This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.0.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
{
"resourceType" : "ValueSet",
"id" : "mcode-genomic-molecular-consequence-vs",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include codes from <code>http://www.sequenceontology.org/</code> where concept descends from SO:0001537</li></ul></div>"
},
"url" : "http://hl7.org/fhir/us/mcode/ValueSet/mcode-genomic-molecular-consequence-vs",
"version" : "2.0.0",
"name" : "GenomicMolecularConsequenceVS",
"title" : "Genomic Molecular Consequence Value Set",
"status" : "active",
"date" : "2022-01-18T03:17:40+00:00",
"publisher" : "HL7 International Clinical Interoperability Council",
"contact" : [
{
"name" : "HL7 International Clinical Interoperability Council",
"telecom" : [
{
"system" : "url",
"value" : "http://www.hl7.org/Special/committees/cic"
},
{
"system" : "email",
"value" : "ciclist@lists.HL7.org"
}
]
}
],
"description" : "Changes in a structural features of a sequence due to the observed variant.",
"jurisdiction" : [
{
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US",
"display" : "United States of America"
}
]
}
],
"compose" : {
"include" : [
{
"system" : "http://www.sequenceontology.org/",
"filter" : [
{
"property" : "concept",
"op" : "descendent-of",
"value" : "SO:0001537"
}
]
}
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}
}