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Definition for Code SystemGenomicStudyChangeType
{
"resourceType" : "CodeSystem",
"id" : "genomicstudy-changetype",
"meta" : {
"lastUpdated" : "2024-10-02T12:31:51.554-05:00",
"profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem genomicstudy-changetype</b></p><a name=\"genomicstudy-changetype\"> </a><a name=\"hcgenomicstudy-changetype\"> </a><a name=\"genomicstudy-changetype-en-US\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Last updated: 2022-08-17T15:47:24.148-05:00</p><p style=\"margin-bottom: 0px\">Profile: <a href=\"shareablecodesystem.html\">Shareable CodeSystem</a></p></div><p>This case-sensitive code system <code>http://hl7.org/fhir/genomicstudy-changetype</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style=\"white-space:nowrap\">DNA<a name=\"genomicstudy-changetype-DNA\"> </a></td><td>DNA change</td><td>Change that involves Deoxyribonucleic acid (DNA) sequences.</td></tr><tr><td style=\"white-space:nowrap\">RNA<a name=\"genomicstudy-changetype-RNA\"> </a></td><td>RNA change</td><td>Change that involves Ribonucleic Acid (RNA) sequences.</td></tr><tr><td style=\"white-space:nowrap\">AA<a name=\"genomicstudy-changetype-AA\"> </a></td><td>Protein/amino Acids change </td><td>Change that involves Amino Acid (AA) or protein sequences.</td></tr><tr><td style=\"white-space:nowrap\">CHR<a name=\"genomicstudy-changetype-CHR\"> </a></td><td>Chromosomal changes</td><td>Change that involves number or strcture of chromosomes.</td></tr><tr><td style=\"white-space:nowrap\">CNV<a name=\"genomicstudy-changetype-CNV\"> </a></td><td>Copy number variations</td><td>Change that involves copy number variations among various genomes.</td></tr></table></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" : 1
}],
"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" : "6.0.0-ballot2",
"name" : "GenomicStudyChangeType",
"title" : "Genomic Study Change Type",
"status" : "active",
"experimental" : true,
"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.",
"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."
}]
}
Usage note: every effort has been made to ensure that the
examples are correct and useful, but they are not a normative part
of the specification.