Mobile Antepartum Summary
1.0.0-comment - ballot
Mobile Antepartum Summary
1.0.0-comment - ballot
This page is part of the Mobile Antepartum Summary (v1.0.0-comment: Publication Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
| Active as of 2024-06-04 |
<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/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS"/>
<version value="1.0.0-comment"/>
<name value="Antepartum_Family_History_and_Genetic_Screening_VS"/>
<title value="Antepartum Family History and Genetic Screening"/>
<status value="active"/>
<experimental value="false"/>
<date value="2024-06-04T15:40:08-05:00"/>
<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="This value set includes the type of genetic-related risks identified through screening of the patient’s and biological father’s family history."/>
<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>
IG © 2021+ IHE Patient Care Coordination Committee. Package ihe.pcc.maps#1.0.0-comment based on FHIR 4.0.1. Generated 2024-06-04
Links: Table of Contents |
QA Report
| New Issue | Issues
Version History |
|
Propose a change