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Resource CodeSystem/FHIR Server from package hl7.fhir.uv.genomics-reporting#current (172 ms)

Package hl7.fhir.uv.genomics-reporting
Type CodeSystem
Id Id
FHIR Version R4
Source http://hl7.org/fhir/uv/genomics-reporting/https://build.fhir.org/ig/HL7/genomics-reporting/CodeSystem-genomic-study-change-type-cs.html
Url http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs
Version 3.0.1-SNAPSHOT
Status active
Date 2024-10-03T13:33:58+00:00
Name GenomicStudyChangeTypeCS
Title Genomic Study Change Type CodeSystem
Experimental True
Realm uv
Authority hl7
Description Backport of http://hl7.org/fhir/genomicstudy-changetype
Content complete

Resources that use this resource

ValueSet
genomic-study-change-type-vs Genomic Study Change Type ValueSet

Resources that this resource uses

No resources found



Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: CodeSystem genomic-study-change-type-cs

This case-sensitive code system http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs defines the following codes:

CodeDisplayDefinition
DNA DNA changeChange that involves Deoxyribonucleic acid (DNA) sequences.
RNA RNA changeChange that involves Ribonucleic Acid (RNA) sequences.
AA Protein/amino Acids changeChange that involves Amino Acid (AA) or protein sequences.
CHR Chromosomal changesChange that involves number or strcture of chromosomes.
CNV Copy number variationsChange that involves copy number variations among various genomes.

Source

{
  "resourceType" : "CodeSystem",
  "id" : "genomic-study-change-type-cs",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem genomic-study-change-type-cs</b></p><a name=\"genomic-study-change-type-cs\"> </a><a name=\"hcgenomic-study-change-type-cs\"> </a><a name=\"genomic-study-change-type-cs-en-US\"> </a><p>This case-sensitive code system <code>http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs</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=\"genomic-study-change-type-cs-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=\"genomic-study-change-type-cs-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=\"genomic-study-change-type-cs-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=\"genomic-study-change-type-cs-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=\"genomic-study-change-type-cs-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/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs",
  "version" : "3.0.1-SNAPSHOT",
  "name" : "GenomicStudyChangeTypeCS",
  "title" : "Genomic Study Change Type CodeSystem",
  "status" : "active",
  "experimental" : true,
  "date" : "2024-10-03T13:33:58+00:00",
  "publisher" : "HL7 International / Clinical Genomics",
  "contact" : [
    {
      "name" : "HL7 International / Clinical Genomics",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://www.hl7.org/Special/committees/clingenomics"
        },
        {
          "system" : "email",
          "value" : "cg@lists.HL7.org"
        }
      ]
    }
  ],
  "description" : "Backport of http://hl7.org/fhir/genomicstudy-changetype",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001",
          "display" : "World"
        }
      ]
    }
  ],
  "caseSensitive" : true,
  "content" : "complete",
  "count" : 5,
  "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."
    }
  ]
}

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