Genomic Sequence Analysis Panel_EGFR

{
  "description" : "Clone of value set Genomic Sequence Analysis Panel to avoid duplication in NSCLC biomarker measure 2021",
  "compose" : {
    "exclude" : [ ],
    "include" : [ {
      "system" : "http://www.ama-assn.org/go/cpt",
      "extension" : [ {
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          "url" : "path"
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        "url" : "http://health-samurai.io/extensions/excised-data"
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  "date" : "2020-11-11T01:00:26-05:00",
  "meta" : {
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    "lastUpdated" : "2020-11-11T01:00:26.000-05:00",
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      "valueString" : "UNKNOWN",
      "url" : "http://hl7.org/fhir/StructureDefinition/data-absent-reason"
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  "purpose" : "(Clinical Focus: Targeted genomic sequence analysis panel, solid organ neoplasm, DNA analysis and RNA analysis when performed),(Data Element Scope: CPT Codes for targeted genomic sequence analysis panels, any number of genes >5),(Inclusion Criteria: Genomic sequence analysis panels, any genes, any number of genes > 5),(Exclusion Criteria: Analysis of individual genes; non-solid organ neoplasms (ie blood cancers))",
  "name" : "GenomicSequenceAnalysisPanel_EGFR",
  "experimental" : false,
  "resourceType" : "ValueSet",
  "expansion" : {
    "contains" : [ {
      "system" : "http://www.ama-assn.org/go/cpt",
      "code" : "81445",
      "display" : "Targeted genomic sequence analysis panel, solid organ neoplasm, 5-50 genes (eg, ALK, BRAF, CDKN2A, EGFR, ERBB2, KIT, KRAS, MET, NRAS, PDGFRA, PDGFRB, PGR, PIK3CA, PTEN, RET), interrogation for sequence variants and copy number variants or rearrangements, if performed; DNA analysis or combined DNA and RNA analysis",
      "version" : "2023"
    }, {
      "system" : "http://www.ama-assn.org/go/cpt",
      "code" : "81455",
      "display" : "Targeted genomic sequence analysis panel, solid organ or hematolymphoid neoplasm or disorder, 51 or greater genes (eg, ALK, BRAF, CDKN2A, CEBPA, DNMT3A, EGFR, ERBB2, EZH2, FLT3, IDH1, IDH2, JAK2, KIT, KRAS, MET, MLL, NOTCH1, NPM1, NRAS, PDGFRA, PDGFRB, PGR, PIK3CA, PTEN, RET), interrogation for sequence variants and copy number variants or rearrangements, or isoform expression or mRNA expression levels, if performed; DNA analysis or combined DNA and RNA analysis",
      "version" : "2023"
    } ],
    "offset" : 0,
    "total" : 2,
    "identifier" : "urn:uuid:8ceeec74-64ff-4b63-9da5-a018adcd41e9",
    "timestamp" : "2023-06-29T17:32:31-04:00",
    "parameter" : [ {
      "name" : "count",
      "valueInteger" : 1000
    }, {
      "name" : "offset",
      "valueInteger" : 0
    } ]
  },
  "title" : "Genomic Sequence Analysis Panel_EGFR",
  "extension" : [ {
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  }, {
    "valueDate" : "2022-12-15",
    "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate"
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    "valueDate" : "2020-11-11",
    "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate"
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  "status" : "active",
  "id" : "ae351e74-8bd3-4f5b-821f-91ae163955f5",
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1131.19",
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    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113762.1.4.1131.19"
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  "version" : "20201111"
}