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 - TTL Representation

Draft as of 2023-10-24

Raw ttl | Download

    @prefix fhir: <http://hl7.org/fhir/> .
    @prefix owl: <http://www.w3.org/2002/07/owl#> .
    @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
    @prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

    # - resource -------------------------------------------------------------------

     a fhir:ValueSet ;
      fhir:nodeRole fhir:treeRoot ;
      fhir:id [ fhir:v "Antepartum.Family.History.and.Genetic.Screening.VS"] ; #
      fhir:text [
    fhir:status [ fhir:v "generated" ] ;
    fhir:div "<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>"
      ] ; #
      fhir:url [ fhir:v "https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS"^^xsd:anyURI] ; #
      fhir:version [ fhir:v "0.0.1-current"] ; #
      fhir:name [ fhir:v "Antepartum_Family_History_and_Genetic_Screening_VS"] ; #
      fhir:title [ fhir:v "Antepartum Family History and Genetic Screening"] ; #
      fhir:status [ fhir:v "draft"] ; #
      fhir:experimental [ fhir:v "false"^^xsd:boolean] ; #
      fhir:date [ fhir:v "2023-10-24T22:43:25+00:00"^^xsd:dateTime] ; #
      fhir:publisher [ fhir:v "IHE Patient Care Coordination Committee"] ; #
      fhir:contact ( [
        ( fhir:telecom [
    fhir:system [ fhir:v "url" ] ;
    fhir:value [ fhir:v "https://www.ihe.net/ihe_domains/patient_care_coordination/" ]     ] )
      ] [
        ( fhir:telecom [
    fhir:system [ fhir:v "email" ] ;
    fhir:value [ fhir:v "pcc@ihe.net" ]     ] )
      ] [
    fhir:name [ fhir:v "IHE Patient Care Coordination Committee" ] ;
        ( fhir:telecom [
    fhir:system [ fhir:v "email" ] ;
    fhir:value [ fhir:v "pcc@ihe.net" ]     ] )
      ] ) ; #
      fhir:description [ fhir:v "TBD"] ; #
      fhir:jurisdiction ( [
        ( fhir:coding [
    fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm"^^xsd:anyURI ] ;
    fhir:code [ fhir:v "001" ]     ] )
      ] ) ; #
      fhir:compose [
        ( fhir:include [
    fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
          ( fhir:concept [
    fhir:code [ fhir:v "408856003" ] ;
    fhir:display [ fhir:v "Autism" ]       ] [
    fhir:code [ fhir:v "414022008" ] ;
    fhir:display [ fhir:v "Blood Disorders" ]       ] [
    fhir:code [ fhir:v "80544005" ] ;
    fhir:display [ fhir:v "Canavan Disease" ]       ] [
    fhir:code [ fhir:v "409709004" ] ;
    fhir:display [ fhir:v "Chromosomal Disorder Includes any inherited genetic or chromosomal disorders" ]       ] [
    fhir:code [ fhir:v "13213009" ] ;
    fhir:display [ fhir:v "Congenital Heart Defect" ]       ] [
    fhir:code [ fhir:v "190905008" ] ;
    fhir:display [ fhir:v "Cystic Fibrosis" ]       ] [
    fhir:code [ fhir:v "276720006" ] ;
    fhir:display [ fhir:v "Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects" ]       ] [
    fhir:code [ fhir:v "41040004" ] ;
    fhir:display [ fhir:v "Down Syndrome" ]       ] [
    fhir:code [ fhir:v "29159009" ] ;
    fhir:display [ fhir:v "Familial Dysautonomia" ]       ] [
    fhir:code [ fhir:v "90935002" ] ;
    fhir:display [ fhir:v "Hemophilia" ]       ] [
    fhir:code [ fhir:v "58756001" ] ;
    fhir:display [ fhir:v "Huntington's Chorea" ]       ] [
    fhir:code [ fhir:v "75934005" ] ;
    fhir:display [ fhir:v "Maternal Metabolic Disorder" ]       ] [
    fhir:code [ fhir:v "91138005" ] ;
    fhir:display [ fhir:v "Mental Retardation" ]       ] [
    fhir:code [ fhir:v "73297009" ] ;
    fhir:display [ fhir:v "Muscular Dystrophy" ]       ] [
    fhir:code [ fhir:v "253098009" ] ;
    fhir:display [ fhir:v "Neural Tube Defect" ]       ] [
    fhir:code [ fhir:v "102878001" ] ;
    fhir:display [ fhir:v "Recurrent pregnancy loss/stillbirth" ]       ] [
    fhir:code [ fhir:v "417357006" ] ;
    fhir:display [ fhir:v "Sickle Cell Disease" ]       ] [
    fhir:code [ fhir:v "16402000" ] ;
    fhir:display [ fhir:v "Sickle Cell Trait" ]       ] [
    fhir:code [ fhir:v "111385000" ] ;
    fhir:display [ fhir:v "Tay-Sachs" ]       ] [
    fhir:code [ fhir:v "40108008" ] ;
    fhir:display [ fhir:v "Thalassemia" ]       ] )     ] )
      ] . #