Definition for Code SystemGenomicStudyChangeType

{
  "resourceType" : "CodeSystem",
  "id" : "genomicstudy-changetype",
  "meta" : {
    "lastUpdated" : "2022-09-06T19:58:29.429-05:00",
    "profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div>!-- Snipped for Brevity --></div>"
  },
  "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" : 0
  }],
  "url" : "http://hl7.org/fhir/genomicstudy-changetype",
  "identifier" : [{
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113883.4.642.4.1977"
  }],
  "version" : "5.0.0-ballot",
  "name" : "GenomicStudyChangeType",
  "title" : "GenomicStudyChangeType",
  "status" : "draft",
  "experimental" : false,
  "date" : "2022-08-17T15:48:24-05:00",
  "publisher" : "HL7 (FHIR Project)",
  "contact" : [{
    "telecom" : [{
      "system" : "url",
      "value" : "http://hl7.org/fhir"
    },
    {
      "system" : "email",
      "value" : "fhir@lists.hl7.org"
    }]
  }],
  "description" : "The change type relevant to GenomicStudy analysis.",
  "caseSensitive" : true,
  "valueSet" : "http://hl7.org/fhir/ValueSet/genomicstudy-changetype",
  "content" : "complete",
  "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."
  }]
}