FHIR © HL7.org  |  Server Home  |  XIG Home  |  XIG Stats  |  Server Source  |  FHIR  

FHIR IG Statistics: CodeSystem/genomic-study-change-type-cs

Packagehl7.fhir.uv.genomics-reporting
Resource TypeCodeSystem
Idgenomic-study-change-type-cs
FHIR VersionR4
Sourcehttp://hl7.org/fhir/uv/genomics-reporting/https://build.fhir.org/ig/HL7/genomics-reporting/CodeSystem-genomic-study-change-type-cs.html
URLhttp://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs
Version4.0.0-ballot
Statusactive
Date2025-06-24T17:31:37+00:00
NameGenomicStudyChangeTypeCS
TitleGenomic Study Change Type CodeSystem
Realmuv
Authorityhl7
DescriptionBackport of http://hl7.org/fhir/genomicstudy-changetype
Contentcomplete

Resources that use this resource

ValueSet
genomic-study-change-type-vsGenomic 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": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "cg"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode": "informative",
      "_valueCode": {
        "extension": [
          {
            "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-conformance-derivedFrom",
            "valueCanonical": "http://hl7.org/fhir/uv/genomics-reporting/ImplementationGuide/genomics-reporting"
          }
        ]
      }
    }
  ],
  "url": "http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-change-type-cs",
  "version": "4.0.0-ballot",
  "name": "GenomicStudyChangeTypeCS",
  "title": "Genomic Study Change Type CodeSystem",
  "status": "active",
  "experimental": true,
  "date": "2025-06-24T17:31:37+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."
    }
  ]
}