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

ValueSet: Annat medicinskt tillstånd ICD-10-SE

Official URL: http://hl7.se/fhir/r4/ig/medicalalertinformation/ValueSet/1.2.752.116.3.1.16.1.1.1 Version: 0.1.0
Draft as of 2025-08-26 Computable Name: SEAlertInformationOtherMedicalConditionICDVS

References

Logical Definition (CLD)

  • Include these codes as defined in http://hl7.org/fhir/sid/icd-10
    CodeDisplay
    T78.3Angioneurotiskt ödem
    I49.8ELångt QT-syndrom
    I27.0Primär pulmonell hypertoni
    I27.2Annan sekundär pulmonell hypertoni
    E27.1Primär binjurebarksinsufficiens
    T88.3Malign hypertermi orsakad av anestesi
    D66.9Ärftlig brist på faktor VIII
    D67.9Ärftlig brist på faktor IX
    D68.0von Willebrands sjukdom
    D68.1Hereditär brist på faktor XI
    D68.2Hereditär brist på andra koagulationsfaktorer
    D68.3Hemorragisk sjukdom orsakad av cirkulerande antikoagulantia
    D68.4Förvärvad brist på koagulationsfaktor
    D68.5Primär trombofili
    D68.6Annan trombofili
    D68.8Andra specificerade koagulationsrubbningar
    D68.9Koagulationsrubbning, ospecificerad
    D69.0Allergisk purpura
    D69.1Kvalitativa trombocytdefekter
    D69.3Idiopatisk trombocytopen purpura
    D69.4Annan primär trombocytopeni
    D69.5Sekundär trombocytopeni
    D69.6Trombocytopeni, ospecificerad
    M31.1Trombotisk mikroangiopati
    G70.0Myasthenia gravis
    E80.2AAkut intermittent porfyri (hepatisk)
    E80.2DPorphyria variegata
    E80.2BHereditär koproporfyri
    E80.2WAnnan specificerad porfyri
    E88.0Rubbningar i plasmaproteinomsättningen som ej klassificeras på annan plats
    E88.0WAnnan specificerad rubbning i plasmaproteinomsättningen som ej klassificeras på annan plats
    T88.2Chock orsakad av anestesi
    T88.5Andra komplikationer till anestesi
    T88.4Misslyckad eller försvårad intubation
    D73.0Hyposplenism
    Q89.0Medfödda missbildningar av mjälten
    D81Kombinerade immunbristtillstånd
    D70.9AAgranulocytos
    D70.9BKostmanns sjukdom
    D70.9DShwachmans syndrom
    D71.9Funktionella rubbningar hos polymorfkärniga neutrofila celler (vissa vita blodkroppar)
    I77.0Arteriovenös fistel, förvärvad
    E71.0Maple-syrup-urine disease
    E71.2Disorder of branched-chain amino-acid metabolism, unspecified
    E71.3Disorders of fatty-acid metabolism
    E71.1A
    E71.1B
    E71.1C
    E71.1D
    E71.3A
    E71.3B
    E71.3C
    E72.2Disorders of urea cycle metabolism
    E72.3Disorders of lysine and hydroxylysine metabolism
    E72.2B
    E72.2C
    E74.0Glycogen storage disease
    E74.1Disorders of fructose metabolism
    E74.4Disorders of pyruvate metabolism and gluconeogenesis
    E88.9Metabolic disorder, unspecified
    E79.8Other disorders of purine and pyrimidine metabolism
    G71.3Mitochondrial myopathy, not elsewhere classified
    E25.0Congenital adrenogenital disorders associated with enzyme deficiency
    K52.2Allergic and dietetic gastroenteritis and colitis

 

Expansion

Expansion from tx.fhir.org based on codesystem ICD-10 version2019-covid-expanded

This value set contains 43 concepts

CodeSystemDisplay
  T78.3http://hl7.org/fhir/sid/icd-10Angioneurotic oedema
  I27.0http://hl7.org/fhir/sid/icd-10Primary pulmonary hypertension
  I27.2http://hl7.org/fhir/sid/icd-10Other secondary pulmonary hypertension
  E27.1http://hl7.org/fhir/sid/icd-10Primary adrenocortical insufficiency
  T88.3http://hl7.org/fhir/sid/icd-10Malignant hyperthermia due to anaesthesia
  D68.0http://hl7.org/fhir/sid/icd-10Von Willebrand disease
  D68.1http://hl7.org/fhir/sid/icd-10Hereditary factor XI deficiency
  D68.2http://hl7.org/fhir/sid/icd-10Hereditary deficiency of other clotting factors
  D68.3http://hl7.org/fhir/sid/icd-10Haemorrhagic disorder due to circulating anticoagulants
  D68.4http://hl7.org/fhir/sid/icd-10Acquired coagulation factor deficiency
  D68.5http://hl7.org/fhir/sid/icd-10Primary thrombophilia
  D68.6http://hl7.org/fhir/sid/icd-10Other thrombophilia
  D68.8http://hl7.org/fhir/sid/icd-10Other specified coagulation defects
  D68.9http://hl7.org/fhir/sid/icd-10Coagulation defect, unspecified
  D69.0http://hl7.org/fhir/sid/icd-10Allergic purpura
  D69.1http://hl7.org/fhir/sid/icd-10Qualitative platelet defects
  D69.3http://hl7.org/fhir/sid/icd-10Idiopathic thrombocytopenic purpura
  D69.4http://hl7.org/fhir/sid/icd-10Other primary thrombocytopenia
  D69.5http://hl7.org/fhir/sid/icd-10Secondary thrombocytopenia
  D69.6http://hl7.org/fhir/sid/icd-10Thrombocytopenia, unspecified
  M31.1http://hl7.org/fhir/sid/icd-10Thrombotic microangiopathy
  G70.0http://hl7.org/fhir/sid/icd-10Myasthenia gravis
  E88.0http://hl7.org/fhir/sid/icd-10Disorders of plasma-protein metabolism, not elsewhere classified
  T88.2http://hl7.org/fhir/sid/icd-10Shock due to anaesthesia
  T88.5http://hl7.org/fhir/sid/icd-10Other complications of anaesthesia
  T88.4http://hl7.org/fhir/sid/icd-10Failed or difficult intubation
  D73.0http://hl7.org/fhir/sid/icd-10Hyposplenism
  Q89.0http://hl7.org/fhir/sid/icd-10Congenital malformations of spleen
  D81http://hl7.org/fhir/sid/icd-10Combined immunodeficiencies
  I77.0http://hl7.org/fhir/sid/icd-10Arteriovenous fistula, acquired
  E71.0http://hl7.org/fhir/sid/icd-10Maple-syrup-urine disease
  E71.2http://hl7.org/fhir/sid/icd-10Disorder of branched-chain amino-acid metabolism, unspecified
  E71.3http://hl7.org/fhir/sid/icd-10Disorders of fatty-acid metabolism
  E72.2http://hl7.org/fhir/sid/icd-10Disorders of urea cycle metabolism
  E72.3http://hl7.org/fhir/sid/icd-10Disorders of lysine and hydroxylysine metabolism
  E74.0http://hl7.org/fhir/sid/icd-10Glycogen storage disease
  E74.1http://hl7.org/fhir/sid/icd-10Disorders of fructose metabolism
  E74.4http://hl7.org/fhir/sid/icd-10Disorders of pyruvate metabolism and gluconeogenesis
  E88.9http://hl7.org/fhir/sid/icd-10Metabolic disorder, unspecified
  E79.8http://hl7.org/fhir/sid/icd-10Other disorders of purine and pyrimidine metabolism
  G71.3http://hl7.org/fhir/sid/icd-10Mitochondrial myopathy, not elsewhere classified
  E25.0http://hl7.org/fhir/sid/icd-10Congenital adrenogenital disorders associated with enzyme deficiency
  K52.2http://hl7.org/fhir/sid/icd-10Allergic and dietetic gastroenteritis and colitis

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code