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

• Narrative Content
• XML
• JSON
• TTL

: Annat medicinskt tillstånd ICD-10-SE - TTL Representation

Draft as of 2025-08-26

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@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 "1.2.752.116.3.1.16.1.1.1"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet 1.2.752.116.3.1.16.1.1.1</b></p><a name=\"1.2.752.116.3.1.16.1.1.1\"> </a><a name=\"hc1.2.752.116.3.1.16.1.1.1\"> </a><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/6.5.0/CodeSystem-icd10.html\"><code>http://hl7.org/fhir/sid/icd-10</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>T78.3</td><td>Angioneurotiskt ödem</td></tr><tr><td>I49.8E</td><td>Långt QT-syndrom</td></tr><tr><td>I27.0</td><td>Primär pulmonell hypertoni</td></tr><tr><td>I27.2</td><td>Annan sekundär pulmonell hypertoni</td></tr><tr><td>E27.1</td><td>Primär binjurebarksinsufficiens</td></tr><tr><td>T88.3</td><td>Malign hypertermi orsakad av anestesi</td></tr><tr><td>D66.9</td><td>Ärftlig brist på faktor VIII</td></tr><tr><td>D67.9</td><td>Ärftlig brist på faktor IX</td></tr><tr><td>D68.0</td><td>von Willebrands sjukdom</td></tr><tr><td>D68.1</td><td>Hereditär brist på faktor XI</td></tr><tr><td>D68.2</td><td>Hereditär brist på andra koagulationsfaktorer</td></tr><tr><td>D68.3</td><td>Hemorragisk sjukdom orsakad av cirkulerande antikoagulantia</td></tr><tr><td>D68.4</td><td>Förvärvad brist på koagulationsfaktor</td></tr><tr><td>D68.5</td><td>Primär trombofili</td></tr><tr><td>D68.6</td><td>Annan trombofili</td></tr><tr><td>D68.8</td><td>Andra specificerade koagulationsrubbningar</td></tr><tr><td>D68.9</td><td>Koagulationsrubbning, ospecificerad</td></tr><tr><td>D69.0</td><td>Allergisk purpura</td></tr><tr><td>D69.1</td><td>Kvalitativa trombocytdefekter</td></tr><tr><td>D69.3</td><td>Idiopatisk trombocytopen purpura</td></tr><tr><td>D69.4</td><td>Annan primär trombocytopeni</td></tr><tr><td>D69.5</td><td>Sekundär trombocytopeni</td></tr><tr><td>D69.6</td><td>Trombocytopeni, ospecificerad</td></tr><tr><td>M31.1</td><td>Trombotisk mikroangiopati</td></tr><tr><td>G70.0</td><td>Myasthenia gravis</td></tr><tr><td>E80.2A</td><td>Akut intermittent porfyri (hepatisk)</td></tr><tr><td>E80.2D</td><td>Porphyria variegata</td></tr><tr><td>E80.2B</td><td>Hereditär koproporfyri</td></tr><tr><td>E80.2W</td><td>Annan specificerad porfyri</td></tr><tr><td>E88.0</td><td>Rubbningar i plasmaproteinomsättningen som ej klassificeras på annan plats</td></tr><tr><td>E88.0W</td><td>Annan specificerad rubbning i plasmaproteinomsättningen som ej klassificeras på annan plats</td></tr><tr><td>T88.2</td><td>Chock orsakad av anestesi</td></tr><tr><td>T88.5</td><td>Andra komplikationer till anestesi</td></tr><tr><td>T88.4</td><td>Misslyckad eller försvårad intubation</td></tr><tr><td>D73.0</td><td>Hyposplenism</td></tr><tr><td>Q89.0</td><td>Medfödda missbildningar av mjälten</td></tr><tr><td>D81</td><td>Kombinerade immunbristtillstånd</td></tr><tr><td>D70.9A</td><td>Agranulocytos</td></tr><tr><td>D70.9B</td><td>Kostmanns sjukdom</td></tr><tr><td>D70.9D</td><td>Shwachmans syndrom</td></tr><tr><td>D71.9</td><td>Funktionella rubbningar hos polymorfkärniga neutrofila celler (vissa vita blodkroppar)</td></tr><tr><td>I77.0</td><td>Arteriovenös fistel, förvärvad</td></tr><tr><td>E71.0</td><td style=\"color: #cccccc\">Maple-syrup-urine disease</td></tr><tr><td>E71.2</td><td style=\"color: #cccccc\">Disorder of branched-chain amino-acid metabolism, unspecified</td></tr><tr><td>E71.3</td><td style=\"color: #cccccc\">Disorders of fatty-acid metabolism</td></tr><tr><td>E71.1A</td><td/></tr><tr><td>E71.1B</td><td/></tr><tr><td>E71.1C</td><td/></tr><tr><td>E71.1D</td><td/></tr><tr><td>E71.3A</td><td/></tr><tr><td>E71.3B</td><td/></tr><tr><td>E71.3C</td><td/></tr><tr><td>E72.2</td><td style=\"color: #cccccc\">Disorders of urea cycle metabolism</td></tr><tr><td>E72.3</td><td style=\"color: #cccccc\">Disorders of lysine and hydroxylysine metabolism</td></tr><tr><td>E72.2B</td><td/></tr><tr><td>E72.2C</td><td/></tr><tr><td>E74.0</td><td style=\"color: #cccccc\">Glycogen storage disease</td></tr><tr><td>E74.1</td><td style=\"color: #cccccc\">Disorders of fructose metabolism</td></tr><tr><td>E74.4</td><td style=\"color: #cccccc\">Disorders of pyruvate metabolism and gluconeogenesis</td></tr><tr><td>E88.9</td><td style=\"color: #cccccc\">Metabolic disorder, unspecified</td></tr><tr><td>E79.8</td><td style=\"color: #cccccc\">Other disorders of purine and pyrimidine metabolism</td></tr><tr><td>G71.3</td><td style=\"color: #cccccc\">Mitochondrial myopathy, not elsewhere classified</td></tr><tr><td>E25.0</td><td style=\"color: #cccccc\">Congenital adrenogenital disorders associated with enzyme deficiency</td></tr><tr><td>K52.2</td><td style=\"color: #cccccc\">Allergic and dietetic gastroenteritis and colitis</td></tr></table></li></ul></div>"^^rdf:XMLLiteral
  ] ; # 
  fhir:url [ fhir:v "http://hl7.se/fhir/r4/ig/medicalalertinformation/ValueSet/1.2.752.116.3.1.16.1.1.1"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "0.1.0"] ; # 
  fhir:name [ fhir:v "SEAlertInformationOtherMedicalConditionICDVS"] ; # 
  fhir:title [ fhir:v "Annat medicinskt tillstånd ICD-10-SE"] ; # 
  fhir:status [ fhir:v "draft"] ; # 
  fhir:date [ fhir:v "2025-08-26T12:10:55+00:00"^^xsd:dateTime] ; # 
  fhir:publisher [ fhir:v "HL7 Sweden"] ; # 
  fhir:contact ( [
fhir:name [ fhir:v "HL7 Sweden" ] ;
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://hl7.se/" ]     ] [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "info@hl7.se" ]     ] )
  ] ) ; # 
  fhir:compose [
    ( fhir:include [
fhir:system [ fhir:v "http://hl7.org/fhir/sid/icd-10"^^xsd:anyURI ] ;
      ( fhir:concept [
fhir:code [ fhir:v "T78.3" ] ;
fhir:display [ fhir:v "Angioneurotiskt ödem" ]       ] [
fhir:code [ fhir:v "I49.8E" ] ;
fhir:display [ fhir:v "Långt QT-syndrom" ]       ] [
fhir:code [ fhir:v "I27.0" ] ;
fhir:display [ fhir:v "Primär pulmonell hypertoni" ]       ] [
fhir:code [ fhir:v "I27.2" ] ;
fhir:display [ fhir:v "Annan sekundär pulmonell hypertoni" ]       ] [
fhir:code [ fhir:v "E27.1" ] ;
fhir:display [ fhir:v "Primär binjurebarksinsufficiens" ]       ] [
fhir:code [ fhir:v "T88.3" ] ;
fhir:display [ fhir:v "Malign hypertermi orsakad av anestesi" ]       ] [
fhir:code [ fhir:v "D66.9" ] ;
fhir:display [ fhir:v "Ärftlig brist på faktor VIII" ]       ] [
fhir:code [ fhir:v "D67.9" ] ;
fhir:display [ fhir:v "Ärftlig brist på faktor IX" ]       ] [
fhir:code [ fhir:v "D68.0" ] ;
fhir:display [ fhir:v "von Willebrands sjukdom" ]       ] [
fhir:code [ fhir:v "D68.1" ] ;
fhir:display [ fhir:v "Hereditär brist på faktor XI" ]       ] [
fhir:code [ fhir:v "D68.2" ] ;
fhir:display [ fhir:v "Hereditär brist på andra koagulationsfaktorer" ]       ] [
fhir:code [ fhir:v "D68.3" ] ;
fhir:display [ fhir:v "Hemorragisk sjukdom orsakad av cirkulerande antikoagulantia" ]       ] [
fhir:code [ fhir:v "D68.4" ] ;
fhir:display [ fhir:v "Förvärvad brist på koagulationsfaktor" ]       ] [
fhir:code [ fhir:v "D68.5" ] ;
fhir:display [ fhir:v "Primär trombofili" ]       ] [
fhir:code [ fhir:v "D68.6" ] ;
fhir:display [ fhir:v "Annan trombofili" ]       ] [
fhir:code [ fhir:v "D68.8" ] ;
fhir:display [ fhir:v "Andra specificerade koagulationsrubbningar" ]       ] [
fhir:code [ fhir:v "D68.9" ] ;
fhir:display [ fhir:v "Koagulationsrubbning, ospecificerad" ]       ] [
fhir:code [ fhir:v "D69.0" ] ;
fhir:display [ fhir:v "Allergisk purpura" ]       ] [
fhir:code [ fhir:v "D69.1" ] ;
fhir:display [ fhir:v "Kvalitativa trombocytdefekter" ]       ] [
fhir:code [ fhir:v "D69.3" ] ;
fhir:display [ fhir:v "Idiopatisk trombocytopen purpura" ]       ] [
fhir:code [ fhir:v "D69.4" ] ;
fhir:display [ fhir:v "Annan primär trombocytopeni" ]       ] [
fhir:code [ fhir:v "D69.5" ] ;
fhir:display [ fhir:v "Sekundär trombocytopeni" ]       ] [
fhir:code [ fhir:v "D69.6" ] ;
fhir:display [ fhir:v "Trombocytopeni, ospecificerad" ]       ] [
fhir:code [ fhir:v "M31.1" ] ;
fhir:display [ fhir:v "Trombotisk mikroangiopati" ]       ] [
fhir:code [ fhir:v "G70.0" ] ;
fhir:display [ fhir:v "Myasthenia gravis" ]       ] [
fhir:code [ fhir:v "E80.2A" ] ;
fhir:display [ fhir:v "Akut intermittent porfyri (hepatisk)" ]       ] [
fhir:code [ fhir:v "E80.2D" ] ;
fhir:display [ fhir:v "Porphyria variegata" ]       ] [
fhir:code [ fhir:v "E80.2B" ] ;
fhir:display [ fhir:v "Hereditär koproporfyri" ]       ] [
fhir:code [ fhir:v "E80.2W" ] ;
fhir:display [ fhir:v "Annan specificerad porfyri" ]       ] [
fhir:code [ fhir:v "E88.0" ] ;
fhir:display [ fhir:v "Rubbningar i plasmaproteinomsättningen som ej klassificeras på annan plats" ]       ] [
fhir:code [ fhir:v "E88.0W" ] ;
fhir:display [ fhir:v "Annan specificerad rubbning i plasmaproteinomsättningen som ej klassificeras på annan plats" ]       ] [
fhir:code [ fhir:v "T88.2" ] ;
fhir:display [ fhir:v "Chock orsakad av anestesi" ]       ] [
fhir:code [ fhir:v "T88.5" ] ;
fhir:display [ fhir:v "Andra komplikationer till anestesi" ]       ] [
fhir:code [ fhir:v "T88.4" ] ;
fhir:display [ fhir:v "Misslyckad eller försvårad intubation" ]       ] [
fhir:code [ fhir:v "D73.0" ] ;
fhir:display [ fhir:v "Hyposplenism" ]       ] [
fhir:code [ fhir:v "Q89.0" ] ;
fhir:display [ fhir:v "Medfödda missbildningar av mjälten" ]       ] [
fhir:code [ fhir:v "D81" ] ;
fhir:display [ fhir:v "Kombinerade immunbristtillstånd" ]       ] [
fhir:code [ fhir:v "D70.9A" ] ;
fhir:display [ fhir:v "Agranulocytos" ]       ] [
fhir:code [ fhir:v "D70.9B" ] ;
fhir:display [ fhir:v "Kostmanns sjukdom" ]       ] [
fhir:code [ fhir:v "D70.9D" ] ;
fhir:display [ fhir:v "Shwachmans syndrom" ]       ] [
fhir:code [ fhir:v "D71.9" ] ;
fhir:display [ fhir:v "Funktionella rubbningar hos polymorfkärniga neutrofila celler (vissa vita blodkroppar)" ]       ] [
fhir:code [ fhir:v "I77.0" ] ;
fhir:display [ fhir:v "Arteriovenös fistel, förvärvad" ]       ] [
fhir:code [ fhir:v "E71.0" ]       ] [
fhir:code [ fhir:v "E71.2" ]       ] [
fhir:code [ fhir:v "E71.3" ]       ] [
fhir:code [ fhir:v "E71.1A" ]       ] [
fhir:code [ fhir:v "E71.1B" ]       ] [
fhir:code [ fhir:v "E71.1C" ]       ] [
fhir:code [ fhir:v "E71.1D" ]       ] [
fhir:code [ fhir:v "E71.3A" ]       ] [
fhir:code [ fhir:v "E71.3B" ]       ] [
fhir:code [ fhir:v "E71.3C" ]       ] [
fhir:code [ fhir:v "E72.2" ]       ] [
fhir:code [ fhir:v "E72.3" ]       ] [
fhir:code [ fhir:v "E72.2B" ]       ] [
fhir:code [ fhir:v "E72.2C" ]       ] [
fhir:code [ fhir:v "E74.0" ]       ] [
fhir:code [ fhir:v "E74.1" ]       ] [
fhir:code [ fhir:v "E74.4" ]       ] [
fhir:code [ fhir:v "E88.9" ]       ] [
fhir:code [ fhir:v "E79.8" ]       ] [
fhir:code [ fhir:v "G71.3" ]       ] [
fhir:code [ fhir:v "E25.0" ]       ] [
fhir:code [ fhir:v "K52.2" ]       ] )     ] )
  ] . #