FHIR Cross-Version Extensions package for FHIR R4 from FHIR R5 - Version 0.0.1-snapshot-2. See the Directory of published versions

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: Genomic Study Change Type - JSON Representation

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{
  "resourceType" : "CodeSystem",
  "id" : "genomicstudy-changetype",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\">\n            <p>This code system \n              <code>http://hl7.org/fhir/genomicstudy-changetype</code> defines the following codes:\n            </p>\n            <table class=\"codes\">\n              <tr>\n                <td style=\"white-space:nowrap\">\n                  <b>Code</b>\n                </td>\n                <td>\n                  <b>Display</b>\n                </td>\n                <td>\n                  <b>Definition</b>\n                </td>\n              </tr>\n              <tr>\n                <td style=\"white-space:nowrap\">DNA\n                  <a name=\"genomicstudy-changetype-DNA\"> </a>\n                </td>\n                <td>DNA change</td>\n                <td>Change that involves Deoxyribonucleic acid (DNA) sequences.</td>\n              </tr>\n              <tr>\n                <td style=\"white-space:nowrap\">RNA\n                  <a name=\"genomicstudy-changetype-RNA\"> </a>\n                </td>\n                <td>RNA change</td>\n                <td>Change that involves Ribonucleic Acid (RNA) sequences.</td>\n              </tr>\n              <tr>\n                <td style=\"white-space:nowrap\">AA\n                  <a name=\"genomicstudy-changetype-AA\"> </a>\n                </td>\n                <td>Protein/amino Acids change </td>\n                <td>Change that involves Amino Acid (AA) or protein sequences.</td>\n              </tr>\n              <tr>\n                <td style=\"white-space:nowrap\">CHR\n                  <a name=\"genomicstudy-changetype-CHR\"> </a>\n                </td>\n                <td>Chromosomal changes</td>\n                <td>Change that involves number or strcture of chromosomes.</td>\n              </tr>\n              <tr>\n                <td style=\"white-space:nowrap\">CNV\n                  <a name=\"genomicstudy-changetype-CNV\"> </a>\n                </td>\n                <td>Copy number variations</td>\n                <td>Change that involves copy number variations among various genomes.</td>\n              </tr>\n            </table>\n          </div>"
  },
  "extension" : [
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode" : "informative"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
      "valueInteger" : 1
    },
    {
      "extension" : [
        {
          "url" : "packageId",
          "valueId" : "hl7.fhir.uv.xver-r5.r4"
        },
        {
          "url" : "version",
          "valueString" : "0.0.1-snapshot-2"
        }
      ],
      "url" : "http://hl7.org/fhir/StructureDefinition/package-source"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode" : "cg"
    }
  ],
  "url" : "http://hl7.org/fhir/genomicstudy-changetype",
  "version" : "5.0.0",
  "name" : "GenomicStudyChangeType",
  "title" : "Genomic Study Change Type",
  "status" : "active",
  "experimental" : true,
  "date" : "2022-08-18T06:48:24+10:00",
  "publisher" : "Clinical Genomics",
  "contact" : [
    {
      "name" : "Clinical Genomics",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://www.hl7.org/Special/committees/clingenomics"
        }
      ]
    }
  ],
  "description" : "The change type relevant to GenomicStudy analysis.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001",
          "display" : "World"
        }
      ]
    }
  ],
  "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."
    }
  ]
}