Antepartum Summary
0.0.1-current - ci-build

Antepartum Summary, published by IHE Patient Care Coordination Committee. This is not an authorized publication; it is the continuous build for version 0.0.1-current). This version is based on the current content of https://github.com/IHE/PCC.APS/ and changes regularly. See the Directory of published versions

## : Antepartum Family History and Genetic Screening - XML Representation

Draft as of 2023-10-24

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    <ValueSet xmlns="http://hl7.org/fhir">
      <id value="Antepartum.Family.History.and.Genetic.Screening.VS"/>
      <text>
        <status value="generated"/>
        <div xmlns="http://www.w3.org/1999/xhtml"><ul><li>Include these codes as defined in <a href="http://www.snomed.org/"><code>http://snomed.info/sct</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href="http://snomed.info/id/408856003">408856003</a></td><td>Autism</td></tr><tr><td><a href="http://snomed.info/id/414022008">414022008</a></td><td>Blood Disorders</td></tr><tr><td><a href="http://snomed.info/id/80544005">80544005</a></td><td>Canavan Disease</td></tr><tr><td><a href="http://snomed.info/id/409709004">409709004</a></td><td>Chromosomal Disorder Includes any inherited genetic or chromosomal disorders</td></tr><tr><td><a href="http://snomed.info/id/13213009">13213009</a></td><td>Congenital Heart Defect</td></tr><tr><td><a href="http://snomed.info/id/190905008">190905008</a></td><td>Cystic Fibrosis</td></tr><tr><td><a href="http://snomed.info/id/276720006">276720006</a></td><td>Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects</td></tr><tr><td><a href="http://snomed.info/id/41040004">41040004</a></td><td>Down Syndrome</td></tr><tr><td><a href="http://snomed.info/id/29159009">29159009</a></td><td>Familial Dysautonomia</td></tr><tr><td><a href="http://snomed.info/id/90935002">90935002</a></td><td>Hemophilia</td></tr><tr><td><a href="http://snomed.info/id/58756001">58756001</a></td><td>Huntington's Chorea</td></tr><tr><td><a href="http://snomed.info/id/75934005">75934005</a></td><td>Maternal Metabolic Disorder</td></tr><tr><td><a href="http://snomed.info/id/91138005">91138005</a></td><td>Mental Retardation</td></tr><tr><td><a href="http://snomed.info/id/73297009">73297009</a></td><td>Muscular Dystrophy</td></tr><tr><td><a href="http://snomed.info/id/253098009">253098009</a></td><td>Neural Tube Defect</td></tr><tr><td><a href="http://snomed.info/id/102878001">102878001</a></td><td>Recurrent pregnancy loss/stillbirth</td></tr><tr><td><a href="http://snomed.info/id/417357006">417357006</a></td><td>Sickle Cell Disease</td></tr><tr><td><a href="http://snomed.info/id/16402000">16402000</a></td><td>Sickle Cell Trait</td></tr><tr><td><a href="http://snomed.info/id/111385000">111385000</a></td><td>Tay-Sachs</td></tr><tr><td><a href="http://snomed.info/id/40108008">40108008</a></td><td>Thalassemia</td></tr></table></li></ul></div>
      </text>
      <url
           value="https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS"/>
      <version value="0.0.1-current"/>
      <name value="Antepartum_Family_History_and_Genetic_Screening_VS"/>
      <title value="Antepartum Family History and Genetic Screening"/>
      <status value="draft"/>
      <experimental value="false"/>
      <date value="2023-10-24T22:43:25+00:00"/>
      <publisher value="IHE Patient Care Coordination Committee"/>
      <contact>
        <telecom>
          <system value="url"/>
          <value
                 value="https://www.ihe.net/ihe_domains/patient_care_coordination/"/>
        </telecom>
      </contact>
      <contact>
        <telecom>
          <system value="email"/>
          <value value="pcc@ihe.net"/>
        </telecom>
      </contact>
      <contact>
        <name value="IHE Patient Care Coordination Committee"/>
        <telecom>
          <system value="email"/>
          <value value="pcc@ihe.net"/>
        </telecom>
      </contact>
      <description value="TBD"/>
      <jurisdiction>
        <coding>
          <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
          <code value="001"/>
        </coding>
      </jurisdiction>
      <compose>
        <include>
          <system value="http://snomed.info/sct"/>
          <concept>
            <code value="408856003"/>
            <display value="Autism"/>
          </concept>
          <concept>
            <code value="414022008"/>
            <display value="Blood Disorders"/>
          </concept>
          <concept>
            <code value="80544005"/>
            <display value="Canavan Disease"/>
          </concept>
          <concept>
            <code value="409709004"/>
            <display
                     value="Chromosomal Disorder Includes any inherited genetic or chromosomal disorders"/>
          </concept>
          <concept>
            <code value="13213009"/>
            <display value="Congenital Heart Defect"/>
          </concept>
          <concept>
            <code value="190905008"/>
            <display value="Cystic Fibrosis"/>
          </concept>
          <concept>
            <code value="276720006"/>
            <display
                     value="Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects"/>
          </concept>
          <concept>
            <code value="41040004"/>
            <display value="Down Syndrome"/>
          </concept>
          <concept>
            <code value="29159009"/>
            <display value="Familial Dysautonomia"/>
          </concept>
          <concept>
            <code value="90935002"/>
            <display value="Hemophilia"/>
          </concept>
          <concept>
            <code value="58756001"/>
            <display value="Huntington's Chorea"/>
          </concept>
          <concept>
            <code value="75934005"/>
            <display value="Maternal Metabolic Disorder"/>
          </concept>
          <concept>
            <code value="91138005"/>
            <display value="Mental Retardation"/>
          </concept>
          <concept>
            <code value="73297009"/>
            <display value="Muscular Dystrophy"/>
          </concept>
          <concept>
            <code value="253098009"/>
            <display value="Neural Tube Defect"/>
          </concept>
          <concept>
            <code value="102878001"/>
            <display value="Recurrent pregnancy loss/stillbirth"/>
          </concept>
          <concept>
            <code value="417357006"/>
            <display value="Sickle Cell Disease"/>
          </concept>
          <concept>
            <code value="16402000"/>
            <display value="Sickle Cell Trait"/>
          </concept>
          <concept>
            <code value="111385000"/>
            <display value="Tay-Sachs"/>
          </concept>
          <concept>
            <code value="40108008"/>
            <display value="Thalassemia"/>
          </concept>
        </include>
      </compose>
    </ValueSet>