FHIR © HL7.org  |  FHIRsmith 4.0.1  |  Server Home  |  XIG Home  |  XIG Stats  | 

FHIR IG analytics

Packagehl7.fhir.uv.xver-r5.r4b
Resource TypeCodeSystem
IdCodeSystem-genomicstudy-changetype.json
FHIR VersionR4B
Sourcehttp://hl7.org/fhir/uv/xver-r5.r4b/0.0.1-snapshot-2/CodeSystem-genomicstudy-changetype.html
URLhttp://hl7.org/fhir/genomicstudy-changetype
Version5.0.0
Statusactive
Date2022-08-18T06:48:24+10:00
NameGenomicStudyChangeType
TitleGenomic Study Change Type
Realmuv
Authorityhl7
DescriptionThe change type relevant to GenomicStudy analysis.
Contentcomplete

Resources that use this resource

ValueSet
R5-genomicstudy-changetype-for-R4BCross-version VS for R5.GenomicStudyChangeType for use in FHIR R4B
R5-genomicstudy-changetype-for-R4Cross-version VS for R5.GenomicStudyChangeType for use in FHIR R4

Resources that this resource uses

No resources found

Narrative

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

This code system http://hl7.org/fhir/genomicstudy-changetype defines the following codes:

Code Display Definition
DNA DNA change Change that involves Deoxyribonucleic acid (DNA) sequences.
RNA RNA change Change that involves Ribonucleic Acid (RNA) sequences.
AA Protein/amino Acids change Change that involves Amino Acid (AA) or protein sequences.
CHR Chromosomal changes Change that involves number or strcture of chromosomes.
CNV Copy number variations Change that involves copy number variations among various genomes.

Source1

{
  "resourceType": "CodeSystem",
  "id": "genomicstudy-changetype",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode": "trial-use"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
      "valueInteger": 1
    },
    {
      "extension": [
        {
          "url": "packageId",
          "valueId": "hl7.fhir.uv.xver-r5.r4b"
        },
        {
          "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."
    }
  ]
}