Birth Defects Reporting - STU1
0.1.2 - draft United States of America flag

Birth Defects Reporting - STU1, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 0.1.2 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-birthdefectsreporting-ig/ and changes regularly. See the Directory of published versions

: ReportableDiagnosisExample - XML Representation

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<Condition xmlns="http://hl7.org/fhir">
  <id value="ReportableDiagnosisExample"/>
  <meta>
    <profile
             value="http://hl7.org/fhir/us/birthdefectreporting/StructureDefinition/bdr-reportablediagnosis"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: Condition ReportableDiagnosisExample</b></p><a name="ReportableDiagnosisExample"> </a><a name="hcReportableDiagnosisExample"> </a><a name="ReportableDiagnosisExample-en-US"> </a><p><b>clinicalStatus</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}">Active</span></p><p><b>verificationStatus</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-ver-status confirmed}">Confirmed</span></p><p><b>category</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-category encounter-diagnosis}">Encounter Diagnosis</span></p><p><b>code</b>: <span title="Codes:{http://snomed.info/sct 719046005}">12q14 microdeletion syndrome (disorder)</span></p><p><b>subject</b>: <a href="Patient-PatientChildExample.html">Gene Austin Wellington (official) Male, DoB: 2020-04-28 ( Medical record number)</a></p><p><b>onset</b>: 2020-07-15</p><h3>Evidences</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Detail</b></td></tr><tr><td style="display: none">*</td><td><a href="Procedure-ConfirmatoryTestExampleWES.html">Procedure Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis</a></td></tr></table></div>
  </text>
  <clinicalStatus>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-clinical"/>
      <code value="active"/>
      <display value="Active"/>
    </coding>
  </clinicalStatus>
  <verificationStatus>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-ver-status"/>
      <code value="confirmed"/>
      <display value="Confirmed"/>
    </coding>
  </verificationStatus>
  <category>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-category"/>
      <code value="encounter-diagnosis"/>
    </coding>
  </category>
  <code>
    <coding>
      <system value="http://snomed.info/sct"/>
      <code value="719046005"/>
      <display value="12q14 microdeletion syndrome (disorder)"/>
    </coding>
  </code>
  <subject>🔗 
    <reference value="Patient/PatientChildExample"/>
  </subject>
  <onsetDateTime value="2020-07-15"/>
  <evidence>
    <detail>🔗 
      <reference value="Procedure/ConfirmatoryTestExampleWES"/>
    </detail>
  </evidence>
</Condition>