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

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

Draft as of 2025-08-26

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{
  "resourceType" : "ValueSet",
  "id" : "1.2.752.116.3.1.16.1.1.1",
  "text" : {
    "status" : "generated",
    "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>"
  },
  "url" : "http://hl7.se/fhir/r4/ig/medicalalertinformation/ValueSet/1.2.752.116.3.1.16.1.1.1",
  "version" : "0.1.0",
  "name" : "SEAlertInformationOtherMedicalConditionICDVS",
  "title" : "Annat medicinskt tillstånd ICD-10-SE",
  "status" : "draft",
  "date" : "2025-08-26T12:10:55+00:00",
  "publisher" : "HL7 Sweden",
  "contact" : [
    {
      "name" : "HL7 Sweden",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://hl7.se/"
        },
        {
          "system" : "email",
          "value" : "info@hl7.se"
        }
      ]
    }
  ],
  "compose" : {
    "include" : [
      {
        "system" : "http://hl7.org/fhir/sid/icd-10",
        "concept" : [
          {
            "code" : "T78.3",
            "display" : "Angioneurotiskt ödem"
          },
          {
            "code" : "I49.8E",
            "display" : "Långt QT-syndrom"
          },
          {
            "code" : "I27.0",
            "display" : "Primär pulmonell hypertoni"
          },
          {
            "code" : "I27.2",
            "display" : "Annan sekundär pulmonell hypertoni"
          },
          {
            "code" : "E27.1",
            "display" : "Primär binjurebarksinsufficiens"
          },
          {
            "code" : "T88.3",
            "display" : "Malign hypertermi orsakad av anestesi"
          },
          {
            "code" : "D66.9",
            "display" : "Ärftlig brist på faktor VIII"
          },
          {
            "code" : "D67.9",
            "display" : "Ärftlig brist på faktor IX"
          },
          {
            "code" : "D68.0",
            "display" : "von Willebrands sjukdom"
          },
          {
            "code" : "D68.1",
            "display" : "Hereditär brist på faktor XI"
          },
          {
            "code" : "D68.2",
            "display" : "Hereditär brist på andra koagulationsfaktorer"
          },
          {
            "code" : "D68.3",
            "display" : "Hemorragisk sjukdom orsakad av cirkulerande antikoagulantia"
          },
          {
            "code" : "D68.4",
            "display" : "Förvärvad brist på koagulationsfaktor"
          },
          {
            "code" : "D68.5",
            "display" : "Primär trombofili"
          },
          {
            "code" : "D68.6",
            "display" : "Annan trombofili"
          },
          {
            "code" : "D68.8",
            "display" : "Andra specificerade koagulationsrubbningar"
          },
          {
            "code" : "D68.9",
            "display" : "Koagulationsrubbning, ospecificerad"
          },
          {
            "code" : "D69.0",
            "display" : "Allergisk purpura"
          },
          {
            "code" : "D69.1",
            "display" : "Kvalitativa trombocytdefekter"
          },
          {
            "code" : "D69.3",
            "display" : "Idiopatisk trombocytopen purpura"
          },
          {
            "code" : "D69.4",
            "display" : "Annan primär trombocytopeni"
          },
          {
            "code" : "D69.5",
            "display" : "Sekundär trombocytopeni"
          },
          {
            "code" : "D69.6",
            "display" : "Trombocytopeni, ospecificerad"
          },
          {
            "code" : "M31.1",
            "display" : "Trombotisk mikroangiopati"
          },
          {
            "code" : "G70.0",
            "display" : "Myasthenia gravis"
          },
          {
            "code" : "E80.2A",
            "display" : "Akut intermittent porfyri (hepatisk)"
          },
          {
            "code" : "E80.2D",
            "display" : "Porphyria variegata"
          },
          {
            "code" : "E80.2B",
            "display" : "Hereditär koproporfyri"
          },
          {
            "code" : "E80.2W",
            "display" : "Annan specificerad porfyri"
          },
          {
            "code" : "E88.0",
            "display" : "Rubbningar i plasmaproteinomsättningen som ej klassificeras på annan plats"
          },
          {
            "code" : "E88.0W",
            "display" : "Annan specificerad rubbning i plasmaproteinomsättningen som ej klassificeras på annan plats"
          },
          {
            "code" : "T88.2",
            "display" : "Chock orsakad av anestesi"
          },
          {
            "code" : "T88.5",
            "display" : "Andra komplikationer till anestesi"
          },
          {
            "code" : "T88.4",
            "display" : "Misslyckad eller försvårad intubation"
          },
          {
            "code" : "D73.0",
            "display" : "Hyposplenism"
          },
          {
            "code" : "Q89.0",
            "display" : "Medfödda missbildningar av mjälten"
          },
          {
            "code" : "D81",
            "display" : "Kombinerade immunbristtillstånd"
          },
          {
            "code" : "D70.9A",
            "display" : "Agranulocytos"
          },
          {
            "code" : "D70.9B",
            "display" : "Kostmanns sjukdom"
          },
          {
            "code" : "D70.9D",
            "display" : "Shwachmans syndrom"
          },
          {
            "code" : "D71.9",
            "display" : "Funktionella rubbningar hos polymorfkärniga neutrofila celler (vissa vita blodkroppar)"
          },
          {
            "code" : "I77.0",
            "display" : "Arteriovenös fistel, förvärvad"
          },
          {
            "code" : "E71.0"
          },
          {
            "code" : "E71.2"
          },
          {
            "code" : "E71.3"
          },
          {
            "code" : "E71.1A"
          },
          {
            "code" : "E71.1B"
          },
          {
            "code" : "E71.1C"
          },
          {
            "code" : "E71.1D"
          },
          {
            "code" : "E71.3A"
          },
          {
            "code" : "E71.3B"
          },
          {
            "code" : "E71.3C"
          },
          {
            "code" : "E72.2"
          },
          {
            "code" : "E72.3"
          },
          {
            "code" : "E72.2B"
          },
          {
            "code" : "E72.2C"
          },
          {
            "code" : "E74.0"
          },
          {
            "code" : "E74.1"
          },
          {
            "code" : "E74.4"
          },
          {
            "code" : "E88.9"
          },
          {
            "code" : "E79.8"
          },
          {
            "code" : "G71.3"
          },
          {
            "code" : "E25.0"
          },
          {
            "code" : "K52.2"
          }
        ]
      }
    ]
  }
}