0.1.0 - ci-build
0.1.0 - ci-build
SEMedicalAlertInformationImplementationGuide, published by HL7 Sweden. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7Sweden/hl7.fhir.r4.ig.medicalalertinformation/ and changes regularly. See the Directory of published versions
| Draft as of 2025-08-26 |
<ValueSet xmlns="http://hl7.org/fhir">
<id value="59821000052101"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ValueSet 59821000052101</b></p><a name="59821000052101"> </a><a name="hc59821000052101"> </a><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/41291007">41291007</a></td><td>angioödem</td></tr><tr><td><a href="http://snomed.info/id/9651007">9651007</a></td><td>långt QT-syndrom</td></tr><tr><td><a href="http://snomed.info/id/70995007">70995007</a></td><td>pulmonell hypertoni</td></tr><tr><td><a href="http://snomed.info/id/373662000">373662000</a></td><td>primär binjurebarksinsufficiens</td></tr><tr><td><a href="http://snomed.info/id/405501007">405501007</a></td><td>malign hypertermi</td></tr><tr><td><a href="http://snomed.info/id/64779008">64779008</a></td><td>blodkoagulationssjukdom</td></tr><tr><td><a href="http://snomed.info/id/53891000052101">53891000052101</a></td><td>trombocytrelaterad sjukdom med ökad blödningstendens</td></tr><tr><td><a href="http://snomed.info/id/126729006">126729006</a></td><td>trombotisk mikroangiopati</td></tr><tr><td><a href="http://snomed.info/id/234467004">234467004</a></td><td>trombofili</td></tr><tr><td><a href="http://snomed.info/id/91637004">91637004</a></td><td>myasthenia gravis</td></tr><tr><td><a href="http://snomed.info/id/234422006">234422006</a></td><td>akut intermittent porfyri</td></tr><tr><td><a href="http://snomed.info/id/58275005">58275005</a></td><td>porphyria variegata</td></tr><tr><td><a href="http://snomed.info/id/7425008">7425008</a></td><td>hereditär koproporfyri</td></tr><tr><td><a href="http://snomed.info/id/64081000">64081000</a></td><td>brist på porfobilinogensyntetas</td></tr><tr><td><a href="http://snomed.info/id/360631004">360631004</a></td><td>brist på kolinesteras 2, ospecifik</td></tr><tr><td><a href="http://snomed.info/id/33211000">33211000</a></td><td>komplikation till anestesi</td></tr><tr><td><a href="http://snomed.info/id/718447001">718447001</a></td><td>svår intubation</td></tr><tr><td><a href="http://snomed.info/id/707147002">707147002</a></td><td>aspleni</td></tr><tr><td><a href="http://snomed.info/id/31323000">31323000</a></td><td>svår kombinerad immunbrist</td></tr><tr><td><a href="http://snomed.info/id/17182001">17182001</a></td><td>agranulocytos</td></tr><tr><td><a href="http://snomed.info/id/770942003">770942003</a></td><td>Kostmanns syndrom</td></tr><tr><td><a href="http://snomed.info/id/89454001">89454001</a></td><td>Shwachmans syndrom</td></tr><tr><td><a href="http://snomed.info/id/203551000052109">203551000052109</a></td><td>störning av neutrofilfunktion</td></tr><tr><td><a href="http://snomed.info/id/439784005">439784005</a></td><td>kirurgiskt anlagd arteriovenös fistel</td></tr><tr><td><a href="http://snomed.info/id/27718001">27718001</a></td><td>Maple syrup urine disease</td></tr><tr><td><a href="http://snomed.info/id/116020001">116020001</a></td><td>rubbning i omsättningen av förgrenade aminosyror</td></tr><tr><td><a href="http://snomed.info/id/39929009">39929009</a></td><td>rubbning i fettsyraomsättningen</td></tr><tr><td><a href="http://snomed.info/id/7046009">7046009</a></td><td>hyperleucin-isoleucinemi</td></tr><tr><td><a href="http://snomed.info/id/87827003">87827003</a></td><td>brist på isovaleryl-CoA-dehydrogenas</td></tr><tr><td><a href="http://snomed.info/id/42393006">42393006</a></td><td>metylmalonisk acidemi</td></tr><tr><td><a href="http://snomed.info/id/69080001">69080001</a></td><td>brist på propionyl-CoA-karboxylas</td></tr><tr><td><a href="http://snomed.info/id/1156591005">1156591005</a></td><td>fettsyreoxidationsdefekt</td></tr><tr><td><a href="http://snomed.info/id/82319005">82319005</a></td><td>brist på acyl-CoA-dehydrogenas</td></tr><tr><td><a href="http://snomed.info/id/36444000">36444000</a></td><td>rubbning i ureaomsättningscykeln</td></tr><tr><td><a href="http://snomed.info/id/237929000">237929000</a></td><td>rubbning i lysin- och hydroxilysinomsättningen</td></tr><tr><td><a href="http://snomed.info/id/41013004">41013004</a></td><td>brist på argininosuccinatlyas</td></tr><tr><td><a href="http://snomed.info/id/398680004">398680004</a></td><td>citrullinemi</td></tr><tr><td><a href="http://snomed.info/id/29633007">29633007</a></td><td>glykogeninlagringssjukdom</td></tr><tr><td><a href="http://snomed.info/id/39452003">39452003</a></td><td>rubbning i fruktosomsättningen</td></tr><tr><td><a href="http://snomed.info/id/190760009">190760009</a></td><td>rubbningar i pyruvatomsättningen och glukoneogenesen</td></tr><tr><td><a href="http://snomed.info/id/75934005">75934005</a></td><td>ämnesomsättningssjukdom</td></tr><tr><td><a href="http://snomed.info/id/238006008">238006008</a></td><td>rubbning i purin- och pyrimidinomsättningen</td></tr><tr><td><a href="http://snomed.info/id/16851005">16851005</a></td><td>mitokondriell myopati</td></tr><tr><td><a href="http://snomed.info/id/237751000">237751000</a></td><td>kongenital adrenal hyperplasi</td></tr><tr><td><a href="http://snomed.info/id/737315000">737315000</a></td><td>enterokolit utlöst av födoämnesprotein</td></tr><tr><td><a href="http://snomed.info/id/439218000">439218000</a></td><td>kirurgiskt anlagt arteriovenöst graft</td></tr></table></li></ul></div>
</text>
<url
value="http://hl7.se/fhir/r4/ig/medicalalertinformation/ValueSet/59821000052101"/>
<version value="0.1.0"/>
<name value="SEAlertInformationMedicalConditionSnomedVS"/>
<title value="Urval medicinska tillstånd, uppmärksamhetsinformation"/>
<status value="draft"/>
<date value="2025-08-26T12:10:55+00:00"/>
<publisher value="HL7 Sweden"/>
<contact>
<name value="HL7 Sweden"/>
<telecom>
<system value="url"/>
<value value="http://hl7.se/"/>
</telecom>
<telecom>
<system value="email"/>
<value value="info@hl7.se"/>
</telecom>
</contact>
<compose>
<include>
<system value="http://snomed.info/sct"/>
<concept>
<code value="41291007"/>
<display value="angioödem"/>
</concept>
<concept>
<code value="9651007"/>
<display value="långt QT-syndrom"/>
</concept>
<concept>
<code value="70995007"/>
<display value="pulmonell hypertoni"/>
</concept>
<concept>
<code value="373662000"/>
<display value="primär binjurebarksinsufficiens"/>
</concept>
<concept>
<code value="405501007"/>
<display value="malign hypertermi"/>
</concept>
<concept>
<code value="64779008"/>
<display value="blodkoagulationssjukdom"/>
</concept>
<concept>
<code value="53891000052101"/>
<display
value="trombocytrelaterad sjukdom med ökad blödningstendens"/>
</concept>
<concept>
<code value="126729006"/>
<display value="trombotisk mikroangiopati"/>
</concept>
<concept>
<code value="234467004"/>
<display value="trombofili"/>
</concept>
<concept>
<code value="91637004"/>
<display value="myasthenia gravis"/>
</concept>
<concept>
<code value="234422006"/>
<display value="akut intermittent porfyri"/>
</concept>
<concept>
<code value="58275005"/>
<display value="porphyria variegata"/>
</concept>
<concept>
<code value="7425008"/>
<display value="hereditär koproporfyri"/>
</concept>
<concept>
<code value="64081000"/>
<display value="brist på porfobilinogensyntetas"/>
</concept>
<concept>
<code value="360631004"/>
<display value="brist på kolinesteras 2, ospecifik"/>
</concept>
<concept>
<code value="33211000"/>
<display value="komplikation till anestesi"/>
</concept>
<concept>
<code value="718447001"/>
<display value="svår intubation"/>
</concept>
<concept>
<code value="707147002"/>
<display value="aspleni"/>
</concept>
<concept>
<code value="31323000"/>
<display value="svår kombinerad immunbrist"/>
</concept>
<concept>
<code value="17182001"/>
<display value="agranulocytos"/>
</concept>
<concept>
<code value="770942003"/>
<display value="Kostmanns syndrom"/>
</concept>
<concept>
<code value="89454001"/>
<display value="Shwachmans syndrom"/>
</concept>
<concept>
<code value="203551000052109"/>
<display value="störning av neutrofilfunktion"/>
</concept>
<concept>
<code value="439784005"/>
<display value="kirurgiskt anlagd arteriovenös fistel"/>
</concept>
<concept>
<code value="27718001"/>
<display value="Maple syrup urine disease"/>
</concept>
<concept>
<code value="116020001"/>
<display value="rubbning i omsättningen av förgrenade aminosyror"/>
</concept>
<concept>
<code value="39929009"/>
<display value="rubbning i fettsyraomsättningen"/>
</concept>
<concept>
<code value="7046009"/>
<display value="hyperleucin-isoleucinemi"/>
</concept>
<concept>
<code value="87827003"/>
<display value="brist på isovaleryl-CoA-dehydrogenas"/>
</concept>
<concept>
<code value="42393006"/>
<display value="metylmalonisk acidemi"/>
</concept>
<concept>
<code value="69080001"/>
<display value="brist på propionyl-CoA-karboxylas"/>
</concept>
<concept>
<code value="1156591005"/>
<display value="fettsyreoxidationsdefekt"/>
</concept>
<concept>
<code value="82319005"/>
<display value="brist på acyl-CoA-dehydrogenas"/>
</concept>
<concept>
<code value="36444000"/>
<display value="rubbning i ureaomsättningscykeln"/>
</concept>
<concept>
<code value="237929000"/>
<display value="rubbning i lysin- och hydroxilysinomsättningen"/>
</concept>
<concept>
<code value="41013004"/>
<display value="brist på argininosuccinatlyas"/>
</concept>
<concept>
<code value="398680004"/>
<display value="citrullinemi"/>
</concept>
<concept>
<code value="29633007"/>
<display value="glykogeninlagringssjukdom"/>
</concept>
<concept>
<code value="39452003"/>
<display value="rubbning i fruktosomsättningen"/>
</concept>
<concept>
<code value="190760009"/>
<display
value="rubbningar i pyruvatomsättningen och glukoneogenesen"/>
</concept>
<concept>
<code value="75934005"/>
<display value="ämnesomsättningssjukdom"/>
</concept>
<concept>
<code value="238006008"/>
<display value="rubbning i purin- och pyrimidinomsättningen"/>
</concept>
<concept>
<code value="16851005"/>
<display value="mitokondriell myopati"/>
</concept>
<concept>
<code value="237751000"/>
<display value="kongenital adrenal hyperplasi"/>
</concept>
<concept>
<code value="737315000"/>
<display value="enterokolit utlöst av födoämnesprotein"/>
</concept>
<concept>
<code value="439218000"/>
<display value="kirurgiskt anlagt arteriovenöst graft"/>
</concept>
</include>
</compose>
</ValueSet>