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FHIR IG Statistics: ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418

Packagenictiz.fhir.nl.stu3.geboortezorg
Resource TypeValueSet
Id2.16.840.1.113883.2.4.11.198--20161026164418
FHIR VersionR3
Sourcehttps://simplifier.net/resolve?scope=nictiz.fhir.nl.stu3.geboortezorg@1.3.3-rc7&canonical=http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418
URLhttp://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418
Version2.3.0
Statusactive
NameChromosomaleAfwijkingen22
TitleChromosomaleAfwijkingen
Realmnl
DescriptionChromosomaleAfwijkingen
CopyrightThis artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org. <div data-source="inherited" style="border-top: 1px solid black">This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.</div>

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
sctSNOMED CT International Edition

Narrative

No narrative content found in resource


Source

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113883.2.4.11.198--20161026164418",
  "meta": {
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-effectivePeriod",
      "valuePeriod": {
        "start": "2016-10-26T16:44:18Z"
      }
    }
  ],
  "url": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418",
  "identifier": [
    {
      "use": "official",
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.2.4.11.198"
    }
  ],
  "version": "2.3.0",
  "name": "ChromosomaleAfwijkingen22",
  "title": "ChromosomaleAfwijkingen",
  "status": "active",
  "experimental": false,
  "publisher": "Nictiz",
  "contact": [
    {
      "name": "Nictiz",
      "telecom": [
        {
          "system": "phone",
          "value": "070-3173450"
        }
      ]
    }
  ],
  "description": "ChromosomaleAfwijkingen",
  "immutable": false,
  "copyright": "This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org. <div data-source=\"inherited\" style=\"border-top: 1px solid black\">This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.</div>",
  "compose": {
    "include": [
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.22",
        "concept": [
          {
            "code": "7",
            "display": "Andere numerieke chromosomale afwijkingen"
          }
        ]
      },
      {
        "system": "http://hl7.org/fhir/v3/NullFlavor",
        "concept": [
          {
            "code": "OTH",
            "display": "Overige chromosomale afwijkingen"
          },
          {
            "code": "NI",
            "display": "Geen informatie"
          }
        ]
      },
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "41040004",
            "display": "Down-syndroom (aandoening)"
          },
          {
            "code": "51500006",
            "display": "trisomie 18 (aandoening)"
          },
          {
            "code": "21111006",
            "display": "trisomie 13 (aandoening)"
          }
        ]
      }
    ]
  }
}