http://hl7.org/fhir/genomicstudy-changetype|5.0.0

{
  "description" : "The change type relevant to GenomicStudy analysis.",
  "compose" : null,
  "package" : "hl7.fhir.r5.core@5.0.0",
  "date" : "2022-08-17T20:48:24Z",
  "meta" : {
    "profile" : [ "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ],
    "lastUpdated" : "2023-03-25T23:21:02.749-05:00"
  },
  "publisher" : "HL7 (FHIR Project)",
  "jurisdiction" : [ {
    "coding" : [ {
      "code" : "001",
      "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
      "display" : "World"
    } ]
  } ],
  "content" : "complete",
  "name" : "GenomicStudyChangeType",
  "experimental" : true,
  "resourceType" : "CodeSystem",
  "title" : "Genomic Study Change Type",
  "supliment" : null,
  "extension" : [ {
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
    "valueCode" : "cg"
  }, {
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
    "valueCode" : "trial-use"
  }, {
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
    "valueInteger" : 1
  } ],
  "status" : "active",
  "id" : "75e3ffa5-1e85-59ab-bb88-785e7d05be90",
  "valueSet" : "http://hl7.org/fhir/ValueSet/genomicstudy-changetype",
  "url" : "http://hl7.org/fhir/genomicstudy-changetype",
  "identifier" : [ {
    "value" : "urn:oid:2.16.840.1.113883.4.642.4.1977",
    "system" : "urn:ietf:rfc:3986"
  } ],
  "concept" : [ {
    "code" : "DNA",
    "display" : "DNA change",
    "definition" : "Change that involves Deoxyribonucleic acid (DNA) sequences."
  }, {
    "code" : "RNA",
    "display" : "RNA change",
    "definition" : "Change that involves Ribonucleic Acid (RNA) sequences."
  }, {
    "code" : "AA",
    "display" : "Protein/amino Acids change ",
    "definition" : "Change that involves Amino Acid (AA) or protein sequences."
  }, {
    "code" : "CHR",
    "display" : "Chromosomal changes",
    "definition" : "Change that involves number or strcture of chromosomes."
  }, {
    "code" : "CNV",
    "display" : "Copy number variations",
    "definition" : "Change that involves copy number variations among various genomes."
  } ],
  "caseSensitive" : true,
  "version" : "5.0.0",
  "contact" : [ {
    "telecom" : [ {
      "value" : "http://hl7.org/fhir",
      "system" : "url"
    }, {
      "value" : "fhir@lists.hl7.org",
      "system" : "email"
    } ]
  } ]
}