cancer, ROS1 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M4.7"/>
    <display
             value="Non-Small Cell Lung Cancer, RET rearrangement FISH/RT-PC"/>
  </concept>
  <concept>
    <code value="M4.8"/>
    <display value="Non-Small Cell Lung Cancer, MET copy number FISH"/>
  </concept>
  <concept>
    <code value="M42.1"/>
    <display value="Alveolar Rhabdomyosarcoma, FOXO1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M42.2"/>
    <display
             value="Alveolar Rhabdomyosarcoma, PAX3-FOXO1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M42.3"/>
    <display
             value="Alveolar Rhabdomyosarcoma, PAX7-FOXO1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M42.4"/>
    <display value="Alveolar Rhabdomyosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M42.5"/>
    <display
             value="Alveolar Rhabdomyosarcoma, Multi-target NGS panel, structural variant (FOXO1, PAX3-FOXO1, PAX7-FOXO1  NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M43.1"/>
    <display
             value="Alveolar Soft Part Sarcoma, TFE3 rearrangement FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M43.2"/>
    <display value="Alveolar Soft Part Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M43.3"/>
    <display
             value="Alveolar Soft Part Sarcoma, Multi-target NGS panel, structural variant (TFE3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M44.1"/>
    <display value="Aneurysmal Bone Cyst, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M44.2"/>
    <display
             value="Aneurysmal Bone Cyst, Multi-target NGS panel, structural variant (USP6)"/>
  </concept>
  <concept>
    <code value="M45.1"/>
    <display
             value="Angiomatoid Fibrous Histiocytoma, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M45.2"/>
    <display
             value="Angiomatoid Fibrous Histiocytoma, FUS rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M45.3"/>
    <display
             value="Angiomatoid Fibrous Histiocytoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M45.4"/>
    <display
             value="Angiomatoid Fibrous Histiocytoma, Multi-target NGS panel, structural variant (EWSR1, FUS, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M46.1"/>
    <display
             value="Chondrosarcoma Conventional Central, Multi-target NGS panel, small variant (IDH1, IDH2)"/>
  </concept>
  <concept>
    <code value="M46.2"/>
    <display
             value="Chondrosarcoma Conventional Central, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M46.3"/>
    <display
             value="Chondrosarcoma Conventional Central, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M47.1"/>
    <display value="Chondroblastoma, SNP Array"/>
  </concept>
  <concept>
    <code value="M47.2"/>
    <display value="Chondroblastoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M47.3"/>
    <display
             value="Chondroblastoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M48.1"/>
    <display
             value="Clear Cell Sarcoma of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M48.2"/>
    <display
             value="Clear Cell Sarcoma of Soft Tissue, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M48.3"/>
    <display
             value="Clear Cell Sarcoma of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M49.1"/>
    <display
             value="CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M49.2"/>
    <display
             value="CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M5.1"/>
    <display value="Mesothelioma, CDKN2A copy number FISH"/>
  </concept>
  <concept>
    <code value="M5.2"/>
    <display
             value="Mesothelioma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M5.3"/>
    <display
             value="Mesothelioma, Multi-target NGS panel, copy number variant (CDKN2A)"/>
  </concept>
  <concept>
    <code value="M50.1"/>
    <display
             value="Dermatofibrosarcoma Protuberans, COL1A1-PDGFB rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M50.2"/>
    <display value="Dermatofibrosarcoma Protuberans, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M50.3"/>
    <display
             value="Dermatofibrosarcoma Protuberans, Multi-target NGS panel, structural variant (COL1A1-PDGFB, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M51.1"/>
    <display
             value="Desmoid-Type Fibromatosis, Multi-target NGS panel, small variant (APC, CTNNB1)"/>
  </concept>
  <concept>
    <code value="M52.1"/>
    <display
             value="Desmoplastic Small Round Cell Tumour, WT1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M52.2"/>
    <display
             value="Desmoplastic Small Round Cell Tumour, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M52.3"/>
    <display
             value="Desmoplastic Small Round Cell Tumour, Multi-target NGS panel, structural variant (WT1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M53.1"/>
    <display
             value="Endometrial Stromal Sarcoma, EPC1-PHF1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M53.2"/>
    <display
             value="Endometrial Stromal Sarcoma, JAZF1-PHF1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M53.3"/>
    <display
             value="Endometrial Stromal Sarcoma, JAZF1-SUZ12 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M53.4"/>
    <display value="Endometrial Stromal Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M53.5"/>
    <display
             value="Endometrial Stromal Sarcoma, Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NTRK1, NTRK2, NTRK3, ZC3H7B-BCOR)"/>
  </concept>
  <concept>
    <code value="M53.7"/>
    <display
             value="Endometrial Stromal Sarcoma, ZC3H7B-BCOR rearrangment FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M54.1"/>
    <display value="Epithelioid Haemangioendothelioma, WWTR1-CAMTA1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M54.2"/>
    <display
             value="Epithelioid Haemangioendothelioma, Multi-target NGS panel, structural variant (WWTR1-CAMTA1)"/>
  </concept>
  <concept>
    <code value="M55.1"/>
    <display
             value="Ewing Like Sarcoma/PNET, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M55.2"/>
    <display value="Ewing Like Sarcoma/PNET, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M55.3"/>
    <display value="Ewing Like Sarcoma/PNET, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M56.1"/>
    <display
             value="Ewing Sarcoma of Bone, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M56.2"/>
    <display value="Ewing Sarcoma of Bone, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M56.3"/>
    <display
             value="Ewing Sarcoma of Bone, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M57.1"/>
    <display
             value="Ewing-Like Soft-Tissue Sarcoma, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M57.2"/>
    <display value="Ewing-Like Soft-Tissue Sarcoma, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M57.3"/>
    <display value="Ewing-Like Soft-Tissue Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M58.1"/>
    <display
             value="Extraskeletal Myxoid Chondrosarcoma, NR4A3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M58.2"/>
    <display
             value="Extraskeletal Myxoid Chondrosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M58.3"/>
    <display
             value="Extraskeletal Myxoid Chondrosarcoma, Multi-target NGS panel, structural variant (NR4A3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M59.1"/>
    <display
             value="Fibrous Dysplasia/Myxomas (Mazabraud Syndrome), Multi-target NGS panel, small variant (GNAS)"/>
  </concept>
  <concept>
    <code value="M6.1"/>
    <display value="Mucoepidermoid Carcinoma, MAML2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M6.2"/>
    <display
             value="Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M6.3"/>
    <display
             value="Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2)"/>
  </concept>
  <concept>
    <code value="M6.5"/>
    <display value="Mucoepidermoid Carcinoma, DPYD hotspot"/>
  </concept>
  <concept>
    <code value="M60.1"/>
    <display value="Giant Cell Tumour of Bone, H3-3B hotspot"/>
  </concept>
  <concept>
    <code value="M60.2"/>
    <display value="Giant Cell Tumour of Bone, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M60.3"/>
    <display
             value="Giant Cell Tumour of Bone, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M61.1"/>
    <display
             value="High-Grade Neuroepithelial Tumour-Bcor Group, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M61.2"/>
    <display
             value="High-Grade Neuroepithelial Tumour-Bcor Group, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M61.3"/>
    <display
             value="High-Grade Neuroepithelial Tumour-Bcor Group, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M62.1"/>
    <display value="Infantile Fibrosarcoma, ETV6-NTRK3 RT-PCR or FISH"/>
  </concept>
  <concept>
    <code value="M62.2"/>
    <display value="Infantile Fibrosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M62.3"/>
    <display
             value="Infantile Fibrosarcoma, Multi-target NGS panel, structural variant (ETV6-NTRK3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M63.1"/>
    <display
             value="Inflammatory Myofibroblastic Tumour, TPM4-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M63.2"/>
    <display
             value="Inflammatory Myofibroblastic Tumour, TPM3-ALK FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M63.3"/>
    <display
             value="Inflammatory Myofibroblastic Tumour, Multi-target NGS panel, structural variant (ALK, TPM4-ALK, TPM3-ALK, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M63.4"/>
    <display
             value="Inflammatory Myofibroblastic Tumour, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M64.1"/>
    <display
             value="Low Grade Fibromyxoid Sarcoma, FUS rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M64.2"/>
    <display value="Low Grade Fibromyxoid Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M64.3"/>
    <display
             value="Low Grade Fibromyxoid Sarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M65.1"/>
    <display value="Mesenchymal Chondrosarcoma, HEY1-NCOA2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M65.2"/>
    <display value="Mesenchymal Chondrosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M65.3"/>
    <display
             value="Mesenchymal Chondrosarcoma, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M66.1"/>
    <display
             value="Myoepithelial Tumours of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M66.2"/>
    <display
             value="Myoepithelial Tumours of Soft Tissue, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M66.3"/>
    <display
             value="Myoepithelial Tumours of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M67.1"/>
    <display
             value="Myxoid/Round Cell Liposarcoma, DDIT3 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M67.2"/>
    <display value="Myxoid/Round Cell Liposarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M67.3"/>
    <display
             value="Myxoid/Round Cell Liposarcoma, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M67.4"/>
    <display value="Myxoid/Round Cell Lipsarcoma, MDM2 amplification FISH"/>
  </concept>
  <concept>
    <code value="M68.1"/>
    <display
             value="Myxoinflammatory Fibroblastic Sarcoma, TGFBR3-OGA FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M68.2"/>
    <display
             value="Myxoinflammatory Fibroblastic Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M68.3"/>
    <display
             value="Myxoinflammatory Fibroblastic Sarcoma, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M68.4"/>
    <display
             value="Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, structural variant (TGFBR3-OGA, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M68.5"/>
    <display
             value="Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M69.1"/>
    <display value="Nodular Fasciitis, USP6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M69.2"/>
    <display
             value="Nodular Fasciitis, Multi-target NGS panel, structural variant (USP6)"/>
  </concept>
  <concept>
    <code value="M7.1"/>
    <display
             value="Melanoma, Adult, Multi-target NGS panel, small variant (BRAF, KIT, NRAS)"/>
  </concept>
  <concept>
    <code value="M7.10"/>
    <display
             value="Melanoma, Adult, Copy number variant detection to genomewide resolution"/>
  </concept>
  <concept>
    <code value="M7.2"/>
    <display value="Melanoma, Adult, BRAF hotspot"/>
  </concept>
  <concept>
    <code value="M7.3"/>
    <display
             value="Melanoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M7.5"/>
    <display value="Melanoma, Adult, MYB &amp; 6cen (FISH)"/>
  </concept>
  <concept>
    <code value="M7.6"/>
    <display value="Melanoma, Adult, RREB1 (6p25)"/>
  </concept>
  <concept>
    <code value="M7.7"/>
    <display value="Melanoma, Adult, CCND1 (11q13)"/>
  </concept>
  <concept>
    <code value="M7.8"/>
    <display value="Melanoma, Adult, MYC &amp; 8cen"/>
  </concept>
  <concept>
    <code value="M7.9"/>
    <display value="Melanoma, Adult, CDKN2A &amp; 9cen"/>
  </concept>
  <concept>
    <code value="M70.1"/>
    <display value="Osteosarcoma, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M70.2"/>
    <display value="Osteosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M70.3"/>
    <display
             value="Osteosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M70.4"/>
    <display
             value="Osteosarcoma, Multi-target NGS panel, copy number variant (MDM2)"/>
  </concept>
  <concept>
    <code value="M71.1"/>
    <display value="Phosphaturic Mesenchymal Tumour, FN1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M71.2"/>
    <display value="Phosphaturic Mesenchymal Tumour, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M71.3"/>
    <display
             value="Phosphaturic Mesenchymal Tumour, Multi-target NGS panel, structural variant (FN1, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M72.1"/>
    <display
             value="Primitive Mesenchymal Myxoid Tumour of Infancy, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M72.2"/>
    <display
             value="Primitive Mesenchymal Myxoid Tumour of Infancy, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M72.3"/>
    <display
             value="Primitive Mesenchymal Myxoid Tumour of Infancy, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M73.1"/>
    <display
             value="Pseudomyogenic Haemangioendothelioma, SERPINE1-FOSB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M73.2"/>
    <display
             value="Pseudomyogenic Haemangioendothelioma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M73.3"/>
    <display
             value="Pseudomyogenic Haemangioendothelioma, Multi-target NGS panel, structural variant (SERPINE1-FOSB, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M74.1"/>
    <display value="Radiation Induced Angiosarcoma, MYC copy number FISH"/>
  </concept>
  <concept>
    <code value="M74.2"/>
    <display value="Radiation Induced Angiosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M74.3"/>
    <display
             value="Radiation Induced Angiosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M74.4"/>
    <display
             value="Radiation Induced Angiosarcoma, Multi-target NGS panel, copy number variant (MYC)"/>
  </concept>
  <concept>
    <code value="M75.1"/>
    <display
             value="Round Cell Sarcoma Nos, Multi-target NGS panel, structural variant (BCOR, CIC, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M75.2"/>
    <display value="Round Cell Sarcoma Nos, BCOR-CCNB3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M75.3"/>
    <display value="Round Cell Sarcoma Nos, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M76.1"/>
    <display
             value="Sclerosing Epithelioid Fibrosarcoma, FUS rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M76.2"/>
    <display
             value="Sclerosing Epithelioid Fibrosarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M76.3"/>
    <display
             value="Sclerosing Epithelioid Fibrosarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M77.1"/>
    <display value="Synovial Sarcoma, SS18 rearrangement FISH or RT-PCR"/>
  </concept>
  <concept>
    <code value="M77.2"/>
    <display value="Synovial Sarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M77.3"/>
    <display
             value="Synovial Sarcoma, Multi-target NGS panel, structural variant (SS18, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M78.1"/>
    <display
             value="Undifferentiated Round Cell Sarcoma of Infancy, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M78.2"/>
    <display
             value="Undifferentiated Round Cell Sarcoma of Infancy, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M79.1"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, MDM2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M79.2"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M79.3"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M79.4"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, copy number variant (MDM2, DDIT3)"/>
  </concept>
  <concept>
    <code value="M79.6"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number FISH"/>
  </concept>
  <concept>
    <code value="M79.7"/>
    <display
             value="Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number RT-PCR/ddPCR"/>
  </concept>
  <concept>
    <code value="M8.1"/>
    <display
             value="Gastrointestinal Stromal Tumour, Multi-target NGS panel, small variant (KIT, PDGFRA)"/>
  </concept>
  <concept>
    <code value="M8.2"/>
    <display
             value="Gastrointestinal Stromal Tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M80.1"/>
    <display value="Acute Myeloid Leukaemia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M80.10"/>
    <display value="Acute Myeloid Leukaemia, MRD PML-RARA RT-qPCR"/>
  </concept>
  <concept>
    <code value="M80.11"/>
    <display value="Acute Myeloid Leukaemia, MRD RUNX1-RUNX1T1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M80.12"/>
    <display value="Acute Myeloid Leukaemia, MRD CBFB-MYH11 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M80.13"/>
    <display value="Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M80.14"/>
    <display value="Acute Myeloid Leukaemia, MRD other QF-PCR"/>
  </concept>
  <concept>
    <code value="M80.15"/>
    <display value="Acute Myeloid Leukaemia, BCR-ABL1 TKD NGS"/>
  </concept>
  <concept>
    <code value="M80.18"/>
    <display value="Acute Myeloid Leukaemia, FLT3 ITD"/>
  </concept>
  <concept>
    <code value="M80.19"/>
    <display
             value="Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (GATA1)"/>
  </concept>
  <concept>
    <code value="M80.2"/>
    <display
             value="Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD), PPM1D, DDX41, PHF6, CUX1"/>
  </concept>
  <concept>
    <code value="M80.21"/>
    <display value="Acute Myeloid Leukaemia, FLT3 TKD hotspot"/>
  </concept>
  <concept>
    <code value="M80.22"/>
    <display value="Acute Myeloid Leukaemia, NPM1 exon 12 hotspot"/>
  </concept>
  <concept>
    <code value="M80.23"/>
    <display value="Acute Myeloid Leukaemia, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M80.24"/>
    <display value="Acute Myeloid Leukaemia, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M80.25"/>
    <display value="Acute Myeloid Leukaemia, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M80.26"/>
    <display value="Acute Myeloid Leukaemia, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M80.27"/>
    <display value="Acute Myeloid Leukaemia, Chr17/Chr17p copy number FISH"/>
  </concept>
  <concept>
    <code value="M80.28"/>
    <display value="Acute Myeloid Leukaemia, Chr12/Chr12p copy number FISH"/>
  </concept>
  <concept>
    <code value="M80.29"/>
    <display
             value="Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA FISH"/>
  </concept>
  <concept>
    <code value="M80.3"/>
    <display
             value="Acute Myeloid Leukaemia, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)"/>
  </concept>
  <concept>
    <code value="M80.30"/>
    <display
             value="Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH"/>
  </concept>
  <concept>
    <code value="M80.31"/>
    <display
             value="Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 FISH"/>
  </concept>
  <concept>
    <code value="M80.32"/>
    <display
             value="Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH"/>
  </concept>
  <concept>
    <code value="M80.33"/>
    <display
             value="Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 FISH"/>
  </concept>
  <concept>
    <code value="M80.34"/>
    <display
             value="Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM FISH"/>
  </concept>
  <concept>
    <code value="M80.35"/>
    <display
             value="Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA FISH"/>
  </concept>
  <concept>
    <code value="M80.36"/>
    <display value="Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M80.37"/>
    <display value="Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 FISH"/>
  </concept>
  <concept>
    <code value="M80.38"/>
    <display
             value="Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 FISH"/>
  </concept>
  <concept>
    <code value="M80.39"/>
    <display
             value="Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 FISH"/>
  </concept>
  <concept>
    <code value="M80.40"/>
    <display
             value="Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH"/>
  </concept>
  <concept>
    <code value="M80.41"/>
    <display
             value="Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.42"/>
    <display
             value="Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.43"/>
    <display
             value="Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.44"/>
    <display
             value="Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.45"/>
    <display
             value="Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.46"/>
    <display
             value="Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.47"/>
    <display
             value="Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.48"/>
    <display
             value="Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.49"/>
    <display
             value="Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.5"/>
    <display
             value="Acute Myeloid Leukaemia, Other: See tests M80.25-M80.40 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M80.50"/>
    <display
             value="Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.51"/>
    <display
             value="Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.52"/>
    <display
             value="Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M80.53"/>
    <display
             value="Acute Myeloid Leukaemia, Multi-target NGS panel, copy number variant (Monosomal karyotype, del5/del5q, del7/del7q, del17/del17p, del12/del12p)"/>
  </concept>
  <concept>
    <code value="M80.54"/>
    <display value="Acute Myeloid Leukaemia, NUP98 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M80.55"/>
    <display value="Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M80.56"/>
    <display value="Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M80.57"/>
    <display value="Acute Myeloid Leukaemia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M80.58"/>
    <display value="Acute Myeloid Leukaemia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M80.7"/>
    <display
             value="Acute Myeloid Leukaemia, Other RT-PCR: See tests M80.41-80.52 for individual specified RT-PCR targets."/>
  </concept>
  <concept>
    <code value="M80.8"/>
    <display
             value="Acute Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of  Complex karyotype)"/>
  </concept>
  <concept>
    <code value="M80.9"/>
    <display value="Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M81.1"/>
    <display
             value="Transient Abnormal Myelopoiesis, Multi-target NGS panel, small variant (GATA1)"/>
  </concept>
  <concept>
    <code value="M82.1"/>
    <display
             value="Myelodysplasia, Multi-target NGS panel, small variant (TP53, SF3B1, IDH1, IDH2, NRAS, KRAS, TET2, SRSF2, ASXL1, DNMT3A, RUNX1, U2AF1, EZH2, BCOR, PTPN11, JAK2, SETBP1, PPM1D, DDX41, PHF6, CUX1, UBA1)"/>
  </concept>
  <concept>
    <code value="M82.10"/>
    <display value="Myelodysplasia, Chr13/Chr13q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.11"/>
    <display value="Myelodysplasia, Chr11q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.12"/>
    <display
             value="Myelodysplasia, Chr12p copy number FISH, t(12p) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M82.13"/>
    <display value="Myelodysplasia, Chr9q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.14"/>
    <display value="Myelodysplasia, Chr17/Chr17p copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.15"/>
    <display value="Myelodysplasia, idic(X)(q13) FISH"/>
  </concept>
  <concept>
    <code value="M82.16"/>
    <display
             value="Myelodysplasia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p &amp; idic(X)(q13);-Y; del 20q; +8; +19,del(3q)"/>
  </concept>
  <concept>
    <code value="M82.17"/>
    <display
             value="Myelodysplasia, Multi-target NGS panel, structural variant (t(12p), t(17p);inv(3)/t(3q)/del(3q)"/>
  </concept>
  <concept>
    <code value="M82.18"/>
    <display value="Myelodysplasia, ChrY copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.19"/>
    <display value="Myelodysplasia, Chr20/20q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.2"/>
    <display
             value="Myelodysplasia, Karyotype (To include detection of complex karyotype, -7/del7q, -5/del5q, i(17q)/t(17p), -13/del13q, del11q, del12p/t(12p), del9q, del17/del17p &amp; idic(X)(q13)); -Y; del 20q; +8; +19,(inv(3)/t(3q)/del(3q))"/>
  </concept>
  <concept>
    <code value="M82.20"/>
    <display value="Myelodysplasia, Chr8 copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.21"/>
    <display value="Myelodysplasia, Chr19 copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.22"/>
    <display value="Myelodysplasia, inv(3)/t(3q)/del(3q)"/>
  </concept>
  <concept>
    <code value="M82.23"/>
    <display value="Myelodysplasia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M82.24"/>
    <display value="Myelodysplasia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M82.4"/>
    <display
             value="Myelodysplasia, FISH copy number and rearrangement Other: See tests M82.7 -M82.22 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M82.6"/>
    <display value="Myelodysplasia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M82.7"/>
    <display value="Myelodysplasia, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.8"/>
    <display value="Myelodysplasia, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M82.9"/>
    <display value="Myelodysplasia, i(17q)/t(17p) FISH"/>
  </concept>
  <concept>
    <code value="M83.1"/>
    <display value="Aplastic Anaemia, Karyotype (Genomewide)"/>
  </concept>
  <concept>
    <code value="M83.3"/>
    <display value="Aplastic Anaemia, FISH copy number and rearrangement"/>
  </concept>
  <concept>
    <code value="M83.4"/>
    <display value="Aplastic Anaemia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M83.5"/>
    <display value="Aplastic Anaemia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M83.6"/>
    <display value="Aplastic Anaemia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M84.1"/>
    <display value="Chronic Myeloid Leukaemia, BCR-ABL1 multiplex"/>
  </concept>
  <concept>
    <code value="M84.11"/>
    <display value="Chronic Myeloid Leukaemia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M84.12"/>
    <display value="Chronic Myeloid Leukaemia, Chr8 copy number FISH"/>
  </concept>
  <concept>
    <code value="M84.13"/>
    <display value="Chronic Myeloid Leukaemia, Chr19 copy number FISH"/>
  </concept>
  <concept>
    <code value="M84.14"/>
    <display value="Chronic Myeloid Leukaemia, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M84.15"/>
    <display value="Chronic Myeloid Leukaemia, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M84.16"/>
    <display value="Chronic Myeloid Leukaemia, i(17q) FISH"/>
  </concept>
  <concept>
    <code value="M84.17"/>
    <display value="Chronic Myeloid Leukaemia, Chr12p copy number FISH"/>
  </concept>
  <concept>
    <code value="M84.18"/>
    <display
             value="Chronic Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH and related abnormalities i.e. 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11)"/>
  </concept>
  <concept>
    <code value="M84.19"/>
    <display value="Chronic Myeloid Leukaemia, Inv(3) MECOM FISH"/>
  </concept>
  <concept>
    <code value="M84.2"/>
    <display value="Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M84.20"/>
    <display
             value="Chronic Myeloid Leukaemia, 11q23 (KMT2A) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M84.21"/>
    <display
             value="Chronic Myeloid Leukaemia, Multi-target NGS panel, copy number variant (trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-)"/>
  </concept>
  <concept>
    <code value="M84.22"/>
    <display
             value="Chronic Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)"/>
  </concept>
  <concept>
    <code value="M84.23"/>
    <display value="Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M84.24"/>
    <display value="Chronic Myeloid Leukaemia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M84.25"/>
    <display value="Chronic Myeloid Leukaemia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M84.3"/>
    <display value="Chronic Myeloid Leukaemia, BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M84.4"/>
    <display
             value="Chronic Myeloid Leukaemia, Karyotype (To include detection of trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-&amp; t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)"/>
  </concept>
  <concept>
    <code value="M84.6"/>
    <display
             value="Chronic Myeloid Leukaemia, FISH copy number and rearrangement Other: See tests M84.12 M84.20 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M84.8"/>
    <display value="Chronic Myeloid Leukaemia, BCR-ABL1 TKD NGS"/>
  </concept>
  <concept>
    <code value="M85.1"/>
    <display
             value="Myeloproliferative Neoplasm, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)"/>
  </concept>
  <concept>
    <code value="M85.10"/>
    <display value="Myeloproliferative Neoplasm, PCM1-JAK2 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M85.11"/>
    <display value="Myeloproliferative Neoplasm, BCR-ABL1 multiplex"/>
  </concept>
  <concept>
    <code value="M85.12"/>
    <display value="Myeloproliferative Neoplasm, Other RT-PCR"/>
  </concept>
  <concept>
    <code value="M85.13"/>
    <display value="Myeloproliferative Neoplasm, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M85.14"/>
    <display value="Myeloproliferative Neoplasm, JAK2 V617F hotspot"/>
  </concept>
  <concept>
    <code value="M85.15"/>
    <display value="Myeloproliferative Neoplasm, JAK2  exon 12 hotspot"/>
  </concept>
  <concept>
    <code value="M85.16"/>
    <display value="Myeloproliferative Neoplasm, CALR exon 9 hotspot"/>
  </concept>
  <concept>
    <code value="M85.17"/>
    <display value="Myeloproliferative Neoplasm, MPL exon 10 hotspot"/>
  </concept>
  <concept>
    <code value="M85.19"/>
    <display value="Myeloproliferative Neoplasm, Chr8 copy number FISH"/>
  </concept>
  <concept>
    <code value="M85.2"/>
    <display
             value="Myeloproliferative Neoplasm, Multi-target NGS panel, small variant"/>
  </concept>
  <concept>
    <code value="M85.20"/>
    <display
             value="Myeloproliferative Neoplasm, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M85.21"/>
    <display
             value="Myeloproliferative Neoplasm, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M85.22"/>
    <display value="Myeloproliferative Neoplasm, i(17q) FISH"/>
  </concept>
  <concept>
    <code value="M85.23"/>
    <display value="Myeloproliferative Neoplasm, Chr12p copy number FISH"/>
  </concept>
  <concept>
    <code value="M85.24"/>
    <display
             value="Myeloproliferative Neoplasm, t(9;22)(q34;q11) BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M85.25"/>
    <display
             value="Myeloproliferative Neoplasm, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)"/>
  </concept>
  <concept>
    <code value="M85.26"/>
    <display
             value="Myeloproliferative Neoplasm, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)"/>
  </concept>
  <concept>
    <code value="M85.27"/>
    <display value="Myeloproliferative Neoplasm, FGFR1 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M85.28"/>
    <display
             value="Myeloproliferative Neoplasm, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)"/>
  </concept>
  <concept>
    <code value="M85.29"/>
    <display value="Myeloproliferative Neoplasm, inv(3)/t(3;3) FISH"/>
  </concept>
  <concept>
    <code value="M85.3"/>
    <display
             value="Myeloproliferative Neoplasm, Karyotype (To include detection of complex karyotype)"/>
  </concept>
  <concept>
    <code value="M85.30"/>
    <display value="Myeloproliferative Neoplasm, 11q23 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M85.31"/>
    <display
             value="Myeloproliferative Neoplasm, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)"/>
  </concept>
  <concept>
    <code value="M85.32"/>
    <display value="Myeloproliferative Neoplasm, FLT3 rearragement FISH"/>
  </concept>
  <concept>
    <code value="M85.33"/>
    <display value="Myeloproliferative Neoplasm, RET rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M85.34"/>
    <display value="Myeloproliferative Neoplasm, NTRK3 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M85.35"/>
    <display
             value="Myeloproliferative Neoplasm, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M85.36"/>
    <display
             value="Myeloproliferative Neoplasm, Multi-target NGS panel, copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)"/>
  </concept>
  <concept>
    <code value="M85.37"/>
    <display value="Myeloproliferative Neoplasm, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M85.38"/>
    <display value="Myeloproliferative Neoplasm, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M85.5"/>
    <display
             value="Myeloproliferative Neoplasm, FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M85.7"/>
    <display
             value="Myeloproliferative Neoplasm, FIP1L1-PDGFRA (4q12) FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M85.8"/>
    <display value="Myeloproliferative Neoplasm, FIP1L1-PDGFRA RT-qPCR"/>
  </concept>
  <concept>
    <code value="M85.9"/>
    <display value="Myeloproliferative Neoplasm, ETV6-PDGFRB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M86.1"/>
    <display
             value="Systemic Mastocytosis, Multi-target NGS panel, small variant (KIT)"/>
  </concept>
  <concept>
    <code value="M86.2"/>
    <display value="Systemic Mastocytosis, KIT D816 QF-PCR"/>
  </concept>
  <concept>
    <code value="M86.3"/>
    <display value="Systemic Mastocytosis, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M86.4"/>
    <display value="Systemic Mastocytosis, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M86.5"/>
    <display value="Systemic Mastocytosis, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M87.1"/>
    <display
             value="Chronic Neutrophilic Leukaemia, Multi-target NGS panel, small variant (CSF3R)"/>
  </concept>
  <concept>
    <code value="M88.1"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant (PTPN11, KRAS, NRAS, NF1, CBL)"/>
  </concept>
  <concept>
    <code value="M88.10"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, trisomy 8)"/>
  </concept>
  <concept>
    <code value="M88.11"/>
    <display value="Juvenile Myelomonocytic Leukaemia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M88.12"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M88.2"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M88.3"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant"/>
  </concept>
  <concept>
    <code value="M88.4"/>
    <display value="Juvenile Myelomonocytic Leukaemia, Karyotype"/>
  </concept>
  <concept>
    <code value="M88.5"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, FISH copy number and rearrangement Other: See tests M88.7-M88.9 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M88.7"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Chr8 copy number FISH"/>
  </concept>
  <concept>
    <code value="M88.8"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M88.9"/>
    <display
             value="Juvenile Myelomonocytic Leukaemia, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M89.1"/>
    <display value="Acute Leukaemia Other, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M89.10"/>
    <display value="Acute Leukaemia Other, MRD PML-RARA RT-qPCR"/>
  </concept>
  <concept>
    <code value="M89.100"/>
    <display
             value="Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.101"/>
    <display
             value="Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.102"/>
    <display value="Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.103"/>
    <display
             value="Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.104"/>
    <display
             value="Acute Leukaemia Other, Multi-target NGS panel, copy number variant"/>
  </concept>
  <concept>
    <code value="M89.105"/>
    <display value="Acute Leukaemia Other, NUP98 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.106"/>
    <display value="Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M89.107"/>
    <display value="Acute Leukaemia Other, MRD NPM1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M89.108"/>
    <display value="Acute Leukaemia Other, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M89.109"/>
    <display value="Acute Leukaemia Other, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M89.11"/>
    <display value="Acute Leukaemia Other, MRD RUNX1-RUNX1T1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M89.12"/>
    <display value="Acute Leukaemia Other, MRD CBFB-MYH11 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M89.13"/>
    <display value="Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M89.14"/>
    <display value="Acute Leukaemia Other, MRD other QF-PCR"/>
  </concept>
  <concept>
    <code value="M89.15"/>
    <display
             value="Acute Leukaemia Other, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)"/>
  </concept>
  <concept>
    <code value="M89.16"/>
    <display
             value="Acute Leukaemia Other, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR )"/>
  </concept>
  <concept>
    <code value="M89.17"/>
    <display value="Acute Leukaemia Other, BCR-ABL1 TKD NGS"/>
  </concept>
  <concept>
    <code value="M89.2"/>
    <display
             value="Acute Leukaemia Other, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)"/>
  </concept>
  <concept>
    <code value="M89.20"/>
    <display value="Acute Leukaemia Other, FLT3 TKD hotspot"/>
  </concept>
  <concept>
    <code value="M89.21"/>
    <display value="Acute Leukaemia Other, NPM1 exon 12 hotspot"/>
  </concept>
  <concept>
    <code value="M89.22"/>
    <display value="Acute Leukaemia Other, IDH1 hotspot"/>
  </concept>
  <concept>
    <code value="M89.23"/>
    <display value="Acute Leukaemia Other, IDH2 hotspot"/>
  </concept>
  <concept>
    <code value="M89.24"/>
    <display value="Acute Leukaemia Other, Chr5/Chr5q copy number FISH"/>
  </concept>
  <concept>
    <code value="M89.25"/>
    <display value="Acute Leukaemia Other, Chr7/Chr7q copy number FISH"/>
  </concept>
  <concept>
    <code value="M89.26"/>
    <display value="Acute Leukaemia Other, Chr17/Chr17p copy number FISH"/>
  </concept>
  <concept>
    <code value="M89.27"/>
    <display value="Acute Leukaemia Other, Chr12/Chr12p copy number FISH"/>
  </concept>
  <concept>
    <code value="M89.28"/>
    <display value="Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA FISH"/>
  </concept>
  <concept>
    <code value="M89.29"/>
    <display
             value="Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH"/>
  </concept>
  <concept>
    <code value="M89.3"/>
    <display
             value="Acute Leukaemia Other, FISH copy number and rearrangement other"/>
  </concept>
  <concept>
    <code value="M89.30"/>
    <display
             value="Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 FISH"/>
  </concept>
  <concept>
    <code value="M89.31"/>
    <display
             value="Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH"/>
  </concept>
  <concept>
    <code value="M89.32"/>
    <display value="Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 FISH"/>
  </concept>
  <concept>
    <code value="M89.33"/>
    <display value="Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM FISH"/>
  </concept>
  <concept>
    <code value="M89.34"/>
    <display
             value="Acute Leukaemia Other, t(1;22)(p13;q13) RBM15-MRTFA FISH"/>
  </concept>
  <concept>
    <code value="M89.35"/>
    <display value="Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M89.36"/>
    <display value="Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 FISH"/>
  </concept>
  <concept>
    <code value="M89.37"/>
    <display
             value="Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 FISH"/>
  </concept>
  <concept>
    <code value="M89.38"/>
    <display value="Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 FISH"/>
  </concept>
  <concept>
    <code value="M89.39"/>
    <display
             value="Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH"/>
  </concept>
  <concept>
    <code value="M89.4"/>
    <display
             value="Acute Leukaemia Other, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD, PPM1D, ETV6, NOTCH1, FBXW7, PTEN,  HRAS)"/>
  </concept>
  <concept>
    <code value="M89.40"/>
    <display
             value="Acute Leukaemia Other, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)"/>
  </concept>
  <concept>
    <code value="M89.41"/>
    <display value="Acute Leukaemia Other, del(1)(p33p33) FISH"/>
  </concept>
  <concept>
    <code value="M89.42"/>
    <display value="Acute Leukaemia Other, iAMP21 FISH"/>
  </concept>
  <concept>
    <code value="M89.5"/>
    <display value="Acute Leukaemia Other, FLT3 ITD"/>
  </concept>
  <concept>
    <code value="M89.52"/>
    <display
             value="Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 FISH"/>
  </concept>
  <concept>
    <code value="M89.53"/>
    <display value="Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 FISH"/>
  </concept>
  <concept>
    <code value="M89.54"/>
    <display value="Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF FISH"/>
  </concept>
  <concept>
    <code value="M89.55"/>
    <display value="Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 FISH"/>
  </concept>
  <concept>
    <code value="M89.56"/>
    <display
             value="Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH"/>
  </concept>
  <concept>
    <code value="M89.57"/>
    <display value="Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN FISH"/>
  </concept>
  <concept>
    <code value="M89.58"/>
    <display
             value="Acute Leukaemia Other,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH"/>
  </concept>
  <concept>
    <code value="M89.59"/>
    <display
             value="Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL FISH"/>
  </concept>
  <concept>
    <code value="M89.6"/>
    <display value="Acute Leukaemia Other, Other RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.60"/>
    <display value="Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 FISH"/>
  </concept>
  <concept>
    <code value="M89.61"/>
    <display value="Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 FISH"/>
  </concept>
  <concept>
    <code value="M89.62"/>
    <display
             value="Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 FISH"/>
  </concept>
  <concept>
    <code value="M89.63"/>
    <display value="Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD FISH"/>
  </concept>
  <concept>
    <code value="M89.64"/>
    <display value="Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 FISH"/>
  </concept>
  <concept>
    <code value="M89.65"/>
    <display
             value="Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH"/>
  </concept>
  <concept>
    <code value="M89.66"/>
    <display
             value="Acute Leukaemia Other, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)"/>
  </concept>
  <concept>
    <code value="M89.67"/>
    <display
             value="Acute Leukaemia Other, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)"/>
  </concept>
  <concept>
    <code value="M89.68"/>
    <display value="Acute Leukaemia Other, PDGFRA rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.69"/>
    <display value="Acute Leukaemia Other, PDGFRB rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.7"/>
    <display
             value="Acute Leukaemia Other, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M89.70"/>
    <display
             value="Acute Leukaemia Other, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)"/>
  </concept>
  <concept>
    <code value="M89.71"/>
    <display value="Acute Leukaemia Other, JAK2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.72"/>
    <display
             value="Acute Leukaemia Other, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)"/>
  </concept>
  <concept>
    <code value="M89.73"/>
    <display value="Acute Leukaemia Other, ABL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.74"/>
    <display value="Acute Leukaemia Other, CSF1R rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.75"/>
    <display value="Acute Leukaemia Other, 14q32 (IGH) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.76"/>
    <display value="Acute Leukaemia Other, CRLF2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.77"/>
    <display value="Acute Leukaemia Other, EPOR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M89.78"/>
    <display
             value="Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.79"/>
    <display
             value="Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.8"/>
    <display value="Acute Leukaemia Other, BCR-ABL1 multiplex"/>
  </concept>
  <concept>
    <code value="M89.80"/>
    <display
             value="Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.81"/>
    <display
             value="Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.82"/>
    <display
             value="Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.83"/>
    <display
             value="Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.84"/>
    <display
             value="Acute Leukaemia Other, t(1;22)(p13;q13)  RBM15-MRTFA RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.85"/>
    <display value="Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.86"/>
    <display value="Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.87"/>
    <display
             value="Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.88"/>
    <display
             value="Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.89"/>
    <display
             value="Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.9"/>
    <display value="Acute Leukaemia Other, MRD NPM1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M89.90"/>
    <display
             value="Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.91"/>
    <display
             value="Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.92"/>
    <display
             value="Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.93"/>
    <display
             value="Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.94"/>
    <display
             value="Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.95"/>
    <display
             value="Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.96"/>
    <display
             value="Acute Leukaemia Other, t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.97"/>
    <display
             value="Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.98"/>
    <display value="Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M89.99"/>
    <display
             value="Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M9.1"/>
    <display
             value="Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, small variant (BRAF, KRAS, NRAS, HRAS, TERT promoter)"/>
  </concept>
  <concept>
    <code value="M9.2"/>
    <display
             value="Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M9.3"/>
    <display
             value="Thyroid Papillary Carcinoma, Adult, RET rearrangement FISH/RT-PC"/>
  </concept>
  <concept>
    <code value="M9.4"/>
    <display
             value="Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"/>
  </concept>
  <concept>
    <code value="M9.6"/>
    <display
             value="Thyroid Papillary Carcinoma, Adult, TERT promoter hotspot"/>
  </concept>
  <concept>
    <code value="M90.1"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M90.2"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, Karyotype (Genomewide)"/>
  </concept>
  <concept>
    <code value="M90.3"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, FISH copy number and rearrangement"/>
  </concept>
  <concept>
    <code value="M90.4"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD)"/>
  </concept>
  <concept>
    <code value="M90.5"/>
    <display value="Blastic Plasmacytoid Dendritic Cell Neoplasm, FLT3 ITD"/>
  </concept>
  <concept>
    <code value="M90.6"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M90.7"/>
    <display
             value="Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M91.1"/>
    <display value="Acute Lymphoblastic Leukaemia, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M91.10"/>
    <display value="Acute Lymphoblastic Leukaemia, BCR-ABL1 FISH"/>
  </concept>
  <concept>
    <code value="M91.11"/>
    <display value="Acute Lymphoblastic Leukaemia, BCR-ABL1 TKD NGS"/>
  </concept>
  <concept>
    <code value="M91.14"/>
    <display value="Acute Lymphoblastic Leukaemia, MRD ALL RT-qPCR"/>
  </concept>
  <concept>
    <code value="M91.15"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Multi-target NGS panel, small variant (ETV6, NOTCH1, FBXW7, TP53, PTEN, KRAS, NRAS, HRAS)"/>
  </concept>
  <concept>
    <code value="M91.2"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Karyotype (To include detection of complex karyotype, hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc)"/>
  </concept>
  <concept>
    <code value="M91.22"/>
    <display
             value="Acute Lymphoblastic Leukaemia, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)"/>
  </concept>
  <concept>
    <code value="M91.23"/>
    <display
             value="Acute Lymphoblastic Leukaemia, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR)"/>
  </concept>
  <concept>
    <code value="M91.24"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)"/>
  </concept>
  <concept>
    <code value="M91.25"/>
    <display value="Acute Lymphoblastic Leukaemia, del(1)(p33p33) FISH"/>
  </concept>
  <concept>
    <code value="M91.26"/>
    <display value="Acute Lymphoblastic Leukaemia, iAMP21 FISH"/>
  </concept>
  <concept>
    <code value="M91.36"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 FISH"/>
  </concept>
  <concept>
    <code value="M91.37"/>
    <display
             value="Acute Lymphoblastic Leukaemia,  t(1;19)(q23;p13) TCF3-PBX1 FISH"/>
  </concept>
  <concept>
    <code value="M91.38"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF FISH"/>
  </concept>
  <concept>
    <code value="M91.39"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 FISH"/>
  </concept>
  <concept>
    <code value="M91.4"/>
    <display
             value="Acute Lymphoblastic Leukaemia, FISH copy number and rearrangement other: See tests M91.24-M91.62 for individual specified FISH targets."/>
  </concept>
  <concept>
    <code value="M91.40"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH"/>
  </concept>
  <concept>
    <code value="M91.41"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN FISH"/>
  </concept>
  <concept>
    <code value="M91.42"/>
    <display
             value="Acute Lymphoblastic Leukaemia,  t(9;11)(p21;q23) KMT2A-MLLT3 FISH"/>
  </concept>
  <concept>
    <code value="M91.43"/>
    <display
             value="Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH"/>
  </concept>
  <concept>
    <code value="M91.44"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL FISH"/>
  </concept>
  <concept>
    <code value="M91.45"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 FISH"/>
  </concept>
  <concept>
    <code value="M91.46"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 FISH"/>
  </concept>
  <concept>
    <code value="M91.47"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 FISH"/>
  </concept>
  <concept>
    <code value="M91.48"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD FISH"/>
  </concept>
  <concept>
    <code value="M91.49"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(7;10)(q34;q24) TRB-TLX1 FISH"/>
  </concept>
  <concept>
    <code value="M91.50"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH"/>
  </concept>
  <concept>
    <code value="M91.51"/>
    <display
             value="Acute Lymphoblastic Leukaemia, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)"/>
  </concept>
  <concept>
    <code value="M91.52"/>
    <display
             value="Acute Lymphoblastic Leukaemia, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)"/>
  </concept>
  <concept>
    <code value="M91.53"/>
    <display
             value="Acute Lymphoblastic Leukaemia, PDGFRA rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.54"/>
    <display
             value="Acute Lymphoblastic Leukaemia, PDGFRB rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.55"/>
    <display
             value="Acute Lymphoblastic Leukaemia, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)"/>
  </concept>
  <concept>
    <code value="M91.56"/>
    <display value="Acute Lymphoblastic Leukaemia, JAK2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.57"/>
    <display
             value="Acute Lymphoblastic Leukaemia, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)"/>
  </concept>
  <concept>
    <code value="M91.58"/>
    <display value="Acute Lymphoblastic Leukaemia, ABL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.59"/>
    <display value="Acute Lymphoblastic Leukaemia, CSF1R rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.6"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Other RT-PCR: See tests M91-63-M91.77 for individual specified RT-PCR targets"/>
  </concept>
  <concept>
    <code value="M91.60"/>
    <display
             value="Acute Lymphoblastic Leukaemia, 14q32(IGH) rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.61"/>
    <display value="Acute Lymphoblastic Leukaemia, CRLF2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.62"/>
    <display value="Acute Lymphoblastic Leukaemia, EPOR rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.63"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.64"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(1;19)(q23;p13) TCF3-PBX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.65"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.66"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.67"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.68"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.69"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(9;11)(p21;q23) KMT2A-MLLT3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.7"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Multi-target NGS panel, structural variant"/>
  </concept>
  <concept>
    <code value="M91.70"/>
    <display
             value="Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.71"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.72"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.73"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.74"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.75"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.76"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(7;10)q34;q24) TRB-TLX1 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.77"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR"/>
  </concept>
  <concept>
    <code value="M91.78"/>
    <display
             value="Acute Lymphoblastic Leukaemia, Multi-target NGS panel, copy number variant (to include hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc.)"/>
  </concept>
  <concept>
    <code value="M91.79"/>
    <display
             value="Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR rare"/>
  </concept>
  <concept>
    <code value="M91.8"/>
    <display value="Acute Lymphoblastic Leukaemia, BCR-ABL1 multiplex"/>
  </concept>
  <concept>
    <code value="M91.80"/>
    <display value="Acute Lymphoblastic Leukaemia, TPMT"/>
  </concept>
  <concept>
    <code value="M91.81"/>
    <display value="Acute Lymphoblastic Leukaemia, NUDT15"/>
  </concept>
  <concept>
    <code value="M91.82"/>
    <display value="Acute Lymphoblastic Leukaemia, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M91.83"/>
    <display value="Acute Lymphoblastic Leukaemia, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M91.84"/>
    <display value="Acute Lymphoblastic Leukaemia, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.85"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(8;14)(q34;q32) IGH-MYC FISH"/>
  </concept>
  <concept>
    <code value="M91.86"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(2;8)(p12;q24) IGK-MYC FISH"/>
  </concept>
  <concept>
    <code value="M91.87"/>
    <display
             value="Acute Lymphoblastic Leukaemia, t(8;22)(q24;q11) IGL-MYC FISH"/>
  </concept>
  <concept>
    <code value="M91.88"/>
    <display value="Acute Lymphoblastic Leukaemia, BCL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.89"/>
    <display value="Acute Lymphoblastic Leukaemia, BCL6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M91.9"/>
    <display value="Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR"/>
  </concept>
  <concept>
    <code value="M92.1"/>
    <display
             value="Plasma Cell Dyscrasia, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF, TP53, DIS3, TENT5C, IRF4)"/>
  </concept>
  <concept>
    <code value="M92.10"/>
    <display value="Plasma Cell Dyscrasia, del(1p) copy number FISH"/>
  </concept>
  <concept>
    <code value="M92.11"/>
    <display value="Plasma Cell Dyscrasia, gain(1q) copy number FISH"/>
  </concept>
  <concept>
    <code value="M92.12"/>
    <display value="Plasma Cell Dyscrasia, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M92.13"/>
    <display
             value="Plasma Cell Dyscrasia, Multi-target NGS panel (To include hyperdiploidy, del(1p), gain(1q), del17p)"/>
  </concept>
  <concept>
    <code value="M92.14"/>
    <display value="Plasma Cell Dyscrasia, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M92.2"/>
    <display value="Plasma Cell Dyscrasia, t(4;14) IGH-FGFR3FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M92.3"/>
    <display value="Plasma Cell Dyscrasia, t(6;14)  IGH-CCND3 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M92.4"/>
    <display
             value="Plasma Cell Dyscrasia, t(11;14)(q13;q32)  IGH-CCND1 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M92.5"/>
    <display value="Plasma Cell Dyscrasia, t(14;16) IGH-MAF FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M92.6"/>
    <display value="Plasma Cell Dyscrasia, t(14;20)  IGH-MAFB FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M92.7"/>
    <display
             value="Plasma Cell Dyscrasia, Multi-target NGS panel, structural variant (To include IGH-FGFR3, IGH-CCND3, IGH-CCND1, IGH-MAF, IGH-MAFB, MYC rearrangements)"/>
  </concept>
  <concept>
    <code value="M92.8"/>
    <display value="Plasma Cell Dyscrasia, IGH rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M92.9"/>
    <display value="Plasma Cell Dyscrasia, Hyperdiploidy copy number FISH"/>
  </concept>
  <concept>
    <code value="M93.3"/>
    <display value="Lymphoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M93.4"/>
    <display value="Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M93.5"/>
    <display value="Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M93.6"/>
    <display
             value="Lymphoma, Multi-target NGS panel-small variant (BTK, PLCG2, RAS, MAP2K1, BCL2)"/>
  </concept>
  <concept>
    <code value="M94.1"/>
    <display
             value="Chronic Lymphocytic Leukaemia, Multi-target NGS panel, small variant (TP53,BTK, PLCG2, BCL2)"/>
  </concept>
  <concept>
    <code value="M94.10"/>
    <display
             value="Chronic Lymphocytic Leukaemia, chromosome 12 copy number FISH"/>
  </concept>
  <concept>
    <code value="M94.2"/>
    <display
             value="Chronic Lymphocytic Leukaemia, Multi-target NGS panel, copy number variant (TP53,ATM, DLEU2/7, RB1, trisomy 12)"/>
  </concept>
  <concept>
    <code value="M94.4"/>
    <display
             value="Chronic Lymphocytic Leukaemia, del(17p) TP53 copy number FISH"/>
  </concept>
  <concept>
    <code value="M94.5"/>
    <display
             value="Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M94.6"/>
    <display
             value="Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS"/>
  </concept>
  <concept>
    <code value="M94.7"/>
    <display value="Chronic Lymphocytic Leukaemia, TP53 seq"/>
  </concept>
  <concept>
    <code value="M94.8"/>
    <display value="Chronic Lymphocytic Leukaemia, 11q copy number FISH"/>
  </concept>
  <concept>
    <code value="M94.9"/>
    <display value="Chronic Lymphocytic Leukaemia, 13q copy number FISH"/>
  </concept>
  <concept>
    <code value="M95.1"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq"/>
  </concept>
  <concept>
    <code value="M95.10"/>
    <display value="B Cell Non-Hodgkin Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M95.11"/>
    <display value="B Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M95.12"/>
    <display value="B cell Non-Hodgkin Lymphoma, MYD88 (L265P) hotspot"/>
  </concept>
  <concept>
    <code value="M95.2"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS"/>
  </concept>
  <concept>
    <code value="M95.3"/>
    <display value="B Cell Non-Hodgkin Lymphoma, Ig rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M95.4"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (EZH2)"/>
  </concept>
  <concept>
    <code value="M95.5"/>
    <display value="B Cell Non-Hodgkin Lymphoma, EZH2 copy number FISH"/>
  </concept>
  <concept>
    <code value="M95.6"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (BTK, PLCG2)"/>
  </concept>
  <concept>
    <code value="M95.7"/>
    <display value="B Cell Non-Hodgkin Lymphoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M95.8"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (Ig)"/>
  </concept>
  <concept>
    <code value="M95.9"/>
    <display
             value="B Cell Non-Hodgkin Lymphoma, Mutli-target NGS panel, copy number (EZH2)"/>
  </concept>
  <concept>
    <code value="M96.1"/>
    <display value="Burkitt Lymphoma, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M96.10"/>
    <display value="Burkitt Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M96.2"/>
    <display value="Burkitt Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M96.3"/>
    <display value="Burkitt Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M96.4"/>
    <display value="Burkitt Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M96.5"/>
    <display value="Burkitt Lymphoma, BCL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M96.6"/>
    <display value="Burkitt Lymphoma, BCL6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M96.7"/>
    <display value="Burkitt Lymphoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M96.8"/>
    <display
             value="Burkitt Lymphoma, Multi-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, other rearrangements of MYC,  BCL2, BCL6)"/>
  </concept>
  <concept>
    <code value="M96.9"/>
    <display value="Burkitt Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M97.1"/>
    <display
             value="Burkitt Like Lymphoma with 11q Abnormalities, 11q copy number FISH"/>
  </concept>
  <concept>
    <code value="M97.2"/>
    <display
             value="Burkitt Like Lymphoma with 11q Abnormalities, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M97.3"/>
    <display
             value="Burkitt Like Lymphoma with 11q Abnormalities, Multi-target NGS panel, copy number variant (11q)"/>
  </concept>
  <concept>
    <code value="M97.4"/>
    <display
             value="Burkitt Like Lymphoma with 11q Abnormalities, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M97.5"/>
    <display
             value="Burkitt Like Lymphoma with 11q Abnormalities, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M98.1"/>
    <display
             value="Large B Cell Like Lymphoma with IRF4 Rearrangement, IRF4 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M98.2"/>
    <display
             value="Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M98.3"/>
    <display
             value="Large B Cell Like Lymphoma with IRF4 Rearrangement, Multi-target NGS panel, structural variant (IRF4)"/>
  </concept>
  <concept>
    <code value="M98.4"/>
    <display
             value="Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M98.5"/>
    <display
             value="Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M99.1"/>
    <display value="High Grade Lymphoma, MYC rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M99.10"/>
    <display value="High Grade Lymphoma, WGS Tumour First"/>
  </concept>
  <concept>
    <code value="M99.11"/>
    <display value="High Grade Lymphoma, WGS Follow-up Germline"/>
  </concept>
  <concept>
    <code value="M99.2"/>
    <display
             value="High Grade Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M99.3"/>
    <display
             value="High Grade Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M99.4"/>
    <display
             value="High Grade Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M99.5"/>
    <display value="High Grade Lymphoma, BCL2 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M99.6"/>
    <display
             value="High Grade Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR"/>
  </concept>
  <concept>
    <code value="M99.7"/>
    <display value="High Grade Lymphoma, BCL6 rearrangement FISH"/>
  </concept>
  <concept>
    <code value="M99.8"/>
    <display value="High Grade Lymphoma, WGS Germline and Tumor"/>
  </concept>
  <concept>
    <code value="M99.9"/>
    <display
             value="High Grade Lymphoma, Mutli-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, IGH-BCL2, other rearrangements of MYC, BCL2, BCL6)"/>
  </concept>
  <concept>
    <code value="R100.3"/>
    <display
             value="Rare syndromic craniosynostosis or isolated multisuture synostosis (WGS)"/>
  </concept>
  <concept>
    <code value="R101.1"/>
    <display
             value="Ehlers Danlos syndrome with a likely monogenic cause (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R102.1"/>
    <display value="Osteogenesis imperfecta (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R104.3"/>
    <display value="Skeletal dysplasia (WGS)"/>
  </concept>
  <concept>
    <code value="R104.4"/>
    <display value="Skeletal dysplasia (Small Panel)"/>
  </concept>
  <concept>
    <code value="R105.1"/>
    <display
             value="MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ common variant newborn screening follow up (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R106.1"/>
    <display
             value="Alstrom syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R107.1"/>
    <display value="Bardet-Biedl syndrome (WES or Large Panel)"/>
  </concept>
  <concept>
    <code value="R109.3"/>
    <display value="Childhood onset leukodystrophy (WGS)"/>
  </concept>
  <concept>
    <code value="R110.1"/>
    <display
             value="Segmental overgrowth disorders Deep sequencing (Small panel)"/>
  </concept>
  <concept>
    <code value="R111.1"/>
    <display value="X-inactivation testing (X-inactivation testing)"/>
  </concept>
  <concept>
    <code value="R112.1"/>
    <display
             value="Factor II deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R115.1"/>
    <display
             value="Factor V deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R115.2"/>
    <display value="Factor V deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R116.1"/>
    <display
             value="Factor VII deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R116.2"/>
    <display value="Factor VII deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R117.1"/>
    <display value="Factor VIII deficiency (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R117.2"/>
    <display
             value="Factor VIII deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R117.3"/>
    <display value="Factor VIII deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R118.1"/>
    <display
             value="Factor IX deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R118.2"/>
    <display value="Factor IX deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R119.1"/>
    <display
             value="Factor X deficiency (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R119.2"/>
    <display value="Factor X deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R120.1"/>
    <display
             value="Factor XI deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R120.2"/>
    <display value="Factor XI deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R121.1"/>
    <display
             value="von Willebrand disease (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R121.2"/>
    <display value="von Willebrand disease (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R122.1"/>
    <display value="Factor XIII deficiency (Small panel)"/>
  </concept>
  <concept>
    <code value="R123.1"/>
    <display
             value="Combined vitamin K-dependent clotting factor deficiency (Small panel)"/>
  </concept>
  <concept>
    <code value="R124.1"/>
    <display value="Combined factor V and VIII deficiency (Small panel)"/>
  </concept>
  <concept>
    <code value="R125.1"/>
    <display
             value="Thoracic aortic aneurysm or dissection (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R127.1"/>
    <display value="Long QT syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R128.1"/>
    <display
             value="Brugada syndrome and cardiac sodium channel disease (Small panel)"/>
  </concept>
  <concept>
    <code value="R129.1"/>
    <display value="Catecholaminergic polymorphic VT (Small panel)"/>
  </concept>
  <concept>
    <code value="R130.1"/>
    <display value="Short QT syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R131.1"/>
    <display value="Hypertrophic cardiomyopathy (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R132.1"/>
    <display
             value="Dilated and Arrhythmogenic cardiomyopathy (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R133.1"/>
    <display
             value="Arrhythmogenic right ventricular cardiomyopathy (Small panel)"/>
  </concept>
  <concept>
    <code value="R134.1"/>
    <display value="Familial hypercholesterolaemia (Small panel)"/>
  </concept>
  <concept>
    <code value="R135.2"/>
    <display value="Paediatric or syndromic cardiomyopathy (WGS)"/>
  </concept>
  <concept>
    <code value="R135.3"/>
    <display value="Paediatric or syndromic cardiomyopathy (WES)"/>
  </concept>
  <concept>
    <code value="R136.1"/>
    <display value="Primary lymphoedema (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R137.1"/>
    <display value="Congenital heart disease microarray (Microarray)"/>
  </concept>
  <concept>
    <code value="R138.1"/>
    <display
             value="Sudden unexplained death or survivors of a cardiac event (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R139.1"/>
    <display
             value="Laterality disorders and isomerism (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R14.1"/>
    <display
             value="Acutely unwell children with a likely monogenic disorder (WGS)"/>
  </concept>
  <concept>
    <code value="R140.1"/>
    <display
             value="Elastin-related phenotypes (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R141.1"/>
    <display value="Monogenic diabetes (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R142.1"/>
    <display
             value="Glucokinase-related fasting hyperglycaemia (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R143.1"/>
    <display value="Neonatal diabetes (Small panel)"/>
  </concept>
  <concept>
    <code value="R143.3"/>
    <display value="Neonatal diabetes (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R143.4"/>
    <display value="Neonatal diabetes (WGS)"/>
  </concept>
  <concept>
    <code value="R144.1"/>
    <display
             value="Congenital hyperinsulinism (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R144.2"/>
    <display value="Congenital hyperinsulinism (Small panel)"/>
  </concept>
  <concept>
    <code value="R145.1"/>
    <display value="Congenital hypothyroidism (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R146.1"/>
    <display value="Differences in sex development (Microarray)"/>
  </concept>
  <concept>
    <code value="R146.2"/>
    <display value="Differences of sex development (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R148.1"/>
    <display value="Hypogonadotropic hypogonadism (Small panel)"/>
  </concept>
  <concept>
    <code value="R149.1"/>
    <display value="Severe early-onset obesity (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R15.4"/>
    <display
             value="Primary immunodeficiency or monogenic inflammatory bowel disease (WGS)"/>
  </concept>
  <concept>
    <code value="R15.5"/>
    <display
             value="Primary immunodeficiency or monogenic inflammatory bowel disease (WES)"/>
  </concept>
  <concept>
    <code value="R150.1"/>
    <display value="Congenital adrenal hypoplasia (Small panel)"/>
  </concept>
  <concept>
    <code value="R151.1"/>
    <display
             value="Familial hyperparathyroidism or Hypocalciuric hypercalcaemia (Small panel)"/>
  </concept>
  <concept>
    <code value="R153.1"/>
    <display value="Familial hypoparathyroidism (Small panel)"/>
  </concept>
  <concept>
    <code value="R154.1"/>
    <display value="Hypophosphataemia or rickets (Small panel)"/>
  </concept>
  <concept>
    <code value="R155.1"/>
    <display
             value="Autoimmune Polyendocrine Syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R156.1"/>
    <display
             value="Carney complex (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R157.1"/>
    <display
             value="IPEX Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R158.1"/>
    <display
             value="Severe insulin resistance and lipodystrophy syndromes (Small panel)"/>
  </concept>
  <concept>
    <code value="R159.1"/>
    <display value="Pituitary hormone deficiency (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R16.1"/>
    <display
             value="Severe combined immunodeficiency with adenosine deaminase deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R160.1"/>
    <display
             value="Primary pigmented nodular adrenocortical disease (Small panel)"/>
  </concept>
  <concept>
    <code value="R162.1"/>
    <display value="Familial tumoral calcinosis (Small panel)"/>
  </concept>
  <concept>
    <code value="R163.1"/>
    <display value="Ectodermal dysplasia (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R164.1"/>
    <display
             value="Epidermolysis bullosa and congenital skin fragility (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R165.1"/>
    <display value="Ichthyosis and erythrokeratoderma (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R166.1"/>
    <display value="Palmoplantar keratodermas (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R167.1"/>
    <display
             value="Autosomal recessive primary hypertrophic osteoarthropathy (Small panel)"/>
  </concept>
  <concept>
    <code value="R168.1"/>
    <display value="Non-acute porphyrias (Small panel)"/>
  </concept>
  <concept>
    <code value="R169.1"/>
    <display
             value="Acute intermittent porphyria (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R17.1"/>
    <display
             value="Lymphoproliferative syndrome with absent SAP expression (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R170.1"/>
    <display
             value="Variegate porphyria (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R171.1"/>
    <display value="Cholestasis (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R172.1"/>
    <display
             value="Wilson disease (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R173.1"/>
    <display value="Polycystic liver disease (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R175.1"/>
    <display value="Pancreatitis (Small panel)"/>
  </concept>
  <concept>
    <code value="R176.1"/>
    <display value="Gilbert syndrome (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R18.1"/>
    <display
             value="Haemophagocytic syndrome with absent XIAP expression (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R180.1"/>
    <display
             value="Congenital adrenal hyperplasia diagnostic test (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R180.2"/>
    <display
             value="Congenital adrenal hyperplasia diagnostic test (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R181.1"/>
    <display
             value="Congenital adrenal hyperplasia carrier testing (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R181.2"/>
    <display
             value="Congenital adrenal hyperplasia carrier testing (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R182.1"/>
    <display value="Hyperthyroidism (Small panel)"/>
  </concept>
  <concept>
    <code value="R183.1"/>
    <display
             value="Glucocorticoid-remediable aldosteronism (GRA) (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R184.1"/>
    <display
             value="Cystic fibrosis diagnostic test (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R184.2"/>
    <display
             value="Cystic fibrosis diagnostic test (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R184.3"/>
    <display value="Cystic fibrosis diagnostic test (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R185.1"/>
    <display
             value="Cystic fibrosis carrier testing (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R186.1"/>
    <display value="Hereditary haemorrhagic telangiectasia (Small panel)"/>
  </concept>
  <concept>
    <code value="R188.1"/>
    <display value="Pulmonary arterial hypertension (Small panel)"/>
  </concept>
  <concept>
    <code value="R189.1"/>
    <display
             value="Respiratory ciliopathies including non-CF bronchiectasis (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R19.1"/>
    <display
             value="Autoimmune lymphoproliferative syndrome with defective apoptosis (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R190.1"/>
    <display value="Pneumothorax familial (Small panel)"/>
  </concept>
  <concept>
    <code value="R191.1"/>
    <display
             value="Alpha-1-antitrypsin deficiency (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R193.4"/>
    <display value="Cystic renal disease (WGS)"/>
  </concept>
  <concept>
    <code value="R194.1"/>
    <display value="Haematuria (Small panel)"/>
  </concept>
  <concept>
    <code value="R195.3"/>
    <display value="Proteinuric renal disease (WGS)"/>
  </concept>
  <concept>
    <code value="R196.1"/>
    <display value="CFHR5 nephropathy (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R197.1"/>
    <display
             value="Membranoproliferative glomerulonephritis including C3 glomerulopathy (Small panel)"/>
  </concept>
  <concept>
    <code value="R197.2"/>
    <display
             value="Membranoproliferative glomerulonephritis including C3 glomerulopathy (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R198.1"/>
    <display value="Renal tubulopathies (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R199.1"/>
    <display
             value="Congenital anomalies of the kidney and urinary tract familial (Microarray)"/>
  </concept>
  <concept>
    <code value="R20.1"/>
    <display
             value="Wiskott-Aldrich syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R201.1"/>
    <display value="Atypical haemolytic uraemic syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R202.1"/>
    <display value="Tubulointerstitial kidney disease (Small panel)"/>
  </concept>
  <concept>
    <code value="R204.1"/>
    <display value="Hereditary Systemic Amyloidosis  (Small panel)"/>
  </concept>
  <concept>
    <code value="R207.1"/>
    <display
             value="Inherited ovarian cancer (without breast cancer) (Small panel)"/>
  </concept>
  <concept>
    <code value="R208.1"/>
    <display
             value="Inherited breast cancer and ovarian cancer (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R21.1"/>
    <display
             value="Fetal anomalies with a likely genetic cause (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R21.2"/>
    <display
             value="Fetal anomalies with a likely genetic cause (WES or Large Panel)"/>
  </concept>
  <concept>
    <code value="R21.3"/>
    <display
             value="Fetal anomalies with a likely genetic cause (Microarray)"/>
  </concept>
  <concept>
    <code value="R210.2"/>
    <display value="Inherited MMR deficiency (Lynch syndrome) (Small panel)"/>
  </concept>
  <concept>
    <code value="R210.4"/>
    <display
             value="Inherited MMR deficiency (Lynch syndrome) (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R210.6"/>
    <display
             value="Inherited MMR deficiency (Lynch syndrome) (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R211.1"/>
    <display
             value="Inherited polyposis and early onset colorectal cancer germline testing (Small panel)"/>
  </concept>
  <concept>
    <code value="R211.3"/>
    <display
             value="Inherited polyposis and early onset colorectal cancer germline testing (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R212.1"/>
    <display
             value="Peutz Jeghers Syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R213.1"/>
    <display
             value="PTEN Hamartoma Tumor Syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R214.1"/>
    <display
             value="Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R215.1"/>
    <display
             value="Hereditary diffuse gastric cancer (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R216.1"/>
    <display
             value="Li Fraumeni Syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R217.1"/>
    <display value="Endocrine neoplasia (Small panel)"/>
  </concept>
  <concept>
    <code value="R218.1"/>
    <display
             value="Multiple endocrine neoplasia type 2 (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R219.1"/>
    <display
             value="Retinoblastoma (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R219.2"/>
    <display value="Retinoblastoma (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R22.1"/>
    <display
             value="Fetus with a likely chromosomal abnormality (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R22.2"/>
    <display
             value="Fetus with a likely chromosomal abnormality (Microarray)"/>
  </concept>
  <concept>
    <code value="R221.1"/>
    <display value="Familial tumours of the nervous system (Small panel)"/>
  </concept>
  <concept>
    <code value="R221.2"/>
    <display
             value="Familial tumours of the nervous system (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R222.1"/>
    <display value="Neurofibromatosis type 1 (Small panel)"/>
  </concept>
  <concept>
    <code value="R222.2"/>
    <display value="Neurofibromatosis type 1 (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R223.1"/>
    <display
             value="Inherited phaeochromocytoma and paraganglioma excluding NF1 (Small panel)"/>
  </concept>
  <concept>
    <code value="R224.1"/>
    <display value="Inherited renal cancer (Small panel)"/>
  </concept>
  <concept>
    <code value="R225.1"/>
    <display
             value="Von Hippel Lindau syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R226.1"/>
    <display
             value="Inherited parathyroid cancer (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R227.1"/>
    <display
             value="Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R227.2"/>
    <display
             value="Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (DNA repair defect testing)"/>
  </concept>
  <concept>
    <code value="R228.1"/>
    <display value="Tuberous sclerosis (Small panel)"/>
  </concept>
  <concept>
    <code value="R228.2"/>
    <display value="Tuberous sclerosis (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R228.3"/>
    <display value="Tuberous sclerosis (Small panel deep sequencing)"/>
  </concept>
  <concept>
    <code value="R229.1"/>
    <display
             value="Confirmed Fanconi anaemia or Bloom syndrome variant testing (Small panel)"/>
  </concept>
  <concept>
    <code value="R23.1"/>
    <display value="Apert syndrome (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R230.1"/>
    <display value="Multiple monogenic benign skin tumours (Small panel)"/>
  </concept>
  <concept>
    <code value="R231.2"/>
    <display value="Neuronal ceroid lipofuscinosis (Small panel)"/>
  </concept>
  <concept>
    <code value="R232.1"/>
    <display
             value="Haemophagocytic syndrome with absent perforin expression (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R233.1"/>
    <display
             value="Agammaglobulinaemia with absent BTK expression (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R234.1"/>
    <display
             value="Severe combined immunodeficiency with PNP deficiency (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R235.1"/>
    <display
             value="SCID with features of gamma chain deficiency (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R236.1"/>
    <display value="Pigmentary skin disorders (WES or Large panel)"/>
  </concept>
  <concept>
    <code value="R236.2"/>
    <display value="Pigmentary skin disorders (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R237.1"/>
    <display
             value="Cutaneous photosensitivity with a likely genetic cause (Small panel)"/>
  </concept>
  <concept>
    <code value="R239.1"/>
    <display
             value="Incontinentia pigmenti (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R239.2"/>
    <display value="Incontinentia pigmenti (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R24.1"/>
    <display value="Achondroplasia (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R240.1"/>
    <display
             value="Diagnostic testing for known variant(s) (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R242.1"/>
    <display
             value="Predictive testing for known familial variant(s) (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R244.1"/>
    <display
             value="Carrier testing for known familial variant(s) (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R246.1"/>
    <display
             value="Carrier testing at population risk for partners of known carriers of nationally agreed autosomal recessive disorders (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R249.1"/>
    <display
             value="NIPD using paternal exclusion testing for very rare conditions where familial variant is known (NIPD)"/>
  </concept>
  <concept>
    <code value="R25.1"/>
    <display
             value="Thanatophoric dysplasia (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R250.1"/>
    <display
             value="NIPD for congenital adrenal hyperplasia CYP21A2 haplotype testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R251.1"/>
    <display value="Non-invasive prenatal sexing (NIPD)"/>
  </concept>
  <concept>
    <code value="R252.1"/>
    <display
             value="SMA carrier testing at population risk for partners of known carriers (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R253.1"/>
    <display
             value="Cystic fibrosis newborn screening follow-up (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R254.1"/>
    <display value="Familial melanoma (Small panel)"/>
  </concept>
  <concept>
    <code value="R255.1"/>
    <display value="Epidermodysplasia verruciformis (Small panel)"/>
  </concept>
  <concept>
    <code value="R256.1"/>
    <display
             value="Nephrocalcinosis or nephrolithiasis (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R257.2"/>
    <display value="Unexplained young onset end-stage renal disease (WGS)"/>
  </concept>
  <concept>
    <code value="R257.3"/>
    <display value="Unexplained young onset end-stage renal disease (WES)"/>
  </concept>
  <concept>
    <code value="R258.1"/>
    <display
             value="Cytopenia Fanconi breakage testing indicated (DNA repair defect testing)"/>
  </concept>
  <concept>
    <code value="R258.2"/>
    <display
             value="Cytopenia Fanconi breakage testing indicated (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R259.1"/>
    <display value="Nijmegen breakage syndrome (DNA repair defect testing)"/>
  </concept>
  <concept>
    <code value="R259.2"/>
    <display
             value="Nijmegen breakage syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R26.1"/>
    <display value="Likely common aneuploidy (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R260.1"/>
    <display
             value="Fanconi anaemia or Bloom syndrome chromosome breakage testing (DNA repair defect testing)"/>
  </concept>
  <concept>
    <code value="R262.1"/>
    <display value="Corneal dystrophy (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R263.1"/>
    <display value="Confirmation of uniparental disomy (UPD testing)"/>
  </concept>
  <concept>
    <code value="R264.1"/>
    <display value="Identity testing (Identity testing)"/>
  </concept>
  <concept>
    <code value="R265.1"/>
    <display
             value="Chromosomal mosaicism â€“ karyotype / Targeted Chromosome Analysis (Karyotype)"/>
  </concept>
  <concept>
    <code value="R268.1"/>
    <display
             value="Kagami-Ogata syndrome paternal uniparental disomy 14 (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R27.3,"/>
    <display value="Paediatric disorders (WGS)"/>
  </concept>
  <concept>
    <code value="R270.1"/>
    <display
             value="Smith-Lemli-Opitz syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R270.2"/>
    <display value="Smith-Lemli-Opitz syndrome (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R271.1"/>
    <display
             value="Neuronal ceroid lipofuscinosis type 2 (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R272.1"/>
    <display
             value="Gaucher disease (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R273.1"/>
    <display
             value="Glycogen storage disease V (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R274.1"/>
    <display value="Glycogen storage disease (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R275.1"/>
    <display
             value="Glutaric acidaemia I newborn screening follow up (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R276.1"/>
    <display value="Lysosomal storage disorder (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R277.1"/>
    <display
             value="Mucopolysaccharidosis type IH/S (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R278.1"/>
    <display
             value="Mucopolysaccharidosis type II (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R278.2"/>
    <display
             value="Mucopolysaccharidosis type II (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R279.1"/>
    <display
             value="Isovaleric acidaemia newborn screening follow up (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R28.1"/>
    <display
             value="Congenital malformation and dysmorphism syndromes â€“ microarray only (Microarray)"/>
  </concept>
  <concept>
    <code value="R280.1"/>
    <display
             value="Krabbe disease â€“ GALC deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R280.2"/>
    <display value="Krabbe disease â€“ GALC deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R281.1"/>
    <display
             value="Krabbe disease Saposin A deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R282.1"/>
    <display
             value="Niemann-Pick disease type A or B (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R283.1"/>
    <display
             value="Phenylketonuria (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R285.1"/>
    <display
             value="Sandhoff disease (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R286.1"/>
    <display
             value="Tay-Sachs disease (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R287.1"/>
    <display
             value="Mucopolysaccharidosis type IVA (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R288.1"/>
    <display
             value="GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R289.1"/>
    <display
             value="Mucolipidosis II and III Alpha/Beta (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R290.1"/>
    <display
             value="Mucopolysaccharidosis type VI (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R291.1"/>
    <display
             value="Mucopolysaccharidosis type IIIA (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R292.1"/>
    <display
             value="Mucopolysaccharidosis type IIIB (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R293.1"/>
    <display
             value="Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Small Panel)"/>
  </concept>
  <concept>
    <code value="R293.2"/>
    <display
             value="Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R294.1"/>
    <display
             value="Ataxia telangiectasia DNA repair testing (DNA repair defect testing)"/>
  </concept>
  <concept>
    <code value="R295.1"/>
    <display
             value="Ataxia telangiectasia variant testing (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R296.1"/>
    <display value="RNA analysis of variants (Other)"/>
  </concept>
  <concept>
    <code value="R298.1"/>
    <display
             value="Possible structural or mosaic chromosomal abnormality FISH (FISH)"/>
  </concept>
  <concept>
    <code value="R299.1"/>
    <display
             value="Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Other)"/>
  </concept>
  <concept>
    <code value="R299.2"/>
    <display
             value="Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Heteroplasmy assessment mitochondrial genome)"/>
  </concept>
  <concept>
    <code value="R299.3"/>
    <display
             value="Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Breakpoint mapping mitochondrial genome)"/>
  </concept>
  <concept>
    <code value="R300.1"/>
    <display
             value="Possible mitochondrial disorder whole mitochondrial genome sequencing (Other)"/>
  </concept>
  <concept>
    <code value="R301.1"/>
    <display
             value="Possible mitochondrial disorder, mitochondrial DNA depletion testing (Other)"/>
  </concept>
  <concept>
    <code value="R304.1"/>
    <display value="NIPD for cystic fibrosis haplotype testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R305.1"/>
    <display value="NIPD for cystic fibrosis variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R306.1"/>
    <display value="NIPD for Apert syndrome variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R307.1"/>
    <display
             value="NIPD for Crouzon syndrome with acanthosis nigricans variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R308.1"/>
    <display
             value="NIPD for FGFR2-related craniosynostosis syndromes variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R309.1"/>
    <display
             value="NIPD for FGFR3-related skeletal dysplasias variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R31.3"/>
    <display value="Bilateral congenital or childhood onset cataracts (WGS)"/>
  </concept>
  <concept>
    <code value="R310.1"/>
    <display
             value="NIPD for Duchenne and Becker muscular dystrophy haplotype testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R311.1"/>
    <display value="NIPD for spinal muscular atrophy variant testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R312.1"/>
    <display
             value="Parental sequencing for lethal autosomal recessive disorders (WES or Large penel)"/>
  </concept>
  <concept>
    <code value="R313.1"/>
    <display
             value="Neutropaenia consistent with ELANE variants (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R314.1"/>
    <display value="Ambiguous genitalia (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R314.2"/>
    <display value="Ambiguous genitalia (Karyotype)"/>
  </concept>
  <concept>
    <code value="R315.1"/>
    <display value="POLG-related disorder (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R315.2"/>
    <display
             value="POLG-related disorder (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R316.1"/>
    <display
             value="Pyruvate dehydrogenase (PDH) deficiency (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R317.1"/>
    <display
             value="Mitochondrial liver disease, including transient infantile liver failure (Small panel)"/>
  </concept>
  <concept>
    <code value="R318.1"/>
    <display
             value="Recurrent miscarriage with products of conception available for testing (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R318.2"/>
    <display
             value="Recurrent miscarriage with products of conception available for testing (Microarray)"/>
  </concept>
  <concept>
    <code value="R319.1"/>
    <display
             value="Calcium-sensing receptor phenotypes (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R32.2"/>
    <display value="Retinal disorders (WGS)"/>
  </concept>
  <concept>
    <code value="R320.1"/>
    <display
             value="Invasive prenatal diagnosis requiring fetal sexing (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R321.1"/>
    <display value="Maternal cell contamination testing (Identity testing)"/>
  </concept>
  <concept>
    <code value="R322.1"/>
    <display value="Skin fibroblasts to be cultured and stored (Other)"/>
  </concept>
  <concept>
    <code value="R323.1"/>
    <display value="Sitosterolaemia (Small panel)"/>
  </concept>
  <concept>
    <code value="R324.1"/>
    <display value="Familial Chylomicronaemia Syndrome (FCS) (Small panel)"/>
  </concept>
  <concept>
    <code value="R325.1"/>
    <display
             value="Lysosomal acid lipase deficiency (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R326.1"/>
    <display value="Vascular skin disorders (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R327.1"/>
    <display value="Mosaic skin disorders deep sequencing (Medium panel)"/>
  </concept>
  <concept>
    <code value="R328.1"/>
    <display
             value="Progressive cardiac conduction disease (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R329.1"/>
    <display
             value="Familial dysalbuminaemic hyperthyroxinaemia (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R33.1"/>
    <display
             value="Possible X-linked retinitis pigmentosa (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R330.1"/>
    <display
             value="Alveolar capillary dysplasia with misalignment of pulmonary veins (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R331.1"/>
    <display
             value="Intestinal failure or congenital diarrhoea (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R332.1"/>
    <display
             value="Rare genetic inflammatory skin disorders (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R333.1"/>
    <display value="Central congenital hypoventilation (STR testing)"/>
  </concept>
  <concept>
    <code value="R333.2"/>
    <display
             value="Central congenital hypoventilation (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R334.1"/>
    <display value="Cystinosis (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R335.1"/>
    <display value="Fabry disease (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R335.2"/>
    <display value="Fabry disease (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R336.1"/>
    <display value="Cerebral vascular malformations (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R337.1"/>
    <display value="CADASIL (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R338.1"/>
    <display
             value="Monitoring for G(M)CSF escape variants (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R340.1"/>
    <display value="Amelogenesis imperfecta (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R341.1"/>
    <display
             value="Hereditary angioedema types I and II (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R343.1"/>
    <display value="Chromosomal mosaicism microarray (Microarray)"/>
  </concept>
  <concept>
    <code value="R344.1"/>
    <display
             value="Primary hyperaldosteronism KCNJ5 (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R345.1"/>
    <display
             value="Facioscapulohumeral muscular dystrophy extended testing (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R345.2"/>
    <display
             value="Facioscapulohumeral muscular dystrophy extended testing (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R345.3"/>
    <display
             value="Facioscapulohumeral muscular dystrophy extended testing (Other)"/>
  </concept>
  <concept>
    <code value="R346.1"/>
    <display value="DNA to be stored (Other)"/>
  </concept>
  <concept>
    <code value="R347.1"/>
    <display
             value="Inherited predisposition to acute myeloid leukaemia (AML) (Small panel)"/>
  </concept>
  <concept>
    <code value="R350.1"/>
    <display value="MERRF syndrome (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R351.1"/>
    <display
             value="NARP syndrome or maternally inherited Leigh syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R351.2"/>
    <display
             value="NARP syndrome or maternally inherited Leigh syndrome (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R352.1"/>
    <display
             value="Mitochondrial DNA maintenance disorder (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R353.1"/>
    <display
             value="Mitochondrial disorder with complex I deficiency (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R354.1"/>
    <display
             value="Mitochondrial disorder with complex II deficiency (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R355.1"/>
    <display
             value="Mitochondrial disorder with complex III deficiency (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R356.1"/>
    <display
             value="Mitochondrial disorder with complex IV deficiency (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R357.1"/>
    <display
             value="Mitochondrial disorder with complex V deficiency (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R36.2,"/>
    <display value="structural eye disease (WGS)"/>
  </concept>
  <concept>
    <code value="R361.1"/>
    <display
             value="Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (Small panel)"/>
  </concept>
  <concept>
    <code value="R361.2"/>
    <display
             value="Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R363.1"/>
    <display value="Inherited predisposition to GIST (Small panel)"/>
  </concept>
  <concept>
    <code value="R364.1"/>
    <display
             value="DICER1-related cancer predisposition (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R365.1"/>
    <display
             value="Fumarate hydratase-related tumour syndromes (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R366.1"/>
    <display
             value="Inherited susceptibility to acute lymphoblastoid leukaemia (ALL) (Small panel)"/>
  </concept>
  <concept>
    <code value="R367.1"/>
    <display value="Inherited pancreatic cancer (Small panel)"/>
  </concept>
  <concept>
    <code value="R368.1"/>
    <display
             value="Hereditary angioedema type III (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R370.1"/>
    <display
             value="Validation of unaccredited findings (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R371.1"/>
    <display value="Malignant hyperthermia (small panel)"/>
  </concept>
  <concept>
    <code value="R372.1"/>
    <display
             value="Newborn screening for sickle cell disease in a transfused baby (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R373.1"/>
    <display value="RNA to be stored (Other)"/>
  </concept>
  <concept>
    <code value="R374.1"/>
    <display value="Other sample to be stored (Other)"/>
  </concept>
  <concept>
    <code value="R375.1"/>
    <display
             value="Family follow-up testing to aid variant interpretation (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R376.1"/>
    <display
             value="Segmental or atypical neurofibromatosis type 1 testing (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R376.2"/>
    <display
             value="Segmental or atypical neurofibromatosis type 1 testing (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R38.2"/>
    <display value="Sporadic aniridia (Small panel)"/>
  </concept>
  <concept>
    <code value="R380.1"/>
    <display value="Niemann Pick disease type C (Small panel)"/>
  </concept>
  <concept>
    <code value="R380.2"/>
    <display value="Niemann Pick disease type C (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R381.2"/>
    <display value="Other rare neuromuscular disorders (WGS)"/>
  </concept>
  <concept>
    <code value="R382.1"/>
    <display value="Hypochondroplasia (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R383.1"/>
    <display value="Linkage testing for Huntington disease (Other)"/>
  </concept>
  <concept>
    <code value="R384.1"/>
    <display
             value="Generalised arterial calcification in infancy (Small panel)"/>
  </concept>
  <concept>
    <code value="R387.1"/>
    <display value="Reanalysis of existing data (Other)"/>
  </concept>
  <concept>
    <code value="R389.1"/>
    <display value="NIPD pre-pregnancy test work-up (NIPD)"/>
  </concept>
  <concept>
    <code value="R39.1"/>
    <display value="Albinism or congenital nystagmus (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R390.1"/>
    <display value="Multiple exostoses (Small panel)"/>
  </concept>
  <concept>
    <code value="R390.2"/>
    <display value="Multiple exostoses (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R391.1"/>
    <display
             value="Barth syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R394.1"/>
    <display
             value="Mitochondrial neurogastrointestinal encephalopathy (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R395.1"/>
    <display
             value="Thiamine metabolism dysfunction syndrome 2 (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R396.1"/>
    <display
             value="Mitochondrial Complex V deficiency, TMEM70 type (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R397.1"/>
    <display
             value="Maternally inherited cardiomyopathy (Targeted mutation testing)"/>
  </concept>
  <concept>
    <code value="R401.1"/>
    <display
             value="Common aneuploidy testing prenatal (Common aneuploidy testing)"/>
  </concept>
  <concept>
    <code value="R402.1"/>
    <display
             value="Premature ovarian insufficiency (Karyotype or equivalent)"/>
  </concept>
  <concept>
    <code value="R402.2"/>
    <display value="Premature ovarian insufficiency (STR testing)"/>
  </concept>
  <concept>
    <code value="R403.1"/>
    <display
             value="MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing newborn screening follow up (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R404.1"/>
    <display
             value="Testing of unaffected individuals for inherited cancer predisposition syndromes (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R404.3"/>
    <display
             value="Testing of unaffected individuals for inherited cancer predisposition syndromes (Small panel)"/>
  </concept>
  <concept>
    <code value="R405.1"/>
    <display value="Hereditary Erythrocytosis (Small panel)"/>
  </concept>
  <concept>
    <code value="R406.1"/>
    <display value="Thrombocythaemia (Small panel)"/>
  </concept>
  <concept>
    <code value="R409.1"/>
    <display
             value="Linkage testing for recognisable Mendelian disorders (Other)"/>
  </concept>
  <concept>
    <code value="R41.1"/>
    <display value="Optic neuropathy (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R41.3"/>
    <display value="Optic neuropathy (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R410.1"/>
    <display value="Myotonic dystrophy type 2 (DM2) (STR testing)"/>
  </concept>
  <concept>
    <code value="R411.1"/>
    <display
             value="Y chromosome microdeletion (Targeted mutation testing or equivalent)"/>
  </concept>
  <concept>
    <code value="R412.1"/>
    <display
             value="Fetal anomalies with a likely genetic cause non urgent (WES or Large Panel)"/>
  </concept>
  <concept>
    <code value="R413.1"/>
    <display value="Autoinflammatory Disorders (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R414.1"/>
    <display
             value="APC associated Polyposis  (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R416.1"/>
    <display
             value="Syndromic and non syndromic craniosynostosis involving midline sutures only (metopic, sagittal, metopic &amp; sagittal)  (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R417.1"/>
    <display value="Multi Locus Imprinting Disorder (MLPA)"/>
  </concept>
  <concept>
    <code value="R417.2"/>
    <display value="Multi Locus Imprinting Disorder (Small Panel)"/>
  </concept>
  <concept>
    <code value="R419.1"/>
    <display value="Acute Rhabdomyolysis (Medium Panel)"/>
  </concept>
  <concept>
    <code value="R42.1"/>
    <display
             value="Leber hereditary optic neuropathy (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R42.2"/>
    <display value="Leber hereditary optic neuropathy (Other)"/>
  </concept>
  <concept>
    <code value="R420.1"/>
    <display value="Pseudoxanthoma elasticum (Small Panel)"/>
  </concept>
  <concept>
    <code value="R421.1"/>
    <display value="Pulmonary Fibrosis, Familial (Medium panel)"/>
  </concept>
  <concept>
    <code value="R422.1"/>
    <display
             value="BAP1 associated tumour predisposition syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R423.1"/>
    <display value="NIPD for Retinoblastoma haplotype testing (NIPD)"/>
  </concept>
  <concept>
    <code value="R424.1"/>
    <display
             value="Subcutaneous panniculitis T-cell lymphoma (Single gene sequencing &lt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R426.1"/>
    <display
             value="Pulmonary alveolar microlithiasis (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R428.1"/>
    <display
             value="Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (STR testing)"/>
  </concept>
  <concept>
    <code value="R428.2"/>
    <display
             value="Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (FISH)"/>
  </concept>
  <concept>
    <code value="R43.1"/>
    <display
             value="Blepharophimosis ptosis and epicanthus inversus (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R43.2"/>
    <display
             value="Blepharophimosis ptosis and epicanthus inversus (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R43.3"/>
    <display
             value="Blepharophimosis ptosis and epicanthus inversus (STR testing)"/>
  </concept>
  <concept>
    <code value="R430.1"/>
    <display value="Inherited prostate cancer (Small panel)"/>
  </concept>
  <concept>
    <code value="R431.1"/>
    <display
             value="Genome-wide DNA Methylation Profiling to Aid Variant Interpretation (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R433.1"/>
    <display value="Monogenic diabetes, subtype glucokinase NIPT (NIPT)"/>
  </concept>
  <concept>
    <code value="R436.1"/>
    <display
             value="Hereditary alpha tryptasaemia (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R438.1,"/>
    <display
             value="Paediatric pseudo-obstruction syndrome (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R440.1"/>
    <display value="Hereditary isolated diabetes insipidus (Small panel)"/>
  </concept>
  <concept>
    <code value="R441.1"/>
    <display
             value="Unexplained death in infancy and sudden unexplained death in childhood (WGS)"/>
  </concept>
  <concept>
    <code value="R442.1"/>
    <display value="Variant Re-interpretation (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R443.1"/>
    <display value="Confirmation test (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R444.1"/>
    <display value="NICE approved PARP inhibitor treatment (Small panel)"/>
  </concept>
  <concept>
    <code value="R444.2"/>
    <display value="NICE approved PARP inhibitor treatment (Small panel)"/>
  </concept>
  <concept>
    <code value="R445.1"/>
    <display
             value="T21, T18 and T13 aneuploidy testing NIPT (previous history) (NIPT)"/>
  </concept>
  <concept>
    <code value="R446.1"/>
    <display
             value="APOL1 kidney donor testing (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R447.1"/>
    <display
             value="Validation of WGS Diagnostic discovery (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R448.1"/>
    <display value="Prenatal testing (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R449.1"/>
    <display
             value="Diagnostic testing for Glutaric acidaemia I (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R45.1"/>
    <display value="Stickler syndrome (Small panel)"/>
  </concept>
  <concept>
    <code value="R450.1"/>
    <display
             value="Diagnostic testing for Isovaleric acidaemia (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R451.1"/>
    <display
             value="Diagnostic testing for MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R452.1"/>
    <display
             value="Silver russell syndrome and Temple Syndrome (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R453.1"/>
    <display value="Monogenic short stature (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R454.1"/>
    <display
             value="Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R456.1"/>
    <display
             value="Embryonal tumour of possible germline origin (WES or Medium panel)"/>
  </concept>
  <concept>
    <code value="R456.2"/>
    <display
             value="Embryonal tumour of possible germline origin (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R457.1"/>
    <display value="Sarcoma of possible germline origin (Small panel)"/>
  </concept>
  <concept>
    <code value="R458.1"/>
    <display value="Young onset or familial dementia (WGS)"/>
  </concept>
  <concept>
    <code value="R459.1"/>
    <display value="Young onset or complex Parkinson disease (WGS)"/>
  </concept>
  <concept>
    <code value="R46.1"/>
    <display
             value="Congenital fibrosis of the extraocular muscles (Small panel)"/>
  </concept>
  <concept>
    <code value="R460.1"/>
    <display
             value="Amyotrophic lateral sclerosis / Motor Neurone Disease (WGS)"/>
  </concept>
  <concept>
    <code value="R461.1"/>
    <display value="Cerebral amyloid angiopathy (WGS)"/>
  </concept>
  <concept>
    <code value="R462.1"/>
    <display value="Childhood interstitial lung disease (Medium panel)"/>
  </concept>
  <concept>
    <code value="R463.1"/>
    <display
             value="Cytogenetic characterisation of a genomic abnormality â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"/>
  </concept>
  <concept>
    <code value="R464.1"/>
    <display
             value="Recurrent miscarriage where products of conception are not available for testing parental karyotype (Karyotype)"/>
  </concept>
  <concept>
    <code value="R465.1"/>
    <display
             value="Familial cytogenetic rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"/>
  </concept>
  <concept>
    <code value="R466.1"/>
    <display value="Unexplained infertility (Karyotype)"/>
  </concept>
  <concept>
    <code value="R467.1"/>
    <display value="Gamete donors (Karyotype)"/>
  </concept>
  <concept>
    <code value="R468.1"/>
    <display
             value="Possible sex chromosome aneuploidy or structural rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"/>
  </concept>
  <concept>
    <code value="R47.1"/>
    <display value="Angelman syndrome (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R471.1"/>
    <display
             value="Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing C9orf72 haplotype (Linkage analysis)"/>
  </concept>
  <concept>
    <code value="R471.2"/>
    <display
             value="Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing SOD1 haplotype (Linkage analysis)"/>
  </concept>
  <concept>
    <code value="R471.3"/>
    <display
             value="Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing MAPT haplotype (Linkage analysis)"/>
  </concept>
  <concept>
    <code value="R471.4"/>
    <display
             value="Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing PSEN1 haplotype (Linkage analysis)"/>
  </concept>
  <concept>
    <code value="R48.1"/>
    <display value="Prader-Willi syndrome (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R49.1"/>
    <display value="Beckwith-Wiedemann syndrome (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R49.3"/>
    <display
             value="Beckwith-Wiedemann syndrome (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R50.1"/>
    <display
             value="Isolated hemihypertrophy or macroglossia (Methylation testing)"/>
  </concept>
  <concept>
    <code value="R52.1"/>
    <display value="Short stature SHOX deficiency (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R52.2"/>
    <display
             value="Short stature SHOX deficiency (Single gene sequencing &lt;10 amplicons)"/>
  </concept>
  <concept>
    <code value="R54.3"/>
    <display value="Hereditary ataxia with onset in adulthood (WGS)"/>
  </concept>
  <concept>
    <code value="R54.4"/>
    <display
             value="Hereditary ataxia with onset in adulthood (RFC1 STR testing)"/>
  </concept>
  <concept>
    <code value="R55.4"/>
    <display value="Hereditary ataxia with onset in childhood (WGS)"/>
  </concept>
  <concept>
    <code value="R56.3"/>
    <display
             value="Adult onset dystonia, chorea or related movement disorder (WGS)"/>
  </concept>
  <concept>
    <code value="R57.5"/>
    <display
             value="Childhood onset dystonia, chorea or related movement disorder (WGS)"/>
  </concept>
  <concept>
    <code value="R60.3"/>
    <display value="Adult onset hereditary spastic paraplegia (WGS)"/>
  </concept>
  <concept>
    <code value="R61.4"/>
    <display value="Childhood onset hereditary spastic paraplegia (WGS)"/>
  </concept>
  <concept>
    <code value="R62.2"/>
    <display value="Adult onset leukodystrophy (WGS)"/>
  </concept>
  <concept>
    <code value="R63.1"/>
    <display
             value="Possible mitochondrial disorder nuclear genes (WES or Large Panel)"/>
  </concept>
  <concept>
    <code value="R64.1"/>
    <display value="MELAS or MIDD (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R65.1"/>
    <display
             value="Aminoglycoside exposure posing risk to hearing (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R66.1"/>
    <display
             value="Paroxysmal central nervous system disorders (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R67.1"/>
    <display value="Monogenic hearing loss (WES or Large Panel)"/>
  </concept>
  <concept>
    <code value="R68.1"/>
    <display value="Huntington disease (STR testing)"/>
  </concept>
  <concept>
    <code value="R69.5"/>
    <display value="Hypotonic infant  (WGS)"/>
  </concept>
  <concept>
    <code value="R70.1"/>
    <display
             value="Spinal muscular atrophy type 1 diagnostic test (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R71.1"/>
    <display
             value="Spinal muscular atrophy type 1 rare variant testing (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R72.1"/>
    <display value="Myotonic dystrophy type 1 (STR testing)"/>
  </concept>
  <concept>
    <code value="R73.1"/>
    <display
             value="Duchenne or Becker muscular dystrophy (Single gene sequencing &gt;=10 amplicons)"/>
  </concept>
  <concept>
    <code value="R73.2"/>
    <display
             value="Duchenne or Becker muscular dystrophy (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R74.1"/>
    <display value="Facioscapulohumeral muscular dystrophy (Other)"/>
  </concept>
  <concept>
    <code value="R75.1"/>
    <display value="Oculopharyngeal muscular dystrophy (STR testing)"/>
  </concept>
  <concept>
    <code value="R76.1"/>
    <display value="Skeletal muscle channelopathy (Small panel)"/>
  </concept>
  <concept>
    <code value="R77.1"/>
    <display
             value="Hereditary neuropathy PMP22 copy number (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R78.4"/>
    <display
             value="Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (WGS)"/>
  </concept>
  <concept>
    <code value="R78.5"/>
    <display
             value="Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (RFC1 STR testing)"/>
  </concept>
  <concept>
    <code value="R79.1"/>
    <display value="Congenital muscular dystrophy (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R80.1"/>
    <display value="Congenital myaesthenic syndrome (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R81.1"/>
    <display value="Congenital myopathy (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R82.1"/>
    <display
             value="Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R83.3"/>
    <display value="Arthrogryposis (WGS)"/>
  </concept>
  <concept>
    <code value="R84.4"/>
    <display value="Cerebellar anomalies (WGS)"/>
  </concept>
  <concept>
    <code value="R85.2"/>
    <display value="Holoprosencephaly (WGS)"/>
  </concept>
  <concept>
    <code value="R86.3"/>
    <display value="Hydrocephalus (WGS)"/>
  </concept>
  <concept>
    <code value="R87.3"/>
    <display value="Cerebral malformation (WGS)"/>
  </concept>
  <concept>
    <code value="R88.3"/>
    <display value="Severe microcephaly (WGS)"/>
  </concept>
  <concept>
    <code value="R89.3"/>
    <display value="Ultra-rare and atypical monogenic disorders (WGS)"/>
  </concept>
  <concept>
    <code value="R90.1"/>
    <display value="Bleeding and platelet disorders (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R91.1"/>
    <display value="Cytopenia NOT Fanconi anaemia (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R91.2"/>
    <display value="Cytopenia NOT Fanconi anaemia (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R92.1"/>
    <display value="Rare anaemia (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R92.2"/>
    <display value="Rare anaemia (Small panel)"/>
  </concept>
  <concept>
    <code value="R92.3"/>
    <display value="Rare anaemia (WES or Medium Panel)"/>
  </concept>
  <concept>
    <code value="R93.1"/>
    <display
             value="Sickle cell, thalassaemia and other haemoglobinopathies (MLPA or equivalent)"/>
  </concept>
  <concept>
    <code value="R93.2"/>
    <display
             value="Sickle cell, thalassaemia and other haemoglobinopathies (Small panel)"/>
  </concept>
  <concept>
    <code value="R95.1"/>
    <display
             value="Iron overload hereditary haemochromatosis testing (Targeted variant testing)"/>
  </concept>
  <concept>
    <code value="R96.1"/>
    <display
             value="Iron metabolism disorders NOT common HFE variants (Small panel)"/>
  </concept>
  <concept>
    <code value="R97.1"/>
    <display
             value="Thrombophilia with a likely monogenic cause (WES or Small Panel)"/>
  </concept>
  <concept>
    <code value="R98.2"/>
    <display value="Likely inborn error of metabolism (WGS)"/>
  </concept>
  <concept>
    <code value="R98.3"/>
    <display value="Likely inborn error of metabolism (WES)"/>
  </concept>
  <concept>
    <code value="R99.1"/>
    <display value="Common craniosynostosis syndromes (Small panel)"/>
  </concept>
  <concept>
    <code value="R99.2"/>
    <display
             value="Common craniosynostosis syndromes (Exon level CNV detection by MLPA or equivalent)"/>
  </concept>
</CodeSystem>