FHIR IG analytics| Package | hl7.fhir.uv.cg-incubator |
| Resource Type | CodeSystem |
| Id | CodeSystem-genomicstudy-changetype.json |
| FHIR Version | R6 |
| Source | https://build.fhir.org/ig/HL7/cg-incubator/CodeSystem-genomicstudy-changetype.html |
| URL | http://hl7.org/fhir/genomicstudy-changetype |
| Version | 0.1.0 |
| Status | draft |
| Date | 2022-08-17T15:48:24-05:00 |
| Name | GenomicStudyChangeType |
| Title | Genomic Study Change Type |
| Realm | uv |
| Authority | hl7 |
| Description | The change type relevant to GenomicStudy analysis. |
| Content | complete |
| ValueSet | |
| genomicstudy-changetype-vs | Genomic Study Change Type VS |
| R5-genomicstudy-changetype-for-R4B | Cross-version VS for R5.GenomicStudyChangeType for use in FHIR R4B |
| R5-genomicstudy-changetype-for-R4 | Cross-version VS for R5.GenomicStudyChangeType for use in FHIR R4 |
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: CodeSystem genomicstudy-changetype
Last updated: 2022-08-17 15:47:24-0500
Profile: Shareable CodeSystem
This case-sensitive code system http://hl7.org/fhir/genomicstudy-changetype defines the following codes:
{
"resourceType": "CodeSystem",
"id": "genomicstudy-changetype",
"meta": {
"lastUpdated": "2022-08-17T15:47:24.148-05:00",
"profile": [
"http://hl7.org/fhir/StructureDefinition/shareablecodesystem"
]
},
"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": "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": "0.1.0",
"name": "GenomicStudyChangeType",
"title": "Genomic Study Change Type",
"status": "draft",
"experimental": true,
"date": "2022-08-17T15:48:24-05:00",
"publisher": "HL7 International / Clinical Genomics",
"contact": [
{
"name": "HL7 International / Clinical Genomics",
"telecom": [
{
"system": "url",
"value": "http://www.hl7.org/Special/committees/cg"
},
{
"system": "email",
"value": "clingenomics@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."
}
]
}