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

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: NHS England Genomic Test Code - TTL Representation

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

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 a fhir:CodeSystem ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "GenomicTestCode"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div [ fhir:v "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem GenomicTestCode</b></p><a name=\"GenomicTestCode\"> </a><a name=\"hcGenomicTestCode\"> </a><p>This case-sensitive code system <code>https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory</code> provides <b>a fragment</b> that includes following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">M1.1<a name=\"GenomicTestCode-M1.461\"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M1.2<a name=\"GenomicTestCode-M1.462\"> </a></td><td>Colorectal Carcinoma, KRAS hotspot</td></tr><tr><td style=\"white-space:nowrap\">M1.3<a name=\"GenomicTestCode-M1.463\"> </a></td><td>Colorectal Carcinoma, NRAS hotspot</td></tr><tr><td style=\"white-space:nowrap\">M1.4<a name=\"GenomicTestCode-M1.464\"> </a></td><td>Colorectal Carcinoma, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M1.5<a name=\"GenomicTestCode-M1.465\"> </a></td><td>Colorectal Carcinoma, MLH1 promoter hypermethylation</td></tr><tr><td style=\"white-space:nowrap\">M1.6<a name=\"GenomicTestCode-M1.466\"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M1.7<a name=\"GenomicTestCode-M1.467\"> </a></td><td>Colorectal Carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M1.9<a name=\"GenomicTestCode-M1.469\"> </a></td><td>Colorectal Carcinoma, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2, POLE, POLD1)</td></tr><tr><td style=\"white-space:nowrap\">M10.1<a name=\"GenomicTestCode-M10.461\"> </a></td><td>Thyroid Follicular Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, HRAS)</td></tr><tr><td style=\"white-space:nowrap\">M10.2<a name=\"GenomicTestCode-M10.462\"> </a></td><td>Thyroid Follicular Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET)</td></tr><tr><td style=\"white-space:nowrap\">M100.1<a name=\"GenomicTestCode-M100.461\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M100.2<a name=\"GenomicTestCode-M100.462\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 Copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M100.3<a name=\"GenomicTestCode-M100.463\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, REL copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M100.4<a name=\"GenomicTestCode-M100.464\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M100.5<a name=\"GenomicTestCode-M100.465\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, copy number variant (CD274, PDCD1LG2, REL)</td></tr><tr><td style=\"white-space:nowrap\">M100.6<a name=\"GenomicTestCode-M100.466\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, rearrangement (CD274, PDCD1LG2)</td></tr><tr><td style=\"white-space:nowrap\">M100.7<a name=\"GenomicTestCode-M100.467\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M100.8<a name=\"GenomicTestCode-M100.468\"> </a></td><td>Primary Mediastinal B Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M101.1<a name=\"GenomicTestCode-M101.461\"> </a></td><td>ALK Positive Large B Cell Lymphoma, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M101.2<a name=\"GenomicTestCode-M101.462\"> </a></td><td>ALK Positive Large B Cell Lymphoma, t(2;17)(p23;q23) CLTC-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M101.3<a name=\"GenomicTestCode-M101.463\"> </a></td><td>ALK Positive Large B Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M101.4<a name=\"GenomicTestCode-M101.464\"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M101.5<a name=\"GenomicTestCode-M101.465\"> </a></td><td>ALK Positive Large B Cell Lymphoma, Multi-target NGS panel, structural variant (CLTC-ALK, ALK-NPM1, other ALK rearrangements)</td></tr><tr><td style=\"white-space:nowrap\">M101.6<a name=\"GenomicTestCode-M101.466\"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M101.7<a name=\"GenomicTestCode-M101.467\"> </a></td><td>ALK Positive Large B Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M102.1<a name=\"GenomicTestCode-M102.461\"> </a></td><td>Mantle Cell Lymphoma, t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M102.2<a name=\"GenomicTestCode-M102.462\"> </a></td><td>Mantle Cell Lymphoma, CCND1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M102.3<a name=\"GenomicTestCode-M102.463\"> </a></td><td>Mantle Cell Lymphoma, CCND2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M102.4<a name=\"GenomicTestCode-M102.464\"> </a></td><td>Mantle Cell Lymphoma, Multi-target NGS panel, structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)</td></tr><tr><td style=\"white-space:nowrap\">M102.5<a name=\"GenomicTestCode-M102.465\"> </a></td><td>Mantle Cell Lymphoma, Multi-target NGS panel, small variant (TP53)</td></tr><tr><td style=\"white-space:nowrap\">M103.1<a name=\"GenomicTestCode-M103.461\"> </a></td><td>Follicular Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M103.2<a name=\"GenomicTestCode-M103.462\"> </a></td><td>Follicular Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M103.3<a name=\"GenomicTestCode-M103.463\"> </a></td><td>Follicular Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M103.4<a name=\"GenomicTestCode-M103.464\"> </a></td><td>Follicular Lymphoma, Multi-target NGS panel, small variant (CARD11, CREBBP, EZH2, ARID1A, EP300, MEF2B, FOXO1)</td></tr><tr><td style=\"white-space:nowrap\">M103.5<a name=\"GenomicTestCode-M103.465\"> </a></td><td>Follicular Lymphoma, Multi-target NGS panel, structural variant (IGH-BCL2, BCL2, BCL6)</td></tr><tr><td style=\"white-space:nowrap\">M104.1<a name=\"GenomicTestCode-M104.461\"> </a></td><td>Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, Multi-target NGS panel, small variant (MYD88, CXCR4)</td></tr><tr><td style=\"white-space:nowrap\">M104.2<a name=\"GenomicTestCode-M104.462\"> </a></td><td>Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, MYD88 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M105.1<a name=\"GenomicTestCode-M105.461\"> </a></td><td>Igm Monoclonal Gammopathy of Uncertain Significance, Multi-target NGS panel, small variant (MYD88, CXCR4)</td></tr><tr><td style=\"white-space:nowrap\">M105.2<a name=\"GenomicTestCode-M105.462\"> </a></td><td>Igm Monoclonal Gammopathy of Uncertain Significance, MYD88 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M106.1<a name=\"GenomicTestCode-M106.461\"> </a></td><td>Intra-Ocular Lymphoma, MYD88 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M107.1<a name=\"GenomicTestCode-M107.461\"> </a></td><td>Malt-Lymphoma, t(11;18)(q21;q21) BIRC3-MALT1  FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M107.10<a name=\"GenomicTestCode-M107.4610\"> </a></td><td>Malt-Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M107.2<a name=\"GenomicTestCode-M107.462\"> </a></td><td>Malt-Lymphoma, t(1;14)(p22;q32) IGH-BCL10 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M107.3<a name=\"GenomicTestCode-M107.463\"> </a></td><td>Malt-Lymphoma, t(14;18)(q32;q21) IGH-MALT1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M107.4<a name=\"GenomicTestCode-M107.464\"> </a></td><td>Malt-Lymphoma, MALT1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M107.5<a name=\"GenomicTestCode-M107.465\"> </a></td><td>Malt-Lymphoma, BCL10 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M107.6<a name=\"GenomicTestCode-M107.466\"> </a></td><td>Malt-Lymphoma, FOXP1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M107.7<a name=\"GenomicTestCode-M107.467\"> </a></td><td>Malt-Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M107.8<a name=\"GenomicTestCode-M107.468\"> </a></td><td>Malt-Lymphoma, Multi-target NGS panel, structural variant (BIRC3-MALT1, IGH-BCL10, IGH-MALT1, other MALT rearrangements, other BCL10 rearrangements, FOXP1)</td></tr><tr><td style=\"white-space:nowrap\">M107.9<a name=\"GenomicTestCode-M107.469\"> </a></td><td>Malt-Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M108.1<a name=\"GenomicTestCode-M108.461\"> </a></td><td>Hairy Cell Leukaemia, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M108.2<a name=\"GenomicTestCode-M108.462\"> </a></td><td>Hairy Cell Leukaemia, BRAF V600 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M108.5<a name=\"GenomicTestCode-M108.465\"> </a></td><td>Hairy Cell Leukaemia, Ig gene hypermutation detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M108.6<a name=\"GenomicTestCode-M108.466\"> </a></td><td>Hairy Cell Leukaemia, Ig gene hypermutation detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M109.1<a name=\"GenomicTestCode-M109.461\"> </a></td><td>Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M109.2<a name=\"GenomicTestCode-M109.462\"> </a></td><td>Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M11.1<a name=\"GenomicTestCode-M11.461\"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, small variant (TP53, BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M11.2<a name=\"GenomicTestCode-M11.462\"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, copy number variant (TP53)</td></tr><tr><td style=\"white-space:nowrap\">M11.3<a name=\"GenomicTestCode-M11.463\"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M11.4<a name=\"GenomicTestCode-M11.464\"> </a></td><td>Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET, ALK)</td></tr><tr><td style=\"white-space:nowrap\">M110.1,<a name=\"GenomicTestCode-M110.461.44\"> </a></td><td>Paediatric Type Follicular Lymphoma, Multi-target NGS panel, small variant (MAP2K1)</td></tr><tr><td style=\"white-space:nowrap\">M110.2,<a name=\"GenomicTestCode-M110.462.44\"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M110.3,<a name=\"GenomicTestCode-M110.463.44\"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M110.4,<a name=\"GenomicTestCode-M110.464.44\"> </a></td><td>Paediatric Type Follicular Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M111.1<a name=\"GenomicTestCode-M111.461\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (RHOA, DNMT3A, IDH2, TET2)</td></tr><tr><td style=\"white-space:nowrap\">M111.2<a name=\"GenomicTestCode-M111.462\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M111.3<a name=\"GenomicTestCode-M111.463\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M111.4<a name=\"GenomicTestCode-M111.464\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, TCR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M111.5<a name=\"GenomicTestCode-M111.465\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M111.6<a name=\"GenomicTestCode-M111.466\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (TCR rearrangement)</td></tr><tr><td style=\"white-space:nowrap\">M111.7<a name=\"GenomicTestCode-M111.467\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M111.8<a name=\"GenomicTestCode-M111.468\"> </a></td><td>T Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M112.3<a name=\"GenomicTestCode-M112.463\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), IRF4/DUSP22 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M112.4<a name=\"GenomicTestCode-M112.464\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), TP63 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M112.5<a name=\"GenomicTestCode-M112.465\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M112.6<a name=\"GenomicTestCode-M112.466\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), Multi-target NGS panel, structural variant (IRF4/DUSP22, TP63)</td></tr><tr><td style=\"white-space:nowrap\">M112.7<a name=\"GenomicTestCode-M112.467\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M112.8<a name=\"GenomicTestCode-M112.468\"> </a></td><td>ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M113.1<a name=\"GenomicTestCode-M113.461\"> </a></td><td>T Prolymphocytic Leukaemia, TCL1A rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M113.2<a name=\"GenomicTestCode-M113.462\"> </a></td><td>T Prolymphocytic Leukaemia, Chr8 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M113.3<a name=\"GenomicTestCode-M113.463\"> </a></td><td>T Prolymphocytic Leukaemia, Multi-target NGS panel, structural variant (TCL1A, Chr8)</td></tr><tr><td style=\"white-space:nowrap\">M113.6<a name=\"GenomicTestCode-M113.466\"> </a></td><td>T Prolymphocytic Leukaemia, Karyotype (to include TCL1 rearrangements t(X;14))</td></tr><tr><td style=\"white-space:nowrap\">M114.1<a name=\"GenomicTestCode-M114.461\"> </a></td><td>Large Granular Lymphocyte Leukaemia, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style=\"white-space:nowrap\">M115.1<a name=\"GenomicTestCode-M115.461\"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style=\"white-space:nowrap\">M115.2<a name=\"GenomicTestCode-M115.462\"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M115.3<a name=\"GenomicTestCode-M115.463\"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M115.4<a name=\"GenomicTestCode-M115.464\"> </a></td><td>NK Cell/Gamma-Delta T Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M116.1<a name=\"GenomicTestCode-M116.461\"> </a></td><td>Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)</td></tr><tr><td style=\"white-space:nowrap\">M116.2<a name=\"GenomicTestCode-M116.462\"> </a></td><td>Hepatosplenic T Cell Lymphoma, i7q rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M116.3<a name=\"GenomicTestCode-M116.463\"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M116.4<a name=\"GenomicTestCode-M116.464\"> </a></td><td>Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, structural variant (i17q)</td></tr><tr><td style=\"white-space:nowrap\">M116.5<a name=\"GenomicTestCode-M116.465\"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M116.6<a name=\"GenomicTestCode-M116.466\"> </a></td><td>Hepatosplenic T Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M117.1<a name=\"GenomicTestCode-M117.461\"> </a></td><td>Histiocytosis, Multi-target NGS panel, small variant (BRAF, MAP2K1, NRAS, KRAS, HRAS, ERBB3, ARAF, MAP3K1, PIK3CA, PIK3CD)</td></tr><tr><td style=\"white-space:nowrap\">M117.12<a name=\"GenomicTestCode-M117.4612\"> </a></td><td>Histiocytosis, NTRK1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M117.16<a name=\"GenomicTestCode-M117.4616\"> </a></td><td>Histiocytosis, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M117.17<a name=\"GenomicTestCode-M117.4617\"> </a></td><td>Histiocytosis, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M117.18<a name=\"GenomicTestCode-M117.4618\"> </a></td><td>Histiocytosis, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M117.19<a name=\"GenomicTestCode-M117.4619\"> </a></td><td>Histiocytosis, High Sensitivity BRAF</td></tr><tr><td style=\"white-space:nowrap\">M117.2<a name=\"GenomicTestCode-M117.462\"> </a></td><td>Histiocytosis, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M117.3<a name=\"GenomicTestCode-M117.463\"> </a></td><td>Histiocytosis, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M117.7<a name=\"GenomicTestCode-M117.467\"> </a></td><td>Histiocytosis, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M118.1<a name=\"GenomicTestCode-M118.461\"> </a></td><td>Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, STR Testing</td></tr><tr><td style=\"white-space:nowrap\">M118.2<a name=\"GenomicTestCode-M118.462\"> </a></td><td>Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, Sex chromosome FISH</td></tr><tr><td style=\"white-space:nowrap\">M119.1,<a name=\"GenomicTestCode-M119.461.44\"> </a></td><td>Paediatric Tumours, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M119.2,<a name=\"GenomicTestCode-M119.462.44\"> </a></td><td>Paediatric Tumours, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M119.4,<a name=\"GenomicTestCode-M119.464.44\"> </a></td><td>Paediatric Tumours, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M119.5,<a name=\"GenomicTestCode-M119.465.44\"> </a></td><td>Paediatric Tumours, Multi-target NGS-small variant</td></tr><tr><td style=\"white-space:nowrap\">M12.1<a name=\"GenomicTestCode-M12.461\"> </a></td><td>Thyroid Medullary Carcinoma, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style=\"white-space:nowrap\">M12.2<a name=\"GenomicTestCode-M12.462\"> </a></td><td>Thyroid Medullary Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M120.1<a name=\"GenomicTestCode-M120.461\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M120.10<a name=\"GenomicTestCode-M120.4610\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.11<a name=\"GenomicTestCode-M120.4611\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.12<a name=\"GenomicTestCode-M120.4612\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.13<a name=\"GenomicTestCode-M120.4613\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.14<a name=\"GenomicTestCode-M120.4614\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.15<a name=\"GenomicTestCode-M120.4615\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M120.16<a name=\"GenomicTestCode-M120.4616\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M120.17<a name=\"GenomicTestCode-M120.4617\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M120.18<a name=\"GenomicTestCode-M120.4618\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M120.2<a name=\"GenomicTestCode-M120.462\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 seq</td></tr><tr><td style=\"white-space:nowrap\">M120.3<a name=\"GenomicTestCode-M120.463\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M120.4<a name=\"GenomicTestCode-M120.464\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M120.5<a name=\"GenomicTestCode-M120.465\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M120.6<a name=\"GenomicTestCode-M120.466\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M120.7<a name=\"GenomicTestCode-M120.467\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.8<a name=\"GenomicTestCode-M120.468\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M120.9<a name=\"GenomicTestCode-M120.469\"> </a></td><td>Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M124.1<a name=\"GenomicTestCode-M124.461\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, small variant (BCOR)</td></tr><tr><td style=\"white-space:nowrap\">M124.10<a name=\"GenomicTestCode-M124.4610\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, structural variant (BCOR, NUTM2B-YWHAE, NUTM2E-YWHAE, NUTM1-YWHAE, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M124.11<a name=\"GenomicTestCode-M124.4611\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, copy number variant (BCOR, YWHAE)</td></tr><tr><td style=\"white-space:nowrap\">M124.2<a name=\"GenomicTestCode-M124.462\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR seq</td></tr><tr><td style=\"white-space:nowrap\">M124.3<a name=\"GenomicTestCode-M124.463\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M124.4<a name=\"GenomicTestCode-M124.464\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, BCOR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M124.5<a name=\"GenomicTestCode-M124.465\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM2B-YWHAE FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M124.6<a name=\"GenomicTestCode-M124.466\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM2E-YWHAE FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M124.7<a name=\"GenomicTestCode-M124.467\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, NUTM1-YWHAE FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M124.8<a name=\"GenomicTestCode-M124.468\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, YWHAE copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M124.9<a name=\"GenomicTestCode-M124.469\"> </a></td><td>Clear Cell Kidney Sarcoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M126.1<a name=\"GenomicTestCode-M126.461\"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, MN1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M126.2<a name=\"GenomicTestCode-M126.462\"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M126.3<a name=\"GenomicTestCode-M126.463\"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, Multi-target NGS panel, structural variant (MN1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M126.4<a name=\"GenomicTestCode-M126.464\"> </a></td><td>CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M127.1<a name=\"GenomicTestCode-M127.461\"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, NTRK3-ETV6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M127.3<a name=\"GenomicTestCode-M127.463\"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M127.4<a name=\"GenomicTestCode-M127.464\"> </a></td><td>Congenital Mesoblastic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK3-ETV6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M13.1<a name=\"GenomicTestCode-M13.461\"> </a></td><td>Phaeochromocytoma, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style=\"white-space:nowrap\">M13.2<a name=\"GenomicTestCode-M13.462\"> </a></td><td>Phaeochromocytoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M130.1<a name=\"GenomicTestCode-M130.461\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M130.2<a name=\"GenomicTestCode-M130.462\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M130.3<a name=\"GenomicTestCode-M130.463\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M130.4<a name=\"GenomicTestCode-M130.464\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M130.5<a name=\"GenomicTestCode-M130.465\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M130.6<a name=\"GenomicTestCode-M130.466\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M130.7<a name=\"GenomicTestCode-M130.467\"> </a></td><td>Cribriform Neuroepithelial Tumour, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M131.1<a name=\"GenomicTestCode-M131.461\"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M131.2<a name=\"GenomicTestCode-M131.462\"> </a></td><td>Cystic Nephroma, Paediatric, DICER1 seq</td></tr><tr><td style=\"white-space:nowrap\">M131.3<a name=\"GenomicTestCode-M131.463\"> </a></td><td>Cystic Nephroma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M131.4<a name=\"GenomicTestCode-M131.464\"> </a></td><td>Cystic Nephroma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M131.5<a name=\"GenomicTestCode-M131.465\"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M131.6<a name=\"GenomicTestCode-M131.466\"> </a></td><td>Cystic Nephroma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M132.1<a name=\"GenomicTestCode-M132.461\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M132.10<a name=\"GenomicTestCode-M132.4610\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.11<a name=\"GenomicTestCode-M132.4611\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M132.12<a name=\"GenomicTestCode-M132.4612\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M132.13<a name=\"GenomicTestCode-M132.4613\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M132.2<a name=\"GenomicTestCode-M132.462\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M132.3<a name=\"GenomicTestCode-M132.463\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.4<a name=\"GenomicTestCode-M132.464\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.5<a name=\"GenomicTestCode-M132.465\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.6<a name=\"GenomicTestCode-M132.466\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.7<a name=\"GenomicTestCode-M132.467\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.8<a name=\"GenomicTestCode-M132.468\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M132.9<a name=\"GenomicTestCode-M132.469\"> </a></td><td>Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M133.1<a name=\"GenomicTestCode-M133.461\"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SUFU)</td></tr><tr><td style=\"white-space:nowrap\">M133.2<a name=\"GenomicTestCode-M133.462\"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, SUFU seq</td></tr><tr><td style=\"white-space:nowrap\">M133.3<a name=\"GenomicTestCode-M133.463\"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M133.4<a name=\"GenomicTestCode-M133.464\"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M133.5<a name=\"GenomicTestCode-M133.465\"> </a></td><td>Desmoplastic Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M136.1<a name=\"GenomicTestCode-M136.461\"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, DNAJB1-PRKACA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M136.2<a name=\"GenomicTestCode-M136.462\"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M136.3<a name=\"GenomicTestCode-M136.463\"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, Multi-target NGS panel, structural variant (DNAJB1-PRKACA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M136.5<a name=\"GenomicTestCode-M136.465\"> </a></td><td>Fibrolamellar Hepatocellular Carcinoma, Paediatric, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M137.1<a name=\"GenomicTestCode-M137.461\"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M137.10<a name=\"GenomicTestCode-M137.4610\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.11<a name=\"GenomicTestCode-M137.4611\"> </a></td><td>Ganglioglioma, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M137.12<a name=\"GenomicTestCode-M137.4612\"> </a></td><td>Ganglioglioma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M137.13<a name=\"GenomicTestCode-M137.4613\"> </a></td><td>Ganglioglioma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M137.14<a name=\"GenomicTestCode-M137.4614\"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)</td></tr><tr><td style=\"white-space:nowrap\">M137.15<a name=\"GenomicTestCode-M137.4615\"> </a></td><td>Ganglioglioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M137.2<a name=\"GenomicTestCode-M137.462\"> </a></td><td>Ganglioglioma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M137.3<a name=\"GenomicTestCode-M137.463\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.4<a name=\"GenomicTestCode-M137.464\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.5<a name=\"GenomicTestCode-M137.465\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.6<a name=\"GenomicTestCode-M137.466\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.7<a name=\"GenomicTestCode-M137.467\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.8<a name=\"GenomicTestCode-M137.468\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M137.9<a name=\"GenomicTestCode-M137.469\"> </a></td><td>Ganglioglioma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M138.1<a name=\"GenomicTestCode-M138.461\"> </a></td><td>Glial Tumours, Paediatric, Multi-target NGS panel, small variant (ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M138.2<a name=\"GenomicTestCode-M138.462\"> </a></td><td>Glial Tumours, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M138.3<a name=\"GenomicTestCode-M138.463\"> </a></td><td>Glial Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M138.4<a name=\"GenomicTestCode-M138.464\"> </a></td><td>Glial Tumours, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M139.1<a name=\"GenomicTestCode-M139.461\"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, small variant (BRAF, CDKN2A, FGFR4)</td></tr><tr><td style=\"white-space:nowrap\">M139.10<a name=\"GenomicTestCode-M139.4610\"> </a></td><td>Glioblastoma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.12<a name=\"GenomicTestCode-M139.4612\"> </a></td><td>Glioblastoma, Paediatric, CDKN2A seq</td></tr><tr><td style=\"white-space:nowrap\">M139.13<a name=\"GenomicTestCode-M139.4613\"> </a></td><td>Glioblastoma, Paediatric, FGFR4 seq</td></tr><tr><td style=\"white-space:nowrap\">M139.14<a name=\"GenomicTestCode-M139.4614\"> </a></td><td>Glioblastoma, Paediatric, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M139.15<a name=\"GenomicTestCode-M139.4615\"> </a></td><td>Glioblastoma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M139.16<a name=\"GenomicTestCode-M139.4616\"> </a></td><td>Glioblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M139.17<a name=\"GenomicTestCode-M139.4617\"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, copy number variant (CDKN2A)</td></tr><tr><td style=\"white-space:nowrap\">M139.18<a name=\"GenomicTestCode-M139.4618\"> </a></td><td>Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M139.2<a name=\"GenomicTestCode-M139.462\"> </a></td><td>Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-FXR1, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B,  BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M139.3<a name=\"GenomicTestCode-M139.463\"> </a></td><td>Glioblastoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.4<a name=\"GenomicTestCode-M139.464\"> </a></td><td>Glioblastoma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.5<a name=\"GenomicTestCode-M139.465\"> </a></td><td>Glioblastoma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.6<a name=\"GenomicTestCode-M139.466\"> </a></td><td>Glioblastoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.7<a name=\"GenomicTestCode-M139.467\"> </a></td><td>Glioblastoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.8<a name=\"GenomicTestCode-M139.468\"> </a></td><td>Glioblastoma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M139.9<a name=\"GenomicTestCode-M139.469\"> </a></td><td>Glioblastoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M14.1<a name=\"GenomicTestCode-M14.461\"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, small variant (TP53)</td></tr><tr><td style=\"white-space:nowrap\">M14.2<a name=\"GenomicTestCode-M14.462\"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, copy number variant (TP53)</td></tr><tr><td style=\"white-space:nowrap\">M14.3<a name=\"GenomicTestCode-M14.463\"> </a></td><td>Adrenal Cortical Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M14.4<a name=\"GenomicTestCode-M14.464\"> </a></td><td>Adrenal Cortical Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M14.5<a name=\"GenomicTestCode-M14.465\"> </a></td><td>Adrenal Cortical Carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M143.1<a name=\"GenomicTestCode-M143.461\"> </a></td><td>Lung, Paediatric, Multi-target NGS panel, small variant (H3-3A, H3-3B)</td></tr><tr><td style=\"white-space:nowrap\">M143.2<a name=\"GenomicTestCode-M143.462\"> </a></td><td>Lung, Paediatric, H3-3A seq</td></tr><tr><td style=\"white-space:nowrap\">M143.3<a name=\"GenomicTestCode-M143.463\"> </a></td><td>Lung, Paediatric, H3-3B seq</td></tr><tr><td style=\"white-space:nowrap\">M143.4<a name=\"GenomicTestCode-M143.464\"> </a></td><td>Lung, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M143.5<a name=\"GenomicTestCode-M143.465\"> </a></td><td>Lung, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M145.1<a name=\"GenomicTestCode-M145.461\"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, BCOR, PTCH1, PTCH2, PTEN, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M145.10<a name=\"GenomicTestCode-M145.4610\"> </a></td><td>Medulloblastoma, Paediatric, BCOR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M145.11<a name=\"GenomicTestCode-M145.4611\"> </a></td><td>Medulloblastoma, Paediatric, C19MC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M145.12<a name=\"GenomicTestCode-M145.4612\"> </a></td><td>Medulloblastoma, Paediatric, PTEN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M145.13<a name=\"GenomicTestCode-M145.4613\"> </a></td><td>Medulloblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M145.14<a name=\"GenomicTestCode-M145.4614\"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (ALK, BCOR, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M145.15<a name=\"GenomicTestCode-M145.4615\"> </a></td><td>Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (ALK, BCOR, C19MC, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M145.16<a name=\"GenomicTestCode-M145.4616\"> </a></td><td>Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M145.2<a name=\"GenomicTestCode-M145.462\"> </a></td><td>Medulloblastoma, Paediatric, ALK seq</td></tr><tr><td style=\"white-space:nowrap\">M145.3<a name=\"GenomicTestCode-M145.463\"> </a></td><td>Medulloblastoma, Paediatric, BCOR seq</td></tr><tr><td style=\"white-space:nowrap\">M145.4<a name=\"GenomicTestCode-M145.464\"> </a></td><td>Medulloblastoma, Paediatric, PTCH1 seq</td></tr><tr><td style=\"white-space:nowrap\">M145.5<a name=\"GenomicTestCode-M145.465\"> </a></td><td>Medulloblastoma, Paediatric, PTCH2 seq</td></tr><tr><td style=\"white-space:nowrap\">M145.6<a name=\"GenomicTestCode-M145.466\"> </a></td><td>Medulloblastoma, Paediatric, TERT promoter seq</td></tr><tr><td style=\"white-space:nowrap\">M145.7<a name=\"GenomicTestCode-M145.467\"> </a></td><td>Medulloblastoma, Paediatric, ALK copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M145.8<a name=\"GenomicTestCode-M145.468\"> </a></td><td>Medulloblastoma, Paediatric, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M145.9<a name=\"GenomicTestCode-M145.469\"> </a></td><td>Medulloblastoma, Paediatric, BCOR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M146.1<a name=\"GenomicTestCode-M146.461\"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, small variant (SMARCA4, DDX3X)</td></tr><tr><td style=\"white-space:nowrap\">M146.2<a name=\"GenomicTestCode-M146.462\"> </a></td><td>Medulloblastoma Group 3, Paediatric, SMARCA4 seq</td></tr><tr><td style=\"white-space:nowrap\">M146.3<a name=\"GenomicTestCode-M146.463\"> </a></td><td>Medulloblastoma Group 3, Paediatric, DDX3X seq</td></tr><tr><td style=\"white-space:nowrap\">M146.4<a name=\"GenomicTestCode-M146.464\"> </a></td><td>Medulloblastoma Group 3, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M146.5<a name=\"GenomicTestCode-M146.465\"> </a></td><td>Medulloblastoma Group 3, Paediatric, PVT1-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M146.6<a name=\"GenomicTestCode-M146.466\"> </a></td><td>Medulloblastoma Group 3, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M146.7<a name=\"GenomicTestCode-M146.467\"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, structural variant (PVT1-MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M146.8<a name=\"GenomicTestCode-M146.468\"> </a></td><td>Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4)</td></tr><tr><td style=\"white-space:nowrap\">M146.9<a name=\"GenomicTestCode-M146.469\"> </a></td><td>Medulloblastoma Group 3, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M147.1<a name=\"GenomicTestCode-M147.461\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, small variant (MYCN, EZH2)</td></tr><tr><td style=\"white-space:nowrap\">M147.10<a name=\"GenomicTestCode-M147.4610\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M147.2<a name=\"GenomicTestCode-M147.462\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYCN seq</td></tr><tr><td style=\"white-space:nowrap\">M147.3<a name=\"GenomicTestCode-M147.463\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, EZH2 seq</td></tr><tr><td style=\"white-space:nowrap\">M147.4<a name=\"GenomicTestCode-M147.464\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M147.5<a name=\"GenomicTestCode-M147.465\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M147.6<a name=\"GenomicTestCode-M147.466\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M147.7<a name=\"GenomicTestCode-M147.467\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M147.8<a name=\"GenomicTestCode-M147.468\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M147.9<a name=\"GenomicTestCode-M147.469\"> </a></td><td>Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, copy number variant (MYCN, MYC)</td></tr><tr><td style=\"white-space:nowrap\">M148.1<a name=\"GenomicTestCode-M148.461\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, small variant (YAP1, PTCH1)</td></tr><tr><td style=\"white-space:nowrap\">M148.10<a name=\"GenomicTestCode-M148.4610\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (YAP1, PTCH1)</td></tr><tr><td style=\"white-space:nowrap\">M148.11<a name=\"GenomicTestCode-M148.4611\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M148.2<a name=\"GenomicTestCode-M148.462\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1 seq</td></tr><tr><td style=\"white-space:nowrap\">M148.3<a name=\"GenomicTestCode-M148.463\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, PTCH1 seq</td></tr><tr><td style=\"white-space:nowrap\">M148.4<a name=\"GenomicTestCode-M148.464\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M148.5<a name=\"GenomicTestCode-M148.465\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M148.6<a name=\"GenomicTestCode-M148.466\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, YAP1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M148.7<a name=\"GenomicTestCode-M148.467\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, PTCH1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M148.8<a name=\"GenomicTestCode-M148.468\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M148.9<a name=\"GenomicTestCode-M148.469\"> </a></td><td>Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, structural variant (YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M149.1<a name=\"GenomicTestCode-M149.461\"> </a></td><td>Melanotic Tumours, Paediatric, Multi-target NGS panel, small variant (NRAS)</td></tr><tr><td style=\"white-space:nowrap\">M149.2<a name=\"GenomicTestCode-M149.462\"> </a></td><td>Melanotic Tumours, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M149.3<a name=\"GenomicTestCode-M149.463\"> </a></td><td>Melanotic Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M15.1<a name=\"GenomicTestCode-M15.461\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, small variant (CDKN2A, EGFR, TP53)</td></tr><tr><td style=\"white-space:nowrap\">M15.2<a name=\"GenomicTestCode-M15.462\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M15.3<a name=\"GenomicTestCode-M15.463\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, copy number variant (CDKN2A, TP53)</td></tr><tr><td style=\"white-space:nowrap\">M15.4<a name=\"GenomicTestCode-M15.464\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, RET rearrangement FISH/RT-PC</td></tr><tr><td style=\"white-space:nowrap\">M15.5<a name=\"GenomicTestCode-M15.465\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M15.6<a name=\"GenomicTestCode-M15.466\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M15.7<a name=\"GenomicTestCode-M15.467\"> </a></td><td>Head and Neck Squamous Cell Carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M150.1<a name=\"GenomicTestCode-M150.461\"> </a></td><td>Meningioma, Paediatric, Multi-target NGS panel, small variant (SMARCE1, AKT1, NF2, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M150.2<a name=\"GenomicTestCode-M150.462\"> </a></td><td>Meningioma, Paediatric, SMARCE1 seq</td></tr><tr><td style=\"white-space:nowrap\">M150.3<a name=\"GenomicTestCode-M150.463\"> </a></td><td>Meningioma, Paediatric, AKT1 seq</td></tr><tr><td style=\"white-space:nowrap\">M150.4<a name=\"GenomicTestCode-M150.464\"> </a></td><td>Meningioma, Paediatric, NF2 seq</td></tr><tr><td style=\"white-space:nowrap\">M150.5<a name=\"GenomicTestCode-M150.465\"> </a></td><td>Meningioma, Paediatric, TERT promoter seq</td></tr><tr><td style=\"white-space:nowrap\">M150.6<a name=\"GenomicTestCode-M150.466\"> </a></td><td>Meningioma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M150.7<a name=\"GenomicTestCode-M150.467\"> </a></td><td>Meningioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M150.8<a name=\"GenomicTestCode-M150.468\"> </a></td><td>Meningioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M151.1<a name=\"GenomicTestCode-M151.461\"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD2 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M151.2<a name=\"GenomicTestCode-M151.462\"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M151.3<a name=\"GenomicTestCode-M151.463\"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-BRD4 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M151.4<a name=\"GenomicTestCode-M151.464\"> </a></td><td>Midline Carcinoma, Paediatric, NUTM1-CIC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M151.5<a name=\"GenomicTestCode-M151.465\"> </a></td><td>Midline Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M151.6<a name=\"GenomicTestCode-M151.466\"> </a></td><td>Midline Carcinoma, Paediatric, Multi-target NGS panel, structural variant (NUTM1-BRD2, NUTM1-BRD3, NUTM1-BRD4, NUTM1-CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M152.1<a name=\"GenomicTestCode-M152.461\"> </a></td><td>Neuroblastoma, Paediatric, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M152.10<a name=\"GenomicTestCode-M152.4610\"> </a></td><td>Neuroblastoma, Paediatric, 17q rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.11<a name=\"GenomicTestCode-M152.4611\"> </a></td><td>Neuroblastoma, Paediatric, 11q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.12<a name=\"GenomicTestCode-M152.4612\"> </a></td><td>Neuroblastoma, Paediatric, 1p36 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.13<a name=\"GenomicTestCode-M152.4613\"> </a></td><td>Neuroblastoma, Paediatric, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.14<a name=\"GenomicTestCode-M152.4614\"> </a></td><td>Neuroblastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M152.15<a name=\"GenomicTestCode-M152.4615\"> </a></td><td>Neuroblastoma, Paediatric, MYCN seq</td></tr><tr><td style=\"white-space:nowrap\">M152.16<a name=\"GenomicTestCode-M152.4616\"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, structural variant (17q, ALK, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M152.17<a name=\"GenomicTestCode-M152.4617\"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, copy number variant (MYCN, ALK, 17q, 11q, 1p36)</td></tr><tr><td style=\"white-space:nowrap\">M152.18<a name=\"GenomicTestCode-M152.4618\"> </a></td><td>Neuroblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M152.19<a name=\"GenomicTestCode-M152.4619\"> </a></td><td>Neuroblastoma, Paediatric, TERT promoter rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.2<a name=\"GenomicTestCode-M152.462\"> </a></td><td>Neuroblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, ATRX, FGFR1, MYCN, NRAS, PHOX2B, TP53)</td></tr><tr><td style=\"white-space:nowrap\">M152.3<a name=\"GenomicTestCode-M152.463\"> </a></td><td>Neuroblastoma, Paediatric, ALK seq</td></tr><tr><td style=\"white-space:nowrap\">M152.4<a name=\"GenomicTestCode-M152.464\"> </a></td><td>Neuroblastoma, Paediatric, FGFR1 seq</td></tr><tr><td style=\"white-space:nowrap\">M152.5<a name=\"GenomicTestCode-M152.465\"> </a></td><td>Neuroblastoma, Paediatric, PHOX2B seq</td></tr><tr><td style=\"white-space:nowrap\">M152.6<a name=\"GenomicTestCode-M152.466\"> </a></td><td>Neuroblastoma, Paediatric, TP53 seq</td></tr><tr><td style=\"white-space:nowrap\">M152.7<a name=\"GenomicTestCode-M152.467\"> </a></td><td>Neuroblastoma, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.8<a name=\"GenomicTestCode-M152.468\"> </a></td><td>Neuroblastoma, Paediatric, ALK copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M152.9<a name=\"GenomicTestCode-M152.469\"> </a></td><td>Neuroblastoma, Paediatric, 17q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M153.1<a name=\"GenomicTestCode-M153.461\"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, small variant (SMO)</td></tr><tr><td style=\"white-space:nowrap\">M153.2<a name=\"GenomicTestCode-M153.462\"> </a></td><td>Nodular Brain Tumour, Paediatric, SMO seq</td></tr><tr><td style=\"white-space:nowrap\">M153.3<a name=\"GenomicTestCode-M153.463\"> </a></td><td>Nodular Brain Tumour, Paediatric, SMO copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M153.4<a name=\"GenomicTestCode-M153.464\"> </a></td><td>Nodular Brain Tumour, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M153.5<a name=\"GenomicTestCode-M153.465\"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M153.6<a name=\"GenomicTestCode-M153.466\"> </a></td><td>Nodular Brain Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMO)</td></tr><tr><td style=\"white-space:nowrap\">M153.7<a name=\"GenomicTestCode-M153.467\"> </a></td><td>Nodular Brain Tumour, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M155.1<a name=\"GenomicTestCode-M155.461\"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, small variant (KIT)</td></tr><tr><td style=\"white-space:nowrap\">M155.2<a name=\"GenomicTestCode-M155.462\"> </a></td><td>Oligoastrocytoma, Paediatric, KIT copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M155.3<a name=\"GenomicTestCode-M155.463\"> </a></td><td>Oligoastrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M155.4<a name=\"GenomicTestCode-M155.464\"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M155.5<a name=\"GenomicTestCode-M155.465\"> </a></td><td>Oligoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIT)</td></tr><tr><td style=\"white-space:nowrap\">M155.6<a name=\"GenomicTestCode-M155.466\"> </a></td><td>Oligoastrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M156.1<a name=\"GenomicTestCode-M156.461\"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, small variant (RB1, ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M156.10<a name=\"GenomicTestCode-M156.4610\"> </a></td><td>Oligodendroglioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M156.2<a name=\"GenomicTestCode-M156.462\"> </a></td><td>Oligodendroglioma, Paediatric, ATRX seq</td></tr><tr><td style=\"white-space:nowrap\">M156.3<a name=\"GenomicTestCode-M156.463\"> </a></td><td>Oligodendroglioma, Paediatric, RB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M156.4<a name=\"GenomicTestCode-M156.464\"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, copy number variant (1p19q, RB1, ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M156.5<a name=\"GenomicTestCode-M156.465\"> </a></td><td>Oligodendroglioma, Paediatric, 1p19q codel FISH</td></tr><tr><td style=\"white-space:nowrap\">M156.6<a name=\"GenomicTestCode-M156.466\"> </a></td><td>Oligodendroglioma, Paediatric, RB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M156.7<a name=\"GenomicTestCode-M156.467\"> </a></td><td>Oligodendroglioma, Paediatric, ATRX copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M156.8<a name=\"GenomicTestCode-M156.468\"> </a></td><td>Oligodendroglioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M156.9<a name=\"GenomicTestCode-M156.469\"> </a></td><td>Oligodendroglioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M157.1<a name=\"GenomicTestCode-M157.461\"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, small variant (RET)</td></tr><tr><td style=\"white-space:nowrap\">M157.2<a name=\"GenomicTestCode-M157.462\"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, RET seq</td></tr><tr><td style=\"white-space:nowrap\">M157.3<a name=\"GenomicTestCode-M157.463\"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M157.4<a name=\"GenomicTestCode-M157.464\"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, RET rearrangement FISH/RT-PC</td></tr><tr><td style=\"white-space:nowrap\">M157.5<a name=\"GenomicTestCode-M157.465\"> </a></td><td>Thyroid Papillary Carcinoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M158.1<a name=\"GenomicTestCode-M158.461\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (RAF1)</td></tr><tr><td style=\"white-space:nowrap\">M158.2<a name=\"GenomicTestCode-M158.462\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1 seq</td></tr><tr><td style=\"white-space:nowrap\">M158.3<a name=\"GenomicTestCode-M158.463\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1-SRGAP3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M158.4<a name=\"GenomicTestCode-M158.464\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, RAF1-NF1A FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M158.5<a name=\"GenomicTestCode-M158.465\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M158.6<a name=\"GenomicTestCode-M158.466\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant (RAF1-SRGAP3, RAF1-NF1A, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M158.7<a name=\"GenomicTestCode-M158.467\"> </a></td><td>Pilocytic Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M159.1<a name=\"GenomicTestCode-M159.461\"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M159.2<a name=\"GenomicTestCode-M159.462\"> </a></td><td>Pituitary Blastoma, Paediatric, DICER1 seq</td></tr><tr><td style=\"white-space:nowrap\">M159.3<a name=\"GenomicTestCode-M159.463\"> </a></td><td>Pituitary Blastoma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M159.4<a name=\"GenomicTestCode-M159.464\"> </a></td><td>Pituitary Blastoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M159.5<a name=\"GenomicTestCode-M159.465\"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M159.6<a name=\"GenomicTestCode-M159.466\"> </a></td><td>Pituitary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M159.7<a name=\"GenomicTestCode-M159.467\"> </a></td><td>Pituitary Blastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M16.1<a name=\"GenomicTestCode-M16.461\"> </a></td><td>Adenoid Cystic Carcinoma, MYB-NFIB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M16.2<a name=\"GenomicTestCode-M16.462\"> </a></td><td>Adenoid Cystic Carcinoma, Multi-target NGS panel, structural variant (MYB-NFIB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M16.4<a name=\"GenomicTestCode-M16.464\"> </a></td><td>Adenoid Cystic Carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M160.1<a name=\"GenomicTestCode-M160.461\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF, H3-3A)</td></tr><tr><td style=\"white-space:nowrap\">M160.10<a name=\"GenomicTestCode-M160.4610\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.11<a name=\"GenomicTestCode-M160.4611\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, H3-3A seq</td></tr><tr><td style=\"white-space:nowrap\">M160.12<a name=\"GenomicTestCode-M160.4612\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M160.13<a name=\"GenomicTestCode-M160.4613\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M160.14<a name=\"GenomicTestCode-M160.4614\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, WGS Germline and Tumour</td></tr><tr><td style=\"white-space:nowrap\">M160.15<a name=\"GenomicTestCode-M160.4615\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)</td></tr><tr><td style=\"white-space:nowrap\">M160.16<a name=\"GenomicTestCode-M160.4616\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M160.2<a name=\"GenomicTestCode-M160.462\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M160.3<a name=\"GenomicTestCode-M160.463\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.4<a name=\"GenomicTestCode-M160.464\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.5<a name=\"GenomicTestCode-M160.465\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.6<a name=\"GenomicTestCode-M160.466\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.7<a name=\"GenomicTestCode-M160.467\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.8<a name=\"GenomicTestCode-M160.468\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M160.9<a name=\"GenomicTestCode-M160.469\"> </a></td><td>Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M161.1<a name=\"GenomicTestCode-M161.461\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M161.2<a name=\"GenomicTestCode-M161.462\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, DICER1 seq</td></tr><tr><td style=\"white-space:nowrap\">M161.3<a name=\"GenomicTestCode-M161.463\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, DICER1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M161.4<a name=\"GenomicTestCode-M161.464\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M161.5<a name=\"GenomicTestCode-M161.465\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M161.6<a name=\"GenomicTestCode-M161.466\"> </a></td><td>Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M162.1<a name=\"GenomicTestCode-M162.461\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, small variant (MSH6, PMS2, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M162.10<a name=\"GenomicTestCode-M162.4610\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, copy number variant (MYC, MSH6, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M162.11<a name=\"GenomicTestCode-M162.4611\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M162.2<a name=\"GenomicTestCode-M162.462\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MSH6 seq</td></tr><tr><td style=\"white-space:nowrap\">M162.3<a name=\"GenomicTestCode-M162.463\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, PMS2 seq</td></tr><tr><td style=\"white-space:nowrap\">M162.4<a name=\"GenomicTestCode-M162.464\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M162.5<a name=\"GenomicTestCode-M162.465\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M162.6<a name=\"GenomicTestCode-M162.466\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, MSH6 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M162.7<a name=\"GenomicTestCode-M162.467\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, PTEN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M162.8<a name=\"GenomicTestCode-M162.468\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M162.9<a name=\"GenomicTestCode-M162.469\"> </a></td><td>Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M165.1<a name=\"GenomicTestCode-M165.461\"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M165.2<a name=\"GenomicTestCode-M165.462\"> </a></td><td>Renal Tumours, Paediatric, ATRX seq</td></tr><tr><td style=\"white-space:nowrap\">M165.3<a name=\"GenomicTestCode-M165.463\"> </a></td><td>Renal Tumours, Paediatric, CTNNB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M165.4<a name=\"GenomicTestCode-M165.464\"> </a></td><td>Renal Tumours, Paediatric, DAXX seq</td></tr><tr><td style=\"white-space:nowrap\">M165.5<a name=\"GenomicTestCode-M165.465\"> </a></td><td>Renal Tumours, Paediatric, ATRX copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M165.6<a name=\"GenomicTestCode-M165.466\"> </a></td><td>Renal Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M165.7<a name=\"GenomicTestCode-M165.467\"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M165.8<a name=\"GenomicTestCode-M165.468\"> </a></td><td>Renal Tumours, Paediatric, Multi-target NGS panel, copy number variant (ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M166.1<a name=\"GenomicTestCode-M166.461\"> </a></td><td>Retinoblastoma, Paediatric, Multi-target NGS panel, small variant (RB1)</td></tr><tr><td style=\"white-space:nowrap\">M166.2<a name=\"GenomicTestCode-M166.462\"> </a></td><td>Retinoblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M166.3<a name=\"GenomicTestCode-M166.463\"> </a></td><td>Retinoblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M166.4<a name=\"GenomicTestCode-M166.464\"> </a></td><td>Retinoblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M167.1<a name=\"GenomicTestCode-M167.461\"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, small variant (SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M167.2<a name=\"GenomicTestCode-M167.462\"> </a></td><td>Rhabdoid Tumours, Paediatric, SMARCB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M167.3<a name=\"GenomicTestCode-M167.463\"> </a></td><td>Rhabdoid Tumours, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M167.4<a name=\"GenomicTestCode-M167.464\"> </a></td><td>Rhabdoid Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M167.5<a name=\"GenomicTestCode-M167.465\"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M167.6<a name=\"GenomicTestCode-M167.466\"> </a></td><td>Rhabdoid Tumours, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M168.1<a name=\"GenomicTestCode-M168.461\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, small variant (PIK3CA, FGFR1)</td></tr><tr><td style=\"white-space:nowrap\">M168.2<a name=\"GenomicTestCode-M168.462\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 seq</td></tr><tr><td style=\"white-space:nowrap\">M168.3<a name=\"GenomicTestCode-M168.463\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M168.4<a name=\"GenomicTestCode-M168.464\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 ITD FISH</td></tr><tr><td style=\"white-space:nowrap\">M168.5<a name=\"GenomicTestCode-M168.465\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M168.6<a name=\"GenomicTestCode-M168.466\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, structural variant (FGFR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M168.7<a name=\"GenomicTestCode-M168.467\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, copy number variant (FGFR1 ITD)</td></tr><tr><td style=\"white-space:nowrap\">M168.8<a name=\"GenomicTestCode-M168.468\"> </a></td><td>Rosette-Forming Glioneuronal Tumour, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M169.1<a name=\"GenomicTestCode-M169.461\"> </a></td><td>Secondary Glioblastoma, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2)</td></tr><tr><td style=\"white-space:nowrap\">M169.2<a name=\"GenomicTestCode-M169.462\"> </a></td><td>Secondary Glioblastoma, Paediatric, IDH1 seq</td></tr><tr><td style=\"white-space:nowrap\">M169.3<a name=\"GenomicTestCode-M169.463\"> </a></td><td>Secondary Glioblastoma, Paediatric, IDH2 seq</td></tr><tr><td style=\"white-space:nowrap\">M169.4<a name=\"GenomicTestCode-M169.464\"> </a></td><td>Secondary Glioblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M169.5<a name=\"GenomicTestCode-M169.465\"> </a></td><td>Secondary Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M169.6<a name=\"GenomicTestCode-M169.466\"> </a></td><td>Secondary Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M17.1<a name=\"GenomicTestCode-M17.461\"> </a></td><td>Secretory Carcinoma (Salivary Gland), ETV6-NTRK3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M17.2<a name=\"GenomicTestCode-M17.462\"> </a></td><td>Secretory Carcinoma (Salivary Gland), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M17.4<a name=\"GenomicTestCode-M17.464\"> </a></td><td>Secretory Carcinoma (Salivary Gland), DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M170.1<a name=\"GenomicTestCode-M170.461\"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SMO, DDX3X)</td></tr><tr><td style=\"white-space:nowrap\">M170.2<a name=\"GenomicTestCode-M170.462\"> </a></td><td>SHH Medulloblastoma, Paediatric, SMO seq</td></tr><tr><td style=\"white-space:nowrap\">M170.3<a name=\"GenomicTestCode-M170.463\"> </a></td><td>SHH Medulloblastoma, Paediatric, DDX3X seq</td></tr><tr><td style=\"white-space:nowrap\">M170.4<a name=\"GenomicTestCode-M170.464\"> </a></td><td>SHH Medulloblastoma, Paediatric, SMO copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M170.5<a name=\"GenomicTestCode-M170.465\"> </a></td><td>SHH Medulloblastoma, Paediatric, DDX3X copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M170.6<a name=\"GenomicTestCode-M170.466\"> </a></td><td>SHH Medulloblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M170.7<a name=\"GenomicTestCode-M170.467\"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M170.8<a name=\"GenomicTestCode-M170.468\"> </a></td><td>SHH Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMO, DDX3X)</td></tr><tr><td style=\"white-space:nowrap\">M170.9<a name=\"GenomicTestCode-M170.469\"> </a></td><td>SHH Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M171.1<a name=\"GenomicTestCode-M171.461\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, small variant (SUFU, TERT promoter, PTCH1)</td></tr><tr><td style=\"white-space:nowrap\">M171.10<a name=\"GenomicTestCode-M171.4610\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M171.2<a name=\"GenomicTestCode-M171.462\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 seq</td></tr><tr><td style=\"white-space:nowrap\">M171.3<a name=\"GenomicTestCode-M171.463\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, SUFU seq</td></tr><tr><td style=\"white-space:nowrap\">M171.4<a name=\"GenomicTestCode-M171.464\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, TERT promoter seq</td></tr><tr><td style=\"white-space:nowrap\">M171.5<a name=\"GenomicTestCode-M171.465\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M171.6<a name=\"GenomicTestCode-M171.466\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, TERT copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M171.7<a name=\"GenomicTestCode-M171.467\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M171.8<a name=\"GenomicTestCode-M171.468\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M171.9<a name=\"GenomicTestCode-M171.469\"> </a></td><td>SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (PTCH1, TERT)</td></tr><tr><td style=\"white-space:nowrap\">M172.1<a name=\"GenomicTestCode-M172.461\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, small variant (TP53, MYCN)</td></tr><tr><td style=\"white-space:nowrap\">M172.2<a name=\"GenomicTestCode-M172.462\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, TP53 seq</td></tr><tr><td style=\"white-space:nowrap\">M172.3<a name=\"GenomicTestCode-M172.463\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN seq</td></tr><tr><td style=\"white-space:nowrap\">M172.4<a name=\"GenomicTestCode-M172.464\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M172.5<a name=\"GenomicTestCode-M172.465\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M172.6<a name=\"GenomicTestCode-M172.466\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M172.7<a name=\"GenomicTestCode-M172.467\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M172.8<a name=\"GenomicTestCode-M172.468\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, copy number variant (TP53, MYCN)</td></tr><tr><td style=\"white-space:nowrap\">M172.9<a name=\"GenomicTestCode-M172.469\"> </a></td><td>SHH Medulloblastoma, TP53 MUTANT, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M173.1<a name=\"GenomicTestCode-M173.461\"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, TFEB-MALAT1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M173.2<a name=\"GenomicTestCode-M173.462\"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M173.3<a name=\"GenomicTestCode-M173.463\"> </a></td><td>t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M174.1<a name=\"GenomicTestCode-M174.461\"> </a></td><td>Testicular, Paediatric, Multi-target NGS panel, small variant (PRKAR1A)</td></tr><tr><td style=\"white-space:nowrap\">M174.2<a name=\"GenomicTestCode-M174.462\"> </a></td><td>Testicular, Paediatric, PRKAR1A seq</td></tr><tr><td style=\"white-space:nowrap\">M174.3<a name=\"GenomicTestCode-M174.463\"> </a></td><td>Testicular, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M174.4<a name=\"GenomicTestCode-M174.464\"> </a></td><td>Testicular, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M178.1<a name=\"GenomicTestCode-M178.461\"> </a></td><td>Wilms Tumours, Paediatric, Multi-target NGS panel, small variant (DROSHA)</td></tr><tr><td style=\"white-space:nowrap\">M178.2<a name=\"GenomicTestCode-M178.462\"> </a></td><td>Wilms Tumours, Paediatric, DROSHA seq</td></tr><tr><td style=\"white-space:nowrap\">M178.3<a name=\"GenomicTestCode-M178.463\"> </a></td><td>Wilms Tumours, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M178.4<a name=\"GenomicTestCode-M178.464\"> </a></td><td>Wilms Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M179.1<a name=\"GenomicTestCode-M179.461\"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (DDX3X, CTNNB1, SMARCA4, TP53)</td></tr><tr><td style=\"white-space:nowrap\">M179.10<a name=\"GenomicTestCode-M179.4610\"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, TP53)</td></tr><tr><td style=\"white-space:nowrap\">M179.11<a name=\"GenomicTestCode-M179.4611\"> </a></td><td>WNT Medulloblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M179.2<a name=\"GenomicTestCode-M179.462\"> </a></td><td>WNT Medulloblastoma, Paediatric, DDX3X seq</td></tr><tr><td style=\"white-space:nowrap\">M179.3<a name=\"GenomicTestCode-M179.463\"> </a></td><td>WNT Medulloblastoma, Paediatric, CTNNB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M179.4<a name=\"GenomicTestCode-M179.464\"> </a></td><td>WNT Medulloblastoma, Paediatric, SMARCA4 seq</td></tr><tr><td style=\"white-space:nowrap\">M179.5<a name=\"GenomicTestCode-M179.465\"> </a></td><td>WNT Medulloblastoma, Paediatric, TP53 seq</td></tr><tr><td style=\"white-space:nowrap\">M179.6<a name=\"GenomicTestCode-M179.466\"> </a></td><td>WNT Medulloblastoma, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M179.7<a name=\"GenomicTestCode-M179.467\"> </a></td><td>WNT Medulloblastoma, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M179.8<a name=\"GenomicTestCode-M179.468\"> </a></td><td>WNT Medulloblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M179.9<a name=\"GenomicTestCode-M179.469\"> </a></td><td>WNT Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M18.1<a name=\"GenomicTestCode-M18.461\"> </a></td><td>Renal Cell Carcinoma, Adult, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M18.2<a name=\"GenomicTestCode-M18.462\"> </a></td><td>Renal Cell Carcinoma,Adult, Multi-target NGS panel small variant (FH, SDHA, SDHB, SDHC, SDHD, VHL, ELOC (TCEB-1), TSC1/2, MET, BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M18.3<a name=\"GenomicTestCode-M18.463\"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 3 FISH</td></tr><tr><td style=\"white-space:nowrap\">M18.4<a name=\"GenomicTestCode-M18.464\"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 8 FISH</td></tr><tr><td style=\"white-space:nowrap\">M18.5<a name=\"GenomicTestCode-M18.465\"> </a></td><td>Renal Cell Carcinoma, Adult, Chromosome 7 &amp; 17 FISH</td></tr><tr><td style=\"white-space:nowrap\">M18.6<a name=\"GenomicTestCode-M18.466\"> </a></td><td>Renal Cell Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, TFE3, TFEB)</td></tr><tr><td style=\"white-space:nowrap\">M18.7<a name=\"GenomicTestCode-M18.467\"> </a></td><td>Renal Cell Carcinoma, Adult, TFEB rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M180.1<a name=\"GenomicTestCode-M180.461\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, small variant (TFE3)</td></tr><tr><td style=\"white-space:nowrap\">M180.2<a name=\"GenomicTestCode-M180.462\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3 seq</td></tr><tr><td style=\"white-space:nowrap\">M180.3<a name=\"GenomicTestCode-M180.463\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M180.4<a name=\"GenomicTestCode-M180.464\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-MITF FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M180.5<a name=\"GenomicTestCode-M180.465\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-PRCC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M180.6<a name=\"GenomicTestCode-M180.466\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M180.7<a name=\"GenomicTestCode-M180.467\"> </a></td><td>Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFE3-ASPSCR1, TFE3-MITF,  TFE3-PRCC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M181.1<a name=\"GenomicTestCode-M181.461\"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Multi-target NGS panel, small variant (MAP2K1)</td></tr><tr><td style=\"white-space:nowrap\">M181.4<a name=\"GenomicTestCode-M181.464\"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M181.5<a name=\"GenomicTestCode-M181.465\"> </a></td><td>Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M182.1<a name=\"GenomicTestCode-M182.461\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M182.2<a name=\"GenomicTestCode-M182.462\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M182.3<a name=\"GenomicTestCode-M182.463\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M182.4<a name=\"GenomicTestCode-M182.464\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, Multi-target NGS panel, structural variant (ALK-NPM1, other ALK rearrangements)</td></tr><tr><td style=\"white-space:nowrap\">M182.5<a name=\"GenomicTestCode-M182.465\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M182.6<a name=\"GenomicTestCode-M182.466\"> </a></td><td>ALK Positive Anaplastic Large Cell Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M183.1<a name=\"GenomicTestCode-M183.461\"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3A, NF1, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M183.2<a name=\"GenomicTestCode-M183.462\"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M183.3<a name=\"GenomicTestCode-M183.463\"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M183.4<a name=\"GenomicTestCode-M183.464\"> </a></td><td>Diffuse Midline Glioma, Paediatric, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M183.5<a name=\"GenomicTestCode-M183.465\"> </a></td><td>Diffuse Midline Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M183.6<a name=\"GenomicTestCode-M183.466\"> </a></td><td>Diffuse Midline Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M183.7<a name=\"GenomicTestCode-M183.467\"> </a></td><td>Diffuse Midline Glioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M183.8<a name=\"GenomicTestCode-M183.468\"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, MYC, MYCN)</td></tr><tr><td style=\"white-space:nowrap\">M183.9<a name=\"GenomicTestCode-M183.469\"> </a></td><td>Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M184.1<a name=\"GenomicTestCode-M184.461\"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3B, H3C2, H3C3, H3C14, IDH1, IDH2, TP53, VHL)</td></tr><tr><td style=\"white-space:nowrap\">M184.2<a name=\"GenomicTestCode-M184.462\"> </a></td><td>Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M184.3<a name=\"GenomicTestCode-M184.463\"> </a></td><td>Glioma, Paediatric, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M184.4<a name=\"GenomicTestCode-M184.464\"> </a></td><td>Glioma, Paediatric, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M184.5<a name=\"GenomicTestCode-M184.465\"> </a></td><td>Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M184.6<a name=\"GenomicTestCode-M184.466\"> </a></td><td>Glioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M184.7<a name=\"GenomicTestCode-M184.467\"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M184.8<a name=\"GenomicTestCode-M184.468\"> </a></td><td>Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M185.1<a name=\"GenomicTestCode-M185.461\"> </a></td><td>High Grade Glioma, Paediatric, Multi-target NGS panel, small variant (CDKN2B)</td></tr><tr><td style=\"white-space:nowrap\">M185.2<a name=\"GenomicTestCode-M185.462\"> </a></td><td>High Grade Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M185.3<a name=\"GenomicTestCode-M185.463\"> </a></td><td>High Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M185.4<a name=\"GenomicTestCode-M185.464\"> </a></td><td>High Grade Glioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M185.5<a name=\"GenomicTestCode-M185.465\"> </a></td><td>High Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M186.1<a name=\"GenomicTestCode-M186.461\"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, small variant (TSC1, TSC2, IDH1, IDH2, FGFR1)</td></tr><tr><td style=\"white-space:nowrap\">M186.2<a name=\"GenomicTestCode-M186.462\"> </a></td><td>Low Grade Glioma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M186.3<a name=\"GenomicTestCode-M186.463\"> </a></td><td>Low Grade Glioma, Paediatric, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M186.4<a name=\"GenomicTestCode-M186.464\"> </a></td><td>Low Grade Glioma, Paediatric, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M186.5<a name=\"GenomicTestCode-M186.465\"> </a></td><td>Low Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M186.6<a name=\"GenomicTestCode-M186.466\"> </a></td><td>Low Grade Glioma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M186.7<a name=\"GenomicTestCode-M186.467\"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M186.8<a name=\"GenomicTestCode-M186.468\"> </a></td><td>Low Grade Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M187.1<a name=\"GenomicTestCode-M187.461\"> </a></td><td>Uveal melanoma, 1p, 3, 6, 8 MLPA</td></tr><tr><td style=\"white-space:nowrap\">M187.2<a name=\"GenomicTestCode-M187.462\"> </a></td><td>Uveal melanoma, BRAF hotspot</td></tr><tr><td style=\"white-space:nowrap\">M187.3<a name=\"GenomicTestCode-M187.463\"> </a></td><td>Uveal melanoma, Multi-target NGS panel, small variant (BRAF, NRAS, NF1)</td></tr><tr><td style=\"white-space:nowrap\">M187.4<a name=\"GenomicTestCode-M187.464\"> </a></td><td>Uveal melanoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M189.1<a name=\"GenomicTestCode-M189.461\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2, BRAF, H3C2, H3C3, H3C14, H3-3A, H3-3B, TERT promoter, TP53, VHL, YAP1, SMARCA4, SMARCB1, DDX3X, CTNNB1)</td></tr><tr><td style=\"white-space:nowrap\">M189.10<a name=\"GenomicTestCode-M189.4610\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M189.11<a name=\"GenomicTestCode-M189.4611\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M189.12<a name=\"GenomicTestCode-M189.4612\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, C19MC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.13<a name=\"GenomicTestCode-M189.4613\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.14<a name=\"GenomicTestCode-M189.4614\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.15<a name=\"GenomicTestCode-M189.4615\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.16<a name=\"GenomicTestCode-M189.4616\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M189.17<a name=\"GenomicTestCode-M189.4617\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M189.18<a name=\"GenomicTestCode-M189.4618\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M189.19<a name=\"GenomicTestCode-M189.4619\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M189.2<a name=\"GenomicTestCode-M189.462\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, structural variant (CIC, BCOR, BCOR-CCNB3, C11orf95-RELA, YAP1-C11orf95, YAP1-TFE3, EWSR1, MN1, RELA, YAP1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M189.20<a name=\"GenomicTestCode-M189.4620\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M189.21<a name=\"GenomicTestCode-M189.4621\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, copy number variant  (C19MC, SMARCA4, SMARCB1, YAP1)</td></tr><tr><td style=\"white-space:nowrap\">M189.3<a name=\"GenomicTestCode-M189.463\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M189.4<a name=\"GenomicTestCode-M189.464\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M189.5<a name=\"GenomicTestCode-M189.465\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M189.6<a name=\"GenomicTestCode-M189.466\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M189.7<a name=\"GenomicTestCode-M189.467\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, EWSR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.8<a name=\"GenomicTestCode-M189.468\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, MN1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M189.9<a name=\"GenomicTestCode-M189.469\"> </a></td><td>Brain Tumour, No Further Morphological Classification, Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.1<a name=\"GenomicTestCode-M190.461\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, small variant (CDKN2A, DICER1, RB1, YAP1, SMARCA4, SMARCB1, MSH6, PMS2, PTEN, ATRX)</td></tr><tr><td style=\"white-space:nowrap\">M190.10<a name=\"GenomicTestCode-M190.4610\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.11<a name=\"GenomicTestCode-M190.4611\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.12<a name=\"GenomicTestCode-M190.4612\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.13<a name=\"GenomicTestCode-M190.4613\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.14<a name=\"GenomicTestCode-M190.4614\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.15<a name=\"GenomicTestCode-M190.4615\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, TTYH1-C19MC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.16<a name=\"GenomicTestCode-M190.4616\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.17<a name=\"GenomicTestCode-M190.4617\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.18<a name=\"GenomicTestCode-M190.4618\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.19<a name=\"GenomicTestCode-M190.4619\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.2<a name=\"GenomicTestCode-M190.462\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M190.20<a name=\"GenomicTestCode-M190.4620\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MN1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.21<a name=\"GenomicTestCode-M190.4621\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M190.22<a name=\"GenomicTestCode-M190.4622\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, C19MC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.23<a name=\"GenomicTestCode-M190.4623\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, DICER1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.24<a name=\"GenomicTestCode-M190.4624\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MSH6 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.25<a name=\"GenomicTestCode-M190.4625\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.26<a name=\"GenomicTestCode-M190.4626\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.27<a name=\"GenomicTestCode-M190.4627\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.28<a name=\"GenomicTestCode-M190.4628\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M190.3<a name=\"GenomicTestCode-M190.463\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.30<a name=\"GenomicTestCode-M190.4630\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M190.31<a name=\"GenomicTestCode-M190.4631\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M190.32<a name=\"GenomicTestCode-M190.4632\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, copy number variant  (C19MC, DICER1, MSH6, MYC, PTEN, SMARCA4, SMARCB1)</td></tr><tr><td style=\"white-space:nowrap\">M190.4<a name=\"GenomicTestCode-M190.464\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.5<a name=\"GenomicTestCode-M190.465\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.6<a name=\"GenomicTestCode-M190.466\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.7<a name=\"GenomicTestCode-M190.467\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.8<a name=\"GenomicTestCode-M190.468\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-FRX1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M190.9<a name=\"GenomicTestCode-M190.469\"> </a></td><td>Embryonal Tumour Differential, Adult and Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.1<a name=\"GenomicTestCode-M191.461\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style=\"white-space:nowrap\">M191.10<a name=\"GenomicTestCode-M191.4610\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M191.11<a name=\"GenomicTestCode-M191.4611\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M191.12<a name=\"GenomicTestCode-M191.4612\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.13<a name=\"GenomicTestCode-M191.4613\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M191.14<a name=\"GenomicTestCode-M191.4614\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M191.15<a name=\"GenomicTestCode-M191.4615\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.16<a name=\"GenomicTestCode-M191.4616\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.17<a name=\"GenomicTestCode-M191.4617\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M191.18<a name=\"GenomicTestCode-M191.4618\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M191.19<a name=\"GenomicTestCode-M191.4619\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M191.2<a name=\"GenomicTestCode-M191.462\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.20<a name=\"GenomicTestCode-M191.4620\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M191.21<a name=\"GenomicTestCode-M191.4621\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M191.22<a name=\"GenomicTestCode-M191.4622\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M191.3<a name=\"GenomicTestCode-M191.463\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.4<a name=\"GenomicTestCode-M191.464\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.5<a name=\"GenomicTestCode-M191.465\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.6<a name=\"GenomicTestCode-M191.466\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.7<a name=\"GenomicTestCode-M191.467\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.8<a name=\"GenomicTestCode-M191.468\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M191.9<a name=\"GenomicTestCode-M191.469\"> </a></td><td>Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.1<a name=\"GenomicTestCode-M192.461\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX,  H3-3A, H3-3B, H3C2, H3C3,  H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style=\"white-space:nowrap\">M192.10<a name=\"GenomicTestCode-M192.4610\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M192.11<a name=\"GenomicTestCode-M192.4611\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style=\"white-space:nowrap\">M192.12<a name=\"GenomicTestCode-M192.4612\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.13<a name=\"GenomicTestCode-M192.4613\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M192.14<a name=\"GenomicTestCode-M192.4614\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M192.15<a name=\"GenomicTestCode-M192.4615\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.16<a name=\"GenomicTestCode-M192.4616\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.17<a name=\"GenomicTestCode-M192.4617\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M192.18<a name=\"GenomicTestCode-M192.4618\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M192.19<a name=\"GenomicTestCode-M192.4619\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M192.2<a name=\"GenomicTestCode-M192.462\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.20<a name=\"GenomicTestCode-M192.4620\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M192.21<a name=\"GenomicTestCode-M192.4621\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M192.22<a name=\"GenomicTestCode-M192.4622\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M192.23<a name=\"GenomicTestCode-M192.4623\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M192.3<a name=\"GenomicTestCode-M192.463\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.4<a name=\"GenomicTestCode-M192.464\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.5<a name=\"GenomicTestCode-M192.465\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.6<a name=\"GenomicTestCode-M192.466\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.7<a name=\"GenomicTestCode-M192.467\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.8<a name=\"GenomicTestCode-M192.468\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M192.9<a name=\"GenomicTestCode-M192.469\"> </a></td><td>High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.1<a name=\"GenomicTestCode-M193.461\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3-3B, H3C2, H3C3, H3C14, BRAF, TERT promoter, CDKN2B, TP53, VHL, NF1)</td></tr><tr><td style=\"white-space:nowrap\">M193.10<a name=\"GenomicTestCode-M193.4610\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M193.11<a name=\"GenomicTestCode-M193.4611\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style=\"white-space:nowrap\">M193.12<a name=\"GenomicTestCode-M193.4612\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.13<a name=\"GenomicTestCode-M193.4613\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M193.14<a name=\"GenomicTestCode-M193.4614\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M193.15<a name=\"GenomicTestCode-M193.4615\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.16<a name=\"GenomicTestCode-M193.4616\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.17<a name=\"GenomicTestCode-M193.4617\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M193.18<a name=\"GenomicTestCode-M193.4618\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M193.19<a name=\"GenomicTestCode-M193.4619\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M193.2<a name=\"GenomicTestCode-M193.462\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.20<a name=\"GenomicTestCode-M193.4620\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M193.21<a name=\"GenomicTestCode-M193.4621\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M193.22<a name=\"GenomicTestCode-M193.4622\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)</td></tr><tr><td style=\"white-space:nowrap\">M193.23<a name=\"GenomicTestCode-M193.4623\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M193.3<a name=\"GenomicTestCode-M193.463\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.4<a name=\"GenomicTestCode-M193.464\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.5<a name=\"GenomicTestCode-M193.465\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.6<a name=\"GenomicTestCode-M193.466\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.7<a name=\"GenomicTestCode-M193.467\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.8<a name=\"GenomicTestCode-M193.468\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M193.9<a name=\"GenomicTestCode-M193.469\"> </a></td><td>Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M194.1<a name=\"GenomicTestCode-M194.461\"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, small variant (ALK, BCOR, CTNNB1, DDX3X, DDX3X, EZH2, MYCN,  PTCH1, PTCH2, PTEN, SMARCA4, SMO, SUFU, TERT promoter, TP53,  YAP1)</td></tr><tr><td style=\"white-space:nowrap\">M194.10<a name=\"GenomicTestCode-M194.4610\"> </a></td><td>Medulloblastoma all Subtypes, BCOR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.11<a name=\"GenomicTestCode-M194.4611\"> </a></td><td>Medulloblastoma all Subtypes, C19MC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.12<a name=\"GenomicTestCode-M194.4612\"> </a></td><td>Medulloblastoma all Subtypes, DDX3X copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.13<a name=\"GenomicTestCode-M194.4613\"> </a></td><td>Medulloblastoma all Subtypes, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.14<a name=\"GenomicTestCode-M194.4614\"> </a></td><td>Medulloblastoma all Subtypes, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.15<a name=\"GenomicTestCode-M194.4615\"> </a></td><td>Medulloblastoma all Subtypes, PTCH1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.16<a name=\"GenomicTestCode-M194.4616\"> </a></td><td>Medulloblastoma all Subtypes, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M194.17<a name=\"GenomicTestCode-M194.4617\"> </a></td><td>Medulloblastoma all Subtypes, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.18<a name=\"GenomicTestCode-M194.4618\"> </a></td><td>Medulloblastoma all Subtypes, SMO copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.19<a name=\"GenomicTestCode-M194.4619\"> </a></td><td>Medulloblastoma all Subtypes, TERT copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.2<a name=\"GenomicTestCode-M194.462\"> </a></td><td>Medulloblastoma all Subtypes, ALK rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.20<a name=\"GenomicTestCode-M194.4620\"> </a></td><td>Medulloblastoma all Subtypes, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.21<a name=\"GenomicTestCode-M194.4621\"> </a></td><td>Medulloblastoma all Subtypes, YAP1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.22<a name=\"GenomicTestCode-M194.4622\"> </a></td><td>Medulloblastoma all Subtypes, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M194.23<a name=\"GenomicTestCode-M194.4623\"> </a></td><td>Medulloblastoma all Subtypes, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M194.24<a name=\"GenomicTestCode-M194.4624\"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, structural variant (ALK, BCOR, MYC, PVT1-MYC, YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M194.25<a name=\"GenomicTestCode-M194.4625\"> </a></td><td>Medulloblastoma all Subtypes, Multi-target NGS panel, copy number variant  (ALK, BCOR, C19MC, DDX3X, MYC, MYCN, PTCH1, PTEN, SMARCA4, SMO, TERT, TP53, YAP1)</td></tr><tr><td style=\"white-space:nowrap\">M194.3<a name=\"GenomicTestCode-M194.463\"> </a></td><td>Medulloblastoma all Subtypes, BCOR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.4<a name=\"GenomicTestCode-M194.464\"> </a></td><td>Medulloblastoma all Subtypes, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M194.5<a name=\"GenomicTestCode-M194.465\"> </a></td><td>Medulloblastoma all Subtypes, PVT1-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M194.6<a name=\"GenomicTestCode-M194.466\"> </a></td><td>Medulloblastoma all Subtypes, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M194.7<a name=\"GenomicTestCode-M194.467\"> </a></td><td>Medulloblastoma all Subtypes, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M194.8<a name=\"GenomicTestCode-M194.468\"> </a></td><td>Medulloblastoma all Subtypes, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M194.9<a name=\"GenomicTestCode-M194.469\"> </a></td><td>Medulloblastoma all Subtypes, ALK copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M195.1<a name=\"GenomicTestCode-M195.461\"> </a></td><td>Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, small variant (BRAF, CTNNB1)</td></tr><tr><td style=\"white-space:nowrap\">M195.2<a name=\"GenomicTestCode-M195.462\"> </a></td><td>Craniopharyngioma, Adult and Paediatric, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M195.3<a name=\"GenomicTestCode-M195.463\"> </a></td><td>Craniopharyngioma, Adult and Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M195.4<a name=\"GenomicTestCode-M195.464\"> </a></td><td>Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M195.5<a name=\"GenomicTestCode-M195.465\"> </a></td><td>Craniopharyngioma, Adult and Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M196.1<a name=\"GenomicTestCode-M196.461\"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M196.2<a name=\"GenomicTestCode-M196.462\"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M196.3<a name=\"GenomicTestCode-M196.463\"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M196.4<a name=\"GenomicTestCode-M196.464\"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M196.5<a name=\"GenomicTestCode-M196.465\"> </a></td><td>Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M197.1<a name=\"GenomicTestCode-M197.461\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, Multi-target NGS panel, structural variant (BCOR, CIC, DDIT3, EWSR1, FOXO1, WT1, BCOR-CCNB3, HEY1-NCOA2, PAX3-FOXO1, PAX7-FOXO1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M197.10<a name=\"GenomicTestCode-M197.4610\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M197.2<a name=\"GenomicTestCode-M197.462\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.3<a name=\"GenomicTestCode-M197.463\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.4<a name=\"GenomicTestCode-M197.464\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.5<a name=\"GenomicTestCode-M197.465\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.6<a name=\"GenomicTestCode-M197.466\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.7<a name=\"GenomicTestCode-M197.467\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.8<a name=\"GenomicTestCode-M197.468\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, PAX3-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M197.9<a name=\"GenomicTestCode-M197.469\"> </a></td><td>Round Cell Sarcoma of Soft Tissue Differential, PAX7-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M198.1<a name=\"GenomicTestCode-M198.461\"> </a></td><td>Vascular Soft Tissue Tumour Differential, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M198.2<a name=\"GenomicTestCode-M198.462\"> </a></td><td>Vascular Soft Tissue Tumour Differential, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M198.3<a name=\"GenomicTestCode-M198.463\"> </a></td><td>Vascular Soft Tissue Tumour Differential, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M198.4<a name=\"GenomicTestCode-M198.464\"> </a></td><td>Vascular Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M198.5<a name=\"GenomicTestCode-M198.465\"> </a></td><td>Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M198.6<a name=\"GenomicTestCode-M198.466\"> </a></td><td>Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style=\"white-space:nowrap\">M199.1<a name=\"GenomicTestCode-M199.461\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, small variant (APC, CTNNB1)</td></tr><tr><td style=\"white-space:nowrap\">M199.10<a name=\"GenomicTestCode-M199.4610\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, TPM4-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M199.11<a name=\"GenomicTestCode-M199.4611\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, ETV6-NTRK3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M199.12<a name=\"GenomicTestCode-M199.4612\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M199.13<a name=\"GenomicTestCode-M199.4613\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M199.2<a name=\"GenomicTestCode-M199.462\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, SS18, USP6, COL1A1-PDGFB, TPM3-ALK, TPM4-ALK, ETV6-NTRK3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M199.3<a name=\"GenomicTestCode-M199.463\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M199.4<a name=\"GenomicTestCode-M199.464\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, FUS rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M199.5<a name=\"GenomicTestCode-M199.465\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M199.6<a name=\"GenomicTestCode-M199.466\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M199.7<a name=\"GenomicTestCode-M199.467\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M199.8<a name=\"GenomicTestCode-M199.468\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, COL1A1-PDGFB rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M199.9<a name=\"GenomicTestCode-M199.469\"> </a></td><td>Spindle Cell Soft Tissue Tumour Differential, TPM3-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M2.1<a name=\"GenomicTestCode-M2.461\"> </a></td><td>Ovarian Carcinoma, Multi-target NGS panel, small variant (BRCA1, BRCA2, SMARCA4)</td></tr><tr><td style=\"white-space:nowrap\">M2.3<a name=\"GenomicTestCode-M2.463\"> </a></td><td>Ovarian Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M2.5<a name=\"GenomicTestCode-M2.465\"> </a></td><td>Ovarian Carcinoma, HRD status (either positive for BRCA 1 and/or 2, or HRD positive)</td></tr><tr><td style=\"white-space:nowrap\">M20.1<a name=\"GenomicTestCode-M20.461\"> </a></td><td>Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF)</td></tr><tr><td style=\"white-space:nowrap\">M20.2<a name=\"GenomicTestCode-M20.462\"> </a></td><td>Anaplastic Astrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M20.3<a name=\"GenomicTestCode-M20.463\"> </a></td><td>Anaplastic Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M20.4<a name=\"GenomicTestCode-M20.464\"> </a></td><td>Anaplastic Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M20.5<a name=\"GenomicTestCode-M20.465\"> </a></td><td>Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M200.1<a name=\"GenomicTestCode-M200.461\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (BCOR, DDIT3, FUS, NR4A3, TGFBR3-OGA, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M200.2<a name=\"GenomicTestCode-M200.462\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M200.3<a name=\"GenomicTestCode-M200.463\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M200.4<a name=\"GenomicTestCode-M200.464\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, NR4A3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M200.5<a name=\"GenomicTestCode-M200.465\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, TGFBR3-OGA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M200.6<a name=\"GenomicTestCode-M200.466\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M200.7<a name=\"GenomicTestCode-M200.467\"> </a></td><td>Myxoid Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M201.1<a name=\"GenomicTestCode-M201.461\"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M201.2<a name=\"GenomicTestCode-M201.462\"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M201.3<a name=\"GenomicTestCode-M201.463\"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M201.4<a name=\"GenomicTestCode-M201.464\"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M201.5<a name=\"GenomicTestCode-M201.465\"> </a></td><td>Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M202.1<a name=\"GenomicTestCode-M202.461\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M202.2<a name=\"GenomicTestCode-M202.462\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M202.3<a name=\"GenomicTestCode-M202.463\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M202.4<a name=\"GenomicTestCode-M202.464\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M202.5<a name=\"GenomicTestCode-M202.465\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, WWTR1-CAMTA1  RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M202.6<a name=\"GenomicTestCode-M202.466\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M202.7<a name=\"GenomicTestCode-M202.467\"> </a></td><td>Epithelioid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (EWSR1, FUS, SS18, TFE3, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M203.1<a name=\"GenomicTestCode-M203.461\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), EPC1-PHF1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M203.2<a name=\"GenomicTestCode-M203.462\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), JAZF1-PHF1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M203.3<a name=\"GenomicTestCode-M203.463\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), JAZF1-SUZ12 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M203.4<a name=\"GenomicTestCode-M203.464\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), NUTM2B-YWHAE FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M203.5<a name=\"GenomicTestCode-M203.465\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M203.6<a name=\"GenomicTestCode-M203.466\"> </a></td><td>Uterine Sarcomas (Inc Endometrial), Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NUTM2B-YWHAE, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M204.1<a name=\"GenomicTestCode-M204.461\"> </a></td><td>Undifferentiated tumour, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M204.2<a name=\"GenomicTestCode-M204.462\"> </a></td><td>Undifferentiated tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M205.1<a name=\"GenomicTestCode-M205.461\"> </a></td><td>Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B, IDH1, IDH2)</td></tr><tr><td style=\"white-space:nowrap\">M205.2<a name=\"GenomicTestCode-M205.462\"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style=\"white-space:nowrap\">M205.3<a name=\"GenomicTestCode-M205.463\"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3A seq</td></tr><tr><td style=\"white-space:nowrap\">M205.4<a name=\"GenomicTestCode-M205.464\"> </a></td><td>Cartilage Forming Bone Tumour Differential, H3-3B seq</td></tr><tr><td style=\"white-space:nowrap\">M205.5<a name=\"GenomicTestCode-M205.465\"> </a></td><td>Cartilage Forming Bone Tumour Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M205.6<a name=\"GenomicTestCode-M205.466\"> </a></td><td>Cartilage Forming Bone Tumour Differential, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M205.7<a name=\"GenomicTestCode-M205.467\"> </a></td><td>Cartilage Forming Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M205.8<a name=\"GenomicTestCode-M205.468\"> </a></td><td>Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M206.1<a name=\"GenomicTestCode-M206.461\"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B)</td></tr><tr><td style=\"white-space:nowrap\">M206.2<a name=\"GenomicTestCode-M206.462\"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style=\"white-space:nowrap\">M206.3<a name=\"GenomicTestCode-M206.463\"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3A seq</td></tr><tr><td style=\"white-space:nowrap\">M206.4<a name=\"GenomicTestCode-M206.464\"> </a></td><td>Bone Forming Bone Tumour Differential, H3-3B seq</td></tr><tr><td style=\"white-space:nowrap\">M206.5<a name=\"GenomicTestCode-M206.465\"> </a></td><td>Bone Forming Bone Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M206.6<a name=\"GenomicTestCode-M206.466\"> </a></td><td>Bone Forming Bone Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M206.7<a name=\"GenomicTestCode-M206.467\"> </a></td><td>Bone Forming Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M206.8<a name=\"GenomicTestCode-M206.468\"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M206.9<a name=\"GenomicTestCode-M206.469\"> </a></td><td>Bone Forming Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M207.1<a name=\"GenomicTestCode-M207.461\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3B)</td></tr><tr><td style=\"white-space:nowrap\">M207.2<a name=\"GenomicTestCode-M207.462\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, H3-3B seq</td></tr><tr><td style=\"white-space:nowrap\">M207.3<a name=\"GenomicTestCode-M207.463\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, H3-3B hotspot</td></tr><tr><td style=\"white-space:nowrap\">M207.4<a name=\"GenomicTestCode-M207.464\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M207.5<a name=\"GenomicTestCode-M207.465\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M207.6<a name=\"GenomicTestCode-M207.466\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M207.7<a name=\"GenomicTestCode-M207.467\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M207.8<a name=\"GenomicTestCode-M207.468\"> </a></td><td>Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M208.1<a name=\"GenomicTestCode-M208.461\"> </a></td><td>Round Cell Sarcoma of Bone Differential, Multi-target NGS panel, structural variant (BCOR, CIC, EWSR1, WT1, BCOR-CCNB3, HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M208.2<a name=\"GenomicTestCode-M208.462\"> </a></td><td>Round Cell Sarcoma of Bone Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M208.3<a name=\"GenomicTestCode-M208.463\"> </a></td><td>Round Cell Sarcoma of Bone Differential, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M208.4<a name=\"GenomicTestCode-M208.464\"> </a></td><td>Round Cell Sarcoma of Bone Differential, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M208.5<a name=\"GenomicTestCode-M208.465\"> </a></td><td>Round Cell Sarcoma of Bone Differential, HEY1-NCOA2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M208.6<a name=\"GenomicTestCode-M208.466\"> </a></td><td>Round Cell Sarcoma of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M209.1<a name=\"GenomicTestCode-M209.461\"> </a></td><td>Vascular Tumour of Bone Differential, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M209.2<a name=\"GenomicTestCode-M209.462\"> </a></td><td>Vascular Tumour of Bone Differential, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M209.3<a name=\"GenomicTestCode-M209.463\"> </a></td><td>Vascular Tumour of Bone Differential, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M209.4<a name=\"GenomicTestCode-M209.464\"> </a></td><td>Vascular Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M209.5<a name=\"GenomicTestCode-M209.465\"> </a></td><td>Vascular Tumour of Bone Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M209.6<a name=\"GenomicTestCode-M209.466\"> </a></td><td>Vascular Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style=\"white-space:nowrap\">M21.1<a name=\"GenomicTestCode-M21.461\"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A,H3C2, BRAF, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M21.2<a name=\"GenomicTestCode-M21.462\"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, copy number variant (EGFR, CDKN2A, CDKN2B)</td></tr><tr><td style=\"white-space:nowrap\">M21.20<a name=\"GenomicTestCode-M21.4620\"> </a></td><td>Astrocytoma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M21.21<a name=\"GenomicTestCode-M21.4621\"> </a></td><td>Astrocytoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M21.22<a name=\"GenomicTestCode-M21.4622\"> </a></td><td>Astrocytoma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M21.23<a name=\"GenomicTestCode-M21.4623\"> </a></td><td>Astrocytoma, Adult, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M21.24<a name=\"GenomicTestCode-M21.4624\"> </a></td><td>Astrocytoma, Adult, CDKN2B copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M21.3<a name=\"GenomicTestCode-M21.463\"> </a></td><td>Astrocytoma, Adult, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M21.5<a name=\"GenomicTestCode-M21.465\"> </a></td><td>Astrocytoma, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M21.6<a name=\"GenomicTestCode-M21.466\"> </a></td><td>Astrocytoma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M21.8<a name=\"GenomicTestCode-M21.468\"> </a></td><td>Astrocytoma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M21.9<a name=\"GenomicTestCode-M21.469\"> </a></td><td>Astrocytoma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M210.1<a name=\"GenomicTestCode-M210.461\"> </a></td><td>Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M210.2<a name=\"GenomicTestCode-M210.462\"> </a></td><td>Spindle Cell Tumour of Bone Differential, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M210.3<a name=\"GenomicTestCode-M210.463\"> </a></td><td>Spindle Cell Tumour of Bone Differential, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M210.4<a name=\"GenomicTestCode-M210.464\"> </a></td><td>Spindle Cell Tumour of Bone Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M210.5<a name=\"GenomicTestCode-M210.465\"> </a></td><td>Spindle Cell Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M210.6<a name=\"GenomicTestCode-M210.466\"> </a></td><td>Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M211.1<a name=\"GenomicTestCode-M211.461\"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, small variant (GNAS)</td></tr><tr><td style=\"white-space:nowrap\">M211.2<a name=\"GenomicTestCode-M211.462\"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M211.3<a name=\"GenomicTestCode-M211.463\"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M211.4<a name=\"GenomicTestCode-M211.464\"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M211.5<a name=\"GenomicTestCode-M211.465\"> </a></td><td>Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M212.1<a name=\"GenomicTestCode-M212.461\"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX, TP53, TFE3)</td></tr><tr><td style=\"white-space:nowrap\">M212.10<a name=\"GenomicTestCode-M212.4610\"> </a></td><td>Renal Tumour Differential, Paediatric, TFEB-MALAT1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M212.11<a name=\"GenomicTestCode-M212.4611\"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M212.12<a name=\"GenomicTestCode-M212.4612\"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-MITF FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M212.13<a name=\"GenomicTestCode-M212.4613\"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3-PRCC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M212.14<a name=\"GenomicTestCode-M212.4614\"> </a></td><td>Renal Tumour Differential, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M212.15<a name=\"GenomicTestCode-M212.4615\"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, TFE3-ASPSCR1, TFE3-MITF, TFE3-PRCC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M212.16<a name=\"GenomicTestCode-M212.4616\"> </a></td><td>Renal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (ATRX, TP53, WT1)</td></tr><tr><td style=\"white-space:nowrap\">M212.2<a name=\"GenomicTestCode-M212.462\"> </a></td><td>Renal Tumour Differential, Paediatric, ATRX seq</td></tr><tr><td style=\"white-space:nowrap\">M212.3<a name=\"GenomicTestCode-M212.463\"> </a></td><td>Renal Tumour Differential, Paediatric, CTNNB1 seq</td></tr><tr><td style=\"white-space:nowrap\">M212.4<a name=\"GenomicTestCode-M212.464\"> </a></td><td>Renal Tumour Differential, Paediatric, DAXX seq</td></tr><tr><td style=\"white-space:nowrap\">M212.5<a name=\"GenomicTestCode-M212.465\"> </a></td><td>Renal Tumour Differential, Paediatric, TFE3 seq</td></tr><tr><td style=\"white-space:nowrap\">M212.6<a name=\"GenomicTestCode-M212.466\"> </a></td><td>Renal Tumour Differential, Paediatric, TP53 seq</td></tr><tr><td style=\"white-space:nowrap\">M212.7<a name=\"GenomicTestCode-M212.467\"> </a></td><td>Renal Tumour Differential, Paediatric, ATRX copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M212.8<a name=\"GenomicTestCode-M212.468\"> </a></td><td>Renal Tumour Differential, Paediatric, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M212.9<a name=\"GenomicTestCode-M212.469\"> </a></td><td>Renal Tumour Differential, Paediatric, WT1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.1<a name=\"GenomicTestCode-M213.461\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1, DDX3X, CTNNB1, CDKN2A, TP53, RAF1, PIK3CA, FGFR1, FGFR4, KIT,  BRAF, H3-3A, ALK, ATRX, NRAS, PHOX2B)</td></tr><tr><td style=\"white-space:nowrap\">M213.10<a name=\"GenomicTestCode-M213.4610\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.11<a name=\"GenomicTestCode-M213.4611\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.12<a name=\"GenomicTestCode-M213.4612\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, ALK-NPM1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.13<a name=\"GenomicTestCode-M213.4613\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.14<a name=\"GenomicTestCode-M213.4614\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EWSR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.15<a name=\"GenomicTestCode-M213.4615\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.16<a name=\"GenomicTestCode-M213.4616\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-NF1A FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.17<a name=\"GenomicTestCode-M213.4617\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-SRGAP3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.18<a name=\"GenomicTestCode-M213.4618\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.19<a name=\"GenomicTestCode-M213.4619\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.2<a name=\"GenomicTestCode-M213.462\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, ALK, C1</td></tr><tr><td style=\"white-space:nowrap\">M213.20<a name=\"GenomicTestCode-M213.4620\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.21<a name=\"GenomicTestCode-M213.4621\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.22<a name=\"GenomicTestCode-M213.4622\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, EGFR, ALK, C19MC, CDKN2A,  FGFR1, KIAA1549, KIT, MYCN, PDGFRA, SMARCA4, SMARCB1, YAP1)</td></tr><tr><td style=\"white-space:nowrap\">M213.23<a name=\"GenomicTestCode-M213.4623\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.24<a name=\"GenomicTestCode-M213.4624\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, ALK copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.25<a name=\"GenomicTestCode-M213.4625\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, C19MC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.26<a name=\"GenomicTestCode-M213.4626\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.27<a name=\"GenomicTestCode-M213.4627\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.28<a name=\"GenomicTestCode-M213.4628\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 ITD FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.29<a name=\"GenomicTestCode-M213.4629\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, KIAA1549 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.3<a name=\"GenomicTestCode-M213.463\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.30<a name=\"GenomicTestCode-M213.4630\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, KIT copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.31<a name=\"GenomicTestCode-M213.4631\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.32<a name=\"GenomicTestCode-M213.4632\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, PDGFRA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.33<a name=\"GenomicTestCode-M213.4633\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, SMARCA4 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.34<a name=\"GenomicTestCode-M213.4634\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, SMARCB1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.35<a name=\"GenomicTestCode-M213.4635\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M213.36<a name=\"GenomicTestCode-M213.4636\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.37<a name=\"GenomicTestCode-M213.4637\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M213.38<a name=\"GenomicTestCode-M213.4638\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M213.4<a name=\"GenomicTestCode-M213.464\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.5<a name=\"GenomicTestCode-M213.465\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.6<a name=\"GenomicTestCode-M213.466\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.7<a name=\"GenomicTestCode-M213.467\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.8<a name=\"GenomicTestCode-M213.468\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FRX1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M213.9<a name=\"GenomicTestCode-M213.469\"> </a></td><td>Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M215.1<a name=\"GenomicTestCode-M215.461\"> </a></td><td>Endometrial Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M215.2<a name=\"GenomicTestCode-M215.462\"> </a></td><td>Endometrial Cancer, MLH1 promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M215.4<a name=\"GenomicTestCode-M215.464\"> </a></td><td>Endometrial Cancer, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2)</td></tr><tr><td style=\"white-space:nowrap\">M215.5<a name=\"GenomicTestCode-M215.465\"> </a></td><td>Endometrial Cancer, Multi-target NGS panel-small variant detection POLE</td></tr><tr><td style=\"white-space:nowrap\">M217.1<a name=\"GenomicTestCode-M217.461\"> </a></td><td>Urothelial Cancer, Multi-target NGS panel, small variant (FGFR3, FGFR2)</td></tr><tr><td style=\"white-space:nowrap\">M217.2<a name=\"GenomicTestCode-M217.462\"> </a></td><td>Bladder Cancer, Multi-target NGS panel, copy number variant (FGFR3, FGFR2)</td></tr><tr><td style=\"white-space:nowrap\">M217.3<a name=\"GenomicTestCode-M217.463\"> </a></td><td>Bladder Cancer, Multi-target NGS panel, structural variant (FGFR3, FGFR2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M218.1<a name=\"GenomicTestCode-M218.461\"> </a></td><td>Prostate Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2, ATM, CDK12)</td></tr><tr><td style=\"white-space:nowrap\">M218.2<a name=\"GenomicTestCode-M218.462\"> </a></td><td>Prostate Cancer, Multi-target NGS panel, structural variant (TMPRSS2-ERG, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M218.3<a name=\"GenomicTestCode-M218.463\"> </a></td><td>Prostate Cancer, TMPRSS2-ERG FISH</td></tr><tr><td style=\"white-space:nowrap\">M219.1<a name=\"GenomicTestCode-M219.461\"> </a></td><td>Pancreatic Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2)</td></tr><tr><td style=\"white-space:nowrap\">M219.2<a name=\"GenomicTestCode-M219.462\"> </a></td><td>Pancreatic Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M219.3<a name=\"GenomicTestCode-M219.463\"> </a></td><td>Pancreatic Cancer, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M219.5<a name=\"GenomicTestCode-M219.465\"> </a></td><td>Pancreatic Cancer, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M22.1<a name=\"GenomicTestCode-M22.461\"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, small variant (H3C2, H3C14, IDH1, IDH2)</td></tr><tr><td style=\"white-space:nowrap\">M22.10<a name=\"GenomicTestCode-M22.4610\"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYB rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M22.11<a name=\"GenomicTestCode-M22.4611\"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYBL1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M22.12<a name=\"GenomicTestCode-M22.4612\"> </a></td><td>Diffuse Astrocytoma, Paediatric, MN1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M22.2<a name=\"GenomicTestCode-M22.462\"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M22.3<a name=\"GenomicTestCode-M22.463\"> </a></td><td>Diffuse Astrocytoma, Paediatric, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M22.4<a name=\"GenomicTestCode-M22.464\"> </a></td><td>Diffuse Astrocytoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M22.5<a name=\"GenomicTestCode-M22.465\"> </a></td><td>Diffuse Astrocytoma, Paediatric, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M22.6<a name=\"GenomicTestCode-M22.466\"> </a></td><td>Diffuse Astrocytoma, Paediatric, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M22.7<a name=\"GenomicTestCode-M22.467\"> </a></td><td>Diffuse Astrocytoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M22.8<a name=\"GenomicTestCode-M22.468\"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style=\"white-space:nowrap\">M22.9<a name=\"GenomicTestCode-M22.469\"> </a></td><td>Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (MYC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M220.1<a name=\"GenomicTestCode-M220.461\"> </a></td><td>Cholangiocarcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, FGFR2)</td></tr><tr><td style=\"white-space:nowrap\">M220.3<a name=\"GenomicTestCode-M220.463\"> </a></td><td>Cholangiocarcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M220.5<a name=\"GenomicTestCode-M220.465\"> </a></td><td>Cholangiocarcinoma, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M220.6<a name=\"GenomicTestCode-M220.466\"> </a></td><td>Cholangiocarcinoma, Multi-target NGS panel -small variant (IDH1)</td></tr><tr><td style=\"white-space:nowrap\">M220.7<a name=\"GenomicTestCode-M220.467\"> </a></td><td>Cholangiocarcinoma, FGFR2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M221.1<a name=\"GenomicTestCode-M221.461\"> </a></td><td>Spitzoid tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M222.2<a name=\"GenomicTestCode-M222.462\"> </a></td><td>Hepatocellular carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M222.4<a name=\"GenomicTestCode-M222.464\"> </a></td><td>Hepatocellular carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M224.1<a name=\"GenomicTestCode-M224.461\"> </a></td><td>MDS/MPN, Multi-target NGS panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">M224.10<a name=\"GenomicTestCode-M224.4610\"> </a></td><td>MDS/MPN, BCR-ABL1 multiplex</td></tr><tr><td style=\"white-space:nowrap\">M224.11<a name=\"GenomicTestCode-M224.4611\"> </a></td><td>MDS/MPN, Other RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M224.13<a name=\"GenomicTestCode-M224.4613\"> </a></td><td>MDS/MPN, JAK2 V617F hotspot</td></tr><tr><td style=\"white-space:nowrap\">M224.14<a name=\"GenomicTestCode-M224.4614\"> </a></td><td>MDS/MPN, JAK2 exon 12 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M224.15<a name=\"GenomicTestCode-M224.4615\"> </a></td><td>MDS/MPN, CALR exon 9 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M224.16<a name=\"GenomicTestCode-M224.4616\"> </a></td><td>MDS/MPN, MPL exon 10 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M224.18<a name=\"GenomicTestCode-M224.4618\"> </a></td><td>MDS/MPN, Chr8 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.19<a name=\"GenomicTestCode-M224.4619\"> </a></td><td>MDS/MPN, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.2<a name=\"GenomicTestCode-M224.462\"> </a></td><td>MDS/MPN, Karyotype (To include detection of complex karyotype)</td></tr><tr><td style=\"white-space:nowrap\">M224.20<a name=\"GenomicTestCode-M224.4620\"> </a></td><td>MDS/MPN, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.21<a name=\"GenomicTestCode-M224.4621\"> </a></td><td>MDS/MPN, i(17q)/t(17p) FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.22<a name=\"GenomicTestCode-M224.4622\"> </a></td><td>MDS/MPN, Chr12p copy number FISH, t(12p) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.23<a name=\"GenomicTestCode-M224.4623\"> </a></td><td>MDS/MPN, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.24<a name=\"GenomicTestCode-M224.4624\"> </a></td><td>MDS/MPN, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)</td></tr><tr><td style=\"white-space:nowrap\">M224.25<a name=\"GenomicTestCode-M224.4625\"> </a></td><td>MDS/MPN, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)</td></tr><tr><td style=\"white-space:nowrap\">M224.26<a name=\"GenomicTestCode-M224.4626\"> </a></td><td>MDS/MPN, FGFR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.27<a name=\"GenomicTestCode-M224.4627\"> </a></td><td>MDS/MPN, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)</td></tr><tr><td style=\"white-space:nowrap\">M224.28<a name=\"GenomicTestCode-M224.4628\"> </a></td><td>MDS/MPN, inv(3)/t(3;3) FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.29<a name=\"GenomicTestCode-M224.4629\"> </a></td><td>MDS/MPN, 11q23 (KMT2A) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.3<a name=\"GenomicTestCode-M224.463\"> </a></td><td>MDS/MPN, FISH copy number and rearrangement Other: See tests M224. -M224. for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M224.30<a name=\"GenomicTestCode-M224.4630\"> </a></td><td>MDS/MPN, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)</td></tr><tr><td style=\"white-space:nowrap\">M224.31<a name=\"GenomicTestCode-M224.4631\"> </a></td><td>MDS/MPN, FLT3 rearragement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.32<a name=\"GenomicTestCode-M224.4632\"> </a></td><td>MDS/MPN, RET rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.33<a name=\"GenomicTestCode-M224.4633\"> </a></td><td>MDS/MPN, NTRK3 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.34<a name=\"GenomicTestCode-M224.4634\"> </a></td><td>MDS/MPN, Chr13/Chr13q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.35<a name=\"GenomicTestCode-M224.4635\"> </a></td><td>MDS/MPN, Chr11q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.36<a name=\"GenomicTestCode-M224.4636\"> </a></td><td>MDS/MPN, Chr9q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.37<a name=\"GenomicTestCode-M224.4637\"> </a></td><td>MDS/MPN, Chr17/Chr17p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.38<a name=\"GenomicTestCode-M224.4638\"> </a></td><td>MDS/MPN, idic(X)(q13) FISH</td></tr><tr><td style=\"white-space:nowrap\">M224.39<a name=\"GenomicTestCode-M224.4639\"> </a></td><td>MDS/MPN, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p/i(17q) &amp; idic(X)(q13), cryptic deletion of 4q12, trisomy 8)</td></tr><tr><td style=\"white-space:nowrap\">M224.4<a name=\"GenomicTestCode-M224.464\"> </a></td><td>MDS/MPN, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M224.40<a name=\"GenomicTestCode-M224.4640\"> </a></td><td>MDS/MPN, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M224.41<a name=\"GenomicTestCode-M224.4641\"> </a></td><td>MDS/MPN, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M224.42<a name=\"GenomicTestCode-M224.4642\"> </a></td><td>MDS/MPN, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M224.5<a name=\"GenomicTestCode-M224.465\"> </a></td><td>MDS/MPN, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)</td></tr><tr><td style=\"white-space:nowrap\">M224.6<a name=\"GenomicTestCode-M224.466\"> </a></td><td>MDS/MPN, FIP1L1-PDGFRA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M224.7<a name=\"GenomicTestCode-M224.467\"> </a></td><td>MDS/MPN, FIP1L1-PDGFRA RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M224.8<a name=\"GenomicTestCode-M224.468\"> </a></td><td>MDS/MPN, ETV6-PDGFRB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M224.9<a name=\"GenomicTestCode-M224.469\"> </a></td><td>MDS/MPN, PCM1-JAK2 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M225.1<a name=\"GenomicTestCode-M225.461\"> </a></td><td>Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M225.2<a name=\"GenomicTestCode-M225.462\"> </a></td><td>Suspected Lymphoma, Ig gene (heavy &amp; light chain) rearrangement detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M225.3<a name=\"GenomicTestCode-M225.463\"> </a></td><td>Suspected Lymphoma, TCR gene rearrangement detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M225.4<a name=\"GenomicTestCode-M225.464\"> </a></td><td>Suspected Lymphoma, TCR gene rearrangement detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M225.5<a name=\"GenomicTestCode-M225.465\"> </a></td><td>Suspected Lymphoma, Karyotype</td></tr><tr><td style=\"white-space:nowrap\">M226.1<a name=\"GenomicTestCode-M226.461\"> </a></td><td>Cancer of Unknown Primary, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M226.3<a name=\"GenomicTestCode-M226.463\"> </a></td><td>Cancer of Unknown Primary, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M226.4<a name=\"GenomicTestCode-M226.464\"> </a></td><td>Cancer of Unknown Primary, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M227.1<a name=\"GenomicTestCode-M227.461\"> </a></td><td>Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M227.3<a name=\"GenomicTestCode-M227.463\"> </a></td><td>Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M23.1<a name=\"GenomicTestCode-M23.461\"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter,  H3-3A)</td></tr><tr><td style=\"white-space:nowrap\">M23.10<a name=\"GenomicTestCode-M23.4610\"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M23.11<a name=\"GenomicTestCode-M23.4611\"> </a></td><td>Diffuse Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M23.12<a name=\"GenomicTestCode-M23.4612\"> </a></td><td>Diffuse Midline Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M23.6<a name=\"GenomicTestCode-M23.466\"> </a></td><td>Diffuse Midline Glioma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M23.7<a name=\"GenomicTestCode-M23.467\"> </a></td><td>Diffuse Midline Glioma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M23.8<a name=\"GenomicTestCode-M23.468\"> </a></td><td>Diffuse Midline Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M23.9<a name=\"GenomicTestCode-M23.469\"> </a></td><td>Diffuse Midline Glioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M231.1,<a name=\"GenomicTestCode-M231.461.44\"> </a></td><td>small cell lung cancer, Multi-target NGS panel, copy number variant (RB1)</td></tr><tr><td style=\"white-space:nowrap\">M231.2,<a name=\"GenomicTestCode-M231.462.44\"> </a></td><td>small cell lung cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M232.1<a name=\"GenomicTestCode-M232.461\"> </a></td><td>Solid Tumour Exhausted all Standards of Care Testing and Treatment- Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M233.1<a name=\"GenomicTestCode-M233.461\"> </a></td><td>High Grade Serous Ovarian Carcinoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M234.1<a name=\"GenomicTestCode-M234.461\"> </a></td><td>Triple Negative Breast Cancer, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M235.1<a name=\"GenomicTestCode-M235.461\"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M235.2<a name=\"GenomicTestCode-M235.462\"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M235.3<a name=\"GenomicTestCode-M235.463\"> </a></td><td>Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M236.1<a name=\"GenomicTestCode-M236.461\"> </a></td><td>Oesophageal Cancer, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M236.2<a name=\"GenomicTestCode-M236.462\"> </a></td><td>Oesophageal Cancer, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M237.1<a name=\"GenomicTestCode-M237.461\"> </a></td><td>Gastric Cancer, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M237.2<a name=\"GenomicTestCode-M237.462\"> </a></td><td>Gastric Cancer, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M238.1,<a name=\"GenomicTestCode-M238.461.44\"> </a></td><td>small Bowel Cancer, MSI Testing</td></tr><tr><td style=\"white-space:nowrap\">M238.2,<a name=\"GenomicTestCode-M238.462.44\"> </a></td><td>small Bowel Cancer, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M239.1<a name=\"GenomicTestCode-M239.461\"> </a></td><td>Thyroid Hurtle Cell Carcinoma, Multi-target NGS panel, structural variant (RET)</td></tr><tr><td style=\"white-space:nowrap\">M24.1<a name=\"GenomicTestCode-M24.461\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, C19MC copy number  FISH</td></tr><tr><td style=\"white-space:nowrap\">M24.2<a name=\"GenomicTestCode-M24.462\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, TTYH1-C19MC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M24.3<a name=\"GenomicTestCode-M24.463\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M24.4<a name=\"GenomicTestCode-M24.464\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M24.5<a name=\"GenomicTestCode-M24.465\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, copy number variant (C19MC)</td></tr><tr><td style=\"white-space:nowrap\">M24.6<a name=\"GenomicTestCode-M24.466\"> </a></td><td>Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, structural variant  (TTYH1-C19MC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M240.1<a name=\"GenomicTestCode-M240.461\"> </a></td><td>Non-invasive follicular thyroid neoplasm with papillary like nuclei, Multi-target NGS panel, small variant (BRAF,HRAS,NRAS,KRAS)</td></tr><tr><td style=\"white-space:nowrap\">M241.1<a name=\"GenomicTestCode-M241.461\"> </a></td><td>Conjunctival melanoma, MYB &amp; 6cen (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M241.2<a name=\"GenomicTestCode-M241.462\"> </a></td><td>Conjunctival melanoma, RREB1 (6p25) (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M241.3<a name=\"GenomicTestCode-M241.463\"> </a></td><td>Conjunctival melanoma, CCND1 (11q13) (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M241.4<a name=\"GenomicTestCode-M241.464\"> </a></td><td>Conjunctival melanoma, MYC &amp; 8cen (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M241.5<a name=\"GenomicTestCode-M241.465\"> </a></td><td>Conjunctival melanoma, CDKN2A &amp; 9cen (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M242.1<a name=\"GenomicTestCode-M242.461\"> </a></td><td>Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), STR Testing</td></tr><tr><td style=\"white-space:nowrap\">M242.2<a name=\"GenomicTestCode-M242.462\"> </a></td><td>Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), Sex chromosome FISH</td></tr><tr><td style=\"white-space:nowrap\">M243.1<a name=\"GenomicTestCode-M243.461\"> </a></td><td>Thymic Carcinoma, Multi-target NGS panel (KIT)</td></tr><tr><td style=\"white-space:nowrap\">M244.1<a name=\"GenomicTestCode-M244.461\"> </a></td><td>In all tumours elligible for NTRK1/2/3 testing, FISH</td></tr><tr><td style=\"white-space:nowrap\">M245.1<a name=\"GenomicTestCode-M245.461\"> </a></td><td>Ovarian sex cord stromal tumuors, Multi-target NGS panel-small variant (FOXL2, CTNNB1, APC, DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M25.1<a name=\"GenomicTestCode-M25.461\"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, small variant (YAP1)</td></tr><tr><td style=\"white-space:nowrap\">M25.10<a name=\"GenomicTestCode-M25.4610\"> </a></td><td>Ependymoma, Paediatric, MYCN copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M25.11<a name=\"GenomicTestCode-M25.4611\"> </a></td><td>Ependymoma, Paediatric, ZFTA rearrangements (several fusion partners)</td></tr><tr><td style=\"white-space:nowrap\">M25.2<a name=\"GenomicTestCode-M25.462\"> </a></td><td>Ependymoma, Paediatric, YAP1 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M25.3<a name=\"GenomicTestCode-M25.463\"> </a></td><td>Ependymoma, Paediatric, YAP1-C11orf95 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M25.4<a name=\"GenomicTestCode-M25.464\"> </a></td><td>Ependymoma, Paediatric, YAP1-TFE3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M25.5<a name=\"GenomicTestCode-M25.465\"> </a></td><td>Ependymoma, Paediatric, C11orf95-RELA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M25.6<a name=\"GenomicTestCode-M25.466\"> </a></td><td>Ependymoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M25.7<a name=\"GenomicTestCode-M25.467\"> </a></td><td>Ependymoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M25.8<a name=\"GenomicTestCode-M25.468\"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, copy number variant (YAP1, MYCN)</td></tr><tr><td style=\"white-space:nowrap\">M25.9<a name=\"GenomicTestCode-M25.469\"> </a></td><td>Ependymoma, Paediatric, Multi-target NGS panel, structural variant  (YAP1-C11orf95, YAP1-TFE3, C11orf95-RELA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M26.1<a name=\"GenomicTestCode-M26.461\"> </a></td><td>Ependymoma Supratentorial, Adult, YAP1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M26.2<a name=\"GenomicTestCode-M26.462\"> </a></td><td>Ependymoma, Adult, RELA rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M26.3<a name=\"GenomicTestCode-M26.463\"> </a></td><td>Ependymoma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M26.4<a name=\"GenomicTestCode-M26.464\"> </a></td><td>Ependymoma, Adult, Multi-target NGS panel, structural variant  (YAP1, RELA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M26.5<a name=\"GenomicTestCode-M26.465\"> </a></td><td>Ependymoma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M26.6<a name=\"GenomicTestCode-M26.466\"> </a></td><td>Ependymoma, Adult, ZFTA rearrangements (several fusion partners)</td></tr><tr><td style=\"white-space:nowrap\">M27.1<a name=\"GenomicTestCode-M27.461\"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M27.10<a name=\"GenomicTestCode-M27.4610\"> </a></td><td>Glioblastoma, Adult, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M27.11<a name=\"GenomicTestCode-M27.4611\"> </a></td><td>Glioblastoma, Adult, PTEN (10q23) copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M27.12<a name=\"GenomicTestCode-M27.4612\"> </a></td><td>Glioblastoma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M27.13<a name=\"GenomicTestCode-M27.4613\"> </a></td><td>Glioblastoma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M27.14<a name=\"GenomicTestCode-M27.4614\"> </a></td><td>Glioblastoma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M27.15<a name=\"GenomicTestCode-M27.4615\"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M27.16<a name=\"GenomicTestCode-M27.4616\"> </a></td><td>Glioblastoma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M27.2<a name=\"GenomicTestCode-M27.462\"> </a></td><td>Glioblastoma, Adult, Multi-target NGS panel, copy number variant (EGFR, PDGFRA, MYC, PTEN, 1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M27.3<a name=\"GenomicTestCode-M27.463\"> </a></td><td>Glioblastoma, Adult, EGFRvIII RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M27.5<a name=\"GenomicTestCode-M27.465\"> </a></td><td>Glioblastoma, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M27.6<a name=\"GenomicTestCode-M27.466\"> </a></td><td>Glioblastoma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M27.7<a name=\"GenomicTestCode-M27.467\"> </a></td><td>Glioblastoma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M27.9<a name=\"GenomicTestCode-M27.469\"> </a></td><td>Glioblastoma, Adult, PDGFRA copy number FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M28.1<a name=\"GenomicTestCode-M28.461\"> </a></td><td>Glioma, Adult, Multi-target NGS panel, small variant (H3C2, H3C3, H3C14, H3-3A, H3-3B, IDH1, IDH2, TP53, VHL, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M28.2<a name=\"GenomicTestCode-M28.462\"> </a></td><td>Glioma, Adult, Multi-target NGS panel, copy number variant (EGFR, 1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M28.3<a name=\"GenomicTestCode-M28.463\"> </a></td><td>Glioma, Adult, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M28.4<a name=\"GenomicTestCode-M28.464\"> </a></td><td>Glioma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M28.5<a name=\"GenomicTestCode-M28.465\"> </a></td><td>Glioma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M28.6<a name=\"GenomicTestCode-M28.466\"> </a></td><td>Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M28.7<a name=\"GenomicTestCode-M28.467\"> </a></td><td>Glioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M28.8<a name=\"GenomicTestCode-M28.468\"> </a></td><td>Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M28.9<a name=\"GenomicTestCode-M28.469\"> </a></td><td>Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M29.1<a name=\"GenomicTestCode-M29.461\"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style=\"white-space:nowrap\">M29.2<a name=\"GenomicTestCode-M29.462\"> </a></td><td>High Grade Glioma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M29.3<a name=\"GenomicTestCode-M29.463\"> </a></td><td>High Grade Glioma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M29.4<a name=\"GenomicTestCode-M29.464\"> </a></td><td>High Grade Glioma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M29.5<a name=\"GenomicTestCode-M29.465\"> </a></td><td>High Grade Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M29.6<a name=\"GenomicTestCode-M29.466\"> </a></td><td>High Grade Glioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M29.7<a name=\"GenomicTestCode-M29.467\"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M29.8<a name=\"GenomicTestCode-M29.468\"> </a></td><td>High Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M29.9<a name=\"GenomicTestCode-M29.469\"> </a></td><td>High Grade Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M3.12<a name=\"GenomicTestCode-M3.4612\"> </a></td><td>Breast Cancer, Tumour profiling tests to guide adjuvant chemotherapy decisions in early breast cancer</td></tr><tr><td style=\"white-space:nowrap\">M3.13<a name=\"GenomicTestCode-M3.4613\"> </a></td><td>Breast Cancer, Multi-target ctDNA NGS panel, small variant (ESR1)</td></tr><tr><td style=\"white-space:nowrap\">M3.5<a name=\"GenomicTestCode-M3.465\"> </a></td><td>Breast Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M3.6<a name=\"GenomicTestCode-M3.466\"> </a></td><td>Breast Cancer, Multi-target NGS panel, small variant (PIK3CA)</td></tr><tr><td style=\"white-space:nowrap\">M3.7<a name=\"GenomicTestCode-M3.467\"> </a></td><td>Breast Cancer, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M3.9<a name=\"GenomicTestCode-M3.469\"> </a></td><td>Breast Cancer, ETV6-NTRK3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M30.1<a name=\"GenomicTestCode-M30.461\"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, small variant (RB1, NF1)</td></tr><tr><td style=\"white-space:nowrap\">M30.2<a name=\"GenomicTestCode-M30.462\"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M30.3<a name=\"GenomicTestCode-M30.463\"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M30.4<a name=\"GenomicTestCode-M30.464\"> </a></td><td>IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M31.1<a name=\"GenomicTestCode-M31.461\"> </a></td><td>Low Grade Glioma, Adult, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M31.2<a name=\"GenomicTestCode-M31.462\"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style=\"white-space:nowrap\">M31.3<a name=\"GenomicTestCode-M31.463\"> </a></td><td>Low Grade Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M31.4<a name=\"GenomicTestCode-M31.464\"> </a></td><td>Low Grade Glioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M31.5<a name=\"GenomicTestCode-M31.465\"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M31.6<a name=\"GenomicTestCode-M31.466\"> </a></td><td>Low Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M31.7<a name=\"GenomicTestCode-M31.467\"> </a></td><td>Low Grade Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M32.1<a name=\"GenomicTestCode-M32.461\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, small variant (BRAF, IDH1, IDH2, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style=\"white-space:nowrap\">M32.2<a name=\"GenomicTestCode-M32.462\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M32.3<a name=\"GenomicTestCode-M32.463\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M32.4<a name=\"GenomicTestCode-M32.464\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M32.5<a name=\"GenomicTestCode-M32.465\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M32.6<a name=\"GenomicTestCode-M32.466\"> </a></td><td>Low Grade Glioma/Glioneuronal Tumours, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M33.3<a name=\"GenomicTestCode-M33.463\"> </a></td><td>Meningioma, Adult, Multi-target NGS panel, small variant (TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M33.4<a name=\"GenomicTestCode-M33.464\"> </a></td><td>Meningioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M33.5<a name=\"GenomicTestCode-M33.465\"> </a></td><td>Meningioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M34.1<a name=\"GenomicTestCode-M34.461\"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)</td></tr><tr><td style=\"white-space:nowrap\">M34.2<a name=\"GenomicTestCode-M34.462\"> </a></td><td>Non-Midline Glioma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M34.3<a name=\"GenomicTestCode-M34.463\"> </a></td><td>Non-Midline Glioma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M34.4<a name=\"GenomicTestCode-M34.464\"> </a></td><td>Non-Midline Glioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M34.5<a name=\"GenomicTestCode-M34.465\"> </a></td><td>Non-Midline Glioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M34.6<a name=\"GenomicTestCode-M34.466\"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M34.7<a name=\"GenomicTestCode-M34.467\"> </a></td><td>Non-Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M34.8<a name=\"GenomicTestCode-M34.468\"> </a></td><td>Non-Midline Glioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M35.1<a name=\"GenomicTestCode-M35.461\"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M35.2<a name=\"GenomicTestCode-M35.462\"> </a></td><td>OligodendroGlioma, Adult, 1p19q codel FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M35.4<a name=\"GenomicTestCode-M35.464\"> </a></td><td>OligodendroGlioma, Adult, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M35.5<a name=\"GenomicTestCode-M35.465\"> </a></td><td>OligodendroGlioma, Adult, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M35.6<a name=\"GenomicTestCode-M35.466\"> </a></td><td>OligodendroGlioma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M35.7<a name=\"GenomicTestCode-M35.467\"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)</td></tr><tr><td style=\"white-space:nowrap\">M35.8<a name=\"GenomicTestCode-M35.468\"> </a></td><td>OligodendroGlioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M35.9<a name=\"GenomicTestCode-M35.469\"> </a></td><td>OligodendroGlioma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M36.1<a name=\"GenomicTestCode-M36.461\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-KIAA1549 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.10<a name=\"GenomicTestCode-M36.4610\"> </a></td><td>Pilocytic Astrocytoma, Adult, KIAA1549 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M36.11<a name=\"GenomicTestCode-M36.4611\"> </a></td><td>Pilocytic Astrocytoma, Adult, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M36.12<a name=\"GenomicTestCode-M36.4612\"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, small variant (BRAF, CDKN2A)</td></tr><tr><td style=\"white-space:nowrap\">M36.13<a name=\"GenomicTestCode-M36.4613\"> </a></td><td>Pilocytic Astrocytoma, Adult, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M36.14<a name=\"GenomicTestCode-M36.4614\"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, BRAF-AGK, BRAF-AKAP9, BRAF-CCDC6, BRAF-FAM118B, BRAF-FXR1, BRAF-GNAI1, BRAF-MACF1, other rearrangements of BRAF, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M36.15<a name=\"GenomicTestCode-M36.4615\"> </a></td><td>Pilocytic Astrocytoma, Adult, Multi-target NGS panel, copy number variant (KIAA1549, CDKN2A)</td></tr><tr><td style=\"white-space:nowrap\">M36.16<a name=\"GenomicTestCode-M36.4616\"> </a></td><td>Pilocytic Astrocytoma, Adult, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M36.2<a name=\"GenomicTestCode-M36.462\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-AGK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.3<a name=\"GenomicTestCode-M36.463\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-AKAP9 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.4<a name=\"GenomicTestCode-M36.464\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-CCDC6 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.5<a name=\"GenomicTestCode-M36.465\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-FAM118B FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.6<a name=\"GenomicTestCode-M36.466\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-FXR1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.7<a name=\"GenomicTestCode-M36.467\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-GNAI1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.8<a name=\"GenomicTestCode-M36.468\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF-MACF1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M36.9<a name=\"GenomicTestCode-M36.469\"> </a></td><td>Pilocytic Astrocytoma, Adult, BRAF rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M37.1<a name=\"GenomicTestCode-M37.461\"> </a></td><td>Pineoblastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)</td></tr><tr><td style=\"white-space:nowrap\">M37.2<a name=\"GenomicTestCode-M37.462\"> </a></td><td>Pineoblastoma, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M37.3<a name=\"GenomicTestCode-M37.463\"> </a></td><td>Pineoblastoma, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M37.4<a name=\"GenomicTestCode-M37.464\"> </a></td><td>Pineoblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M38.1<a name=\"GenomicTestCode-M38.461\"> </a></td><td>Pituitary Tumours, MGMT promoter hyperMethylation</td></tr><tr><td style=\"white-space:nowrap\">M38.2<a name=\"GenomicTestCode-M38.462\"> </a></td><td>Pituitary Tumours, Multi-target NGS panel, copy number variant (EGFR)</td></tr><tr><td style=\"white-space:nowrap\">M38.3<a name=\"GenomicTestCode-M38.463\"> </a></td><td>Pituitary Tumours, EGFR copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M38.4<a name=\"GenomicTestCode-M38.464\"> </a></td><td>Pituitary Tumours, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M38.5<a name=\"GenomicTestCode-M38.465\"> </a></td><td>Pituitary Tumours, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M38.6<a name=\"GenomicTestCode-M38.466\"> </a></td><td>Pituitary Tumours, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M39.1<a name=\"GenomicTestCode-M39.461\"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, small variant (CDKN2A)</td></tr><tr><td style=\"white-space:nowrap\">M39.2<a name=\"GenomicTestCode-M39.462\"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M39.3<a name=\"GenomicTestCode-M39.463\"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, DNA Methylation</td></tr><tr><td style=\"white-space:nowrap\">M39.4<a name=\"GenomicTestCode-M39.464\"> </a></td><td>Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M4.1<a name=\"GenomicTestCode-M4.461\"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET)</td></tr><tr><td style=\"white-space:nowrap\">M4.10<a name=\"GenomicTestCode-M4.4610\"> </a></td><td>Non-Small Cell Lung Cancer, EML4-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M4.11<a name=\"GenomicTestCode-M4.4611\"> </a></td><td>Non-Small Cell Lung Cancer, ALK hotspot cDNA</td></tr><tr><td style=\"white-space:nowrap\">M4.13<a name=\"GenomicTestCode-M4.4613\"> </a></td><td>Non-Small Cell Lung Cancer, Combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping, ERBB2*) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon 14 skipping)</td></tr><tr><td style=\"white-space:nowrap\">M4.14<a name=\"GenomicTestCode-M4.4614\"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target ctDNA combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping and copy number variations) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon</td></tr><tr><td style=\"white-space:nowrap\">M4.2<a name=\"GenomicTestCode-M4.462\"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, structural variant (ROS1, RET, EML4-ALK, NTRK1, NTRK1, NTRK3, MET)</td></tr><tr><td style=\"white-space:nowrap\">M4.3<a name=\"GenomicTestCode-M4.463\"> </a></td><td>Non-Small Cell Lung Cancer, Multi-target NGS panel, copy number variant (MET)</td></tr><tr><td style=\"white-space:nowrap\">M4.4<a name=\"GenomicTestCode-M4.464\"> </a></td><td>Non-Small Cell Lung Cancer, EGFR hotspot Tumor</td></tr><tr><td style=\"white-space:nowrap\">M4.5<a name=\"GenomicTestCode-M4.465\"> </a></td><td>Non-Small Cell Lung Cancer, EGFR hotspot ctDNA</td></tr><tr><td style=\"white-space:nowrap\">M4.6<a name=\"GenomicTestCode-M4.466\"> </a></td><td>Non-Small Cell Lung Cancer, ROS1 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M4.7<a name=\"GenomicTestCode-M4.467\"> </a></td><td>Non-Small Cell Lung Cancer, RET rearrangement FISH/RT-PC</td></tr><tr><td style=\"white-space:nowrap\">M4.8<a name=\"GenomicTestCode-M4.468\"> </a></td><td>Non-Small Cell Lung Cancer, MET copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M42.1<a name=\"GenomicTestCode-M42.461\"> </a></td><td>Alveolar Rhabdomyosarcoma, FOXO1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M42.2<a name=\"GenomicTestCode-M42.462\"> </a></td><td>Alveolar Rhabdomyosarcoma, PAX3-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M42.3<a name=\"GenomicTestCode-M42.463\"> </a></td><td>Alveolar Rhabdomyosarcoma, PAX7-FOXO1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M42.4<a name=\"GenomicTestCode-M42.464\"> </a></td><td>Alveolar Rhabdomyosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M42.5<a name=\"GenomicTestCode-M42.465\"> </a></td><td>Alveolar Rhabdomyosarcoma, Multi-target NGS panel, structural variant (FOXO1, PAX3-FOXO1, PAX7-FOXO1  NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M43.1<a name=\"GenomicTestCode-M43.461\"> </a></td><td>Alveolar Soft Part Sarcoma, TFE3 rearrangement FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M43.2<a name=\"GenomicTestCode-M43.462\"> </a></td><td>Alveolar Soft Part Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M43.3<a name=\"GenomicTestCode-M43.463\"> </a></td><td>Alveolar Soft Part Sarcoma, Multi-target NGS panel, structural variant (TFE3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M44.1<a name=\"GenomicTestCode-M44.461\"> </a></td><td>Aneurysmal Bone Cyst, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M44.2<a name=\"GenomicTestCode-M44.462\"> </a></td><td>Aneurysmal Bone Cyst, Multi-target NGS panel, structural variant (USP6)</td></tr><tr><td style=\"white-space:nowrap\">M45.1<a name=\"GenomicTestCode-M45.461\"> </a></td><td>Angiomatoid Fibrous Histiocytoma, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M45.2<a name=\"GenomicTestCode-M45.462\"> </a></td><td>Angiomatoid Fibrous Histiocytoma, FUS rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M45.3<a name=\"GenomicTestCode-M45.463\"> </a></td><td>Angiomatoid Fibrous Histiocytoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M45.4<a name=\"GenomicTestCode-M45.464\"> </a></td><td>Angiomatoid Fibrous Histiocytoma, Multi-target NGS panel, structural variant (EWSR1, FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M46.1<a name=\"GenomicTestCode-M46.461\"> </a></td><td>Chondrosarcoma Conventional Central, Multi-target NGS panel, small variant (IDH1, IDH2)</td></tr><tr><td style=\"white-space:nowrap\">M46.2<a name=\"GenomicTestCode-M46.462\"> </a></td><td>Chondrosarcoma Conventional Central, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M46.3<a name=\"GenomicTestCode-M46.463\"> </a></td><td>Chondrosarcoma Conventional Central, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M47.1<a name=\"GenomicTestCode-M47.461\"> </a></td><td>Chondroblastoma, SNP Array</td></tr><tr><td style=\"white-space:nowrap\">M47.2<a name=\"GenomicTestCode-M47.462\"> </a></td><td>Chondroblastoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M47.3<a name=\"GenomicTestCode-M47.463\"> </a></td><td>Chondroblastoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M48.1<a name=\"GenomicTestCode-M48.461\"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M48.2<a name=\"GenomicTestCode-M48.462\"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M48.3<a name=\"GenomicTestCode-M48.463\"> </a></td><td>Clear Cell Sarcoma of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M49.1<a name=\"GenomicTestCode-M49.461\"> </a></td><td>CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M49.2<a name=\"GenomicTestCode-M49.462\"> </a></td><td>CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M5.1<a name=\"GenomicTestCode-M5.461\"> </a></td><td>Mesothelioma, CDKN2A copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M5.2<a name=\"GenomicTestCode-M5.462\"> </a></td><td>Mesothelioma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M5.3<a name=\"GenomicTestCode-M5.463\"> </a></td><td>Mesothelioma, Multi-target NGS panel, copy number variant (CDKN2A)</td></tr><tr><td style=\"white-space:nowrap\">M50.1<a name=\"GenomicTestCode-M50.461\"> </a></td><td>Dermatofibrosarcoma Protuberans, COL1A1-PDGFB rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M50.2<a name=\"GenomicTestCode-M50.462\"> </a></td><td>Dermatofibrosarcoma Protuberans, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M50.3<a name=\"GenomicTestCode-M50.463\"> </a></td><td>Dermatofibrosarcoma Protuberans, Multi-target NGS panel, structural variant (COL1A1-PDGFB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M51.1<a name=\"GenomicTestCode-M51.461\"> </a></td><td>Desmoid-Type Fibromatosis, Multi-target NGS panel, small variant (APC, CTNNB1)</td></tr><tr><td style=\"white-space:nowrap\">M52.1<a name=\"GenomicTestCode-M52.461\"> </a></td><td>Desmoplastic Small Round Cell Tumour, WT1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M52.2<a name=\"GenomicTestCode-M52.462\"> </a></td><td>Desmoplastic Small Round Cell Tumour, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M52.3<a name=\"GenomicTestCode-M52.463\"> </a></td><td>Desmoplastic Small Round Cell Tumour, Multi-target NGS panel, structural variant (WT1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M53.1<a name=\"GenomicTestCode-M53.461\"> </a></td><td>Endometrial Stromal Sarcoma, EPC1-PHF1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M53.2<a name=\"GenomicTestCode-M53.462\"> </a></td><td>Endometrial Stromal Sarcoma, JAZF1-PHF1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M53.3<a name=\"GenomicTestCode-M53.463\"> </a></td><td>Endometrial Stromal Sarcoma, JAZF1-SUZ12 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M53.4<a name=\"GenomicTestCode-M53.464\"> </a></td><td>Endometrial Stromal Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M53.5<a name=\"GenomicTestCode-M53.465\"> </a></td><td>Endometrial Stromal Sarcoma, Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NTRK1, NTRK2, NTRK3, ZC3H7B-BCOR)</td></tr><tr><td style=\"white-space:nowrap\">M53.7<a name=\"GenomicTestCode-M53.467\"> </a></td><td>Endometrial Stromal Sarcoma, ZC3H7B-BCOR rearrangment FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M54.1<a name=\"GenomicTestCode-M54.461\"> </a></td><td>Epithelioid Haemangioendothelioma, WWTR1-CAMTA1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M54.2<a name=\"GenomicTestCode-M54.462\"> </a></td><td>Epithelioid Haemangioendothelioma, Multi-target NGS panel, structural variant (WWTR1-CAMTA1)</td></tr><tr><td style=\"white-space:nowrap\">M55.1<a name=\"GenomicTestCode-M55.461\"> </a></td><td>Ewing Like Sarcoma/PNET, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M55.2<a name=\"GenomicTestCode-M55.462\"> </a></td><td>Ewing Like Sarcoma/PNET, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M55.3<a name=\"GenomicTestCode-M55.463\"> </a></td><td>Ewing Like Sarcoma/PNET, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M56.1<a name=\"GenomicTestCode-M56.461\"> </a></td><td>Ewing Sarcoma of Bone, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M56.2<a name=\"GenomicTestCode-M56.462\"> </a></td><td>Ewing Sarcoma of Bone, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M56.3<a name=\"GenomicTestCode-M56.463\"> </a></td><td>Ewing Sarcoma of Bone, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M57.1<a name=\"GenomicTestCode-M57.461\"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M57.2<a name=\"GenomicTestCode-M57.462\"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M57.3<a name=\"GenomicTestCode-M57.463\"> </a></td><td>Ewing-Like Soft-Tissue Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M58.1<a name=\"GenomicTestCode-M58.461\"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, NR4A3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M58.2<a name=\"GenomicTestCode-M58.462\"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M58.3<a name=\"GenomicTestCode-M58.463\"> </a></td><td>Extraskeletal Myxoid Chondrosarcoma, Multi-target NGS panel, structural variant (NR4A3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M59.1<a name=\"GenomicTestCode-M59.461\"> </a></td><td>Fibrous Dysplasia/Myxomas (Mazabraud Syndrome), Multi-target NGS panel, small variant (GNAS)</td></tr><tr><td style=\"white-space:nowrap\">M6.1<a name=\"GenomicTestCode-M6.461\"> </a></td><td>Mucoepidermoid Carcinoma, MAML2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M6.2<a name=\"GenomicTestCode-M6.462\"> </a></td><td>Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M6.3<a name=\"GenomicTestCode-M6.463\"> </a></td><td>Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2)</td></tr><tr><td style=\"white-space:nowrap\">M6.5<a name=\"GenomicTestCode-M6.465\"> </a></td><td>Mucoepidermoid Carcinoma, DPYD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M60.1<a name=\"GenomicTestCode-M60.461\"> </a></td><td>Giant Cell Tumour of Bone, H3-3B hotspot</td></tr><tr><td style=\"white-space:nowrap\">M60.2<a name=\"GenomicTestCode-M60.462\"> </a></td><td>Giant Cell Tumour of Bone, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M60.3<a name=\"GenomicTestCode-M60.463\"> </a></td><td>Giant Cell Tumour of Bone, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M61.1<a name=\"GenomicTestCode-M61.461\"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M61.2<a name=\"GenomicTestCode-M61.462\"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M61.3<a name=\"GenomicTestCode-M61.463\"> </a></td><td>High-Grade Neuroepithelial Tumour-Bcor Group, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M62.1<a name=\"GenomicTestCode-M62.461\"> </a></td><td>Infantile Fibrosarcoma, ETV6-NTRK3 RT-PCR or FISH</td></tr><tr><td style=\"white-space:nowrap\">M62.2<a name=\"GenomicTestCode-M62.462\"> </a></td><td>Infantile Fibrosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M62.3<a name=\"GenomicTestCode-M62.463\"> </a></td><td>Infantile Fibrosarcoma, Multi-target NGS panel, structural variant (ETV6-NTRK3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M63.1<a name=\"GenomicTestCode-M63.461\"> </a></td><td>Inflammatory Myofibroblastic Tumour, TPM4-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M63.2<a name=\"GenomicTestCode-M63.462\"> </a></td><td>Inflammatory Myofibroblastic Tumour, TPM3-ALK FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M63.3<a name=\"GenomicTestCode-M63.463\"> </a></td><td>Inflammatory Myofibroblastic Tumour, Multi-target NGS panel, structural variant (ALK, TPM4-ALK, TPM3-ALK, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M63.4<a name=\"GenomicTestCode-M63.464\"> </a></td><td>Inflammatory Myofibroblastic Tumour, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M64.1<a name=\"GenomicTestCode-M64.461\"> </a></td><td>Low Grade Fibromyxoid Sarcoma, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M64.2<a name=\"GenomicTestCode-M64.462\"> </a></td><td>Low Grade Fibromyxoid Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M64.3<a name=\"GenomicTestCode-M64.463\"> </a></td><td>Low Grade Fibromyxoid Sarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M65.1<a name=\"GenomicTestCode-M65.461\"> </a></td><td>Mesenchymal Chondrosarcoma, HEY1-NCOA2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M65.2<a name=\"GenomicTestCode-M65.462\"> </a></td><td>Mesenchymal Chondrosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M65.3<a name=\"GenomicTestCode-M65.463\"> </a></td><td>Mesenchymal Chondrosarcoma, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M66.1<a name=\"GenomicTestCode-M66.461\"> </a></td><td>Myoepithelial Tumours of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M66.2<a name=\"GenomicTestCode-M66.462\"> </a></td><td>Myoepithelial Tumours of Soft Tissue, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M66.3<a name=\"GenomicTestCode-M66.463\"> </a></td><td>Myoepithelial Tumours of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M67.1<a name=\"GenomicTestCode-M67.461\"> </a></td><td>Myxoid/Round Cell Liposarcoma, DDIT3 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M67.2<a name=\"GenomicTestCode-M67.462\"> </a></td><td>Myxoid/Round Cell Liposarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M67.3<a name=\"GenomicTestCode-M67.463\"> </a></td><td>Myxoid/Round Cell Liposarcoma, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M67.4<a name=\"GenomicTestCode-M67.464\"> </a></td><td>Myxoid/Round Cell Lipsarcoma, MDM2 amplification FISH</td></tr><tr><td style=\"white-space:nowrap\">M68.1<a name=\"GenomicTestCode-M68.461\"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, TGFBR3-OGA FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M68.2<a name=\"GenomicTestCode-M68.462\"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M68.3<a name=\"GenomicTestCode-M68.463\"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M68.4<a name=\"GenomicTestCode-M68.464\"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, structural variant (TGFBR3-OGA, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M68.5<a name=\"GenomicTestCode-M68.465\"> </a></td><td>Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M69.1<a name=\"GenomicTestCode-M69.461\"> </a></td><td>Nodular Fasciitis, USP6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M69.2<a name=\"GenomicTestCode-M69.462\"> </a></td><td>Nodular Fasciitis, Multi-target NGS panel, structural variant (USP6)</td></tr><tr><td style=\"white-space:nowrap\">M7.1<a name=\"GenomicTestCode-M7.461\"> </a></td><td>Melanoma, Adult, Multi-target NGS panel, small variant (BRAF, KIT, NRAS)</td></tr><tr><td style=\"white-space:nowrap\">M7.10<a name=\"GenomicTestCode-M7.4610\"> </a></td><td>Melanoma, Adult, Copy number variant detection to genomewide resolution</td></tr><tr><td style=\"white-space:nowrap\">M7.2<a name=\"GenomicTestCode-M7.462\"> </a></td><td>Melanoma, Adult, BRAF hotspot</td></tr><tr><td style=\"white-space:nowrap\">M7.3<a name=\"GenomicTestCode-M7.463\"> </a></td><td>Melanoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M7.5<a name=\"GenomicTestCode-M7.465\"> </a></td><td>Melanoma, Adult, MYB &amp; 6cen (FISH)</td></tr><tr><td style=\"white-space:nowrap\">M7.6<a name=\"GenomicTestCode-M7.466\"> </a></td><td>Melanoma, Adult, RREB1 (6p25)</td></tr><tr><td style=\"white-space:nowrap\">M7.7<a name=\"GenomicTestCode-M7.467\"> </a></td><td>Melanoma, Adult, CCND1 (11q13)</td></tr><tr><td style=\"white-space:nowrap\">M7.8<a name=\"GenomicTestCode-M7.468\"> </a></td><td>Melanoma, Adult, MYC &amp; 8cen</td></tr><tr><td style=\"white-space:nowrap\">M7.9<a name=\"GenomicTestCode-M7.469\"> </a></td><td>Melanoma, Adult, CDKN2A &amp; 9cen</td></tr><tr><td style=\"white-space:nowrap\">M70.1<a name=\"GenomicTestCode-M70.461\"> </a></td><td>Osteosarcoma, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M70.2<a name=\"GenomicTestCode-M70.462\"> </a></td><td>Osteosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M70.3<a name=\"GenomicTestCode-M70.463\"> </a></td><td>Osteosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M70.4<a name=\"GenomicTestCode-M70.464\"> </a></td><td>Osteosarcoma, Multi-target NGS panel, copy number variant (MDM2)</td></tr><tr><td style=\"white-space:nowrap\">M71.1<a name=\"GenomicTestCode-M71.461\"> </a></td><td>Phosphaturic Mesenchymal Tumour, FN1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M71.2<a name=\"GenomicTestCode-M71.462\"> </a></td><td>Phosphaturic Mesenchymal Tumour, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M71.3<a name=\"GenomicTestCode-M71.463\"> </a></td><td>Phosphaturic Mesenchymal Tumour, Multi-target NGS panel, structural variant (FN1, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M72.1<a name=\"GenomicTestCode-M72.461\"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M72.2<a name=\"GenomicTestCode-M72.462\"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M72.3<a name=\"GenomicTestCode-M72.463\"> </a></td><td>Primitive Mesenchymal Myxoid Tumour of Infancy, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M73.1<a name=\"GenomicTestCode-M73.461\"> </a></td><td>Pseudomyogenic Haemangioendothelioma, SERPINE1-FOSB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M73.2<a name=\"GenomicTestCode-M73.462\"> </a></td><td>Pseudomyogenic Haemangioendothelioma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M73.3<a name=\"GenomicTestCode-M73.463\"> </a></td><td>Pseudomyogenic Haemangioendothelioma, Multi-target NGS panel, structural variant (SERPINE1-FOSB, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M74.1<a name=\"GenomicTestCode-M74.461\"> </a></td><td>Radiation Induced Angiosarcoma, MYC copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M74.2<a name=\"GenomicTestCode-M74.462\"> </a></td><td>Radiation Induced Angiosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M74.3<a name=\"GenomicTestCode-M74.463\"> </a></td><td>Radiation Induced Angiosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M74.4<a name=\"GenomicTestCode-M74.464\"> </a></td><td>Radiation Induced Angiosarcoma, Multi-target NGS panel, copy number variant (MYC)</td></tr><tr><td style=\"white-space:nowrap\">M75.1<a name=\"GenomicTestCode-M75.461\"> </a></td><td>Round Cell Sarcoma Nos, Multi-target NGS panel, structural variant (BCOR, CIC, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M75.2<a name=\"GenomicTestCode-M75.462\"> </a></td><td>Round Cell Sarcoma Nos, BCOR-CCNB3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M75.3<a name=\"GenomicTestCode-M75.463\"> </a></td><td>Round Cell Sarcoma Nos, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M76.1<a name=\"GenomicTestCode-M76.461\"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, FUS rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M76.2<a name=\"GenomicTestCode-M76.462\"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M76.3<a name=\"GenomicTestCode-M76.463\"> </a></td><td>Sclerosing Epithelioid Fibrosarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M77.1<a name=\"GenomicTestCode-M77.461\"> </a></td><td>Synovial Sarcoma, SS18 rearrangement FISH or RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M77.2<a name=\"GenomicTestCode-M77.462\"> </a></td><td>Synovial Sarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M77.3<a name=\"GenomicTestCode-M77.463\"> </a></td><td>Synovial Sarcoma, Multi-target NGS panel, structural variant (SS18, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M78.1<a name=\"GenomicTestCode-M78.461\"> </a></td><td>Undifferentiated Round Cell Sarcoma of Infancy, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M78.2<a name=\"GenomicTestCode-M78.462\"> </a></td><td>Undifferentiated Round Cell Sarcoma of Infancy, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M79.1<a name=\"GenomicTestCode-M79.461\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, MDM2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M79.2<a name=\"GenomicTestCode-M79.462\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M79.3<a name=\"GenomicTestCode-M79.463\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M79.4<a name=\"GenomicTestCode-M79.464\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, copy number variant (MDM2, DDIT3)</td></tr><tr><td style=\"white-space:nowrap\">M79.6<a name=\"GenomicTestCode-M79.466\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M79.7<a name=\"GenomicTestCode-M79.467\"> </a></td><td>Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number RT-PCR/ddPCR</td></tr><tr><td style=\"white-space:nowrap\">M8.1<a name=\"GenomicTestCode-M8.461\"> </a></td><td>Gastrointestinal Stromal Tumour, Multi-target NGS panel, small variant (KIT, PDGFRA)</td></tr><tr><td style=\"white-space:nowrap\">M8.2<a name=\"GenomicTestCode-M8.462\"> </a></td><td>Gastrointestinal Stromal Tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M80.1<a name=\"GenomicTestCode-M80.461\"> </a></td><td>Acute Myeloid Leukaemia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M80.10<a name=\"GenomicTestCode-M80.4610\"> </a></td><td>Acute Myeloid Leukaemia, MRD PML-RARA RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M80.11<a name=\"GenomicTestCode-M80.4611\"> </a></td><td>Acute Myeloid Leukaemia, MRD RUNX1-RUNX1T1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M80.12<a name=\"GenomicTestCode-M80.4612\"> </a></td><td>Acute Myeloid Leukaemia, MRD CBFB-MYH11 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M80.13<a name=\"GenomicTestCode-M80.4613\"> </a></td><td>Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M80.14<a name=\"GenomicTestCode-M80.4614\"> </a></td><td>Acute Myeloid Leukaemia, MRD other QF-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.15<a name=\"GenomicTestCode-M80.4615\"> </a></td><td>Acute Myeloid Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style=\"white-space:nowrap\">M80.18<a name=\"GenomicTestCode-M80.4618\"> </a></td><td>Acute Myeloid Leukaemia, FLT3 ITD</td></tr><tr><td style=\"white-space:nowrap\">M80.19<a name=\"GenomicTestCode-M80.4619\"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (GATA1)</td></tr><tr><td style=\"white-space:nowrap\">M80.2<a name=\"GenomicTestCode-M80.462\"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD), PPM1D, DDX41, PHF6, CUX1</td></tr><tr><td style=\"white-space:nowrap\">M80.21<a name=\"GenomicTestCode-M80.4621\"> </a></td><td>Acute Myeloid Leukaemia, FLT3 TKD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M80.22<a name=\"GenomicTestCode-M80.4622\"> </a></td><td>Acute Myeloid Leukaemia, NPM1 exon 12 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M80.23<a name=\"GenomicTestCode-M80.4623\"> </a></td><td>Acute Myeloid Leukaemia, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M80.24<a name=\"GenomicTestCode-M80.4624\"> </a></td><td>Acute Myeloid Leukaemia, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M80.25<a name=\"GenomicTestCode-M80.4625\"> </a></td><td>Acute Myeloid Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.26<a name=\"GenomicTestCode-M80.4626\"> </a></td><td>Acute Myeloid Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.27<a name=\"GenomicTestCode-M80.4627\"> </a></td><td>Acute Myeloid Leukaemia, Chr17/Chr17p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.28<a name=\"GenomicTestCode-M80.4628\"> </a></td><td>Acute Myeloid Leukaemia, Chr12/Chr12p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.29<a name=\"GenomicTestCode-M80.4629\"> </a></td><td>Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.3<a name=\"GenomicTestCode-M80.463\"> </a></td><td>Acute Myeloid Leukaemia, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)</td></tr><tr><td style=\"white-space:nowrap\">M80.30<a name=\"GenomicTestCode-M80.4630\"> </a></td><td>Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.31<a name=\"GenomicTestCode-M80.4631\"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.32<a name=\"GenomicTestCode-M80.4632\"> </a></td><td>Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.33<a name=\"GenomicTestCode-M80.4633\"> </a></td><td>Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.34<a name=\"GenomicTestCode-M80.4634\"> </a></td><td>Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.35<a name=\"GenomicTestCode-M80.4635\"> </a></td><td>Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.36<a name=\"GenomicTestCode-M80.4636\"> </a></td><td>Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.37<a name=\"GenomicTestCode-M80.4637\"> </a></td><td>Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.38<a name=\"GenomicTestCode-M80.4638\"> </a></td><td>Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.39<a name=\"GenomicTestCode-M80.4639\"> </a></td><td>Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.40<a name=\"GenomicTestCode-M80.4640\"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.41<a name=\"GenomicTestCode-M80.4641\"> </a></td><td>Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.42<a name=\"GenomicTestCode-M80.4642\"> </a></td><td>Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.43<a name=\"GenomicTestCode-M80.4643\"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.44<a name=\"GenomicTestCode-M80.4644\"> </a></td><td>Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.45<a name=\"GenomicTestCode-M80.4645\"> </a></td><td>Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.46<a name=\"GenomicTestCode-M80.4646\"> </a></td><td>Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.47<a name=\"GenomicTestCode-M80.4647\"> </a></td><td>Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.48<a name=\"GenomicTestCode-M80.4648\"> </a></td><td>Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.49<a name=\"GenomicTestCode-M80.4649\"> </a></td><td>Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.5<a name=\"GenomicTestCode-M80.465\"> </a></td><td>Acute Myeloid Leukaemia, Other: See tests M80.25-M80.40 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M80.50<a name=\"GenomicTestCode-M80.4650\"> </a></td><td>Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.51<a name=\"GenomicTestCode-M80.4651\"> </a></td><td>Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.52<a name=\"GenomicTestCode-M80.4652\"> </a></td><td>Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M80.53<a name=\"GenomicTestCode-M80.4653\"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, copy number variant (Monosomal karyotype, del5/del5q, del7/del7q, del17/del17p, del12/del12p)</td></tr><tr><td style=\"white-space:nowrap\">M80.54<a name=\"GenomicTestCode-M80.4654\"> </a></td><td>Acute Myeloid Leukaemia, NUP98 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M80.55<a name=\"GenomicTestCode-M80.4655\"> </a></td><td>Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M80.56<a name=\"GenomicTestCode-M80.4656\"> </a></td><td>Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M80.57<a name=\"GenomicTestCode-M80.4657\"> </a></td><td>Acute Myeloid Leukaemia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M80.58<a name=\"GenomicTestCode-M80.4658\"> </a></td><td>Acute Myeloid Leukaemia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M80.7<a name=\"GenomicTestCode-M80.467\"> </a></td><td>Acute Myeloid Leukaemia, Other RT-PCR: See tests M80.41-80.52 for individual specified RT-PCR targets.</td></tr><tr><td style=\"white-space:nowrap\">M80.8<a name=\"GenomicTestCode-M80.468\"> </a></td><td>Acute Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of  Complex karyotype)</td></tr><tr><td style=\"white-space:nowrap\">M80.9<a name=\"GenomicTestCode-M80.469\"> </a></td><td>Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M81.1<a name=\"GenomicTestCode-M81.461\"> </a></td><td>Transient Abnormal Myelopoiesis, Multi-target NGS panel, small variant (GATA1)</td></tr><tr><td style=\"white-space:nowrap\">M82.1<a name=\"GenomicTestCode-M82.461\"> </a></td><td>Myelodysplasia, Multi-target NGS panel, small variant (TP53, SF3B1, IDH1, IDH2, NRAS, KRAS, TET2, SRSF2, ASXL1, DNMT3A, RUNX1, U2AF1, EZH2, BCOR, PTPN11, JAK2, SETBP1, PPM1D, DDX41, PHF6, CUX1, UBA1)</td></tr><tr><td style=\"white-space:nowrap\">M82.10<a name=\"GenomicTestCode-M82.4610\"> </a></td><td>Myelodysplasia, Chr13/Chr13q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.11<a name=\"GenomicTestCode-M82.4611\"> </a></td><td>Myelodysplasia, Chr11q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.12<a name=\"GenomicTestCode-M82.4612\"> </a></td><td>Myelodysplasia, Chr12p copy number FISH, t(12p) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.13<a name=\"GenomicTestCode-M82.4613\"> </a></td><td>Myelodysplasia, Chr9q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.14<a name=\"GenomicTestCode-M82.4614\"> </a></td><td>Myelodysplasia, Chr17/Chr17p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.15<a name=\"GenomicTestCode-M82.4615\"> </a></td><td>Myelodysplasia, idic(X)(q13) FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.16<a name=\"GenomicTestCode-M82.4616\"> </a></td><td>Myelodysplasia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, -13/del13q, del11q, del12p, del9q, del17/del17p &amp; idic(X)(q13);-Y; del 20q; +8; +19,del(3q)</td></tr><tr><td style=\"white-space:nowrap\">M82.17<a name=\"GenomicTestCode-M82.4617\"> </a></td><td>Myelodysplasia, Multi-target NGS panel, structural variant (t(12p), t(17p);inv(3)/t(3q)/del(3q)</td></tr><tr><td style=\"white-space:nowrap\">M82.18<a name=\"GenomicTestCode-M82.4618\"> </a></td><td>Myelodysplasia, ChrY copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.19<a name=\"GenomicTestCode-M82.4619\"> </a></td><td>Myelodysplasia, Chr20/20q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.2<a name=\"GenomicTestCode-M82.462\"> </a></td><td>Myelodysplasia, Karyotype (To include detection of complex karyotype, -7/del7q, -5/del5q, i(17q)/t(17p), -13/del13q, del11q, del12p/t(12p), del9q, del17/del17p &amp; idic(X)(q13)); -Y; del 20q; +8; +19,(inv(3)/t(3q)/del(3q))</td></tr><tr><td style=\"white-space:nowrap\">M82.20<a name=\"GenomicTestCode-M82.4620\"> </a></td><td>Myelodysplasia, Chr8 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.21<a name=\"GenomicTestCode-M82.4621\"> </a></td><td>Myelodysplasia, Chr19 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.22<a name=\"GenomicTestCode-M82.4622\"> </a></td><td>Myelodysplasia, inv(3)/t(3q)/del(3q)</td></tr><tr><td style=\"white-space:nowrap\">M82.23<a name=\"GenomicTestCode-M82.4623\"> </a></td><td>Myelodysplasia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M82.24<a name=\"GenomicTestCode-M82.4624\"> </a></td><td>Myelodysplasia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M82.4<a name=\"GenomicTestCode-M82.464\"> </a></td><td>Myelodysplasia, FISH copy number and rearrangement Other: See tests M82.7 -M82.22 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M82.6<a name=\"GenomicTestCode-M82.466\"> </a></td><td>Myelodysplasia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M82.7<a name=\"GenomicTestCode-M82.467\"> </a></td><td>Myelodysplasia, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.8<a name=\"GenomicTestCode-M82.468\"> </a></td><td>Myelodysplasia, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M82.9<a name=\"GenomicTestCode-M82.469\"> </a></td><td>Myelodysplasia, i(17q)/t(17p) FISH</td></tr><tr><td style=\"white-space:nowrap\">M83.1<a name=\"GenomicTestCode-M83.461\"> </a></td><td>Aplastic Anaemia, Karyotype (Genomewide)</td></tr><tr><td style=\"white-space:nowrap\">M83.3<a name=\"GenomicTestCode-M83.463\"> </a></td><td>Aplastic Anaemia, FISH copy number and rearrangement</td></tr><tr><td style=\"white-space:nowrap\">M83.4<a name=\"GenomicTestCode-M83.464\"> </a></td><td>Aplastic Anaemia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M83.5<a name=\"GenomicTestCode-M83.465\"> </a></td><td>Aplastic Anaemia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M83.6<a name=\"GenomicTestCode-M83.466\"> </a></td><td>Aplastic Anaemia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M84.1<a name=\"GenomicTestCode-M84.461\"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 multiplex</td></tr><tr><td style=\"white-space:nowrap\">M84.11<a name=\"GenomicTestCode-M84.4611\"> </a></td><td>Chronic Myeloid Leukaemia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M84.12<a name=\"GenomicTestCode-M84.4612\"> </a></td><td>Chronic Myeloid Leukaemia, Chr8 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.13<a name=\"GenomicTestCode-M84.4613\"> </a></td><td>Chronic Myeloid Leukaemia, Chr19 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.14<a name=\"GenomicTestCode-M84.4614\"> </a></td><td>Chronic Myeloid Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.15<a name=\"GenomicTestCode-M84.4615\"> </a></td><td>Chronic Myeloid Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.16<a name=\"GenomicTestCode-M84.4616\"> </a></td><td>Chronic Myeloid Leukaemia, i(17q) FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.17<a name=\"GenomicTestCode-M84.4617\"> </a></td><td>Chronic Myeloid Leukaemia, Chr12p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.18<a name=\"GenomicTestCode-M84.4618\"> </a></td><td>Chronic Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH and related abnormalities i.e. 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11)</td></tr><tr><td style=\"white-space:nowrap\">M84.19<a name=\"GenomicTestCode-M84.4619\"> </a></td><td>Chronic Myeloid Leukaemia, Inv(3) MECOM FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.2<a name=\"GenomicTestCode-M84.462\"> </a></td><td>Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M84.20<a name=\"GenomicTestCode-M84.4620\"> </a></td><td>Chronic Myeloid Leukaemia, 11q23 (KMT2A) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.21<a name=\"GenomicTestCode-M84.4621\"> </a></td><td>Chronic Myeloid Leukaemia, Multi-target NGS panel, copy number variant (trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-)</td></tr><tr><td style=\"white-space:nowrap\">M84.22<a name=\"GenomicTestCode-M84.4622\"> </a></td><td>Chronic Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], Ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)</td></tr><tr><td style=\"white-space:nowrap\">M84.23<a name=\"GenomicTestCode-M84.4623\"> </a></td><td>Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M84.24<a name=\"GenomicTestCode-M84.4624\"> </a></td><td>Chronic Myeloid Leukaemia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M84.25<a name=\"GenomicTestCode-M84.4625\"> </a></td><td>Chronic Myeloid Leukaemia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M84.3<a name=\"GenomicTestCode-M84.463\"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M84.4<a name=\"GenomicTestCode-M84.464\"> </a></td><td>Chronic Myeloid Leukaemia, Karyotype (To include detection of trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-&amp; t(9;22)(q34;q11) BCR-ABL1, 2nd Ph+[+der(22)t(9;22)(q34;q11)], ider(22)(q10)t(9;22)(q34;q11), inv(3), 11q23 rearrangements)</td></tr><tr><td style=\"white-space:nowrap\">M84.6<a name=\"GenomicTestCode-M84.466\"> </a></td><td>Chronic Myeloid Leukaemia, FISH copy number and rearrangement Other: See tests M84.12 M84.20 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M84.8<a name=\"GenomicTestCode-M84.468\"> </a></td><td>Chronic Myeloid Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style=\"white-space:nowrap\">M85.1<a name=\"GenomicTestCode-M85.461\"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)</td></tr><tr><td style=\"white-space:nowrap\">M85.10<a name=\"GenomicTestCode-M85.4610\"> </a></td><td>Myeloproliferative Neoplasm, PCM1-JAK2 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M85.11<a name=\"GenomicTestCode-M85.4611\"> </a></td><td>Myeloproliferative Neoplasm, BCR-ABL1 multiplex</td></tr><tr><td style=\"white-space:nowrap\">M85.12<a name=\"GenomicTestCode-M85.4612\"> </a></td><td>Myeloproliferative Neoplasm, Other RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M85.13<a name=\"GenomicTestCode-M85.4613\"> </a></td><td>Myeloproliferative Neoplasm, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M85.14<a name=\"GenomicTestCode-M85.4614\"> </a></td><td>Myeloproliferative Neoplasm, JAK2 V617F hotspot</td></tr><tr><td style=\"white-space:nowrap\">M85.15<a name=\"GenomicTestCode-M85.4615\"> </a></td><td>Myeloproliferative Neoplasm, JAK2  exon 12 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M85.16<a name=\"GenomicTestCode-M85.4616\"> </a></td><td>Myeloproliferative Neoplasm, CALR exon 9 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M85.17<a name=\"GenomicTestCode-M85.4617\"> </a></td><td>Myeloproliferative Neoplasm, MPL exon 10 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M85.19<a name=\"GenomicTestCode-M85.4619\"> </a></td><td>Myeloproliferative Neoplasm, Chr8 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.2<a name=\"GenomicTestCode-M85.462\"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">M85.20<a name=\"GenomicTestCode-M85.4620\"> </a></td><td>Myeloproliferative Neoplasm, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.21<a name=\"GenomicTestCode-M85.4621\"> </a></td><td>Myeloproliferative Neoplasm, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.22<a name=\"GenomicTestCode-M85.4622\"> </a></td><td>Myeloproliferative Neoplasm, i(17q) FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.23<a name=\"GenomicTestCode-M85.4623\"> </a></td><td>Myeloproliferative Neoplasm, Chr12p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.24<a name=\"GenomicTestCode-M85.4624\"> </a></td><td>Myeloproliferative Neoplasm, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.25<a name=\"GenomicTestCode-M85.4625\"> </a></td><td>Myeloproliferative Neoplasm, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)</td></tr><tr><td style=\"white-space:nowrap\">M85.26<a name=\"GenomicTestCode-M85.4626\"> </a></td><td>Myeloproliferative Neoplasm, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)</td></tr><tr><td style=\"white-space:nowrap\">M85.27<a name=\"GenomicTestCode-M85.4627\"> </a></td><td>Myeloproliferative Neoplasm, FGFR1 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.28<a name=\"GenomicTestCode-M85.4628\"> </a></td><td>Myeloproliferative Neoplasm, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)</td></tr><tr><td style=\"white-space:nowrap\">M85.29<a name=\"GenomicTestCode-M85.4629\"> </a></td><td>Myeloproliferative Neoplasm, inv(3)/t(3;3) FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.3<a name=\"GenomicTestCode-M85.463\"> </a></td><td>Myeloproliferative Neoplasm, Karyotype (To include detection of complex karyotype)</td></tr><tr><td style=\"white-space:nowrap\">M85.30<a name=\"GenomicTestCode-M85.4630\"> </a></td><td>Myeloproliferative Neoplasm, 11q23 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.31<a name=\"GenomicTestCode-M85.4631\"> </a></td><td>Myeloproliferative Neoplasm, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)</td></tr><tr><td style=\"white-space:nowrap\">M85.32<a name=\"GenomicTestCode-M85.4632\"> </a></td><td>Myeloproliferative Neoplasm, FLT3 rearragement FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.33<a name=\"GenomicTestCode-M85.4633\"> </a></td><td>Myeloproliferative Neoplasm, RET rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.34<a name=\"GenomicTestCode-M85.4634\"> </a></td><td>Myeloproliferative Neoplasm, NTRK3 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M85.35<a name=\"GenomicTestCode-M85.4635\"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M85.36<a name=\"GenomicTestCode-M85.4636\"> </a></td><td>Myeloproliferative Neoplasm, Multi-target NGS panel, copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)</td></tr><tr><td style=\"white-space:nowrap\">M85.37<a name=\"GenomicTestCode-M85.4637\"> </a></td><td>Myeloproliferative Neoplasm, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M85.38<a name=\"GenomicTestCode-M85.4638\"> </a></td><td>Myeloproliferative Neoplasm, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M85.5<a name=\"GenomicTestCode-M85.465\"> </a></td><td>Myeloproliferative Neoplasm, FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M85.7<a name=\"GenomicTestCode-M85.467\"> </a></td><td>Myeloproliferative Neoplasm, FIP1L1-PDGFRA (4q12) FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M85.8<a name=\"GenomicTestCode-M85.468\"> </a></td><td>Myeloproliferative Neoplasm, FIP1L1-PDGFRA RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M85.9<a name=\"GenomicTestCode-M85.469\"> </a></td><td>Myeloproliferative Neoplasm, ETV6-PDGFRB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M86.1<a name=\"GenomicTestCode-M86.461\"> </a></td><td>Systemic Mastocytosis, Multi-target NGS panel, small variant (KIT)</td></tr><tr><td style=\"white-space:nowrap\">M86.2<a name=\"GenomicTestCode-M86.462\"> </a></td><td>Systemic Mastocytosis, KIT D816 QF-PCR</td></tr><tr><td style=\"white-space:nowrap\">M86.3<a name=\"GenomicTestCode-M86.463\"> </a></td><td>Systemic Mastocytosis, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M86.4<a name=\"GenomicTestCode-M86.464\"> </a></td><td>Systemic Mastocytosis, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M86.5<a name=\"GenomicTestCode-M86.465\"> </a></td><td>Systemic Mastocytosis, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M87.1<a name=\"GenomicTestCode-M87.461\"> </a></td><td>Chronic Neutrophilic Leukaemia, Multi-target NGS panel, small variant (CSF3R)</td></tr><tr><td style=\"white-space:nowrap\">M88.1<a name=\"GenomicTestCode-M88.461\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant (PTPN11, KRAS, NRAS, NF1, CBL)</td></tr><tr><td style=\"white-space:nowrap\">M88.10<a name=\"GenomicTestCode-M88.4610\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, trisomy 8)</td></tr><tr><td style=\"white-space:nowrap\">M88.11<a name=\"GenomicTestCode-M88.4611\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M88.12<a name=\"GenomicTestCode-M88.4612\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M88.2<a name=\"GenomicTestCode-M88.462\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M88.3<a name=\"GenomicTestCode-M88.463\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant</td></tr><tr><td style=\"white-space:nowrap\">M88.4<a name=\"GenomicTestCode-M88.464\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Karyotype</td></tr><tr><td style=\"white-space:nowrap\">M88.5<a name=\"GenomicTestCode-M88.465\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, FISH copy number and rearrangement Other: See tests M88.7-M88.9 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M88.7<a name=\"GenomicTestCode-M88.467\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr8 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M88.8<a name=\"GenomicTestCode-M88.468\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M88.9<a name=\"GenomicTestCode-M88.469\"> </a></td><td>Juvenile Myelomonocytic Leukaemia, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.1<a name=\"GenomicTestCode-M89.461\"> </a></td><td>Acute Leukaemia Other, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M89.10<a name=\"GenomicTestCode-M89.4610\"> </a></td><td>Acute Leukaemia Other, MRD PML-RARA RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M89.100<a name=\"GenomicTestCode-M89.46100\"> </a></td><td>Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.101<a name=\"GenomicTestCode-M89.46101\"> </a></td><td>Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.102<a name=\"GenomicTestCode-M89.46102\"> </a></td><td>Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.103<a name=\"GenomicTestCode-M89.46103\"> </a></td><td>Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.104<a name=\"GenomicTestCode-M89.46104\"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, copy number variant</td></tr><tr><td style=\"white-space:nowrap\">M89.105<a name=\"GenomicTestCode-M89.46105\"> </a></td><td>Acute Leukaemia Other, NUP98 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.106<a name=\"GenomicTestCode-M89.46106\"> </a></td><td>Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M89.107<a name=\"GenomicTestCode-M89.46107\"> </a></td><td>Acute Leukaemia Other, MRD NPM1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M89.108<a name=\"GenomicTestCode-M89.46108\"> </a></td><td>Acute Leukaemia Other, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M89.109<a name=\"GenomicTestCode-M89.46109\"> </a></td><td>Acute Leukaemia Other, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M89.11<a name=\"GenomicTestCode-M89.4611\"> </a></td><td>Acute Leukaemia Other, MRD RUNX1-RUNX1T1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M89.12<a name=\"GenomicTestCode-M89.4612\"> </a></td><td>Acute Leukaemia Other, MRD CBFB-MYH11 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M89.13<a name=\"GenomicTestCode-M89.4613\"> </a></td><td>Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M89.14<a name=\"GenomicTestCode-M89.4614\"> </a></td><td>Acute Leukaemia Other, MRD other QF-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.15<a name=\"GenomicTestCode-M89.4615\"> </a></td><td>Acute Leukaemia Other, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)</td></tr><tr><td style=\"white-space:nowrap\">M89.16<a name=\"GenomicTestCode-M89.4616\"> </a></td><td>Acute Leukaemia Other, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR )</td></tr><tr><td style=\"white-space:nowrap\">M89.17<a name=\"GenomicTestCode-M89.4617\"> </a></td><td>Acute Leukaemia Other, BCR-ABL1 TKD NGS</td></tr><tr><td style=\"white-space:nowrap\">M89.2<a name=\"GenomicTestCode-M89.462\"> </a></td><td>Acute Leukaemia Other, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)</td></tr><tr><td style=\"white-space:nowrap\">M89.20<a name=\"GenomicTestCode-M89.4620\"> </a></td><td>Acute Leukaemia Other, FLT3 TKD hotspot</td></tr><tr><td style=\"white-space:nowrap\">M89.21<a name=\"GenomicTestCode-M89.4621\"> </a></td><td>Acute Leukaemia Other, NPM1 exon 12 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M89.22<a name=\"GenomicTestCode-M89.4622\"> </a></td><td>Acute Leukaemia Other, IDH1 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M89.23<a name=\"GenomicTestCode-M89.4623\"> </a></td><td>Acute Leukaemia Other, IDH2 hotspot</td></tr><tr><td style=\"white-space:nowrap\">M89.24<a name=\"GenomicTestCode-M89.4624\"> </a></td><td>Acute Leukaemia Other, Chr5/Chr5q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.25<a name=\"GenomicTestCode-M89.4625\"> </a></td><td>Acute Leukaemia Other, Chr7/Chr7q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.26<a name=\"GenomicTestCode-M89.4626\"> </a></td><td>Acute Leukaemia Other, Chr17/Chr17p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.27<a name=\"GenomicTestCode-M89.4627\"> </a></td><td>Acute Leukaemia Other, Chr12/Chr12p copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.28<a name=\"GenomicTestCode-M89.4628\"> </a></td><td>Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.29<a name=\"GenomicTestCode-M89.4629\"> </a></td><td>Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.3<a name=\"GenomicTestCode-M89.463\"> </a></td><td>Acute Leukaemia Other, FISH copy number and rearrangement other</td></tr><tr><td style=\"white-space:nowrap\">M89.30<a name=\"GenomicTestCode-M89.4630\"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.31<a name=\"GenomicTestCode-M89.4631\"> </a></td><td>Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 ( KMT2A) rearrangements FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.32<a name=\"GenomicTestCode-M89.4632\"> </a></td><td>Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.33<a name=\"GenomicTestCode-M89.4633\"> </a></td><td>Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.34<a name=\"GenomicTestCode-M89.4634\"> </a></td><td>Acute Leukaemia Other, t(1;22)(p13;q13) RBM15-MRTFA FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.35<a name=\"GenomicTestCode-M89.4635\"> </a></td><td>Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.36<a name=\"GenomicTestCode-M89.4636\"> </a></td><td>Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.37<a name=\"GenomicTestCode-M89.4637\"> </a></td><td>Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.38<a name=\"GenomicTestCode-M89.4638\"> </a></td><td>Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.39<a name=\"GenomicTestCode-M89.4639\"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.4<a name=\"GenomicTestCode-M89.464\"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD, PPM1D, ETV6, NOTCH1, FBXW7, PTEN,  HRAS)</td></tr><tr><td style=\"white-space:nowrap\">M89.40<a name=\"GenomicTestCode-M89.4640\"> </a></td><td>Acute Leukaemia Other, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)</td></tr><tr><td style=\"white-space:nowrap\">M89.41<a name=\"GenomicTestCode-M89.4641\"> </a></td><td>Acute Leukaemia Other, del(1)(p33p33) FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.42<a name=\"GenomicTestCode-M89.4642\"> </a></td><td>Acute Leukaemia Other, iAMP21 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.5<a name=\"GenomicTestCode-M89.465\"> </a></td><td>Acute Leukaemia Other, FLT3 ITD</td></tr><tr><td style=\"white-space:nowrap\">M89.52<a name=\"GenomicTestCode-M89.4652\"> </a></td><td>Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.53<a name=\"GenomicTestCode-M89.4653\"> </a></td><td>Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.54<a name=\"GenomicTestCode-M89.4654\"> </a></td><td>Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.55<a name=\"GenomicTestCode-M89.4655\"> </a></td><td>Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.56<a name=\"GenomicTestCode-M89.4656\"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.57<a name=\"GenomicTestCode-M89.4657\"> </a></td><td>Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.58<a name=\"GenomicTestCode-M89.4658\"> </a></td><td>Acute Leukaemia Other,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.59<a name=\"GenomicTestCode-M89.4659\"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.6<a name=\"GenomicTestCode-M89.466\"> </a></td><td>Acute Leukaemia Other, Other RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.60<a name=\"GenomicTestCode-M89.4660\"> </a></td><td>Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.61<a name=\"GenomicTestCode-M89.4661\"> </a></td><td>Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.62<a name=\"GenomicTestCode-M89.4662\"> </a></td><td>Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.63<a name=\"GenomicTestCode-M89.4663\"> </a></td><td>Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.64<a name=\"GenomicTestCode-M89.4664\"> </a></td><td>Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.65<a name=\"GenomicTestCode-M89.4665\"> </a></td><td>Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.66<a name=\"GenomicTestCode-M89.4666\"> </a></td><td>Acute Leukaemia Other, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)</td></tr><tr><td style=\"white-space:nowrap\">M89.67<a name=\"GenomicTestCode-M89.4667\"> </a></td><td>Acute Leukaemia Other, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)</td></tr><tr><td style=\"white-space:nowrap\">M89.68<a name=\"GenomicTestCode-M89.4668\"> </a></td><td>Acute Leukaemia Other, PDGFRA rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.69<a name=\"GenomicTestCode-M89.4669\"> </a></td><td>Acute Leukaemia Other, PDGFRB rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.7<a name=\"GenomicTestCode-M89.467\"> </a></td><td>Acute Leukaemia Other, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M89.70<a name=\"GenomicTestCode-M89.4670\"> </a></td><td>Acute Leukaemia Other, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)</td></tr><tr><td style=\"white-space:nowrap\">M89.71<a name=\"GenomicTestCode-M89.4671\"> </a></td><td>Acute Leukaemia Other, JAK2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.72<a name=\"GenomicTestCode-M89.4672\"> </a></td><td>Acute Leukaemia Other, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)</td></tr><tr><td style=\"white-space:nowrap\">M89.73<a name=\"GenomicTestCode-M89.4673\"> </a></td><td>Acute Leukaemia Other, ABL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.74<a name=\"GenomicTestCode-M89.4674\"> </a></td><td>Acute Leukaemia Other, CSF1R rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.75<a name=\"GenomicTestCode-M89.4675\"> </a></td><td>Acute Leukaemia Other, 14q32 (IGH) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.76<a name=\"GenomicTestCode-M89.4676\"> </a></td><td>Acute Leukaemia Other, CRLF2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.77<a name=\"GenomicTestCode-M89.4677\"> </a></td><td>Acute Leukaemia Other, EPOR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M89.78<a name=\"GenomicTestCode-M89.4678\"> </a></td><td>Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.79<a name=\"GenomicTestCode-M89.4679\"> </a></td><td>Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.8<a name=\"GenomicTestCode-M89.468\"> </a></td><td>Acute Leukaemia Other, BCR-ABL1 multiplex</td></tr><tr><td style=\"white-space:nowrap\">M89.80<a name=\"GenomicTestCode-M89.4680\"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.81<a name=\"GenomicTestCode-M89.4681\"> </a></td><td>Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A &amp; other 11q23.3 (KMT2A) rearrangements RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.82<a name=\"GenomicTestCode-M89.4682\"> </a></td><td>Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.83<a name=\"GenomicTestCode-M89.4683\"> </a></td><td>Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.84<a name=\"GenomicTestCode-M89.4684\"> </a></td><td>Acute Leukaemia Other, t(1;22)(p13;q13)  RBM15-MRTFA RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.85<a name=\"GenomicTestCode-M89.4685\"> </a></td><td>Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.86<a name=\"GenomicTestCode-M89.4686\"> </a></td><td>Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.87<a name=\"GenomicTestCode-M89.4687\"> </a></td><td>Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.88<a name=\"GenomicTestCode-M89.4688\"> </a></td><td>Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.89<a name=\"GenomicTestCode-M89.4689\"> </a></td><td>Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.9<a name=\"GenomicTestCode-M89.469\"> </a></td><td>Acute Leukaemia Other, MRD NPM1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M89.90<a name=\"GenomicTestCode-M89.4690\"> </a></td><td>Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.91<a name=\"GenomicTestCode-M89.4691\"> </a></td><td>Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.92<a name=\"GenomicTestCode-M89.4692\"> </a></td><td>Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.93<a name=\"GenomicTestCode-M89.4693\"> </a></td><td>Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.94<a name=\"GenomicTestCode-M89.4694\"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.95<a name=\"GenomicTestCode-M89.4695\"> </a></td><td>Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.96<a name=\"GenomicTestCode-M89.4696\"> </a></td><td>Acute Leukaemia Other, t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.97<a name=\"GenomicTestCode-M89.4697\"> </a></td><td>Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.98<a name=\"GenomicTestCode-M89.4698\"> </a></td><td>Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M89.99<a name=\"GenomicTestCode-M89.4699\"> </a></td><td>Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M9.1<a name=\"GenomicTestCode-M9.461\"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, small variant (BRAF, KRAS, NRAS, HRAS, TERT promoter)</td></tr><tr><td style=\"white-space:nowrap\">M9.2<a name=\"GenomicTestCode-M9.462\"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M9.3<a name=\"GenomicTestCode-M9.463\"> </a></td><td>Thyroid Papillary Carcinoma, Adult, RET rearrangement FISH/RT-PC</td></tr><tr><td style=\"white-space:nowrap\">M9.4<a name=\"GenomicTestCode-M9.464\"> </a></td><td>Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)</td></tr><tr><td style=\"white-space:nowrap\">M9.6<a name=\"GenomicTestCode-M9.466\"> </a></td><td>Thyroid Papillary Carcinoma, Adult, TERT promoter hotspot</td></tr><tr><td style=\"white-space:nowrap\">M90.1<a name=\"GenomicTestCode-M90.461\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M90.2<a name=\"GenomicTestCode-M90.462\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, Karyotype (Genomewide)</td></tr><tr><td style=\"white-space:nowrap\">M90.3<a name=\"GenomicTestCode-M90.463\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, FISH copy number and rearrangement</td></tr><tr><td style=\"white-space:nowrap\">M90.4<a name=\"GenomicTestCode-M90.464\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, Multi-target NGS panel, small variant (NPM1, CEBPA, RUNX1, FLT3, IDH1, IDH2, KIT, WT1, ASXL1, SRSF2, STAG2, RAD21, TP53, KRAS, NRAS, KMT2A(MLL)-PTD)</td></tr><tr><td style=\"white-space:nowrap\">M90.5<a name=\"GenomicTestCode-M90.465\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, FLT3 ITD</td></tr><tr><td style=\"white-space:nowrap\">M90.6<a name=\"GenomicTestCode-M90.466\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M90.7<a name=\"GenomicTestCode-M90.467\"> </a></td><td>Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M91.1<a name=\"GenomicTestCode-M91.461\"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M91.10<a name=\"GenomicTestCode-M91.4610\"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.11<a name=\"GenomicTestCode-M91.4611\"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 TKD NGS</td></tr><tr><td style=\"white-space:nowrap\">M91.14<a name=\"GenomicTestCode-M91.4614\"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD ALL RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M91.15<a name=\"GenomicTestCode-M91.4615\"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, small variant (ETV6, NOTCH1, FBXW7, TP53, PTEN, KRAS, NRAS, HRAS)</td></tr><tr><td style=\"white-space:nowrap\">M91.2<a name=\"GenomicTestCode-M91.462\"> </a></td><td>Acute Lymphoblastic Leukaemia, Karyotype (To include detection of complex karyotype, hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc)</td></tr><tr><td style=\"white-space:nowrap\">M91.22<a name=\"GenomicTestCode-M91.4622\"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD target identification (Ig/TCR gene rearrangement by PCR &amp; sequencing with MRD workup via QF-PCR)</td></tr><tr><td style=\"white-space:nowrap\">M91.23<a name=\"GenomicTestCode-M91.4623\"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR)</td></tr><tr><td style=\"white-space:nowrap\">M91.24<a name=\"GenomicTestCode-M91.4624\"> </a></td><td>Acute Lymphoblastic Leukaemia, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)</td></tr><tr><td style=\"white-space:nowrap\">M91.25<a name=\"GenomicTestCode-M91.4625\"> </a></td><td>Acute Lymphoblastic Leukaemia, del(1)(p33p33) FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.26<a name=\"GenomicTestCode-M91.4626\"> </a></td><td>Acute Lymphoblastic Leukaemia, iAMP21 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.36<a name=\"GenomicTestCode-M91.4636\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.37<a name=\"GenomicTestCode-M91.4637\"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(1;19)(q23;p13) TCF3-PBX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.38<a name=\"GenomicTestCode-M91.4638\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.39<a name=\"GenomicTestCode-M91.4639\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.4<a name=\"GenomicTestCode-M91.464\"> </a></td><td>Acute Lymphoblastic Leukaemia, FISH copy number and rearrangement other: See tests M91.24-M91.62 for individual specified FISH targets.</td></tr><tr><td style=\"white-space:nowrap\">M91.40<a name=\"GenomicTestCode-M91.4640\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.41<a name=\"GenomicTestCode-M91.4641\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.42<a name=\"GenomicTestCode-M91.4642\"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(9;11)(p21;q23) KMT2A-MLLT3 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.43<a name=\"GenomicTestCode-M91.4643\"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.44<a name=\"GenomicTestCode-M91.4644\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.45<a name=\"GenomicTestCode-M91.4645\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.46<a name=\"GenomicTestCode-M91.4646\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.47<a name=\"GenomicTestCode-M91.4647\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.48<a name=\"GenomicTestCode-M91.4648\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.49<a name=\"GenomicTestCode-M91.4649\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;10)(q34;q24) TRB-TLX1 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.50<a name=\"GenomicTestCode-M91.4650\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.51<a name=\"GenomicTestCode-M91.4651\"> </a></td><td>Acute Lymphoblastic Leukaemia, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)</td></tr><tr><td style=\"white-space:nowrap\">M91.52<a name=\"GenomicTestCode-M91.4652\"> </a></td><td>Acute Lymphoblastic Leukaemia, TLX1 rearrangement FISH (other than TLX1-TRD &amp; TRB-TLX1 see M91.48 &amp; M91.49)</td></tr><tr><td style=\"white-space:nowrap\">M91.53<a name=\"GenomicTestCode-M91.4653\"> </a></td><td>Acute Lymphoblastic Leukaemia, PDGFRA rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.54<a name=\"GenomicTestCode-M91.4654\"> </a></td><td>Acute Lymphoblastic Leukaemia, PDGFRB rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.55<a name=\"GenomicTestCode-M91.4655\"> </a></td><td>Acute Lymphoblastic Leukaemia, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)</td></tr><tr><td style=\"white-space:nowrap\">M91.56<a name=\"GenomicTestCode-M91.4656\"> </a></td><td>Acute Lymphoblastic Leukaemia, JAK2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.57<a name=\"GenomicTestCode-M91.4657\"> </a></td><td>Acute Lymphoblastic Leukaemia, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)</td></tr><tr><td style=\"white-space:nowrap\">M91.58<a name=\"GenomicTestCode-M91.4658\"> </a></td><td>Acute Lymphoblastic Leukaemia, ABL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.59<a name=\"GenomicTestCode-M91.4659\"> </a></td><td>Acute Lymphoblastic Leukaemia, CSF1R rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.6<a name=\"GenomicTestCode-M91.466\"> </a></td><td>Acute Lymphoblastic Leukaemia, Other RT-PCR: See tests M91-63-M91.77 for individual specified RT-PCR targets</td></tr><tr><td style=\"white-space:nowrap\">M91.60<a name=\"GenomicTestCode-M91.4660\"> </a></td><td>Acute Lymphoblastic Leukaemia, 14q32(IGH) rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.61<a name=\"GenomicTestCode-M91.4661\"> </a></td><td>Acute Lymphoblastic Leukaemia, CRLF2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.62<a name=\"GenomicTestCode-M91.4662\"> </a></td><td>Acute Lymphoblastic Leukaemia, EPOR rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.63<a name=\"GenomicTestCode-M91.4663\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.64<a name=\"GenomicTestCode-M91.4664\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;19)(q23;p13) TCF3-PBX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.65<a name=\"GenomicTestCode-M91.4665\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.66<a name=\"GenomicTestCode-M91.4666\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.67<a name=\"GenomicTestCode-M91.4667\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.68<a name=\"GenomicTestCode-M91.4668\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.69<a name=\"GenomicTestCode-M91.4669\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(9;11)(p21;q23) KMT2A-MLLT3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.7<a name=\"GenomicTestCode-M91.467\"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, structural variant</td></tr><tr><td style=\"white-space:nowrap\">M91.70<a name=\"GenomicTestCode-M91.4670\"> </a></td><td>Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.71<a name=\"GenomicTestCode-M91.4671\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.72<a name=\"GenomicTestCode-M91.4672\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.73<a name=\"GenomicTestCode-M91.4673\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.74<a name=\"GenomicTestCode-M91.4674\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.75<a name=\"GenomicTestCode-M91.4675\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.76<a name=\"GenomicTestCode-M91.4676\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(7;10)q34;q24) TRB-TLX1 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.77<a name=\"GenomicTestCode-M91.4677\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M91.78<a name=\"GenomicTestCode-M91.4678\"> </a></td><td>Acute Lymphoblastic Leukaemia, Multi-target NGS panel, copy number variant (to include hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc.)</td></tr><tr><td style=\"white-space:nowrap\">M91.79<a name=\"GenomicTestCode-M91.4679\"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR rare</td></tr><tr><td style=\"white-space:nowrap\">M91.8<a name=\"GenomicTestCode-M91.468\"> </a></td><td>Acute Lymphoblastic Leukaemia, BCR-ABL1 multiplex</td></tr><tr><td style=\"white-space:nowrap\">M91.80<a name=\"GenomicTestCode-M91.4680\"> </a></td><td>Acute Lymphoblastic Leukaemia, TPMT</td></tr><tr><td style=\"white-space:nowrap\">M91.81<a name=\"GenomicTestCode-M91.4681\"> </a></td><td>Acute Lymphoblastic Leukaemia, NUDT15</td></tr><tr><td style=\"white-space:nowrap\">M91.82<a name=\"GenomicTestCode-M91.4682\"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M91.83<a name=\"GenomicTestCode-M91.4683\"> </a></td><td>Acute Lymphoblastic Leukaemia, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M91.84<a name=\"GenomicTestCode-M91.4684\"> </a></td><td>Acute Lymphoblastic Leukaemia, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.85<a name=\"GenomicTestCode-M91.4685\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(8;14)(q34;q32) IGH-MYC FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.86<a name=\"GenomicTestCode-M91.4686\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(2;8)(p12;q24) IGK-MYC FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.87<a name=\"GenomicTestCode-M91.4687\"> </a></td><td>Acute Lymphoblastic Leukaemia, t(8;22)(q24;q11) IGL-MYC FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.88<a name=\"GenomicTestCode-M91.4688\"> </a></td><td>Acute Lymphoblastic Leukaemia, BCL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.89<a name=\"GenomicTestCode-M91.4689\"> </a></td><td>Acute Lymphoblastic Leukaemia, BCL6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M91.9<a name=\"GenomicTestCode-M91.469\"> </a></td><td>Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">M92.1<a name=\"GenomicTestCode-M92.461\"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF, TP53, DIS3, TENT5C, IRF4)</td></tr><tr><td style=\"white-space:nowrap\">M92.10<a name=\"GenomicTestCode-M92.4610\"> </a></td><td>Plasma Cell Dyscrasia, del(1p) copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M92.11<a name=\"GenomicTestCode-M92.4611\"> </a></td><td>Plasma Cell Dyscrasia, gain(1q) copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M92.12<a name=\"GenomicTestCode-M92.4612\"> </a></td><td>Plasma Cell Dyscrasia, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M92.13<a name=\"GenomicTestCode-M92.4613\"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel (To include hyperdiploidy, del(1p), gain(1q), del17p)</td></tr><tr><td style=\"white-space:nowrap\">M92.14<a name=\"GenomicTestCode-M92.4614\"> </a></td><td>Plasma Cell Dyscrasia, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M92.2<a name=\"GenomicTestCode-M92.462\"> </a></td><td>Plasma Cell Dyscrasia, t(4;14) IGH-FGFR3FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M92.3<a name=\"GenomicTestCode-M92.463\"> </a></td><td>Plasma Cell Dyscrasia, t(6;14)  IGH-CCND3 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M92.4<a name=\"GenomicTestCode-M92.464\"> </a></td><td>Plasma Cell Dyscrasia, t(11;14)(q13;q32)  IGH-CCND1 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M92.5<a name=\"GenomicTestCode-M92.465\"> </a></td><td>Plasma Cell Dyscrasia, t(14;16) IGH-MAF FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M92.6<a name=\"GenomicTestCode-M92.466\"> </a></td><td>Plasma Cell Dyscrasia, t(14;20)  IGH-MAFB FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M92.7<a name=\"GenomicTestCode-M92.467\"> </a></td><td>Plasma Cell Dyscrasia, Multi-target NGS panel, structural variant (To include IGH-FGFR3, IGH-CCND3, IGH-CCND1, IGH-MAF, IGH-MAFB, MYC rearrangements)</td></tr><tr><td style=\"white-space:nowrap\">M92.8<a name=\"GenomicTestCode-M92.468\"> </a></td><td>Plasma Cell Dyscrasia, IGH rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M92.9<a name=\"GenomicTestCode-M92.469\"> </a></td><td>Plasma Cell Dyscrasia, Hyperdiploidy copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M93.3<a name=\"GenomicTestCode-M93.463\"> </a></td><td>Lymphoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M93.4<a name=\"GenomicTestCode-M93.464\"> </a></td><td>Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M93.5<a name=\"GenomicTestCode-M93.465\"> </a></td><td>Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M93.6<a name=\"GenomicTestCode-M93.466\"> </a></td><td>Lymphoma, Multi-target NGS panel-small variant (BTK, PLCG2, RAS, MAP2K1, BCL2)</td></tr><tr><td style=\"white-space:nowrap\">M94.1<a name=\"GenomicTestCode-M94.461\"> </a></td><td>Chronic Lymphocytic Leukaemia, Multi-target NGS panel, small variant (TP53,BTK, PLCG2, BCL2)</td></tr><tr><td style=\"white-space:nowrap\">M94.10<a name=\"GenomicTestCode-M94.4610\"> </a></td><td>Chronic Lymphocytic Leukaemia, chromosome 12 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M94.2<a name=\"GenomicTestCode-M94.462\"> </a></td><td>Chronic Lymphocytic Leukaemia, Multi-target NGS panel, copy number variant (TP53,ATM, DLEU2/7, RB1, trisomy 12)</td></tr><tr><td style=\"white-space:nowrap\">M94.4<a name=\"GenomicTestCode-M94.464\"> </a></td><td>Chronic Lymphocytic Leukaemia, del(17p) TP53 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M94.5<a name=\"GenomicTestCode-M94.465\"> </a></td><td>Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M94.6<a name=\"GenomicTestCode-M94.466\"> </a></td><td>Chronic Lymphocytic Leukaemia, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M94.7<a name=\"GenomicTestCode-M94.467\"> </a></td><td>Chronic Lymphocytic Leukaemia, TP53 seq</td></tr><tr><td style=\"white-space:nowrap\">M94.8<a name=\"GenomicTestCode-M94.468\"> </a></td><td>Chronic Lymphocytic Leukaemia, 11q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M94.9<a name=\"GenomicTestCode-M94.469\"> </a></td><td>Chronic Lymphocytic Leukaemia, 13q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M95.1<a name=\"GenomicTestCode-M95.461\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection multiplex seq</td></tr><tr><td style=\"white-space:nowrap\">M95.10<a name=\"GenomicTestCode-M95.4610\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M95.11<a name=\"GenomicTestCode-M95.4611\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M95.12<a name=\"GenomicTestCode-M95.4612\"> </a></td><td>B cell Non-Hodgkin Lymphoma, MYD88 (L265P) hotspot</td></tr><tr><td style=\"white-space:nowrap\">M95.2<a name=\"GenomicTestCode-M95.462\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig gene (heavy &amp; light chain) rearrangement &amp; hypermutation detection NGS</td></tr><tr><td style=\"white-space:nowrap\">M95.3<a name=\"GenomicTestCode-M95.463\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Ig rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M95.4<a name=\"GenomicTestCode-M95.464\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (EZH2)</td></tr><tr><td style=\"white-space:nowrap\">M95.5<a name=\"GenomicTestCode-M95.465\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, EZH2 copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M95.6<a name=\"GenomicTestCode-M95.466\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (BTK, PLCG2)</td></tr><tr><td style=\"white-space:nowrap\">M95.7<a name=\"GenomicTestCode-M95.467\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M95.8<a name=\"GenomicTestCode-M95.468\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (Ig)</td></tr><tr><td style=\"white-space:nowrap\">M95.9<a name=\"GenomicTestCode-M95.469\"> </a></td><td>B Cell Non-Hodgkin Lymphoma, Mutli-target NGS panel, copy number (EZH2)</td></tr><tr><td style=\"white-space:nowrap\">M96.1<a name=\"GenomicTestCode-M96.461\"> </a></td><td>Burkitt Lymphoma, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M96.10<a name=\"GenomicTestCode-M96.4610\"> </a></td><td>Burkitt Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M96.2<a name=\"GenomicTestCode-M96.462\"> </a></td><td>Burkitt Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M96.3<a name=\"GenomicTestCode-M96.463\"> </a></td><td>Burkitt Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M96.4<a name=\"GenomicTestCode-M96.464\"> </a></td><td>Burkitt Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M96.5<a name=\"GenomicTestCode-M96.465\"> </a></td><td>Burkitt Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M96.6<a name=\"GenomicTestCode-M96.466\"> </a></td><td>Burkitt Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M96.7<a name=\"GenomicTestCode-M96.467\"> </a></td><td>Burkitt Lymphoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M96.8<a name=\"GenomicTestCode-M96.468\"> </a></td><td>Burkitt Lymphoma, Multi-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, other rearrangements of MYC,  BCL2, BCL6)</td></tr><tr><td style=\"white-space:nowrap\">M96.9<a name=\"GenomicTestCode-M96.469\"> </a></td><td>Burkitt Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M97.1<a name=\"GenomicTestCode-M97.461\"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, 11q copy number FISH</td></tr><tr><td style=\"white-space:nowrap\">M97.2<a name=\"GenomicTestCode-M97.462\"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M97.3<a name=\"GenomicTestCode-M97.463\"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, Multi-target NGS panel, copy number variant (11q)</td></tr><tr><td style=\"white-space:nowrap\">M97.4<a name=\"GenomicTestCode-M97.464\"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M97.5<a name=\"GenomicTestCode-M97.465\"> </a></td><td>Burkitt Like Lymphoma with 11q Abnormalities, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M98.1<a name=\"GenomicTestCode-M98.461\"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, IRF4 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M98.2<a name=\"GenomicTestCode-M98.462\"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M98.3<a name=\"GenomicTestCode-M98.463\"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, Multi-target NGS panel, structural variant (IRF4)</td></tr><tr><td style=\"white-space:nowrap\">M98.4<a name=\"GenomicTestCode-M98.464\"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M98.5<a name=\"GenomicTestCode-M98.465\"> </a></td><td>Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M99.1<a name=\"GenomicTestCode-M99.461\"> </a></td><td>High Grade Lymphoma, MYC rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M99.10<a name=\"GenomicTestCode-M99.4610\"> </a></td><td>High Grade Lymphoma, WGS Tumour First</td></tr><tr><td style=\"white-space:nowrap\">M99.11<a name=\"GenomicTestCode-M99.4611\"> </a></td><td>High Grade Lymphoma, WGS Follow-up Germline</td></tr><tr><td style=\"white-space:nowrap\">M99.2<a name=\"GenomicTestCode-M99.462\"> </a></td><td>High Grade Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M99.3<a name=\"GenomicTestCode-M99.463\"> </a></td><td>High Grade Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M99.4<a name=\"GenomicTestCode-M99.464\"> </a></td><td>High Grade Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M99.5<a name=\"GenomicTestCode-M99.465\"> </a></td><td>High Grade Lymphoma, BCL2 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M99.6<a name=\"GenomicTestCode-M99.466\"> </a></td><td>High Grade Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">M99.7<a name=\"GenomicTestCode-M99.467\"> </a></td><td>High Grade Lymphoma, BCL6 rearrangement FISH</td></tr><tr><td style=\"white-space:nowrap\">M99.8<a name=\"GenomicTestCode-M99.468\"> </a></td><td>High Grade Lymphoma, WGS Germline and Tumor</td></tr><tr><td style=\"white-space:nowrap\">M99.9<a name=\"GenomicTestCode-M99.469\"> </a></td><td>High Grade Lymphoma, Mutli-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, IGH-BCL2, other rearrangements of MYC, BCL2, BCL6)</td></tr><tr><td style=\"white-space:nowrap\">R100.3<a name=\"GenomicTestCode-R100.463\"> </a></td><td>Rare syndromic craniosynostosis or isolated multisuture synostosis (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R101.1<a name=\"GenomicTestCode-R101.461\"> </a></td><td>Ehlers Danlos syndrome with a likely monogenic cause (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R102.1<a name=\"GenomicTestCode-R102.461\"> </a></td><td>Osteogenesis imperfecta (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R104.3<a name=\"GenomicTestCode-R104.463\"> </a></td><td>Skeletal dysplasia (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R104.4<a name=\"GenomicTestCode-R104.464\"> </a></td><td>Skeletal dysplasia (Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R105.1<a name=\"GenomicTestCode-R105.461\"> </a></td><td>MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ common variant newborn screening follow up (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R106.1<a name=\"GenomicTestCode-R106.461\"> </a></td><td>Alstrom syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R107.1<a name=\"GenomicTestCode-R107.461\"> </a></td><td>Bardet-Biedl syndrome (WES or Large Panel)</td></tr><tr><td style=\"white-space:nowrap\">R109.3<a name=\"GenomicTestCode-R109.463\"> </a></td><td>Childhood onset leukodystrophy (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R110.1<a name=\"GenomicTestCode-R110.461\"> </a></td><td>Segmental overgrowth disorders Deep sequencing (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R111.1<a name=\"GenomicTestCode-R111.461\"> </a></td><td>X-inactivation testing (X-inactivation testing)</td></tr><tr><td style=\"white-space:nowrap\">R112.1<a name=\"GenomicTestCode-R112.461\"> </a></td><td>Factor II deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R115.1<a name=\"GenomicTestCode-R115.461\"> </a></td><td>Factor V deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R115.2<a name=\"GenomicTestCode-R115.462\"> </a></td><td>Factor V deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R116.1<a name=\"GenomicTestCode-R116.461\"> </a></td><td>Factor VII deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R116.2<a name=\"GenomicTestCode-R116.462\"> </a></td><td>Factor VII deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R117.1<a name=\"GenomicTestCode-R117.461\"> </a></td><td>Factor VIII deficiency (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R117.2<a name=\"GenomicTestCode-R117.462\"> </a></td><td>Factor VIII deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R117.3<a name=\"GenomicTestCode-R117.463\"> </a></td><td>Factor VIII deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R118.1<a name=\"GenomicTestCode-R118.461\"> </a></td><td>Factor IX deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R118.2<a name=\"GenomicTestCode-R118.462\"> </a></td><td>Factor IX deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R119.1<a name=\"GenomicTestCode-R119.461\"> </a></td><td>Factor X deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R119.2<a name=\"GenomicTestCode-R119.462\"> </a></td><td>Factor X deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R120.1<a name=\"GenomicTestCode-R120.461\"> </a></td><td>Factor XI deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R120.2<a name=\"GenomicTestCode-R120.462\"> </a></td><td>Factor XI deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R121.1<a name=\"GenomicTestCode-R121.461\"> </a></td><td>von Willebrand disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R121.2<a name=\"GenomicTestCode-R121.462\"> </a></td><td>von Willebrand disease (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R122.1<a name=\"GenomicTestCode-R122.461\"> </a></td><td>Factor XIII deficiency (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R123.1<a name=\"GenomicTestCode-R123.461\"> </a></td><td>Combined vitamin K-dependent clotting factor deficiency (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R124.1<a name=\"GenomicTestCode-R124.461\"> </a></td><td>Combined factor V and VIII deficiency (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R125.1<a name=\"GenomicTestCode-R125.461\"> </a></td><td>Thoracic aortic aneurysm or dissection (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R127.1<a name=\"GenomicTestCode-R127.461\"> </a></td><td>Long QT syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R128.1<a name=\"GenomicTestCode-R128.461\"> </a></td><td>Brugada syndrome and cardiac sodium channel disease (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R129.1<a name=\"GenomicTestCode-R129.461\"> </a></td><td>Catecholaminergic polymorphic VT (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R130.1<a name=\"GenomicTestCode-R130.461\"> </a></td><td>Short QT syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R131.1<a name=\"GenomicTestCode-R131.461\"> </a></td><td>Hypertrophic cardiomyopathy (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R132.1<a name=\"GenomicTestCode-R132.461\"> </a></td><td>Dilated and Arrhythmogenic cardiomyopathy (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R133.1<a name=\"GenomicTestCode-R133.461\"> </a></td><td>Arrhythmogenic right ventricular cardiomyopathy (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R134.1<a name=\"GenomicTestCode-R134.461\"> </a></td><td>Familial hypercholesterolaemia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R135.2<a name=\"GenomicTestCode-R135.462\"> </a></td><td>Paediatric or syndromic cardiomyopathy (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R135.3<a name=\"GenomicTestCode-R135.463\"> </a></td><td>Paediatric or syndromic cardiomyopathy (WES)</td></tr><tr><td style=\"white-space:nowrap\">R136.1<a name=\"GenomicTestCode-R136.461\"> </a></td><td>Primary lymphoedema (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R137.1<a name=\"GenomicTestCode-R137.461\"> </a></td><td>Congenital heart disease microarray (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R138.1<a name=\"GenomicTestCode-R138.461\"> </a></td><td>Sudden unexplained death or survivors of a cardiac event (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R139.1<a name=\"GenomicTestCode-R139.461\"> </a></td><td>Laterality disorders and isomerism (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R14.1<a name=\"GenomicTestCode-R14.461\"> </a></td><td>Acutely unwell children with a likely monogenic disorder (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R140.1<a name=\"GenomicTestCode-R140.461\"> </a></td><td>Elastin-related phenotypes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R141.1<a name=\"GenomicTestCode-R141.461\"> </a></td><td>Monogenic diabetes (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R142.1<a name=\"GenomicTestCode-R142.461\"> </a></td><td>Glucokinase-related fasting hyperglycaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R143.1<a name=\"GenomicTestCode-R143.461\"> </a></td><td>Neonatal diabetes (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R143.3<a name=\"GenomicTestCode-R143.463\"> </a></td><td>Neonatal diabetes (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R143.4<a name=\"GenomicTestCode-R143.464\"> </a></td><td>Neonatal diabetes (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R144.1<a name=\"GenomicTestCode-R144.461\"> </a></td><td>Congenital hyperinsulinism (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R144.2<a name=\"GenomicTestCode-R144.462\"> </a></td><td>Congenital hyperinsulinism (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R145.1<a name=\"GenomicTestCode-R145.461\"> </a></td><td>Congenital hypothyroidism (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R146.1<a name=\"GenomicTestCode-R146.461\"> </a></td><td>Differences in sex development (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R146.2<a name=\"GenomicTestCode-R146.462\"> </a></td><td>Differences of sex development (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R148.1<a name=\"GenomicTestCode-R148.461\"> </a></td><td>Hypogonadotropic hypogonadism (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R149.1<a name=\"GenomicTestCode-R149.461\"> </a></td><td>Severe early-onset obesity (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R15.4<a name=\"GenomicTestCode-R15.464\"> </a></td><td>Primary immunodeficiency or monogenic inflammatory bowel disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R15.5<a name=\"GenomicTestCode-R15.465\"> </a></td><td>Primary immunodeficiency or monogenic inflammatory bowel disease (WES)</td></tr><tr><td style=\"white-space:nowrap\">R150.1<a name=\"GenomicTestCode-R150.461\"> </a></td><td>Congenital adrenal hypoplasia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R151.1<a name=\"GenomicTestCode-R151.461\"> </a></td><td>Familial hyperparathyroidism or Hypocalciuric hypercalcaemia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R153.1<a name=\"GenomicTestCode-R153.461\"> </a></td><td>Familial hypoparathyroidism (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R154.1<a name=\"GenomicTestCode-R154.461\"> </a></td><td>Hypophosphataemia or rickets (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R155.1<a name=\"GenomicTestCode-R155.461\"> </a></td><td>Autoimmune Polyendocrine Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R156.1<a name=\"GenomicTestCode-R156.461\"> </a></td><td>Carney complex (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R157.1<a name=\"GenomicTestCode-R157.461\"> </a></td><td>IPEX Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R158.1<a name=\"GenomicTestCode-R158.461\"> </a></td><td>Severe insulin resistance and lipodystrophy syndromes (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R159.1<a name=\"GenomicTestCode-R159.461\"> </a></td><td>Pituitary hormone deficiency (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R16.1<a name=\"GenomicTestCode-R16.461\"> </a></td><td>Severe combined immunodeficiency with adenosine deaminase deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R160.1<a name=\"GenomicTestCode-R160.461\"> </a></td><td>Primary pigmented nodular adrenocortical disease (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R162.1<a name=\"GenomicTestCode-R162.461\"> </a></td><td>Familial tumoral calcinosis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R163.1<a name=\"GenomicTestCode-R163.461\"> </a></td><td>Ectodermal dysplasia (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R164.1<a name=\"GenomicTestCode-R164.461\"> </a></td><td>Epidermolysis bullosa and congenital skin fragility (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R165.1<a name=\"GenomicTestCode-R165.461\"> </a></td><td>Ichthyosis and erythrokeratoderma (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R166.1<a name=\"GenomicTestCode-R166.461\"> </a></td><td>Palmoplantar keratodermas (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R167.1<a name=\"GenomicTestCode-R167.461\"> </a></td><td>Autosomal recessive primary hypertrophic osteoarthropathy (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R168.1<a name=\"GenomicTestCode-R168.461\"> </a></td><td>Non-acute porphyrias (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R169.1<a name=\"GenomicTestCode-R169.461\"> </a></td><td>Acute intermittent porphyria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R17.1<a name=\"GenomicTestCode-R17.461\"> </a></td><td>Lymphoproliferative syndrome with absent SAP expression (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R170.1<a name=\"GenomicTestCode-R170.461\"> </a></td><td>Variegate porphyria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R171.1<a name=\"GenomicTestCode-R171.461\"> </a></td><td>Cholestasis (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R172.1<a name=\"GenomicTestCode-R172.461\"> </a></td><td>Wilson disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R173.1<a name=\"GenomicTestCode-R173.461\"> </a></td><td>Polycystic liver disease (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R175.1<a name=\"GenomicTestCode-R175.461\"> </a></td><td>Pancreatitis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R176.1<a name=\"GenomicTestCode-R176.461\"> </a></td><td>Gilbert syndrome (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R18.1<a name=\"GenomicTestCode-R18.461\"> </a></td><td>Haemophagocytic syndrome with absent XIAP expression (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R180.1<a name=\"GenomicTestCode-R180.461\"> </a></td><td>Congenital adrenal hyperplasia diagnostic test (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R180.2<a name=\"GenomicTestCode-R180.462\"> </a></td><td>Congenital adrenal hyperplasia diagnostic test (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R181.1<a name=\"GenomicTestCode-R181.461\"> </a></td><td>Congenital adrenal hyperplasia carrier testing (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R181.2<a name=\"GenomicTestCode-R181.462\"> </a></td><td>Congenital adrenal hyperplasia carrier testing (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R182.1<a name=\"GenomicTestCode-R182.461\"> </a></td><td>Hyperthyroidism (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R183.1<a name=\"GenomicTestCode-R183.461\"> </a></td><td>Glucocorticoid-remediable aldosteronism (GRA) (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R184.1<a name=\"GenomicTestCode-R184.461\"> </a></td><td>Cystic fibrosis diagnostic test (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R184.2<a name=\"GenomicTestCode-R184.462\"> </a></td><td>Cystic fibrosis diagnostic test (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R184.3<a name=\"GenomicTestCode-R184.463\"> </a></td><td>Cystic fibrosis diagnostic test (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R185.1<a name=\"GenomicTestCode-R185.461\"> </a></td><td>Cystic fibrosis carrier testing (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R186.1<a name=\"GenomicTestCode-R186.461\"> </a></td><td>Hereditary haemorrhagic telangiectasia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R188.1<a name=\"GenomicTestCode-R188.461\"> </a></td><td>Pulmonary arterial hypertension (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R189.1<a name=\"GenomicTestCode-R189.461\"> </a></td><td>Respiratory ciliopathies including non-CF bronchiectasis (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R19.1<a name=\"GenomicTestCode-R19.461\"> </a></td><td>Autoimmune lymphoproliferative syndrome with defective apoptosis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R190.1<a name=\"GenomicTestCode-R190.461\"> </a></td><td>Pneumothorax familial (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R191.1<a name=\"GenomicTestCode-R191.461\"> </a></td><td>Alpha-1-antitrypsin deficiency (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R193.4<a name=\"GenomicTestCode-R193.464\"> </a></td><td>Cystic renal disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R194.1<a name=\"GenomicTestCode-R194.461\"> </a></td><td>Haematuria (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R195.3<a name=\"GenomicTestCode-R195.463\"> </a></td><td>Proteinuric renal disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R196.1<a name=\"GenomicTestCode-R196.461\"> </a></td><td>CFHR5 nephropathy (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R197.1<a name=\"GenomicTestCode-R197.461\"> </a></td><td>Membranoproliferative glomerulonephritis including C3 glomerulopathy (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R197.2<a name=\"GenomicTestCode-R197.462\"> </a></td><td>Membranoproliferative glomerulonephritis including C3 glomerulopathy (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R198.1<a name=\"GenomicTestCode-R198.461\"> </a></td><td>Renal tubulopathies (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R199.1<a name=\"GenomicTestCode-R199.461\"> </a></td><td>Congenital anomalies of the kidney and urinary tract familial (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R20.1<a name=\"GenomicTestCode-R20.461\"> </a></td><td>Wiskott-Aldrich syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R201.1<a name=\"GenomicTestCode-R201.461\"> </a></td><td>Atypical haemolytic uraemic syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R202.1<a name=\"GenomicTestCode-R202.461\"> </a></td><td>Tubulointerstitial kidney disease (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R204.1<a name=\"GenomicTestCode-R204.461\"> </a></td><td>Hereditary Systemic Amyloidosis  (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R207.1<a name=\"GenomicTestCode-R207.461\"> </a></td><td>Inherited ovarian cancer (without breast cancer) (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R208.1<a name=\"GenomicTestCode-R208.461\"> </a></td><td>Inherited breast cancer and ovarian cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R21.1<a name=\"GenomicTestCode-R21.461\"> </a></td><td>Fetal anomalies with a likely genetic cause (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R21.2<a name=\"GenomicTestCode-R21.462\"> </a></td><td>Fetal anomalies with a likely genetic cause (WES or Large Panel)</td></tr><tr><td style=\"white-space:nowrap\">R21.3<a name=\"GenomicTestCode-R21.463\"> </a></td><td>Fetal anomalies with a likely genetic cause (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R210.2<a name=\"GenomicTestCode-R210.462\"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R210.4<a name=\"GenomicTestCode-R210.464\"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R210.6<a name=\"GenomicTestCode-R210.466\"> </a></td><td>Inherited MMR deficiency (Lynch syndrome) (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R211.1<a name=\"GenomicTestCode-R211.461\"> </a></td><td>Inherited polyposis and early onset colorectal cancer germline testing (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R211.3<a name=\"GenomicTestCode-R211.463\"> </a></td><td>Inherited polyposis and early onset colorectal cancer germline testing (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R212.1<a name=\"GenomicTestCode-R212.461\"> </a></td><td>Peutz Jeghers Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R213.1<a name=\"GenomicTestCode-R213.461\"> </a></td><td>PTEN Hamartoma Tumor Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R214.1<a name=\"GenomicTestCode-R214.461\"> </a></td><td>Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R215.1<a name=\"GenomicTestCode-R215.461\"> </a></td><td>Hereditary diffuse gastric cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R216.1<a name=\"GenomicTestCode-R216.461\"> </a></td><td>Li Fraumeni Syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R217.1<a name=\"GenomicTestCode-R217.461\"> </a></td><td>Endocrine neoplasia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R218.1<a name=\"GenomicTestCode-R218.461\"> </a></td><td>Multiple endocrine neoplasia type 2 (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R219.1<a name=\"GenomicTestCode-R219.461\"> </a></td><td>Retinoblastoma (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R219.2<a name=\"GenomicTestCode-R219.462\"> </a></td><td>Retinoblastoma (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R22.1<a name=\"GenomicTestCode-R22.461\"> </a></td><td>Fetus with a likely chromosomal abnormality (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R22.2<a name=\"GenomicTestCode-R22.462\"> </a></td><td>Fetus with a likely chromosomal abnormality (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R221.1<a name=\"GenomicTestCode-R221.461\"> </a></td><td>Familial tumours of the nervous system (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R221.2<a name=\"GenomicTestCode-R221.462\"> </a></td><td>Familial tumours of the nervous system (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R222.1<a name=\"GenomicTestCode-R222.461\"> </a></td><td>Neurofibromatosis type 1 (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R222.2<a name=\"GenomicTestCode-R222.462\"> </a></td><td>Neurofibromatosis type 1 (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R223.1<a name=\"GenomicTestCode-R223.461\"> </a></td><td>Inherited phaeochromocytoma and paraganglioma excluding NF1 (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R224.1<a name=\"GenomicTestCode-R224.461\"> </a></td><td>Inherited renal cancer (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R225.1<a name=\"GenomicTestCode-R225.461\"> </a></td><td>Von Hippel Lindau syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R226.1<a name=\"GenomicTestCode-R226.461\"> </a></td><td>Inherited parathyroid cancer (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R227.1<a name=\"GenomicTestCode-R227.461\"> </a></td><td>Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R227.2<a name=\"GenomicTestCode-R227.462\"> </a></td><td>Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (DNA repair defect testing)</td></tr><tr><td style=\"white-space:nowrap\">R228.1<a name=\"GenomicTestCode-R228.461\"> </a></td><td>Tuberous sclerosis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R228.2<a name=\"GenomicTestCode-R228.462\"> </a></td><td>Tuberous sclerosis (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R228.3<a name=\"GenomicTestCode-R228.463\"> </a></td><td>Tuberous sclerosis (Small panel deep sequencing)</td></tr><tr><td style=\"white-space:nowrap\">R229.1<a name=\"GenomicTestCode-R229.461\"> </a></td><td>Confirmed Fanconi anaemia or Bloom syndrome variant testing (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R23.1<a name=\"GenomicTestCode-R23.461\"> </a></td><td>Apert syndrome (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R230.1<a name=\"GenomicTestCode-R230.461\"> </a></td><td>Multiple monogenic benign skin tumours (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R231.2<a name=\"GenomicTestCode-R231.462\"> </a></td><td>Neuronal ceroid lipofuscinosis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R232.1<a name=\"GenomicTestCode-R232.461\"> </a></td><td>Haemophagocytic syndrome with absent perforin expression (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R233.1<a name=\"GenomicTestCode-R233.461\"> </a></td><td>Agammaglobulinaemia with absent BTK expression (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R234.1<a name=\"GenomicTestCode-R234.461\"> </a></td><td>Severe combined immunodeficiency with PNP deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R235.1<a name=\"GenomicTestCode-R235.461\"> </a></td><td>SCID with features of gamma chain deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R236.1<a name=\"GenomicTestCode-R236.461\"> </a></td><td>Pigmentary skin disorders (WES or Large panel)</td></tr><tr><td style=\"white-space:nowrap\">R236.2<a name=\"GenomicTestCode-R236.462\"> </a></td><td>Pigmentary skin disorders (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R237.1<a name=\"GenomicTestCode-R237.461\"> </a></td><td>Cutaneous photosensitivity with a likely genetic cause (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R239.1<a name=\"GenomicTestCode-R239.461\"> </a></td><td>Incontinentia pigmenti (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R239.2<a name=\"GenomicTestCode-R239.462\"> </a></td><td>Incontinentia pigmenti (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R24.1<a name=\"GenomicTestCode-R24.461\"> </a></td><td>Achondroplasia (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R240.1<a name=\"GenomicTestCode-R240.461\"> </a></td><td>Diagnostic testing for known variant(s) (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R242.1<a name=\"GenomicTestCode-R242.461\"> </a></td><td>Predictive testing for known familial variant(s) (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R244.1<a name=\"GenomicTestCode-R244.461\"> </a></td><td>Carrier testing for known familial variant(s) (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R246.1<a name=\"GenomicTestCode-R246.461\"> </a></td><td>Carrier testing at population risk for partners of known carriers of nationally agreed autosomal recessive disorders (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R249.1<a name=\"GenomicTestCode-R249.461\"> </a></td><td>NIPD using paternal exclusion testing for very rare conditions where familial variant is known (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R25.1<a name=\"GenomicTestCode-R25.461\"> </a></td><td>Thanatophoric dysplasia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R250.1<a name=\"GenomicTestCode-R250.461\"> </a></td><td>NIPD for congenital adrenal hyperplasia CYP21A2 haplotype testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R251.1<a name=\"GenomicTestCode-R251.461\"> </a></td><td>Non-invasive prenatal sexing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R252.1<a name=\"GenomicTestCode-R252.461\"> </a></td><td>SMA carrier testing at population risk for partners of known carriers (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R253.1<a name=\"GenomicTestCode-R253.461\"> </a></td><td>Cystic fibrosis newborn screening follow-up (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R254.1<a name=\"GenomicTestCode-R254.461\"> </a></td><td>Familial melanoma (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R255.1<a name=\"GenomicTestCode-R255.461\"> </a></td><td>Epidermodysplasia verruciformis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R256.1<a name=\"GenomicTestCode-R256.461\"> </a></td><td>Nephrocalcinosis or nephrolithiasis (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R257.2<a name=\"GenomicTestCode-R257.462\"> </a></td><td>Unexplained young onset end-stage renal disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R257.3<a name=\"GenomicTestCode-R257.463\"> </a></td><td>Unexplained young onset end-stage renal disease (WES)</td></tr><tr><td style=\"white-space:nowrap\">R258.1<a name=\"GenomicTestCode-R258.461\"> </a></td><td>Cytopenia Fanconi breakage testing indicated (DNA repair defect testing)</td></tr><tr><td style=\"white-space:nowrap\">R258.2<a name=\"GenomicTestCode-R258.462\"> </a></td><td>Cytopenia Fanconi breakage testing indicated (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R259.1<a name=\"GenomicTestCode-R259.461\"> </a></td><td>Nijmegen breakage syndrome (DNA repair defect testing)</td></tr><tr><td style=\"white-space:nowrap\">R259.2<a name=\"GenomicTestCode-R259.462\"> </a></td><td>Nijmegen breakage syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R26.1<a name=\"GenomicTestCode-R26.461\"> </a></td><td>Likely common aneuploidy (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R260.1<a name=\"GenomicTestCode-R260.461\"> </a></td><td>Fanconi anaemia or Bloom syndrome chromosome breakage testing (DNA repair defect testing)</td></tr><tr><td style=\"white-space:nowrap\">R262.1<a name=\"GenomicTestCode-R262.461\"> </a></td><td>Corneal dystrophy (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R263.1<a name=\"GenomicTestCode-R263.461\"> </a></td><td>Confirmation of uniparental disomy (UPD testing)</td></tr><tr><td style=\"white-space:nowrap\">R264.1<a name=\"GenomicTestCode-R264.461\"> </a></td><td>Identity testing (Identity testing)</td></tr><tr><td style=\"white-space:nowrap\">R265.1<a name=\"GenomicTestCode-R265.461\"> </a></td><td>Chromosomal mosaicism â€“ karyotype / Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R268.1<a name=\"GenomicTestCode-R268.461\"> </a></td><td>Kagami-Ogata syndrome paternal uniparental disomy 14 (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R27.3,<a name=\"GenomicTestCode-R27.463.44\"> </a></td><td>Paediatric disorders (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R270.1<a name=\"GenomicTestCode-R270.461\"> </a></td><td>Smith-Lemli-Opitz syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R270.2<a name=\"GenomicTestCode-R270.462\"> </a></td><td>Smith-Lemli-Opitz syndrome (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R271.1<a name=\"GenomicTestCode-R271.461\"> </a></td><td>Neuronal ceroid lipofuscinosis type 2 (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R272.1<a name=\"GenomicTestCode-R272.461\"> </a></td><td>Gaucher disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R273.1<a name=\"GenomicTestCode-R273.461\"> </a></td><td>Glycogen storage disease V (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R274.1<a name=\"GenomicTestCode-R274.461\"> </a></td><td>Glycogen storage disease (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R275.1<a name=\"GenomicTestCode-R275.461\"> </a></td><td>Glutaric acidaemia I newborn screening follow up (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R276.1<a name=\"GenomicTestCode-R276.461\"> </a></td><td>Lysosomal storage disorder (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R277.1<a name=\"GenomicTestCode-R277.461\"> </a></td><td>Mucopolysaccharidosis type IH/S (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R278.1<a name=\"GenomicTestCode-R278.461\"> </a></td><td>Mucopolysaccharidosis type II (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R278.2<a name=\"GenomicTestCode-R278.462\"> </a></td><td>Mucopolysaccharidosis type II (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R279.1<a name=\"GenomicTestCode-R279.461\"> </a></td><td>Isovaleric acidaemia newborn screening follow up (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R28.1<a name=\"GenomicTestCode-R28.461\"> </a></td><td>Congenital malformation and dysmorphism syndromes â€“ microarray only (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R280.1<a name=\"GenomicTestCode-R280.461\"> </a></td><td>Krabbe disease â€“ GALC deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R280.2<a name=\"GenomicTestCode-R280.462\"> </a></td><td>Krabbe disease â€“ GALC deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R281.1<a name=\"GenomicTestCode-R281.461\"> </a></td><td>Krabbe disease Saposin A deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R282.1<a name=\"GenomicTestCode-R282.461\"> </a></td><td>Niemann-Pick disease type A or B (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R283.1<a name=\"GenomicTestCode-R283.461\"> </a></td><td>Phenylketonuria (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R285.1<a name=\"GenomicTestCode-R285.461\"> </a></td><td>Sandhoff disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R286.1<a name=\"GenomicTestCode-R286.461\"> </a></td><td>Tay-Sachs disease (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R287.1<a name=\"GenomicTestCode-R287.461\"> </a></td><td>Mucopolysaccharidosis type IVA (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R288.1<a name=\"GenomicTestCode-R288.461\"> </a></td><td>GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R289.1<a name=\"GenomicTestCode-R289.461\"> </a></td><td>Mucolipidosis II and III Alpha/Beta (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R290.1<a name=\"GenomicTestCode-R290.461\"> </a></td><td>Mucopolysaccharidosis type VI (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R291.1<a name=\"GenomicTestCode-R291.461\"> </a></td><td>Mucopolysaccharidosis type IIIA (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R292.1<a name=\"GenomicTestCode-R292.461\"> </a></td><td>Mucopolysaccharidosis type IIIB (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R293.1<a name=\"GenomicTestCode-R293.461\"> </a></td><td>Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R293.2<a name=\"GenomicTestCode-R293.462\"> </a></td><td>Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R294.1<a name=\"GenomicTestCode-R294.461\"> </a></td><td>Ataxia telangiectasia DNA repair testing (DNA repair defect testing)</td></tr><tr><td style=\"white-space:nowrap\">R295.1<a name=\"GenomicTestCode-R295.461\"> </a></td><td>Ataxia telangiectasia variant testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R296.1<a name=\"GenomicTestCode-R296.461\"> </a></td><td>RNA analysis of variants (Other)</td></tr><tr><td style=\"white-space:nowrap\">R298.1<a name=\"GenomicTestCode-R298.461\"> </a></td><td>Possible structural or mosaic chromosomal abnormality FISH (FISH)</td></tr><tr><td style=\"white-space:nowrap\">R299.1<a name=\"GenomicTestCode-R299.461\"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Other)</td></tr><tr><td style=\"white-space:nowrap\">R299.2<a name=\"GenomicTestCode-R299.462\"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Heteroplasmy assessment mitochondrial genome)</td></tr><tr><td style=\"white-space:nowrap\">R299.3<a name=\"GenomicTestCode-R299.463\"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Breakpoint mapping mitochondrial genome)</td></tr><tr><td style=\"white-space:nowrap\">R300.1<a name=\"GenomicTestCode-R300.461\"> </a></td><td>Possible mitochondrial disorder whole mitochondrial genome sequencing (Other)</td></tr><tr><td style=\"white-space:nowrap\">R301.1<a name=\"GenomicTestCode-R301.461\"> </a></td><td>Possible mitochondrial disorder, mitochondrial DNA depletion testing (Other)</td></tr><tr><td style=\"white-space:nowrap\">R304.1<a name=\"GenomicTestCode-R304.461\"> </a></td><td>NIPD for cystic fibrosis haplotype testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R305.1<a name=\"GenomicTestCode-R305.461\"> </a></td><td>NIPD for cystic fibrosis variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R306.1<a name=\"GenomicTestCode-R306.461\"> </a></td><td>NIPD for Apert syndrome variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R307.1<a name=\"GenomicTestCode-R307.461\"> </a></td><td>NIPD for Crouzon syndrome with acanthosis nigricans variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R308.1<a name=\"GenomicTestCode-R308.461\"> </a></td><td>NIPD for FGFR2-related craniosynostosis syndromes variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R309.1<a name=\"GenomicTestCode-R309.461\"> </a></td><td>NIPD for FGFR3-related skeletal dysplasias variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R31.3<a name=\"GenomicTestCode-R31.463\"> </a></td><td>Bilateral congenital or childhood onset cataracts (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R310.1<a name=\"GenomicTestCode-R310.461\"> </a></td><td>NIPD for Duchenne and Becker muscular dystrophy haplotype testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R311.1<a name=\"GenomicTestCode-R311.461\"> </a></td><td>NIPD for spinal muscular atrophy variant testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R312.1<a name=\"GenomicTestCode-R312.461\"> </a></td><td>Parental sequencing for lethal autosomal recessive disorders (WES or Large penel)</td></tr><tr><td style=\"white-space:nowrap\">R313.1<a name=\"GenomicTestCode-R313.461\"> </a></td><td>Neutropaenia consistent with ELANE variants (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R314.1<a name=\"GenomicTestCode-R314.461\"> </a></td><td>Ambiguous genitalia (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R314.2<a name=\"GenomicTestCode-R314.462\"> </a></td><td>Ambiguous genitalia (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R315.1<a name=\"GenomicTestCode-R315.461\"> </a></td><td>POLG-related disorder (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R315.2<a name=\"GenomicTestCode-R315.462\"> </a></td><td>POLG-related disorder (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R316.1<a name=\"GenomicTestCode-R316.461\"> </a></td><td>Pyruvate dehydrogenase (PDH) deficiency (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R317.1<a name=\"GenomicTestCode-R317.461\"> </a></td><td>Mitochondrial liver disease, including transient infantile liver failure (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R318.1<a name=\"GenomicTestCode-R318.461\"> </a></td><td>Recurrent miscarriage with products of conception available for testing (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R318.2<a name=\"GenomicTestCode-R318.462\"> </a></td><td>Recurrent miscarriage with products of conception available for testing (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R319.1<a name=\"GenomicTestCode-R319.461\"> </a></td><td>Calcium-sensing receptor phenotypes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R32.2<a name=\"GenomicTestCode-R32.462\"> </a></td><td>Retinal disorders (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R320.1<a name=\"GenomicTestCode-R320.461\"> </a></td><td>Invasive prenatal diagnosis requiring fetal sexing (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R321.1<a name=\"GenomicTestCode-R321.461\"> </a></td><td>Maternal cell contamination testing (Identity testing)</td></tr><tr><td style=\"white-space:nowrap\">R322.1<a name=\"GenomicTestCode-R322.461\"> </a></td><td>Skin fibroblasts to be cultured and stored (Other)</td></tr><tr><td style=\"white-space:nowrap\">R323.1<a name=\"GenomicTestCode-R323.461\"> </a></td><td>Sitosterolaemia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R324.1<a name=\"GenomicTestCode-R324.461\"> </a></td><td>Familial Chylomicronaemia Syndrome (FCS) (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R325.1<a name=\"GenomicTestCode-R325.461\"> </a></td><td>Lysosomal acid lipase deficiency (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R326.1<a name=\"GenomicTestCode-R326.461\"> </a></td><td>Vascular skin disorders (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R327.1<a name=\"GenomicTestCode-R327.461\"> </a></td><td>Mosaic skin disorders deep sequencing (Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R328.1<a name=\"GenomicTestCode-R328.461\"> </a></td><td>Progressive cardiac conduction disease (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R329.1<a name=\"GenomicTestCode-R329.461\"> </a></td><td>Familial dysalbuminaemic hyperthyroxinaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R33.1<a name=\"GenomicTestCode-R33.461\"> </a></td><td>Possible X-linked retinitis pigmentosa (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R330.1<a name=\"GenomicTestCode-R330.461\"> </a></td><td>Alveolar capillary dysplasia with misalignment of pulmonary veins (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R331.1<a name=\"GenomicTestCode-R331.461\"> </a></td><td>Intestinal failure or congenital diarrhoea (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R332.1<a name=\"GenomicTestCode-R332.461\"> </a></td><td>Rare genetic inflammatory skin disorders (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R333.1<a name=\"GenomicTestCode-R333.461\"> </a></td><td>Central congenital hypoventilation (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R333.2<a name=\"GenomicTestCode-R333.462\"> </a></td><td>Central congenital hypoventilation (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R334.1<a name=\"GenomicTestCode-R334.461\"> </a></td><td>Cystinosis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R335.1<a name=\"GenomicTestCode-R335.461\"> </a></td><td>Fabry disease (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R335.2<a name=\"GenomicTestCode-R335.462\"> </a></td><td>Fabry disease (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R336.1<a name=\"GenomicTestCode-R336.461\"> </a></td><td>Cerebral vascular malformations (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R337.1<a name=\"GenomicTestCode-R337.461\"> </a></td><td>CADASIL (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R338.1<a name=\"GenomicTestCode-R338.461\"> </a></td><td>Monitoring for G(M)CSF escape variants (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R340.1<a name=\"GenomicTestCode-R340.461\"> </a></td><td>Amelogenesis imperfecta (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R341.1<a name=\"GenomicTestCode-R341.461\"> </a></td><td>Hereditary angioedema types I and II (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R343.1<a name=\"GenomicTestCode-R343.461\"> </a></td><td>Chromosomal mosaicism microarray (Microarray)</td></tr><tr><td style=\"white-space:nowrap\">R344.1<a name=\"GenomicTestCode-R344.461\"> </a></td><td>Primary hyperaldosteronism KCNJ5 (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R345.1<a name=\"GenomicTestCode-R345.461\"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R345.2<a name=\"GenomicTestCode-R345.462\"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R345.3<a name=\"GenomicTestCode-R345.463\"> </a></td><td>Facioscapulohumeral muscular dystrophy extended testing (Other)</td></tr><tr><td style=\"white-space:nowrap\">R346.1<a name=\"GenomicTestCode-R346.461\"> </a></td><td>DNA to be stored (Other)</td></tr><tr><td style=\"white-space:nowrap\">R347.1<a name=\"GenomicTestCode-R347.461\"> </a></td><td>Inherited predisposition to acute myeloid leukaemia (AML) (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R350.1<a name=\"GenomicTestCode-R350.461\"> </a></td><td>MERRF syndrome (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R351.1<a name=\"GenomicTestCode-R351.461\"> </a></td><td>NARP syndrome or maternally inherited Leigh syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R351.2<a name=\"GenomicTestCode-R351.462\"> </a></td><td>NARP syndrome or maternally inherited Leigh syndrome (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R352.1<a name=\"GenomicTestCode-R352.461\"> </a></td><td>Mitochondrial DNA maintenance disorder (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R353.1<a name=\"GenomicTestCode-R353.461\"> </a></td><td>Mitochondrial disorder with complex I deficiency (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R354.1<a name=\"GenomicTestCode-R354.461\"> </a></td><td>Mitochondrial disorder with complex II deficiency (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R355.1<a name=\"GenomicTestCode-R355.461\"> </a></td><td>Mitochondrial disorder with complex III deficiency (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R356.1<a name=\"GenomicTestCode-R356.461\"> </a></td><td>Mitochondrial disorder with complex IV deficiency (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R357.1<a name=\"GenomicTestCode-R357.461\"> </a></td><td>Mitochondrial disorder with complex V deficiency (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R36.2,<a name=\"GenomicTestCode-R36.462.44\"> </a></td><td>structural eye disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R361.1<a name=\"GenomicTestCode-R361.461\"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R361.2<a name=\"GenomicTestCode-R361.462\"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R363.1<a name=\"GenomicTestCode-R363.461\"> </a></td><td>Inherited predisposition to GIST (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R364.1<a name=\"GenomicTestCode-R364.461\"> </a></td><td>DICER1-related cancer predisposition (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R365.1<a name=\"GenomicTestCode-R365.461\"> </a></td><td>Fumarate hydratase-related tumour syndromes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R366.1<a name=\"GenomicTestCode-R366.461\"> </a></td><td>Inherited susceptibility to acute lymphoblastoid leukaemia (ALL) (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R367.1<a name=\"GenomicTestCode-R367.461\"> </a></td><td>Inherited pancreatic cancer (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R368.1<a name=\"GenomicTestCode-R368.461\"> </a></td><td>Hereditary angioedema type III (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R370.1<a name=\"GenomicTestCode-R370.461\"> </a></td><td>Validation of unaccredited findings (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R371.1<a name=\"GenomicTestCode-R371.461\"> </a></td><td>Malignant hyperthermia (small panel)</td></tr><tr><td style=\"white-space:nowrap\">R372.1<a name=\"GenomicTestCode-R372.461\"> </a></td><td>Newborn screening for sickle cell disease in a transfused baby (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R373.1<a name=\"GenomicTestCode-R373.461\"> </a></td><td>RNA to be stored (Other)</td></tr><tr><td style=\"white-space:nowrap\">R374.1<a name=\"GenomicTestCode-R374.461\"> </a></td><td>Other sample to be stored (Other)</td></tr><tr><td style=\"white-space:nowrap\">R375.1<a name=\"GenomicTestCode-R375.461\"> </a></td><td>Family follow-up testing to aid variant interpretation (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R376.1<a name=\"GenomicTestCode-R376.461\"> </a></td><td>Segmental or atypical neurofibromatosis type 1 testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R376.2<a name=\"GenomicTestCode-R376.462\"> </a></td><td>Segmental or atypical neurofibromatosis type 1 testing (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R38.2<a name=\"GenomicTestCode-R38.462\"> </a></td><td>Sporadic aniridia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R380.1<a name=\"GenomicTestCode-R380.461\"> </a></td><td>Niemann Pick disease type C (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R380.2<a name=\"GenomicTestCode-R380.462\"> </a></td><td>Niemann Pick disease type C (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R381.2<a name=\"GenomicTestCode-R381.462\"> </a></td><td>Other rare neuromuscular disorders (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R382.1<a name=\"GenomicTestCode-R382.461\"> </a></td><td>Hypochondroplasia (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R383.1<a name=\"GenomicTestCode-R383.461\"> </a></td><td>Linkage testing for Huntington disease (Other)</td></tr><tr><td style=\"white-space:nowrap\">R384.1<a name=\"GenomicTestCode-R384.461\"> </a></td><td>Generalised arterial calcification in infancy (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R387.1<a name=\"GenomicTestCode-R387.461\"> </a></td><td>Reanalysis of existing data (Other)</td></tr><tr><td style=\"white-space:nowrap\">R389.1<a name=\"GenomicTestCode-R389.461\"> </a></td><td>NIPD pre-pregnancy test work-up (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R39.1<a name=\"GenomicTestCode-R39.461\"> </a></td><td>Albinism or congenital nystagmus (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R390.1<a name=\"GenomicTestCode-R390.461\"> </a></td><td>Multiple exostoses (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R390.2<a name=\"GenomicTestCode-R390.462\"> </a></td><td>Multiple exostoses (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R391.1<a name=\"GenomicTestCode-R391.461\"> </a></td><td>Barth syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R394.1<a name=\"GenomicTestCode-R394.461\"> </a></td><td>Mitochondrial neurogastrointestinal encephalopathy (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R395.1<a name=\"GenomicTestCode-R395.461\"> </a></td><td>Thiamine metabolism dysfunction syndrome 2 (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R396.1<a name=\"GenomicTestCode-R396.461\"> </a></td><td>Mitochondrial Complex V deficiency, TMEM70 type (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R397.1<a name=\"GenomicTestCode-R397.461\"> </a></td><td>Maternally inherited cardiomyopathy (Targeted mutation testing)</td></tr><tr><td style=\"white-space:nowrap\">R401.1<a name=\"GenomicTestCode-R401.461\"> </a></td><td>Common aneuploidy testing prenatal (Common aneuploidy testing)</td></tr><tr><td style=\"white-space:nowrap\">R402.1<a name=\"GenomicTestCode-R402.461\"> </a></td><td>Premature ovarian insufficiency (Karyotype or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R402.2<a name=\"GenomicTestCode-R402.462\"> </a></td><td>Premature ovarian insufficiency (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R403.1<a name=\"GenomicTestCode-R403.461\"> </a></td><td>MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing newborn screening follow up (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R404.1<a name=\"GenomicTestCode-R404.461\"> </a></td><td>Testing of unaffected individuals for inherited cancer predisposition syndromes (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R404.3<a name=\"GenomicTestCode-R404.463\"> </a></td><td>Testing of unaffected individuals for inherited cancer predisposition syndromes (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R405.1<a name=\"GenomicTestCode-R405.461\"> </a></td><td>Hereditary Erythrocytosis (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R406.1<a name=\"GenomicTestCode-R406.461\"> </a></td><td>Thrombocythaemia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R409.1<a name=\"GenomicTestCode-R409.461\"> </a></td><td>Linkage testing for recognisable Mendelian disorders (Other)</td></tr><tr><td style=\"white-space:nowrap\">R41.1<a name=\"GenomicTestCode-R41.461\"> </a></td><td>Optic neuropathy (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R41.3<a name=\"GenomicTestCode-R41.463\"> </a></td><td>Optic neuropathy (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R410.1<a name=\"GenomicTestCode-R410.461\"> </a></td><td>Myotonic dystrophy type 2 (DM2) (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R411.1<a name=\"GenomicTestCode-R411.461\"> </a></td><td>Y chromosome microdeletion (Targeted mutation testing or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R412.1<a name=\"GenomicTestCode-R412.461\"> </a></td><td>Fetal anomalies with a likely genetic cause non urgent (WES or Large Panel)</td></tr><tr><td style=\"white-space:nowrap\">R413.1<a name=\"GenomicTestCode-R413.461\"> </a></td><td>Autoinflammatory Disorders (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R414.1<a name=\"GenomicTestCode-R414.461\"> </a></td><td>APC associated Polyposis  (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R416.1<a name=\"GenomicTestCode-R416.461\"> </a></td><td>Syndromic and non syndromic craniosynostosis involving midline sutures only (metopic, sagittal, metopic &amp; sagittal)  (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R417.1<a name=\"GenomicTestCode-R417.461\"> </a></td><td>Multi Locus Imprinting Disorder (MLPA)</td></tr><tr><td style=\"white-space:nowrap\">R417.2<a name=\"GenomicTestCode-R417.462\"> </a></td><td>Multi Locus Imprinting Disorder (Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R419.1<a name=\"GenomicTestCode-R419.461\"> </a></td><td>Acute Rhabdomyolysis (Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R42.1<a name=\"GenomicTestCode-R42.461\"> </a></td><td>Leber hereditary optic neuropathy (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R42.2<a name=\"GenomicTestCode-R42.462\"> </a></td><td>Leber hereditary optic neuropathy (Other)</td></tr><tr><td style=\"white-space:nowrap\">R420.1<a name=\"GenomicTestCode-R420.461\"> </a></td><td>Pseudoxanthoma elasticum (Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R421.1<a name=\"GenomicTestCode-R421.461\"> </a></td><td>Pulmonary Fibrosis, Familial (Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R422.1<a name=\"GenomicTestCode-R422.461\"> </a></td><td>BAP1 associated tumour predisposition syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R423.1<a name=\"GenomicTestCode-R423.461\"> </a></td><td>NIPD for Retinoblastoma haplotype testing (NIPD)</td></tr><tr><td style=\"white-space:nowrap\">R424.1<a name=\"GenomicTestCode-R424.461\"> </a></td><td>Subcutaneous panniculitis T-cell lymphoma (Single gene sequencing &lt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R426.1<a name=\"GenomicTestCode-R426.461\"> </a></td><td>Pulmonary alveolar microlithiasis (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R428.1<a name=\"GenomicTestCode-R428.461\"> </a></td><td>Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R428.2<a name=\"GenomicTestCode-R428.462\"> </a></td><td>Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (FISH)</td></tr><tr><td style=\"white-space:nowrap\">R43.1<a name=\"GenomicTestCode-R43.461\"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R43.2<a name=\"GenomicTestCode-R43.462\"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R43.3<a name=\"GenomicTestCode-R43.463\"> </a></td><td>Blepharophimosis ptosis and epicanthus inversus (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R430.1<a name=\"GenomicTestCode-R430.461\"> </a></td><td>Inherited prostate cancer (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R431.1<a name=\"GenomicTestCode-R431.461\"> </a></td><td>Genome-wide DNA Methylation Profiling to Aid Variant Interpretation (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R433.1<a name=\"GenomicTestCode-R433.461\"> </a></td><td>Monogenic diabetes, subtype glucokinase NIPT (NIPT)</td></tr><tr><td style=\"white-space:nowrap\">R436.1<a name=\"GenomicTestCode-R436.461\"> </a></td><td>Hereditary alpha tryptasaemia (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R438.1,<a name=\"GenomicTestCode-R438.461.44\"> </a></td><td>Paediatric pseudo-obstruction syndrome (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R440.1<a name=\"GenomicTestCode-R440.461\"> </a></td><td>Hereditary isolated diabetes insipidus (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R441.1<a name=\"GenomicTestCode-R441.461\"> </a></td><td>Unexplained death in infancy and sudden unexplained death in childhood (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R442.1<a name=\"GenomicTestCode-R442.461\"> </a></td><td>Variant Re-interpretation (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R443.1<a name=\"GenomicTestCode-R443.461\"> </a></td><td>Confirmation test (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R444.1<a name=\"GenomicTestCode-R444.461\"> </a></td><td>NICE approved PARP inhibitor treatment (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R444.2<a name=\"GenomicTestCode-R444.462\"> </a></td><td>NICE approved PARP inhibitor treatment (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R445.1<a name=\"GenomicTestCode-R445.461\"> </a></td><td>T21, T18 and T13 aneuploidy testing NIPT (previous history) (NIPT)</td></tr><tr><td style=\"white-space:nowrap\">R446.1<a name=\"GenomicTestCode-R446.461\"> </a></td><td>APOL1 kidney donor testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R447.1<a name=\"GenomicTestCode-R447.461\"> </a></td><td>Validation of WGS Diagnostic discovery (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R448.1<a name=\"GenomicTestCode-R448.461\"> </a></td><td>Prenatal testing (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R449.1<a name=\"GenomicTestCode-R449.461\"> </a></td><td>Diagnostic testing for Glutaric acidaemia I (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R45.1<a name=\"GenomicTestCode-R45.461\"> </a></td><td>Stickler syndrome (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R450.1<a name=\"GenomicTestCode-R450.461\"> </a></td><td>Diagnostic testing for Isovaleric acidaemia (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R451.1<a name=\"GenomicTestCode-R451.461\"> </a></td><td>Diagnostic testing for MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R452.1<a name=\"GenomicTestCode-R452.461\"> </a></td><td>Silver russell syndrome and Temple Syndrome (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R453.1<a name=\"GenomicTestCode-R453.461\"> </a></td><td>Monogenic short stature (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R454.1<a name=\"GenomicTestCode-R454.461\"> </a></td><td>Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R456.1<a name=\"GenomicTestCode-R456.461\"> </a></td><td>Embryonal tumour of possible germline origin (WES or Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R456.2<a name=\"GenomicTestCode-R456.462\"> </a></td><td>Embryonal tumour of possible germline origin (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R457.1<a name=\"GenomicTestCode-R457.461\"> </a></td><td>Sarcoma of possible germline origin (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R458.1<a name=\"GenomicTestCode-R458.461\"> </a></td><td>Young onset or familial dementia (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R459.1<a name=\"GenomicTestCode-R459.461\"> </a></td><td>Young onset or complex Parkinson disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R46.1<a name=\"GenomicTestCode-R46.461\"> </a></td><td>Congenital fibrosis of the extraocular muscles (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R460.1<a name=\"GenomicTestCode-R460.461\"> </a></td><td>Amyotrophic lateral sclerosis / Motor Neurone Disease (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R461.1<a name=\"GenomicTestCode-R461.461\"> </a></td><td>Cerebral amyloid angiopathy (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R462.1<a name=\"GenomicTestCode-R462.461\"> </a></td><td>Childhood interstitial lung disease (Medium panel)</td></tr><tr><td style=\"white-space:nowrap\">R463.1<a name=\"GenomicTestCode-R463.461\"> </a></td><td>Cytogenetic characterisation of a genomic abnormality â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R464.1<a name=\"GenomicTestCode-R464.461\"> </a></td><td>Recurrent miscarriage where products of conception are not available for testing parental karyotype (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R465.1<a name=\"GenomicTestCode-R465.461\"> </a></td><td>Familial cytogenetic rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R466.1<a name=\"GenomicTestCode-R466.461\"> </a></td><td>Unexplained infertility (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R467.1<a name=\"GenomicTestCode-R467.461\"> </a></td><td>Gamete donors (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R468.1<a name=\"GenomicTestCode-R468.461\"> </a></td><td>Possible sex chromosome aneuploidy or structural rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)</td></tr><tr><td style=\"white-space:nowrap\">R47.1<a name=\"GenomicTestCode-R47.461\"> </a></td><td>Angelman syndrome (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R471.1<a name=\"GenomicTestCode-R471.461\"> </a></td><td>Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing C9orf72 haplotype (Linkage analysis)</td></tr><tr><td style=\"white-space:nowrap\">R471.2<a name=\"GenomicTestCode-R471.462\"> </a></td><td>Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing SOD1 haplotype (Linkage analysis)</td></tr><tr><td style=\"white-space:nowrap\">R471.3<a name=\"GenomicTestCode-R471.463\"> </a></td><td>Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing MAPT haplotype (Linkage analysis)</td></tr><tr><td style=\"white-space:nowrap\">R471.4<a name=\"GenomicTestCode-R471.464\"> </a></td><td>Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing PSEN1 haplotype (Linkage analysis)</td></tr><tr><td style=\"white-space:nowrap\">R48.1<a name=\"GenomicTestCode-R48.461\"> </a></td><td>Prader-Willi syndrome (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R49.1<a name=\"GenomicTestCode-R49.461\"> </a></td><td>Beckwith-Wiedemann syndrome (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R49.3<a name=\"GenomicTestCode-R49.463\"> </a></td><td>Beckwith-Wiedemann syndrome (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R50.1<a name=\"GenomicTestCode-R50.461\"> </a></td><td>Isolated hemihypertrophy or macroglossia (Methylation testing)</td></tr><tr><td style=\"white-space:nowrap\">R52.1<a name=\"GenomicTestCode-R52.461\"> </a></td><td>Short stature SHOX deficiency (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R52.2<a name=\"GenomicTestCode-R52.462\"> </a></td><td>Short stature SHOX deficiency (Single gene sequencing &lt;10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R54.3<a name=\"GenomicTestCode-R54.463\"> </a></td><td>Hereditary ataxia with onset in adulthood (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R54.4<a name=\"GenomicTestCode-R54.464\"> </a></td><td>Hereditary ataxia with onset in adulthood (RFC1 STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R55.4<a name=\"GenomicTestCode-R55.464\"> </a></td><td>Hereditary ataxia with onset in childhood (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R56.3<a name=\"GenomicTestCode-R56.463\"> </a></td><td>Adult onset dystonia, chorea or related movement disorder (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R57.5<a name=\"GenomicTestCode-R57.465\"> </a></td><td>Childhood onset dystonia, chorea or related movement disorder (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R60.3<a name=\"GenomicTestCode-R60.463\"> </a></td><td>Adult onset hereditary spastic paraplegia (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R61.4<a name=\"GenomicTestCode-R61.464\"> </a></td><td>Childhood onset hereditary spastic paraplegia (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R62.2<a name=\"GenomicTestCode-R62.462\"> </a></td><td>Adult onset leukodystrophy (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R63.1<a name=\"GenomicTestCode-R63.461\"> </a></td><td>Possible mitochondrial disorder nuclear genes (WES or Large Panel)</td></tr><tr><td style=\"white-space:nowrap\">R64.1<a name=\"GenomicTestCode-R64.461\"> </a></td><td>MELAS or MIDD (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R65.1<a name=\"GenomicTestCode-R65.461\"> </a></td><td>Aminoglycoside exposure posing risk to hearing (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R66.1<a name=\"GenomicTestCode-R66.461\"> </a></td><td>Paroxysmal central nervous system disorders (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R67.1<a name=\"GenomicTestCode-R67.461\"> </a></td><td>Monogenic hearing loss (WES or Large Panel)</td></tr><tr><td style=\"white-space:nowrap\">R68.1<a name=\"GenomicTestCode-R68.461\"> </a></td><td>Huntington disease (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R69.5<a name=\"GenomicTestCode-R69.465\"> </a></td><td>Hypotonic infant  (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R70.1<a name=\"GenomicTestCode-R70.461\"> </a></td><td>Spinal muscular atrophy type 1 diagnostic test (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R71.1<a name=\"GenomicTestCode-R71.461\"> </a></td><td>Spinal muscular atrophy type 1 rare variant testing (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R72.1<a name=\"GenomicTestCode-R72.461\"> </a></td><td>Myotonic dystrophy type 1 (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R73.1<a name=\"GenomicTestCode-R73.461\"> </a></td><td>Duchenne or Becker muscular dystrophy (Single gene sequencing &gt;=10 amplicons)</td></tr><tr><td style=\"white-space:nowrap\">R73.2<a name=\"GenomicTestCode-R73.462\"> </a></td><td>Duchenne or Becker muscular dystrophy (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R74.1<a name=\"GenomicTestCode-R74.461\"> </a></td><td>Facioscapulohumeral muscular dystrophy (Other)</td></tr><tr><td style=\"white-space:nowrap\">R75.1<a name=\"GenomicTestCode-R75.461\"> </a></td><td>Oculopharyngeal muscular dystrophy (STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R76.1<a name=\"GenomicTestCode-R76.461\"> </a></td><td>Skeletal muscle channelopathy (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R77.1<a name=\"GenomicTestCode-R77.461\"> </a></td><td>Hereditary neuropathy PMP22 copy number (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R78.4<a name=\"GenomicTestCode-R78.464\"> </a></td><td>Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R78.5<a name=\"GenomicTestCode-R78.465\"> </a></td><td>Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (RFC1 STR testing)</td></tr><tr><td style=\"white-space:nowrap\">R79.1<a name=\"GenomicTestCode-R79.461\"> </a></td><td>Congenital muscular dystrophy (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R80.1<a name=\"GenomicTestCode-R80.461\"> </a></td><td>Congenital myaesthenic syndrome (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R81.1<a name=\"GenomicTestCode-R81.461\"> </a></td><td>Congenital myopathy (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R82.1<a name=\"GenomicTestCode-R82.461\"> </a></td><td>Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R83.3<a name=\"GenomicTestCode-R83.463\"> </a></td><td>Arthrogryposis (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R84.4<a name=\"GenomicTestCode-R84.464\"> </a></td><td>Cerebellar anomalies (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R85.2<a name=\"GenomicTestCode-R85.462\"> </a></td><td>Holoprosencephaly (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R86.3<a name=\"GenomicTestCode-R86.463\"> </a></td><td>Hydrocephalus (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R87.3<a name=\"GenomicTestCode-R87.463\"> </a></td><td>Cerebral malformation (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R88.3<a name=\"GenomicTestCode-R88.463\"> </a></td><td>Severe microcephaly (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R89.3<a name=\"GenomicTestCode-R89.463\"> </a></td><td>Ultra-rare and atypical monogenic disorders (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R90.1<a name=\"GenomicTestCode-R90.461\"> </a></td><td>Bleeding and platelet disorders (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R91.1<a name=\"GenomicTestCode-R91.461\"> </a></td><td>Cytopenia NOT Fanconi anaemia (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R91.2<a name=\"GenomicTestCode-R91.462\"> </a></td><td>Cytopenia NOT Fanconi anaemia (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R92.1<a name=\"GenomicTestCode-R92.461\"> </a></td><td>Rare anaemia (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R92.2<a name=\"GenomicTestCode-R92.462\"> </a></td><td>Rare anaemia (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R92.3<a name=\"GenomicTestCode-R92.463\"> </a></td><td>Rare anaemia (WES or Medium Panel)</td></tr><tr><td style=\"white-space:nowrap\">R93.1<a name=\"GenomicTestCode-R93.461\"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies (MLPA or equivalent)</td></tr><tr><td style=\"white-space:nowrap\">R93.2<a name=\"GenomicTestCode-R93.462\"> </a></td><td>Sickle cell, thalassaemia and other haemoglobinopathies (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R95.1<a name=\"GenomicTestCode-R95.461\"> </a></td><td>Iron overload hereditary haemochromatosis testing (Targeted variant testing)</td></tr><tr><td style=\"white-space:nowrap\">R96.1<a name=\"GenomicTestCode-R96.461\"> </a></td><td>Iron metabolism disorders NOT common HFE variants (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R97.1<a name=\"GenomicTestCode-R97.461\"> </a></td><td>Thrombophilia with a likely monogenic cause (WES or Small Panel)</td></tr><tr><td style=\"white-space:nowrap\">R98.2<a name=\"GenomicTestCode-R98.462\"> </a></td><td>Likely inborn error of metabolism (WGS)</td></tr><tr><td style=\"white-space:nowrap\">R98.3<a name=\"GenomicTestCode-R98.463\"> </a></td><td>Likely inborn error of metabolism (WES)</td></tr><tr><td style=\"white-space:nowrap\">R99.1<a name=\"GenomicTestCode-R99.461\"> </a></td><td>Common craniosynostosis syndromes (Small panel)</td></tr><tr><td style=\"white-space:nowrap\">R99.2<a name=\"GenomicTestCode-R99.462\"> </a></td><td>Common craniosynostosis syndromes (Exon level CNV detection by MLPA or equivalent)</td></tr></table></div>"^^rdf:XMLLiteral ]
  ] ; # 
  fhir:url [
fhir:v "https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory"^^xsd:anyURI ;
fhir:l <https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory>
  ] ; # 
  fhir:version [ fhir:v "2.0.12"] ; # 
  fhir:name [ fhir:v "GenomicTestCode"] ; # 
  fhir:title [ fhir:v "NHS England Genomic Test Code"] ; # 
  fhir:status [ fhir:v "active"] ; # 
  fhir:experimental [ fhir:v false] ; # 
  fhir:date [ fhir:v "2026-06-04"^^xsd:date] ; # 
  fhir:publisher [ fhir:v "NHS North West Genomics"] ; # 
  fhir:contact ( [
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "https://www.nwgenomics.nhs.uk/contact-us" ]     ] )
  ] ) ; # 
  fhir:description [ fhir:v "- [Genomic Test Directory](https://www.england.nhs.uk/publication/national-genomic-test-directories)\"\n\nHL7 v2 CodeSystem : England-GenomicTestDirectory"] ; # 
  fhir:jurisdiction ( [
    ( fhir:coding [
fhir:system [
fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ;
fhir:l <urn:iso:std:iso:3166>       ] ;
fhir:code [ fhir:v "GB" ] ;
fhir:display [ fhir:v "United Kingdom of Great Britain and Northern Ireland" ]     ] )
  ] ) ; # 
  fhir:caseSensitive [ fhir:v true] ; # 
  fhir:content [ fhir:v "fragment"] ; # 
  fhir:concept ( [
fhir:code [ fhir:v "M1.1" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF)" ]
  ] [
fhir:code [ fhir:v "M1.2" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, KRAS hotspot" ]
  ] [
fhir:code [ fhir:v "M1.3" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, NRAS hotspot" ]
  ] [
fhir:code [ fhir:v "M1.4" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M1.5" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, MLH1 promoter hypermethylation" ]
  ] [
fhir:code [ fhir:v "M1.6" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M1.7" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M1.9" ] ;
fhir:display [ fhir:v "Colorectal Carcinoma, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2, POLE, POLD1)" ]
  ] [
fhir:code [ fhir:v "M10.1" ] ;
fhir:display [ fhir:v "Thyroid Follicular Carcinoma, Multi-target NGS panel, small variant (KRAS, NRAS, HRAS)" ]
  ] [
fhir:code [ fhir:v "M10.2" ] ;
fhir:display [ fhir:v "Thyroid Follicular Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET)" ]
  ] [
fhir:code [ fhir:v "M100.1" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M100.2" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, CD274, PDCD1LG2 Copy number FISH" ]
  ] [
fhir:code [ fhir:v "M100.3" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, REL copy number FISH" ]
  ] [
fhir:code [ fhir:v "M100.4" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M100.5" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, copy number variant (CD274, PDCD1LG2, REL)" ]
  ] [
fhir:code [ fhir:v "M100.6" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, Multi-target NGS panel, rearrangement (CD274, PDCD1LG2)" ]
  ] [
fhir:code [ fhir:v "M100.7" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M100.8" ] ;
fhir:display [ fhir:v "Primary Mediastinal B Cell Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M101.1" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M101.2" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, t(2;17)(p23;q23) CLTC-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M101.3" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M101.4" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M101.5" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, Multi-target NGS panel, structural variant (CLTC-ALK, ALK-NPM1, other ALK rearrangements)" ]
  ] [
fhir:code [ fhir:v "M101.6" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M101.7" ] ;
fhir:display [ fhir:v "ALK Positive Large B Cell Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M102.1" ] ;
fhir:display [ fhir:v "Mantle Cell Lymphoma, t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M102.2" ] ;
fhir:display [ fhir:v "Mantle Cell Lymphoma, CCND1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M102.3" ] ;
fhir:display [ fhir:v "Mantle Cell Lymphoma, CCND2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M102.4" ] ;
fhir:display [ fhir:v "Mantle Cell Lymphoma, Multi-target NGS panel, structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)" ]
  ] [
fhir:code [ fhir:v "M102.5" ] ;
fhir:display [ fhir:v "Mantle Cell Lymphoma, Multi-target NGS panel, small variant (TP53)" ]
  ] [
fhir:code [ fhir:v "M103.1" ] ;
fhir:display [ fhir:v "Follicular Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M103.2" ] ;
fhir:display [ fhir:v "Follicular Lymphoma, BCL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M103.3" ] ;
fhir:display [ fhir:v "Follicular Lymphoma, BCL6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M103.4" ] ;
fhir:display [ fhir:v "Follicular Lymphoma, Multi-target NGS panel, small variant (CARD11, CREBBP, EZH2, ARID1A, EP300, MEF2B, FOXO1)" ]
  ] [
fhir:code [ fhir:v "M103.5" ] ;
fhir:display [ fhir:v "Follicular Lymphoma, Multi-target NGS panel, structural variant (IGH-BCL2, BCL2, BCL6)" ]
  ] [
fhir:code [ fhir:v "M104.1" ] ;
fhir:display [ fhir:v "Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, Multi-target NGS panel, small variant (MYD88, CXCR4)" ]
  ] [
fhir:code [ fhir:v "M104.2" ] ;
fhir:display [ fhir:v "Lymphoplasmacytic Lymphoma/Waldenstrom Macroglobulinaemia, MYD88 hotspot" ]
  ] [
fhir:code [ fhir:v "M105.1" ] ;
fhir:display [ fhir:v "Igm Monoclonal Gammopathy of Uncertain Significance, Multi-target NGS panel, small variant (MYD88, CXCR4)" ]
  ] [
fhir:code [ fhir:v "M105.2" ] ;
fhir:display [ fhir:v "Igm Monoclonal Gammopathy of Uncertain Significance, MYD88 hotspot" ]
  ] [
fhir:code [ fhir:v "M106.1" ] ;
fhir:display [ fhir:v "Intra-Ocular Lymphoma, MYD88 hotspot" ]
  ] [
fhir:code [ fhir:v "M107.1" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, t(11;18)(q21;q21) BIRC3-MALT1  FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M107.10" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M107.2" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, t(1;14)(p22;q32) IGH-BCL10 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M107.3" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, t(14;18)(q32;q21) IGH-MALT1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M107.4" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, MALT1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M107.5" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, BCL10 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M107.6" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, FOXP1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M107.7" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M107.8" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, Multi-target NGS panel, structural variant (BIRC3-MALT1, IGH-BCL10, IGH-MALT1, other MALT rearrangements, other BCL10 rearrangements, FOXP1)" ]
  ] [
fhir:code [ fhir:v "M107.9" ] ;
fhir:display [ fhir:v "Malt-Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M108.1" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Multi-target NGS panel, small variant (BRAF)" ]
  ] [
fhir:code [ fhir:v "M108.2" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, BRAF V600 hotspot" ]
  ] [
fhir:code [ fhir:v "M108.5" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Ig gene hypermutation detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M108.6" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Ig gene hypermutation detection NGS" ]
  ] [
fhir:code [ fhir:v "M109.1" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M109.2" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Vh4-34 Variant, Ig gene (heavy chain) rearrangement detection NGS" ]
  ] [
fhir:code [ fhir:v "M11.1" ] ;
fhir:display [ fhir:v "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, small variant (TP53, BRAF)" ]
  ] [
fhir:code [ fhir:v "M11.2" ] ;
fhir:display [ fhir:v "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, copy number variant (TP53)" ]
  ] [
fhir:code [ fhir:v "M11.3" ] ;
fhir:display [ fhir:v "Poorly Differentiated Anaplastic Thyroid Carcinoma, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M11.4" ] ;
fhir:display [ fhir:v "Poorly Differentiated Anaplastic Thyroid Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, RET, ALK)" ]
  ] [
fhir:code [ fhir:v "M110.1," ] ;
fhir:display [ fhir:v "Paediatric Type Follicular Lymphoma, Multi-target NGS panel, small variant (MAP2K1)" ]
  ] [
fhir:code [ fhir:v "M110.2," ] ;
fhir:display [ fhir:v "Paediatric Type Follicular Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M110.3," ] ;
fhir:display [ fhir:v "Paediatric Type Follicular Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M110.4," ] ;
fhir:display [ fhir:v "Paediatric Type Follicular Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M111.1" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (RHOA, DNMT3A, IDH2, TET2)" ]
  ] [
fhir:code [ fhir:v "M111.2" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M111.3" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, TCR gene rearrangement detection NGS" ]
  ] [
fhir:code [ fhir:v "M111.4" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, TCR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M111.5" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M111.6" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (TCR rearrangement)" ]
  ] [
fhir:code [ fhir:v "M111.7" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M111.8" ] ;
fhir:display [ fhir:v "T Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M112.3" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), IRF4/DUSP22 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M112.4" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), TP63 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M112.5" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M112.6" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), Multi-target NGS panel, structural variant (IRF4/DUSP22, TP63)" ]
  ] [
fhir:code [ fhir:v "M112.7" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M112.8" ] ;
fhir:display [ fhir:v "ALK Negative Anaplastic Large Cell Lymphoma (Including Primary Cutaneous Subtypes), WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M113.1" ] ;
fhir:display [ fhir:v "T Prolymphocytic Leukaemia, TCL1A rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M113.2" ] ;
fhir:display [ fhir:v "T Prolymphocytic Leukaemia, Chr8 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M113.3" ] ;
fhir:display [ fhir:v "T Prolymphocytic Leukaemia, Multi-target NGS panel, structural variant (TCL1A, Chr8)" ]
  ] [
fhir:code [ fhir:v "M113.6" ] ;
fhir:display [ fhir:v "T Prolymphocytic Leukaemia, Karyotype (to include TCL1 rearrangements t(X;14))" ]
  ] [
fhir:code [ fhir:v "M114.1" ] ;
fhir:display [ fhir:v "Large Granular Lymphocyte Leukaemia, Multi-target NGS panel, small variant (STAT3, STAT5B)" ]
  ] [
fhir:code [ fhir:v "M115.1" ] ;
fhir:display [ fhir:v "NK Cell/Gamma-Delta T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)" ]
  ] [
fhir:code [ fhir:v "M115.2" ] ;
fhir:display [ fhir:v "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M115.3" ] ;
fhir:display [ fhir:v "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M115.4" ] ;
fhir:display [ fhir:v "NK Cell/Gamma-Delta T Cell Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M116.1" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, small variant (STAT3, STAT5B)" ]
  ] [
fhir:code [ fhir:v "M116.2" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, i7q rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M116.3" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M116.4" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, Multi-target NGS panel, structural variant (i17q)" ]
  ] [
fhir:code [ fhir:v "M116.5" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M116.6" ] ;
fhir:display [ fhir:v "Hepatosplenic T Cell Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M117.1" ] ;
fhir:display [ fhir:v "Histiocytosis, Multi-target NGS panel, small variant (BRAF, MAP2K1, NRAS, KRAS, HRAS, ERBB3, ARAF, MAP3K1, PIK3CA, PIK3CD)" ]
  ] [
fhir:code [ fhir:v "M117.12" ] ;
fhir:display [ fhir:v "Histiocytosis, NTRK1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M117.16" ] ;
fhir:display [ fhir:v "Histiocytosis, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M117.17" ] ;
fhir:display [ fhir:v "Histiocytosis, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M117.18" ] ;
fhir:display [ fhir:v "Histiocytosis, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M117.19" ] ;
fhir:display [ fhir:v "Histiocytosis, High Sensitivity BRAF" ]
  ] [
fhir:code [ fhir:v "M117.2" ] ;
fhir:display [ fhir:v "Histiocytosis, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M117.3" ] ;
fhir:display [ fhir:v "Histiocytosis, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M117.7" ] ;
fhir:display [ fhir:v "Histiocytosis, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M118.1" ] ;
fhir:display [ fhir:v "Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, STR Testing" ]
  ] [
fhir:code [ fhir:v "M118.2" ] ;
fhir:display [ fhir:v "Any patient undergoing Allogeneic Haematopoietic Stem Cell transplantation, Sex chromosome FISH" ]
  ] [
fhir:code [ fhir:v "M119.1," ] ;
fhir:display [ fhir:v "Paediatric Tumours, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M119.2," ] ;
fhir:display [ fhir:v "Paediatric Tumours, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M119.4," ] ;
fhir:display [ fhir:v "Paediatric Tumours, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M119.5," ] ;
fhir:display [ fhir:v "Paediatric Tumours, Multi-target NGS-small variant" ]
  ] [
fhir:code [ fhir:v "M12.1" ] ;
fhir:display [ fhir:v "Thyroid Medullary Carcinoma, Multi-target NGS panel, small variant (RET)" ]
  ] [
fhir:code [ fhir:v "M12.2" ] ;
fhir:display [ fhir:v "Thyroid Medullary Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M120.1" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCA4, SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M120.10" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.11" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.12" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.13" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.14" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.15" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M120.16" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M120.17" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M120.18" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M120.2" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 seq" ]
  ] [
fhir:code [ fhir:v "M120.3" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 seq" ]
  ] [
fhir:code [ fhir:v "M120.4" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M120.5" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M120.6" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M120.7" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.8" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M120.9" ] ;
fhir:display [ fhir:v "Atypical Teratoid/Rhabdoid Tumour, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M124.1" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, small variant (BCOR)" ]
  ] [
fhir:code [ fhir:v "M124.10" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, structural variant (BCOR, NUTM2B-YWHAE, NUTM2E-YWHAE, NUTM1-YWHAE, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M124.11" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, Multi-target NGS panel, copy number variant (BCOR, YWHAE)" ]
  ] [
fhir:code [ fhir:v "M124.2" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, BCOR seq" ]
  ] [
fhir:code [ fhir:v "M124.3" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, BCOR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M124.4" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, BCOR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M124.5" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, NUTM2B-YWHAE FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M124.6" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, NUTM2E-YWHAE FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M124.7" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, NUTM1-YWHAE FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M124.8" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, YWHAE copy number FISH" ]
  ] [
fhir:code [ fhir:v "M124.9" ] ;
fhir:display [ fhir:v "Clear Cell Kidney Sarcoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M126.1" ] ;
fhir:display [ fhir:v "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, MN1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M126.2" ] ;
fhir:display [ fhir:v "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M126.3" ] ;
fhir:display [ fhir:v "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, Multi-target NGS panel, structural variant (MN1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M126.4" ] ;
fhir:display [ fhir:v "CNS High-Grade Neuroepithelial Tumour with MN1 Alteration, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M127.1" ] ;
fhir:display [ fhir:v "Congenital Mesoblastic Nephroma, Paediatric, NTRK3-ETV6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M127.3" ] ;
fhir:display [ fhir:v "Congenital Mesoblastic Nephroma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M127.4" ] ;
fhir:display [ fhir:v "Congenital Mesoblastic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK3-ETV6, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M13.1" ] ;
fhir:display [ fhir:v "Phaeochromocytoma, Multi-target NGS panel, small variant (RET)" ]
  ] [
fhir:code [ fhir:v "M13.2" ] ;
fhir:display [ fhir:v "Phaeochromocytoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M130.1" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, small variant (SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M130.2" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 seq" ]
  ] [
fhir:code [ fhir:v "M130.3" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M130.4" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M130.5" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M130.6" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M130.7" ] ;
fhir:display [ fhir:v "Cribriform Neuroepithelial Tumour, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M131.1" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, Multi-target NGS panel, small variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M131.2" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, DICER1 seq" ]
  ] [
fhir:code [ fhir:v "M131.3" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, DICER1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M131.4" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M131.5" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M131.6" ] ;
fhir:display [ fhir:v "Cystic Nephroma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M132.1" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, small variant (BRAF)" ]
  ] [
fhir:code [ fhir:v "M132.10" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.11" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M132.12" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M132.13" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M132.2" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M132.3" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.4" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.5" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.6" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.7" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.8" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M132.9" ] ;
fhir:display [ fhir:v "Desmoplastic Infantile Gangliogliomas, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M133.1" ] ;
fhir:display [ fhir:v "Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SUFU)" ]
  ] [
fhir:code [ fhir:v "M133.2" ] ;
fhir:display [ fhir:v "Desmoplastic Medulloblastoma, Paediatric, SUFU seq" ]
  ] [
fhir:code [ fhir:v "M133.3" ] ;
fhir:display [ fhir:v "Desmoplastic Medulloblastoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M133.4" ] ;
fhir:display [ fhir:v "Desmoplastic Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M133.5" ] ;
fhir:display [ fhir:v "Desmoplastic Medulloblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M136.1" ] ;
fhir:display [ fhir:v "Fibrolamellar Hepatocellular Carcinoma, Paediatric, DNAJB1-PRKACA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M136.2" ] ;
fhir:display [ fhir:v "Fibrolamellar Hepatocellular Carcinoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M136.3" ] ;
fhir:display [ fhir:v "Fibrolamellar Hepatocellular Carcinoma, Paediatric, Multi-target NGS panel, structural variant (DNAJB1-PRKACA, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M136.5" ] ;
fhir:display [ fhir:v "Fibrolamellar Hepatocellular Carcinoma, Paediatric, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M137.1" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, Multi-target NGS panel, small variant (BRAF)" ]
  ] [
fhir:code [ fhir:v "M137.10" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.11" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, KIAA1549 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M137.12" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M137.13" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M137.14" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)" ]
  ] [
fhir:code [ fhir:v "M137.15" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M137.2" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M137.3" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.4" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.5" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.6" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.7" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.8" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M137.9" ] ;
fhir:display [ fhir:v "Ganglioglioma, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M138.1" ] ;
fhir:display [ fhir:v "Glial Tumours, Paediatric, Multi-target NGS panel, small variant (ATRX)" ]
  ] [
fhir:code [ fhir:v "M138.2" ] ;
fhir:display [ fhir:v "Glial Tumours, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M138.3" ] ;
fhir:display [ fhir:v "Glial Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M138.4" ] ;
fhir:display [ fhir:v "Glial Tumours, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M139.1" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, Multi-target NGS panel, small variant (BRAF, CDKN2A, FGFR4)" ]
  ] [
fhir:code [ fhir:v "M139.10" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.12" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, CDKN2A seq" ]
  ] [
fhir:code [ fhir:v "M139.13" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, FGFR4 seq" ]
  ] [
fhir:code [ fhir:v "M139.14" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M139.15" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M139.16" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M139.17" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, Multi-target NGS panel, copy number variant (CDKN2A)" ]
  ] [
fhir:code [ fhir:v "M139.18" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M139.2" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M139.3" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.4" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.5" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.6" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.7" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.8" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M139.9" ] ;
fhir:display [ fhir:v "Glioblastoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M14.1" ] ;
fhir:display [ fhir:v "Adrenal Cortical Carcinoma, Multi-target NGS panel, small variant (TP53)" ]
  ] [
fhir:code [ fhir:v "M14.2" ] ;
fhir:display [ fhir:v "Adrenal Cortical Carcinoma, Multi-target NGS panel, copy number variant (TP53)" ]
  ] [
fhir:code [ fhir:v "M14.3" ] ;
fhir:display [ fhir:v "Adrenal Cortical Carcinoma, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M14.4" ] ;
fhir:display [ fhir:v "Adrenal Cortical Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M14.5" ] ;
fhir:display [ fhir:v "Adrenal Cortical Carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M143.1" ] ;
fhir:display [ fhir:v "Lung, Paediatric, Multi-target NGS panel, small variant (H3-3A, H3-3B)" ]
  ] [
fhir:code [ fhir:v "M143.2" ] ;
fhir:display [ fhir:v "Lung, Paediatric, H3-3A seq" ]
  ] [
fhir:code [ fhir:v "M143.3" ] ;
fhir:display [ fhir:v "Lung, Paediatric, H3-3B seq" ]
  ] [
fhir:code [ fhir:v "M143.4" ] ;
fhir:display [ fhir:v "Lung, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M143.5" ] ;
fhir:display [ fhir:v "Lung, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M145.1" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, BCOR, PTCH1, PTCH2, PTEN, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M145.10" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, BCOR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M145.11" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, C19MC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M145.12" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, PTEN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M145.13" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M145.14" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (ALK, BCOR, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M145.15" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (ALK, BCOR, C19MC, PTEN)" ]
  ] [
fhir:code [ fhir:v "M145.16" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M145.2" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, ALK seq" ]
  ] [
fhir:code [ fhir:v "M145.3" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, BCOR seq" ]
  ] [
fhir:code [ fhir:v "M145.4" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, PTCH1 seq" ]
  ] [
fhir:code [ fhir:v "M145.5" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, PTCH2 seq" ]
  ] [
fhir:code [ fhir:v "M145.6" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, TERT promoter seq" ]
  ] [
fhir:code [ fhir:v "M145.7" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, ALK copy number FISH" ]
  ] [
fhir:code [ fhir:v "M145.8" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M145.9" ] ;
fhir:display [ fhir:v "Medulloblastoma, Paediatric, BCOR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M146.1" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, small variant (SMARCA4, DDX3X)" ]
  ] [
fhir:code [ fhir:v "M146.2" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, SMARCA4 seq" ]
  ] [
fhir:code [ fhir:v "M146.3" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, DDX3X seq" ]
  ] [
fhir:code [ fhir:v "M146.4" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M146.5" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, PVT1-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M146.6" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M146.7" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, structural variant (PVT1-MYC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M146.8" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4)" ]
  ] [
fhir:code [ fhir:v "M146.9" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M147.1" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, small variant (MYCN, EZH2)" ]
  ] [
fhir:code [ fhir:v "M147.10" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M147.2" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, MYCN seq" ]
  ] [
fhir:code [ fhir:v "M147.3" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, EZH2 seq" ]
  ] [
fhir:code [ fhir:v "M147.4" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M147.5" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M147.6" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M147.7" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M147.8" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M147.9" ] ;
fhir:display [ fhir:v "Medulloblastoma Group 3/4, Paediatric, Multi-target NGS panel, copy number variant (MYCN, MYC)" ]
  ] [
fhir:code [ fhir:v "M148.1" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, small variant (YAP1, PTCH1)" ]
  ] [
fhir:code [ fhir:v "M148.10" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (YAP1, PTCH1)" ]
  ] [
fhir:code [ fhir:v "M148.11" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M148.2" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, YAP1 seq" ]
  ] [
fhir:code [ fhir:v "M148.3" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, PTCH1 seq" ]
  ] [
fhir:code [ fhir:v "M148.4" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M148.5" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M148.6" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, YAP1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M148.7" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, PTCH1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M148.8" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M148.9" ] ;
fhir:display [ fhir:v "Medulloblastoma TP53 WT, Paediatric, Multi-target NGS panel, structural variant (YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M149.1" ] ;
fhir:display [ fhir:v "Melanotic Tumours, Paediatric, Multi-target NGS panel, small variant (NRAS)" ]
  ] [
fhir:code [ fhir:v "M149.2" ] ;
fhir:display [ fhir:v "Melanotic Tumours, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M149.3" ] ;
fhir:display [ fhir:v "Melanotic Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M15.1" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, small variant (CDKN2A, EGFR, TP53)" ]
  ] [
fhir:code [ fhir:v "M15.2" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M15.3" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, copy number variant (CDKN2A, TP53)" ]
  ] [
fhir:code [ fhir:v "M15.4" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, RET rearrangement FISH/RT-PC" ]
  ] [
fhir:code [ fhir:v "M15.5" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M15.6" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M15.7" ] ;
fhir:display [ fhir:v "Head and Neck Squamous Cell Carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M150.1" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, Multi-target NGS panel, small variant (SMARCE1, AKT1, NF2, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M150.2" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, SMARCE1 seq" ]
  ] [
fhir:code [ fhir:v "M150.3" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, AKT1 seq" ]
  ] [
fhir:code [ fhir:v "M150.4" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, NF2 seq" ]
  ] [
fhir:code [ fhir:v "M150.5" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, TERT promoter seq" ]
  ] [
fhir:code [ fhir:v "M150.6" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M150.7" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M150.8" ] ;
fhir:display [ fhir:v "Meningioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M151.1" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, NUTM1-BRD2 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M151.2" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, NUTM1-BRD3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M151.3" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, NUTM1-BRD4 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M151.4" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, NUTM1-CIC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M151.5" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M151.6" ] ;
fhir:display [ fhir:v "Midline Carcinoma, Paediatric, Multi-target NGS panel, structural variant (NUTM1-BRD2, NUTM1-BRD3, NUTM1-BRD4, NUTM1-CIC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M152.1" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, SNP Array" ]
  ] [
fhir:code [ fhir:v "M152.10" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, 17q rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M152.11" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, 11q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M152.12" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, 1p36 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M152.13" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M152.14" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M152.15" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, MYCN seq" ]
  ] [
fhir:code [ fhir:v "M152.16" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, Multi-target NGS panel, structural variant (17q, ALK, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M152.17" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, Multi-target NGS panel, copy number variant (MYCN, ALK, 17q, 11q, 1p36)" ]
  ] [
fhir:code [ fhir:v "M152.18" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M152.19" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, TERT promoter rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M152.2" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, Multi-target NGS panel, small variant (ALK, ATRX, FGFR1, MYCN, NRAS, PHOX2B, TP53)" ]
  ] [
fhir:code [ fhir:v "M152.3" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, ALK seq" ]
  ] [
fhir:code [ fhir:v "M152.4" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, FGFR1 seq" ]
  ] [
fhir:code [ fhir:v "M152.5" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, PHOX2B seq" ]
  ] [
fhir:code [ fhir:v "M152.6" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, TP53 seq" ]
  ] [
fhir:code [ fhir:v "M152.7" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M152.8" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, ALK copy number FISH" ]
  ] [
fhir:code [ fhir:v "M152.9" ] ;
fhir:display [ fhir:v "Neuroblastoma, Paediatric, 17q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M153.1" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, small variant (SMO)" ]
  ] [
fhir:code [ fhir:v "M153.2" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, SMO seq" ]
  ] [
fhir:code [ fhir:v "M153.3" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, SMO copy number FISH" ]
  ] [
fhir:code [ fhir:v "M153.4" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M153.5" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M153.6" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, Multi-target NGS panel, copy number variant (SMO)" ]
  ] [
fhir:code [ fhir:v "M153.7" ] ;
fhir:display [ fhir:v "Nodular Brain Tumour, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M155.1" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, Multi-target NGS panel, small variant (KIT)" ]
  ] [
fhir:code [ fhir:v "M155.2" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, KIT copy number FISH" ]
  ] [
fhir:code [ fhir:v "M155.3" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M155.4" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M155.5" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIT)" ]
  ] [
fhir:code [ fhir:v "M155.6" ] ;
fhir:display [ fhir:v "Oligoastrocytoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M156.1" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, Multi-target NGS panel, small variant (RB1, ATRX)" ]
  ] [
fhir:code [ fhir:v "M156.10" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M156.2" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, ATRX seq" ]
  ] [
fhir:code [ fhir:v "M156.3" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, RB1 seq" ]
  ] [
fhir:code [ fhir:v "M156.4" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, Multi-target NGS panel, copy number variant (1p19q, RB1, ATRX)" ]
  ] [
fhir:code [ fhir:v "M156.5" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, 1p19q codel FISH" ]
  ] [
fhir:code [ fhir:v "M156.6" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, RB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M156.7" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, ATRX copy number FISH" ]
  ] [
fhir:code [ fhir:v "M156.8" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M156.9" ] ;
fhir:display [ fhir:v "Oligodendroglioma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M157.1" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, small variant (RET)" ]
  ] [
fhir:code [ fhir:v "M157.2" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Paediatric, RET seq" ]
  ] [
fhir:code [ fhir:v "M157.3" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Paediatric, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M157.4" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Paediatric, RET rearrangement FISH/RT-PC" ]
  ] [
fhir:code [ fhir:v "M157.5" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M158.1" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (RAF1)" ]
  ] [
fhir:code [ fhir:v "M158.2" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, RAF1 seq" ]
  ] [
fhir:code [ fhir:v "M158.3" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, RAF1-SRGAP3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M158.4" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, RAF1-NF1A FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M158.5" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M158.6" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant (RAF1-SRGAP3, RAF1-NF1A, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M158.7" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M159.1" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M159.2" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, DICER1 seq" ]
  ] [
fhir:code [ fhir:v "M159.3" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, DICER1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M159.4" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M159.5" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M159.6" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M159.7" ] ;
fhir:display [ fhir:v "Pituitary Blastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M16.1" ] ;
fhir:display [ fhir:v "Adenoid Cystic Carcinoma, MYB-NFIB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M16.2" ] ;
fhir:display [ fhir:v "Adenoid Cystic Carcinoma, Multi-target NGS panel, structural variant (MYB-NFIB, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M16.4" ] ;
fhir:display [ fhir:v "Adenoid Cystic Carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M160.1" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF, H3-3A)" ]
  ] [
fhir:code [ fhir:v "M160.10" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.11" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, H3-3A seq" ]
  ] [
fhir:code [ fhir:v "M160.12" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, KIAA1549 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M160.13" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M160.14" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, WGS Germline and Tumour" ]
  ] [
fhir:code [ fhir:v "M160.15" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, copy number variant (KIAA1549)" ]
  ] [
fhir:code [ fhir:v "M160.16" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M160.2" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M160.3" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.4" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.5" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.6" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.7" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.8" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M160.9" ] ;
fhir:display [ fhir:v "Pleomorphic Xanthoastrocytoma, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M161.1" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M161.2" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, DICER1 seq" ]
  ] [
fhir:code [ fhir:v "M161.3" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, DICER1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M161.4" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M161.5" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M161.6" ] ;
fhir:display [ fhir:v "Pleuropulmonary Blastoma, Paediatric, Multi-target NGS panel, copy number variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M162.1" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, small variant (MSH6, PMS2, PTEN)" ]
  ] [
fhir:code [ fhir:v "M162.10" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, copy number variant (MYC, MSH6, PTEN)" ]
  ] [
fhir:code [ fhir:v "M162.11" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M162.2" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, MSH6 seq" ]
  ] [
fhir:code [ fhir:v "M162.3" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, PMS2 seq" ]
  ] [
fhir:code [ fhir:v "M162.4" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M162.5" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M162.6" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, MSH6 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M162.7" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, PTEN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M162.8" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M162.9" ] ;
fhir:display [ fhir:v "Primitive Neuroectodermal Tumours, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M165.1" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX)" ]
  ] [
fhir:code [ fhir:v "M165.2" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, ATRX seq" ]
  ] [
fhir:code [ fhir:v "M165.3" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, CTNNB1 seq" ]
  ] [
fhir:code [ fhir:v "M165.4" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, DAXX seq" ]
  ] [
fhir:code [ fhir:v "M165.5" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, ATRX copy number FISH" ]
  ] [
fhir:code [ fhir:v "M165.6" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M165.7" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M165.8" ] ;
fhir:display [ fhir:v "Renal Tumours, Paediatric, Multi-target NGS panel, copy number variant (ATRX)" ]
  ] [
fhir:code [ fhir:v "M166.1" ] ;
fhir:display [ fhir:v "Retinoblastoma, Paediatric, Multi-target NGS panel, small variant (RB1)" ]
  ] [
fhir:code [ fhir:v "M166.2" ] ;
fhir:display [ fhir:v "Retinoblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M166.3" ] ;
fhir:display [ fhir:v "Retinoblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M166.4" ] ;
fhir:display [ fhir:v "Retinoblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M167.1" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, small variant (SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M167.2" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, SMARCB1 seq" ]
  ] [
fhir:code [ fhir:v "M167.3" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M167.4" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M167.5" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M167.6" ] ;
fhir:display [ fhir:v "Rhabdoid Tumours, Paediatric, Multi-target NGS panel, copy number variant (SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M168.1" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, small variant (PIK3CA, FGFR1)" ]
  ] [
fhir:code [ fhir:v "M168.2" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 seq" ]
  ] [
fhir:code [ fhir:v "M168.3" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M168.4" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, FGFR1 ITD FISH" ]
  ] [
fhir:code [ fhir:v "M168.5" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M168.6" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, structural variant (FGFR1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M168.7" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, Multi-target NGS panel, copy number variant (FGFR1 ITD)" ]
  ] [
fhir:code [ fhir:v "M168.8" ] ;
fhir:display [ fhir:v "Rosette-Forming Glioneuronal Tumour, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M169.1" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, Multi-target NGS panel, small variant (IDH1, IDH2)" ]
  ] [
fhir:code [ fhir:v "M169.2" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, IDH1 seq" ]
  ] [
fhir:code [ fhir:v "M169.3" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, IDH2 seq" ]
  ] [
fhir:code [ fhir:v "M169.4" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M169.5" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M169.6" ] ;
fhir:display [ fhir:v "Secondary Glioblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M17.1" ] ;
fhir:display [ fhir:v "Secretory Carcinoma (Salivary Gland), ETV6-NTRK3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M17.2" ] ;
fhir:display [ fhir:v "Secretory Carcinoma (Salivary Gland), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M17.4" ] ;
fhir:display [ fhir:v "Secretory Carcinoma (Salivary Gland), DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M170.1" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (SMO, DDX3X)" ]
  ] [
fhir:code [ fhir:v "M170.2" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, SMO seq" ]
  ] [
fhir:code [ fhir:v "M170.3" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, DDX3X seq" ]
  ] [
fhir:code [ fhir:v "M170.4" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, SMO copy number FISH" ]
  ] [
fhir:code [ fhir:v "M170.5" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, DDX3X copy number FISH" ]
  ] [
fhir:code [ fhir:v "M170.6" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M170.7" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M170.8" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMO, DDX3X)" ]
  ] [
fhir:code [ fhir:v "M170.9" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M171.1" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, small variant (SUFU, TERT promoter, PTCH1)" ]
  ] [
fhir:code [ fhir:v "M171.10" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M171.2" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 seq" ]
  ] [
fhir:code [ fhir:v "M171.3" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, SUFU seq" ]
  ] [
fhir:code [ fhir:v "M171.4" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, TERT promoter seq" ]
  ] [
fhir:code [ fhir:v "M171.5" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, PTCH1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M171.6" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, TERT copy number FISH" ]
  ] [
fhir:code [ fhir:v "M171.7" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M171.8" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M171.9" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 WT, Paediatric, Multi-target NGS panel, copy number variant (PTCH1, TERT)" ]
  ] [
fhir:code [ fhir:v "M172.1" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, small variant (TP53, MYCN)" ]
  ] [
fhir:code [ fhir:v "M172.2" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, TP53 seq" ]
  ] [
fhir:code [ fhir:v "M172.3" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN seq" ]
  ] [
fhir:code [ fhir:v "M172.4" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M172.5" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M172.6" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M172.7" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M172.8" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, Multi-target NGS panel, copy number variant (TP53, MYCN)" ]
  ] [
fhir:code [ fhir:v "M172.9" ] ;
fhir:display [ fhir:v "SHH Medulloblastoma, TP53 MUTANT, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M173.1" ] ;
fhir:display [ fhir:v "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, TFEB-MALAT1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M173.2" ] ;
fhir:display [ fhir:v "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M173.3" ] ;
fhir:display [ fhir:v "t(6;11) Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M174.1" ] ;
fhir:display [ fhir:v "Testicular, Paediatric, Multi-target NGS panel, small variant (PRKAR1A)" ]
  ] [
fhir:code [ fhir:v "M174.2" ] ;
fhir:display [ fhir:v "Testicular, Paediatric, PRKAR1A seq" ]
  ] [
fhir:code [ fhir:v "M174.3" ] ;
fhir:display [ fhir:v "Testicular, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M174.4" ] ;
fhir:display [ fhir:v "Testicular, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M178.1" ] ;
fhir:display [ fhir:v "Wilms Tumours, Paediatric, Multi-target NGS panel, small variant (DROSHA)" ]
  ] [
fhir:code [ fhir:v "M178.2" ] ;
fhir:display [ fhir:v "Wilms Tumours, Paediatric, DROSHA seq" ]
  ] [
fhir:code [ fhir:v "M178.3" ] ;
fhir:display [ fhir:v "Wilms Tumours, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M178.4" ] ;
fhir:display [ fhir:v "Wilms Tumours, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M179.1" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, small variant (DDX3X, CTNNB1, SMARCA4, TP53)" ]
  ] [
fhir:code [ fhir:v "M179.10" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, copy number variant (SMARCA4, TP53)" ]
  ] [
fhir:code [ fhir:v "M179.11" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M179.2" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, DDX3X seq" ]
  ] [
fhir:code [ fhir:v "M179.3" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, CTNNB1 seq" ]
  ] [
fhir:code [ fhir:v "M179.4" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, SMARCA4 seq" ]
  ] [
fhir:code [ fhir:v "M179.5" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, TP53 seq" ]
  ] [
fhir:code [ fhir:v "M179.6" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M179.7" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M179.8" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M179.9" ] ;
fhir:display [ fhir:v "WNT Medulloblastoma, Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M18.1" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, TFE3 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M18.2" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma,Adult, Multi-target NGS panel small variant (FH, SDHA, SDHB, SDHC, SDHD, VHL, ELOC (TCEB-1), TSC1/2, MET, BRAF)" ]
  ] [
fhir:code [ fhir:v "M18.3" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, Chromosome 3 FISH" ]
  ] [
fhir:code [ fhir:v "M18.4" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, Chromosome 8 FISH" ]
  ] [
fhir:code [ fhir:v "M18.5" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, Chromosome 7 & 17 FISH" ]
  ] [
fhir:code [ fhir:v "M18.6" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, TFE3, TFEB)" ]
  ] [
fhir:code [ fhir:v "M18.7" ] ;
fhir:display [ fhir:v "Renal Cell Carcinoma, Adult, TFEB rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M180.1" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, small variant (TFE3)" ]
  ] [
fhir:code [ fhir:v "M180.2" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3 seq" ]
  ] [
fhir:code [ fhir:v "M180.3" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M180.4" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-MITF FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M180.5" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, TFE3-PRCC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M180.6" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M180.7" ] ;
fhir:display [ fhir:v "Xp11.2 Translocation-Associated Renal Cell Carcinoma, Paediatric, Multi-target NGS panel, structural variant (TFE3-ASPSCR1, TFE3-MITF,  TFE3-PRCC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M181.1" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Non-Classical Variant, Multi-target NGS panel, small variant (MAP2K1)" ]
  ] [
fhir:code [ fhir:v "M181.4" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M181.5" ] ;
fhir:display [ fhir:v "Hairy Cell Leukaemia, Non-Classical Variant, Ig gene hypermutation detection NGS" ]
  ] [
fhir:code [ fhir:v "M182.1" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, t(2;5)(p23;q35) ALK-NPM1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M182.2" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M182.3" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M182.4" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, Multi-target NGS panel, structural variant (ALK-NPM1, other ALK rearrangements)" ]
  ] [
fhir:code [ fhir:v "M182.5" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M182.6" ] ;
fhir:display [ fhir:v "ALK Positive Anaplastic Large Cell Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M183.1" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3A, NF1, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M183.2" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M183.3" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M183.4" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M183.5" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M183.6" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M183.7" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M183.8" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q, MYC, MYCN)" ]
  ] [
fhir:code [ fhir:v "M183.9" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Paediatric, Multi-target NGS panel, structural variant (MYC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M184.1" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, Multi-target NGS panel, small variant (H3-3B, H3C2, H3C3, H3C14, IDH1, IDH2, TP53, VHL)" ]
  ] [
fhir:code [ fhir:v "M184.2" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M184.3" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M184.4" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M184.5" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M184.6" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M184.7" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M184.8" ] ;
fhir:display [ fhir:v "Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M185.1" ] ;
fhir:display [ fhir:v "High Grade Glioma, Paediatric, Multi-target NGS panel, small variant (CDKN2B)" ]
  ] [
fhir:code [ fhir:v "M185.2" ] ;
fhir:display [ fhir:v "High Grade Glioma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M185.3" ] ;
fhir:display [ fhir:v "High Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M185.4" ] ;
fhir:display [ fhir:v "High Grade Glioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M185.5" ] ;
fhir:display [ fhir:v "High Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M186.1" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, Multi-target NGS panel, small variant (TSC1, TSC2, IDH1, IDH2, FGFR1)" ]
  ] [
fhir:code [ fhir:v "M186.2" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M186.3" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M186.4" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M186.5" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M186.6" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M186.7" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M186.8" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M187.1" ] ;
fhir:display [ fhir:v "Uveal melanoma, 1p, 3, 6, 8 MLPA" ]
  ] [
fhir:code [ fhir:v "M187.2" ] ;
fhir:display [ fhir:v "Uveal melanoma, BRAF hotspot" ]
  ] [
fhir:code [ fhir:v "M187.3" ] ;
fhir:display [ fhir:v "Uveal melanoma, Multi-target NGS panel, small variant (BRAF, NRAS, NF1)" ]
  ] [
fhir:code [ fhir:v "M187.4" ] ;
fhir:display [ fhir:v "Uveal melanoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M189.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M189.10" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M189.11" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, SNP Array" ]
  ] [
fhir:code [ fhir:v "M189.12" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, C19MC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M189.13" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M189.14" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M189.15" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M189.16" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M189.17" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M189.18" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M189.19" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M189.2" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M189.20" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M189.21" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, Multi-target NGS panel, copy number variant  (C19MC, SMARCA4, SMARCB1, YAP1)" ]
  ] [
fhir:code [ fhir:v "M189.3" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M189.4" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, C11orf95-RELA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M189.5" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M189.6" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M189.7" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, EWSR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M189.8" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, MN1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M189.9" ] ;
fhir:display [ fhir:v "Brain Tumour, No Further Morphological Classification, Paediatric, RELA rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.1" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, small variant (CDKN2A, DICER1, RB1, YAP1, SMARCA4, SMARCB1, MSH6, PMS2, PTEN, ATRX)" ]
  ] [
fhir:code [ fhir:v "M190.10" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.11" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.12" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M190.13" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, C11orf95-RELA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.14" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, RELA rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.15" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, TTYH1-C19MC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.16" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, YAP1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.17" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.18" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.19" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M190.2" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M190.20" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, MN1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M190.21" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, SNP Array" ]
  ] [
fhir:code [ fhir:v "M190.22" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, C19MC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.23" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, DICER1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.24" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, MSH6 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.25" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.26" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.27" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.28" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M190.3" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.30" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M190.31" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M190.32" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, Multi-target NGS panel, copy number variant  (C19MC, DICER1, MSH6, MYC, PTEN, SMARCA4, SMARCB1)" ]
  ] [
fhir:code [ fhir:v "M190.4" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.5" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.6" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.7" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.8" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-FRX1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M190.9" ] ;
fhir:display [ fhir:v "Embryonal Tumour Differential, Adult and Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M191.10" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M191.11" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)" ]
  ] [
fhir:code [ fhir:v "M191.12" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.13" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M191.14" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M191.15" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.16" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.17" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M191.18" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M191.19" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M191.2" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.20" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M191.21" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M191.22" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M191.3" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.4" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.5" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.6" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.7" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.8" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M191.9" ] ;
fhir:display [ fhir:v "Low Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M192.10" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M192.11" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant (EGFR)" ]
  ] [
fhir:code [ fhir:v "M192.12" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.13" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M192.14" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M192.15" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.16" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.17" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M192.18" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M192.19" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M192.2" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.20" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M192.21" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M192.22" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)" ]
  ] [
fhir:code [ fhir:v "M192.23" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M192.3" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.4" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.5" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.6" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.7" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.8" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M192.9" ] ;
fhir:display [ fhir:v "High Grade Intrinsic Brain Tumour Differential, Adult, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M193.10" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M193.11" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant (EGFR)" ]
  ] [
fhir:code [ fhir:v "M193.12" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.13" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M193.14" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M193.15" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.16" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.17" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M193.18" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M193.19" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M193.2" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.20" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M193.21" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M193.22" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, Multi-target NGS panel, copy number variant  (1p, 19q, EGFR, CDKN2A, PTEN)" ]
  ] [
fhir:code [ fhir:v "M193.23" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M193.3" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.4" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.5" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.6" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.7" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.8" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M193.9" ] ;
fhir:display [ fhir:v "Unable To Grade Intrinsic Brain Tumour, Adult, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M194.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M194.10" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, BCOR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.11" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, C19MC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.12" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, DDX3X copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.13" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.14" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.15" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, PTCH1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.16" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M194.17" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.18" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, SMO copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.19" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, TERT copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.2" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, ALK rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M194.20" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.21" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, YAP1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M194.22" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M194.23" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M194.24" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, Multi-target NGS panel, structural variant (ALK, BCOR, MYC, PVT1-MYC, YAP1-C11orf95, YAP1-TFE3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M194.25" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, Multi-target NGS panel, copy number variant  (ALK, BCOR, C19MC, DDX3X, MYC, MYCN, PTCH1, PTEN, SMARCA4, SMO, TERT, TP53, YAP1)" ]
  ] [
fhir:code [ fhir:v "M194.3" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, BCOR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M194.4" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M194.5" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, PVT1-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M194.6" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M194.7" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M194.8" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, SNP Array" ]
  ] [
fhir:code [ fhir:v "M194.9" ] ;
fhir:display [ fhir:v "Medulloblastoma all Subtypes, ALK copy number FISH" ]
  ] [
fhir:code [ fhir:v "M195.1" ] ;
fhir:display [ fhir:v "Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, small variant (BRAF, CTNNB1)" ]
  ] [
fhir:code [ fhir:v "M195.2" ] ;
fhir:display [ fhir:v "Craniopharyngioma, Adult and Paediatric, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M195.3" ] ;
fhir:display [ fhir:v "Craniopharyngioma, Adult and Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M195.4" ] ;
fhir:display [ fhir:v "Craniopharyngioma, Adult and Paediatric, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M195.5" ] ;
fhir:display [ fhir:v "Craniopharyngioma, Adult and Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M196.1" ] ;
fhir:display [ fhir:v "Bone Forming Soft Tissue Tumour Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M196.2" ] ;
fhir:display [ fhir:v "Bone Forming Soft Tissue Tumour Differential, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M196.3" ] ;
fhir:display [ fhir:v "Bone Forming Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M196.4" ] ;
fhir:display [ fhir:v "Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M196.5" ] ;
fhir:display [ fhir:v "Bone Forming Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M197.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M197.10" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M197.2" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, DDIT3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.3" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.4" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, FOXO1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.5" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, WT1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.6" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.7" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, HEY1-NCOA2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.8" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, PAX3-FOXO1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M197.9" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Soft Tissue Differential, PAX7-FOXO1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M198.1" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M198.2" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, SERPINE1-FOSB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M198.3" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, WWTR1-CAMTA1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M198.4" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M198.5" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M198.6" ] ;
fhir:display [ fhir:v "Vascular Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MYC)" ]
  ] [
fhir:code [ fhir:v "M199.1" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, small variant (APC, CTNNB1)" ]
  ] [
fhir:code [ fhir:v "M199.10" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, TPM4-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M199.11" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, ETV6-NTRK3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M199.12" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M199.13" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M199.2" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M199.3" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M199.4" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, FUS rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M199.5" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M199.6" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M199.7" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M199.8" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, COL1A1-PDGFB rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M199.9" ] ;
fhir:display [ fhir:v "Spindle Cell Soft Tissue Tumour Differential, TPM3-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M2.1" ] ;
fhir:display [ fhir:v "Ovarian Carcinoma, Multi-target NGS panel, small variant (BRCA1, BRCA2, SMARCA4)" ]
  ] [
fhir:code [ fhir:v "M2.3" ] ;
fhir:display [ fhir:v "Ovarian Carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M2.5" ] ;
fhir:display [ fhir:v "Ovarian Carcinoma, HRD status (either positive for BRCA 1 and/or 2, or HRD positive)" ]
  ] [
fhir:code [ fhir:v "M20.1" ] ;
fhir:display [ fhir:v "Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, small variant (BRAF)" ]
  ] [
fhir:code [ fhir:v "M20.2" ] ;
fhir:display [ fhir:v "Anaplastic Astrocytoma, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M20.3" ] ;
fhir:display [ fhir:v "Anaplastic Astrocytoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M20.4" ] ;
fhir:display [ fhir:v "Anaplastic Astrocytoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M20.5" ] ;
fhir:display [ fhir:v "Anaplastic Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (BRAF-KIAA1549, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M200.1" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (BCOR, DDIT3, FUS, NR4A3, TGFBR3-OGA, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M200.2" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M200.3" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M200.4" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, NR4A3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M200.5" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, TGFBR3-OGA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M200.6" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M200.7" ] ;
fhir:display [ fhir:v "Myxoid Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M201.1" ] ;
fhir:display [ fhir:v "Adipocytic Soft Tissue Tumour Differential, DDIT3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M201.2" ] ;
fhir:display [ fhir:v "Adipocytic Soft Tissue Tumour Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M201.3" ] ;
fhir:display [ fhir:v "Adipocytic Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M201.4" ] ;
fhir:display [ fhir:v "Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M201.5" ] ;
fhir:display [ fhir:v "Adipocytic Soft Tissue Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M202.1" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M202.2" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, FUS rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M202.3" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, SS18 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M202.4" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, TFE3 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M202.5" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, WWTR1-CAMTA1  RT-PCR" ]
  ] [
fhir:code [ fhir:v "M202.6" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M202.7" ] ;
fhir:display [ fhir:v "Epithelioid Soft Tissue Tumour Differential, Multi-target NGS panel, structural variant (EWSR1, FUS, SS18, TFE3, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M203.1" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), EPC1-PHF1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M203.2" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), JAZF1-PHF1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M203.3" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), JAZF1-SUZ12 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M203.4" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), NUTM2B-YWHAE FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M203.5" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M203.6" ] ;
fhir:display [ fhir:v "Uterine Sarcomas (Inc Endometrial), Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NUTM2B-YWHAE, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M204.1" ] ;
fhir:display [ fhir:v "Undifferentiated tumour, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M204.2" ] ;
fhir:display [ fhir:v "Undifferentiated tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M205.1" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B, IDH1, IDH2)" ]
  ] [
fhir:code [ fhir:v "M205.2" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, H3-3B hotspot" ]
  ] [
fhir:code [ fhir:v "M205.3" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, H3-3A seq" ]
  ] [
fhir:code [ fhir:v "M205.4" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, H3-3B seq" ]
  ] [
fhir:code [ fhir:v "M205.5" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, HEY1-NCOA2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M205.6" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, SNP Array" ]
  ] [
fhir:code [ fhir:v "M205.7" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M205.8" ] ;
fhir:display [ fhir:v "Cartilage Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M206.1" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3A, H3-3B)" ]
  ] [
fhir:code [ fhir:v "M206.2" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, H3-3B hotspot" ]
  ] [
fhir:code [ fhir:v "M206.3" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, H3-3A seq" ]
  ] [
fhir:code [ fhir:v "M206.4" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, H3-3B seq" ]
  ] [
fhir:code [ fhir:v "M206.5" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M206.6" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M206.7" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M206.8" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M206.9" ] ;
fhir:display [ fhir:v "Bone Forming Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M207.1" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, small variant (H3-3B)" ]
  ] [
fhir:code [ fhir:v "M207.2" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, H3-3B seq" ]
  ] [
fhir:code [ fhir:v "M207.3" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, H3-3B hotspot" ]
  ] [
fhir:code [ fhir:v "M207.4" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M207.5" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M207.6" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M207.7" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, structural variant (USP6, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M207.8" ] ;
fhir:display [ fhir:v "Osteoclast-Rich Bone Tumour Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M208.1" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, Multi-target NGS panel, structural variant (BCOR, CIC, EWSR1, WT1, BCOR-CCNB3, HEY1-NCOA2, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M208.2" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M208.3" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, WT1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M208.4" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M208.5" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, HEY1-NCOA2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M208.6" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma of Bone Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M209.1" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M209.2" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, SERPINE1-FOSB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M209.3" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, WWTR1-CAMTA1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M209.4" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M209.5" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, Multi-target NGS panel, structural variant (SERPINE1-FOSB, WWTR1-CAMTA1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M209.6" ] ;
fhir:display [ fhir:v "Vascular Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MYC)" ]
  ] [
fhir:code [ fhir:v "M21.1" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A,H3C2, BRAF, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M21.2" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, Multi-target NGS panel, copy number variant (EGFR, CDKN2A, CDKN2B)" ]
  ] [
fhir:code [ fhir:v "M21.20" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M21.21" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M21.22" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M21.23" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M21.24" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, CDKN2B copy number FISH" ]
  ] [
fhir:code [ fhir:v "M21.3" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M21.5" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M21.6" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M21.8" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M21.9" ] ;
fhir:display [ fhir:v "Astrocytoma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M210.1" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, structural variant (ALK, BCOR, CIC, EWSR1, FUS, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M210.2" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M210.3" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, FUS rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M210.4" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M210.5" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M210.6" ] ;
fhir:display [ fhir:v "Spindle Cell Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M211.1" ] ;
fhir:display [ fhir:v "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, small variant (GNAS)" ]
  ] [
fhir:code [ fhir:v "M211.2" ] ;
fhir:display [ fhir:v "Fibro-Osseous Tumour of Bone Differential, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M211.3" ] ;
fhir:display [ fhir:v "Fibro-Osseous Tumour of Bone Differential, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M211.4" ] ;
fhir:display [ fhir:v "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M211.5" ] ;
fhir:display [ fhir:v "Fibro-Osseous Tumour of Bone Differential, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M212.1" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, Multi-target NGS panel, small variant (CTNNB1, DAXX, ATRX, TP53, TFE3)" ]
  ] [
fhir:code [ fhir:v "M212.10" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TFEB-MALAT1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M212.11" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TFE3-ASPSCR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M212.12" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TFE3-MITF FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M212.13" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TFE3-PRCC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M212.14" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M212.15" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, Multi-target NGS panel, structural variant (TFEB-MALAT1, TFE3-ASPSCR1, TFE3-MITF, TFE3-PRCC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M212.16" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, Multi-target NGS panel, copy number variant (ATRX, TP53, WT1)" ]
  ] [
fhir:code [ fhir:v "M212.2" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, ATRX seq" ]
  ] [
fhir:code [ fhir:v "M212.3" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, CTNNB1 seq" ]
  ] [
fhir:code [ fhir:v "M212.4" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, DAXX seq" ]
  ] [
fhir:code [ fhir:v "M212.5" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TFE3 seq" ]
  ] [
fhir:code [ fhir:v "M212.6" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, TP53 seq" ]
  ] [
fhir:code [ fhir:v "M212.7" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, ATRX copy number FISH" ]
  ] [
fhir:code [ fhir:v "M212.8" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M212.9" ] ;
fhir:display [ fhir:v "Renal Tumour Differential, Paediatric, WT1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M213.10" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.11" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.12" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, ALK-NPM1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M213.13" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, C11orf95-RELA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.14" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, EWSR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M213.15" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M213.16" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-NF1A FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.17" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, RAF1-SRGAP3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.18" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, RELA rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.19" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.2" ] ;
fhir:display [ fhir:v "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" ]
  ] [
fhir:code [ fhir:v "M213.20" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.21" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.22" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M213.23" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.24" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, ALK copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.25" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, C19MC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.26" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.27" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.28" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, FGFR1 ITD FISH" ]
  ] [
fhir:code [ fhir:v "M213.29" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, KIAA1549 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.3" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M213.30" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, KIT copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.31" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.32" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, PDGFRA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.33" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, SMARCA4 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.34" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, SMARCB1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.35" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, YAP1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M213.36" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.37" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M213.38" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M213.4" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.5" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.6" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.7" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.8" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-FRX1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M213.9" ] ;
fhir:display [ fhir:v "Glial and Glioneuronal Tumour Differential, Paediatric, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M215.1" ] ;
fhir:display [ fhir:v "Endometrial Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M215.2" ] ;
fhir:display [ fhir:v "Endometrial Cancer, MLH1 promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M215.4" ] ;
fhir:display [ fhir:v "Endometrial Cancer, Multi-target NGS panel, small variant (MLH1, MSH2, MSH6, PMS2)" ]
  ] [
fhir:code [ fhir:v "M215.5" ] ;
fhir:display [ fhir:v "Endometrial Cancer, Multi-target NGS panel-small variant detection POLE" ]
  ] [
fhir:code [ fhir:v "M217.1" ] ;
fhir:display [ fhir:v "Urothelial Cancer, Multi-target NGS panel, small variant (FGFR3, FGFR2)" ]
  ] [
fhir:code [ fhir:v "M217.2" ] ;
fhir:display [ fhir:v "Bladder Cancer, Multi-target NGS panel, copy number variant (FGFR3, FGFR2)" ]
  ] [
fhir:code [ fhir:v "M217.3" ] ;
fhir:display [ fhir:v "Bladder Cancer, Multi-target NGS panel, structural variant (FGFR3, FGFR2, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M218.1" ] ;
fhir:display [ fhir:v "Prostate Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2, ATM, CDK12)" ]
  ] [
fhir:code [ fhir:v "M218.2" ] ;
fhir:display [ fhir:v "Prostate Cancer, Multi-target NGS panel, structural variant (TMPRSS2-ERG, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M218.3" ] ;
fhir:display [ fhir:v "Prostate Cancer, TMPRSS2-ERG FISH" ]
  ] [
fhir:code [ fhir:v "M219.1" ] ;
fhir:display [ fhir:v "Pancreatic Cancer, Multi-target NGS panel, small variant (BRCA1, BRCA2)" ]
  ] [
fhir:code [ fhir:v "M219.2" ] ;
fhir:display [ fhir:v "Pancreatic Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M219.3" ] ;
fhir:display [ fhir:v "Pancreatic Cancer, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M219.5" ] ;
fhir:display [ fhir:v "Pancreatic Cancer, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M22.1" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, small variant (H3C2, H3C14, IDH1, IDH2)" ]
  ] [
fhir:code [ fhir:v "M22.10" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, MYB rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M22.11" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, MYBL1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M22.12" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, MN1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M22.2" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M22.3" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M22.4" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M22.5" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M22.6" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M22.7" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M22.8" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, copy number variant (MYC)" ]
  ] [
fhir:code [ fhir:v "M22.9" ] ;
fhir:display [ fhir:v "Diffuse Astrocytoma, Paediatric, Multi-target NGS panel, structural variant  (MYC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M220.1" ] ;
fhir:display [ fhir:v "Cholangiocarcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3, FGFR2)" ]
  ] [
fhir:code [ fhir:v "M220.3" ] ;
fhir:display [ fhir:v "Cholangiocarcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M220.5" ] ;
fhir:display [ fhir:v "Cholangiocarcinoma, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M220.6" ] ;
fhir:display [ fhir:v "Cholangiocarcinoma, Multi-target NGS panel -small variant (IDH1)" ]
  ] [
fhir:code [ fhir:v "M220.7" ] ;
fhir:display [ fhir:v "Cholangiocarcinoma, FGFR2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M221.1" ] ;
fhir:display [ fhir:v "Spitzoid tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M222.2" ] ;
fhir:display [ fhir:v "Hepatocellular carcinoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M222.4" ] ;
fhir:display [ fhir:v "Hepatocellular carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M224.1" ] ;
fhir:display [ fhir:v "MDS/MPN, Multi-target NGS panel, small variant" ]
  ] [
fhir:code [ fhir:v "M224.10" ] ;
fhir:display [ fhir:v "MDS/MPN, BCR-ABL1 multiplex" ]
  ] [
fhir:code [ fhir:v "M224.11" ] ;
fhir:display [ fhir:v "MDS/MPN, Other RT-PCR" ]
  ] [
fhir:code [ fhir:v "M224.13" ] ;
fhir:display [ fhir:v "MDS/MPN, JAK2 V617F hotspot" ]
  ] [
fhir:code [ fhir:v "M224.14" ] ;
fhir:display [ fhir:v "MDS/MPN, JAK2 exon 12 hotspot" ]
  ] [
fhir:code [ fhir:v "M224.15" ] ;
fhir:display [ fhir:v "MDS/MPN, CALR exon 9 hotspot" ]
  ] [
fhir:code [ fhir:v "M224.16" ] ;
fhir:display [ fhir:v "MDS/MPN, MPL exon 10 hotspot" ]
  ] [
fhir:code [ fhir:v "M224.18" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr8 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.19" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.2" ] ;
fhir:display [ fhir:v "MDS/MPN, Karyotype (To include detection of complex karyotype)" ]
  ] [
fhir:code [ fhir:v "M224.20" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.21" ] ;
fhir:display [ fhir:v "MDS/MPN, i(17q)/t(17p) FISH" ]
  ] [
fhir:code [ fhir:v "M224.22" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr12p copy number FISH, t(12p) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M224.23" ] ;
fhir:display [ fhir:v "MDS/MPN, t(9;22)(q34;q11) BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M224.24" ] ;
fhir:display [ fhir:v "MDS/MPN, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)" ]
  ] [
fhir:code [ fhir:v "M224.25" ] ;
fhir:display [ fhir:v "MDS/MPN, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)" ]
  ] [
fhir:code [ fhir:v "M224.26" ] ;
fhir:display [ fhir:v "MDS/MPN, FGFR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M224.27" ] ;
fhir:display [ fhir:v "MDS/MPN, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)" ]
  ] [
fhir:code [ fhir:v "M224.28" ] ;
fhir:display [ fhir:v "MDS/MPN, inv(3)/t(3;3) FISH" ]
  ] [
fhir:code [ fhir:v "M224.29" ] ;
fhir:display [ fhir:v "MDS/MPN, 11q23 (KMT2A) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M224.3" ] ;
fhir:display [ fhir:v "MDS/MPN, FISH copy number and rearrangement Other: See tests M224. -M224. for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M224.30" ] ;
fhir:display [ fhir:v "MDS/MPN, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)" ]
  ] [
fhir:code [ fhir:v "M224.31" ] ;
fhir:display [ fhir:v "MDS/MPN, FLT3 rearragement FISH" ]
  ] [
fhir:code [ fhir:v "M224.32" ] ;
fhir:display [ fhir:v "MDS/MPN, RET rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M224.33" ] ;
fhir:display [ fhir:v "MDS/MPN, NTRK3 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M224.34" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr13/Chr13q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.35" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr11q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.36" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr9q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.37" ] ;
fhir:display [ fhir:v "MDS/MPN, Chr17/Chr17p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M224.38" ] ;
fhir:display [ fhir:v "MDS/MPN, idic(X)(q13) FISH" ]
  ] [
fhir:code [ fhir:v "M224.39" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M224.4" ] ;
fhir:display [ fhir:v "MDS/MPN, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M224.40" ] ;
fhir:display [ fhir:v "MDS/MPN, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M224.41" ] ;
fhir:display [ fhir:v "MDS/MPN, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M224.42" ] ;
fhir:display [ fhir:v "MDS/MPN, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M224.5" ] ;
fhir:display [ fhir:v "MDS/MPN, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)" ]
  ] [
fhir:code [ fhir:v "M224.6" ] ;
fhir:display [ fhir:v "MDS/MPN, FIP1L1-PDGFRA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M224.7" ] ;
fhir:display [ fhir:v "MDS/MPN, FIP1L1-PDGFRA RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M224.8" ] ;
fhir:display [ fhir:v "MDS/MPN, ETV6-PDGFRB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M224.9" ] ;
fhir:display [ fhir:v "MDS/MPN, PCM1-JAK2 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M225.1" ] ;
fhir:display [ fhir:v "Suspected Lymphoma, Ig gene (heavy & light chain) rearrangement detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M225.2" ] ;
fhir:display [ fhir:v "Suspected Lymphoma, Ig gene (heavy & light chain) rearrangement detection NGS" ]
  ] [
fhir:code [ fhir:v "M225.3" ] ;
fhir:display [ fhir:v "Suspected Lymphoma, TCR gene rearrangement detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M225.4" ] ;
fhir:display [ fhir:v "Suspected Lymphoma, TCR gene rearrangement detection NGS" ]
  ] [
fhir:code [ fhir:v "M225.5" ] ;
fhir:display [ fhir:v "Suspected Lymphoma, Karyotype" ]
  ] [
fhir:code [ fhir:v "M226.1" ] ;
fhir:display [ fhir:v "Cancer of Unknown Primary, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M226.3" ] ;
fhir:display [ fhir:v "Cancer of Unknown Primary, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M226.4" ] ;
fhir:display [ fhir:v "Cancer of Unknown Primary, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M227.1" ] ;
fhir:display [ fhir:v "Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M227.3" ] ;
fhir:display [ fhir:v "Solid tumour other (i.e. specific histology not listed elsewhere in the test directory), DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M23.1" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter,  H3-3A)" ]
  ] [
fhir:code [ fhir:v "M23.10" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M23.11" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M23.12" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M23.6" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M23.7" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M23.8" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M23.9" ] ;
fhir:display [ fhir:v "Diffuse Midline Glioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M231.1," ] ;
fhir:display [ fhir:v "small cell lung cancer, Multi-target NGS panel, copy number variant (RB1)" ]
  ] [
fhir:code [ fhir:v "M231.2," ] ;
fhir:display [ fhir:v "small cell lung cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M232.1" ] ;
fhir:display [ fhir:v "Solid Tumour Exhausted all Standards of Care Testing and Treatment- Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M233.1" ] ;
fhir:display [ fhir:v "High Grade Serous Ovarian Carcinoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M234.1" ] ;
fhir:display [ fhir:v "Triple Negative Breast Cancer, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M235.1" ] ;
fhir:display [ fhir:v "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M235.2" ] ;
fhir:display [ fhir:v "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M235.3" ] ;
fhir:display [ fhir:v "Proven or Suspected Haematological Tumours Exhausted all Standard of Care Testing and Treatment, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M236.1" ] ;
fhir:display [ fhir:v "Oesophageal Cancer, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M236.2" ] ;
fhir:display [ fhir:v "Oesophageal Cancer, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M237.1" ] ;
fhir:display [ fhir:v "Gastric Cancer, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M237.2" ] ;
fhir:display [ fhir:v "Gastric Cancer, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M238.1," ] ;
fhir:display [ fhir:v "small Bowel Cancer, MSI Testing" ]
  ] [
fhir:code [ fhir:v "M238.2," ] ;
fhir:display [ fhir:v "small Bowel Cancer, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M239.1" ] ;
fhir:display [ fhir:v "Thyroid Hurtle Cell Carcinoma, Multi-target NGS panel, structural variant (RET)" ]
  ] [
fhir:code [ fhir:v "M24.1" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, C19MC copy number  FISH" ]
  ] [
fhir:code [ fhir:v "M24.2" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, TTYH1-C19MC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M24.3" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M24.4" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M24.5" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, copy number variant (C19MC)" ]
  ] [
fhir:code [ fhir:v "M24.6" ] ;
fhir:display [ fhir:v "Embryonal Tumours with Multi-Layered Rosettes, Paediatric, Multi-target NGS panel, structural variant  (TTYH1-C19MC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M240.1" ] ;
fhir:display [ fhir:v "Non-invasive follicular thyroid neoplasm with papillary like nuclei, Multi-target NGS panel, small variant (BRAF,HRAS,NRAS,KRAS)" ]
  ] [
fhir:code [ fhir:v "M241.1" ] ;
fhir:display [ fhir:v "Conjunctival melanoma, MYB & 6cen (FISH)" ]
  ] [
fhir:code [ fhir:v "M241.2" ] ;
fhir:display [ fhir:v "Conjunctival melanoma, RREB1 (6p25) (FISH)" ]
  ] [
fhir:code [ fhir:v "M241.3" ] ;
fhir:display [ fhir:v "Conjunctival melanoma, CCND1 (11q13) (FISH)" ]
  ] [
fhir:code [ fhir:v "M241.4" ] ;
fhir:display [ fhir:v "Conjunctival melanoma, MYC & 8cen (FISH)" ]
  ] [
fhir:code [ fhir:v "M241.5" ] ;
fhir:display [ fhir:v "Conjunctival melanoma, CDKN2A & 9cen (FISH)" ]
  ] [
fhir:code [ fhir:v "M242.1" ] ;
fhir:display [ fhir:v "Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), STR Testing" ]
  ] [
fhir:code [ fhir:v "M242.2" ] ;
fhir:display [ fhir:v "Any patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected), Sex chromosome FISH" ]
  ] [
fhir:code [ fhir:v "M243.1" ] ;
fhir:display [ fhir:v "Thymic Carcinoma, Multi-target NGS panel (KIT)" ]
  ] [
fhir:code [ fhir:v "M244.1" ] ;
fhir:display [ fhir:v "In all tumours elligible for NTRK1/2/3 testing, FISH" ]
  ] [
fhir:code [ fhir:v "M245.1" ] ;
fhir:display [ fhir:v "Ovarian sex cord stromal tumuors, Multi-target NGS panel-small variant (FOXL2, CTNNB1, APC, DICER1)" ]
  ] [
fhir:code [ fhir:v "M25.1" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, Multi-target NGS panel, small variant (YAP1)" ]
  ] [
fhir:code [ fhir:v "M25.10" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, MYCN copy number FISH" ]
  ] [
fhir:code [ fhir:v "M25.11" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, ZFTA rearrangements (several fusion partners)" ]
  ] [
fhir:code [ fhir:v "M25.2" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, YAP1 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M25.3" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, YAP1-C11orf95 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M25.4" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, YAP1-TFE3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M25.5" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, C11orf95-RELA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M25.6" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M25.7" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M25.8" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, Multi-target NGS panel, copy number variant (YAP1, MYCN)" ]
  ] [
fhir:code [ fhir:v "M25.9" ] ;
fhir:display [ fhir:v "Ependymoma, Paediatric, Multi-target NGS panel, structural variant  (YAP1-C11orf95, YAP1-TFE3, C11orf95-RELA, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M26.1" ] ;
fhir:display [ fhir:v "Ependymoma Supratentorial, Adult, YAP1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M26.2" ] ;
fhir:display [ fhir:v "Ependymoma, Adult, RELA rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M26.3" ] ;
fhir:display [ fhir:v "Ependymoma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M26.4" ] ;
fhir:display [ fhir:v "Ependymoma, Adult, Multi-target NGS panel, structural variant  (YAP1, RELA, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M26.5" ] ;
fhir:display [ fhir:v "Ependymoma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M26.6" ] ;
fhir:display [ fhir:v "Ependymoma, Adult, ZFTA rearrangements (several fusion partners)" ]
  ] [
fhir:code [ fhir:v "M27.1" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M27.10" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M27.11" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, PTEN (10q23) copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M27.12" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M27.13" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M27.14" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M27.15" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, Multi-target NGS panel, structural variant (EGFRvIII, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M27.16" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M27.2" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, Multi-target NGS panel, copy number variant (EGFR, PDGFRA, MYC, PTEN, 1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M27.3" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, EGFRvIII RT-PCR" ]
  ] [
fhir:code [ fhir:v "M27.5" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M27.6" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M27.7" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M27.9" ] ;
fhir:display [ fhir:v "Glioblastoma, Adult, PDGFRA copy number FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M28.1" ] ;
fhir:display [ fhir:v "Glioma, Adult, Multi-target NGS panel, small variant (H3C2, H3C3, H3C14, H3-3A, H3-3B, IDH1, IDH2, TP53, VHL, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M28.2" ] ;
fhir:display [ fhir:v "Glioma, Adult, Multi-target NGS panel, copy number variant (EGFR, 1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M28.3" ] ;
fhir:display [ fhir:v "Glioma, Adult, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M28.4" ] ;
fhir:display [ fhir:v "Glioma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M28.5" ] ;
fhir:display [ fhir:v "Glioma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M28.6" ] ;
fhir:display [ fhir:v "Glioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M28.7" ] ;
fhir:display [ fhir:v "Glioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M28.8" ] ;
fhir:display [ fhir:v "Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M28.9" ] ;
fhir:display [ fhir:v "Glioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M29.1" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)" ]
  ] [
fhir:code [ fhir:v "M29.2" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M29.3" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M29.4" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M29.5" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M29.6" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M29.7" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M29.8" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M29.9" ] ;
fhir:display [ fhir:v "High Grade Glioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M3.12" ] ;
fhir:display [ fhir:v "Breast Cancer, Tumour profiling tests to guide adjuvant chemotherapy decisions in early breast cancer" ]
  ] [
fhir:code [ fhir:v "M3.13" ] ;
fhir:display [ fhir:v "Breast Cancer, Multi-target ctDNA NGS panel, small variant (ESR1)" ]
  ] [
fhir:code [ fhir:v "M3.5" ] ;
fhir:display [ fhir:v "Breast Cancer, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M3.6" ] ;
fhir:display [ fhir:v "Breast Cancer, Multi-target NGS panel, small variant (PIK3CA)" ]
  ] [
fhir:code [ fhir:v "M3.7" ] ;
fhir:display [ fhir:v "Breast Cancer, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M3.9" ] ;
fhir:display [ fhir:v "Breast Cancer, ETV6-NTRK3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M30.1" ] ;
fhir:display [ fhir:v "IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, small variant (RB1, NF1)" ]
  ] [
fhir:code [ fhir:v "M30.2" ] ;
fhir:display [ fhir:v "IDH-Wildtype Glioblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M30.3" ] ;
fhir:display [ fhir:v "IDH-Wildtype Glioblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M30.4" ] ;
fhir:display [ fhir:v "IDH-Wildtype Glioblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M31.1" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M31.2" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, TERT promoter, H3-3A, H3C2)" ]
  ] [
fhir:code [ fhir:v "M31.3" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M31.4" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M31.5" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M31.6" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M31.7" ] ;
fhir:display [ fhir:v "Low Grade Glioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M32.1" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, small variant (BRAF, IDH1, IDH2, TERT promoter, H3-3A, H3C2)" ]
  ] [
fhir:code [ fhir:v "M32.2" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M32.3" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M32.4" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M32.5" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M32.6" ] ;
fhir:display [ fhir:v "Low Grade Glioma/Glioneuronal Tumours, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M33.3" ] ;
fhir:display [ fhir:v "Meningioma, Adult, Multi-target NGS panel, small variant (TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M33.4" ] ;
fhir:display [ fhir:v "Meningioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M33.5" ] ;
fhir:display [ fhir:v "Meningioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M34.1" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, TERT promoter, H3-3A, H3C2)" ]
  ] [
fhir:code [ fhir:v "M34.2" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M34.3" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M34.4" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M34.5" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M34.6" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M34.7" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M34.8" ] ;
fhir:display [ fhir:v "Non-Midline Glioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M35.1" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, Multi-target NGS panel, small variant (IDH1, IDH2, ATRX, H3-3A, H3C2, BRAF, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M35.2" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, 1p19q codel FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M35.4" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M35.5" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M35.6" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M35.7" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, Multi-target NGS panel, copy number variant (1p, 19q)" ]
  ] [
fhir:code [ fhir:v "M35.8" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M35.9" ] ;
fhir:display [ fhir:v "OligodendroGlioma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M36.1" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-KIAA1549 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.10" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, KIAA1549 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M36.11" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M36.12" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, Multi-target NGS panel, small variant (BRAF, CDKN2A)" ]
  ] [
fhir:code [ fhir:v "M36.13" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M36.14" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M36.15" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, Multi-target NGS panel, copy number variant (KIAA1549, CDKN2A)" ]
  ] [
fhir:code [ fhir:v "M36.16" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M36.2" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-AGK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.3" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-AKAP9 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.4" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-CCDC6 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.5" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-FAM118B FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.6" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-FXR1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.7" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-GNAI1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.8" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF-MACF1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M36.9" ] ;
fhir:display [ fhir:v "Pilocytic Astrocytoma, Adult, BRAF rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M37.1" ] ;
fhir:display [ fhir:v "Pineoblastoma, Paediatric, Multi-target NGS panel, small variant (DICER1)" ]
  ] [
fhir:code [ fhir:v "M37.2" ] ;
fhir:display [ fhir:v "Pineoblastoma, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M37.3" ] ;
fhir:display [ fhir:v "Pineoblastoma, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M37.4" ] ;
fhir:display [ fhir:v "Pineoblastoma, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M38.1" ] ;
fhir:display [ fhir:v "Pituitary Tumours, MGMT promoter hyperMethylation" ]
  ] [
fhir:code [ fhir:v "M38.2" ] ;
fhir:display [ fhir:v "Pituitary Tumours, Multi-target NGS panel, copy number variant (EGFR)" ]
  ] [
fhir:code [ fhir:v "M38.3" ] ;
fhir:display [ fhir:v "Pituitary Tumours, EGFR copy number FISH" ]
  ] [
fhir:code [ fhir:v "M38.4" ] ;
fhir:display [ fhir:v "Pituitary Tumours, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M38.5" ] ;
fhir:display [ fhir:v "Pituitary Tumours, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M38.6" ] ;
fhir:display [ fhir:v "Pituitary Tumours, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M39.1" ] ;
fhir:display [ fhir:v "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, small variant (CDKN2A)" ]
  ] [
fhir:code [ fhir:v "M39.2" ] ;
fhir:display [ fhir:v "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M39.3" ] ;
fhir:display [ fhir:v "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, DNA Methylation" ]
  ] [
fhir:code [ fhir:v "M39.4" ] ;
fhir:display [ fhir:v "Rare Primitive Neuroectodermal Tumours Groups 2/3, Paediatric, Multi-target NGS panel, structural variant  (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M4.1" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET)" ]
  ] [
fhir:code [ fhir:v "M4.10" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, EML4-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M4.11" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, ALK hotspot cDNA" ]
  ] [
fhir:code [ fhir:v "M4.13" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M4.14" ] ;
fhir:display [ fhir:v "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" ]
  ] [
fhir:code [ fhir:v "M4.2" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, Multi-target NGS panel, structural variant (ROS1, RET, EML4-ALK, NTRK1, NTRK1, NTRK3, MET)" ]
  ] [
fhir:code [ fhir:v "M4.3" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, Multi-target NGS panel, copy number variant (MET)" ]
  ] [
fhir:code [ fhir:v "M4.4" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, EGFR hotspot Tumor" ]
  ] [
fhir:code [ fhir:v "M4.5" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, EGFR hotspot ctDNA" ]
  ] [
fhir:code [ fhir:v "M4.6" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, ROS1 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M4.7" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, RET rearrangement FISH/RT-PC" ]
  ] [
fhir:code [ fhir:v "M4.8" ] ;
fhir:display [ fhir:v "Non-Small Cell Lung Cancer, MET copy number FISH" ]
  ] [
fhir:code [ fhir:v "M42.1" ] ;
fhir:display [ fhir:v "Alveolar Rhabdomyosarcoma, FOXO1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M42.2" ] ;
fhir:display [ fhir:v "Alveolar Rhabdomyosarcoma, PAX3-FOXO1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M42.3" ] ;
fhir:display [ fhir:v "Alveolar Rhabdomyosarcoma, PAX7-FOXO1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M42.4" ] ;
fhir:display [ fhir:v "Alveolar Rhabdomyosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M42.5" ] ;
fhir:display [ fhir:v "Alveolar Rhabdomyosarcoma, Multi-target NGS panel, structural variant (FOXO1, PAX3-FOXO1, PAX7-FOXO1  NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M43.1" ] ;
fhir:display [ fhir:v "Alveolar Soft Part Sarcoma, TFE3 rearrangement FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M43.2" ] ;
fhir:display [ fhir:v "Alveolar Soft Part Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M43.3" ] ;
fhir:display [ fhir:v "Alveolar Soft Part Sarcoma, Multi-target NGS panel, structural variant (TFE3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M44.1" ] ;
fhir:display [ fhir:v "Aneurysmal Bone Cyst, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M44.2" ] ;
fhir:display [ fhir:v "Aneurysmal Bone Cyst, Multi-target NGS panel, structural variant (USP6)" ]
  ] [
fhir:code [ fhir:v "M45.1" ] ;
fhir:display [ fhir:v "Angiomatoid Fibrous Histiocytoma, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M45.2" ] ;
fhir:display [ fhir:v "Angiomatoid Fibrous Histiocytoma, FUS rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M45.3" ] ;
fhir:display [ fhir:v "Angiomatoid Fibrous Histiocytoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M45.4" ] ;
fhir:display [ fhir:v "Angiomatoid Fibrous Histiocytoma, Multi-target NGS panel, structural variant (EWSR1, FUS, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M46.1" ] ;
fhir:display [ fhir:v "Chondrosarcoma Conventional Central, Multi-target NGS panel, small variant (IDH1, IDH2)" ]
  ] [
fhir:code [ fhir:v "M46.2" ] ;
fhir:display [ fhir:v "Chondrosarcoma Conventional Central, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M46.3" ] ;
fhir:display [ fhir:v "Chondrosarcoma Conventional Central, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M47.1" ] ;
fhir:display [ fhir:v "Chondroblastoma, SNP Array" ]
  ] [
fhir:code [ fhir:v "M47.2" ] ;
fhir:display [ fhir:v "Chondroblastoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M47.3" ] ;
fhir:display [ fhir:v "Chondroblastoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M48.1" ] ;
fhir:display [ fhir:v "Clear Cell Sarcoma of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M48.2" ] ;
fhir:display [ fhir:v "Clear Cell Sarcoma of Soft Tissue, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M48.3" ] ;
fhir:display [ fhir:v "Clear Cell Sarcoma of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M49.1" ] ;
fhir:display [ fhir:v "CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M49.2" ] ;
fhir:display [ fhir:v "CNS Ewing Sarcoma Family Tumour WithÂ CICÂ Alteration, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M5.1" ] ;
fhir:display [ fhir:v "Mesothelioma, CDKN2A copy number FISH" ]
  ] [
fhir:code [ fhir:v "M5.2" ] ;
fhir:display [ fhir:v "Mesothelioma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M5.3" ] ;
fhir:display [ fhir:v "Mesothelioma, Multi-target NGS panel, copy number variant (CDKN2A)" ]
  ] [
fhir:code [ fhir:v "M50.1" ] ;
fhir:display [ fhir:v "Dermatofibrosarcoma Protuberans, COL1A1-PDGFB rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M50.2" ] ;
fhir:display [ fhir:v "Dermatofibrosarcoma Protuberans, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M50.3" ] ;
fhir:display [ fhir:v "Dermatofibrosarcoma Protuberans, Multi-target NGS panel, structural variant (COL1A1-PDGFB, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M51.1" ] ;
fhir:display [ fhir:v "Desmoid-Type Fibromatosis, Multi-target NGS panel, small variant (APC, CTNNB1)" ]
  ] [
fhir:code [ fhir:v "M52.1" ] ;
fhir:display [ fhir:v "Desmoplastic Small Round Cell Tumour, WT1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M52.2" ] ;
fhir:display [ fhir:v "Desmoplastic Small Round Cell Tumour, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M52.3" ] ;
fhir:display [ fhir:v "Desmoplastic Small Round Cell Tumour, Multi-target NGS panel, structural variant (WT1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M53.1" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, EPC1-PHF1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M53.2" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, JAZF1-PHF1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M53.3" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, JAZF1-SUZ12 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M53.4" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M53.5" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, Multi-target NGS panel, structural variant (EPC1-PHF1, JAZF1-PHF1, JAZF1-SUZ12, NTRK1, NTRK2, NTRK3, ZC3H7B-BCOR)" ]
  ] [
fhir:code [ fhir:v "M53.7" ] ;
fhir:display [ fhir:v "Endometrial Stromal Sarcoma, ZC3H7B-BCOR rearrangment FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M54.1" ] ;
fhir:display [ fhir:v "Epithelioid Haemangioendothelioma, WWTR1-CAMTA1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M54.2" ] ;
fhir:display [ fhir:v "Epithelioid Haemangioendothelioma, Multi-target NGS panel, structural variant (WWTR1-CAMTA1)" ]
  ] [
fhir:code [ fhir:v "M55.1" ] ;
fhir:display [ fhir:v "Ewing Like Sarcoma/PNET, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M55.2" ] ;
fhir:display [ fhir:v "Ewing Like Sarcoma/PNET, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M55.3" ] ;
fhir:display [ fhir:v "Ewing Like Sarcoma/PNET, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M56.1" ] ;
fhir:display [ fhir:v "Ewing Sarcoma of Bone, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M56.2" ] ;
fhir:display [ fhir:v "Ewing Sarcoma of Bone, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M56.3" ] ;
fhir:display [ fhir:v "Ewing Sarcoma of Bone, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M57.1" ] ;
fhir:display [ fhir:v "Ewing-Like Soft-Tissue Sarcoma, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M57.2" ] ;
fhir:display [ fhir:v "Ewing-Like Soft-Tissue Sarcoma, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M57.3" ] ;
fhir:display [ fhir:v "Ewing-Like Soft-Tissue Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M58.1" ] ;
fhir:display [ fhir:v "Extraskeletal Myxoid Chondrosarcoma, NR4A3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M58.2" ] ;
fhir:display [ fhir:v "Extraskeletal Myxoid Chondrosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M58.3" ] ;
fhir:display [ fhir:v "Extraskeletal Myxoid Chondrosarcoma, Multi-target NGS panel, structural variant (NR4A3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M59.1" ] ;
fhir:display [ fhir:v "Fibrous Dysplasia/Myxomas (Mazabraud Syndrome), Multi-target NGS panel, small variant (GNAS)" ]
  ] [
fhir:code [ fhir:v "M6.1" ] ;
fhir:display [ fhir:v "Mucoepidermoid Carcinoma, MAML2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M6.2" ] ;
fhir:display [ fhir:v "Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M6.3" ] ;
fhir:display [ fhir:v "Mucoepidermoid Carcinoma, Multi-target NGS panel, structural variant (MAML2)" ]
  ] [
fhir:code [ fhir:v "M6.5" ] ;
fhir:display [ fhir:v "Mucoepidermoid Carcinoma, DPYD hotspot" ]
  ] [
fhir:code [ fhir:v "M60.1" ] ;
fhir:display [ fhir:v "Giant Cell Tumour of Bone, H3-3B hotspot" ]
  ] [
fhir:code [ fhir:v "M60.2" ] ;
fhir:display [ fhir:v "Giant Cell Tumour of Bone, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M60.3" ] ;
fhir:display [ fhir:v "Giant Cell Tumour of Bone, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M61.1" ] ;
fhir:display [ fhir:v "High-Grade Neuroepithelial Tumour-Bcor Group, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M61.2" ] ;
fhir:display [ fhir:v "High-Grade Neuroepithelial Tumour-Bcor Group, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M61.3" ] ;
fhir:display [ fhir:v "High-Grade Neuroepithelial Tumour-Bcor Group, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M62.1" ] ;
fhir:display [ fhir:v "Infantile Fibrosarcoma, ETV6-NTRK3 RT-PCR or FISH" ]
  ] [
fhir:code [ fhir:v "M62.2" ] ;
fhir:display [ fhir:v "Infantile Fibrosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M62.3" ] ;
fhir:display [ fhir:v "Infantile Fibrosarcoma, Multi-target NGS panel, structural variant (ETV6-NTRK3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M63.1" ] ;
fhir:display [ fhir:v "Inflammatory Myofibroblastic Tumour, TPM4-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M63.2" ] ;
fhir:display [ fhir:v "Inflammatory Myofibroblastic Tumour, TPM3-ALK FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M63.3" ] ;
fhir:display [ fhir:v "Inflammatory Myofibroblastic Tumour, Multi-target NGS panel, structural variant (ALK, TPM4-ALK, TPM3-ALK, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M63.4" ] ;
fhir:display [ fhir:v "Inflammatory Myofibroblastic Tumour, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M64.1" ] ;
fhir:display [ fhir:v "Low Grade Fibromyxoid Sarcoma, FUS rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M64.2" ] ;
fhir:display [ fhir:v "Low Grade Fibromyxoid Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M64.3" ] ;
fhir:display [ fhir:v "Low Grade Fibromyxoid Sarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M65.1" ] ;
fhir:display [ fhir:v "Mesenchymal Chondrosarcoma, HEY1-NCOA2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M65.2" ] ;
fhir:display [ fhir:v "Mesenchymal Chondrosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M65.3" ] ;
fhir:display [ fhir:v "Mesenchymal Chondrosarcoma, Multi-target NGS panel, structural variant (HEY1-NCOA2, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M66.1" ] ;
fhir:display [ fhir:v "Myoepithelial Tumours of Soft Tissue, EWSR1 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M66.2" ] ;
fhir:display [ fhir:v "Myoepithelial Tumours of Soft Tissue, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M66.3" ] ;
fhir:display [ fhir:v "Myoepithelial Tumours of Soft Tissue, Multi-target NGS panel, structural variant (EWSR1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M67.1" ] ;
fhir:display [ fhir:v "Myxoid/Round Cell Liposarcoma, DDIT3 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M67.2" ] ;
fhir:display [ fhir:v "Myxoid/Round Cell Liposarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M67.3" ] ;
fhir:display [ fhir:v "Myxoid/Round Cell Liposarcoma, Multi-target NGS panel, structural variant (DDIT3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M67.4" ] ;
fhir:display [ fhir:v "Myxoid/Round Cell Lipsarcoma, MDM2 amplification FISH" ]
  ] [
fhir:code [ fhir:v "M68.1" ] ;
fhir:display [ fhir:v "Myxoinflammatory Fibroblastic Sarcoma, TGFBR3-OGA FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M68.2" ] ;
fhir:display [ fhir:v "Myxoinflammatory Fibroblastic Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M68.3" ] ;
fhir:display [ fhir:v "Myxoinflammatory Fibroblastic Sarcoma, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M68.4" ] ;
fhir:display [ fhir:v "Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, structural variant (TGFBR3-OGA, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M68.5" ] ;
fhir:display [ fhir:v "Myxoinflammatory Fibroblastic Sarcoma, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M69.1" ] ;
fhir:display [ fhir:v "Nodular Fasciitis, USP6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M69.2" ] ;
fhir:display [ fhir:v "Nodular Fasciitis, Multi-target NGS panel, structural variant (USP6)" ]
  ] [
fhir:code [ fhir:v "M7.1" ] ;
fhir:display [ fhir:v "Melanoma, Adult, Multi-target NGS panel, small variant (BRAF, KIT, NRAS)" ]
  ] [
fhir:code [ fhir:v "M7.10" ] ;
fhir:display [ fhir:v "Melanoma, Adult, Copy number variant detection to genomewide resolution" ]
  ] [
fhir:code [ fhir:v "M7.2" ] ;
fhir:display [ fhir:v "Melanoma, Adult, BRAF hotspot" ]
  ] [
fhir:code [ fhir:v "M7.3" ] ;
fhir:display [ fhir:v "Melanoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M7.5" ] ;
fhir:display [ fhir:v "Melanoma, Adult, MYB & 6cen (FISH)" ]
  ] [
fhir:code [ fhir:v "M7.6" ] ;
fhir:display [ fhir:v "Melanoma, Adult, RREB1 (6p25)" ]
  ] [
fhir:code [ fhir:v "M7.7" ] ;
fhir:display [ fhir:v "Melanoma, Adult, CCND1 (11q13)" ]
  ] [
fhir:code [ fhir:v "M7.8" ] ;
fhir:display [ fhir:v "Melanoma, Adult, MYC & 8cen" ]
  ] [
fhir:code [ fhir:v "M7.9" ] ;
fhir:display [ fhir:v "Melanoma, Adult, CDKN2A & 9cen" ]
  ] [
fhir:code [ fhir:v "M70.1" ] ;
fhir:display [ fhir:v "Osteosarcoma, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M70.2" ] ;
fhir:display [ fhir:v "Osteosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M70.3" ] ;
fhir:display [ fhir:v "Osteosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M70.4" ] ;
fhir:display [ fhir:v "Osteosarcoma, Multi-target NGS panel, copy number variant (MDM2)" ]
  ] [
fhir:code [ fhir:v "M71.1" ] ;
fhir:display [ fhir:v "Phosphaturic Mesenchymal Tumour, FN1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M71.2" ] ;
fhir:display [ fhir:v "Phosphaturic Mesenchymal Tumour, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M71.3" ] ;
fhir:display [ fhir:v "Phosphaturic Mesenchymal Tumour, Multi-target NGS panel, structural variant (FN1, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M72.1" ] ;
fhir:display [ fhir:v "Primitive Mesenchymal Myxoid Tumour of Infancy, Multi-target NGS panel, structural variant (BCOR, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M72.2" ] ;
fhir:display [ fhir:v "Primitive Mesenchymal Myxoid Tumour of Infancy, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M72.3" ] ;
fhir:display [ fhir:v "Primitive Mesenchymal Myxoid Tumour of Infancy, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M73.1" ] ;
fhir:display [ fhir:v "Pseudomyogenic Haemangioendothelioma, SERPINE1-FOSB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M73.2" ] ;
fhir:display [ fhir:v "Pseudomyogenic Haemangioendothelioma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M73.3" ] ;
fhir:display [ fhir:v "Pseudomyogenic Haemangioendothelioma, Multi-target NGS panel, structural variant (SERPINE1-FOSB, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M74.1" ] ;
fhir:display [ fhir:v "Radiation Induced Angiosarcoma, MYC copy number FISH" ]
  ] [
fhir:code [ fhir:v "M74.2" ] ;
fhir:display [ fhir:v "Radiation Induced Angiosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M74.3" ] ;
fhir:display [ fhir:v "Radiation Induced Angiosarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M74.4" ] ;
fhir:display [ fhir:v "Radiation Induced Angiosarcoma, Multi-target NGS panel, copy number variant (MYC)" ]
  ] [
fhir:code [ fhir:v "M75.1" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma Nos, Multi-target NGS panel, structural variant (BCOR, CIC, BCOR-CCNB3, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M75.2" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma Nos, BCOR-CCNB3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M75.3" ] ;
fhir:display [ fhir:v "Round Cell Sarcoma Nos, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M76.1" ] ;
fhir:display [ fhir:v "Sclerosing Epithelioid Fibrosarcoma, FUS rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M76.2" ] ;
fhir:display [ fhir:v "Sclerosing Epithelioid Fibrosarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M76.3" ] ;
fhir:display [ fhir:v "Sclerosing Epithelioid Fibrosarcoma, Multi-target NGS panel, structural variant (FUS, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M77.1" ] ;
fhir:display [ fhir:v "Synovial Sarcoma, SS18 rearrangement FISH or RT-PCR" ]
  ] [
fhir:code [ fhir:v "M77.2" ] ;
fhir:display [ fhir:v "Synovial Sarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M77.3" ] ;
fhir:display [ fhir:v "Synovial Sarcoma, Multi-target NGS panel, structural variant (SS18, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M78.1" ] ;
fhir:display [ fhir:v "Undifferentiated Round Cell Sarcoma of Infancy, Multi-target NGS panel, structural variant (CIC, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M78.2" ] ;
fhir:display [ fhir:v "Undifferentiated Round Cell Sarcoma of Infancy, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M79.1" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, MDM2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M79.2" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M79.3" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M79.4" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, Multi-target NGS panel, copy number variant (MDM2, DDIT3)" ]
  ] [
fhir:code [ fhir:v "M79.6" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M79.7" ] ;
fhir:display [ fhir:v "Well Differentiated/Dedifferentiated Liposarcoma, DDIT3 copy number RT-PCR/ddPCR" ]
  ] [
fhir:code [ fhir:v "M8.1" ] ;
fhir:display [ fhir:v "Gastrointestinal Stromal Tumour, Multi-target NGS panel, small variant (KIT, PDGFRA)" ]
  ] [
fhir:code [ fhir:v "M8.2" ] ;
fhir:display [ fhir:v "Gastrointestinal Stromal Tumour, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M80.1" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M80.10" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD PML-RARA RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M80.11" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD RUNX1-RUNX1T1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M80.12" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD CBFB-MYH11 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M80.13" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M80.14" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD other QF-PCR" ]
  ] [
fhir:code [ fhir:v "M80.15" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, BCR-ABL1 TKD NGS" ]
  ] [
fhir:code [ fhir:v "M80.18" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, FLT3 ITD" ]
  ] [
fhir:code [ fhir:v "M80.19" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Multi-target NGS panel, small variant (GATA1)" ]
  ] [
fhir:code [ fhir:v "M80.2" ] ;
fhir:display [ fhir:v "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" ]
  ] [
fhir:code [ fhir:v "M80.21" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, FLT3 TKD hotspot" ]
  ] [
fhir:code [ fhir:v "M80.22" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, NPM1 exon 12 hotspot" ]
  ] [
fhir:code [ fhir:v "M80.23" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M80.24" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M80.25" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M80.26" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M80.27" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Chr17/Chr17p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M80.28" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Chr12/Chr12p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M80.29" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA FISH" ]
  ] [
fhir:code [ fhir:v "M80.3" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)" ]
  ] [
fhir:code [ fhir:v "M80.30" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH" ]
  ] [
fhir:code [ fhir:v "M80.31" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 FISH" ]
  ] [
fhir:code [ fhir:v "M80.32" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 ( KMT2A) rearrangements FISH" ]
  ] [
fhir:code [ fhir:v "M80.33" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 FISH" ]
  ] [
fhir:code [ fhir:v "M80.34" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM FISH" ]
  ] [
fhir:code [ fhir:v "M80.35" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA FISH" ]
  ] [
fhir:code [ fhir:v "M80.36" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M80.37" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 FISH" ]
  ] [
fhir:code [ fhir:v "M80.38" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 FISH" ]
  ] [
fhir:code [ fhir:v "M80.39" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 FISH" ]
  ] [
fhir:code [ fhir:v "M80.40" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH" ]
  ] [
fhir:code [ fhir:v "M80.41" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(15;17)(q24;q21) PML-RARA RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.42" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.43" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.44" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 (KMT2A) rearrangements RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.45" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(6;9)(p22;q34) DEK-NUP214 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.46" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(3)(q21q26) GATA2-MECOM RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.47" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(1;22)(p13;q13) RBM15-MRTFA RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.48" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(9;22)(q34;q11) BCR-ABL1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.49" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.5" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Other: See tests M80.25-M80.40 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M80.50" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.51" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.52" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M80.53" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Multi-target NGS panel, copy number variant (Monosomal karyotype, del5/del5q, del7/del7q, del17/del17p, del12/del12p)" ]
  ] [
fhir:code [ fhir:v "M80.54" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, NUP98 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M80.55" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M80.56" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M80.57" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M80.58" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M80.7" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Other RT-PCR: See tests M80.41-80.52 for individual specified RT-PCR targets." ]
  ] [
fhir:code [ fhir:v "M80.8" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, Multi-target NGS panel, structural variant (To include detection of  Complex karyotype)" ]
  ] [
fhir:code [ fhir:v "M80.9" ] ;
fhir:display [ fhir:v "Acute Myeloid Leukaemia, MRD NPM1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M81.1" ] ;
fhir:display [ fhir:v "Transient Abnormal Myelopoiesis, Multi-target NGS panel, small variant (GATA1)" ]
  ] [
fhir:code [ fhir:v "M82.1" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M82.10" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr13/Chr13q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.11" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr11q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.12" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr12p copy number FISH, t(12p) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M82.13" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr9q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.14" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr17/Chr17p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.15" ] ;
fhir:display [ fhir:v "Myelodysplasia, idic(X)(q13) FISH" ]
  ] [
fhir:code [ fhir:v "M82.16" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M82.17" ] ;
fhir:display [ fhir:v "Myelodysplasia, Multi-target NGS panel, structural variant (t(12p), t(17p);inv(3)/t(3q)/del(3q)" ]
  ] [
fhir:code [ fhir:v "M82.18" ] ;
fhir:display [ fhir:v "Myelodysplasia, ChrY copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.19" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr20/20q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.2" ] ;
fhir:display [ fhir:v "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))" ]
  ] [
fhir:code [ fhir:v "M82.20" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr8 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.21" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr19 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.22" ] ;
fhir:display [ fhir:v "Myelodysplasia, inv(3)/t(3q)/del(3q)" ]
  ] [
fhir:code [ fhir:v "M82.23" ] ;
fhir:display [ fhir:v "Myelodysplasia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M82.24" ] ;
fhir:display [ fhir:v "Myelodysplasia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M82.4" ] ;
fhir:display [ fhir:v "Myelodysplasia, FISH copy number and rearrangement Other: See tests M82.7 -M82.22 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M82.6" ] ;
fhir:display [ fhir:v "Myelodysplasia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M82.7" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.8" ] ;
fhir:display [ fhir:v "Myelodysplasia, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M82.9" ] ;
fhir:display [ fhir:v "Myelodysplasia, i(17q)/t(17p) FISH" ]
  ] [
fhir:code [ fhir:v "M83.1" ] ;
fhir:display [ fhir:v "Aplastic Anaemia, Karyotype (Genomewide)" ]
  ] [
fhir:code [ fhir:v "M83.3" ] ;
fhir:display [ fhir:v "Aplastic Anaemia, FISH copy number and rearrangement" ]
  ] [
fhir:code [ fhir:v "M83.4" ] ;
fhir:display [ fhir:v "Aplastic Anaemia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M83.5" ] ;
fhir:display [ fhir:v "Aplastic Anaemia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M83.6" ] ;
fhir:display [ fhir:v "Aplastic Anaemia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M84.1" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, BCR-ABL1 multiplex" ]
  ] [
fhir:code [ fhir:v "M84.11" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M84.12" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Chr8 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M84.13" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Chr19 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M84.14" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M84.15" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M84.16" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, i(17q) FISH" ]
  ] [
fhir:code [ fhir:v "M84.17" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Chr12p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M84.18" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M84.19" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Inv(3) MECOM FISH" ]
  ] [
fhir:code [ fhir:v "M84.2" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M84.20" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, 11q23 (KMT2A) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M84.21" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, Multi-target NGS panel, copy number variant (trisomy 8, trisomy 19, -7/7q, -5/5q, i(17q), 12p-)" ]
  ] [
fhir:code [ fhir:v "M84.22" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M84.23" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, MRD BCR-ABL1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M84.24" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M84.25" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M84.3" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M84.4" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M84.6" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, FISH copy number and rearrangement Other: See tests M84.12 M84.20 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M84.8" ] ;
fhir:display [ fhir:v "Chronic Myeloid Leukaemia, BCR-ABL1 TKD NGS" ]
  ] [
fhir:code [ fhir:v "M85.1" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Multi-target NGS limited panel, small variant (JAK2, CALR, MPL)" ]
  ] [
fhir:code [ fhir:v "M85.10" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, PCM1-JAK2 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M85.11" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, BCR-ABL1 multiplex" ]
  ] [
fhir:code [ fhir:v "M85.12" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Other RT-PCR" ]
  ] [
fhir:code [ fhir:v "M85.13" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M85.14" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, JAK2 V617F hotspot" ]
  ] [
fhir:code [ fhir:v "M85.15" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, JAK2  exon 12 hotspot" ]
  ] [
fhir:code [ fhir:v "M85.16" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, CALR exon 9 hotspot" ]
  ] [
fhir:code [ fhir:v "M85.17" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, MPL exon 10 hotspot" ]
  ] [
fhir:code [ fhir:v "M85.19" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Chr8 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M85.2" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Multi-target NGS panel, small variant" ]
  ] [
fhir:code [ fhir:v "M85.20" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M85.21" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M85.22" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, i(17q) FISH" ]
  ] [
fhir:code [ fhir:v "M85.23" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Chr12p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M85.24" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, t(9;22)(q34;q11) BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M85.25" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)" ]
  ] [
fhir:code [ fhir:v "M85.26" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)" ]
  ] [
fhir:code [ fhir:v "M85.27" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, FGFR1 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M85.28" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)" ]
  ] [
fhir:code [ fhir:v "M85.29" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, inv(3)/t(3;3) FISH" ]
  ] [
fhir:code [ fhir:v "M85.3" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Karyotype (To include detection of complex karyotype)" ]
  ] [
fhir:code [ fhir:v "M85.30" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, 11q23 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M85.31" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)" ]
  ] [
fhir:code [ fhir:v "M85.32" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, FLT3 rearragement FISH" ]
  ] [
fhir:code [ fhir:v "M85.33" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, RET rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M85.34" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, NTRK3 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M85.35" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M85.36" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, Multi-target NGS panel, copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)" ]
  ] [
fhir:code [ fhir:v "M85.37" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M85.38" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M85.5" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M85.7" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, FIP1L1-PDGFRA (4q12) FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M85.8" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, FIP1L1-PDGFRA RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M85.9" ] ;
fhir:display [ fhir:v "Myeloproliferative Neoplasm, ETV6-PDGFRB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M86.1" ] ;
fhir:display [ fhir:v "Systemic Mastocytosis, Multi-target NGS panel, small variant (KIT)" ]
  ] [
fhir:code [ fhir:v "M86.2" ] ;
fhir:display [ fhir:v "Systemic Mastocytosis, KIT D816 QF-PCR" ]
  ] [
fhir:code [ fhir:v "M86.3" ] ;
fhir:display [ fhir:v "Systemic Mastocytosis, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M86.4" ] ;
fhir:display [ fhir:v "Systemic Mastocytosis, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M86.5" ] ;
fhir:display [ fhir:v "Systemic Mastocytosis, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M87.1" ] ;
fhir:display [ fhir:v "Chronic Neutrophilic Leukaemia, Multi-target NGS panel, small variant (CSF3R)" ]
  ] [
fhir:code [ fhir:v "M88.1" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant (PTPN11, KRAS, NRAS, NF1, CBL)" ]
  ] [
fhir:code [ fhir:v "M88.10" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, copy number variant (-7/del7q, -5/del5q, trisomy 8)" ]
  ] [
fhir:code [ fhir:v "M88.11" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M88.12" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M88.2" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M88.3" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Multi-target NGS panel, small variant" ]
  ] [
fhir:code [ fhir:v "M88.4" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Karyotype" ]
  ] [
fhir:code [ fhir:v "M88.5" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, FISH copy number and rearrangement Other: See tests M88.7-M88.9 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M88.7" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Chr8 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M88.8" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M88.9" ] ;
fhir:display [ fhir:v "Juvenile Myelomonocytic Leukaemia, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M89.1" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M89.10" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD PML-RARA RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M89.100" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.101" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.102" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.103" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.104" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Multi-target NGS panel, copy number variant" ]
  ] [
fhir:code [ fhir:v "M89.105" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, NUP98 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.106" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M89.107" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD NPM1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M89.108" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M89.109" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M89.11" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD RUNX1-RUNX1T1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M89.12" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD CBFB-MYH11 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M89.13" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD BCR-ABL1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M89.14" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD other QF-PCR" ]
  ] [
fhir:code [ fhir:v "M89.15" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD target identification (Ig/TCR gene rearrangement by PCR & sequencing with MRD workup via QF-PCR)" ]
  ] [
fhir:code [ fhir:v "M89.16" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR )" ]
  ] [
fhir:code [ fhir:v "M89.17" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, BCR-ABL1 TKD NGS" ]
  ] [
fhir:code [ fhir:v "M89.2" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Karyotype (To include detection of Complex karyotype, Monosomal karyotype)" ]
  ] [
fhir:code [ fhir:v "M89.20" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, FLT3 TKD hotspot" ]
  ] [
fhir:code [ fhir:v "M89.21" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, NPM1 exon 12 hotspot" ]
  ] [
fhir:code [ fhir:v "M89.22" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, IDH1 hotspot" ]
  ] [
fhir:code [ fhir:v "M89.23" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, IDH2 hotspot" ]
  ] [
fhir:code [ fhir:v "M89.24" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Chr5/Chr5q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M89.25" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Chr7/Chr7q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M89.26" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Chr17/Chr17p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M89.27" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Chr12/Chr12p copy number FISH" ]
  ] [
fhir:code [ fhir:v "M89.28" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA FISH" ]
  ] [
fhir:code [ fhir:v "M89.29" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.3" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, FISH copy number and rearrangement other" ]
  ] [
fhir:code [ fhir:v "M89.30" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 FISH" ]
  ] [
fhir:code [ fhir:v "M89.31" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 ( KMT2A) rearrangements FISH" ]
  ] [
fhir:code [ fhir:v "M89.32" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 FISH" ]
  ] [
fhir:code [ fhir:v "M89.33" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM FISH" ]
  ] [
fhir:code [ fhir:v "M89.34" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(1;22)(p13;q13) RBM15-MRTFA FISH" ]
  ] [
fhir:code [ fhir:v "M89.35" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.36" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.37" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.38" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 FISH" ]
  ] [
fhir:code [ fhir:v "M89.39" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 FISH" ]
  ] [
fhir:code [ fhir:v "M89.4" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M89.40" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)" ]
  ] [
fhir:code [ fhir:v "M89.41" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, del(1)(p33p33) FISH" ]
  ] [
fhir:code [ fhir:v "M89.42" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, iAMP21 FISH" ]
  ] [
fhir:code [ fhir:v "M89.5" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, FLT3 ITD" ]
  ] [
fhir:code [ fhir:v "M89.52" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.53" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.54" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF FISH" ]
  ] [
fhir:code [ fhir:v "M89.55" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.56" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.57" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN FISH" ]
  ] [
fhir:code [ fhir:v "M89.58" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH" ]
  ] [
fhir:code [ fhir:v "M89.59" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL FISH" ]
  ] [
fhir:code [ fhir:v "M89.6" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Other RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.60" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.61" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.62" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;11)(p15;p15) NUP98-HOXA13 FISH" ]
  ] [
fhir:code [ fhir:v "M89.63" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(10;14)(q24;q11) TLX1-TRD FISH" ]
  ] [
fhir:code [ fhir:v "M89.64" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;10)(q34;q24) TRB-TLX1 FISH" ]
  ] [
fhir:code [ fhir:v "M89.65" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH" ]
  ] [
fhir:code [ fhir:v "M89.66" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)" ]
  ] [
fhir:code [ fhir:v "M89.67" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, TLX1 rearrangement FISH (other than TLX1-TRD & TRB-TLX1 see M91.48 & M91.49)" ]
  ] [
fhir:code [ fhir:v "M89.68" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, PDGFRA rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.69" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, PDGFRB rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.7" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M89.70" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)" ]
  ] [
fhir:code [ fhir:v "M89.71" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, JAK2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.72" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)" ]
  ] [
fhir:code [ fhir:v "M89.73" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, ABL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.74" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, CSF1R rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.75" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, 14q32 (IGH) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.76" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, CRLF2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.77" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, EPOR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M89.78" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(15;17)(q24;q21) PML-RARA RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.79" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(8;21)(q22;q22) RUNX1-RUNX1T1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.8" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, BCR-ABL1 multiplex" ]
  ] [
fhir:code [ fhir:v "M89.80" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(16)(p13.1q22) CBFB-MYH11 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.81" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(9;11)(p21;q23) MLLT3-KMT2A & other 11q23.3 (KMT2A) rearrangements RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.82" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(6;9)(p22;q34) DEK-NUP214 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.83" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(3)(q21q26) GATA2-MECOM RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.84" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(1;22)(p13;q13)  RBM15-MRTFA RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.85" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(9;22)(q34;q11) BCR-ABL1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.86" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(3;5)(q25;q34) NPM1-MLF1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.87" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(5;11)(q35;p15.5) NUP98-NSD1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.88" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(7;12)(q36;p13) MNX1-ETV6 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.89" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, inv(16)(p13.3q24.3) CBFA2T3-GLIS2 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.9" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, MRD NPM1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M89.90" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.91" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other,  t(1;19)(q23;p13) TCF3-PBX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.92" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(17;19)(q22;p13) TCF3-HLF RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.93" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.94" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.95" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.96" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.97" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.98" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(1;7)(p32;q11) TRB-TAL1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M89.99" ] ;
fhir:display [ fhir:v "Acute Leukaemia Other, t(11;14)(p15;q11) TRD-LMO1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M9.1" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, small variant (BRAF, KRAS, NRAS, HRAS, TERT promoter)" ]
  ] [
fhir:code [ fhir:v "M9.2" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (RET, NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M9.3" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Adult, RET rearrangement FISH/RT-PC" ]
  ] [
fhir:code [ fhir:v "M9.4" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Adult, Multi-target NGS panel, structural variant (NTRK1, NTRK2, NTRK3)" ]
  ] [
fhir:code [ fhir:v "M9.6" ] ;
fhir:display [ fhir:v "Thyroid Papillary Carcinoma, Adult, TERT promoter hotspot" ]
  ] [
fhir:code [ fhir:v "M90.1" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M90.2" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, Karyotype (Genomewide)" ]
  ] [
fhir:code [ fhir:v "M90.3" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, FISH copy number and rearrangement" ]
  ] [
fhir:code [ fhir:v "M90.4" ] ;
fhir:display [ fhir:v "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)" ]
  ] [
fhir:code [ fhir:v "M90.5" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, FLT3 ITD" ]
  ] [
fhir:code [ fhir:v "M90.6" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M90.7" ] ;
fhir:display [ fhir:v "Blastic Plasmacytoid Dendritic Cell Neoplasm, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M91.1" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M91.10" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, BCR-ABL1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.11" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, BCR-ABL1 TKD NGS" ]
  ] [
fhir:code [ fhir:v "M91.14" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MRD ALL RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M91.15" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, small variant (ETV6, NOTCH1, FBXW7, TP53, PTEN, KRAS, NRAS, HRAS)" ]
  ] [
fhir:code [ fhir:v "M91.2" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Karyotype (To include detection of complex karyotype, hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc)" ]
  ] [
fhir:code [ fhir:v "M91.22" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MRD target identification (Ig/TCR gene rearrangement by PCR & sequencing with MRD workup via QF-PCR)" ]
  ] [
fhir:code [ fhir:v "M91.23" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MRD quantification (Ig/TCR gene rearrangement MRD QF-PCR)" ]
  ] [
fhir:code [ fhir:v "M91.24" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Global copy number change FISH (i.e. hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy)" ]
  ] [
fhir:code [ fhir:v "M91.25" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, del(1)(p33p33) FISH" ]
  ] [
fhir:code [ fhir:v "M91.26" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, iAMP21 FISH" ]
  ] [
fhir:code [ fhir:v "M91.36" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.37" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia,  t(1;19)(q23;p13) TCF3-PBX1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.38" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF FISH" ]
  ] [
fhir:code [ fhir:v "M91.39" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.4" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, FISH copy number and rearrangement other: See tests M91.24-M91.62 for individual specified FISH targets." ]
  ] [
fhir:code [ fhir:v "M91.40" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.41" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN FISH" ]
  ] [
fhir:code [ fhir:v "M91.42" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia,  t(9;11)(p21;q23) KMT2A-MLLT3 FISH" ]
  ] [
fhir:code [ fhir:v "M91.43" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 FISH" ]
  ] [
fhir:code [ fhir:v "M91.44" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL FISH" ]
  ] [
fhir:code [ fhir:v "M91.45" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.46" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.47" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 FISH" ]
  ] [
fhir:code [ fhir:v "M91.48" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD FISH" ]
  ] [
fhir:code [ fhir:v "M91.49" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(7;10)(q34;q24) TRB-TLX1 FISH" ]
  ] [
fhir:code [ fhir:v "M91.50" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 FISH" ]
  ] [
fhir:code [ fhir:v "M91.51" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, TAL1 rearrangement FISH (other than TRB-TAL1 see M91.45)" ]
  ] [
fhir:code [ fhir:v "M91.52" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, TLX1 rearrangement FISH (other than TLX1-TRD & TRB-TLX1 see M91.48 & M91.49)" ]
  ] [
fhir:code [ fhir:v "M91.53" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, PDGFRA rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.54" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, PDGFRB rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.55" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, ABL1 rearrangement FISH (other than BCR-ABL1 see M91.10)" ]
  ] [
fhir:code [ fhir:v "M91.56" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, JAK2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.57" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, KMT2A rearrangement FISH (other than specific rearrangements described in tests M91.30-91,44)" ]
  ] [
fhir:code [ fhir:v "M91.58" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, ABL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.59" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, CSF1R rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.6" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Other RT-PCR: See tests M91-63-M91.77 for individual specified RT-PCR targets" ]
  ] [
fhir:code [ fhir:v "M91.60" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, 14q32(IGH) rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.61" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, CRLF2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.62" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, EPOR rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.63" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(12;21)(p13;q22) ETV6-RUNX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.64" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(1;19)(q23;p13) TCF3-PBX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.65" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(17;19)(q22;p13) TCF3-HLF RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.66" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(4;11)(q21;q23) KMT2A-AFF1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.67" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.3) KMT2A-MLLT1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.68" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(6;11)(q27;q23) KMT2A-AFDN RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.69" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(9;11)(p21;q23) KMT2A-MLLT3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.7" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, structural variant" ]
  ] [
fhir:code [ fhir:v "M91.70" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia,  t(10;11)(p12;q23) KMT2A-MLLT10 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.71" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;19)(q23;p13.1) KMT2A-ELL RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.72" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(1;7)(p32;q11) TRB-TAL1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.73" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(11;14)(p15;q11) TRD-LMO1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.74" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(7;11)(p15;p15) NUP98-HOXA13 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.75" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(10;14)(q24;q11) TLX1-TRD RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.76" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(7;10)q34;q24) TRB-TLX1 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.77" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(5;14)(q35;q32.2) BCL11B-TLX3 RT-PCR" ]
  ] [
fhir:code [ fhir:v "M91.78" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, Multi-target NGS panel, copy number variant (to include hyperdiploidy, high hyperdiploidy, near haploidy, low hypodiploidy etc.)" ]
  ] [
fhir:code [ fhir:v "M91.79" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR rare" ]
  ] [
fhir:code [ fhir:v "M91.8" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, BCR-ABL1 multiplex" ]
  ] [
fhir:code [ fhir:v "M91.80" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, TPMT" ]
  ] [
fhir:code [ fhir:v "M91.81" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, NUDT15" ]
  ] [
fhir:code [ fhir:v "M91.82" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M91.83" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M91.84" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.85" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(8;14)(q34;q32) IGH-MYC FISH" ]
  ] [
fhir:code [ fhir:v "M91.86" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(2;8)(p12;q24) IGK-MYC FISH" ]
  ] [
fhir:code [ fhir:v "M91.87" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, t(8;22)(q24;q11) IGL-MYC FISH" ]
  ] [
fhir:code [ fhir:v "M91.88" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, BCL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.89" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, BCL6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M91.9" ] ;
fhir:display [ fhir:v "Acute Lymphoblastic Leukaemia, MRD BCR-ABL1 RT-qPCR" ]
  ] [
fhir:code [ fhir:v "M92.1" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, Multi-target NGS panel, small variant (KRAS, NRAS, BRAF, TP53, DIS3, TENT5C, IRF4)" ]
  ] [
fhir:code [ fhir:v "M92.10" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, del(1p) copy number FISH" ]
  ] [
fhir:code [ fhir:v "M92.11" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, gain(1q) copy number FISH" ]
  ] [
fhir:code [ fhir:v "M92.12" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M92.13" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, Multi-target NGS panel (To include hyperdiploidy, del(1p), gain(1q), del17p)" ]
  ] [
fhir:code [ fhir:v "M92.14" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M92.2" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, t(4;14) IGH-FGFR3FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M92.3" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, t(6;14)  IGH-CCND3 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M92.4" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, t(11;14)(q13;q32)  IGH-CCND1 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M92.5" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, t(14;16) IGH-MAF FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M92.6" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, t(14;20)  IGH-MAFB FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M92.7" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, Multi-target NGS panel, structural variant (To include IGH-FGFR3, IGH-CCND3, IGH-CCND1, IGH-MAF, IGH-MAFB, MYC rearrangements)" ]
  ] [
fhir:code [ fhir:v "M92.8" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, IGH rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M92.9" ] ;
fhir:display [ fhir:v "Plasma Cell Dyscrasia, Hyperdiploidy copy number FISH" ]
  ] [
fhir:code [ fhir:v "M93.3" ] ;
fhir:display [ fhir:v "Lymphoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M93.4" ] ;
fhir:display [ fhir:v "Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M93.5" ] ;
fhir:display [ fhir:v "Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M93.6" ] ;
fhir:display [ fhir:v "Lymphoma, Multi-target NGS panel-small variant (BTK, PLCG2, RAS, MAP2K1, BCL2)" ]
  ] [
fhir:code [ fhir:v "M94.1" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, Multi-target NGS panel, small variant (TP53,BTK, PLCG2, BCL2)" ]
  ] [
fhir:code [ fhir:v "M94.10" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, chromosome 12 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M94.2" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, Multi-target NGS panel, copy number variant (TP53,ATM, DLEU2/7, RB1, trisomy 12)" ]
  ] [
fhir:code [ fhir:v "M94.4" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, del(17p) TP53 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M94.5" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, Ig gene (heavy & light chain) rearrangement & hypermutation detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M94.6" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, Ig gene (heavy & light chain) rearrangement & hypermutation detection NGS" ]
  ] [
fhir:code [ fhir:v "M94.7" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, TP53 seq" ]
  ] [
fhir:code [ fhir:v "M94.8" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, 11q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M94.9" ] ;
fhir:display [ fhir:v "Chronic Lymphocytic Leukaemia, 13q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M95.1" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Ig gene (heavy & light chain) rearrangement & hypermutation detection multiplex seq" ]
  ] [
fhir:code [ fhir:v "M95.10" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M95.11" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M95.12" ] ;
fhir:display [ fhir:v "B cell Non-Hodgkin Lymphoma, MYD88 (L265P) hotspot" ]
  ] [
fhir:code [ fhir:v "M95.2" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Ig gene (heavy & light chain) rearrangement & hypermutation detection NGS" ]
  ] [
fhir:code [ fhir:v "M95.3" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Ig rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M95.4" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (EZH2)" ]
  ] [
fhir:code [ fhir:v "M95.5" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, EZH2 copy number FISH" ]
  ] [
fhir:code [ fhir:v "M95.6" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, small variant (BTK, PLCG2)" ]
  ] [
fhir:code [ fhir:v "M95.7" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M95.8" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Multi-target NGS panel, structural variant (Ig)" ]
  ] [
fhir:code [ fhir:v "M95.9" ] ;
fhir:display [ fhir:v "B Cell Non-Hodgkin Lymphoma, Mutli-target NGS panel, copy number (EZH2)" ]
  ] [
fhir:code [ fhir:v "M96.1" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M96.10" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M96.2" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M96.3" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M96.4" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M96.5" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, BCL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M96.6" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, BCL6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M96.7" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M96.8" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, Multi-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, other rearrangements of MYC,  BCL2, BCL6)" ]
  ] [
fhir:code [ fhir:v "M96.9" ] ;
fhir:display [ fhir:v "Burkitt Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M97.1" ] ;
fhir:display [ fhir:v "Burkitt Like Lymphoma with 11q Abnormalities, 11q copy number FISH" ]
  ] [
fhir:code [ fhir:v "M97.2" ] ;
fhir:display [ fhir:v "Burkitt Like Lymphoma with 11q Abnormalities, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M97.3" ] ;
fhir:display [ fhir:v "Burkitt Like Lymphoma with 11q Abnormalities, Multi-target NGS panel, copy number variant (11q)" ]
  ] [
fhir:code [ fhir:v "M97.4" ] ;
fhir:display [ fhir:v "Burkitt Like Lymphoma with 11q Abnormalities, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M97.5" ] ;
fhir:display [ fhir:v "Burkitt Like Lymphoma with 11q Abnormalities, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M98.1" ] ;
fhir:display [ fhir:v "Large B Cell Like Lymphoma with IRF4 Rearrangement, IRF4 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M98.2" ] ;
fhir:display [ fhir:v "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M98.3" ] ;
fhir:display [ fhir:v "Large B Cell Like Lymphoma with IRF4 Rearrangement, Multi-target NGS panel, structural variant (IRF4)" ]
  ] [
fhir:code [ fhir:v "M98.4" ] ;
fhir:display [ fhir:v "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M98.5" ] ;
fhir:display [ fhir:v "Large B Cell Like Lymphoma with IRF4 Rearrangement, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M99.1" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, MYC rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M99.10" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, WGS Tumour First" ]
  ] [
fhir:code [ fhir:v "M99.11" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, WGS Follow-up Germline" ]
  ] [
fhir:code [ fhir:v "M99.2" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, t(8;14)(q34;q32) IGH-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M99.3" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, t(2;8)(p12;q24) IGK-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M99.4" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, t(8;22)(q24;q11) IGL-MYC FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M99.5" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, BCL2 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M99.6" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, t(14;18)(q32;q21) IGH-BCL2 FISH/RT-PCR" ]
  ] [
fhir:code [ fhir:v "M99.7" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, BCL6 rearrangement FISH" ]
  ] [
fhir:code [ fhir:v "M99.8" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, WGS Germline and Tumor" ]
  ] [
fhir:code [ fhir:v "M99.9" ] ;
fhir:display [ fhir:v "High Grade Lymphoma, Mutli-target NGS panel, structural variant (IGH-MYC, IGK-MYC, IGL-MYC, IGH-BCL2, other rearrangements of MYC, BCL2, BCL6)" ]
  ] [
fhir:code [ fhir:v "R100.3" ] ;
fhir:display [ fhir:v "Rare syndromic craniosynostosis or isolated multisuture synostosis (WGS)" ]
  ] [
fhir:code [ fhir:v "R101.1" ] ;
fhir:display [ fhir:v "Ehlers Danlos syndrome with a likely monogenic cause (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R102.1" ] ;
fhir:display [ fhir:v "Osteogenesis imperfecta (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R104.3" ] ;
fhir:display [ fhir:v "Skeletal dysplasia (WGS)" ]
  ] [
fhir:code [ fhir:v "R104.4" ] ;
fhir:display [ fhir:v "Skeletal dysplasia (Small Panel)" ]
  ] [
fhir:code [ fhir:v "R105.1" ] ;
fhir:display [ fhir:v "MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ common variant newborn screening follow up (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R106.1" ] ;
fhir:display [ fhir:v "Alstrom syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R107.1" ] ;
fhir:display [ fhir:v "Bardet-Biedl syndrome (WES or Large Panel)" ]
  ] [
fhir:code [ fhir:v "R109.3" ] ;
fhir:display [ fhir:v "Childhood onset leukodystrophy (WGS)" ]
  ] [
fhir:code [ fhir:v "R110.1" ] ;
fhir:display [ fhir:v "Segmental overgrowth disorders Deep sequencing (Small panel)" ]
  ] [
fhir:code [ fhir:v "R111.1" ] ;
fhir:display [ fhir:v "X-inactivation testing (X-inactivation testing)" ]
  ] [
fhir:code [ fhir:v "R112.1" ] ;
fhir:display [ fhir:v "Factor II deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R115.1" ] ;
fhir:display [ fhir:v "Factor V deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R115.2" ] ;
fhir:display [ fhir:v "Factor V deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R116.1" ] ;
fhir:display [ fhir:v "Factor VII deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R116.2" ] ;
fhir:display [ fhir:v "Factor VII deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R117.1" ] ;
fhir:display [ fhir:v "Factor VIII deficiency (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R117.2" ] ;
fhir:display [ fhir:v "Factor VIII deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R117.3" ] ;
fhir:display [ fhir:v "Factor VIII deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R118.1" ] ;
fhir:display [ fhir:v "Factor IX deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R118.2" ] ;
fhir:display [ fhir:v "Factor IX deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R119.1" ] ;
fhir:display [ fhir:v "Factor X deficiency (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R119.2" ] ;
fhir:display [ fhir:v "Factor X deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R120.1" ] ;
fhir:display [ fhir:v "Factor XI deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R120.2" ] ;
fhir:display [ fhir:v "Factor XI deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R121.1" ] ;
fhir:display [ fhir:v "von Willebrand disease (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R121.2" ] ;
fhir:display [ fhir:v "von Willebrand disease (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R122.1" ] ;
fhir:display [ fhir:v "Factor XIII deficiency (Small panel)" ]
  ] [
fhir:code [ fhir:v "R123.1" ] ;
fhir:display [ fhir:v "Combined vitamin K-dependent clotting factor deficiency (Small panel)" ]
  ] [
fhir:code [ fhir:v "R124.1" ] ;
fhir:display [ fhir:v "Combined factor V and VIII deficiency (Small panel)" ]
  ] [
fhir:code [ fhir:v "R125.1" ] ;
fhir:display [ fhir:v "Thoracic aortic aneurysm or dissection (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R127.1" ] ;
fhir:display [ fhir:v "Long QT syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R128.1" ] ;
fhir:display [ fhir:v "Brugada syndrome and cardiac sodium channel disease (Small panel)" ]
  ] [
fhir:code [ fhir:v "R129.1" ] ;
fhir:display [ fhir:v "Catecholaminergic polymorphic VT (Small panel)" ]
  ] [
fhir:code [ fhir:v "R130.1" ] ;
fhir:display [ fhir:v "Short QT syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R131.1" ] ;
fhir:display [ fhir:v "Hypertrophic cardiomyopathy (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R132.1" ] ;
fhir:display [ fhir:v "Dilated and Arrhythmogenic cardiomyopathy (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R133.1" ] ;
fhir:display [ fhir:v "Arrhythmogenic right ventricular cardiomyopathy (Small panel)" ]
  ] [
fhir:code [ fhir:v "R134.1" ] ;
fhir:display [ fhir:v "Familial hypercholesterolaemia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R135.2" ] ;
fhir:display [ fhir:v "Paediatric or syndromic cardiomyopathy (WGS)" ]
  ] [
fhir:code [ fhir:v "R135.3" ] ;
fhir:display [ fhir:v "Paediatric or syndromic cardiomyopathy (WES)" ]
  ] [
fhir:code [ fhir:v "R136.1" ] ;
fhir:display [ fhir:v "Primary lymphoedema (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R137.1" ] ;
fhir:display [ fhir:v "Congenital heart disease microarray (Microarray)" ]
  ] [
fhir:code [ fhir:v "R138.1" ] ;
fhir:display [ fhir:v "Sudden unexplained death or survivors of a cardiac event (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R139.1" ] ;
fhir:display [ fhir:v "Laterality disorders and isomerism (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R14.1" ] ;
fhir:display [ fhir:v "Acutely unwell children with a likely monogenic disorder (WGS)" ]
  ] [
fhir:code [ fhir:v "R140.1" ] ;
fhir:display [ fhir:v "Elastin-related phenotypes (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R141.1" ] ;
fhir:display [ fhir:v "Monogenic diabetes (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R142.1" ] ;
fhir:display [ fhir:v "Glucokinase-related fasting hyperglycaemia (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R143.1" ] ;
fhir:display [ fhir:v "Neonatal diabetes (Small panel)" ]
  ] [
fhir:code [ fhir:v "R143.3" ] ;
fhir:display [ fhir:v "Neonatal diabetes (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R143.4" ] ;
fhir:display [ fhir:v "Neonatal diabetes (WGS)" ]
  ] [
fhir:code [ fhir:v "R144.1" ] ;
fhir:display [ fhir:v "Congenital hyperinsulinism (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R144.2" ] ;
fhir:display [ fhir:v "Congenital hyperinsulinism (Small panel)" ]
  ] [
fhir:code [ fhir:v "R145.1" ] ;
fhir:display [ fhir:v "Congenital hypothyroidism (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R146.1" ] ;
fhir:display [ fhir:v "Differences in sex development (Microarray)" ]
  ] [
fhir:code [ fhir:v "R146.2" ] ;
fhir:display [ fhir:v "Differences of sex development (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R148.1" ] ;
fhir:display [ fhir:v "Hypogonadotropic hypogonadism (Small panel)" ]
  ] [
fhir:code [ fhir:v "R149.1" ] ;
fhir:display [ fhir:v "Severe early-onset obesity (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R15.4" ] ;
fhir:display [ fhir:v "Primary immunodeficiency or monogenic inflammatory bowel disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R15.5" ] ;
fhir:display [ fhir:v "Primary immunodeficiency or monogenic inflammatory bowel disease (WES)" ]
  ] [
fhir:code [ fhir:v "R150.1" ] ;
fhir:display [ fhir:v "Congenital adrenal hypoplasia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R151.1" ] ;
fhir:display [ fhir:v "Familial hyperparathyroidism or Hypocalciuric hypercalcaemia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R153.1" ] ;
fhir:display [ fhir:v "Familial hypoparathyroidism (Small panel)" ]
  ] [
fhir:code [ fhir:v "R154.1" ] ;
fhir:display [ fhir:v "Hypophosphataemia or rickets (Small panel)" ]
  ] [
fhir:code [ fhir:v "R155.1" ] ;
fhir:display [ fhir:v "Autoimmune Polyendocrine Syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R156.1" ] ;
fhir:display [ fhir:v "Carney complex (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R157.1" ] ;
fhir:display [ fhir:v "IPEX Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R158.1" ] ;
fhir:display [ fhir:v "Severe insulin resistance and lipodystrophy syndromes (Small panel)" ]
  ] [
fhir:code [ fhir:v "R159.1" ] ;
fhir:display [ fhir:v "Pituitary hormone deficiency (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R16.1" ] ;
fhir:display [ fhir:v "Severe combined immunodeficiency with adenosine deaminase deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R160.1" ] ;
fhir:display [ fhir:v "Primary pigmented nodular adrenocortical disease (Small panel)" ]
  ] [
fhir:code [ fhir:v "R162.1" ] ;
fhir:display [ fhir:v "Familial tumoral calcinosis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R163.1" ] ;
fhir:display [ fhir:v "Ectodermal dysplasia (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R164.1" ] ;
fhir:display [ fhir:v "Epidermolysis bullosa and congenital skin fragility (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R165.1" ] ;
fhir:display [ fhir:v "Ichthyosis and erythrokeratoderma (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R166.1" ] ;
fhir:display [ fhir:v "Palmoplantar keratodermas (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R167.1" ] ;
fhir:display [ fhir:v "Autosomal recessive primary hypertrophic osteoarthropathy (Small panel)" ]
  ] [
fhir:code [ fhir:v "R168.1" ] ;
fhir:display [ fhir:v "Non-acute porphyrias (Small panel)" ]
  ] [
fhir:code [ fhir:v "R169.1" ] ;
fhir:display [ fhir:v "Acute intermittent porphyria (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R17.1" ] ;
fhir:display [ fhir:v "Lymphoproliferative syndrome with absent SAP expression (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R170.1" ] ;
fhir:display [ fhir:v "Variegate porphyria (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R171.1" ] ;
fhir:display [ fhir:v "Cholestasis (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R172.1" ] ;
fhir:display [ fhir:v "Wilson disease (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R173.1" ] ;
fhir:display [ fhir:v "Polycystic liver disease (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R175.1" ] ;
fhir:display [ fhir:v "Pancreatitis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R176.1" ] ;
fhir:display [ fhir:v "Gilbert syndrome (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R18.1" ] ;
fhir:display [ fhir:v "Haemophagocytic syndrome with absent XIAP expression (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R180.1" ] ;
fhir:display [ fhir:v "Congenital adrenal hyperplasia diagnostic test (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R180.2" ] ;
fhir:display [ fhir:v "Congenital adrenal hyperplasia diagnostic test (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R181.1" ] ;
fhir:display [ fhir:v "Congenital adrenal hyperplasia carrier testing (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R181.2" ] ;
fhir:display [ fhir:v "Congenital adrenal hyperplasia carrier testing (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R182.1" ] ;
fhir:display [ fhir:v "Hyperthyroidism (Small panel)" ]
  ] [
fhir:code [ fhir:v "R183.1" ] ;
fhir:display [ fhir:v "Glucocorticoid-remediable aldosteronism (GRA) (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R184.1" ] ;
fhir:display [ fhir:v "Cystic fibrosis diagnostic test (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R184.2" ] ;
fhir:display [ fhir:v "Cystic fibrosis diagnostic test (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R184.3" ] ;
fhir:display [ fhir:v "Cystic fibrosis diagnostic test (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R185.1" ] ;
fhir:display [ fhir:v "Cystic fibrosis carrier testing (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R186.1" ] ;
fhir:display [ fhir:v "Hereditary haemorrhagic telangiectasia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R188.1" ] ;
fhir:display [ fhir:v "Pulmonary arterial hypertension (Small panel)" ]
  ] [
fhir:code [ fhir:v "R189.1" ] ;
fhir:display [ fhir:v "Respiratory ciliopathies including non-CF bronchiectasis (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R19.1" ] ;
fhir:display [ fhir:v "Autoimmune lymphoproliferative syndrome with defective apoptosis (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R190.1" ] ;
fhir:display [ fhir:v "Pneumothorax familial (Small panel)" ]
  ] [
fhir:code [ fhir:v "R191.1" ] ;
fhir:display [ fhir:v "Alpha-1-antitrypsin deficiency (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R193.4" ] ;
fhir:display [ fhir:v "Cystic renal disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R194.1" ] ;
fhir:display [ fhir:v "Haematuria (Small panel)" ]
  ] [
fhir:code [ fhir:v "R195.3" ] ;
fhir:display [ fhir:v "Proteinuric renal disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R196.1" ] ;
fhir:display [ fhir:v "CFHR5 nephropathy (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R197.1" ] ;
fhir:display [ fhir:v "Membranoproliferative glomerulonephritis including C3 glomerulopathy (Small panel)" ]
  ] [
fhir:code [ fhir:v "R197.2" ] ;
fhir:display [ fhir:v "Membranoproliferative glomerulonephritis including C3 glomerulopathy (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R198.1" ] ;
fhir:display [ fhir:v "Renal tubulopathies (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R199.1" ] ;
fhir:display [ fhir:v "Congenital anomalies of the kidney and urinary tract familial (Microarray)" ]
  ] [
fhir:code [ fhir:v "R20.1" ] ;
fhir:display [ fhir:v "Wiskott-Aldrich syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R201.1" ] ;
fhir:display [ fhir:v "Atypical haemolytic uraemic syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R202.1" ] ;
fhir:display [ fhir:v "Tubulointerstitial kidney disease (Small panel)" ]
  ] [
fhir:code [ fhir:v "R204.1" ] ;
fhir:display [ fhir:v "Hereditary Systemic Amyloidosis  (Small panel)" ]
  ] [
fhir:code [ fhir:v "R207.1" ] ;
fhir:display [ fhir:v "Inherited ovarian cancer (without breast cancer) (Small panel)" ]
  ] [
fhir:code [ fhir:v "R208.1" ] ;
fhir:display [ fhir:v "Inherited breast cancer and ovarian cancer (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R21.1" ] ;
fhir:display [ fhir:v "Fetal anomalies with a likely genetic cause (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R21.2" ] ;
fhir:display [ fhir:v "Fetal anomalies with a likely genetic cause (WES or Large Panel)" ]
  ] [
fhir:code [ fhir:v "R21.3" ] ;
fhir:display [ fhir:v "Fetal anomalies with a likely genetic cause (Microarray)" ]
  ] [
fhir:code [ fhir:v "R210.2" ] ;
fhir:display [ fhir:v "Inherited MMR deficiency (Lynch syndrome) (Small panel)" ]
  ] [
fhir:code [ fhir:v "R210.4" ] ;
fhir:display [ fhir:v "Inherited MMR deficiency (Lynch syndrome) (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R210.6" ] ;
fhir:display [ fhir:v "Inherited MMR deficiency (Lynch syndrome) (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R211.1" ] ;
fhir:display [ fhir:v "Inherited polyposis and early onset colorectal cancer germline testing (Small panel)" ]
  ] [
fhir:code [ fhir:v "R211.3" ] ;
fhir:display [ fhir:v "Inherited polyposis and early onset colorectal cancer germline testing (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R212.1" ] ;
fhir:display [ fhir:v "Peutz Jeghers Syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R213.1" ] ;
fhir:display [ fhir:v "PTEN Hamartoma Tumor Syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R214.1" ] ;
fhir:display [ fhir:v "Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R215.1" ] ;
fhir:display [ fhir:v "Hereditary diffuse gastric cancer (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R216.1" ] ;
fhir:display [ fhir:v "Li Fraumeni Syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R217.1" ] ;
fhir:display [ fhir:v "Endocrine neoplasia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R218.1" ] ;
fhir:display [ fhir:v "Multiple endocrine neoplasia type 2 (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R219.1" ] ;
fhir:display [ fhir:v "Retinoblastoma (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R219.2" ] ;
fhir:display [ fhir:v "Retinoblastoma (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R22.1" ] ;
fhir:display [ fhir:v "Fetus with a likely chromosomal abnormality (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R22.2" ] ;
fhir:display [ fhir:v "Fetus with a likely chromosomal abnormality (Microarray)" ]
  ] [
fhir:code [ fhir:v "R221.1" ] ;
fhir:display [ fhir:v "Familial tumours of the nervous system (Small panel)" ]
  ] [
fhir:code [ fhir:v "R221.2" ] ;
fhir:display [ fhir:v "Familial tumours of the nervous system (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R222.1" ] ;
fhir:display [ fhir:v "Neurofibromatosis type 1 (Small panel)" ]
  ] [
fhir:code [ fhir:v "R222.2" ] ;
fhir:display [ fhir:v "Neurofibromatosis type 1 (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R223.1" ] ;
fhir:display [ fhir:v "Inherited phaeochromocytoma and paraganglioma excluding NF1 (Small panel)" ]
  ] [
fhir:code [ fhir:v "R224.1" ] ;
fhir:display [ fhir:v "Inherited renal cancer (Small panel)" ]
  ] [
fhir:code [ fhir:v "R225.1" ] ;
fhir:display [ fhir:v "Von Hippel Lindau syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R226.1" ] ;
fhir:display [ fhir:v "Inherited parathyroid cancer (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R227.1" ] ;
fhir:display [ fhir:v "Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R227.2" ] ;
fhir:display [ fhir:v "Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome (DNA repair defect testing)" ]
  ] [
fhir:code [ fhir:v "R228.1" ] ;
fhir:display [ fhir:v "Tuberous sclerosis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R228.2" ] ;
fhir:display [ fhir:v "Tuberous sclerosis (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R228.3" ] ;
fhir:display [ fhir:v "Tuberous sclerosis (Small panel deep sequencing)" ]
  ] [
fhir:code [ fhir:v "R229.1" ] ;
fhir:display [ fhir:v "Confirmed Fanconi anaemia or Bloom syndrome variant testing (Small panel)" ]
  ] [
fhir:code [ fhir:v "R23.1" ] ;
fhir:display [ fhir:v "Apert syndrome (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R230.1" ] ;
fhir:display [ fhir:v "Multiple monogenic benign skin tumours (Small panel)" ]
  ] [
fhir:code [ fhir:v "R231.2" ] ;
fhir:display [ fhir:v "Neuronal ceroid lipofuscinosis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R232.1" ] ;
fhir:display [ fhir:v "Haemophagocytic syndrome with absent perforin expression (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R233.1" ] ;
fhir:display [ fhir:v "Agammaglobulinaemia with absent BTK expression (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R234.1" ] ;
fhir:display [ fhir:v "Severe combined immunodeficiency with PNP deficiency (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R235.1" ] ;
fhir:display [ fhir:v "SCID with features of gamma chain deficiency (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R236.1" ] ;
fhir:display [ fhir:v "Pigmentary skin disorders (WES or Large panel)" ]
  ] [
fhir:code [ fhir:v "R236.2" ] ;
fhir:display [ fhir:v "Pigmentary skin disorders (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R237.1" ] ;
fhir:display [ fhir:v "Cutaneous photosensitivity with a likely genetic cause (Small panel)" ]
  ] [
fhir:code [ fhir:v "R239.1" ] ;
fhir:display [ fhir:v "Incontinentia pigmenti (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R239.2" ] ;
fhir:display [ fhir:v "Incontinentia pigmenti (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R24.1" ] ;
fhir:display [ fhir:v "Achondroplasia (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R240.1" ] ;
fhir:display [ fhir:v "Diagnostic testing for known variant(s) (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R242.1" ] ;
fhir:display [ fhir:v "Predictive testing for known familial variant(s) (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R244.1" ] ;
fhir:display [ fhir:v "Carrier testing for known familial variant(s) (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R246.1" ] ;
fhir:display [ fhir:v "Carrier testing at population risk for partners of known carriers of nationally agreed autosomal recessive disorders (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R249.1" ] ;
fhir:display [ fhir:v "NIPD using paternal exclusion testing for very rare conditions where familial variant is known (NIPD)" ]
  ] [
fhir:code [ fhir:v "R25.1" ] ;
fhir:display [ fhir:v "Thanatophoric dysplasia (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R250.1" ] ;
fhir:display [ fhir:v "NIPD for congenital adrenal hyperplasia CYP21A2 haplotype testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R251.1" ] ;
fhir:display [ fhir:v "Non-invasive prenatal sexing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R252.1" ] ;
fhir:display [ fhir:v "SMA carrier testing at population risk for partners of known carriers (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R253.1" ] ;
fhir:display [ fhir:v "Cystic fibrosis newborn screening follow-up (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R254.1" ] ;
fhir:display [ fhir:v "Familial melanoma (Small panel)" ]
  ] [
fhir:code [ fhir:v "R255.1" ] ;
fhir:display [ fhir:v "Epidermodysplasia verruciformis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R256.1" ] ;
fhir:display [ fhir:v "Nephrocalcinosis or nephrolithiasis (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R257.2" ] ;
fhir:display [ fhir:v "Unexplained young onset end-stage renal disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R257.3" ] ;
fhir:display [ fhir:v "Unexplained young onset end-stage renal disease (WES)" ]
  ] [
fhir:code [ fhir:v "R258.1" ] ;
fhir:display [ fhir:v "Cytopenia Fanconi breakage testing indicated (DNA repair defect testing)" ]
  ] [
fhir:code [ fhir:v "R258.2" ] ;
fhir:display [ fhir:v "Cytopenia Fanconi breakage testing indicated (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R259.1" ] ;
fhir:display [ fhir:v "Nijmegen breakage syndrome (DNA repair defect testing)" ]
  ] [
fhir:code [ fhir:v "R259.2" ] ;
fhir:display [ fhir:v "Nijmegen breakage syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R26.1" ] ;
fhir:display [ fhir:v "Likely common aneuploidy (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R260.1" ] ;
fhir:display [ fhir:v "Fanconi anaemia or Bloom syndrome chromosome breakage testing (DNA repair defect testing)" ]
  ] [
fhir:code [ fhir:v "R262.1" ] ;
fhir:display [ fhir:v "Corneal dystrophy (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R263.1" ] ;
fhir:display [ fhir:v "Confirmation of uniparental disomy (UPD testing)" ]
  ] [
fhir:code [ fhir:v "R264.1" ] ;
fhir:display [ fhir:v "Identity testing (Identity testing)" ]
  ] [
fhir:code [ fhir:v "R265.1" ] ;
fhir:display [ fhir:v "Chromosomal mosaicism â€“ karyotype / Targeted Chromosome Analysis (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R268.1" ] ;
fhir:display [ fhir:v "Kagami-Ogata syndrome paternal uniparental disomy 14 (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R27.3," ] ;
fhir:display [ fhir:v "Paediatric disorders (WGS)" ]
  ] [
fhir:code [ fhir:v "R270.1" ] ;
fhir:display [ fhir:v "Smith-Lemli-Opitz syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R270.2" ] ;
fhir:display [ fhir:v "Smith-Lemli-Opitz syndrome (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R271.1" ] ;
fhir:display [ fhir:v "Neuronal ceroid lipofuscinosis type 2 (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R272.1" ] ;
fhir:display [ fhir:v "Gaucher disease (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R273.1" ] ;
fhir:display [ fhir:v "Glycogen storage disease V (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R274.1" ] ;
fhir:display [ fhir:v "Glycogen storage disease (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R275.1" ] ;
fhir:display [ fhir:v "Glutaric acidaemia I newborn screening follow up (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R276.1" ] ;
fhir:display [ fhir:v "Lysosomal storage disorder (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R277.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type IH/S (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R278.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type II (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R278.2" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type II (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R279.1" ] ;
fhir:display [ fhir:v "Isovaleric acidaemia newborn screening follow up (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R28.1" ] ;
fhir:display [ fhir:v "Congenital malformation and dysmorphism syndromes â€“ microarray only (Microarray)" ]
  ] [
fhir:code [ fhir:v "R280.1" ] ;
fhir:display [ fhir:v "Krabbe disease â€“ GALC deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R280.2" ] ;
fhir:display [ fhir:v "Krabbe disease â€“ GALC deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R281.1" ] ;
fhir:display [ fhir:v "Krabbe disease Saposin A deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R282.1" ] ;
fhir:display [ fhir:v "Niemann-Pick disease type A or B (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R283.1" ] ;
fhir:display [ fhir:v "Phenylketonuria (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R285.1" ] ;
fhir:display [ fhir:v "Sandhoff disease (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R286.1" ] ;
fhir:display [ fhir:v "Tay-Sachs disease (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R287.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type IVA (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R288.1" ] ;
fhir:display [ fhir:v "GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R289.1" ] ;
fhir:display [ fhir:v "Mucolipidosis II and III Alpha/Beta (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R290.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type VI (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R291.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type IIIA (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R292.1" ] ;
fhir:display [ fhir:v "Mucopolysaccharidosis type IIIB (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R293.1" ] ;
fhir:display [ fhir:v "Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Small Panel)" ]
  ] [
fhir:code [ fhir:v "R293.2" ] ;
fhir:display [ fhir:v "Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R294.1" ] ;
fhir:display [ fhir:v "Ataxia telangiectasia DNA repair testing (DNA repair defect testing)" ]
  ] [
fhir:code [ fhir:v "R295.1" ] ;
fhir:display [ fhir:v "Ataxia telangiectasia variant testing (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R296.1" ] ;
fhir:display [ fhir:v "RNA analysis of variants (Other)" ]
  ] [
fhir:code [ fhir:v "R298.1" ] ;
fhir:display [ fhir:v "Possible structural or mosaic chromosomal abnormality FISH (FISH)" ]
  ] [
fhir:code [ fhir:v "R299.1" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Other)" ]
  ] [
fhir:code [ fhir:v "R299.2" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Heteroplasmy assessment mitochondrial genome)" ]
  ] [
fhir:code [ fhir:v "R299.3" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder, mitochondrial DNA rearrangement testing (Breakpoint mapping mitochondrial genome)" ]
  ] [
fhir:code [ fhir:v "R300.1" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder whole mitochondrial genome sequencing (Other)" ]
  ] [
fhir:code [ fhir:v "R301.1" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder, mitochondrial DNA depletion testing (Other)" ]
  ] [
fhir:code [ fhir:v "R304.1" ] ;
fhir:display [ fhir:v "NIPD for cystic fibrosis haplotype testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R305.1" ] ;
fhir:display [ fhir:v "NIPD for cystic fibrosis variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R306.1" ] ;
fhir:display [ fhir:v "NIPD for Apert syndrome variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R307.1" ] ;
fhir:display [ fhir:v "NIPD for Crouzon syndrome with acanthosis nigricans variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R308.1" ] ;
fhir:display [ fhir:v "NIPD for FGFR2-related craniosynostosis syndromes variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R309.1" ] ;
fhir:display [ fhir:v "NIPD for FGFR3-related skeletal dysplasias variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R31.3" ] ;
fhir:display [ fhir:v "Bilateral congenital or childhood onset cataracts (WGS)" ]
  ] [
fhir:code [ fhir:v "R310.1" ] ;
fhir:display [ fhir:v "NIPD for Duchenne and Becker muscular dystrophy haplotype testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R311.1" ] ;
fhir:display [ fhir:v "NIPD for spinal muscular atrophy variant testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R312.1" ] ;
fhir:display [ fhir:v "Parental sequencing for lethal autosomal recessive disorders (WES or Large penel)" ]
  ] [
fhir:code [ fhir:v "R313.1" ] ;
fhir:display [ fhir:v "Neutropaenia consistent with ELANE variants (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R314.1" ] ;
fhir:display [ fhir:v "Ambiguous genitalia (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R314.2" ] ;
fhir:display [ fhir:v "Ambiguous genitalia (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R315.1" ] ;
fhir:display [ fhir:v "POLG-related disorder (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R315.2" ] ;
fhir:display [ fhir:v "POLG-related disorder (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R316.1" ] ;
fhir:display [ fhir:v "Pyruvate dehydrogenase (PDH) deficiency (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R317.1" ] ;
fhir:display [ fhir:v "Mitochondrial liver disease, including transient infantile liver failure (Small panel)" ]
  ] [
fhir:code [ fhir:v "R318.1" ] ;
fhir:display [ fhir:v "Recurrent miscarriage with products of conception available for testing (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R318.2" ] ;
fhir:display [ fhir:v "Recurrent miscarriage with products of conception available for testing (Microarray)" ]
  ] [
fhir:code [ fhir:v "R319.1" ] ;
fhir:display [ fhir:v "Calcium-sensing receptor phenotypes (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R32.2" ] ;
fhir:display [ fhir:v "Retinal disorders (WGS)" ]
  ] [
fhir:code [ fhir:v "R320.1" ] ;
fhir:display [ fhir:v "Invasive prenatal diagnosis requiring fetal sexing (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R321.1" ] ;
fhir:display [ fhir:v "Maternal cell contamination testing (Identity testing)" ]
  ] [
fhir:code [ fhir:v "R322.1" ] ;
fhir:display [ fhir:v "Skin fibroblasts to be cultured and stored (Other)" ]
  ] [
fhir:code [ fhir:v "R323.1" ] ;
fhir:display [ fhir:v "Sitosterolaemia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R324.1" ] ;
fhir:display [ fhir:v "Familial Chylomicronaemia Syndrome (FCS) (Small panel)" ]
  ] [
fhir:code [ fhir:v "R325.1" ] ;
fhir:display [ fhir:v "Lysosomal acid lipase deficiency (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R326.1" ] ;
fhir:display [ fhir:v "Vascular skin disorders (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R327.1" ] ;
fhir:display [ fhir:v "Mosaic skin disorders deep sequencing (Medium panel)" ]
  ] [
fhir:code [ fhir:v "R328.1" ] ;
fhir:display [ fhir:v "Progressive cardiac conduction disease (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R329.1" ] ;
fhir:display [ fhir:v "Familial dysalbuminaemic hyperthyroxinaemia (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R33.1" ] ;
fhir:display [ fhir:v "Possible X-linked retinitis pigmentosa (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R330.1" ] ;
fhir:display [ fhir:v "Alveolar capillary dysplasia with misalignment of pulmonary veins (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R331.1" ] ;
fhir:display [ fhir:v "Intestinal failure or congenital diarrhoea (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R332.1" ] ;
fhir:display [ fhir:v "Rare genetic inflammatory skin disorders (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R333.1" ] ;
fhir:display [ fhir:v "Central congenital hypoventilation (STR testing)" ]
  ] [
fhir:code [ fhir:v "R333.2" ] ;
fhir:display [ fhir:v "Central congenital hypoventilation (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R334.1" ] ;
fhir:display [ fhir:v "Cystinosis (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R335.1" ] ;
fhir:display [ fhir:v "Fabry disease (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R335.2" ] ;
fhir:display [ fhir:v "Fabry disease (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R336.1" ] ;
fhir:display [ fhir:v "Cerebral vascular malformations (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R337.1" ] ;
fhir:display [ fhir:v "CADASIL (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R338.1" ] ;
fhir:display [ fhir:v "Monitoring for G(M)CSF escape variants (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R340.1" ] ;
fhir:display [ fhir:v "Amelogenesis imperfecta (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R341.1" ] ;
fhir:display [ fhir:v "Hereditary angioedema types I and II (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R343.1" ] ;
fhir:display [ fhir:v "Chromosomal mosaicism microarray (Microarray)" ]
  ] [
fhir:code [ fhir:v "R344.1" ] ;
fhir:display [ fhir:v "Primary hyperaldosteronism KCNJ5 (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R345.1" ] ;
fhir:display [ fhir:v "Facioscapulohumeral muscular dystrophy extended testing (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R345.2" ] ;
fhir:display [ fhir:v "Facioscapulohumeral muscular dystrophy extended testing (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R345.3" ] ;
fhir:display [ fhir:v "Facioscapulohumeral muscular dystrophy extended testing (Other)" ]
  ] [
fhir:code [ fhir:v "R346.1" ] ;
fhir:display [ fhir:v "DNA to be stored (Other)" ]
  ] [
fhir:code [ fhir:v "R347.1" ] ;
fhir:display [ fhir:v "Inherited predisposition to acute myeloid leukaemia (AML) (Small panel)" ]
  ] [
fhir:code [ fhir:v "R350.1" ] ;
fhir:display [ fhir:v "MERRF syndrome (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R351.1" ] ;
fhir:display [ fhir:v "NARP syndrome or maternally inherited Leigh syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R351.2" ] ;
fhir:display [ fhir:v "NARP syndrome or maternally inherited Leigh syndrome (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R352.1" ] ;
fhir:display [ fhir:v "Mitochondrial DNA maintenance disorder (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R353.1" ] ;
fhir:display [ fhir:v "Mitochondrial disorder with complex I deficiency (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R354.1" ] ;
fhir:display [ fhir:v "Mitochondrial disorder with complex II deficiency (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R355.1" ] ;
fhir:display [ fhir:v "Mitochondrial disorder with complex III deficiency (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R356.1" ] ;
fhir:display [ fhir:v "Mitochondrial disorder with complex IV deficiency (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R357.1" ] ;
fhir:display [ fhir:v "Mitochondrial disorder with complex V deficiency (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R36.2," ] ;
fhir:display [ fhir:v "structural eye disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R361.1" ] ;
fhir:display [ fhir:v "Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (Small panel)" ]
  ] [
fhir:code [ fhir:v "R361.2" ] ;
fhir:display [ fhir:v "Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R363.1" ] ;
fhir:display [ fhir:v "Inherited predisposition to GIST (Small panel)" ]
  ] [
fhir:code [ fhir:v "R364.1" ] ;
fhir:display [ fhir:v "DICER1-related cancer predisposition (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R365.1" ] ;
fhir:display [ fhir:v "Fumarate hydratase-related tumour syndromes (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R366.1" ] ;
fhir:display [ fhir:v "Inherited susceptibility to acute lymphoblastoid leukaemia (ALL) (Small panel)" ]
  ] [
fhir:code [ fhir:v "R367.1" ] ;
fhir:display [ fhir:v "Inherited pancreatic cancer (Small panel)" ]
  ] [
fhir:code [ fhir:v "R368.1" ] ;
fhir:display [ fhir:v "Hereditary angioedema type III (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R370.1" ] ;
fhir:display [ fhir:v "Validation of unaccredited findings (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R371.1" ] ;
fhir:display [ fhir:v "Malignant hyperthermia (small panel)" ]
  ] [
fhir:code [ fhir:v "R372.1" ] ;
fhir:display [ fhir:v "Newborn screening for sickle cell disease in a transfused baby (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R373.1" ] ;
fhir:display [ fhir:v "RNA to be stored (Other)" ]
  ] [
fhir:code [ fhir:v "R374.1" ] ;
fhir:display [ fhir:v "Other sample to be stored (Other)" ]
  ] [
fhir:code [ fhir:v "R375.1" ] ;
fhir:display [ fhir:v "Family follow-up testing to aid variant interpretation (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R376.1" ] ;
fhir:display [ fhir:v "Segmental or atypical neurofibromatosis type 1 testing (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R376.2" ] ;
fhir:display [ fhir:v "Segmental or atypical neurofibromatosis type 1 testing (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R38.2" ] ;
fhir:display [ fhir:v "Sporadic aniridia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R380.1" ] ;
fhir:display [ fhir:v "Niemann Pick disease type C (Small panel)" ]
  ] [
fhir:code [ fhir:v "R380.2" ] ;
fhir:display [ fhir:v "Niemann Pick disease type C (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R381.2" ] ;
fhir:display [ fhir:v "Other rare neuromuscular disorders (WGS)" ]
  ] [
fhir:code [ fhir:v "R382.1" ] ;
fhir:display [ fhir:v "Hypochondroplasia (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R383.1" ] ;
fhir:display [ fhir:v "Linkage testing for Huntington disease (Other)" ]
  ] [
fhir:code [ fhir:v "R384.1" ] ;
fhir:display [ fhir:v "Generalised arterial calcification in infancy (Small panel)" ]
  ] [
fhir:code [ fhir:v "R387.1" ] ;
fhir:display [ fhir:v "Reanalysis of existing data (Other)" ]
  ] [
fhir:code [ fhir:v "R389.1" ] ;
fhir:display [ fhir:v "NIPD pre-pregnancy test work-up (NIPD)" ]
  ] [
fhir:code [ fhir:v "R39.1" ] ;
fhir:display [ fhir:v "Albinism or congenital nystagmus (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R390.1" ] ;
fhir:display [ fhir:v "Multiple exostoses (Small panel)" ]
  ] [
fhir:code [ fhir:v "R390.2" ] ;
fhir:display [ fhir:v "Multiple exostoses (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R391.1" ] ;
fhir:display [ fhir:v "Barth syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R394.1" ] ;
fhir:display [ fhir:v "Mitochondrial neurogastrointestinal encephalopathy (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R395.1" ] ;
fhir:display [ fhir:v "Thiamine metabolism dysfunction syndrome 2 (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R396.1" ] ;
fhir:display [ fhir:v "Mitochondrial Complex V deficiency, TMEM70 type (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R397.1" ] ;
fhir:display [ fhir:v "Maternally inherited cardiomyopathy (Targeted mutation testing)" ]
  ] [
fhir:code [ fhir:v "R401.1" ] ;
fhir:display [ fhir:v "Common aneuploidy testing prenatal (Common aneuploidy testing)" ]
  ] [
fhir:code [ fhir:v "R402.1" ] ;
fhir:display [ fhir:v "Premature ovarian insufficiency (Karyotype or equivalent)" ]
  ] [
fhir:code [ fhir:v "R402.2" ] ;
fhir:display [ fhir:v "Premature ovarian insufficiency (STR testing)" ]
  ] [
fhir:code [ fhir:v "R403.1" ] ;
fhir:display [ fhir:v "MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing newborn screening follow up (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R404.1" ] ;
fhir:display [ fhir:v "Testing of unaffected individuals for inherited cancer predisposition syndromes (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R404.3" ] ;
fhir:display [ fhir:v "Testing of unaffected individuals for inherited cancer predisposition syndromes (Small panel)" ]
  ] [
fhir:code [ fhir:v "R405.1" ] ;
fhir:display [ fhir:v "Hereditary Erythrocytosis (Small panel)" ]
  ] [
fhir:code [ fhir:v "R406.1" ] ;
fhir:display [ fhir:v "Thrombocythaemia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R409.1" ] ;
fhir:display [ fhir:v "Linkage testing for recognisable Mendelian disorders (Other)" ]
  ] [
fhir:code [ fhir:v "R41.1" ] ;
fhir:display [ fhir:v "Optic neuropathy (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R41.3" ] ;
fhir:display [ fhir:v "Optic neuropathy (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R410.1" ] ;
fhir:display [ fhir:v "Myotonic dystrophy type 2 (DM2) (STR testing)" ]
  ] [
fhir:code [ fhir:v "R411.1" ] ;
fhir:display [ fhir:v "Y chromosome microdeletion (Targeted mutation testing or equivalent)" ]
  ] [
fhir:code [ fhir:v "R412.1" ] ;
fhir:display [ fhir:v "Fetal anomalies with a likely genetic cause non urgent (WES or Large Panel)" ]
  ] [
fhir:code [ fhir:v "R413.1" ] ;
fhir:display [ fhir:v "Autoinflammatory Disorders (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R414.1" ] ;
fhir:display [ fhir:v "APC associated Polyposis  (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R416.1" ] ;
fhir:display [ fhir:v "Syndromic and non syndromic craniosynostosis involving midline sutures only (metopic, sagittal, metopic & sagittal)  (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R417.1" ] ;
fhir:display [ fhir:v "Multi Locus Imprinting Disorder (MLPA)" ]
  ] [
fhir:code [ fhir:v "R417.2" ] ;
fhir:display [ fhir:v "Multi Locus Imprinting Disorder (Small Panel)" ]
  ] [
fhir:code [ fhir:v "R419.1" ] ;
fhir:display [ fhir:v "Acute Rhabdomyolysis (Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R42.1" ] ;
fhir:display [ fhir:v "Leber hereditary optic neuropathy (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R42.2" ] ;
fhir:display [ fhir:v "Leber hereditary optic neuropathy (Other)" ]
  ] [
fhir:code [ fhir:v "R420.1" ] ;
fhir:display [ fhir:v "Pseudoxanthoma elasticum (Small Panel)" ]
  ] [
fhir:code [ fhir:v "R421.1" ] ;
fhir:display [ fhir:v "Pulmonary Fibrosis, Familial (Medium panel)" ]
  ] [
fhir:code [ fhir:v "R422.1" ] ;
fhir:display [ fhir:v "BAP1 associated tumour predisposition syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R423.1" ] ;
fhir:display [ fhir:v "NIPD for Retinoblastoma haplotype testing (NIPD)" ]
  ] [
fhir:code [ fhir:v "R424.1" ] ;
fhir:display [ fhir:v "Subcutaneous panniculitis T-cell lymphoma (Single gene sequencing <=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R426.1" ] ;
fhir:display [ fhir:v "Pulmonary alveolar microlithiasis (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R428.1" ] ;
fhir:display [ fhir:v "Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (STR testing)" ]
  ] [
fhir:code [ fhir:v "R428.2" ] ;
fhir:display [ fhir:v "Patient receiving solid organ transplantation (only in cases where passenger lymphocyte syndrome is suspected) (FISH)" ]
  ] [
fhir:code [ fhir:v "R43.1" ] ;
fhir:display [ fhir:v "Blepharophimosis ptosis and epicanthus inversus (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R43.2" ] ;
fhir:display [ fhir:v "Blepharophimosis ptosis and epicanthus inversus (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R43.3" ] ;
fhir:display [ fhir:v "Blepharophimosis ptosis and epicanthus inversus (STR testing)" ]
  ] [
fhir:code [ fhir:v "R430.1" ] ;
fhir:display [ fhir:v "Inherited prostate cancer (Small panel)" ]
  ] [
fhir:code [ fhir:v "R431.1" ] ;
fhir:display [ fhir:v "Genome-wide DNA Methylation Profiling to Aid Variant Interpretation (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R433.1" ] ;
fhir:display [ fhir:v "Monogenic diabetes, subtype glucokinase NIPT (NIPT)" ]
  ] [
fhir:code [ fhir:v "R436.1" ] ;
fhir:display [ fhir:v "Hereditary alpha tryptasaemia (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R438.1," ] ;
fhir:display [ fhir:v "Paediatric pseudo-obstruction syndrome (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R440.1" ] ;
fhir:display [ fhir:v "Hereditary isolated diabetes insipidus (Small panel)" ]
  ] [
fhir:code [ fhir:v "R441.1" ] ;
fhir:display [ fhir:v "Unexplained death in infancy and sudden unexplained death in childhood (WGS)" ]
  ] [
fhir:code [ fhir:v "R442.1" ] ;
fhir:display [ fhir:v "Variant Re-interpretation (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R443.1" ] ;
fhir:display [ fhir:v "Confirmation test (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R444.1" ] ;
fhir:display [ fhir:v "NICE approved PARP inhibitor treatment (Small panel)" ]
  ] [
fhir:code [ fhir:v "R444.2" ] ;
fhir:display [ fhir:v "NICE approved PARP inhibitor treatment (Small panel)" ]
  ] [
fhir:code [ fhir:v "R445.1" ] ;
fhir:display [ fhir:v "T21, T18 and T13 aneuploidy testing NIPT (previous history) (NIPT)" ]
  ] [
fhir:code [ fhir:v "R446.1" ] ;
fhir:display [ fhir:v "APOL1 kidney donor testing (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R447.1" ] ;
fhir:display [ fhir:v "Validation of WGS Diagnostic discovery (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R448.1" ] ;
fhir:display [ fhir:v "Prenatal testing (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R449.1" ] ;
fhir:display [ fhir:v "Diagnostic testing for Glutaric acidaemia I (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R45.1" ] ;
fhir:display [ fhir:v "Stickler syndrome (Small panel)" ]
  ] [
fhir:code [ fhir:v "R450.1" ] ;
fhir:display [ fhir:v "Diagnostic testing for Isovaleric acidaemia (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R451.1" ] ;
fhir:display [ fhir:v "Diagnostic testing for MCADD Medium-chain acyl-CoA dehydrogenase deficiency â€“ full ACADM sequencing (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R452.1" ] ;
fhir:display [ fhir:v "Silver russell syndrome and Temple Syndrome (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R453.1" ] ;
fhir:display [ fhir:v "Monogenic short stature (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R454.1" ] ;
fhir:display [ fhir:v "Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R456.1" ] ;
fhir:display [ fhir:v "Embryonal tumour of possible germline origin (WES or Medium panel)" ]
  ] [
fhir:code [ fhir:v "R456.2" ] ;
fhir:display [ fhir:v "Embryonal tumour of possible germline origin (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R457.1" ] ;
fhir:display [ fhir:v "Sarcoma of possible germline origin (Small panel)" ]
  ] [
fhir:code [ fhir:v "R458.1" ] ;
fhir:display [ fhir:v "Young onset or familial dementia (WGS)" ]
  ] [
fhir:code [ fhir:v "R459.1" ] ;
fhir:display [ fhir:v "Young onset or complex Parkinson disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R46.1" ] ;
fhir:display [ fhir:v "Congenital fibrosis of the extraocular muscles (Small panel)" ]
  ] [
fhir:code [ fhir:v "R460.1" ] ;
fhir:display [ fhir:v "Amyotrophic lateral sclerosis / Motor Neurone Disease (WGS)" ]
  ] [
fhir:code [ fhir:v "R461.1" ] ;
fhir:display [ fhir:v "Cerebral amyloid angiopathy (WGS)" ]
  ] [
fhir:code [ fhir:v "R462.1" ] ;
fhir:display [ fhir:v "Childhood interstitial lung disease (Medium panel)" ]
  ] [
fhir:code [ fhir:v "R463.1" ] ;
fhir:display [ fhir:v "Cytogenetic characterisation of a genomic abnormality â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R464.1" ] ;
fhir:display [ fhir:v "Recurrent miscarriage where products of conception are not available for testing parental karyotype (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R465.1" ] ;
fhir:display [ fhir:v "Familial cytogenetic rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R466.1" ] ;
fhir:display [ fhir:v "Unexplained infertility (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R467.1" ] ;
fhir:display [ fhir:v "Gamete donors (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R468.1" ] ;
fhir:display [ fhir:v "Possible sex chromosome aneuploidy or structural rearrangement â€“ Karyotype or Targeted Chromosome Analysis (Karyotype)" ]
  ] [
fhir:code [ fhir:v "R47.1" ] ;
fhir:display [ fhir:v "Angelman syndrome (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R471.1" ] ;
fhir:display [ fhir:v "Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing C9orf72 haplotype (Linkage analysis)" ]
  ] [
fhir:code [ fhir:v "R471.2" ] ;
fhir:display [ fhir:v "Neurodegenerative Disorders, adult onset  Prenatal Exclusion Testing SOD1 haplotype (Linkage analysis)" ]
  ] [
fhir:code [ fhir:v "R471.3" ] ;
fhir:display [ fhir:v "Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing MAPT haplotype (Linkage analysis)" ]
  ] [
fhir:code [ fhir:v "R471.4" ] ;
fhir:display [ fhir:v "Neurodegenerative Disorders, adult onset Prenatal Exclusion Testing PSEN1 haplotype (Linkage analysis)" ]
  ] [
fhir:code [ fhir:v "R48.1" ] ;
fhir:display [ fhir:v "Prader-Willi syndrome (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R49.1" ] ;
fhir:display [ fhir:v "Beckwith-Wiedemann syndrome (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R49.3" ] ;
fhir:display [ fhir:v "Beckwith-Wiedemann syndrome (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R50.1" ] ;
fhir:display [ fhir:v "Isolated hemihypertrophy or macroglossia (Methylation testing)" ]
  ] [
fhir:code [ fhir:v "R52.1" ] ;
fhir:display [ fhir:v "Short stature SHOX deficiency (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R52.2" ] ;
fhir:display [ fhir:v "Short stature SHOX deficiency (Single gene sequencing <10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R54.3" ] ;
fhir:display [ fhir:v "Hereditary ataxia with onset in adulthood (WGS)" ]
  ] [
fhir:code [ fhir:v "R54.4" ] ;
fhir:display [ fhir:v "Hereditary ataxia with onset in adulthood (RFC1 STR testing)" ]
  ] [
fhir:code [ fhir:v "R55.4" ] ;
fhir:display [ fhir:v "Hereditary ataxia with onset in childhood (WGS)" ]
  ] [
fhir:code [ fhir:v "R56.3" ] ;
fhir:display [ fhir:v "Adult onset dystonia, chorea or related movement disorder (WGS)" ]
  ] [
fhir:code [ fhir:v "R57.5" ] ;
fhir:display [ fhir:v "Childhood onset dystonia, chorea or related movement disorder (WGS)" ]
  ] [
fhir:code [ fhir:v "R60.3" ] ;
fhir:display [ fhir:v "Adult onset hereditary spastic paraplegia (WGS)" ]
  ] [
fhir:code [ fhir:v "R61.4" ] ;
fhir:display [ fhir:v "Childhood onset hereditary spastic paraplegia (WGS)" ]
  ] [
fhir:code [ fhir:v "R62.2" ] ;
fhir:display [ fhir:v "Adult onset leukodystrophy (WGS)" ]
  ] [
fhir:code [ fhir:v "R63.1" ] ;
fhir:display [ fhir:v "Possible mitochondrial disorder nuclear genes (WES or Large Panel)" ]
  ] [
fhir:code [ fhir:v "R64.1" ] ;
fhir:display [ fhir:v "MELAS or MIDD (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R65.1" ] ;
fhir:display [ fhir:v "Aminoglycoside exposure posing risk to hearing (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R66.1" ] ;
fhir:display [ fhir:v "Paroxysmal central nervous system disorders (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R67.1" ] ;
fhir:display [ fhir:v "Monogenic hearing loss (WES or Large Panel)" ]
  ] [
fhir:code [ fhir:v "R68.1" ] ;
fhir:display [ fhir:v "Huntington disease (STR testing)" ]
  ] [
fhir:code [ fhir:v "R69.5" ] ;
fhir:display [ fhir:v "Hypotonic infant  (WGS)" ]
  ] [
fhir:code [ fhir:v "R70.1" ] ;
fhir:display [ fhir:v "Spinal muscular atrophy type 1 diagnostic test (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R71.1" ] ;
fhir:display [ fhir:v "Spinal muscular atrophy type 1 rare variant testing (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R72.1" ] ;
fhir:display [ fhir:v "Myotonic dystrophy type 1 (STR testing)" ]
  ] [
fhir:code [ fhir:v "R73.1" ] ;
fhir:display [ fhir:v "Duchenne or Becker muscular dystrophy (Single gene sequencing >=10 amplicons)" ]
  ] [
fhir:code [ fhir:v "R73.2" ] ;
fhir:display [ fhir:v "Duchenne or Becker muscular dystrophy (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R74.1" ] ;
fhir:display [ fhir:v "Facioscapulohumeral muscular dystrophy (Other)" ]
  ] [
fhir:code [ fhir:v "R75.1" ] ;
fhir:display [ fhir:v "Oculopharyngeal muscular dystrophy (STR testing)" ]
  ] [
fhir:code [ fhir:v "R76.1" ] ;
fhir:display [ fhir:v "Skeletal muscle channelopathy (Small panel)" ]
  ] [
fhir:code [ fhir:v "R77.1" ] ;
fhir:display [ fhir:v "Hereditary neuropathy PMP22 copy number (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R78.4" ] ;
fhir:display [ fhir:v "Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (WGS)" ]
  ] [
fhir:code [ fhir:v "R78.5" ] ;
fhir:display [ fhir:v "Hereditary neuropathy or pain disorder â€“ NOT PMP22 copy number (RFC1 STR testing)" ]
  ] [
fhir:code [ fhir:v "R79.1" ] ;
fhir:display [ fhir:v "Congenital muscular dystrophy (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R80.1" ] ;
fhir:display [ fhir:v "Congenital myaesthenic syndrome (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R81.1" ] ;
fhir:display [ fhir:v "Congenital myopathy (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R82.1" ] ;
fhir:display [ fhir:v "Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R83.3" ] ;
fhir:display [ fhir:v "Arthrogryposis (WGS)" ]
  ] [
fhir:code [ fhir:v "R84.4" ] ;
fhir:display [ fhir:v "Cerebellar anomalies (WGS)" ]
  ] [
fhir:code [ fhir:v "R85.2" ] ;
fhir:display [ fhir:v "Holoprosencephaly (WGS)" ]
  ] [
fhir:code [ fhir:v "R86.3" ] ;
fhir:display [ fhir:v "Hydrocephalus (WGS)" ]
  ] [
fhir:code [ fhir:v "R87.3" ] ;
fhir:display [ fhir:v "Cerebral malformation (WGS)" ]
  ] [
fhir:code [ fhir:v "R88.3" ] ;
fhir:display [ fhir:v "Severe microcephaly (WGS)" ]
  ] [
fhir:code [ fhir:v "R89.3" ] ;
fhir:display [ fhir:v "Ultra-rare and atypical monogenic disorders (WGS)" ]
  ] [
fhir:code [ fhir:v "R90.1" ] ;
fhir:display [ fhir:v "Bleeding and platelet disorders (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R91.1" ] ;
fhir:display [ fhir:v "Cytopenia NOT Fanconi anaemia (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R91.2" ] ;
fhir:display [ fhir:v "Cytopenia NOT Fanconi anaemia (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R92.1" ] ;
fhir:display [ fhir:v "Rare anaemia (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R92.2" ] ;
fhir:display [ fhir:v "Rare anaemia (Small panel)" ]
  ] [
fhir:code [ fhir:v "R92.3" ] ;
fhir:display [ fhir:v "Rare anaemia (WES or Medium Panel)" ]
  ] [
fhir:code [ fhir:v "R93.1" ] ;
fhir:display [ fhir:v "Sickle cell, thalassaemia and other haemoglobinopathies (MLPA or equivalent)" ]
  ] [
fhir:code [ fhir:v "R93.2" ] ;
fhir:display [ fhir:v "Sickle cell, thalassaemia and other haemoglobinopathies (Small panel)" ]
  ] [
fhir:code [ fhir:v "R95.1" ] ;
fhir:display [ fhir:v "Iron overload hereditary haemochromatosis testing (Targeted variant testing)" ]
  ] [
fhir:code [ fhir:v "R96.1" ] ;
fhir:display [ fhir:v "Iron metabolism disorders NOT common HFE variants (Small panel)" ]
  ] [
fhir:code [ fhir:v "R97.1" ] ;
fhir:display [ fhir:v "Thrombophilia with a likely monogenic cause (WES or Small Panel)" ]
  ] [
fhir:code [ fhir:v "R98.2" ] ;
fhir:display [ fhir:v "Likely inborn error of metabolism (WGS)" ]
  ] [
fhir:code [ fhir:v "R98.3" ] ;
fhir:display [ fhir:v "Likely inborn error of metabolism (WES)" ]
  ] [
fhir:code [ fhir:v "R99.1" ] ;
fhir:display [ fhir:v "Common craniosynostosis syndromes (Small panel)" ]
  ] [
fhir:code [ fhir:v "R99.2" ] ;
fhir:display [ fhir:v "Common craniosynostosis syndromes (Exon level CNV detection by MLPA or equivalent)" ]
  ] ) . #