DSTU2

This page is part of the FHIR Specification (v1.0.2: DSTU 2). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

Obs-genetics-example1-somatic.xml

Raw XML (canonical form)

Genetics Observation of Somatic Variant in Lung Cancer (id = "genetics-example1-somatic")

<Observation xmlns="http://hl7.org/fhir">
    <id value="genetics-example1-somatic"/>
    <text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: genetics-example1-somatic</p><p><b>contained</b>: </p><p><b>status</b>: final</p><p><b>code</b>: Genetic analysis master panel ­Blood or Tissue by Molecular genetics method <span>(Details : {LOINC code '55233-1' = 'Genetic analysis master panel - Blood or Tissue by
           Molecular genetics method', given as 'Genetic analysis master panel ­Blood or Tissue by
           Molecular genetics method'})</span></p><p><b>subject</b>: <a>Molecular Lab Patient ID: HOSP-23456</a></p><p><b>performer</b>: <a>Molecular Diagnostic Laboratory</a></p><p><b>interpretation</b>: positive <span>(Details : {http://hl7.org/fhir/v2/0078 code 'POS' = 'Positive)</span></p><p><b>comments</b>: The EGFR p.L858R mutation has been associated with response to anti-EGFR therapy</p><p><b>specimen</b>: <a>Molecular Specimen ID: MLD45-Z4-1234</a></p></div></text><contained>
        <Condition>
            <id value="c1"/>
            <patient>
                <reference value="Patient/p1"/>
            </patient>
            <code>
                <coding>
                    <system value="http://snomed.info/sct"/>
                    <code value="254626006"/>
                </coding>
                <text value="Adenocarcinoma of lung "/>
            </code>
            <category>
                <coding>
                    <system value="http://hl7.org/fhir/condition-category"/>
                    <code value="finding"/>
                    <display value="Finding"/>
                </coding>
            </category>
            <verificationStatus value="provisional"/>
        </Condition>
    </contained>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsGenomeBuild">
        <valueString value="GRCh 37"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsChromosome">
        <valueCodeableConcept>
            <coding>
                <system value="http://www.ncbi.nlm.nih.gov/gene"/>
                <code value="NC_000007"/>
            </coding>
            <text value="Homo sapiens chromosome 7"/>
        </valueCodeableConcept>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsGenomicStart">
        <valueInteger value="55259515"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsGenomicStop">
        <valueInteger value="55259516"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsSpecies">
        <valueCodeableConcept>
            <coding>
                <system value="http://snomed.info/sct"/>
                <code value="337915000"/>
            </coding>
            <text value="Homo sapiens"/>
        </valueCodeableConcept>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsCIGAR">
        <valueString value="1M"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsAssessedCondition">
        <valueReference>
            <reference value="#c1"/>
        </valueReference>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsReferenceAllele">
        <valueString value="T"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsObservedAllele">
        <valueString value="G"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsGene">
        <valueCodeableConcept>
            <coding>
                <system value="http://www.genenames.org"/>
                <code value="3236"/>
                <display value="EGFR"/>
            </coding>
        </valueCodeableConcept>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsTranscriptReferenceSequenceId">
        <valueCodeableConcept>
            <coding>
                <system value="http://www.ensembl.org"/>
                <code value="ENSESTT00000085772.1"/>
            </coding>
        </valueCodeableConcept>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsDNASequenceVariation">
        <valueString value="c.2573T&gt;G"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsDNASequenceVariationType">
        <valueCodeableConcept>
            <coding>
                <system value="http://loinc.org"/>
                <code value="LA6690-7"/>
                <display value="Substitution"/>
            </coding>
        </valueCodeableConcept>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsAminoAcidChange">
        <valueString value="p.Leu858Arg"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsAlleleName">
        <valueString value="p.L858R"/>
    </extension>
    <extension url="http://hl7.org/fhir/StructureDefinition/geneticsGenomicSourceClass">
        <valueCodeableConcept>
            <coding>
                <system value="http://loinc.org"/>
                <code value="LA6684-0"/>
                <display value="Somatic"/>
            </coding>
        </valueCodeableConcept>
    </extension>


    <status value="final"/>
    <code>
        <coding>
            <system value="http://loinc.org"/>
            <code value="55233-1"/>
            <display value="Genetic analysis master panel ­Blood or Tissue by Molecular genetics method"/>
        </coding>
    </code>
    <subject>
        <reference value="Patient/genetics-example1-somatic"/>
        <display value="Molecular Lab Patient ID: HOSP-23456"/>
    </subject>
    <performer>
        <reference value="Practitioner/genetics-example1-somatic"/>
        <display value="Molecular Diagnostic Laboratory"/>
    </performer>
    <interpretation>
        <coding>
            <system value="http://hl7.org/fhir/v2/0078"/>
            <code value="POS"/>
        </coding>
        <text value="positive"/>
    </interpretation>
    <comments value="The EGFR p.L858R mutation has been associated with response to anti-EGFR therapy"/>
    <specimen>
        <reference value="Specimen/genetics-example1-somatic"/>
        <display value="Molecular Specimen ID: MLD45-Z4-1234"/>
    </specimen>
    

    

</Observation>

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.