NHS England Genomic Test Code - JSON Representation

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: NHS England Genomic Test Code - JSON Representation

Active as of 2026-06-04
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{
  "resourceType" : "CodeSystem",
  "id" : "GenomicTestCode",
  "text" : {
    "status" : "generated",
    "div" : "<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\u00a0CICÂ\u00a0Alteration, 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\u00a0CICÂ\u00a0Alteration, 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>"
  },
  "url" : "https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory",
  "version" : "2.0.12",
  "name" : "GenomicTestCode",
  "title" : "NHS England Genomic Test Code",
  "status" : "active",
  "experimental" : false,
  "date" : "2026-06-04",
  "publisher" : "NHS North West Genomics",
  "contact" : [
    {
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.nwgenomics.nhs.uk/contact-us"
        }
      ]
    }
  ],
  "description" : "- [Genomic Test Directory](https://www.england.nhs.uk/publication/national-genomic-test-directories)\"\n\nHL7 v2 CodeSystem : England-GenomicTestDirectory",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "GB",
          "display" : "United Kingdom of Great Britain and Northern Ireland"
        }
      ]
    }
  ],
  "caseSensitive" : true,
  "content" : "fragment",
  "concept" : [
    {
      "code" : "M1.1",
      "display" : "Colorectal Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF)"
    },
    {
      "code" : "M1.2",
      "display" : "Colorectal Carcinoma, KRAS hotspot"
    },
    {
      "code" : "M1.3",
      "display" : "Colorectal Carcinoma, NRAS hotspot"
    },
    {
      "code" : "M1.4",
      "display" : "Colorectal Carcinoma, MSI Testing"
    },
    {
      "code" : "M1.5",
      "display" : "Colorectal Carcinoma, MLH1 promoter hypermethylation"
    },
    {
      "code" : "M1.6",
      "display" : "Colorectal Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M1.7",
      "display" : "Colorectal Carcinoma, DPYD hotspot"
    },
    {
      "code" : "M1.9",
      "display" : "Colorectal Carcinoma, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2, POLE, POLD1)"
    },
    {
      "code" : "M10.1",
      "display" : "Thyroid Follicular Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, HRAS)"
    },
    {
      "code" : "M10.2",
      "display" : "Thyroid Follicular Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET)"
    },
    {
      "code" : "M100.1",
      "display" : "Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 rearrangement FISH"
    },
    {
      "code" : "M100.2",
      "display" : "Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 Copy number FISH"
    },
    {
      "code" : "M100.3",
      "display" : "Primary Mediastinal B Cell Lymphoma, REL copy number FISH"
    },
    {
      "code" : "M100.4",
      "display" : "Primary Mediastinal B Cell Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M100.5",
      "display" : "Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, copy number variant (CD274, PDCD1LG2, REL)"
    },
    {
      "code" : "M100.6",
      "display" : "Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, rearrangement (CD274, PDCD1LG2)"
    },
    {
      "code" : "M100.7",
      "display" : "Primary Mediastinal B Cell Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M100.8",
      "display" : "Primary Mediastinal B Cell Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M101.1",
      "display" : "ALK Positive Large B Cell Lymphoma, ALK rearrangement FISH"
    },
    {
      "code" : "M101.2",
      "display" : "ALK Positive Large B Cell Lymphoma, t(2;17)(p23;q23) CLTC-ALK FISH/RT-PCR"
    },
    {
      "code" : "M101.3",
      "display" : "ALK Positive Large B Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR"
    },
    {
      "code" : "M101.4",
      "display" : "ALK Positive Large B Cell Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M101.5",
      "display" : "ALK Positive Large B Cell Lymphoma, Multi-target NGS panel, structural variant (CLTC-ALK, ALK-NPM1, other ALK rearrangements)"
    },
    {
      "code" : "M101.6",
      "display" : "ALK Positive Large B Cell Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M101.7",
      "display" : "ALK Positive Large B Cell Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M102.1",
      "display" : "Mantle Cell Lymphoma, t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR"
    },
    {
      "code" : "M102.2",
      "display" : "Mantle Cell Lymphoma, CCND1 rearrangement FISH"
    },
    {
      "code" : "M102.3",
      "display" : "Mantle Cell Lymphoma, CCND2 rearrangement FISH"
    },
    {
      "code" : "M102.4",
      "display" : "Mantle Cell Lymphoma, Multi-target NGS panel, structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)"
    },
    {
      "code" : "M102.5",
      "display" : "Mantle Cell Lymphoma, Multi-target NGS panel, small variant (TP53)"
    },
    {
      "code" : "M103.1",
      "display" : "Follicular Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR"
    },
    {
      "code" : "M103.2",
      "display" : "Follicular Lymphoma, BCL2 rearrangement FISH"
    },
    {
      "code" : "M103.3",
      "display" : "Follicular Lymphoma, BCL6 rearrangement FISH"
    },
    {
      "code" : "M103.4",
      "display" : "Follicular Lymphoma, Multi-target NGS panel, small variant (CARD11, CREBBP, EZH2, ARID1A, EP300, MEF2B, FOXO1)"
    },
    {
      "code" : "M103.5",
      "display" : "Follicular Lymphoma, Multi-target NGS panel, structural variant (IGH-BCL2, BCL2, BCL6)"
    },
    {
      "code" : "M104.1",
      "display" : "Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, Multi-target NGS panel, small variant (MYD88, CXCR4)"
    },
    {
      "code" : "M104.2",
      "display" : "Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, MYD88 hotspot"
    },
    {
      "code" : "M105.1",
      "display" : "Igm Monoclonal Gammopathy of Uncertain Significance, Multi-target NGS panel, small variant (MYD88, CXCR4)"
    },
    {
      "code" : "M105.2",
      "display" : "Igm Monoclonal Gammopathy of Uncertain Significance, MYD88 hotspot"
    },
    {
      "code" : "M106.1",
      "display" : "Intra-Ocular Lymphoma, MYD88 hotspot"
    },
    {
      "code" : "M107.1",
      "display" : "Malt-Lymphoma, t(11;18)(q21;q21) BIRC3-MALT1  FISH/RT-PCR"
    },
    {
      "code" : "M107.10",
      "display" : "Malt-Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M107.2",
      "display" : "Malt-Lymphoma, t(1;14)(p22;q32) IGH-BCL10 FISH/RT-PCR"
    },
    {
      "code" : "M107.3",
      "display" : "Malt-Lymphoma, t(14;18)(q32;q21) IGH-MALT1 FISH/RT-PCR"
    },
    {
      "code" : "M107.4",
      "display" : "Malt-Lymphoma, MALT1 rearrangement FISH"
    },
    {
      "code" : "M107.5",
      "display" : "Malt-Lymphoma, BCL10 rearrangement FISH"
    },
    {
      "code" : "M107.6",
      "display" : "Malt-Lymphoma, FOXP1 rearrangement FISH"
    },
    {
      "code" : "M107.7",
      "display" : "Malt-Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M107.8",
      "display" : "Malt-Lymphoma, Multi-target NGS panel, structural variant (BIRC3-MALT1, IGH-BCL10, IGH-MALT1, other MALT rearrangements, other BCL10 rearrangements, FOXP1)"
    },
    {
      "code" : "M107.9",
      "display" : "Malt-Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M108.1",
      "display" : "Hairy Cell Leukaemia, Multi-target NGS panel, small variant (BRAF)"
    },
    {
      "code" : "M108.2",
      "display" : "Hairy Cell Leukaemia, BRAF V600 hotspot"
    },
    {
      "code" : "M108.5",
      "display" : "Hairy Cell Leukaemia, Ig gene hypermutation detection multiplex seq"
    },
    {
      "code" : "M108.6",
      "display" : "Hairy Cell Leukaemia, Ig gene hypermutation detection NGS"
    },
    {
      "code" : "M109.1",
      "display" : "Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection multiplex seq"
    },
    {
      "code" : "M109.2",
      "display" : "Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection NGS"
    },
    {
      "code" : "M11.1",
      "display" : "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, small variant (TP53, BRAF)"
    },
    {
      "code" : "M11.2",
      "display" : "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, copy number variant (TP53)"
    },
    {
      "code" : "M11.3",
      "display" : "Poorly Differentiated Anaplastic Thyroid Carcinoma, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M11.4",
      "display" : "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET, ALK)"
    },
    {
      "code" : "M110.1,",
      "display" : "Paediatric Type Follicular Lymphoma, Multi-target NGS panel, small variant (MAP2K1)"
    },
    {
      "code" : "M110.2,",
      "display" : "Paediatric Type Follicular Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M110.3,",
      "display" : "Paediatric Type Follicular Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M110.4,",
      "display" : "Paediatric Type Follicular Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M111.1",
      "display" : "T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (RHOA, DNMT3A, IDH2, TET2)"
    },
    {
      "code" : "M111.2",
      "display" : "T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection multiplex seq"
    },
    {
      "code" : "M111.3",
      "display" : "T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection NGS"
    },
    {
      "code" : "M111.4",
      "display" : "T Cell Non-Hodgkin Lymphoma, TCR rearrangement FISH"
    },
    {
      "code" : "M111.5",
      "display" : "T Cell Non-Hodgkin Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M111.6",
      "display" : "T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (TCR rearrangement)"
    },
    {
      "code" : "M111.7",
      "display" : "T Cell Non-Hodgkin Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M111.8",
      "display" : "T Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M112.3",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), IRF4/DUSP22 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M112.4",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), TP63 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M112.5",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Germline and Tumour"
    },
    {
      "code" : "M112.6",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), Multi-target NGS panel, structural variant (IRF4/DUSP22, TP63)"
    },
    {
      "code" : "M112.7",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Tumour First"
    },
    {
      "code" : "M112.8",
      "display" : "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Follow-up Germline"
    },
    {
      "code" : "M113.1",
      "display" : "T Prolymphocytic Leukaemia, TCL1A rearrangement FISH"
    },
    {
      "code" : "M113.2",
      "display" : "T Prolymphocytic Leukaemia, Chr8 rearrangement FISH"
    },
    {
      "code" : "M113.3",
      "display" : "T Prolymphocytic Leukaemia, Multi-target NGS panel, structural variant (TCL1A, Chr8)"
    },
    {
      "code" : "M113.6",
      "display" : "T Prolymphocytic Leukaemia, Karyotype (to include TCL1 rearrangements t(X;14))"
    },
    {
      "code" : "M114.1",
      "display" : "Large Granular Lymphocyte Leukaemia, Multi-target NGS panel, small variant (STAT3, STAT5B)"
    },
    {
      "code" : "M115.1",
      "display" : "NK Cell/Gamma-Delta T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)"
    },
    {
      "code" : "M115.2",
      "display" : "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M115.3",
      "display" : "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M115.4",
      "display" : "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M116.1",
      "display" : "Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)"
    },
    {
      "code" : "M116.2",
      "display" : "Hepatosplenic T Cell Lymphoma, i7q rearrangement FISH"
    },
    {
      "code" : "M116.3",
      "display" : "Hepatosplenic T Cell Lymphoma, WGS Germline and Tumour"
    },
    {
      "code" : "M116.4",
      "display" : "Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, structural variant (i17q)"
    },
    {
      "code" : "M116.5",
      "display" : "Hepatosplenic T Cell Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M116.6",
      "display" : "Hepatosplenic T Cell Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M117.1",
      "display" : "Histiocytosis, Multi-target NGS panel, small variant (BRAF, MAP2K1, NRAS, KRAS, HRAS, ERBB3, ARAF, MAP3K1, PIK3CA, PIK3CD)"
    },
    {
      "code" : "M117.12",
      "display" : "Histiocytosis, NTRK1 rearrangement FISH"
    },
    {
      "code" : "M117.16",
      "display" : "Histiocytosis, WGS Germline and Tumour"
    },
    {
      "code" : "M117.17",
      "display" : "Histiocytosis, WGS Tumour First"
    },
    {
      "code" : "M117.18",
      "display" : "Histiocytosis, WGS Follow-up Germline"
    },
    {
      "code" : "M117.19",
      "display" : "Histiocytosis, High Sensitivity BRAF"
    },
    {
      "code" : "M117.2",
      "display" : "Histiocytosis, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M117.3",
      "display" : "Histiocytosis, ALK rearrangement FISH"
    },
    {
      "code" : "M117.7",
      "display" : "Histiocytosis, BRAF rearrangement FISH"
    },
    {
      "code" : "M118.1",
      "display" : "Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, STR Testing"
    },
    {
      "code" : "M118.2",
      "display" : "Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, Sex chromosome FISH"
    },
    {
      "code" : "M119.1,",
      "display" : "Paediatric Tumours, WGS Germline and Tumour"
    },
    {
      "code" : "M119.2,",
      "display" : "Paediatric Tumours, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M119.4,",
      "display" : "Paediatric Tumours, DPYD hotspot"
    },
    {
      "code" : "M119.5,",
      "display" : "Paediatric Tumours, Multi-target NGS-small variant"
    },
    {
      "code" : "M12.1",
      "display" : "Thyroid Medullary Carcinoma, Multi-target NGS panel, small variant (RET)"
    },
    {
      "code" : "M12.2",
      "display" : "Thyroid Medullary Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M120.1",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1)"
    },
    {
      "code" : "M120.10",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M120.11",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M120.12",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M120.13",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M120.14",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M120.15",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M120.16",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M120.17",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, SMARCB1)"
    },
    {
      "code" : "M120.18",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, DNA Methylation"
    },
    {
      "code" : "M120.2",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 seq"
    },
    {
      "code" : "M120.3",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 seq"
    },
    {
      "code" : "M120.4",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M120.5",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M120.6",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M120.7",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M120.8",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M120.9",
      "display" : "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M124.1",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, small variant (BCOR)"
    },
    {
      "code" : "M124.10",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, structural variant (BCOR, NUTM2B-YWHAE, NUTM2E-YWHAE, NUTM1-YWHAE, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M124.11",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, copy number variant (BCOR, YWHAE)"
    },
    {
      "code" : "M124.2",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, BCOR seq"
    },
    {
      "code" : "M124.3",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, BCOR copy number FISH"
    },
    {
      "code" : "M124.4",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, BCOR rearrangement FISH"
    },
    {
      "code" : "M124.5",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, NUTM2B-YWHAE FISH/RT-PCR"
    },
    {
      "code" : "M124.6",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, NUTM2E-YWHAE FISH/RT-PCR"
    },
    {
      "code" : "M124.7",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, NUTM1-YWHAE FISH/RT-PCR"
    },
    {
      "code" : "M124.8",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, YWHAE copy number FISH"
    },
    {
      "code" : "M124.9",
      "display" : "Clear Cell Kidney Sarcoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M126.1",
      "display" : "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, MN1 rearrangement FISH"
    },
    {
      "code" : "M126.2",
      "display" : "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M126.3",
      "display" : "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, Multi-target NGS panel, structural variant (MN1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M126.4",
      "display" : "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, DNA Methylation"
    },
    {
      "code" : "M127.1",
      "display" : "Congenital Mesoblastic Nephroma, Paediatric, NTRK3-ETV6 FISH/RT-PCR"
    },
    {
      "code" : "M127.3",
      "display" : "Congenital Mesoblastic Nephroma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M127.4",
      "display" : "Congenital Mesoblastic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK3-ETV6, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M13.1",
      "display" : "Phaeochromocytoma, Multi-target NGS panel, small variant (RET)"
    },
    {
      "code" : "M13.2",
      "display" : "Phaeochromocytoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M130.1",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCB1)"
    },
    {
      "code" : "M130.2",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 seq"
    },
    {
      "code" : "M130.3",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M130.4",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M130.5",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M130.6",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)"
    },
    {
      "code" : "M130.7",
      "display" : "Cribriform Neuroepithelial Tumour, Paediatric, DNA Methylation"
    },
    {
      "code" : "M131.1",
      "display" : "Cystic Nephroma, Paediatric, Multi-target NGS panel, small variant (DICER1)"
    },
    {
      "code" : "M131.2",
      "display" : "Cystic Nephroma, Paediatric, DICER1 seq"
    },
    {
      "code" : "M131.3",
      "display" : "Cystic Nephroma, Paediatric, DICER1 copy number FISH"
    },
    {
      "code" : "M131.4",
      "display" : "Cystic Nephroma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M131.5",
      "display" : "Cystic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M131.6",
      "display" : "Cystic Nephroma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"
    },
    {
      "code" : "M132.1",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, small variant (BRAF)"
    },
    {
      "code" : "M132.10",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M132.11",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M132.12",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M132.13",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, DNA Methylation"
    },
    {
      "code" : "M132.2",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M132.3",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M132.4",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M132.5",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M132.6",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M132.7",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M132.8",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M132.9",
      "display" : "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M133.1",
      "display" : "Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SUFU)"
    },
    {
      "code" : "M133.2",
      "display" : "Desmoplastic Medulloblastoma, Paediatric, SUFU seq"
    },
    {
      "code" : "M133.3",
      "display" : "Desmoplastic Medulloblastoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M133.4",
      "display" : "Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M133.5",
      "display" : "Desmoplastic Medulloblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M136.1",
      "display" : "Fibrolamellar Hepatocellular Carcinoma, Paediatric, DNAJB1-PRKACA FISH/RT-PCR"
    },
    {
      "code" : "M136.2",
      "display" : "Fibrolamellar Hepatocellular Carcinoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M136.3",
      "display" : "Fibrolamellar Hepatocellular Carcinoma, Paediatric, Multi-target NGS panel, structural variant (DNAJB1-PRKACA, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M136.5",
      "display" : "Fibrolamellar Hepatocellular Carcinoma, Paediatric, DPYD hotspot"
    },
    {
      "code" : "M137.1",
      "display" : "Ganglioglioma, Paediatric, Multi-target NGS panel, small variant (BRAF)"
    },
    {
      "code" : "M137.10",
      "display" : "Ganglioglioma, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M137.11",
      "display" : "Ganglioglioma, Paediatric, KIAA1549 copy number FISH"
    },
    {
      "code" : "M137.12",
      "display" : "Ganglioglioma, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M137.13",
      "display" : "Ganglioglioma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M137.14",
      "display" : "Ganglioglioma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)"
    },
    {
      "code" : "M137.15",
      "display" : "Ganglioglioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M137.2",
      "display" : "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)"
    },
    {
      "code" : "M137.3",
      "display" : "Ganglioglioma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M137.4",
      "display" : "Ganglioglioma, Paediatric, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M137.5",
      "display" : "Ganglioglioma, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M137.6",
      "display" : "Ganglioglioma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M137.7",
      "display" : "Ganglioglioma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M137.8",
      "display" : "Ganglioglioma, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M137.9",
      "display" : "Ganglioglioma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M138.1",
      "display" : "Glial Tumours, Paediatric, Multi-target NGS panel, small variant (ATRX)"
    },
    {
      "code" : "M138.2",
      "display" : "Glial Tumours, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M138.3",
      "display" : "Glial Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M138.4",
      "display" : "Glial Tumours, Paediatric, DNA Methylation"
    },
    {
      "code" : "M139.1",
      "display" : "Glioblastoma, Paediatric, Multi-target NGS panel, small variant (BRAF, CDKN2A, FGFR4)"
    },
    {
      "code" : "M139.10",
      "display" : "Glioblastoma, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M139.12",
      "display" : "Glioblastoma, Paediatric, CDKN2A seq"
    },
    {
      "code" : "M139.13",
      "display" : "Glioblastoma, Paediatric, FGFR4 seq"
    },
    {
      "code" : "M139.14",
      "display" : "Glioblastoma, Paediatric, CDKN2A copy number FISH"
    },
    {
      "code" : "M139.15",
      "display" : "Glioblastoma, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M139.16",
      "display" : "Glioblastoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M139.17",
      "display" : "Glioblastoma, Paediatric, Multi-target NGS panel, copy number variant (CDKN2A)"
    },
    {
      "code" : "M139.18",
      "display" : "Glioblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M139.2",
      "display" : "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)"
    },
    {
      "code" : "M139.3",
      "display" : "Glioblastoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M139.4",
      "display" : "Glioblastoma, Paediatric, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M139.5",
      "display" : "Glioblastoma, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M139.6",
      "display" : "Glioblastoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M139.7",
      "display" : "Glioblastoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M139.8",
      "display" : "Glioblastoma, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M139.9",
      "display" : "Glioblastoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M14.1",
      "display" : "Adrenal Cortical Carcinoma, Multi-target NGS panel, small variant (TP53)"
    },
    {
      "code" : "M14.2",
      "display" : "Adrenal Cortical Carcinoma, Multi-target NGS panel, copy number variant (TP53)"
    },
    {
      "code" : "M14.3",
      "display" : "Adrenal Cortical Carcinoma, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M14.4",
      "display" : "Adrenal Cortical Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M14.5",
      "display" : "Adrenal Cortical Carcinoma, DPYD hotspot"
    },
    {
      "code" : "M143.1",
      "display" : "Lung, Paediatric, Multi-target NGS panel, small variant (H3-3A, H3-3B)"
    },
    {
      "code" : "M143.2",
      "display" : "Lung, Paediatric, H3-3A seq"
    },
    {
      "code" : "M143.3",
      "display" : "Lung, Paediatric, H3-3B seq"
    },
    {
      "code" : "M143.4",
      "display" : "Lung, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M143.5",
      "display" : "Lung, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M145.1",
      "display" : "Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, BCOR, PTCH1, PTCH2, PTEN, TERT promoter)"
    },
    {
      "code" : "M145.10",
      "display" : "Medulloblastoma, Paediatric, BCOR rearrangement FISH"
    },
    {
      "code" : "M145.11",
      "display" : "Medulloblastoma, Paediatric, C19MC copy number FISH"
    },
    {
      "code" : "M145.12",
      "display" : "Medulloblastoma, Paediatric, PTEN copy number FISH"
    },
    {
      "code" : "M145.13",
      "display" : "Medulloblastoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M145.14",
      "display" : "Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (ALK, BCOR, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M145.15",
      "display" : "Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (ALK, BCOR, C19MC, PTEN)"
    },
    {
      "code" : "M145.16",
      "display" : "Medulloblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M145.2",
      "display" : "Medulloblastoma, Paediatric, ALK seq"
    },
    {
      "code" : "M145.3",
      "display" : "Medulloblastoma, Paediatric, BCOR seq"
    },
    {
      "code" : "M145.4",
      "display" : "Medulloblastoma, Paediatric, PTCH1 seq"
    },
    {
      "code" : "M145.5",
      "display" : "Medulloblastoma, Paediatric, PTCH2 seq"
    },
    {
      "code" : "M145.6",
      "display" : "Medulloblastoma, Paediatric, TERT promoter seq"
    },
    {
      "code" : "M145.7",
      "display" : "Medulloblastoma, Paediatric, ALK copy number FISH"
    },
    {
      "code" : "M145.8",
      "display" : "Medulloblastoma, Paediatric, ALK rearrangement FISH"
    },
    {
      "code" : "M145.9",
      "display" : "Medulloblastoma, Paediatric, BCOR copy number FISH"
    },
    {
      "code" : "M146.1",
      "display" : "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, small variant (SMARCA4, DDX3X)"
    },
    {
      "code" : "M146.2",
      "display" : "Medulloblastoma Group 3, Paediatric, SMARCA4 seq"
    },
    {
      "code" : "M146.3",
      "display" : "Medulloblastoma Group 3, Paediatric, DDX3X seq"
    },
    {
      "code" : "M146.4",
      "display" : "Medulloblastoma Group 3, Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M146.5",
      "display" : "Medulloblastoma Group 3, Paediatric, PVT1-MYC FISH/RT-PCR"
    },
    {
      "code" : "M146.6",
      "display" : "Medulloblastoma Group 3, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M146.7",
      "display" : "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, structural variant (PVT1-MYC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M146.8",
      "display" : "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4)"
    },
    {
      "code" : "M146.9",
      "display" : "Medulloblastoma Group 3, Paediatric, DNA Methylation"
    },
    {
      "code" : "M147.1",
      "display" : "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, small variant (MYCN, EZH2)"
    },
    {
      "code" : "M147.10",
      "display" : "Medulloblastoma Group 3/4, Paediatric, DNA Methylation"
    },
    {
      "code" : "M147.2",
      "display" : "Medulloblastoma Group 3/4, Paediatric, MYCN seq"
    },
    {
      "code" : "M147.3",
      "display" : "Medulloblastoma Group 3/4, Paediatric, EZH2 seq"
    },
    {
      "code" : "M147.4",
      "display" : "Medulloblastoma Group 3/4, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M147.5",
      "display" : "Medulloblastoma Group 3/4, Paediatric, MYC copy number FISH"
    },
    {
      "code" : "M147.6",
      "display" : "Medulloblastoma Group 3/4, Paediatric, MYC rearrangement FISH"
    },
    {
      "code" : "M147.7",
      "display" : "Medulloblastoma Group 3/4, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M147.8",
      "display" : "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M147.9",
      "display" : "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, copy number variant (MYCN, MYC)"
    },
    {
      "code" : "M148.1",
      "display" : "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, small variant (YAP1, PTCH1)"
    },
    {
      "code" : "M148.10",
      "display" : "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (YAP1, PTCH1)"
    },
    {
      "code" : "M148.11",
      "display" : "Medulloblastoma TP53 WT, Paediatric, DNA Methylation"
    },
    {
      "code" : "M148.2",
      "display" : "Medulloblastoma TP53 WT, Paediatric, YAP1 seq"
    },
    {
      "code" : "M148.3",
      "display" : "Medulloblastoma TP53 WT, Paediatric, PTCH1 seq"
    },
    {
      "code" : "M148.4",
      "display" : "Medulloblastoma TP53 WT, Paediatric, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M148.5",
      "display" : "Medulloblastoma TP53 WT, Paediatric, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M148.6",
      "display" : "Medulloblastoma TP53 WT, Paediatric, YAP1 copy number FISH"
    },
    {
      "code" : "M148.7",
      "display" : "Medulloblastoma TP53 WT, Paediatric, PTCH1 copy number FISH"
    },
    {
      "code" : "M148.8",
      "display" : "Medulloblastoma TP53 WT, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M148.9",
      "display" : "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, structural variant (YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M149.1",
      "display" : "Melanotic Tumours, Paediatric, Multi-target NGS panel, small variant (NRAS)"
    },
    {
      "code" : "M149.2",
      "display" : "Melanotic Tumours, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M149.3",
      "display" : "Melanotic Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M15.1",
      "display" : "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, small variant (CDKN2A, EGFR, TP53)"
    },
    {
      "code" : "M15.2",
      "display" : "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M15.3",
      "display" : "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, copy number variant (CDKN2A, TP53)"
    },
    {
      "code" : "M15.4",
      "display" : "Head and Neck Squamous Cell Carcinoma, RET rearrangement FISH/RT-PC"
    },
    {
      "code" : "M15.5",
      "display" : "Head and Neck Squamous Cell Carcinoma, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M15.6",
      "display" : "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M15.7",
      "display" : "Head and Neck Squamous Cell Carcinoma, DPYD hotspot"
    },
    {
      "code" : "M150.1",
      "display" : "Meningioma, Paediatric, Multi-target NGS panel, small variant (SMARCE1, AKT1, NF2, TERT promoter)"
    },
    {
      "code" : "M150.2",
      "display" : "Meningioma, Paediatric, SMARCE1 seq"
    },
    {
      "code" : "M150.3",
      "display" : "Meningioma, Paediatric, AKT1 seq"
    },
    {
      "code" : "M150.4",
      "display" : "Meningioma, Paediatric, NF2 seq"
    },
    {
      "code" : "M150.5",
      "display" : "Meningioma, Paediatric, TERT promoter seq"
    },
    {
      "code" : "M150.6",
      "display" : "Meningioma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M150.7",
      "display" : "Meningioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M150.8",
      "display" : "Meningioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M151.1",
      "display" : "Midline Carcinoma, Paediatric, NUTM1-BRD2 FISH/RT-PCR"
    },
    {
      "code" : "M151.2",
      "display" : "Midline Carcinoma, Paediatric, NUTM1-BRD3 FISH/RT-PCR"
    },
    {
      "code" : "M151.3",
      "display" : "Midline Carcinoma, Paediatric, NUTM1-BRD4 FISH/RT-PCR"
    },
    {
      "code" : "M151.4",
      "display" : "Midline Carcinoma, Paediatric, NUTM1-CIC FISH/RT-PCR"
    },
    {
      "code" : "M151.5",
      "display" : "Midline Carcinoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M151.6",
      "display" : "Midline Carcinoma, Paediatric, Multi-target NGS panel, structural variant (NUTM1-BRD2, NUTM1-BRD3, NUTM1-BRD4, NUTM1-CIC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M152.1",
      "display" : "Neuroblastoma, Paediatric, SNP Array"
    },
    {
      "code" : "M152.10",
      "display" : "Neuroblastoma, Paediatric, 17q rearrangement FISH"
    },
    {
      "code" : "M152.11",
      "display" : "Neuroblastoma, Paediatric, 11q copy number FISH"
    },
    {
      "code" : "M152.12",
      "display" : "Neuroblastoma, Paediatric, 1p36 copy number FISH"
    },
    {
      "code" : "M152.13",
      "display" : "Neuroblastoma, Paediatric, ALK rearrangement FISH"
    },
    {
      "code" : "M152.14",
      "display" : "Neuroblastoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M152.15",
      "display" : "Neuroblastoma, Paediatric, MYCN seq"
    },
    {
      "code" : "M152.16",
      "display" : "Neuroblastoma, Paediatric, Multi-target NGS panel, structural variant (17q, ALK, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M152.17",
      "display" : "Neuroblastoma, Paediatric, Multi-target NGS panel, copy number variant (MYCN, ALK, 17q, 11q, 1p36)"
    },
    {
      "code" : "M152.18",
      "display" : "Neuroblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M152.19",
      "display" : "Neuroblastoma, Paediatric, TERT promoter rearrangement FISH"
    },
    {
      "code" : "M152.2",
      "display" : "Neuroblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, ATRX, FGFR1, MYCN, NRAS, PHOX2B, TP53)"
    },
    {
      "code" : "M152.3",
      "display" : "Neuroblastoma, Paediatric, ALK seq"
    },
    {
      "code" : "M152.4",
      "display" : "Neuroblastoma, Paediatric, FGFR1 seq"
    },
    {
      "code" : "M152.5",
      "display" : "Neuroblastoma, Paediatric, PHOX2B seq"
    },
    {
      "code" : "M152.6",
      "display" : "Neuroblastoma, Paediatric, TP53 seq"
    },
    {
      "code" : "M152.7",
      "display" : "Neuroblastoma, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M152.8",
      "display" : "Neuroblastoma, Paediatric, ALK copy number FISH"
    },
    {
      "code" : "M152.9",
      "display" : "Neuroblastoma, Paediatric, 17q copy number FISH"
    },
    {
      "code" : "M153.1",
      "display" : "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, small variant (SMO)"
    },
    {
      "code" : "M153.2",
      "display" : "Nodular Brain Tumour, Paediatric, SMO seq"
    },
    {
      "code" : "M153.3",
      "display" : "Nodular Brain Tumour, Paediatric, SMO copy number FISH"
    },
    {
      "code" : "M153.4",
      "display" : "Nodular Brain Tumour, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M153.5",
      "display" : "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M153.6",
      "display" : "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMO)"
    },
    {
      "code" : "M153.7",
      "display" : "Nodular Brain Tumour, Paediatric, DNA Methylation"
    },
    {
      "code" : "M155.1",
      "display" : "Oligoastrocytoma, Paediatric, Multi-target NGS panel, small variant (KIT)"
    },
    {
      "code" : "M155.2",
      "display" : "Oligoastrocytoma, Paediatric, KIT copy number FISH"
    },
    {
      "code" : "M155.3",
      "display" : "Oligoastrocytoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M155.4",
      "display" : "Oligoastrocytoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M155.5",
      "display" : "Oligoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIT)"
    },
    {
      "code" : "M155.6",
      "display" : "Oligoastrocytoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M156.1",
      "display" : "Oligodendroglioma, Paediatric, Multi-target NGS panel, small variant (RB1, ATRX)"
    },
    {
      "code" : "M156.10",
      "display" : "Oligodendroglioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M156.2",
      "display" : "Oligodendroglioma, Paediatric, ATRX seq"
    },
    {
      "code" : "M156.3",
      "display" : "Oligodendroglioma, Paediatric, RB1 seq"
    },
    {
      "code" : "M156.4",
      "display" : "Oligodendroglioma, Paediatric, Multi-target NGS panel, copy number variant (1p19q, RB1, ATRX)"
    },
    {
      "code" : "M156.5",
      "display" : "Oligodendroglioma, Paediatric, 1p19q codel FISH"
    },
    {
      "code" : "M156.6",
      "display" : "Oligodendroglioma, Paediatric, RB1 copy number FISH"
    },
    {
      "code" : "M156.7",
      "display" : "Oligodendroglioma, Paediatric, ATRX copy number FISH"
    },
    {
      "code" : "M156.8",
      "display" : "Oligodendroglioma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M156.9",
      "display" : "Oligodendroglioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M157.1",
      "display" : "Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, small variant (RET)"
    },
    {
      "code" : "M157.2",
      "display" : "Thyroid Papillary Carcinoma, Paediatric, RET seq"
    },
    {
      "code" : "M157.3",
      "display" : "Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M157.4",
      "display" : "Thyroid Papillary Carcinoma, Paediatric, RET rearrangement FISH/RT-PC"
    },
    {
      "code" : "M157.5",
      "display" : "Thyroid Papillary Carcinoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M158.1",
      "display" : "Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (RAF1)"
    },
    {
      "code" : "M158.2",
      "display" : "Pilocytic Astrocytoma, Paediatric, RAF1 seq"
    },
    {
      "code" : "M158.3",
      "display" : "Pilocytic Astrocytoma, Paediatric, RAF1-SRGAP3 FISH/RT-PCR"
    },
    {
      "code" : "M158.4",
      "display" : "Pilocytic Astrocytoma, Paediatric, RAF1-NF1A FISH/RT-PCR"
    },
    {
      "code" : "M158.5",
      "display" : "Pilocytic Astrocytoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M158.6",
      "display" : "Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant (RAF1-SRGAP3, RAF1-NF1A, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M158.7",
      "display" : "Pilocytic Astrocytoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M159.1",
      "display" : "Pituitary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"
    },
    {
      "code" : "M159.2",
      "display" : "Pituitary Blastoma, Paediatric, DICER1 seq"
    },
    {
      "code" : "M159.3",
      "display" : "Pituitary Blastoma, Paediatric, DICER1 copy number FISH"
    },
    {
      "code" : "M159.4",
      "display" : "Pituitary Blastoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M159.5",
      "display" : "Pituitary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M159.6",
      "display" : "Pituitary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"
    },
    {
      "code" : "M159.7",
      "display" : "Pituitary Blastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M16.1",
      "display" : "Adenoid Cystic Carcinoma, MYB-NFIB FISH/RT-PCR"
    },
    {
      "code" : "M16.2",
      "display" : "Adenoid Cystic Carcinoma, Multi-target NGS panel, structural variant (MYB-NFIB, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M16.4",
      "display" : "Adenoid Cystic Carcinoma, DPYD hotspot"
    },
    {
      "code" : "M160.1",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF, H3-3A)"
    },
    {
      "code" : "M160.10",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M160.11",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, H3-3A seq"
    },
    {
      "code" : "M160.12",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, KIAA1549 copy number FISH"
    },
    {
      "code" : "M160.13",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M160.14",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, WGS Germline and Tumour"
    },
    {
      "code" : "M160.15",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)"
    },
    {
      "code" : "M160.16",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M160.2",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M160.3",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M160.4",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M160.5",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M160.6",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M160.7",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M160.8",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M160.9",
      "display" : "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M161.1",
      "display" : "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"
    },
    {
      "code" : "M161.2",
      "display" : "Pleuropulmonary Blastoma, Paediatric, DICER1 seq"
    },
    {
      "code" : "M161.3",
      "display" : "Pleuropulmonary Blastoma, Paediatric, DICER1 copy number FISH"
    },
    {
      "code" : "M161.4",
      "display" : "Pleuropulmonary Blastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M161.5",
      "display" : "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M161.6",
      "display" : "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)"
    },
    {
      "code" : "M162.1",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, small variant (MSH6, PMS2, PTEN)"
    },
    {
      "code" : "M162.10",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, copy number variant (MYC, MSH6, PTEN)"
    },
    {
      "code" : "M162.11",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, DNA Methylation"
    },
    {
      "code" : "M162.2",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, MSH6 seq"
    },
    {
      "code" : "M162.3",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, PMS2 seq"
    },
    {
      "code" : "M162.4",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, MYC copy number FISH"
    },
    {
      "code" : "M162.5",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, MYC rearrangement FISH"
    },
    {
      "code" : "M162.6",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, MSH6 copy number FISH"
    },
    {
      "code" : "M162.7",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, PTEN copy number FISH"
    },
    {
      "code" : "M162.8",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M162.9",
      "display" : "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M165.1",
      "display" : "Renal Tumours, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX)"
    },
    {
      "code" : "M165.2",
      "display" : "Renal Tumours, Paediatric, ATRX seq"
    },
    {
      "code" : "M165.3",
      "display" : "Renal Tumours, Paediatric, CTNNB1 seq"
    },
    {
      "code" : "M165.4",
      "display" : "Renal Tumours, Paediatric, DAXX seq"
    },
    {
      "code" : "M165.5",
      "display" : "Renal Tumours, Paediatric, ATRX copy number FISH"
    },
    {
      "code" : "M165.6",
      "display" : "Renal Tumours, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M165.7",
      "display" : "Renal Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M165.8",
      "display" : "Renal Tumours, Paediatric, Multi-target NGS panel, copy number variant (ATRX)"
    },
    {
      "code" : "M166.1",
      "display" : "Retinoblastoma, Paediatric, Multi-target NGS panel, small variant (RB1)"
    },
    {
      "code" : "M166.2",
      "display" : "Retinoblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M166.3",
      "display" : "Retinoblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M166.4",
      "display" : "Retinoblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M167.1",
      "display" : "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, small variant (SMARCB1)"
    },
    {
      "code" : "M167.2",
      "display" : "Rhabdoid Tumours, Paediatric, SMARCB1 seq"
    },
    {
      "code" : "M167.3",
      "display" : "Rhabdoid Tumours, Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M167.4",
      "display" : "Rhabdoid Tumours, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M167.5",
      "display" : "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M167.6",
      "display" : "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)"
    },
    {
      "code" : "M168.1",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, small variant (PIK3CA, FGFR1)"
    },
    {
      "code" : "M168.2",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 seq"
    },
    {
      "code" : "M168.3",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 rearrangement FISH"
    },
    {
      "code" : "M168.4",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 ITD FISH"
    },
    {
      "code" : "M168.5",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M168.6",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, structural variant (FGFR1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M168.7",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, copy number variant (FGFR1 ITD)"
    },
    {
      "code" : "M168.8",
      "display" : "Rosette-Forming Glioneuronal Tumour, Paediatric, DNA Methylation"
    },
    {
      "code" : "M169.1",
      "display" : "Secondary Glioblastoma, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2)"
    },
    {
      "code" : "M169.2",
      "display" : "Secondary Glioblastoma, Paediatric, IDH1 seq"
    },
    {
      "code" : "M169.3",
      "display" : "Secondary Glioblastoma, Paediatric, IDH2 seq"
    },
    {
      "code" : "M169.4",
      "display" : "Secondary Glioblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M169.5",
      "display" : "Secondary Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M169.6",
      "display" : "Secondary Glioblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M17.1",
      "display" : "Secretory Carcinoma (Salivary Gland), ETV6-NTRK3 FISH/RT-PCR"
    },
    {
      "code" : "M17.2",
      "display" : "Secretory Carcinoma (Salivary Gland), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M17.4",
      "display" : "Secretory Carcinoma (Salivary Gland), DPYD hotspot"
    },
    {
      "code" : "M170.1",
      "display" : "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SMO, DDX3X)"
    },
    {
      "code" : "M170.2",
      "display" : "SHH Medulloblastoma, Paediatric, SMO seq"
    },
    {
      "code" : "M170.3",
      "display" : "SHH Medulloblastoma, Paediatric, DDX3X seq"
    },
    {
      "code" : "M170.4",
      "display" : "SHH Medulloblastoma, Paediatric, SMO copy number FISH"
    },
    {
      "code" : "M170.5",
      "display" : "SHH Medulloblastoma, Paediatric, DDX3X copy number FISH"
    },
    {
      "code" : "M170.6",
      "display" : "SHH Medulloblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M170.7",
      "display" : "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M170.8",
      "display" : "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMO, DDX3X)"
    },
    {
      "code" : "M170.9",
      "display" : "SHH Medulloblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M171.1",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, small variant (SUFU, TERT promoter, PTCH1)"
    },
    {
      "code" : "M171.10",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, DNA Methylation"
    },
    {
      "code" : "M171.2",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 seq"
    },
    {
      "code" : "M171.3",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, SUFU seq"
    },
    {
      "code" : "M171.4",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, TERT promoter seq"
    },
    {
      "code" : "M171.5",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 copy number FISH"
    },
    {
      "code" : "M171.6",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, TERT copy number FISH"
    },
    {
      "code" : "M171.7",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M171.8",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M171.9",
      "display" : "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (PTCH1, TERT)"
    },
    {
      "code" : "M172.1",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, small variant (TP53, MYCN)"
    },
    {
      "code" : "M172.2",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, TP53 seq"
    },
    {
      "code" : "M172.3",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN seq"
    },
    {
      "code" : "M172.4",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M172.5",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M172.6",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M172.7",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M172.8",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, copy number variant (TP53, MYCN)"
    },
    {
      "code" : "M172.9",
      "display" : "SHH Medulloblastoma, TP53 MUTANT, Paediatric, DNA Methylation"
    },
    {
      "code" : "M173.1",
      "display" : "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, TFEB-MALAT1 FISH/RT-PCR"
    },
    {
      "code" : "M173.2",
      "display" : "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M173.3",
      "display" : "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M174.1",
      "display" : "Testicular, Paediatric, Multi-target NGS panel, small variant (PRKAR1A)"
    },
    {
      "code" : "M174.2",
      "display" : "Testicular, Paediatric, PRKAR1A seq"
    },
    {
      "code" : "M174.3",
      "display" : "Testicular, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M174.4",
      "display" : "Testicular, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M178.1",
      "display" : "Wilms Tumours, Paediatric, Multi-target NGS panel, small variant (DROSHA)"
    },
    {
      "code" : "M178.2",
      "display" : "Wilms Tumours, Paediatric, DROSHA seq"
    },
    {
      "code" : "M178.3",
      "display" : "Wilms Tumours, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M178.4",
      "display" : "Wilms Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M179.1",
      "display" : "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (DDX3X, CTNNB1, SMARCA4, TP53)"
    },
    {
      "code" : "M179.10",
      "display" : "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, TP53)"
    },
    {
      "code" : "M179.11",
      "display" : "WNT Medulloblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M179.2",
      "display" : "WNT Medulloblastoma, Paediatric, DDX3X seq"
    },
    {
      "code" : "M179.3",
      "display" : "WNT Medulloblastoma, Paediatric, CTNNB1 seq"
    },
    {
      "code" : "M179.4",
      "display" : "WNT Medulloblastoma, Paediatric, SMARCA4 seq"
    },
    {
      "code" : "M179.5",
      "display" : "WNT Medulloblastoma, Paediatric, TP53 seq"
    },
    {
      "code" : "M179.6",
      "display" : "WNT Medulloblastoma, Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M179.7",
      "display" : "WNT Medulloblastoma, Paediatric, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M179.8",
      "display" : "WNT Medulloblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M179.9",
      "display" : "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M18.1",
      "display" : "Renal Cell Carcinoma, Adult, TFE3 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M18.2",
      "display" : "Renal Cell Carcinoma,Adult, Multi-target NGS panel small variant (FH, SDHA, SDHB, SDHC, SDHD, VHL, ELOC (TCEB-1), TSC1/2, MET, BRAF)"
    },
    {
      "code" : "M18.3",
      "display" : "Renal Cell Carcinoma, Adult, Chromosome 3 FISH"
    },
    {
      "code" : "M18.4",
      "display" : "Renal Cell Carcinoma, Adult, Chromosome 8 FISH"
    },
    {
      "code" : "M18.5",
      "display" : "Renal Cell Carcinoma, Adult, Chromosome 7 & 17 FISH"
    },
    {
      "code" : "M18.6",
      "display" : "Renal Cell Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, TFE3, TFEB)"
    },
    {
      "code" : "M18.7",
      "display" : "Renal Cell Carcinoma, Adult, TFEB rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M180.1",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, small variant (TFE3)"
    },
    {
      "code" : "M180.2",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3 seq"
    },
    {
      "code" : "M180.3",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR"
    },
    {
      "code" : "M180.4",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-MITF FISH/RT-PCR"
    },
    {
      "code" : "M180.5",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-PRCC FISH/RT-PCR"
    },
    {
      "code" : "M180.6",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M180.7",
      "display" : "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFE3-ASPSCR1, TFE3-MITF,  TFE3-PRCC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M181.1",
      "display" : "Hairy Cell Leukaemia, Non-Classical Variant, Multi-target NGS panel, small variant (MAP2K1)"
    },
    {
      "code" : "M181.4",
      "display" : "Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection multiplex seq"
    },
    {
      "code" : "M181.5",
      "display" : "Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection NGS"
    },
    {
      "code" : "M182.1",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR"
    },
    {
      "code" : "M182.2",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, ALK rearrangement FISH"
    },
    {
      "code" : "M182.3",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, WGS Germline and Tumor"
    },
    {
      "code" : "M182.4",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, Multi-target NGS panel, structural variant (ALK-NPM1, other ALK rearrangements)"
    },
    {
      "code" : "M182.5",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M182.6",
      "display" : "ALK Positive Anaplastic Large Cell Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M183.1",
      "display" : "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3A, NF1, TERT promoter)"
    },
    {
      "code" : "M183.2",
      "display" : "Diffuse Midline Glioma, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M183.3",
      "display" : "Diffuse Midline Glioma, Paediatric, MYC copy number FISH"
    },
    {
      "code" : "M183.4",
      "display" : "Diffuse Midline Glioma, Paediatric, MYC rearrangement FISH"
    },
    {
      "code" : "M183.5",
      "display" : "Diffuse Midline Glioma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M183.6",
      "display" : "Diffuse Midline Glioma, Paediatric, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M183.7",
      "display" : "Diffuse Midline Glioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M183.8",
      "display" : "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, MYC, MYCN)"
    },
    {
      "code" : "M183.9",
      "display" : "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M184.1",
      "display" : "Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3B, H3C2, H3C3, H3C14, IDH1, IDH2, TP53, VHL)"
    },
    {
      "code" : "M184.2",
      "display" : "Glioma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M184.3",
      "display" : "Glioma, Paediatric, IDH1 hotspot"
    },
    {
      "code" : "M184.4",
      "display" : "Glioma, Paediatric, IDH2 hotspot"
    },
    {
      "code" : "M184.5",
      "display" : "Glioma, Paediatric, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M184.6",
      "display" : "Glioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M184.7",
      "display" : "Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M184.8",
      "display" : "Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M185.1",
      "display" : "High Grade Glioma, Paediatric, Multi-target NGS panel, small variant (CDKN2B)"
    },
    {
      "code" : "M185.2",
      "display" : "High Grade Glioma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M185.3",
      "display" : "High Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M185.4",
      "display" : "High Grade Glioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M185.5",
      "display" : "High Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M186.1",
      "display" : "Low Grade Glioma, Paediatric, Multi-target NGS panel, small variant (TSC1, TSC2, IDH1, IDH2, FGFR1)"
    },
    {
      "code" : "M186.2",
      "display" : "Low Grade Glioma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M186.3",
      "display" : "Low Grade Glioma, Paediatric, IDH1 hotspot"
    },
    {
      "code" : "M186.4",
      "display" : "Low Grade Glioma, Paediatric, IDH2 hotspot"
    },
    {
      "code" : "M186.5",
      "display" : "Low Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M186.6",
      "display" : "Low Grade Glioma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M186.7",
      "display" : "Low Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M186.8",
      "display" : "Low Grade Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M187.1",
      "display" : "Uveal melanoma, 1p, 3, 6, 8 MLPA"
    },
    {
      "code" : "M187.2",
      "display" : "Uveal melanoma, BRAF hotspot"
    },
    {
      "code" : "M187.3",
      "display" : "Uveal melanoma, Multi-target NGS panel, small variant (BRAF, NRAS, NF1)"
    },
    {
      "code" : "M187.4",
      "display" : "Uveal melanoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M189.1",
      "display" : "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)"
    },
    {
      "code" : "M189.10",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M189.11",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, SNP Array"
    },
    {
      "code" : "M189.12",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, C19MC copy number FISH"
    },
    {
      "code" : "M189.13",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M189.14",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M189.15",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 copy number FISH"
    },
    {
      "code" : "M189.16",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M189.17",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M189.18",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, IDH1 hotspot"
    },
    {
      "code" : "M189.19",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, IDH2 hotspot"
    },
    {
      "code" : "M189.2",
      "display" : "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)"
    },
    {
      "code" : "M189.20",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, DNA Methylation"
    },
    {
      "code" : "M189.21",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, copy number variant  (C19MC, SMARCA4, SMARCB1, YAP1)"
    },
    {
      "code" : "M189.3",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M189.4",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, C11orf95-RELA FISH/RT-PCR"
    },
    {
      "code" : "M189.5",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M189.6",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M189.7",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, EWSR1 rearrangement FISH"
    },
    {
      "code" : "M189.8",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, MN1 rearrangement FISH"
    },
    {
      "code" : "M189.9",
      "display" : "Brain Tumour, No Further Morphological Classification, Paediatric, RELA rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M190.1",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, small variant (CDKN2A, DICER1, RB1, YAP1, SMARCA4, SMARCB1, MSH6, PMS2, PTEN, ATRX)"
    },
    {
      "code" : "M190.10",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M190.11",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M190.12",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M190.13",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, C11orf95-RELA FISH/RT-PCR"
    },
    {
      "code" : "M190.14",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, RELA rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M190.15",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, TTYH1-C19MC FISH/RT-PCR"
    },
    {
      "code" : "M190.16",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, YAP1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M190.17",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M190.18",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M190.19",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, MYC rearrangement FISH"
    },
    {
      "code" : "M190.2",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M190.20",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, MN1 rearrangement FISH"
    },
    {
      "code" : "M190.21",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, SNP Array"
    },
    {
      "code" : "M190.22",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, C19MC copy number FISH"
    },
    {
      "code" : "M190.23",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, DICER1 copy number FISH"
    },
    {
      "code" : "M190.24",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, MSH6 copy number FISH"
    },
    {
      "code" : "M190.25",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, MYC copy number FISH"
    },
    {
      "code" : "M190.26",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M190.27",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M190.28",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M190.3",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M190.30",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M190.31",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, DNA Methylation"
    },
    {
      "code" : "M190.32",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, copy number variant  (C19MC, DICER1, MSH6, MYC, PTEN, SMARCA4, SMARCB1)"
    },
    {
      "code" : "M190.4",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M190.5",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M190.6",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M190.7",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M190.8",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-FRX1 FISH/RT-PCR"
    },
    {
      "code" : "M190.9",
      "display" : "Embryonal Tumour Differential, Adult and Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M191.1",
      "display" : "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)"
    },
    {
      "code" : "M191.10",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH"
    },
    {
      "code" : "M191.11",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"
    },
    {
      "code" : "M191.12",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M191.13",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH"
    },
    {
      "code" : "M191.14",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M191.15",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR"
    },
    {
      "code" : "M191.16",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M191.17",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M191.18",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot"
    },
    {
      "code" : "M191.19",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot"
    },
    {
      "code" : "M191.2",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M191.20",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation"
    },
    {
      "code" : "M191.21",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M191.22",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M191.3",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M191.4",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M191.5",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M191.6",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M191.7",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M191.8",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M191.9",
      "display" : "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M192.1",
      "display" : "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)"
    },
    {
      "code" : "M192.10",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH"
    },
    {
      "code" : "M192.11",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant (EGFR)"
    },
    {
      "code" : "M192.12",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M192.13",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH"
    },
    {
      "code" : "M192.14",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M192.15",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR"
    },
    {
      "code" : "M192.16",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M192.17",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M192.18",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot"
    },
    {
      "code" : "M192.19",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot"
    },
    {
      "code" : "M192.2",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M192.20",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation"
    },
    {
      "code" : "M192.21",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M192.22",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"
    },
    {
      "code" : "M192.23",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M192.3",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M192.4",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M192.5",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M192.6",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M192.7",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M192.8",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M192.9",
      "display" : "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M193.1",
      "display" : "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)"
    },
    {
      "code" : "M193.10",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF rearrangement FISH"
    },
    {
      "code" : "M193.11",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant (EGFR)"
    },
    {
      "code" : "M193.12",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M193.13",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, CDKN2A copy number FISH"
    },
    {
      "code" : "M193.14",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M193.15",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, EGFRvIII RT-PCR"
    },
    {
      "code" : "M193.16",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M193.17",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M193.18",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, IDH1 hotspot"
    },
    {
      "code" : "M193.19",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, IDH2 hotspot"
    },
    {
      "code" : "M193.2",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M193.20",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, DNA Methylation"
    },
    {
      "code" : "M193.21",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M193.22",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)"
    },
    {
      "code" : "M193.23",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M193.3",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M193.4",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M193.5",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M193.6",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M193.7",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M193.8",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M193.9",
      "display" : "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M194.1",
      "display" : "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)"
    },
    {
      "code" : "M194.10",
      "display" : "Medulloblastoma all Subtypes, BCOR copy number FISH"
    },
    {
      "code" : "M194.11",
      "display" : "Medulloblastoma all Subtypes, C19MC copy number FISH"
    },
    {
      "code" : "M194.12",
      "display" : "Medulloblastoma all Subtypes, DDX3X copy number FISH"
    },
    {
      "code" : "M194.13",
      "display" : "Medulloblastoma all Subtypes, MYC copy number FISH"
    },
    {
      "code" : "M194.14",
      "display" : "Medulloblastoma all Subtypes, MYCN copy number FISH"
    },
    {
      "code" : "M194.15",
      "display" : "Medulloblastoma all Subtypes, PTCH1 copy number FISH"
    },
    {
      "code" : "M194.16",
      "display" : "Medulloblastoma all Subtypes, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M194.17",
      "display" : "Medulloblastoma all Subtypes, SMARCA4 copy number FISH"
    },
    {
      "code" : "M194.18",
      "display" : "Medulloblastoma all Subtypes, SMO copy number FISH"
    },
    {
      "code" : "M194.19",
      "display" : "Medulloblastoma all Subtypes, TERT copy number FISH"
    },
    {
      "code" : "M194.2",
      "display" : "Medulloblastoma all Subtypes, ALK rearrangement FISH"
    },
    {
      "code" : "M194.20",
      "display" : "Medulloblastoma all Subtypes, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M194.21",
      "display" : "Medulloblastoma all Subtypes, YAP1 copy number FISH"
    },
    {
      "code" : "M194.22",
      "display" : "Medulloblastoma all Subtypes, WGS Germline and Tumor"
    },
    {
      "code" : "M194.23",
      "display" : "Medulloblastoma all Subtypes, DNA Methylation"
    },
    {
      "code" : "M194.24",
      "display" : "Medulloblastoma all Subtypes, Multi-target NGS panel, structural variant (ALK, BCOR, MYC, PVT1-MYC, YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M194.25",
      "display" : "Medulloblastoma all Subtypes, Multi-target NGS panel, copy number variant  (ALK, BCOR, C19MC, DDX3X, MYC, MYCN, PTCH1, PTEN, SMARCA4, SMO, TERT, TP53, YAP1)"
    },
    {
      "code" : "M194.3",
      "display" : "Medulloblastoma all Subtypes, BCOR rearrangement FISH"
    },
    {
      "code" : "M194.4",
      "display" : "Medulloblastoma all Subtypes, MYC rearrangement FISH"
    },
    {
      "code" : "M194.5",
      "display" : "Medulloblastoma all Subtypes, PVT1-MYC FISH/RT-PCR"
    },
    {
      "code" : "M194.6",
      "display" : "Medulloblastoma all Subtypes, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M194.7",
      "display" : "Medulloblastoma all Subtypes, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M194.8",
      "display" : "Medulloblastoma all Subtypes, SNP Array"
    },
    {
      "code" : "M194.9",
      "display" : "Medulloblastoma all Subtypes, ALK copy number FISH"
    },
    {
      "code" : "M195.1",
      "display" : "Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, small variant (BRAF, CTNNB1)"
    },
    {
      "code" : "M195.2",
      "display" : "Craniopharyngioma, Adult and Paediatric, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M195.3",
      "display" : "Craniopharyngioma, Adult and Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M195.4",
      "display" : "Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M195.5",
      "display" : "Craniopharyngioma, Adult and Paediatric, DNA Methylation"
    },
    {
      "code" : "M196.1",
      "display" : "Bone Forming Soft Tissue Tumour Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M196.2",
      "display" : "Bone Forming Soft Tissue Tumour Differential, USP6 rearrangement FISH"
    },
    {
      "code" : "M196.3",
      "display" : "Bone Forming Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M196.4",
      "display" : "Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M196.5",
      "display" : "Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M197.1",
      "display" : "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)"
    },
    {
      "code" : "M197.10",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M197.2",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, DDIT3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M197.3",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M197.4",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, FOXO1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M197.5",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, WT1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M197.6",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M197.7",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, HEY1-NCOA2 RT-PCR"
    },
    {
      "code" : "M197.8",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, PAX3-FOXO1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M197.9",
      "display" : "Round Cell Sarcoma of Soft Tissue Differential, PAX7-FOXO1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M198.1",
      "display" : "Vascular Soft Tissue Tumour Differential, MYC copy number FISH"
    },
    {
      "code" : "M198.2",
      "display" : "Vascular Soft Tissue Tumour Differential, SERPINE1-FOSB FISH/RT-PCR"
    },
    {
      "code" : "M198.3",
      "display" : "Vascular Soft Tissue Tumour Differential, WWTR1-CAMTA1 RT-PCR"
    },
    {
      "code" : "M198.4",
      "display" : "Vascular Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M198.5",
      "display" : "Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M198.6",
      "display" : "Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MYC)"
    },
    {
      "code" : "M199.1",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, small variant (APC, CTNNB1)"
    },
    {
      "code" : "M199.10",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, TPM4-ALK FISH/RT-PCR"
    },
    {
      "code" : "M199.11",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, ETV6-NTRK3 RT-PCR"
    },
    {
      "code" : "M199.12",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M199.13",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M199.2",
      "display" : "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)"
    },
    {
      "code" : "M199.3",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M199.4",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, FUS rearrangement FISH"
    },
    {
      "code" : "M199.5",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M199.6",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M199.7",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, USP6 rearrangement FISH"
    },
    {
      "code" : "M199.8",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, COL1A1-PDGFB rearrangement FISH"
    },
    {
      "code" : "M199.9",
      "display" : "Spindle Cell Soft Tissue Tumour Differential, TPM3-ALK FISH/RT-PCR"
    },
    {
      "code" : "M2.1",
      "display" : "Ovarian Carcinoma, Multi-target NGS panel, small variant (BRCA1, BRCA2, SMARCA4)"
    },
    {
      "code" : "M2.3",
      "display" : "Ovarian Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M2.5",
      "display" : "Ovarian Carcinoma, HRD status (either positive for BRCA 1 and/or 2, or HRD positive)"
    },
    {
      "code" : "M20.1",
      "display" : "Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF)"
    },
    {
      "code" : "M20.2",
      "display" : "Anaplastic Astrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M20.3",
      "display" : "Anaplastic Astrocytoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M20.4",
      "display" : "Anaplastic Astrocytoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M20.5",
      "display" : "Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M200.1",
      "display" : "Myxoid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (BCOR, DDIT3, FUS, NR4A3, TGFBR3-OGA, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M200.2",
      "display" : "Myxoid Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M200.3",
      "display" : "Myxoid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M200.4",
      "display" : "Myxoid Soft Tissue Tumour Differential, NR4A3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M200.5",
      "display" : "Myxoid Soft Tissue Tumour Differential, TGFBR3-OGA FISH/RT-PCR"
    },
    {
      "code" : "M200.6",
      "display" : "Myxoid Soft Tissue Tumour Differential, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M200.7",
      "display" : "Myxoid Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M201.1",
      "display" : "Adipocytic Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M201.2",
      "display" : "Adipocytic Soft Tissue Tumour Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M201.3",
      "display" : "Adipocytic Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M201.4",
      "display" : "Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M201.5",
      "display" : "Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M202.1",
      "display" : "Epithelioid Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M202.2",
      "display" : "Epithelioid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M202.3",
      "display" : "Epithelioid Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M202.4",
      "display" : "Epithelioid Soft Tissue Tumour Differential, TFE3 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M202.5",
      "display" : "Epithelioid Soft Tissue Tumour Differential, WWTR1-CAMTA1  RT-PCR"
    },
    {
      "code" : "M202.6",
      "display" : "Epithelioid Soft Tissue Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M202.7",
      "display" : "Epithelioid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (EWSR1, FUS, SS18, TFE3, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M203.1",
      "display" : "Uterine Sarcomas (Inc Endometrial), EPC1-PHF1 rearrangement FISH"
    },
    {
      "code" : "M203.2",
      "display" : "Uterine Sarcomas (Inc Endometrial), JAZF1-PHF1 rearrangement FISH"
    },
    {
      "code" : "M203.3",
      "display" : "Uterine Sarcomas (Inc Endometrial), JAZF1-SUZ12 rearrangement FISH"
    },
    {
      "code" : "M203.4",
      "display" : "Uterine Sarcomas (Inc Endometrial), NUTM2B-YWHAE FISH/RT-PCR"
    },
    {
      "code" : "M203.5",
      "display" : "Uterine Sarcomas (Inc Endometrial), WGS Germline and Tumor"
    },
    {
      "code" : "M203.6",
      "display" : "Uterine Sarcomas (Inc Endometrial), Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NUTM2B-YWHAE, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M204.1",
      "display" : "Undifferentiated tumour, WGS Germline and Tumor"
    },
    {
      "code" : "M204.2",
      "display" : "Undifferentiated tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M205.1",
      "display" : "Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B, IDH1, IDH2)"
    },
    {
      "code" : "M205.2",
      "display" : "Cartilage Forming Bone Tumour Differential, H3-3B hotspot"
    },
    {
      "code" : "M205.3",
      "display" : "Cartilage Forming Bone Tumour Differential, H3-3A seq"
    },
    {
      "code" : "M205.4",
      "display" : "Cartilage Forming Bone Tumour Differential, H3-3B seq"
    },
    {
      "code" : "M205.5",
      "display" : "Cartilage Forming Bone Tumour Differential, HEY1-NCOA2 RT-PCR"
    },
    {
      "code" : "M205.6",
      "display" : "Cartilage Forming Bone Tumour Differential, SNP Array"
    },
    {
      "code" : "M205.7",
      "display" : "Cartilage Forming Bone Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M205.8",
      "display" : "Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M206.1",
      "display" : "Bone Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B)"
    },
    {
      "code" : "M206.2",
      "display" : "Bone Forming Bone Tumour Differential, H3-3B hotspot"
    },
    {
      "code" : "M206.3",
      "display" : "Bone Forming Bone Tumour Differential, H3-3A seq"
    },
    {
      "code" : "M206.4",
      "display" : "Bone Forming Bone Tumour Differential, H3-3B seq"
    },
    {
      "code" : "M206.5",
      "display" : "Bone Forming Bone Tumour Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M206.6",
      "display" : "Bone Forming Bone Tumour Differential, USP6 rearrangement FISH"
    },
    {
      "code" : "M206.7",
      "display" : "Bone Forming Bone Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M206.8",
      "display" : "Bone Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M206.9",
      "display" : "Bone Forming Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M207.1",
      "display" : "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3B)"
    },
    {
      "code" : "M207.2",
      "display" : "Osteoclast-Rich Bone Tumour Differential, H3-3B seq"
    },
    {
      "code" : "M207.3",
      "display" : "Osteoclast-Rich Bone Tumour Differential, H3-3B hotspot"
    },
    {
      "code" : "M207.4",
      "display" : "Osteoclast-Rich Bone Tumour Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M207.5",
      "display" : "Osteoclast-Rich Bone Tumour Differential, USP6 rearrangement FISH"
    },
    {
      "code" : "M207.6",
      "display" : "Osteoclast-Rich Bone Tumour Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M207.7",
      "display" : "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M207.8",
      "display" : "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M208.1",
      "display" : "Round Cell Sarcoma of Bone Differential, Multi-target NGS panel, structural variant (BCOR, CIC, EWSR1, WT1, BCOR-CCNB3, HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M208.2",
      "display" : "Round Cell Sarcoma of Bone Differential, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M208.3",
      "display" : "Round Cell Sarcoma of Bone Differential, WT1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M208.4",
      "display" : "Round Cell Sarcoma of Bone Differential, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M208.5",
      "display" : "Round Cell Sarcoma of Bone Differential, HEY1-NCOA2 RT-PCR"
    },
    {
      "code" : "M208.6",
      "display" : "Round Cell Sarcoma of Bone Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M209.1",
      "display" : "Vascular Tumour of Bone Differential, MYC copy number FISH"
    },
    {
      "code" : "M209.2",
      "display" : "Vascular Tumour of Bone Differential, SERPINE1-FOSB FISH/RT-PCR"
    },
    {
      "code" : "M209.3",
      "display" : "Vascular Tumour of Bone Differential, WWTR1-CAMTA1 RT-PCR"
    },
    {
      "code" : "M209.4",
      "display" : "Vascular Tumour of Bone Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M209.5",
      "display" : "Vascular Tumour of Bone Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M209.6",
      "display" : "Vascular Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MYC)"
    },
    {
      "code" : "M21.1",
      "display" : "Astrocytoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A,H3C2, BRAF, TERT promoter)"
    },
    {
      "code" : "M21.2",
      "display" : "Astrocytoma, Adult, Multi-target NGS panel, copy number variant (EGFR, CDKN2A, CDKN2B)"
    },
    {
      "code" : "M21.20",
      "display" : "Astrocytoma, Adult, DNA Methylation"
    },
    {
      "code" : "M21.21",
      "display" : "Astrocytoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M21.22",
      "display" : "Astrocytoma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M21.23",
      "display" : "Astrocytoma, Adult, CDKN2A copy number FISH"
    },
    {
      "code" : "M21.24",
      "display" : "Astrocytoma, Adult, CDKN2B copy number FISH"
    },
    {
      "code" : "M21.3",
      "display" : "Astrocytoma, Adult, EGFRvIII RT-PCR"
    },
    {
      "code" : "M21.5",
      "display" : "Astrocytoma, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M21.6",
      "display" : "Astrocytoma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M21.8",
      "display" : "Astrocytoma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M21.9",
      "display" : "Astrocytoma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M210.1",
      "display" : "Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M210.2",
      "display" : "Spindle Cell Tumour of Bone Differential, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M210.3",
      "display" : "Spindle Cell Tumour of Bone Differential, FUS rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M210.4",
      "display" : "Spindle Cell Tumour of Bone Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M210.5",
      "display" : "Spindle Cell Tumour of Bone Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M210.6",
      "display" : "Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M211.1",
      "display" : "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, small variant (GNAS)"
    },
    {
      "code" : "M211.2",
      "display" : "Fibro-Osseous Tumour of Bone Differential, MDM2 copy number FISH"
    },
    {
      "code" : "M211.3",
      "display" : "Fibro-Osseous Tumour of Bone Differential, WGS Germline and Tumor"
    },
    {
      "code" : "M211.4",
      "display" : "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M211.5",
      "display" : "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M212.1",
      "display" : "Renal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX, TP53, TFE3)"
    },
    {
      "code" : "M212.10",
      "display" : "Renal Tumour Differential, Paediatric, TFEB-MALAT1 FISH/RT-PCR"
    },
    {
      "code" : "M212.11",
      "display" : "Renal Tumour Differential, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR"
    },
    {
      "code" : "M212.12",
      "display" : "Renal Tumour Differential, Paediatric, TFE3-MITF FISH/RT-PCR"
    },
    {
      "code" : "M212.13",
      "display" : "Renal Tumour Differential, Paediatric, TFE3-PRCC FISH/RT-PCR"
    },
    {
      "code" : "M212.14",
      "display" : "Renal Tumour Differential, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M212.15",
      "display" : "Renal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, TFE3-ASPSCR1, TFE3-MITF, TFE3-PRCC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M212.16",
      "display" : "Renal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (ATRX, TP53, WT1)"
    },
    {
      "code" : "M212.2",
      "display" : "Renal Tumour Differential, Paediatric, ATRX seq"
    },
    {
      "code" : "M212.3",
      "display" : "Renal Tumour Differential, Paediatric, CTNNB1 seq"
    },
    {
      "code" : "M212.4",
      "display" : "Renal Tumour Differential, Paediatric, DAXX seq"
    },
    {
      "code" : "M212.5",
      "display" : "Renal Tumour Differential, Paediatric, TFE3 seq"
    },
    {
      "code" : "M212.6",
      "display" : "Renal Tumour Differential, Paediatric, TP53 seq"
    },
    {
      "code" : "M212.7",
      "display" : "Renal Tumour Differential, Paediatric, ATRX copy number FISH"
    },
    {
      "code" : "M212.8",
      "display" : "Renal Tumour Differential, Paediatric, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M212.9",
      "display" : "Renal Tumour Differential, Paediatric, WT1 copy number FISH"
    },
    {
      "code" : "M213.1",
      "display" : "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)"
    },
    {
      "code" : "M213.10",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M213.11",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M213.12",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, ALK-NPM1 rearrangement FISH"
    },
    {
      "code" : "M213.13",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, C11orf95-RELA FISH/RT-PCR"
    },
    {
      "code" : "M213.14",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, EWSR1 rearrangement FISH"
    },
    {
      "code" : "M213.15",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 rearrangement FISH"
    },
    {
      "code" : "M213.16",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-NF1A FISH/RT-PCR"
    },
    {
      "code" : "M213.17",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-SRGAP3 FISH/RT-PCR"
    },
    {
      "code" : "M213.18",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, RELA rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M213.19",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M213.2",
      "display" : "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"
    },
    {
      "code" : "M213.20",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M213.21",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M213.22",
      "display" : "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)"
    },
    {
      "code" : "M213.23",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M213.24",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, ALK copy number FISH"
    },
    {
      "code" : "M213.25",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, C19MC copy number FISH"
    },
    {
      "code" : "M213.26",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, CDKN2A copy number FISH"
    },
    {
      "code" : "M213.27",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, EGFR copy number FISH"
    },
    {
      "code" : "M213.28",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 ITD FISH"
    },
    {
      "code" : "M213.29",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, KIAA1549 copy number FISH"
    },
    {
      "code" : "M213.3",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF rearrangement FISH"
    },
    {
      "code" : "M213.30",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, KIT copy number FISH"
    },
    {
      "code" : "M213.31",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M213.32",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, PDGFRA FISH/RT-PCR"
    },
    {
      "code" : "M213.33",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, SMARCA4 copy number FISH"
    },
    {
      "code" : "M213.34",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, SMARCB1 copy number FISH"
    },
    {
      "code" : "M213.35",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 copy number FISH"
    },
    {
      "code" : "M213.36",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, EGFRvIII RT-PCR"
    },
    {
      "code" : "M213.37",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M213.38",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, DNA Methylation"
    },
    {
      "code" : "M213.4",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M213.5",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M213.6",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M213.7",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M213.8",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FRX1 FISH/RT-PCR"
    },
    {
      "code" : "M213.9",
      "display" : "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M215.1",
      "display" : "Endometrial Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M215.2",
      "display" : "Endometrial Cancer, MLH1 promoter hyperMethylation"
    },
    {
      "code" : "M215.4",
      "display" : "Endometrial Cancer, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2)"
    },
    {
      "code" : "M215.5",
      "display" : "Endometrial Cancer, Multi-target NGS panel-small variant detection POLE"
    },
    {
      "code" : "M217.1",
      "display" : "Urothelial Cancer, Multi-target NGS panel, small variant (FGFR3, FGFR2)"
    },
    {
      "code" : "M217.2",
      "display" : "Bladder Cancer, Multi-target NGS panel, copy number variant (FGFR3, FGFR2)"
    },
    {
      "code" : "M217.3",
      "display" : "Bladder Cancer, Multi-target NGS panel, structural variant (FGFR3, FGFR2, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M218.1",
      "display" : "Prostate Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2, ATM, CDK12)"
    },
    {
      "code" : "M218.2",
      "display" : "Prostate Cancer, Multi-target NGS panel, structural variant (TMPRSS2-ERG, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M218.3",
      "display" : "Prostate Cancer, TMPRSS2-ERG FISH"
    },
    {
      "code" : "M219.1",
      "display" : "Pancreatic Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2)"
    },
    {
      "code" : "M219.2",
      "display" : "Pancreatic Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M219.3",
      "display" : "Pancreatic Cancer, DPYD hotspot"
    },
    {
      "code" : "M219.5",
      "display" : "Pancreatic Cancer, MSI Testing"
    },
    {
      "code" : "M22.1",
      "display" : "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, small variant (H3C2, H3C14, IDH1, IDH2)"
    },
    {
      "code" : "M22.10",
      "display" : "Diffuse Astrocytoma, Paediatric, MYB rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M22.11",
      "display" : "Diffuse Astrocytoma, Paediatric, MYBL1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M22.12",
      "display" : "Diffuse Astrocytoma, Paediatric, MN1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M22.2",
      "display" : "Diffuse Astrocytoma, Paediatric, MYC copy number FISH"
    },
    {
      "code" : "M22.3",
      "display" : "Diffuse Astrocytoma, Paediatric, MYC rearrangement FISH"
    },
    {
      "code" : "M22.4",
      "display" : "Diffuse Astrocytoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M22.5",
      "display" : "Diffuse Astrocytoma, Paediatric, IDH1 hotspot"
    },
    {
      "code" : "M22.6",
      "display" : "Diffuse Astrocytoma, Paediatric, IDH2 hotspot"
    },
    {
      "code" : "M22.7",
      "display" : "Diffuse Astrocytoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M22.8",
      "display" : "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, copy number variant (MYC)"
    },
    {
      "code" : "M22.9",
      "display" : "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (MYC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M220.1",
      "display" : "Cholangiocarcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, FGFR2)"
    },
    {
      "code" : "M220.3",
      "display" : "Cholangiocarcinoma, DPYD hotspot"
    },
    {
      "code" : "M220.5",
      "display" : "Cholangiocarcinoma, MSI Testing"
    },
    {
      "code" : "M220.6",
      "display" : "Cholangiocarcinoma, Multi-target NGS panel -small variant (IDH1)"
    },
    {
      "code" : "M220.7",
      "display" : "Cholangiocarcinoma, FGFR2 rearrangement FISH"
    },
    {
      "code" : "M221.1",
      "display" : "Spitzoid tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M222.2",
      "display" : "Hepatocellular carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M222.4",
      "display" : "Hepatocellular carcinoma, DPYD hotspot"
    },
    {
      "code" : "M224.1",
      "display" : "MDS/MPN, Multi-target NGS panel, small variant"
    },
    {
      "code" : "M224.10",
      "display" : "MDS/MPN, BCR-ABL1 multiplex"
    },
    {
      "code" : "M224.11",
      "display" : "MDS/MPN, Other RT-PCR"
    },
    {
      "code" : "M224.13",
      "display" : "MDS/MPN, JAK2 V617F hotspot"
    },
    {
      "code" : "M224.14",
      "display" : "MDS/MPN, JAK2 exon 12 hotspot"
    },
    {
      "code" : "M224.15",
      "display" : "MDS/MPN, CALR exon 9 hotspot"
    },
    {
      "code" : "M224.16",
      "display" : "MDS/MPN, MPL exon 10 hotspot"
    },
    {
      "code" : "M224.18",
      "display" : "MDS/MPN, Chr8 copy number FISH"
    },
    {
      "code" : "M224.19",
      "display" : "MDS/MPN, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M224.2",
      "display" : "MDS/MPN, Karyotype (To include detection of complex karyotype)"
    },
    {
      "code" : "M224.20",
      "display" : "MDS/MPN, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M224.21",
      "display" : "MDS/MPN, i(17q)/t(17p) FISH"
    },
    {
      "code" : "M224.22",
      "display" : "MDS/MPN, Chr12p copy number FISH, t(12p) rearrangement FISH"
    },
    {
      "code" : "M224.23",
      "display" : "MDS/MPN, t(9;22)(q34;q11) BCR-ABL1 FISH"
    },
    {
      "code" : "M224.24",
      "display" : "MDS/MPN, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)"
    },
    {
      "code" : "M224.25",
      "display" : "MDS/MPN, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)"
    },
    {
      "code" : "M224.26",
      "display" : "MDS/MPN, FGFR1 rearrangement FISH"
    },
    {
      "code" : "M224.27",
      "display" : "MDS/MPN, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)"
    },
    {
      "code" : "M224.28",
      "display" : "MDS/MPN, inv(3)/t(3;3) FISH"
    },
    {
      "code" : "M224.29",
      "display" : "MDS/MPN, 11q23 (KMT2A) rearrangement FISH"
    },
    {
      "code" : "M224.3",
      "display" : "MDS/MPN, FISH copy number and rearrangement Other: See tests M224. -M224. for individual specified FISH targets."
    },
    {
      "code" : "M224.30",
      "display" : "MDS/MPN, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)"
    },
    {
      "code" : "M224.31",
      "display" : "MDS/MPN, FLT3 rearragement FISH"
    },
    {
      "code" : "M224.32",
      "display" : "MDS/MPN, RET rearrangement FISH"
    },
    {
      "code" : "M224.33",
      "display" : "MDS/MPN, NTRK3 rearrangement FISH"
    },
    {
      "code" : "M224.34",
      "display" : "MDS/MPN, Chr13/Chr13q copy number FISH"
    },
    {
      "code" : "M224.35",
      "display" : "MDS/MPN, Chr11q copy number FISH"
    },
    {
      "code" : "M224.36",
      "display" : "MDS/MPN, Chr9q copy number FISH"
    },
    {
      "code" : "M224.37",
      "display" : "MDS/MPN, Chr17/Chr17p copy number FISH"
    },
    {
      "code" : "M224.38",
      "display" : "MDS/MPN, idic(X)(q13) FISH"
    },
    {
      "code" : "M224.39",
      "display" : "MDS/MPN, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p/i(17q) & idic(X)(q13), cryptic deletion of 4q12, trisomy 8)"
    },
    {
      "code" : "M224.4",
      "display" : "MDS/MPN, WGS Germline and Tumor"
    },
    {
      "code" : "M224.40",
      "display" : "MDS/MPN, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M224.41",
      "display" : "MDS/MPN, WGS Tumour First"
    },
    {
      "code" : "M224.42",
      "display" : "MDS/MPN, WGS Follow-up Germline"
    },
    {
      "code" : "M224.5",
      "display" : "MDS/MPN, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)"
    },
    {
      "code" : "M224.6",
      "display" : "MDS/MPN, FIP1L1-PDGFRA FISH/RT-PCR"
    },
    {
      "code" : "M224.7",
      "display" : "MDS/MPN, FIP1L1-PDGFRA RT-qPCR"
    },
    {
      "code" : "M224.8",
      "display" : "MDS/MPN, ETV6-PDGFRB FISH/RT-PCR"
    },
    {
      "code" : "M224.9",
      "display" : "MDS/MPN, PCM1-JAK2 FISH/RT-PCR"
    },
    {
      "code" : "M225.1",
      "display" : "Suspected Lymphoma, Ig gene (heavy & light chain) rearrangement detection multiplex seq"
    },
    {
      "code" : "M225.2",
      "display" : "Suspected Lymphoma, Ig gene (heavy & light chain) rearrangement detection NGS"
    },
    {
      "code" : "M225.3",
      "display" : "Suspected Lymphoma, TCR gene rearrangement detection multiplex seq"
    },
    {
      "code" : "M225.4",
      "display" : "Suspected Lymphoma, TCR gene rearrangement detection NGS"
    },
    {
      "code" : "M225.5",
      "display" : "Suspected Lymphoma, Karyotype"
    },
    {
      "code" : "M226.1",
      "display" : "Cancer of Unknown Primary, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M226.3",
      "display" : "Cancer of Unknown Primary, DPYD hotspot"
    },
    {
      "code" : "M226.4",
      "display" : "Cancer of Unknown Primary, WGS Germline and Tumor"
    },
    {
      "code" : "M227.1",
      "display" : "Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M227.3",
      "display" : "Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), DPYD hotspot"
    },
    {
      "code" : "M23.1",
      "display" : "Diffuse Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter,  H3-3A)"
    },
    {
      "code" : "M23.10",
      "display" : "Diffuse Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M23.11",
      "display" : "Diffuse Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M23.12",
      "display" : "Diffuse Midline Glioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M23.6",
      "display" : "Diffuse Midline Glioma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M23.7",
      "display" : "Diffuse Midline Glioma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M23.8",
      "display" : "Diffuse Midline Glioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M23.9",
      "display" : "Diffuse Midline Glioma, Adult, DNA Methylation"
    },
    {
      "code" : "M231.1,",
      "display" : "small cell lung cancer, Multi-target NGS panel, copy number variant (RB1)"
    },
    {
      "code" : "M231.2,",
      "display" : "small cell lung cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M232.1",
      "display" : "Solid Tumour Exhausted all Standards of Care Testing and Treatment- Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M233.1",
      "display" : "High Grade Serous Ovarian Carcinoma, WGS Germline and Tumor"
    },
    {
      "code" : "M234.1",
      "display" : "Triple Negative Breast Cancer, WGS Germline and Tumor"
    },
    {
      "code" : "M235.1",
      "display" : "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Germline and Tumor"
    },
    {
      "code" : "M235.2",
      "display" : "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Tumour First"
    },
    {
      "code" : "M235.3",
      "display" : "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Follow-up Germline"
    },
    {
      "code" : "M236.1",
      "display" : "Oesophageal Cancer, MSI Testing"
    },
    {
      "code" : "M236.2",
      "display" : "Oesophageal Cancer, DPYD hotspot"
    },
    {
      "code" : "M237.1",
      "display" : "Gastric Cancer, MSI Testing"
    },
    {
      "code" : "M237.2",
      "display" : "Gastric Cancer, DPYD hotspot"
    },
    {
      "code" : "M238.1,",
      "display" : "small Bowel Cancer, MSI Testing"
    },
    {
      "code" : "M238.2,",
      "display" : "small Bowel Cancer, DPYD hotspot"
    },
    {
      "code" : "M239.1",
      "display" : "Thyroid Hurtle Cell Carcinoma, Multi-target NGS panel, structural variant (RET)"
    },
    {
      "code" : "M24.1",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, C19MC copy number  FISH"
    },
    {
      "code" : "M24.2",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, TTYH1-C19MC FISH/RT-PCR"
    },
    {
      "code" : "M24.3",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M24.4",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, DNA Methylation"
    },
    {
      "code" : "M24.5",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, copy number variant (C19MC)"
    },
    {
      "code" : "M24.6",
      "display" : "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, structural variant  (TTYH1-C19MC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M240.1",
      "display" : "Non-invasive follicular thyroid neoplasm with papillary like nuclei, Multi-target NGS panel, small variant (BRAF,HRAS,NRAS,KRAS)"
    },
    {
      "code" : "M241.1",
      "display" : "Conjunctival melanoma, MYB & 6cen (FISH)"
    },
    {
      "code" : "M241.2",
      "display" : "Conjunctival melanoma, RREB1 (6p25) (FISH)"
    },
    {
      "code" : "M241.3",
      "display" : "Conjunctival melanoma, CCND1 (11q13) (FISH)"
    },
    {
      "code" : "M241.4",
      "display" : "Conjunctival melanoma, MYC & 8cen (FISH)"
    },
    {
      "code" : "M241.5",
      "display" : "Conjunctival melanoma, CDKN2A & 9cen (FISH)"
    },
    {
      "code" : "M242.1",
      "display" : "Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), STR Testing"
    },
    {
      "code" : "M242.2",
      "display" : "Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), Sex chromosome FISH"
    },
    {
      "code" : "M243.1",
      "display" : "Thymic Carcinoma, Multi-target NGS panel (KIT)"
    },
    {
      "code" : "M244.1",
      "display" : "In all tumours elligible for NTRK1/2/3 testing, FISH"
    },
    {
      "code" : "M245.1",
      "display" : "Ovarian sex cord stromal tumuors, Multi-target NGS panel-small variant (FOXL2, CTNNB1, APC, DICER1)"
    },
    {
      "code" : "M25.1",
      "display" : "Ependymoma, Paediatric, Multi-target NGS panel, small variant (YAP1)"
    },
    {
      "code" : "M25.10",
      "display" : "Ependymoma, Paediatric, MYCN copy number FISH"
    },
    {
      "code" : "M25.11",
      "display" : "Ependymoma, Paediatric, ZFTA rearrangements (several fusion partners)"
    },
    {
      "code" : "M25.2",
      "display" : "Ependymoma, Paediatric, YAP1 copy number FISH"
    },
    {
      "code" : "M25.3",
      "display" : "Ependymoma, Paediatric, YAP1-C11orf95 FISH/RT-PCR"
    },
    {
      "code" : "M25.4",
      "display" : "Ependymoma, Paediatric, YAP1-TFE3 FISH/RT-PCR"
    },
    {
      "code" : "M25.5",
      "display" : "Ependymoma, Paediatric, C11orf95-RELA FISH/RT-PCR"
    },
    {
      "code" : "M25.6",
      "display" : "Ependymoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M25.7",
      "display" : "Ependymoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M25.8",
      "display" : "Ependymoma, Paediatric, Multi-target NGS panel, copy number variant (YAP1, MYCN)"
    },
    {
      "code" : "M25.9",
      "display" : "Ependymoma, Paediatric, Multi-target NGS panel, structural variant  (YAP1-C11orf95, YAP1-TFE3, C11orf95-RELA, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M26.1",
      "display" : "Ependymoma Supratentorial, Adult, YAP1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M26.2",
      "display" : "Ependymoma, Adult, RELA rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M26.3",
      "display" : "Ependymoma, Adult, DNA Methylation"
    },
    {
      "code" : "M26.4",
      "display" : "Ependymoma, Adult, Multi-target NGS panel, structural variant  (YAP1, RELA, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M26.5",
      "display" : "Ependymoma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M26.6",
      "display" : "Ependymoma, Adult, ZFTA rearrangements (several fusion partners)"
    },
    {
      "code" : "M27.1",
      "display" : "Glioblastoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)"
    },
    {
      "code" : "M27.10",
      "display" : "Glioblastoma, Adult, MYC copy number FISH"
    },
    {
      "code" : "M27.11",
      "display" : "Glioblastoma, Adult, PTEN (10q23) copy number FISH/RT-PCR"
    },
    {
      "code" : "M27.12",
      "display" : "Glioblastoma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M27.13",
      "display" : "Glioblastoma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M27.14",
      "display" : "Glioblastoma, Adult, DNA Methylation"
    },
    {
      "code" : "M27.15",
      "display" : "Glioblastoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M27.16",
      "display" : "Glioblastoma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M27.2",
      "display" : "Glioblastoma, Adult, Multi-target NGS panel, copy number variant (EGFR, PDGFRA, MYC, PTEN, 1p, 19q)"
    },
    {
      "code" : "M27.3",
      "display" : "Glioblastoma, Adult, EGFRvIII RT-PCR"
    },
    {
      "code" : "M27.5",
      "display" : "Glioblastoma, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M27.6",
      "display" : "Glioblastoma, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M27.7",
      "display" : "Glioblastoma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M27.9",
      "display" : "Glioblastoma, Adult, PDGFRA copy number FISH/RT-PCR"
    },
    {
      "code" : "M28.1",
      "display" : "Glioma, Adult, Multi-target NGS panel, small variant (H3C2, H3C3, H3C14, H3-3A, H3-3B, IDH1, IDH2, TP53, VHL, TERT promoter)"
    },
    {
      "code" : "M28.2",
      "display" : "Glioma, Adult, Multi-target NGS panel, copy number variant (EGFR, 1p, 19q)"
    },
    {
      "code" : "M28.3",
      "display" : "Glioma, Adult, EGFR copy number FISH"
    },
    {
      "code" : "M28.4",
      "display" : "Glioma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M28.5",
      "display" : "Glioma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M28.6",
      "display" : "Glioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M28.7",
      "display" : "Glioma, Adult, DNA Methylation"
    },
    {
      "code" : "M28.8",
      "display" : "Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M28.9",
      "display" : "Glioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M29.1",
      "display" : "High Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)"
    },
    {
      "code" : "M29.2",
      "display" : "High Grade Glioma, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M29.3",
      "display" : "High Grade Glioma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M29.4",
      "display" : "High Grade Glioma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M29.5",
      "display" : "High Grade Glioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M29.6",
      "display" : "High Grade Glioma, Adult, DNA Methylation"
    },
    {
      "code" : "M29.7",
      "display" : "High Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M29.8",
      "display" : "High Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M29.9",
      "display" : "High Grade Glioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M3.12",
      "display" : "Breast Cancer, Tumour profiling tests to guide adjuvant chemotherapy decisions in early breast cancer"
    },
    {
      "code" : "M3.13",
      "display" : "Breast Cancer, Multi-target ctDNA NGS panel, small variant (ESR1)"
    },
    {
      "code" : "M3.5",
      "display" : "Breast Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M3.6",
      "display" : "Breast Cancer, Multi-target NGS panel, small variant (PIK3CA)"
    },
    {
      "code" : "M3.7",
      "display" : "Breast Cancer, DPYD hotspot"
    },
    {
      "code" : "M3.9",
      "display" : "Breast Cancer, ETV6-NTRK3 FISH/RT-PCR"
    },
    {
      "code" : "M30.1",
      "display" : "IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, small variant (RB1, NF1)"
    },
    {
      "code" : "M30.2",
      "display" : "IDH-Wildtype Glioblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M30.3",
      "display" : "IDH-Wildtype Glioblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M30.4",
      "display" : "IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M31.1",
      "display" : "Low Grade Glioma, Adult, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M31.2",
      "display" : "Low Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, TERT promoter, H3-3A, H3C2)"
    },
    {
      "code" : "M31.3",
      "display" : "Low Grade Glioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M31.4",
      "display" : "Low Grade Glioma, Adult, DNA Methylation"
    },
    {
      "code" : "M31.5",
      "display" : "Low Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M31.6",
      "display" : "Low Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M31.7",
      "display" : "Low Grade Glioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M32.1",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, small variant (BRAF, IDH1, IDH2, TERT promoter, H3-3A, H3C2)"
    },
    {
      "code" : "M32.2",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M32.3",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, DNA Methylation"
    },
    {
      "code" : "M32.4",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M32.5",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M32.6",
      "display" : "Low Grade Glioma/Glioneuronal Tumours, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M33.3",
      "display" : "Meningioma, Adult, Multi-target NGS panel, small variant (TERT promoter)"
    },
    {
      "code" : "M33.4",
      "display" : "Meningioma, Adult, DNA Methylation"
    },
    {
      "code" : "M33.5",
      "display" : "Meningioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M34.1",
      "display" : "Non-Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)"
    },
    {
      "code" : "M34.2",
      "display" : "Non-Midline Glioma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M34.3",
      "display" : "Non-Midline Glioma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M34.4",
      "display" : "Non-Midline Glioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M34.5",
      "display" : "Non-Midline Glioma, Adult, DNA Methylation"
    },
    {
      "code" : "M34.6",
      "display" : "Non-Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M34.7",
      "display" : "Non-Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M34.8",
      "display" : "Non-Midline Glioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M35.1",
      "display" : "OligodendroGlioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)"
    },
    {
      "code" : "M35.2",
      "display" : "OligodendroGlioma, Adult, 1p19q codel FISH/RT-PCR"
    },
    {
      "code" : "M35.4",
      "display" : "OligodendroGlioma, Adult, IDH1 hotspot"
    },
    {
      "code" : "M35.5",
      "display" : "OligodendroGlioma, Adult, IDH2 hotspot"
    },
    {
      "code" : "M35.6",
      "display" : "OligodendroGlioma, Adult, DNA Methylation"
    },
    {
      "code" : "M35.7",
      "display" : "OligodendroGlioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)"
    },
    {
      "code" : "M35.8",
      "display" : "OligodendroGlioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M35.9",
      "display" : "OligodendroGlioma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M36.1",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-KIAA1549 FISH/RT-PCR"
    },
    {
      "code" : "M36.10",
      "display" : "Pilocytic Astrocytoma, Adult, KIAA1549 copy number FISH"
    },
    {
      "code" : "M36.11",
      "display" : "Pilocytic Astrocytoma, Adult, CDKN2A copy number FISH"
    },
    {
      "code" : "M36.12",
      "display" : "Pilocytic Astrocytoma, Adult, Multi-target NGS panel, small variant (BRAF, CDKN2A)"
    },
    {
      "code" : "M36.13",
      "display" : "Pilocytic Astrocytoma, Adult, DNA Methylation"
    },
    {
      "code" : "M36.14",
      "display" : "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)"
    },
    {
      "code" : "M36.15",
      "display" : "Pilocytic Astrocytoma, Adult, Multi-target NGS panel, copy number variant (KIAA1549, CDKN2A)"
    },
    {
      "code" : "M36.16",
      "display" : "Pilocytic Astrocytoma, Adult, WGS Germline and Tumor"
    },
    {
      "code" : "M36.2",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-AGK FISH/RT-PCR"
    },
    {
      "code" : "M36.3",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-AKAP9 FISH/RT-PCR"
    },
    {
      "code" : "M36.4",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-CCDC6 FISH/RT-PCR"
    },
    {
      "code" : "M36.5",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-FAM118B FISH/RT-PCR"
    },
    {
      "code" : "M36.6",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-FXR1 FISH/RT-PCR"
    },
    {
      "code" : "M36.7",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-GNAI1 FISH/RT-PCR"
    },
    {
      "code" : "M36.8",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF-MACF1 FISH/RT-PCR"
    },
    {
      "code" : "M36.9",
      "display" : "Pilocytic Astrocytoma, Adult, BRAF rearrangement FISH"
    },
    {
      "code" : "M37.1",
      "display" : "Pineoblastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)"
    },
    {
      "code" : "M37.2",
      "display" : "Pineoblastoma, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M37.3",
      "display" : "Pineoblastoma, Paediatric, DNA Methylation"
    },
    {
      "code" : "M37.4",
      "display" : "Pineoblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M38.1",
      "display" : "Pituitary Tumours, MGMT promoter hyperMethylation"
    },
    {
      "code" : "M38.2",
      "display" : "Pituitary Tumours, Multi-target NGS panel, copy number variant (EGFR)"
    },
    {
      "code" : "M38.3",
      "display" : "Pituitary Tumours, EGFR copy number FISH"
    },
    {
      "code" : "M38.4",
      "display" : "Pituitary Tumours, DNA Methylation"
    },
    {
      "code" : "M38.5",
      "display" : "Pituitary Tumours, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M38.6",
      "display" : "Pituitary Tumours, WGS Germline and Tumor"
    },
    {
      "code" : "M39.1",
      "display" : "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, small variant (CDKN2A)"
    },
    {
      "code" : "M39.2",
      "display" : "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, WGS Germline and Tumor"
    },
    {
      "code" : "M39.3",
      "display" : "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, DNA Methylation"
    },
    {
      "code" : "M39.4",
      "display" : "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M4.1",
      "display" : "Non-Small Cell Lung Cancer, Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET)"
    },
    {
      "code" : "M4.10",
      "display" : "Non-Small Cell Lung Cancer, EML4-ALK FISH/RT-PCR"
    },
    {
      "code" : "M4.11",
      "display" : "Non-Small Cell Lung Cancer, ALK hotspot cDNA"
    },
    {
      "code" : "M4.13",
      "display" : "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)"
    },
    {
      "code" : "M4.14",
      "display" : "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"
    },
    {
      "code" : "M4.2",
      "display" : "Non-Small Cell Lung Cancer, Multi-target NGS panel, structural variant (ROS1, RET, EML4-ALK, NTRK1, NTRK1, NTRK3, MET)"
    },
    {
      "code" : "M4.3",
      "display" : "Non-Small Cell Lung Cancer, Multi-target NGS panel, copy number variant (MET)"
    },
    {
      "code" : "M4.4",
      "display" : "Non-Small Cell Lung Cancer, EGFR hotspot Tumor"
    },
    {
      "code" : "M4.5",
      "display" : "Non-Small Cell Lung Cancer, EGFR hotspot ctDNA"
    },
    {
      "code" : "M4.6",
      "display" : "Non-Small Cell Lung Cancer, ROS1 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M4.7",
      "display" : "Non-Small Cell Lung Cancer, RET rearrangement FISH/RT-PC"
    },
    {
      "code" : "M4.8",
      "display" : "Non-Small Cell Lung Cancer, MET copy number FISH"
    },
    {
      "code" : "M42.1",
      "display" : "Alveolar Rhabdomyosarcoma, FOXO1 rearrangement FISH"
    },
    {
      "code" : "M42.2",
      "display" : "Alveolar Rhabdomyosarcoma, PAX3-FOXO1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M42.3",
      "display" : "Alveolar Rhabdomyosarcoma, PAX7-FOXO1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M42.4",
      "display" : "Alveolar Rhabdomyosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M42.5",
      "display" : "Alveolar Rhabdomyosarcoma, Multi-target NGS panel, structural variant (FOXO1, PAX3-FOXO1, PAX7-FOXO1  NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M43.1",
      "display" : "Alveolar Soft Part Sarcoma, TFE3 rearrangement FISH/RT-PCR"
    },
    {
      "code" : "M43.2",
      "display" : "Alveolar Soft Part Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M43.3",
      "display" : "Alveolar Soft Part Sarcoma, Multi-target NGS panel, structural variant (TFE3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M44.1",
      "display" : "Aneurysmal Bone Cyst, USP6 rearrangement FISH"
    },
    {
      "code" : "M44.2",
      "display" : "Aneurysmal Bone Cyst, Multi-target NGS panel, structural variant (USP6)"
    },
    {
      "code" : "M45.1",
      "display" : "Angiomatoid Fibrous Histiocytoma, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M45.2",
      "display" : "Angiomatoid Fibrous Histiocytoma, FUS rearrangement FISH"
    },
    {
      "code" : "M45.3",
      "display" : "Angiomatoid Fibrous Histiocytoma, WGS Germline and Tumor"
    },
    {
      "code" : "M45.4",
      "display" : "Angiomatoid Fibrous Histiocytoma, Multi-target NGS panel, structural variant (EWSR1, FUS, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M46.1",
      "display" : "Chondrosarcoma Conventional Central, Multi-target NGS panel, small variant (IDH1, IDH2)"
    },
    {
      "code" : "M46.2",
      "display" : "Chondrosarcoma Conventional Central, WGS Germline and Tumor"
    },
    {
      "code" : "M46.3",
      "display" : "Chondrosarcoma Conventional Central, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M47.1",
      "display" : "Chondroblastoma, SNP Array"
    },
    {
      "code" : "M47.2",
      "display" : "Chondroblastoma, WGS Germline and Tumor"
    },
    {
      "code" : "M47.3",
      "display" : "Chondroblastoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M48.1",
      "display" : "Clear Cell Sarcoma of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M48.2",
      "display" : "Clear Cell Sarcoma of Soft Tissue, WGS Germline and Tumor"
    },
    {
      "code" : "M48.3",
      "display" : "Clear Cell Sarcoma of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M49.1",
      "display" : "CNS Ewing Sarcoma Family Tumour WithÂ\u00a0CICÂ\u00a0Alteration, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M49.2",
      "display" : "CNS Ewing Sarcoma Family Tumour WithÂ\u00a0CICÂ\u00a0Alteration, WGS Germline and Tumor"
    },
    {
      "code" : "M5.1",
      "display" : "Mesothelioma, CDKN2A copy number FISH"
    },
    {
      "code" : "M5.2",
      "display" : "Mesothelioma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M5.3",
      "display" : "Mesothelioma, Multi-target NGS panel, copy number variant (CDKN2A)"
    },
    {
      "code" : "M50.1",
      "display" : "Dermatofibrosarcoma Protuberans, COL1A1-PDGFB rearrangement FISH"
    },
    {
      "code" : "M50.2",
      "display" : "Dermatofibrosarcoma Protuberans, WGS Germline and Tumor"
    },
    {
      "code" : "M50.3",
      "display" : "Dermatofibrosarcoma Protuberans, Multi-target NGS panel, structural variant (COL1A1-PDGFB, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M51.1",
      "display" : "Desmoid-Type Fibromatosis, Multi-target NGS panel, small variant (APC, CTNNB1)"
    },
    {
      "code" : "M52.1",
      "display" : "Desmoplastic Small Round Cell Tumour, WT1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M52.2",
      "display" : "Desmoplastic Small Round Cell Tumour, WGS Germline and Tumor"
    },
    {
      "code" : "M52.3",
      "display" : "Desmoplastic Small Round Cell Tumour, Multi-target NGS panel, structural variant (WT1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M53.1",
      "display" : "Endometrial Stromal Sarcoma, EPC1-PHF1 rearrangement FISH"
    },
    {
      "code" : "M53.2",
      "display" : "Endometrial Stromal Sarcoma, JAZF1-PHF1 rearrangement FISH"
    },
    {
      "code" : "M53.3",
      "display" : "Endometrial Stromal Sarcoma, JAZF1-SUZ12 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M53.4",
      "display" : "Endometrial Stromal Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M53.5",
      "display" : "Endometrial Stromal Sarcoma, Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NTRK1, NTRK2, NTRK3, ZC3H7B-BCOR)"
    },
    {
      "code" : "M53.7",
      "display" : "Endometrial Stromal Sarcoma, ZC3H7B-BCOR rearrangment FISH/RT-PCR"
    },
    {
      "code" : "M54.1",
      "display" : "Epithelioid Haemangioendothelioma, WWTR1-CAMTA1 RT-PCR"
    },
    {
      "code" : "M54.2",
      "display" : "Epithelioid Haemangioendothelioma, Multi-target NGS panel, structural variant (WWTR1-CAMTA1)"
    },
    {
      "code" : "M55.1",
      "display" : "Ewing Like Sarcoma/PNET, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M55.2",
      "display" : "Ewing Like Sarcoma/PNET, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M55.3",
      "display" : "Ewing Like Sarcoma/PNET, WGS Germline and Tumor"
    },
    {
      "code" : "M56.1",
      "display" : "Ewing Sarcoma of Bone, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M56.2",
      "display" : "Ewing Sarcoma of Bone, WGS Germline and Tumor"
    },
    {
      "code" : "M56.3",
      "display" : "Ewing Sarcoma of Bone, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M57.1",
      "display" : "Ewing-Like Soft-Tissue Sarcoma, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M57.2",
      "display" : "Ewing-Like Soft-Tissue Sarcoma, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M57.3",
      "display" : "Ewing-Like Soft-Tissue Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M58.1",
      "display" : "Extraskeletal Myxoid Chondrosarcoma, NR4A3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M58.2",
      "display" : "Extraskeletal Myxoid Chondrosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M58.3",
      "display" : "Extraskeletal Myxoid Chondrosarcoma, Multi-target NGS panel, structural variant (NR4A3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M59.1",
      "display" : "Fibrous Dysplasia/Myxomas (Mazabraud Syndrome), Multi-target NGS panel, small variant (GNAS)"
    },
    {
      "code" : "M6.1",
      "display" : "Mucoepidermoid Carcinoma, MAML2 rearrangement FISH"
    },
    {
      "code" : "M6.2",
      "display" : "Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M6.3",
      "display" : "Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2)"
    },
    {
      "code" : "M6.5",
      "display" : "Mucoepidermoid Carcinoma, DPYD hotspot"
    },
    {
      "code" : "M60.1",
      "display" : "Giant Cell Tumour of Bone, H3-3B hotspot"
    },
    {
      "code" : "M60.2",
      "display" : "Giant Cell Tumour of Bone, WGS Germline and Tumor"
    },
    {
      "code" : "M60.3",
      "display" : "Giant Cell Tumour of Bone, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M61.1",
      "display" : "High-Grade Neuroepithelial Tumour-Bcor Group, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M61.2",
      "display" : "High-Grade Neuroepithelial Tumour-Bcor Group, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M61.3",
      "display" : "High-Grade Neuroepithelial Tumour-Bcor Group, WGS Germline and Tumor"
    },
    {
      "code" : "M62.1",
      "display" : "Infantile Fibrosarcoma, ETV6-NTRK3 RT-PCR or FISH"
    },
    {
      "code" : "M62.2",
      "display" : "Infantile Fibrosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M62.3",
      "display" : "Infantile Fibrosarcoma, Multi-target NGS panel, structural variant (ETV6-NTRK3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M63.1",
      "display" : "Inflammatory Myofibroblastic Tumour, TPM4-ALK FISH/RT-PCR"
    },
    {
      "code" : "M63.2",
      "display" : "Inflammatory Myofibroblastic Tumour, TPM3-ALK FISH/RT-PCR"
    },
    {
      "code" : "M63.3",
      "display" : "Inflammatory Myofibroblastic Tumour, Multi-target NGS panel, structural variant (ALK, TPM4-ALK, TPM3-ALK, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M63.4",
      "display" : "Inflammatory Myofibroblastic Tumour, WGS Germline and Tumor"
    },
    {
      "code" : "M64.1",
      "display" : "Low Grade Fibromyxoid Sarcoma, FUS rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M64.2",
      "display" : "Low Grade Fibromyxoid Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M64.3",
      "display" : "Low Grade Fibromyxoid Sarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M65.1",
      "display" : "Mesenchymal Chondrosarcoma, HEY1-NCOA2 RT-PCR"
    },
    {
      "code" : "M65.2",
      "display" : "Mesenchymal Chondrosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M65.3",
      "display" : "Mesenchymal Chondrosarcoma, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M66.1",
      "display" : "Myoepithelial Tumours of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M66.2",
      "display" : "Myoepithelial Tumours of Soft Tissue, WGS Germline and Tumor"
    },
    {
      "code" : "M66.3",
      "display" : "Myoepithelial Tumours of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M67.1",
      "display" : "Myxoid/Round Cell Liposarcoma, DDIT3 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M67.2",
      "display" : "Myxoid/Round Cell Liposarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M67.3",
      "display" : "Myxoid/Round Cell Liposarcoma, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M67.4",
      "display" : "Myxoid/Round Cell Lipsarcoma, MDM2 amplification FISH"
    },
    {
      "code" : "M68.1",
      "display" : "Myxoinflammatory Fibroblastic Sarcoma, TGFBR3-OGA FISH/RT-PCR"
    },
    {
      "code" : "M68.2",
      "display" : "Myxoinflammatory Fibroblastic Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M68.3",
      "display" : "Myxoinflammatory Fibroblastic Sarcoma, MDM2 copy number FISH"
    },
    {
      "code" : "M68.4",
      "display" : "Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, structural variant (TGFBR3-OGA, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M68.5",
      "display" : "Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M69.1",
      "display" : "Nodular Fasciitis, USP6 rearrangement FISH"
    },
    {
      "code" : "M69.2",
      "display" : "Nodular Fasciitis, Multi-target NGS panel, structural variant (USP6)"
    },
    {
      "code" : "M7.1",
      "display" : "Melanoma, Adult, Multi-target NGS panel, small variant (BRAF, KIT, NRAS)"
    },
    {
      "code" : "M7.10",
      "display" : "Melanoma, Adult, Copy number variant detection to genomewide resolution"
    },
    {
      "code" : "M7.2",
      "display" : "Melanoma, Adult, BRAF hotspot"
    },
    {
      "code" : "M7.3",
      "display" : "Melanoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M7.5",
      "display" : "Melanoma, Adult, MYB & 6cen (FISH)"
    },
    {
      "code" : "M7.6",
      "display" : "Melanoma, Adult, RREB1 (6p25)"
    },
    {
      "code" : "M7.7",
      "display" : "Melanoma, Adult, CCND1 (11q13)"
    },
    {
      "code" : "M7.8",
      "display" : "Melanoma, Adult, MYC & 8cen"
    },
    {
      "code" : "M7.9",
      "display" : "Melanoma, Adult, CDKN2A & 9cen"
    },
    {
      "code" : "M70.1",
      "display" : "Osteosarcoma, MDM2 copy number FISH"
    },
    {
      "code" : "M70.2",
      "display" : "Osteosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M70.3",
      "display" : "Osteosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M70.4",
      "display" : "Osteosarcoma, Multi-target NGS panel, copy number variant (MDM2)"
    },
    {
      "code" : "M71.1",
      "display" : "Phosphaturic Mesenchymal Tumour, FN1 rearrangement FISH"
    },
    {
      "code" : "M71.2",
      "display" : "Phosphaturic Mesenchymal Tumour, WGS Germline and Tumor"
    },
    {
      "code" : "M71.3",
      "display" : "Phosphaturic Mesenchymal Tumour, Multi-target NGS panel, structural variant (FN1, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M72.1",
      "display" : "Primitive Mesenchymal Myxoid Tumour of Infancy, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M72.2",
      "display" : "Primitive Mesenchymal Myxoid Tumour of Infancy, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M72.3",
      "display" : "Primitive Mesenchymal Myxoid Tumour of Infancy, WGS Germline and Tumor"
    },
    {
      "code" : "M73.1",
      "display" : "Pseudomyogenic Haemangioendothelioma, SERPINE1-FOSB FISH/RT-PCR"
    },
    {
      "code" : "M73.2",
      "display" : "Pseudomyogenic Haemangioendothelioma, WGS Germline and Tumor"
    },
    {
      "code" : "M73.3",
      "display" : "Pseudomyogenic Haemangioendothelioma, Multi-target NGS panel, structural variant (SERPINE1-FOSB, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M74.1",
      "display" : "Radiation Induced Angiosarcoma, MYC copy number FISH"
    },
    {
      "code" : "M74.2",
      "display" : "Radiation Induced Angiosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M74.3",
      "display" : "Radiation Induced Angiosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M74.4",
      "display" : "Radiation Induced Angiosarcoma, Multi-target NGS panel, copy number variant (MYC)"
    },
    {
      "code" : "M75.1",
      "display" : "Round Cell Sarcoma Nos, Multi-target NGS panel, structural variant (BCOR, CIC, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M75.2",
      "display" : "Round Cell Sarcoma Nos, BCOR-CCNB3 RT-PCR"
    },
    {
      "code" : "M75.3",
      "display" : "Round Cell Sarcoma Nos, WGS Germline and Tumor"
    },
    {
      "code" : "M76.1",
      "display" : "Sclerosing Epithelioid Fibrosarcoma, FUS rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M76.2",
      "display" : "Sclerosing Epithelioid Fibrosarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M76.3",
      "display" : "Sclerosing Epithelioid Fibrosarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M77.1",
      "display" : "Synovial Sarcoma, SS18 rearrangement FISH or RT-PCR"
    },
    {
      "code" : "M77.2",
      "display" : "Synovial Sarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M77.3",
      "display" : "Synovial Sarcoma, Multi-target NGS panel, structural variant (SS18, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M78.1",
      "display" : "Undifferentiated Round Cell Sarcoma of Infancy, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M78.2",
      "display" : "Undifferentiated Round Cell Sarcoma of Infancy, WGS Germline and Tumor"
    },
    {
      "code" : "M79.1",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, MDM2 copy number FISH"
    },
    {
      "code" : "M79.2",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, WGS Germline and Tumor"
    },
    {
      "code" : "M79.3",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M79.4",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, copy number variant (MDM2, DDIT3)"
    },
    {
      "code" : "M79.6",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number FISH"
    },
    {
      "code" : "M79.7",
      "display" : "Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number RT-PCR/ddPCR"
    },
    {
      "code" : "M8.1",
      "display" : "Gastrointestinal Stromal Tumour, Multi-target NGS panel, small variant (KIT, PDGFRA)"
    },
    {
      "code" : "M8.2",
      "display" : "Gastrointestinal Stromal Tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M80.1",
      "display" : "Acute Myeloid Leukaemia, WGS Germline and Tumor"
    },
    {
      "code" : "M80.10",
      "display" : "Acute Myeloid Leukaemia, MRD PML-RARA RT-qPCR"
    },
    {
      "code" : "M80.11",
      "display" : "Acute Myeloid Leukaemia, MRD RUNX1-RUNX1T1 RT-qPCR"
    },
    {
      "code" : "M80.12",
      "display" : "Acute Myeloid Leukaemia, MRD CBFB-MYH11 RT-qPCR"
    },
    {
      "code" : "M80.13",
      "display" : "Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR"
    },
    {
      "code" : "M80.14",
      "display" : "Acute Myeloid Leukaemia, MRD other QF-PCR"
    },
    {
      "code" : "M80.15",
      "display" : "Acute Myeloid Leukaemia, BCR-ABL1 TKD NGS"
    },
    {
      "code" : "M80.18",
      "display" : "Acute Myeloid Leukaemia, FLT3 ITD"
    },
    {
      "code" : "M80.19",
      "display" : "Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (GATA1)"
    },
    {
      "code" : "M80.2",
      "display" : "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"
    },
    {
      "code" : "M80.21",
      "display" : "Acute Myeloid Leukaemia, FLT3 TKD hotspot"
    },
    {
      "code" : "M80.22",
      "display" : "Acute Myeloid Leukaemia, NPM1 exon 12 hotspot"
    },
    {
      "code" : "M80.23",
      "display" : "Acute Myeloid Leukaemia, IDH1 hotspot"
    },
    {
      "code" : "M80.24",
      "display" : "Acute Myeloid Leukaemia, IDH2 hotspot"
    },
    {
      "code" : "M80.25",
      "display" : "Acute Myeloid Leukaemia, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M80.26",
      "display" : "Acute Myeloid Leukaemia, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M80.27",
      "display" : "Acute Myeloid Leukaemia, Chr17/Chr17p copy number FISH"
    },
    {
      "code" : "M80.28",
      "display" : "Acute Myeloid Leukaemia, Chr12/Chr12p copy number FISH"
    },
    {
      "code" : "M80.29",
      "display" : "Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA FISH"
    },
    {
      "code" : "M80.3",
      "display" : "Acute Myeloid Leukaemia, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)"
    },
    {
      "code" : "M80.30",
      "display" : "Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH"
    },
    {
      "code" : "M80.31",
      "display" : "Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 FISH"
    },
    {
      "code" : "M80.32",
      "display" : "Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 ( KMT2A) rearrangements FISH"
    },
    {
      "code" : "M80.33",
      "display" : "Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 FISH"
    },
    {
      "code" : "M80.34",
      "display" : "Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM FISH"
    },
    {
      "code" : "M80.35",
      "display" : "Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA FISH"
    },
    {
      "code" : "M80.36",
      "display" : "Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH"
    },
    {
      "code" : "M80.37",
      "display" : "Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 FISH"
    },
    {
      "code" : "M80.38",
      "display" : "Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 FISH"
    },
    {
      "code" : "M80.39",
      "display" : "Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 FISH"
    },
    {
      "code" : "M80.40",
      "display" : "Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH"
    },
    {
      "code" : "M80.41",
      "display" : "Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA RT-PCR"
    },
    {
      "code" : "M80.42",
      "display" : "Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR"
    },
    {
      "code" : "M80.43",
      "display" : "Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR"
    },
    {
      "code" : "M80.44",
      "display" : "Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 (KMT2A) rearrangements RT-PCR"
    },
    {
      "code" : "M80.45",
      "display" : "Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 RT-PCR"
    },
    {
      "code" : "M80.46",
      "display" : "Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM RT-PCR"
    },
    {
      "code" : "M80.47",
      "display" : "Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA RT-PCR"
    },
    {
      "code" : "M80.48",
      "display" : "Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 RT-PCR"
    },
    {
      "code" : "M80.49",
      "display" : "Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR"
    },
    {
      "code" : "M80.5",
      "display" : "Acute Myeloid Leukaemia, Other: See tests M80.25-M80.40 for individual specified FISH targets."
    },
    {
      "code" : "M80.50",
      "display" : "Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR"
    },
    {
      "code" : "M80.51",
      "display" : "Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR"
    },
    {
      "code" : "M80.52",
      "display" : "Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR"
    },
    {
      "code" : "M80.53",
      "display" : "Acute Myeloid Leukaemia, Multi-target NGS panel, copy number variant (Monosomal karyotype, del5/del5q, del7/del7q, del17/del17p, del12/del12p)"
    },
    {
      "code" : "M80.54",
      "display" : "Acute Myeloid Leukaemia, NUP98 rearrangement FISH"
    },
    {
      "code" : "M80.55",
      "display" : "Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare"
    },
    {
      "code" : "M80.56",
      "display" : "Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR rare"
    },
    {
      "code" : "M80.57",
      "display" : "Acute Myeloid Leukaemia, WGS Tumour First"
    },
    {
      "code" : "M80.58",
      "display" : "Acute Myeloid Leukaemia, WGS Follow-up Germline"
    },
    {
      "code" : "M80.7",
      "display" : "Acute Myeloid Leukaemia, Other RT-PCR: See tests M80.41-80.52 for individual specified RT-PCR targets."
    },
    {
      "code" : "M80.8",
      "display" : "Acute Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of  Complex karyotype)"
    },
    {
      "code" : "M80.9",
      "display" : "Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR"
    },
    {
      "code" : "M81.1",
      "display" : "Transient Abnormal Myelopoiesis, Multi-target NGS panel, small variant (GATA1)"
    },
    {
      "code" : "M82.1",
      "display" : "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)"
    },
    {
      "code" : "M82.10",
      "display" : "Myelodysplasia, Chr13/Chr13q copy number FISH"
    },
    {
      "code" : "M82.11",
      "display" : "Myelodysplasia, Chr11q copy number FISH"
    },
    {
      "code" : "M82.12",
      "display" : "Myelodysplasia, Chr12p copy number FISH, t(12p) rearrangement FISH"
    },
    {
      "code" : "M82.13",
      "display" : "Myelodysplasia, Chr9q copy number FISH"
    },
    {
      "code" : "M82.14",
      "display" : "Myelodysplasia, Chr17/Chr17p copy number FISH"
    },
    {
      "code" : "M82.15",
      "display" : "Myelodysplasia, idic(X)(q13) FISH"
    },
    {
      "code" : "M82.16",
      "display" : "Myelodysplasia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p & idic(X)(q13);-Y; del 20q; +8; +19,del(3q)"
    },
    {
      "code" : "M82.17",
      "display" : "Myelodysplasia, Multi-target NGS panel, structural variant (t(12p), t(17p);inv(3)/t(3q)/del(3q)"
    },
    {
      "code" : "M82.18",
      "display" : "Myelodysplasia, ChrY copy number FISH"
    },
    {
      "code" : "M82.19",
      "display" : "Myelodysplasia, Chr20/20q copy number FISH"
    },
    {
      "code" : "M82.2",
      "display" : "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 & idic(X)(q13)); -Y; del 20q; +8; +19,(inv(3)/t(3q)/del(3q))"
    },
    {
      "code" : "M82.20",
      "display" : "Myelodysplasia, Chr8 copy number FISH"
    },
    {
      "code" : "M82.21",
      "display" : "Myelodysplasia, Chr19 copy number FISH"
    },
    {
      "code" : "M82.22",
      "display" : "Myelodysplasia, inv(3)/t(3q)/del(3q)"
    },
    {
      "code" : "M82.23",
      "display" : "Myelodysplasia, WGS Tumour First"
    },
    {
      "code" : "M82.24",
      "display" : "Myelodysplasia, WGS Follow-up Germline"
    },
    {
      "code" : "M82.4",
      "display" : "Myelodysplasia, FISH copy number and rearrangement Other: See tests M82.7 -M82.22 for individual specified FISH targets."
    },
    {
      "code" : "M82.6",
      "display" : "Myelodysplasia, WGS Germline and Tumor"
    },
    {
      "code" : "M82.7",
      "display" : "Myelodysplasia, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M82.8",
      "display" : "Myelodysplasia, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M82.9",
      "display" : "Myelodysplasia, i(17q)/t(17p) FISH"
    },
    {
      "code" : "M83.1",
      "display" : "Aplastic Anaemia, Karyotype (Genomewide)"
    },
    {
      "code" : "M83.3",
      "display" : "Aplastic Anaemia, FISH copy number and rearrangement"
    },
    {
      "code" : "M83.4",
      "display" : "Aplastic Anaemia, WGS Germline and Tumor"
    },
    {
      "code" : "M83.5",
      "display" : "Aplastic Anaemia, WGS Tumour First"
    },
    {
      "code" : "M83.6",
      "display" : "Aplastic Anaemia, WGS Follow-up Germline"
    },
    {
      "code" : "M84.1",
      "display" : "Chronic Myeloid Leukaemia, BCR-ABL1 multiplex"
    },
    {
      "code" : "M84.11",
      "display" : "Chronic Myeloid Leukaemia, WGS Germline and Tumor"
    },
    {
      "code" : "M84.12",
      "display" : "Chronic Myeloid Leukaemia, Chr8 copy number FISH"
    },
    {
      "code" : "M84.13",
      "display" : "Chronic Myeloid Leukaemia, Chr19 copy number FISH"
    },
    {
      "code" : "M84.14",
      "display" : "Chronic Myeloid Leukaemia, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M84.15",
      "display" : "Chronic Myeloid Leukaemia, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M84.16",
      "display" : "Chronic Myeloid Leukaemia, i(17q) FISH"
    },
    {
      "code" : "M84.17",
      "display" : "Chronic Myeloid Leukaemia, Chr12p copy number FISH"
    },
    {
      "code" : "M84.18",
      "display" : "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)"
    },
    {
      "code" : "M84.19",
      "display" : "Chronic Myeloid Leukaemia, Inv(3) MECOM FISH"
    },
    {
      "code" : "M84.2",
      "display" : "Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR"
    },
    {
      "code" : "M84.20",
      "display" : "Chronic Myeloid Leukaemia, 11q23 (KMT2A) rearrangement FISH"
    },
    {
      "code" : "M84.21",
      "display" : "Chronic Myeloid Leukaemia, Multi-target NGS panel, copy number variant (trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-)"
    },
    {
      "code" : "M84.22",
      "display" : "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)"
    },
    {
      "code" : "M84.23",
      "display" : "Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare"
    },
    {
      "code" : "M84.24",
      "display" : "Chronic Myeloid Leukaemia, WGS Tumour First"
    },
    {
      "code" : "M84.25",
      "display" : "Chronic Myeloid Leukaemia, WGS Follow-up Germline"
    },
    {
      "code" : "M84.3",
      "display" : "Chronic Myeloid Leukaemia, BCR-ABL1 FISH"
    },
    {
      "code" : "M84.4",
      "display" : "Chronic Myeloid Leukaemia, Karyotype (To include detection of trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-& 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)"
    },
    {
      "code" : "M84.6",
      "display" : "Chronic Myeloid Leukaemia, FISH copy number and rearrangement Other: See tests M84.12 M84.20 for individual specified FISH targets."
    },
    {
      "code" : "M84.8",
      "display" : "Chronic Myeloid Leukaemia, BCR-ABL1 TKD NGS"
    },
    {
      "code" : "M85.1",
      "display" : "Myeloproliferative Neoplasm, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)"
    },
    {
      "code" : "M85.10",
      "display" : "Myeloproliferative Neoplasm, PCM1-JAK2 FISH/RT-PCR"
    },
    {
      "code" : "M85.11",
      "display" : "Myeloproliferative Neoplasm, BCR-ABL1 multiplex"
    },
    {
      "code" : "M85.12",
      "display" : "Myeloproliferative Neoplasm, Other RT-PCR"
    },
    {
      "code" : "M85.13",
      "display" : "Myeloproliferative Neoplasm, WGS Germline and Tumor"
    },
    {
      "code" : "M85.14",
      "display" : "Myeloproliferative Neoplasm, JAK2 V617F hotspot"
    },
    {
      "code" : "M85.15",
      "display" : "Myeloproliferative Neoplasm, JAK2  exon 12 hotspot"
    },
    {
      "code" : "M85.16",
      "display" : "Myeloproliferative Neoplasm, CALR exon 9 hotspot"
    },
    {
      "code" : "M85.17",
      "display" : "Myeloproliferative Neoplasm, MPL exon 10 hotspot"
    },
    {
      "code" : "M85.19",
      "display" : "Myeloproliferative Neoplasm, Chr8 copy number FISH"
    },
    {
      "code" : "M85.2",
      "display" : "Myeloproliferative Neoplasm, Multi-target NGS panel, small variant"
    },
    {
      "code" : "M85.20",
      "display" : "Myeloproliferative Neoplasm, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M85.21",
      "display" : "Myeloproliferative Neoplasm, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M85.22",
      "display" : "Myeloproliferative Neoplasm, i(17q) FISH"
    },
    {
      "code" : "M85.23",
      "display" : "Myeloproliferative Neoplasm, Chr12p copy number FISH"
    },
    {
      "code" : "M85.24",
      "display" : "Myeloproliferative Neoplasm, t(9;22)(q34;q11) BCR-ABL1 FISH"
    },
    {
      "code" : "M85.25",
      "display" : "Myeloproliferative Neoplasm, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)"
    },
    {
      "code" : "M85.26",
      "display" : "Myeloproliferative Neoplasm, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)"
    },
    {
      "code" : "M85.27",
      "display" : "Myeloproliferative Neoplasm, FGFR1 rearrangement FISH"
    },
    {
      "code" : "M85.28",
      "display" : "Myeloproliferative Neoplasm, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)"
    },
    {
      "code" : "M85.29",
      "display" : "Myeloproliferative Neoplasm, inv(3)/t(3;3) FISH"
    },
    {
      "code" : "M85.3",
      "display" : "Myeloproliferative Neoplasm, Karyotype (To include detection of complex karyotype)"
    },
    {
      "code" : "M85.30",
      "display" : "Myeloproliferative Neoplasm, 11q23 rearrangement FISH"
    },
    {
      "code" : "M85.31",
      "display" : "Myeloproliferative Neoplasm, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)"
    },
    {
      "code" : "M85.32",
      "display" : "Myeloproliferative Neoplasm, FLT3 rearragement FISH"
    },
    {
      "code" : "M85.33",
      "display" : "Myeloproliferative Neoplasm, RET rearrangement FISH"
    },
    {
      "code" : "M85.34",
      "display" : "Myeloproliferative Neoplasm, NTRK3 rearrangement FISH"
    },
    {
      "code" : "M85.35",
      "display" : "Myeloproliferative Neoplasm, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M85.36",
      "display" : "Myeloproliferative Neoplasm, Multi-target NGS panel, copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)"
    },
    {
      "code" : "M85.37",
      "display" : "Myeloproliferative Neoplasm, WGS Tumour First"
    },
    {
      "code" : "M85.38",
      "display" : "Myeloproliferative Neoplasm, WGS Follow-up Germline"
    },
    {
      "code" : "M85.5",
      "display" : "Myeloproliferative Neoplasm, FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets."
    },
    {
      "code" : "M85.7",
      "display" : "Myeloproliferative Neoplasm, FIP1L1-PDGFRA (4q12) FISH/RT-PCR"
    },
    {
      "code" : "M85.8",
      "display" : "Myeloproliferative Neoplasm, FIP1L1-PDGFRA RT-qPCR"
    },
    {
      "code" : "M85.9",
      "display" : "Myeloproliferative Neoplasm, ETV6-PDGFRB FISH/RT-PCR"
    },
    {
      "code" : "M86.1",
      "display" : "Systemic Mastocytosis, Multi-target NGS panel, small variant (KIT)"
    },
    {
      "code" : "M86.2",
      "display" : "Systemic Mastocytosis, KIT D816 QF-PCR"
    },
    {
      "code" : "M86.3",
      "display" : "Systemic Mastocytosis, WGS Germline and Tumor"
    },
    {
      "code" : "M86.4",
      "display" : "Systemic Mastocytosis, WGS Tumour First"
    },
    {
      "code" : "M86.5",
      "display" : "Systemic Mastocytosis, WGS Follow-up Germline"
    },
    {
      "code" : "M87.1",
      "display" : "Chronic Neutrophilic Leukaemia, Multi-target NGS panel, small variant (CSF3R)"
    },
    {
      "code" : "M88.1",
      "display" : "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant (PTPN11, KRAS, NRAS, NF1, CBL)"
    },
    {
      "code" : "M88.10",
      "display" : "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, trisomy 8)"
    },
    {
      "code" : "M88.11",
      "display" : "Juvenile Myelomonocytic Leukaemia, WGS Tumour First"
    },
    {
      "code" : "M88.12",
      "display" : "Juvenile Myelomonocytic Leukaemia, WGS Follow-up Germline"
    },
    {
      "code" : "M88.2",
      "display" : "Juvenile Myelomonocytic Leukaemia, WGS Germline and Tumor"
    },
    {
      "code" : "M88.3",
      "display" : "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant"
    },
    {
      "code" : "M88.4",
      "display" : "Juvenile Myelomonocytic Leukaemia, Karyotype"
    },
    {
      "code" : "M88.5",
      "display" : "Juvenile Myelomonocytic Leukaemia, FISH copy number and rearrangement Other: See tests M88.7-M88.9 for individual specified FISH targets."
    },
    {
      "code" : "M88.7",
      "display" : "Juvenile Myelomonocytic Leukaemia, Chr8 copy number FISH"
    },
    {
      "code" : "M88.8",
      "display" : "Juvenile Myelomonocytic Leukaemia, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M88.9",
      "display" : "Juvenile Myelomonocytic Leukaemia, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M89.1",
      "display" : "Acute Leukaemia Other, WGS Germline and Tumor"
    },
    {
      "code" : "M89.10",
      "display" : "Acute Leukaemia Other, MRD PML-RARA RT-qPCR"
    },
    {
      "code" : "M89.100",
      "display" : "Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR"
    },
    {
      "code" : "M89.101",
      "display" : "Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD RT-PCR"
    },
    {
      "code" : "M89.102",
      "display" : "Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 RT-PCR"
    },
    {
      "code" : "M89.103",
      "display" : "Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR"
    },
    {
      "code" : "M89.104",
      "display" : "Acute Leukaemia Other, Multi-target NGS panel, copy number variant"
    },
    {
      "code" : "M89.105",
      "display" : "Acute Leukaemia Other, NUP98 rearrangement FISH"
    },
    {
      "code" : "M89.106",
      "display" : "Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR rare"
    },
    {
      "code" : "M89.107",
      "display" : "Acute Leukaemia Other, MRD NPM1 RT-qPCR rare"
    },
    {
      "code" : "M89.108",
      "display" : "Acute Leukaemia Other, WGS Tumour First"
    },
    {
      "code" : "M89.109",
      "display" : "Acute Leukaemia Other, WGS Follow-up Germline"
    },
    {
      "code" : "M89.11",
      "display" : "Acute Leukaemia Other, MRD RUNX1-RUNX1T1 RT-qPCR"
    },
    {
      "code" : "M89.12",
      "display" : "Acute Leukaemia Other, MRD CBFB-MYH11 RT-qPCR"
    },
    {
      "code" : "M89.13",
      "display" : "Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR"
    },
    {
      "code" : "M89.14",
      "display" : "Acute Leukaemia Other, MRD other QF-PCR"
    },
    {
      "code" : "M89.15",
      "display" : "Acute Leukaemia Other, MRD target identification (Ig/TCR gene rearrangement by PCR & sequencing with MRD workup via QF-PCR)"
    },
    {
      "code" : "M89.16",
      "display" : "Acute Leukaemia Other, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR )"
    },
    {
      "code" : "M89.17",
      "display" : "Acute Leukaemia Other, BCR-ABL1 TKD NGS"
    },
    {
      "code" : "M89.2",
      "display" : "Acute Leukaemia Other, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)"
    },
    {
      "code" : "M89.20",
      "display" : "Acute Leukaemia Other, FLT3 TKD hotspot"
    },
    {
      "code" : "M89.21",
      "display" : "Acute Leukaemia Other, NPM1 exon 12 hotspot"
    },
    {
      "code" : "M89.22",
      "display" : "Acute Leukaemia Other, IDH1 hotspot"
    },
    {
      "code" : "M89.23",
      "display" : "Acute Leukaemia Other, IDH2 hotspot"
    },
    {
      "code" : "M89.24",
      "display" : "Acute Leukaemia Other, Chr5/Chr5q copy number FISH"
    },
    {
      "code" : "M89.25",
      "display" : "Acute Leukaemia Other, Chr7/Chr7q copy number FISH"
    },
    {
      "code" : "M89.26",
      "display" : "Acute Leukaemia Other, Chr17/Chr17p copy number FISH"
    },
    {
      "code" : "M89.27",
      "display" : "Acute Leukaemia Other, Chr12/Chr12p copy number FISH"
    },
    {
      "code" : "M89.28",
      "display" : "Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA FISH"
    },
    {
      "code" : "M89.29",
      "display" : "Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH"
    },
    {
      "code" : "M89.3",
      "display" : "Acute Leukaemia Other, FISH copy number and rearrangement other"
    },
    {
      "code" : "M89.30",
      "display" : "Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 FISH"
    },
    {
      "code" : "M89.31",
      "display" : "Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 ( KMT2A) rearrangements FISH"
    },
    {
      "code" : "M89.32",
      "display" : "Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 FISH"
    },
    {
      "code" : "M89.33",
      "display" : "Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM FISH"
    },
    {
      "code" : "M89.34",
      "display" : "Acute Leukaemia Other, t(1;22)(p13;q13) RBM15-MRTFA FISH"
    },
    {
      "code" : "M89.35",
      "display" : "Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 FISH"
    },
    {
      "code" : "M89.36",
      "display" : "Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 FISH"
    },
    {
      "code" : "M89.37",
      "display" : "Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 FISH"
    },
    {
      "code" : "M89.38",
      "display" : "Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 FISH"
    },
    {
      "code" : "M89.39",
      "display" : "Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH"
    },
    {
      "code" : "M89.4",
      "display" : "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)"
    },
    {
      "code" : "M89.40",
      "display" : "Acute Leukaemia Other, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)"
    },
    {
      "code" : "M89.41",
      "display" : "Acute Leukaemia Other, del(1)(p33p33) FISH"
    },
    {
      "code" : "M89.42",
      "display" : "Acute Leukaemia Other, iAMP21 FISH"
    },
    {
      "code" : "M89.5",
      "display" : "Acute Leukaemia Other, FLT3 ITD"
    },
    {
      "code" : "M89.52",
      "display" : "Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 FISH"
    },
    {
      "code" : "M89.53",
      "display" : "Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 FISH"
    },
    {
      "code" : "M89.54",
      "display" : "Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF FISH"
    },
    {
      "code" : "M89.55",
      "display" : "Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 FISH"
    },
    {
      "code" : "M89.56",
      "display" : "Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH"
    },
    {
      "code" : "M89.57",
      "display" : "Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN FISH"
    },
    {
      "code" : "M89.58",
      "display" : "Acute Leukaemia Other,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH"
    },
    {
      "code" : "M89.59",
      "display" : "Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL FISH"
    },
    {
      "code" : "M89.6",
      "display" : "Acute Leukaemia Other, Other RT-PCR"
    },
    {
      "code" : "M89.60",
      "display" : "Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 FISH"
    },
    {
      "code" : "M89.61",
      "display" : "Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 FISH"
    },
    {
      "code" : "M89.62",
      "display" : "Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 FISH"
    },
    {
      "code" : "M89.63",
      "display" : "Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD FISH"
    },
    {
      "code" : "M89.64",
      "display" : "Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 FISH"
    },
    {
      "code" : "M89.65",
      "display" : "Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH"
    },
    {
      "code" : "M89.66",
      "display" : "Acute Leukaemia Other, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)"
    },
    {
      "code" : "M89.67",
      "display" : "Acute Leukaemia Other, TLX1 rearrangement FISH (other than TLX1-TRD & TRB-TLX1 see M91.48 & M91.49)"
    },
    {
      "code" : "M89.68",
      "display" : "Acute Leukaemia Other, PDGFRA rearrangement FISH"
    },
    {
      "code" : "M89.69",
      "display" : "Acute Leukaemia Other, PDGFRB rearrangement FISH"
    },
    {
      "code" : "M89.7",
      "display" : "Acute Leukaemia Other, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M89.70",
      "display" : "Acute Leukaemia Other, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)"
    },
    {
      "code" : "M89.71",
      "display" : "Acute Leukaemia Other, JAK2 rearrangement FISH"
    },
    {
      "code" : "M89.72",
      "display" : "Acute Leukaemia Other, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)"
    },
    {
      "code" : "M89.73",
      "display" : "Acute Leukaemia Other, ABL2 rearrangement FISH"
    },
    {
      "code" : "M89.74",
      "display" : "Acute Leukaemia Other, CSF1R rearrangement FISH"
    },
    {
      "code" : "M89.75",
      "display" : "Acute Leukaemia Other, 14q32 (IGH) rearrangement FISH"
    },
    {
      "code" : "M89.76",
      "display" : "Acute Leukaemia Other, CRLF2 rearrangement FISH"
    },
    {
      "code" : "M89.77",
      "display" : "Acute Leukaemia Other, EPOR rearrangement FISH"
    },
    {
      "code" : "M89.78",
      "display" : "Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA RT-PCR"
    },
    {
      "code" : "M89.79",
      "display" : "Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR"
    },
    {
      "code" : "M89.8",
      "display" : "Acute Leukaemia Other, BCR-ABL1 multiplex"
    },
    {
      "code" : "M89.80",
      "display" : "Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR"
    },
    {
      "code" : "M89.81",
      "display" : "Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 (KMT2A) rearrangements RT-PCR"
    },
    {
      "code" : "M89.82",
      "display" : "Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 RT-PCR"
    },
    {
      "code" : "M89.83",
      "display" : "Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM RT-PCR"
    },
    {
      "code" : "M89.84",
      "display" : "Acute Leukaemia Other, t(1;22)(p13;q13)  RBM15-MRTFA RT-PCR"
    },
    {
      "code" : "M89.85",
      "display" : "Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 RT-PCR"
    },
    {
      "code" : "M89.86",
      "display" : "Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR"
    },
    {
      "code" : "M89.87",
      "display" : "Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR"
    },
    {
      "code" : "M89.88",
      "display" : "Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR"
    },
    {
      "code" : "M89.89",
      "display" : "Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR"
    },
    {
      "code" : "M89.9",
      "display" : "Acute Leukaemia Other, MRD NPM1 RT-qPCR"
    },
    {
      "code" : "M89.90",
      "display" : "Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR"
    },
    {
      "code" : "M89.91",
      "display" : "Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 RT-PCR"
    },
    {
      "code" : "M89.92",
      "display" : "Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF RT-PCR"
    },
    {
      "code" : "M89.93",
      "display" : "Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR"
    },
    {
      "code" : "M89.94",
      "display" : "Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR"
    },
    {
      "code" : "M89.95",
      "display" : "Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR"
    },
    {
      "code" : "M89.96",
      "display" : "Acute Leukaemia Other, t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR"
    },
    {
      "code" : "M89.97",
      "display" : "Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR"
    },
    {
      "code" : "M89.98",
      "display" : "Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 RT-PCR"
    },
    {
      "code" : "M89.99",
      "display" : "Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 RT-PCR"
    },
    {
      "code" : "M9.1",
      "display" : "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, small variant (BRAF, KRAS, NRAS, HRAS, TERT promoter)"
    },
    {
      "code" : "M9.2",
      "display" : "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M9.3",
      "display" : "Thyroid Papillary Carcinoma, Adult, RET rearrangement FISH/RT-PC"
    },
    {
      "code" : "M9.4",
      "display" : "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)"
    },
    {
      "code" : "M9.6",
      "display" : "Thyroid Papillary Carcinoma, Adult, TERT promoter hotspot"
    },
    {
      "code" : "M90.1",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Germline and Tumor"
    },
    {
      "code" : "M90.2",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, Karyotype (Genomewide)"
    },
    {
      "code" : "M90.3",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, FISH copy number and rearrangement"
    },
    {
      "code" : "M90.4",
      "display" : "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)"
    },
    {
      "code" : "M90.5",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, FLT3 ITD"
    },
    {
      "code" : "M90.6",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Tumour First"
    },
    {
      "code" : "M90.7",
      "display" : "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Follow-up Germline"
    },
    {
      "code" : "M91.1",
      "display" : "Acute Lymphoblastic Leukaemia, WGS Germline and Tumor"
    },
    {
      "code" : "M91.10",
      "display" : "Acute Lymphoblastic Leukaemia, BCR-ABL1 FISH"
    },
    {
      "code" : "M91.11",
      "display" : "Acute Lymphoblastic Leukaemia, BCR-ABL1 TKD NGS"
    },
    {
      "code" : "M91.14",
      "display" : "Acute Lymphoblastic Leukaemia, MRD ALL RT-qPCR"
    },
    {
      "code" : "M91.15",
      "display" : "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, small variant (ETV6, NOTCH1, FBXW7, TP53, PTEN, KRAS, NRAS, HRAS)"
    },
    {
      "code" : "M91.2",
      "display" : "Acute Lymphoblastic Leukaemia, Karyotype (To include detection of complex karyotype, hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc)"
    },
    {
      "code" : "M91.22",
      "display" : "Acute Lymphoblastic Leukaemia, MRD target identification (Ig/TCR gene rearrangement by PCR & sequencing with MRD workup via QF-PCR)"
    },
    {
      "code" : "M91.23",
      "display" : "Acute Lymphoblastic Leukaemia, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR)"
    },
    {
      "code" : "M91.24",
      "display" : "Acute Lymphoblastic Leukaemia, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)"
    },
    {
      "code" : "M91.25",
      "display" : "Acute Lymphoblastic Leukaemia, del(1)(p33p33) FISH"
    },
    {
      "code" : "M91.26",
      "display" : "Acute Lymphoblastic Leukaemia, iAMP21 FISH"
    },
    {
      "code" : "M91.36",
      "display" : "Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 FISH"
    },
    {
      "code" : "M91.37",
      "display" : "Acute Lymphoblastic Leukaemia,  t(1;19)(q23;p13) TCF3-PBX1 FISH"
    },
    {
      "code" : "M91.38",
      "display" : "Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF FISH"
    },
    {
      "code" : "M91.39",
      "display" : "Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 FISH"
    },
    {
      "code" : "M91.4",
      "display" : "Acute Lymphoblastic Leukaemia, FISH copy number and rearrangement other: See tests M91.24-M91.62 for individual specified FISH targets."
    },
    {
      "code" : "M91.40",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH"
    },
    {
      "code" : "M91.41",
      "display" : "Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN FISH"
    },
    {
      "code" : "M91.42",
      "display" : "Acute Lymphoblastic Leukaemia,  t(9;11)(p21;q23) KMT2A-MLLT3 FISH"
    },
    {
      "code" : "M91.43",
      "display" : "Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH"
    },
    {
      "code" : "M91.44",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL FISH"
    },
    {
      "code" : "M91.45",
      "display" : "Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 FISH"
    },
    {
      "code" : "M91.46",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 FISH"
    },
    {
      "code" : "M91.47",
      "display" : "Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 FISH"
    },
    {
      "code" : "M91.48",
      "display" : "Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD FISH"
    },
    {
      "code" : "M91.49",
      "display" : "Acute Lymphoblastic Leukaemia, t(7;10)(q34;q24) TRB-TLX1 FISH"
    },
    {
      "code" : "M91.50",
      "display" : "Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH"
    },
    {
      "code" : "M91.51",
      "display" : "Acute Lymphoblastic Leukaemia, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)"
    },
    {
      "code" : "M91.52",
      "display" : "Acute Lymphoblastic Leukaemia, TLX1 rearrangement FISH (other than TLX1-TRD & TRB-TLX1 see M91.48 & M91.49)"
    },
    {
      "code" : "M91.53",
      "display" : "Acute Lymphoblastic Leukaemia, PDGFRA rearrangement FISH"
    },
    {
      "code" : "M91.54",
      "display" : "Acute Lymphoblastic Leukaemia, PDGFRB rearrangement FISH"
    },
    {
      "code" : "M91.55",
      "display" : "Acute Lymphoblastic Leukaemia, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)"
    },
    {
      "code" : "M91.56",
      "display" : "Acute Lymphoblastic Leukaemia, JAK2 rearrangement FISH"
    },
    {
      "code" : "M91.57",
      "display" : "Acute Lymphoblastic Leukaemia, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)"
    },
    {
      "code" : "M91.58",
      "display" : "Acute Lymphoblastic Leukaemia, ABL2 rearrangement FISH"
    },
    {
      "code" : "M91.59",
      "display" : "Acute Lymphoblastic Leukaemia, CSF1R rearrangement FISH"
    },
    {
      "code" : "M91.6",
      "display" : "Acute Lymphoblastic Leukaemia, Other RT-PCR: See tests M91-63-M91.77 for individual specified RT-PCR targets"
    },
    {
      "code" : "M91.60",
      "display" : "Acute Lymphoblastic Leukaemia, 14q32(IGH) rearrangement FISH"
    },
    {
      "code" : "M91.61",
      "display" : "Acute Lymphoblastic Leukaemia, CRLF2 rearrangement FISH"
    },
    {
      "code" : "M91.62",
      "display" : "Acute Lymphoblastic Leukaemia, EPOR rearrangement FISH"
    },
    {
      "code" : "M91.63",
      "display" : "Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR"
    },
    {
      "code" : "M91.64",
      "display" : "Acute Lymphoblastic Leukaemia, t(1;19)(q23;p13) TCF3-PBX1 RT-PCR"
    },
    {
      "code" : "M91.65",
      "display" : "Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF RT-PCR"
    },
    {
      "code" : "M91.66",
      "display" : "Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR"
    },
    {
      "code" : "M91.67",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR"
    },
    {
      "code" : "M91.68",
      "display" : "Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR"
    },
    {
      "code" : "M91.69",
      "display" : "Acute Lymphoblastic Leukaemia, t(9;11)(p21;q23) KMT2A-MLLT3 RT-PCR"
    },
    {
      "code" : "M91.7",
      "display" : "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, structural variant"
    },
    {
      "code" : "M91.70",
      "display" : "Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR"
    },
    {
      "code" : "M91.71",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR"
    },
    {
      "code" : "M91.72",
      "display" : "Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 RT-PCR"
    },
    {
      "code" : "M91.73",
      "display" : "Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 RT-PCR"
    },
    {
      "code" : "M91.74",
      "display" : "Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR"
    },
    {
      "code" : "M91.75",
      "display" : "Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD RT-PCR"
    },
    {
      "code" : "M91.76",
      "display" : "Acute Lymphoblastic Leukaemia, t(7;10)q34;q24) TRB-TLX1 RT-PCR"
    },
    {
      "code" : "M91.77",
      "display" : "Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR"
    },
    {
      "code" : "M91.78",
      "display" : "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, copy number variant (to include hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc.)"
    },
    {
      "code" : "M91.79",
      "display" : "Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR rare"
    },
    {
      "code" : "M91.8",
      "display" : "Acute Lymphoblastic Leukaemia, BCR-ABL1 multiplex"
    },
    {
      "code" : "M91.80",
      "display" : "Acute Lymphoblastic Leukaemia, TPMT"
    },
    {
      "code" : "M91.81",
      "display" : "Acute Lymphoblastic Leukaemia, NUDT15"
    },
    {
      "code" : "M91.82",
      "display" : "Acute Lymphoblastic Leukaemia, WGS Tumour First"
    },
    {
      "code" : "M91.83",
      "display" : "Acute Lymphoblastic Leukaemia, WGS Follow-up Germline"
    },
    {
      "code" : "M91.84",
      "display" : "Acute Lymphoblastic Leukaemia, MYC rearrangement FISH"
    },
    {
      "code" : "M91.85",
      "display" : "Acute Lymphoblastic Leukaemia, t(8;14)(q34;q32) IGH-MYC FISH"
    },
    {
      "code" : "M91.86",
      "display" : "Acute Lymphoblastic Leukaemia, t(2;8)(p12;q24) IGK-MYC FISH"
    },
    {
      "code" : "M91.87",
      "display" : "Acute Lymphoblastic Leukaemia, t(8;22)(q24;q11) IGL-MYC FISH"
    },
    {
      "code" : "M91.88",
      "display" : "Acute Lymphoblastic Leukaemia, BCL2 rearrangement FISH"
    },
    {
      "code" : "M91.89",
      "display" : "Acute Lymphoblastic Leukaemia, BCL6 rearrangement FISH"
    },
    {
      "code" : "M91.9",
      "display" : "Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR"
    },
    {
      "code" : "M92.1",
      "display" : "Plasma Cell Dyscrasia, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF, TP53, DIS3, TENT5C, IRF4)"
    },
    {
      "code" : "M92.10",
      "display" : "Plasma Cell Dyscrasia, del(1p) copy number FISH"
    },
    {
      "code" : "M92.11",
      "display" : "Plasma Cell Dyscrasia, gain(1q) copy number FISH"
    },
    {
      "code" : "M92.12",
      "display" : "Plasma Cell Dyscrasia, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M92.13",
      "display" : "Plasma Cell Dyscrasia, Multi-target NGS panel (To include hyperdiploidy, del(1p), gain(1q), del17p)"
    },
    {
      "code" : "M92.14",
      "display" : "Plasma Cell Dyscrasia, MYC rearrangement FISH"
    },
    {
      "code" : "M92.2",
      "display" : "Plasma Cell Dyscrasia, t(4;14) IGH-FGFR3FISH/RT-PCR"
    },
    {
      "code" : "M92.3",
      "display" : "Plasma Cell Dyscrasia, t(6;14)  IGH-CCND3 FISH/RT-PCR"
    },
    {
      "code" : "M92.4",
      "display" : "Plasma Cell Dyscrasia, t(11;14)(q13;q32)  IGH-CCND1 FISH/RT-PCR"
    },
    {
      "code" : "M92.5",
      "display" : "Plasma Cell Dyscrasia, t(14;16) IGH-MAF FISH/RT-PCR"
    },
    {
      "code" : "M92.6",
      "display" : "Plasma Cell Dyscrasia, t(14;20)  IGH-MAFB FISH/RT-PCR"
    },
    {
      "code" : "M92.7",
      "display" : "Plasma Cell Dyscrasia, Multi-target NGS panel, structural variant (To include IGH-FGFR3, IGH-CCND3, IGH-CCND1, IGH-MAF, IGH-MAFB, MYC rearrangements)"
    },
    {
      "code" : "M92.8",
      "display" : "Plasma Cell Dyscrasia, IGH rearrangement FISH"
    },
    {
      "code" : "M92.9",
      "display" : "Plasma Cell Dyscrasia, Hyperdiploidy copy number FISH"
    },
    {
      "code" : "M93.3",
      "display" : "Lymphoma, WGS Germline and Tumor"
    },
    {
      "code" : "M93.4",
      "display" : "Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M93.5",
      "display" : "Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M93.6",
      "display" : "Lymphoma, Multi-target NGS panel-small variant (BTK, PLCG2, RAS, MAP2K1, BCL2)"
    },
    {
      "code" : "M94.1",
      "display" : "Chronic Lymphocytic Leukaemia, Multi-target NGS panel, small variant (TP53,BTK, PLCG2, BCL2)"
    },
    {
      "code" : "M94.10",
      "display" : "Chronic Lymphocytic Leukaemia, chromosome 12 copy number FISH"
    },
    {
      "code" : "M94.2",
      "display" : "Chronic Lymphocytic Leukaemia, Multi-target NGS panel, copy number variant (TP53,ATM, DLEU2/7, RB1, trisomy 12)"
    },
    {
      "code" : "M94.4",
      "display" : "Chronic Lymphocytic Leukaemia, del(17p) TP53 copy number FISH"
    },
    {
      "code" : "M94.5",
      "display" : "Chronic Lymphocytic Leukaemia, Ig gene (heavy & light chain) rearrangement & hypermutation detection multiplex seq"
    },
    {
      "code" : "M94.6",
      "display" : "Chronic Lymphocytic Leukaemia, Ig gene (heavy & light chain) rearrangement & hypermutation detection NGS"
    },
    {
      "code" : "M94.7",
      "display" : "Chronic Lymphocytic Leukaemia, TP53 seq"
    },
    {
      "code" : "M94.8",
      "display" : "Chronic Lymphocytic Leukaemia, 11q copy number FISH"
    },
    {
      "code" : "M94.9",
      "display" : "Chronic Lymphocytic Leukaemia, 13q copy number FISH"
    },
    {
      "code" : "M95.1",
      "display" : "B Cell Non-Hodgkin Lymphoma, Ig gene (heavy & light chain) rearrangement & hypermutation detection multiplex seq"
    },
    {
      "code" : "M95.10",
      "display" : "B Cell Non-Hodgkin Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M95.11",
      "display" : "B Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M95.12",
      "display" : "B cell Non-Hodgkin Lymphoma, MYD88 (L265P) hotspot"
    },
    {
      "code" : "M95.2",
      "display" : "B Cell Non-Hodgkin Lymphoma, Ig gene (heavy & light chain) rearrangement & hypermutation detection NGS"
    },
    {
      "code" : "M95.3",
      "display" : "B Cell Non-Hodgkin Lymphoma, Ig rearrangement FISH"
    },
    {
      "code" : "M95.4",
      "display" : "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (EZH2)"
    },
    {
      "code" : "M95.5",
      "display" : "B Cell Non-Hodgkin Lymphoma, EZH2 copy number FISH"
    },
    {
      "code" : "M95.6",
      "display" : "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (BTK, PLCG2)"
    },
    {
      "code" : "M95.7",
      "display" : "B Cell Non-Hodgkin Lymphoma, WGS Germline and Tumor"
    },
    {
      "code" : "M95.8",
      "display" : "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (Ig)"
    },
    {
      "code" : "M95.9",
      "display" : "B Cell Non-Hodgkin Lymphoma, Mutli-target NGS panel, copy number (EZH2)"
    },
    {
      "code" : "M96.1",
      "display" : "Burkitt Lymphoma, MYC rearrangement FISH"
    },
    {
      "code" : "M96.10",
      "display" : "Burkitt Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M96.2",
      "display" : "Burkitt Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR"
    },
    {
      "code" : "M96.3",
      "display" : "Burkitt Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR"
    },
    {
      "code" : "M96.4",
      "display" : "Burkitt Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR"
    },
    {
      "code" : "M96.5",
      "display" : "Burkitt Lymphoma, BCL2 rearrangement FISH"
    },
    {
      "code" : "M96.6",
      "display" : "Burkitt Lymphoma, BCL6 rearrangement FISH"
    },
    {
      "code" : "M96.7",
      "display" : "Burkitt Lymphoma, WGS Germline and Tumor"
    },
    {
      "code" : "M96.8",
      "display" : "Burkitt Lymphoma, Multi-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, other rearrangements of MYC,  BCL2, BCL6)"
    },
    {
      "code" : "M96.9",
      "display" : "Burkitt Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M97.1",
      "display" : "Burkitt Like Lymphoma with 11q Abnormalities, 11q copy number FISH"
    },
    {
      "code" : "M97.2",
      "display" : "Burkitt Like Lymphoma with 11q Abnormalities, WGS Germline and Tumor"
    },
    {
      "code" : "M97.3",
      "display" : "Burkitt Like Lymphoma with 11q Abnormalities, Multi-target NGS panel, copy number variant (11q)"
    },
    {
      "code" : "M97.4",
      "display" : "Burkitt Like Lymphoma with 11q Abnormalities, WGS Tumour First"
    },
    {
      "code" : "M97.5",
      "display" : "Burkitt Like Lymphoma with 11q Abnormalities, WGS Follow-up Germline"
    },
    {
      "code" : "M98.1",
      "display" : "Large B Cell Like Lymphoma with IRF4 Rearrangement, IRF4 rearrangement FISH"
    },
    {
      "code" : "M98.2",
      "display" : "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Germline and Tumor"
    },
    {
      "code" : "M98.3",
      "display" : "Large B Cell Like Lymphoma with IRF4 Rearrangement, Multi-target NGS panel, structural variant (IRF4)"
    },
    {
      "code" : "M98.4",
      "display" : "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Tumour First"
    },
    {
      "code" : "M98.5",
      "display" : "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Follow-up Germline"
    },
    {
      "code" : "M99.1",
      "display" : "High Grade Lymphoma, MYC rearrangement FISH"
    },
    {
      "code" : "M99.10",
      "display" : "High Grade Lymphoma, WGS Tumour First"
    },
    {
      "code" : "M99.11",
      "display" : "High Grade Lymphoma, WGS Follow-up Germline"
    },
    {
      "code" : "M99.2",
      "display" : "High Grade Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR"
    },
    {
      "code" : "M99.3",
      "display" : "High Grade Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR"
    },
    {
      "code" : "M99.4",
      "display" : "High Grade Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR"
    },
    {
      "code" : "M99.5",
      "display" : "High Grade Lymphoma, BCL2 rearrangement FISH"
    },
    {
      "code" : "M99.6",
      "display" : "High Grade Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR"
    },
    {
      "code" : "M99.7",
      "display" : "High Grade Lymphoma, BCL6 rearrangement FISH"
    },
    {
      "code" : "M99.8",
      "display" : "High Grade Lymphoma, WGS Germline and Tumor"
    },
    {
      "code" : "M99.9",
      "display" : "High Grade Lymphoma, Mutli-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, IGH-BCL2, other rearrangements of MYC, BCL2, BCL6)"
    },
    {
      "code" : "R100.3",
      "display" : "Rare syndromic craniosynostosis or isolated multisuture synostosis (WGS)"
    },
    {
      "code" : "R101.1",
      "display" : "Ehlers Danlos syndrome with a likely monogenic cause (WES or Medium Panel)"
    },
    {
      "code" : "R102.1",
      "display" : "Osteogenesis imperfecta (WES or Medium Panel)"
    },
    {
      "code" : "R104.3",
      "display" : "Skeletal dysplasia (WGS)"
    },
    {
      "code" : "R104.4",
      "display" : "Skeletal dysplasia (Small Panel)"
    },
    {
      "code" : "R105.1",
      "display" : "MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ common variant newborn screening follow up (Targeted variant testing)"
    },
    {
      "code" : "R106.1",
      "display" : "Alstrom syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R107.1",
      "display" : "Bardet-Biedl syndrome (WES or Large Panel)"
    },
    {
      "code" : "R109.3",
      "display" : "Childhood onset leukodystrophy (WGS)"
    },
    {
      "code" : "R110.1",
      "display" : "Segmental overgrowth disorders Deep sequencing (Small panel)"
    },
    {
      "code" : "R111.1",
      "display" : "X-inactivation testing (X-inactivation testing)"
    },
    {
      "code" : "R112.1",
      "display" : "Factor II deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R115.1",
      "display" : "Factor V deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R115.2",
      "display" : "Factor V deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R116.1",
      "display" : "Factor VII deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R116.2",
      "display" : "Factor VII deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R117.1",
      "display" : "Factor VIII deficiency (Targeted mutation testing)"
    },
    {
      "code" : "R117.2",
      "display" : "Factor VIII deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R117.3",
      "display" : "Factor VIII deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R118.1",
      "display" : "Factor IX deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R118.2",
      "display" : "Factor IX deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R119.1",
      "display" : "Factor X deficiency (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R119.2",
      "display" : "Factor X deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R120.1",
      "display" : "Factor XI deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R120.2",
      "display" : "Factor XI deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R121.1",
      "display" : "von Willebrand disease (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R121.2",
      "display" : "von Willebrand disease (MLPA or equivalent)"
    },
    {
      "code" : "R122.1",
      "display" : "Factor XIII deficiency (Small panel)"
    },
    {
      "code" : "R123.1",
      "display" : "Combined vitamin K-dependent clotting factor deficiency (Small panel)"
    },
    {
      "code" : "R124.1",
      "display" : "Combined factor V and VIII deficiency (Small panel)"
    },
    {
      "code" : "R125.1",
      "display" : "Thoracic aortic aneurysm or dissection (WES or Medium Panel)"
    },
    {
      "code" : "R127.1",
      "display" : "Long QT syndrome (Small panel)"
    },
    {
      "code" : "R128.1",
      "display" : "Brugada syndrome and cardiac sodium channel disease (Small panel)"
    },
    {
      "code" : "R129.1",
      "display" : "Catecholaminergic polymorphic VT (Small panel)"
    },
    {
      "code" : "R130.1",
      "display" : "Short QT syndrome (Small panel)"
    },
    {
      "code" : "R131.1",
      "display" : "Hypertrophic cardiomyopathy (WES or Medium Panel)"
    },
    {
      "code" : "R132.1",
      "display" : "Dilated and Arrhythmogenic cardiomyopathy (WES or Medium Panel)"
    },
    {
      "code" : "R133.1",
      "display" : "Arrhythmogenic right ventricular cardiomyopathy (Small panel)"
    },
    {
      "code" : "R134.1",
      "display" : "Familial hypercholesterolaemia (Small panel)"
    },
    {
      "code" : "R135.2",
      "display" : "Paediatric or syndromic cardiomyopathy (WGS)"
    },
    {
      "code" : "R135.3",
      "display" : "Paediatric or syndromic cardiomyopathy (WES)"
    },
    {
      "code" : "R136.1",
      "display" : "Primary lymphoedema (WES or Medium Panel)"
    },
    {
      "code" : "R137.1",
      "display" : "Congenital heart disease microarray (Microarray)"
    },
    {
      "code" : "R138.1",
      "display" : "Sudden unexplained death or survivors of a cardiac event (WES or Medium Panel)"
    },
    {
      "code" : "R139.1",
      "display" : "Laterality disorders and isomerism (WES or Medium Panel)"
    },
    {
      "code" : "R14.1",
      "display" : "Acutely unwell children with a likely monogenic disorder (WGS)"
    },
    {
      "code" : "R140.1",
      "display" : "Elastin-related phenotypes (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R141.1",
      "display" : "Monogenic diabetes (WES or Medium Panel)"
    },
    {
      "code" : "R142.1",
      "display" : "Glucokinase-related fasting hyperglycaemia (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R143.1",
      "display" : "Neonatal diabetes (Small panel)"
    },
    {
      "code" : "R143.3",
      "display" : "Neonatal diabetes (Methylation testing)"
    },
    {
      "code" : "R143.4",
      "display" : "Neonatal diabetes (WGS)"
    },
    {
      "code" : "R144.1",
      "display" : "Congenital hyperinsulinism (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R144.2",
      "display" : "Congenital hyperinsulinism (Small panel)"
    },
    {
      "code" : "R145.1",
      "display" : "Congenital hypothyroidism (WES or Medium panel)"
    },
    {
      "code" : "R146.1",
      "display" : "Differences in sex development (Microarray)"
    },
    {
      "code" : "R146.2",
      "display" : "Differences of sex development (WES or Medium Panel)"
    },
    {
      "code" : "R148.1",
      "display" : "Hypogonadotropic hypogonadism (Small panel)"
    },
    {
      "code" : "R149.1",
      "display" : "Severe early-onset obesity (WES or Medium panel)"
    },
    {
      "code" : "R15.4",
      "display" : "Primary immunodeficiency or monogenic inflammatory bowel disease (WGS)"
    },
    {
      "code" : "R15.5",
      "display" : "Primary immunodeficiency or monogenic inflammatory bowel disease (WES)"
    },
    {
      "code" : "R150.1",
      "display" : "Congenital adrenal hypoplasia (Small panel)"
    },
    {
      "code" : "R151.1",
      "display" : "Familial hyperparathyroidism or Hypocalciuric hypercalcaemia (Small panel)"
    },
    {
      "code" : "R153.1",
      "display" : "Familial hypoparathyroidism (Small panel)"
    },
    {
      "code" : "R154.1",
      "display" : "Hypophosphataemia or rickets (Small panel)"
    },
    {
      "code" : "R155.1",
      "display" : "Autoimmune Polyendocrine Syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R156.1",
      "display" : "Carney complex (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R157.1",
      "display" : "IPEX Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R158.1",
      "display" : "Severe insulin resistance and lipodystrophy syndromes (Small panel)"
    },
    {
      "code" : "R159.1",
      "display" : "Pituitary hormone deficiency (WES or Medium panel)"
    },
    {
      "code" : "R16.1",
      "display" : "Severe combined immunodeficiency with adenosine deaminase deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R160.1",
      "display" : "Primary pigmented nodular adrenocortical disease (Small panel)"
    },
    {
      "code" : "R162.1",
      "display" : "Familial tumoral calcinosis (Small panel)"
    },
    {
      "code" : "R163.1",
      "display" : "Ectodermal dysplasia (WES or Medium panel)"
    },
    {
      "code" : "R164.1",
      "display" : "Epidermolysis bullosa and congenital skin fragility (WES or Medium Panel)"
    },
    {
      "code" : "R165.1",
      "display" : "Ichthyosis and erythrokeratoderma (WES or Medium panel)"
    },
    {
      "code" : "R166.1",
      "display" : "Palmoplantar keratodermas (WES or Medium panel)"
    },
    {
      "code" : "R167.1",
      "display" : "Autosomal recessive primary hypertrophic osteoarthropathy (Small panel)"
    },
    {
      "code" : "R168.1",
      "display" : "Non-acute porphyrias (Small panel)"
    },
    {
      "code" : "R169.1",
      "display" : "Acute intermittent porphyria (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R17.1",
      "display" : "Lymphoproliferative syndrome with absent SAP expression (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R170.1",
      "display" : "Variegate porphyria (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R171.1",
      "display" : "Cholestasis (WES or Medium Panel)"
    },
    {
      "code" : "R172.1",
      "display" : "Wilson disease (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R173.1",
      "display" : "Polycystic liver disease (WES or Small Panel)"
    },
    {
      "code" : "R175.1",
      "display" : "Pancreatitis (Small panel)"
    },
    {
      "code" : "R176.1",
      "display" : "Gilbert syndrome (Targeted mutation testing)"
    },
    {
      "code" : "R18.1",
      "display" : "Haemophagocytic syndrome with absent XIAP expression (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R180.1",
      "display" : "Congenital adrenal hyperplasia diagnostic test (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R180.2",
      "display" : "Congenital adrenal hyperplasia diagnostic test (MLPA or equivalent)"
    },
    {
      "code" : "R181.1",
      "display" : "Congenital adrenal hyperplasia carrier testing (Targeted mutation testing)"
    },
    {
      "code" : "R181.2",
      "display" : "Congenital adrenal hyperplasia carrier testing (MLPA or equivalent)"
    },
    {
      "code" : "R182.1",
      "display" : "Hyperthyroidism (Small panel)"
    },
    {
      "code" : "R183.1",
      "display" : "Glucocorticoid-remediable aldosteronism (GRA) (Targeted mutation testing)"
    },
    {
      "code" : "R184.1",
      "display" : "Cystic fibrosis diagnostic test (Targeted variant testing)"
    },
    {
      "code" : "R184.2",
      "display" : "Cystic fibrosis diagnostic test (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R184.3",
      "display" : "Cystic fibrosis diagnostic test (MLPA or equivalent)"
    },
    {
      "code" : "R185.1",
      "display" : "Cystic fibrosis carrier testing (Targeted mutation testing)"
    },
    {
      "code" : "R186.1",
      "display" : "Hereditary haemorrhagic telangiectasia (Small panel)"
    },
    {
      "code" : "R188.1",
      "display" : "Pulmonary arterial hypertension (Small panel)"
    },
    {
      "code" : "R189.1",
      "display" : "Respiratory ciliopathies including non-CF bronchiectasis (WES or Medium Panel)"
    },
    {
      "code" : "R19.1",
      "display" : "Autoimmune lymphoproliferative syndrome with defective apoptosis (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R190.1",
      "display" : "Pneumothorax familial (Small panel)"
    },
    {
      "code" : "R191.1",
      "display" : "Alpha-1-antitrypsin deficiency (Targeted variant testing)"
    },
    {
      "code" : "R193.4",
      "display" : "Cystic renal disease (WGS)"
    },
    {
      "code" : "R194.1",
      "display" : "Haematuria (Small panel)"
    },
    {
      "code" : "R195.3",
      "display" : "Proteinuric renal disease (WGS)"
    },
    {
      "code" : "R196.1",
      "display" : "CFHR5 nephropathy (MLPA or equivalent)"
    },
    {
      "code" : "R197.1",
      "display" : "Membranoproliferative glomerulonephritis including C3 glomerulopathy (Small panel)"
    },
    {
      "code" : "R197.2",
      "display" : "Membranoproliferative glomerulonephritis including C3 glomerulopathy (MLPA or equivalent)"
    },
    {
      "code" : "R198.1",
      "display" : "Renal tubulopathies (WES or Medium Panel)"
    },
    {
      "code" : "R199.1",
      "display" : "Congenital anomalies of the kidney and urinary tract familial (Microarray)"
    },
    {
      "code" : "R20.1",
      "display" : "Wiskott-Aldrich syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R201.1",
      "display" : "Atypical haemolytic uraemic syndrome (Small panel)"
    },
    {
      "code" : "R202.1",
      "display" : "Tubulointerstitial kidney disease (Small panel)"
    },
    {
      "code" : "R204.1",
      "display" : "Hereditary Systemic Amyloidosis  (Small panel)"
    },
    {
      "code" : "R207.1",
      "display" : "Inherited ovarian cancer (without breast cancer) (Small panel)"
    },
    {
      "code" : "R208.1",
      "display" : "Inherited breast cancer and ovarian cancer (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R21.1",
      "display" : "Fetal anomalies with a likely genetic cause (Common aneuploidy testing)"
    },
    {
      "code" : "R21.2",
      "display" : "Fetal anomalies with a likely genetic cause (WES or Large Panel)"
    },
    {
      "code" : "R21.3",
      "display" : "Fetal anomalies with a likely genetic cause (Microarray)"
    },
    {
      "code" : "R210.2",
      "display" : "Inherited MMR deficiency (Lynch syndrome) (Small panel)"
    },
    {
      "code" : "R210.4",
      "display" : "Inherited MMR deficiency (Lynch syndrome) (Methylation testing)"
    },
    {
      "code" : "R210.6",
      "display" : "Inherited MMR deficiency (Lynch syndrome) (MLPA or equivalent)"
    },
    {
      "code" : "R211.1",
      "display" : "Inherited polyposis and early onset colorectal cancer germline testing (Small panel)"
    },
    {
      "code" : "R211.3",
      "display" : "Inherited polyposis and early onset colorectal cancer germline testing (MLPA or equivalent)"
    },
    {
      "code" : "R212.1",
      "display" : "Peutz Jeghers Syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R213.1",
      "display" : "PTEN Hamartoma Tumor Syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R214.1",
      "display" : "Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome (Small panel)"
    },
    {
      "code" : "R215.1",
      "display" : "Hereditary diffuse gastric cancer (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R216.1",
      "display" : "Li Fraumeni Syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R217.1",
      "display" : "Endocrine neoplasia (Small panel)"
    },
    {
      "code" : "R218.1",
      "display" : "Multiple endocrine neoplasia type 2 (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R219.1",
      "display" : "Retinoblastoma (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R219.2",
      "display" : "Retinoblastoma (MLPA or equivalent)"
    },
    {
      "code" : "R22.1",
      "display" : "Fetus with a likely chromosomal abnormality (Common aneuploidy testing)"
    },
    {
      "code" : "R22.2",
      "display" : "Fetus with a likely chromosomal abnormality (Microarray)"
    },
    {
      "code" : "R221.1",
      "display" : "Familial tumours of the nervous system (Small panel)"
    },
    {
      "code" : "R221.2",
      "display" : "Familial tumours of the nervous system (MLPA or equivalent)"
    },
    {
      "code" : "R222.1",
      "display" : "Neurofibromatosis type 1 (Small panel)"
    },
    {
      "code" : "R222.2",
      "display" : "Neurofibromatosis type 1 (MLPA or equivalent)"
    },
    {
      "code" : "R223.1",
      "display" : "Inherited phaeochromocytoma and paraganglioma excluding NF1 (Small panel)"
    },
    {
      "code" : "R224.1",
      "display" : "Inherited renal cancer (Small panel)"
    },
    {
      "code" : "R225.1",
      "display" : "Von Hippel Lindau syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R226.1",
      "display" : "Inherited parathyroid cancer (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R227.1",
      "display" : "Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (Small panel)"
    },
    {
      "code" : "R227.2",
      "display" : "Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (DNA repair defect testing)"
    },
    {
      "code" : "R228.1",
      "display" : "Tuberous sclerosis (Small panel)"
    },
    {
      "code" : "R228.2",
      "display" : "Tuberous sclerosis (MLPA or equivalent)"
    },
    {
      "code" : "R228.3",
      "display" : "Tuberous sclerosis (Small panel deep sequencing)"
    },
    {
      "code" : "R229.1",
      "display" : "Confirmed Fanconi anaemia or Bloom syndrome variant testing (Small panel)"
    },
    {
      "code" : "R23.1",
      "display" : "Apert syndrome (Targeted variant testing)"
    },
    {
      "code" : "R230.1",
      "display" : "Multiple monogenic benign skin tumours (Small panel)"
    },
    {
      "code" : "R231.2",
      "display" : "Neuronal ceroid lipofuscinosis (Small panel)"
    },
    {
      "code" : "R232.1",
      "display" : "Haemophagocytic syndrome with absent perforin expression (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R233.1",
      "display" : "Agammaglobulinaemia with absent BTK expression (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R234.1",
      "display" : "Severe combined immunodeficiency with PNP deficiency (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R235.1",
      "display" : "SCID with features of gamma chain deficiency (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R236.1",
      "display" : "Pigmentary skin disorders (WES or Large panel)"
    },
    {
      "code" : "R236.2",
      "display" : "Pigmentary skin disorders (MLPA or equivalent)"
    },
    {
      "code" : "R237.1",
      "display" : "Cutaneous photosensitivity with a likely genetic cause (Small panel)"
    },
    {
      "code" : "R239.1",
      "display" : "Incontinentia pigmenti (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R239.2",
      "display" : "Incontinentia pigmenti (Targeted variant testing)"
    },
    {
      "code" : "R24.1",
      "display" : "Achondroplasia (Targeted variant testing)"
    },
    {
      "code" : "R240.1",
      "display" : "Diagnostic testing for known variant(s) (Targeted variant testing)"
    },
    {
      "code" : "R242.1",
      "display" : "Predictive testing for known familial variant(s) (Targeted variant testing)"
    },
    {
      "code" : "R244.1",
      "display" : "Carrier testing for known familial variant(s) (Targeted variant testing)"
    },
    {
      "code" : "R246.1",
      "display" : "Carrier testing at population risk for partners of known carriers of nationally agreed autosomal recessive disorders (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R249.1",
      "display" : "NIPD using paternal exclusion testing for very rare conditions where familial variant is known (NIPD)"
    },
    {
      "code" : "R25.1",
      "display" : "Thanatophoric dysplasia (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R250.1",
      "display" : "NIPD for congenital adrenal hyperplasia CYP21A2 haplotype testing (NIPD)"
    },
    {
      "code" : "R251.1",
      "display" : "Non-invasive prenatal sexing (NIPD)"
    },
    {
      "code" : "R252.1",
      "display" : "SMA carrier testing at population risk for partners of known carriers (MLPA or equivalent)"
    },
    {
      "code" : "R253.1",
      "display" : "Cystic fibrosis newborn screening follow-up (Targeted mutation testing)"
    },
    {
      "code" : "R254.1",
      "display" : "Familial melanoma (Small panel)"
    },
    {
      "code" : "R255.1",
      "display" : "Epidermodysplasia verruciformis (Small panel)"
    },
    {
      "code" : "R256.1",
      "display" : "Nephrocalcinosis or nephrolithiasis (WES or Medium Panel)"
    },
    {
      "code" : "R257.2",
      "display" : "Unexplained young onset end-stage renal disease (WGS)"
    },
    {
      "code" : "R257.3",
      "display" : "Unexplained young onset end-stage renal disease (WES)"
    },
    {
      "code" : "R258.1",
      "display" : "Cytopenia Fanconi breakage testing indicated (DNA repair defect testing)"
    },
    {
      "code" : "R258.2",
      "display" : "Cytopenia Fanconi breakage testing indicated (WES or Medium Panel)"
    },
    {
      "code" : "R259.1",
      "display" : "Nijmegen breakage syndrome (DNA repair defect testing)"
    },
    {
      "code" : "R259.2",
      "display" : "Nijmegen breakage syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R26.1",
      "display" : "Likely common aneuploidy (Common aneuploidy testing)"
    },
    {
      "code" : "R260.1",
      "display" : "Fanconi anaemia or Bloom syndrome chromosome breakage testing (DNA repair defect testing)"
    },
    {
      "code" : "R262.1",
      "display" : "Corneal dystrophy (WES or Medium panel)"
    },
    {
      "code" : "R263.1",
      "display" : "Confirmation of uniparental disomy (UPD testing)"
    },
    {
      "code" : "R264.1",
      "display" : "Identity testing (Identity testing)"
    },
    {
      "code" : "R265.1",
      "display" : "Chromosomal mosaicism â€“ karyotype / Targeted Chromosome Analysis (Karyotype)"
    },
    {
      "code" : "R268.1",
      "display" : "Kagami-Ogata syndrome paternal uniparental disomy 14 (Methylation testing)"
    },
    {
      "code" : "R27.3,",
      "display" : "Paediatric disorders (WGS)"
    },
    {
      "code" : "R270.1",
      "display" : "Smith-Lemli-Opitz syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R270.2",
      "display" : "Smith-Lemli-Opitz syndrome (MLPA or equivalent)"
    },
    {
      "code" : "R271.1",
      "display" : "Neuronal ceroid lipofuscinosis type 2 (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R272.1",
      "display" : "Gaucher disease (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R273.1",
      "display" : "Glycogen storage disease V (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R274.1",
      "display" : "Glycogen storage disease (WES or Medium Panel)"
    },
    {
      "code" : "R275.1",
      "display" : "Glutaric acidaemia I newborn screening follow up (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R276.1",
      "display" : "Lysosomal storage disorder (WES or Medium Panel)"
    },
    {
      "code" : "R277.1",
      "display" : "Mucopolysaccharidosis type IH/S (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R278.1",
      "display" : "Mucopolysaccharidosis type II (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R278.2",
      "display" : "Mucopolysaccharidosis type II (Targeted variant testing)"
    },
    {
      "code" : "R279.1",
      "display" : "Isovaleric acidaemia newborn screening follow up (Targeted variant testing)"
    },
    {
      "code" : "R28.1",
      "display" : "Congenital malformation and dysmorphism syndromes â€“ microarray only (Microarray)"
    },
    {
      "code" : "R280.1",
      "display" : "Krabbe disease â€“ GALC deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R280.2",
      "display" : "Krabbe disease â€“ GALC deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R281.1",
      "display" : "Krabbe disease Saposin A deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R282.1",
      "display" : "Niemann-Pick disease type A or B (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R283.1",
      "display" : "Phenylketonuria (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R285.1",
      "display" : "Sandhoff disease (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R286.1",
      "display" : "Tay-Sachs disease (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R287.1",
      "display" : "Mucopolysaccharidosis type IVA (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R288.1",
      "display" : "GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R289.1",
      "display" : "Mucolipidosis II and III Alpha/Beta (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R290.1",
      "display" : "Mucopolysaccharidosis type VI (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R291.1",
      "display" : "Mucopolysaccharidosis type IIIA (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R292.1",
      "display" : "Mucopolysaccharidosis type IIIB (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R293.1",
      "display" : "Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Small Panel)"
    },
    {
      "code" : "R293.2",
      "display" : "Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Methylation testing)"
    },
    {
      "code" : "R294.1",
      "display" : "Ataxia telangiectasia DNA repair testing (DNA repair defect testing)"
    },
    {
      "code" : "R295.1",
      "display" : "Ataxia telangiectasia variant testing (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R296.1",
      "display" : "RNA analysis of variants (Other)"
    },
    {
      "code" : "R298.1",
      "display" : "Possible structural or mosaic chromosomal abnormality FISH (FISH)"
    },
    {
      "code" : "R299.1",
      "display" : "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Other)"
    },
    {
      "code" : "R299.2",
      "display" : "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Heteroplasmy assessment mitochondrial genome)"
    },
    {
      "code" : "R299.3",
      "display" : "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Breakpoint mapping mitochondrial genome)"
    },
    {
      "code" : "R300.1",
      "display" : "Possible mitochondrial disorder whole mitochondrial genome sequencing (Other)"
    },
    {
      "code" : "R301.1",
      "display" : "Possible mitochondrial disorder, mitochondrial DNA depletion testing (Other)"
    },
    {
      "code" : "R304.1",
      "display" : "NIPD for cystic fibrosis haplotype testing (NIPD)"
    },
    {
      "code" : "R305.1",
      "display" : "NIPD for cystic fibrosis variant testing (NIPD)"
    },
    {
      "code" : "R306.1",
      "display" : "NIPD for Apert syndrome variant testing (NIPD)"
    },
    {
      "code" : "R307.1",
      "display" : "NIPD for Crouzon syndrome with acanthosis nigricans variant testing (NIPD)"
    },
    {
      "code" : "R308.1",
      "display" : "NIPD for FGFR2-related craniosynostosis syndromes variant testing (NIPD)"
    },
    {
      "code" : "R309.1",
      "display" : "NIPD for FGFR3-related skeletal dysplasias variant testing (NIPD)"
    },
    {
      "code" : "R31.3",
      "display" : "Bilateral congenital or childhood onset cataracts (WGS)"
    },
    {
      "code" : "R310.1",
      "display" : "NIPD for Duchenne and Becker muscular dystrophy haplotype testing (NIPD)"
    },
    {
      "code" : "R311.1",
      "display" : "NIPD for spinal muscular atrophy variant testing (NIPD)"
    },
    {
      "code" : "R312.1",
      "display" : "Parental sequencing for lethal autosomal recessive disorders (WES or Large penel)"
    },
    {
      "code" : "R313.1",
      "display" : "Neutropaenia consistent with ELANE variants (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R314.1",
      "display" : "Ambiguous genitalia (Common aneuploidy testing)"
    },
    {
      "code" : "R314.2",
      "display" : "Ambiguous genitalia (Karyotype)"
    },
    {
      "code" : "R315.1",
      "display" : "POLG-related disorder (Targeted mutation testing)"
    },
    {
      "code" : "R315.2",
      "display" : "POLG-related disorder (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R316.1",
      "display" : "Pyruvate dehydrogenase (PDH) deficiency (WES or Medium panel)"
    },
    {
      "code" : "R317.1",
      "display" : "Mitochondrial liver disease, including transient infantile liver failure (Small panel)"
    },
    {
      "code" : "R318.1",
      "display" : "Recurrent miscarriage with products of conception available for testing (Common aneuploidy testing)"
    },
    {
      "code" : "R318.2",
      "display" : "Recurrent miscarriage with products of conception available for testing (Microarray)"
    },
    {
      "code" : "R319.1",
      "display" : "Calcium-sensing receptor phenotypes (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R32.2",
      "display" : "Retinal disorders (WGS)"
    },
    {
      "code" : "R320.1",
      "display" : "Invasive prenatal diagnosis requiring fetal sexing (Common aneuploidy testing)"
    },
    {
      "code" : "R321.1",
      "display" : "Maternal cell contamination testing (Identity testing)"
    },
    {
      "code" : "R322.1",
      "display" : "Skin fibroblasts to be cultured and stored (Other)"
    },
    {
      "code" : "R323.1",
      "display" : "Sitosterolaemia (Small panel)"
    },
    {
      "code" : "R324.1",
      "display" : "Familial Chylomicronaemia Syndrome (FCS) (Small panel)"
    },
    {
      "code" : "R325.1",
      "display" : "Lysosomal acid lipase deficiency (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R326.1",
      "display" : "Vascular skin disorders (WES or Medium panel)"
    },
    {
      "code" : "R327.1",
      "display" : "Mosaic skin disorders deep sequencing (Medium panel)"
    },
    {
      "code" : "R328.1",
      "display" : "Progressive cardiac conduction disease (WES or Small Panel)"
    },
    {
      "code" : "R329.1",
      "display" : "Familial dysalbuminaemic hyperthyroxinaemia (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R33.1",
      "display" : "Possible X-linked retinitis pigmentosa (Targeted variant testing)"
    },
    {
      "code" : "R330.1",
      "display" : "Alveolar capillary dysplasia with misalignment of pulmonary veins (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R331.1",
      "display" : "Intestinal failure or congenital diarrhoea (WES or Small Panel)"
    },
    {
      "code" : "R332.1",
      "display" : "Rare genetic inflammatory skin disorders (WES or Medium panel)"
    },
    {
      "code" : "R333.1",
      "display" : "Central congenital hypoventilation (STR testing)"
    },
    {
      "code" : "R333.2",
      "display" : "Central congenital hypoventilation (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R334.1",
      "display" : "Cystinosis (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R335.1",
      "display" : "Fabry disease (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R335.2",
      "display" : "Fabry disease (MLPA or equivalent)"
    },
    {
      "code" : "R336.1",
      "display" : "Cerebral vascular malformations (WES or Medium Panel)"
    },
    {
      "code" : "R337.1",
      "display" : "CADASIL (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R338.1",
      "display" : "Monitoring for G(M)CSF escape variants (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R340.1",
      "display" : "Amelogenesis imperfecta (WES or Medium panel)"
    },
    {
      "code" : "R341.1",
      "display" : "Hereditary angioedema types I and II (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R343.1",
      "display" : "Chromosomal mosaicism microarray (Microarray)"
    },
    {
      "code" : "R344.1",
      "display" : "Primary hyperaldosteronism KCNJ5 (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R345.1",
      "display" : "Facioscapulohumeral muscular dystrophy extended testing (Methylation testing)"
    },
    {
      "code" : "R345.2",
      "display" : "Facioscapulohumeral muscular dystrophy extended testing (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R345.3",
      "display" : "Facioscapulohumeral muscular dystrophy extended testing (Other)"
    },
    {
      "code" : "R346.1",
      "display" : "DNA to be stored (Other)"
    },
    {
      "code" : "R347.1",
      "display" : "Inherited predisposition to acute myeloid leukaemia (AML) (Small panel)"
    },
    {
      "code" : "R350.1",
      "display" : "MERRF syndrome (Targeted mutation testing)"
    },
    {
      "code" : "R351.1",
      "display" : "NARP syndrome or maternally inherited Leigh syndrome (Small panel)"
    },
    {
      "code" : "R351.2",
      "display" : "NARP syndrome or maternally inherited Leigh syndrome (Targeted mutation testing)"
    },
    {
      "code" : "R352.1",
      "display" : "Mitochondrial DNA maintenance disorder (WES or Medium Panel)"
    },
    {
      "code" : "R353.1",
      "display" : "Mitochondrial disorder with complex I deficiency (WES or Medium Panel)"
    },
    {
      "code" : "R354.1",
      "display" : "Mitochondrial disorder with complex II deficiency (WES or Small Panel)"
    },
    {
      "code" : "R355.1",
      "display" : "Mitochondrial disorder with complex III deficiency (WES or Small Panel)"
    },
    {
      "code" : "R356.1",
      "display" : "Mitochondrial disorder with complex IV deficiency (WES or Small Panel)"
    },
    {
      "code" : "R357.1",
      "display" : "Mitochondrial disorder with complex V deficiency (WES or Small Panel)"
    },
    {
      "code" : "R36.2,",
      "display" : "structural eye disease (WGS)"
    },
    {
      "code" : "R361.1",
      "display" : "Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (Small panel)"
    },
    {
      "code" : "R361.2",
      "display" : "Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (MLPA or equivalent)"
    },
    {
      "code" : "R363.1",
      "display" : "Inherited predisposition to GIST (Small panel)"
    },
    {
      "code" : "R364.1",
      "display" : "DICER1-related cancer predisposition (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R365.1",
      "display" : "Fumarate hydratase-related tumour syndromes (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R366.1",
      "display" : "Inherited susceptibility to acute lymphoblastoid leukaemia (ALL) (Small panel)"
    },
    {
      "code" : "R367.1",
      "display" : "Inherited pancreatic cancer (Small panel)"
    },
    {
      "code" : "R368.1",
      "display" : "Hereditary angioedema type III (Targeted variant testing)"
    },
    {
      "code" : "R370.1",
      "display" : "Validation of unaccredited findings (Targeted variant testing)"
    },
    {
      "code" : "R371.1",
      "display" : "Malignant hyperthermia (small panel)"
    },
    {
      "code" : "R372.1",
      "display" : "Newborn screening for sickle cell disease in a transfused baby (Targeted variant testing)"
    },
    {
      "code" : "R373.1",
      "display" : "RNA to be stored (Other)"
    },
    {
      "code" : "R374.1",
      "display" : "Other sample to be stored (Other)"
    },
    {
      "code" : "R375.1",
      "display" : "Family follow-up testing to aid variant interpretation (Targeted variant testing)"
    },
    {
      "code" : "R376.1",
      "display" : "Segmental or atypical neurofibromatosis type 1 testing (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R376.2",
      "display" : "Segmental or atypical neurofibromatosis type 1 testing (MLPA or equivalent)"
    },
    {
      "code" : "R38.2",
      "display" : "Sporadic aniridia (Small panel)"
    },
    {
      "code" : "R380.1",
      "display" : "Niemann Pick disease type C (Small panel)"
    },
    {
      "code" : "R380.2",
      "display" : "Niemann Pick disease type C (MLPA or equivalent)"
    },
    {
      "code" : "R381.2",
      "display" : "Other rare neuromuscular disorders (WGS)"
    },
    {
      "code" : "R382.1",
      "display" : "Hypochondroplasia (Targeted mutation testing)"
    },
    {
      "code" : "R383.1",
      "display" : "Linkage testing for Huntington disease (Other)"
    },
    {
      "code" : "R384.1",
      "display" : "Generalised arterial calcification in infancy (Small panel)"
    },
    {
      "code" : "R387.1",
      "display" : "Reanalysis of existing data (Other)"
    },
    {
      "code" : "R389.1",
      "display" : "NIPD pre-pregnancy test work-up (NIPD)"
    },
    {
      "code" : "R39.1",
      "display" : "Albinism or congenital nystagmus (WES or Medium panel)"
    },
    {
      "code" : "R390.1",
      "display" : "Multiple exostoses (Small panel)"
    },
    {
      "code" : "R390.2",
      "display" : "Multiple exostoses (MLPA or equivalent)"
    },
    {
      "code" : "R391.1",
      "display" : "Barth syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R394.1",
      "display" : "Mitochondrial neurogastrointestinal encephalopathy (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R395.1",
      "display" : "Thiamine metabolism dysfunction syndrome 2 (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R396.1",
      "display" : "Mitochondrial Complex V deficiency, TMEM70 type (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R397.1",
      "display" : "Maternally inherited cardiomyopathy (Targeted mutation testing)"
    },
    {
      "code" : "R401.1",
      "display" : "Common aneuploidy testing prenatal (Common aneuploidy testing)"
    },
    {
      "code" : "R402.1",
      "display" : "Premature ovarian insufficiency (Karyotype or equivalent)"
    },
    {
      "code" : "R402.2",
      "display" : "Premature ovarian insufficiency (STR testing)"
    },
    {
      "code" : "R403.1",
      "display" : "MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing newborn screening follow up (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R404.1",
      "display" : "Testing of unaffected individuals for inherited cancer predisposition syndromes (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R404.3",
      "display" : "Testing of unaffected individuals for inherited cancer predisposition syndromes (Small panel)"
    },
    {
      "code" : "R405.1",
      "display" : "Hereditary Erythrocytosis (Small panel)"
    },
    {
      "code" : "R406.1",
      "display" : "Thrombocythaemia (Small panel)"
    },
    {
      "code" : "R409.1",
      "display" : "Linkage testing for recognisable Mendelian disorders (Other)"
    },
    {
      "code" : "R41.1",
      "display" : "Optic neuropathy (WES or Medium panel)"
    },
    {
      "code" : "R41.3",
      "display" : "Optic neuropathy (Targeted variant testing)"
    },
    {
      "code" : "R410.1",
      "display" : "Myotonic dystrophy type 2 (DM2) (STR testing)"
    },
    {
      "code" : "R411.1",
      "display" : "Y chromosome microdeletion (Targeted mutation testing or equivalent)"
    },
    {
      "code" : "R412.1",
      "display" : "Fetal anomalies with a likely genetic cause non urgent (WES or Large Panel)"
    },
    {
      "code" : "R413.1",
      "display" : "Autoinflammatory Disorders (WES or Medium panel)"
    },
    {
      "code" : "R414.1",
      "display" : "APC associated Polyposis  (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R416.1",
      "display" : "Syndromic and non syndromic craniosynostosis involving midline sutures only (metopic, sagittal, metopic & sagittal)  (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R417.1",
      "display" : "Multi Locus Imprinting Disorder (MLPA)"
    },
    {
      "code" : "R417.2",
      "display" : "Multi Locus Imprinting Disorder (Small Panel)"
    },
    {
      "code" : "R419.1",
      "display" : "Acute Rhabdomyolysis (Medium Panel)"
    },
    {
      "code" : "R42.1",
      "display" : "Leber hereditary optic neuropathy (Targeted variant testing)"
    },
    {
      "code" : "R42.2",
      "display" : "Leber hereditary optic neuropathy (Other)"
    },
    {
      "code" : "R420.1",
      "display" : "Pseudoxanthoma elasticum (Small Panel)"
    },
    {
      "code" : "R421.1",
      "display" : "Pulmonary Fibrosis, Familial (Medium panel)"
    },
    {
      "code" : "R422.1",
      "display" : "BAP1 associated tumour predisposition syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R423.1",
      "display" : "NIPD for Retinoblastoma haplotype testing (NIPD)"
    },
    {
      "code" : "R424.1",
      "display" : "Subcutaneous panniculitis T-cell lymphoma (Single gene sequencing <=10 amplicons)"
    },
    {
      "code" : "R426.1",
      "display" : "Pulmonary alveolar microlithiasis (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R428.1",
      "display" : "Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (STR testing)"
    },
    {
      "code" : "R428.2",
      "display" : "Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (FISH)"
    },
    {
      "code" : "R43.1",
      "display" : "Blepharophimosis ptosis and epicanthus inversus (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R43.2",
      "display" : "Blepharophimosis ptosis and epicanthus inversus (MLPA or equivalent)"
    },
    {
      "code" : "R43.3",
      "display" : "Blepharophimosis ptosis and epicanthus inversus (STR testing)"
    },
    {
      "code" : "R430.1",
      "display" : "Inherited prostate cancer (Small panel)"
    },
    {
      "code" : "R431.1",
      "display" : "Genome-wide DNA Methylation Profiling to Aid Variant Interpretation (Methylation testing)"
    },
    {
      "code" : "R433.1",
      "display" : "Monogenic diabetes, subtype glucokinase NIPT (NIPT)"
    },
    {
      "code" : "R436.1",
      "display" : "Hereditary alpha tryptasaemia (Targeted variant testing)"
    },
    {
      "code" : "R438.1,",
      "display" : "Paediatric pseudo-obstruction syndrome (WES or Medium panel)"
    },
    {
      "code" : "R440.1",
      "display" : "Hereditary isolated diabetes insipidus (Small panel)"
    },
    {
      "code" : "R441.1",
      "display" : "Unexplained death in infancy and sudden unexplained death in childhood (WGS)"
    },
    {
      "code" : "R442.1",
      "display" : "Variant Re-interpretation (Targeted variant testing)"
    },
    {
      "code" : "R443.1",
      "display" : "Confirmation test (Targeted variant testing)"
    },
    {
      "code" : "R444.1",
      "display" : "NICE approved PARP inhibitor treatment (Small panel)"
    },
    {
      "code" : "R444.2",
      "display" : "NICE approved PARP inhibitor treatment (Small panel)"
    },
    {
      "code" : "R445.1",
      "display" : "T21, T18 and T13 aneuploidy testing NIPT (previous history) (NIPT)"
    },
    {
      "code" : "R446.1",
      "display" : "APOL1 kidney donor testing (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R447.1",
      "display" : "Validation of WGS Diagnostic discovery (Targeted variant testing)"
    },
    {
      "code" : "R448.1",
      "display" : "Prenatal testing (Targeted variant testing)"
    },
    {
      "code" : "R449.1",
      "display" : "Diagnostic testing for Glutaric acidaemia I (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R45.1",
      "display" : "Stickler syndrome (Small panel)"
    },
    {
      "code" : "R450.1",
      "display" : "Diagnostic testing for Isovaleric acidaemia (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R451.1",
      "display" : "Diagnostic testing for MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R452.1",
      "display" : "Silver russell syndrome and Temple Syndrome (Methylation testing)"
    },
    {
      "code" : "R453.1",
      "display" : "Monogenic short stature (WES or Medium Panel)"
    },
    {
      "code" : "R454.1",
      "display" : "Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy (Targeted variant testing)"
    },
    {
      "code" : "R456.1",
      "display" : "Embryonal tumour of possible germline origin (WES or Medium panel)"
    },
    {
      "code" : "R456.2",
      "display" : "Embryonal tumour of possible germline origin (Methylation testing)"
    },
    {
      "code" : "R457.1",
      "display" : "Sarcoma of possible germline origin (Small panel)"
    },
    {
      "code" : "R458.1",
      "display" : "Young onset or familial dementia (WGS)"
    },
    {
      "code" : "R459.1",
      "display" : "Young onset or complex Parkinson disease (WGS)"
    },
    {
      "code" : "R46.1",
      "display" : "Congenital fibrosis of the extraocular muscles (Small panel)"
    },
    {
      "code" : "R460.1",
      "display" : "Amyotrophic lateral sclerosis / Motor Neurone Disease (WGS)"
    },
    {
      "code" : "R461.1",
      "display" : "Cerebral amyloid angiopathy (WGS)"
    },
    {
      "code" : "R462.1",
      "display" : "Childhood interstitial lung disease (Medium panel)"
    },
    {
      "code" : "R463.1",
      "display" : "Cytogenetic characterisation of a genomic abnormality â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"
    },
    {
      "code" : "R464.1",
      "display" : "Recurrent miscarriage where products of conception are not available for testing parental karyotype (Karyotype)"
    },
    {
      "code" : "R465.1",
      "display" : "Familial cytogenetic rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"
    },
    {
      "code" : "R466.1",
      "display" : "Unexplained infertility (Karyotype)"
    },
    {
      "code" : "R467.1",
      "display" : "Gamete donors (Karyotype)"
    },
    {
      "code" : "R468.1",
      "display" : "Possible sex chromosome aneuploidy or structural rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)"
    },
    {
      "code" : "R47.1",
      "display" : "Angelman syndrome (Methylation testing)"
    },
    {
      "code" : "R471.1",
      "display" : "Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing C9orf72 haplotype (Linkage analysis)"
    },
    {
      "code" : "R471.2",
      "display" : "Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing SOD1 haplotype (Linkage analysis)"
    },
    {
      "code" : "R471.3",
      "display" : "Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing MAPT haplotype (Linkage analysis)"
    },
    {
      "code" : "R471.4",
      "display" : "Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing PSEN1 haplotype (Linkage analysis)"
    },
    {
      "code" : "R48.1",
      "display" : "Prader-Willi syndrome (Methylation testing)"
    },
    {
      "code" : "R49.1",
      "display" : "Beckwith-Wiedemann syndrome (Methylation testing)"
    },
    {
      "code" : "R49.3",
      "display" : "Beckwith-Wiedemann syndrome (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R50.1",
      "display" : "Isolated hemihypertrophy or macroglossia (Methylation testing)"
    },
    {
      "code" : "R52.1",
      "display" : "Short stature SHOX deficiency (MLPA or equivalent)"
    },
    {
      "code" : "R52.2",
      "display" : "Short stature SHOX deficiency (Single gene sequencing <10 amplicons)"
    },
    {
      "code" : "R54.3",
      "display" : "Hereditary ataxia with onset in adulthood (WGS)"
    },
    {
      "code" : "R54.4",
      "display" : "Hereditary ataxia with onset in adulthood (RFC1 STR testing)"
    },
    {
      "code" : "R55.4",
      "display" : "Hereditary ataxia with onset in childhood (WGS)"
    },
    {
      "code" : "R56.3",
      "display" : "Adult onset dystonia, chorea or related movement disorder (WGS)"
    },
    {
      "code" : "R57.5",
      "display" : "Childhood onset dystonia, chorea or related movement disorder (WGS)"
    },
    {
      "code" : "R60.3",
      "display" : "Adult onset hereditary spastic paraplegia (WGS)"
    },
    {
      "code" : "R61.4",
      "display" : "Childhood onset hereditary spastic paraplegia (WGS)"
    },
    {
      "code" : "R62.2",
      "display" : "Adult onset leukodystrophy (WGS)"
    },
    {
      "code" : "R63.1",
      "display" : "Possible mitochondrial disorder nuclear genes (WES or Large Panel)"
    },
    {
      "code" : "R64.1",
      "display" : "MELAS or MIDD (Targeted variant testing)"
    },
    {
      "code" : "R65.1",
      "display" : "Aminoglycoside exposure posing risk to hearing (Targeted variant testing)"
    },
    {
      "code" : "R66.1",
      "display" : "Paroxysmal central nervous system disorders (WES or Medium Panel)"
    },
    {
      "code" : "R67.1",
      "display" : "Monogenic hearing loss (WES or Large Panel)"
    },
    {
      "code" : "R68.1",
      "display" : "Huntington disease (STR testing)"
    },
    {
      "code" : "R69.5",
      "display" : "Hypotonic infant  (WGS)"
    },
    {
      "code" : "R70.1",
      "display" : "Spinal muscular atrophy type 1 diagnostic test (MLPA or equivalent)"
    },
    {
      "code" : "R71.1",
      "display" : "Spinal muscular atrophy type 1 rare variant testing (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R72.1",
      "display" : "Myotonic dystrophy type 1 (STR testing)"
    },
    {
      "code" : "R73.1",
      "display" : "Duchenne or Becker muscular dystrophy (Single gene sequencing >=10 amplicons)"
    },
    {
      "code" : "R73.2",
      "display" : "Duchenne or Becker muscular dystrophy (MLPA or equivalent)"
    },
    {
      "code" : "R74.1",
      "display" : "Facioscapulohumeral muscular dystrophy (Other)"
    },
    {
      "code" : "R75.1",
      "display" : "Oculopharyngeal muscular dystrophy (STR testing)"
    },
    {
      "code" : "R76.1",
      "display" : "Skeletal muscle channelopathy (Small panel)"
    },
    {
      "code" : "R77.1",
      "display" : "Hereditary neuropathy PMP22 copy number (MLPA or equivalent)"
    },
    {
      "code" : "R78.4",
      "display" : "Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (WGS)"
    },
    {
      "code" : "R78.5",
      "display" : "Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (RFC1 STR testing)"
    },
    {
      "code" : "R79.1",
      "display" : "Congenital muscular dystrophy (WES or Medium Panel)"
    },
    {
      "code" : "R80.1",
      "display" : "Congenital myaesthenic syndrome (WES or Medium Panel)"
    },
    {
      "code" : "R81.1",
      "display" : "Congenital myopathy (WES or Medium Panel)"
    },
    {
      "code" : "R82.1",
      "display" : "Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies (WES or Medium Panel)"
    },
    {
      "code" : "R83.3",
      "display" : "Arthrogryposis (WGS)"
    },
    {
      "code" : "R84.4",
      "display" : "Cerebellar anomalies (WGS)"
    },
    {
      "code" : "R85.2",
      "display" : "Holoprosencephaly (WGS)"
    },
    {
      "code" : "R86.3",
      "display" : "Hydrocephalus (WGS)"
    },
    {
      "code" : "R87.3",
      "display" : "Cerebral malformation (WGS)"
    },
    {
      "code" : "R88.3",
      "display" : "Severe microcephaly (WGS)"
    },
    {
      "code" : "R89.3",
      "display" : "Ultra-rare and atypical monogenic disorders (WGS)"
    },
    {
      "code" : "R90.1",
      "display" : "Bleeding and platelet disorders (WES or Medium Panel)"
    },
    {
      "code" : "R91.1",
      "display" : "Cytopenia NOT Fanconi anaemia (WES or Medium Panel)"
    },
    {
      "code" : "R91.2",
      "display" : "Cytopenia NOT Fanconi anaemia (MLPA or equivalent)"
    },
    {
      "code" : "R92.1",
      "display" : "Rare anaemia (MLPA or equivalent)"
    },
    {
      "code" : "R92.2",
      "display" : "Rare anaemia (Small panel)"
    },
    {
      "code" : "R92.3",
      "display" : "Rare anaemia (WES or Medium Panel)"
    },
    {
      "code" : "R93.1",
      "display" : "Sickle cell, thalassaemia and other haemoglobinopathies (MLPA or equivalent)"
    },
    {
      "code" : "R93.2",
      "display" : "Sickle cell, thalassaemia and other haemoglobinopathies (Small panel)"
    },
    {
      "code" : "R95.1",
      "display" : "Iron overload hereditary haemochromatosis testing (Targeted variant testing)"
    },
    {
      "code" : "R96.1",
      "display" : "Iron metabolism disorders NOT common HFE variants (Small panel)"
    },
    {
      "code" : "R97.1",
      "display" : "Thrombophilia with a likely monogenic cause (WES or Small Panel)"
    },
    {
      "code" : "R98.2",
      "display" : "Likely inborn error of metabolism (WGS)"
    },
    {
      "code" : "R98.3",
      "display" : "Likely inborn error of metabolism (WES)"
    },
    {
      "code" : "R99.1",
      "display" : "Common craniosynostosis syndromes (Small panel)"
    },
    {
      "code" : "R99.2",
      "display" : "Common craniosynostosis syndromes (Exon level CNV detection by MLPA or equivalent)"
    }
  ]
}