{
  "description": "Value Set for terms that describe a predicted ramification based on the presence of associated molecular finding(s).",
  "compose": {
    "include": [ {
      "system": "http://loinc.org",
      "concept": [ {
        "code": "LA10315-2",
        "display": "Ultrarapid metabolizer"
      }, {
        "code": "LA25391-6",
        "display": "Normal metabolizer"
      }, {
        "code": "LA25390-8",
        "display": "Rapid metabolizer"
      }, {
        "code": "LA10317-8",
        "display": "Intermediate metabolizer"
      }, {
        "code": "LA9657-3",
        "display": "Poor metabolizer"
      }, {
        "code": "LA19542-2",
        "display": "Low Risk"
      }, {
        "code": "LA19541-4",
        "display": "High Risk"
      }, {
        "code": "LA6676-6",
        "display": "Resistant"
      }, {
        "code": "LA6677-4",
        "display": "Responsive"
      }, {
        "code": "LA9660-7",
        "display": "Presumed resistant"
      }, {
        "code": "LA9661-5",
        "display": "Presumed responsive"
      }, {
        "code": "LA6682-4",
        "display": "Unknown Significance"
      }, {
        "code": "LA6675-8",
        "display": "Benign"
      }, {
        "code": "LA6674-1",
        "display": "Presumed Benign"
      }, {
        "code": "LA9662-3",
        "display": "Presumed non-responsive"
      }, {
        "code": "LA25392-4",
        "display": "Increased function"
      }, {
        "code": "LA25393-2",
        "display": "Normal function"
      }, {
        "code": "LA25395-7",
        "display": "Decreased function"
      }, {
        "code": "LA25394-0",
        "display": "Poor function"
      } ]
    }, {
      "system": "http://snomed.info/sct",
      "concept": [ {
        "code": "444734003",
        "display": "Does not meet eligibility criteria for clinical trial (finding)"
      }, {
        "code": "399223003",
        "display": "Patient eligible for clinical trial (finding)"
      } ]
    } ]
  },
  "_filename": "ValueSet-genetic-therapeutic-implications-vs.json",
  "package_name": "hl7.fhir.uv.genomics-reporting",
  "date": "2022-05-09T16:53:07+00:00",
  "publisher": "HL7 Clinical Genomics Working Group",
  "jurisdiction": [ {
    "coding": [ {
      "code": "001",
      "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
      "display": "World"
    } ]
  } ],
  "name": "GeneticTherapeuticImplicationsVS",
  "copyright": "This material contains content from LOINC (http://loinc.org). LOINC is copyright © 1995-2020, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license. LOINC® is a registered United States trademark of Regenstrief Institute, Inc.\nThis value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement.",
  "type": null,
  "experimental": null,
  "resourceType": "ValueSet",
  "title": "Genetic Therapeutic Implications",
  "package_version": "2.0.0",
  "status": "active",
  "id": "e892324d-37ae-492c-a4a7-58ee8c928eab",
  "kind": null,
  "url": "http://hl7.org/fhir/uv/genomics-reporting/ValueSet/genetic-therapeutic-implications-vs",
  "version": "2.0.0",
  "contact": [ {
    "name": "HL7 Clinical Genomics Working Group",
    "telecom": [ {
      "value": "http://www.hl7.org/Special/committees/clingenomics",
      "system": "url"
    }, {
      "value": "cg@lists.HL7.org",
      "system": "email"
    } ]
  } ]
}