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Resource ValueSet/FHIR Server from package dk.kip.rkkp.fhir.ig.core#current (16 ms)

Package dk.kip.rkkp.fhir.ig.core
Type ValueSet
Id Id
FHIR Version R4
Source https://kip.rkkp.dk/fhir/https://build.fhir.org/ig/KIP-infrastructure/implementation-guide/ValueSet-CytogeneticCancerChangesALD.html
Url https://kip.rkkp.dk/fhir/ValueSet/CytogeneticCancerChangesALD
Version 2.11.0
Status active
Date 2022-07-13T00:00:00+02:00
Name CytogeneticCancerChangesALD
Title Cytogenetiske kræft forandringer
Experimental True
Description Cytogenetiske WHO specifikke recurrente forandringer i forhold til kræft [ALD]

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
GenericValues Generic values
PatobankSNOMED Den Danske SNOMED for Patologi


Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: ValueSet CytogeneticCancerChangesALD

This value set includes codes based on the following rules:

  • Include these codes as defined in https://kip.rkkp.dk/fhir/CodeSystem/PatobankSNOMED
    CodeDisplayDefinition
    M98963t(8;21)(q22;q22) RUNX1-RUNX1T1AML m. t(8;21); RUNX1-RUNX1T1
    M98713inv(16)(p13.1q22) or t(16;16)(p13.1q22) CBFB-/MYH11AML m. inv(16) el. t(16;16); CBFß-MYH11
    M98663t(15;17)(q22;q21) PML-RARAakut promyelocyt leukæmi m. t(15;17); PML-RARa
    M98973t(9;11)(p22;q23) MLLT3-MLLAML m. t(9;11); KMT2A-MLLT3
    M98653t(6;9)(p22;q34) DEK-NUP214AML m. t(6;9); DEK-NUP214
    M98693inv(3)(q21q26.2) eller t(3;3)(q21q26.2) RPN1-EV1AML m inv(3)(q21q26.2)el t(3;3)(q21;q26.2);RPN1-EVI1
    M99113t(1;22)(p13;q13) RBM15-MKL1AML(megakaryoblastisk)m t(1;22)(p13;q13);RBM15-MLK1
    M98063t(9;22)(q34;q11.2) BCR-ABL1bl. fænotype akut leukæmi m. t(9;22); BCR-ABL1
    M98073t(v;11q23) MLL rearrangeretbl. fænotype akut leukæmi m. t(v;11q); KMT2A rearr.
    M98143t(12;21)(p13;q22) dB-lymfobl. leukæmi/lymfom m. t(12;21); ETV6-RUNX1
    M98173t(5;14)(q31;q32) IL3-IGH@B-lymfobl. leukæmi/lymfom m. t(5;14); IgH/IL3
    M98153B-lymfoblast leukæmi med hyperdiploidiB-lymfobl. leukæmi/lymfom med hyperdiploidi
  • Include these codes as defined in https://kip.rkkp.dk/fhir/CodeSystem/GenericValues
    CodeDisplayDefinition
    noneIngenNone - used to choose none of the available values

Source

{
  "resourceType" : "ValueSet",
  "id" : "CytogeneticCancerChangesALD",
  "text" : {
    "status" : "extensions",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet CytogeneticCancerChangesALD</b></p><a name=\"CytogeneticCancerChangesALD\"> </a><a name=\"hcCytogeneticCancerChangesALD\"> </a><a name=\"CytogeneticCancerChangesALD-en-US\"> </a><p>This value set includes codes based on the following rules:</p><ul><li>Include these codes as defined in <a href=\"CodeSystem-PatobankSNOMED.html\"><code>https://kip.rkkp.dk/fhir/CodeSystem/PatobankSNOMED</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98963\">M98963</a></td><td>t(8;21)(q22;q22) RUNX1-RUNX1T1</td><td>AML m. t(8;21); RUNX1-RUNX1T1</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98713\">M98713</a></td><td>inv(16)(p13.1q22) or t(16;16)(p13.1q22) CBFB-/MYH11</td><td>AML m. inv(16) el. t(16;16); CBFß-MYH11</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98663\">M98663</a></td><td>t(15;17)(q22;q21) PML-RARA</td><td>akut promyelocyt leukæmi m. t(15;17); PML-RARa</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98973\">M98973</a></td><td>t(9;11)(p22;q23) MLLT3-MLL</td><td>AML m. t(9;11); KMT2A-MLLT3</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98653\">M98653</a></td><td>t(6;9)(p22;q34) DEK-NUP214</td><td>AML m. t(6;9); DEK-NUP214</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98693\">M98693</a></td><td>inv(3)(q21q26.2) eller t(3;3)(q21q26.2) RPN1-EV1</td><td>AML m inv(3)(q21q26.2)el t(3;3)(q21;q26.2);RPN1-EVI1</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M99113\">M99113</a></td><td>t(1;22)(p13;q13) RBM15-MKL1</td><td>AML(megakaryoblastisk)m t(1;22)(p13;q13);RBM15-MLK1</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98063\">M98063</a></td><td>t(9;22)(q34;q11.2) BCR-ABL1</td><td>bl. fænotype akut leukæmi m. t(9;22); BCR-ABL1</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98073\">M98073</a></td><td>t(v;11q23) MLL rearrangeret</td><td>bl. fænotype akut leukæmi m. t(v;11q); KMT2A rearr.</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98143\">M98143</a></td><td>t(12;21)(p13;q22) d</td><td>B-lymfobl. leukæmi/lymfom m. t(12;21); ETV6-RUNX1</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98173\">M98173</a></td><td>t(5;14)(q31;q32) IL3-IGH@</td><td>B-lymfobl. leukæmi/lymfom m. t(5;14); IgH/IL3</td></tr><tr><td><a href=\"CodeSystem-PatobankSNOMED.html#PatobankSNOMED-M98153\">M98153</a></td><td>B-lymfoblast leukæmi med hyperdiploidi</td><td>B-lymfobl. leukæmi/lymfom med hyperdiploidi</td></tr></table></li><li>Include these codes as defined in <a href=\"CodeSystem-GenericValues.html\"><code>https://kip.rkkp.dk/fhir/CodeSystem/GenericValues</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href=\"CodeSystem-GenericValues.html#GenericValues-none\">none</a></td><td>Ingen</td><td>None - used to choose none of the available values</td></tr></table></li></ul></div>"
  },
  "url" : "https://kip.rkkp.dk/fhir/ValueSet/CytogeneticCancerChangesALD",
  "version" : "2.11.0",
  "name" : "CytogeneticCancerChangesALD",
  "title" : "Cytogenetiske kræft forandringer",
  "status" : "active",
  "experimental" : true,
  "date" : "2022-07-13T00:00:00+02:00",
  "publisher" : "Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S",
  "contact" : [
    {
      "name" : "Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://trifork.com"
        },
        {
          "system" : "email",
          "value" : "rbk@trifork.com"
        }
      ]
    }
  ],
  "description" : "Cytogenetiske WHO specifikke recurrente forandringer i forhold til kræft [ALD]",
  "compose" : {
    "include" : [
      {
        "system" : "https://kip.rkkp.dk/fhir/CodeSystem/PatobankSNOMED",
        "concept" : [
          {
            "code" : "M98963",
            "display" : "t(8;21)(q22;q22) RUNX1-RUNX1T1"
          },
          {
            "code" : "M98713",
            "display" : "inv(16)(p13.1q22) or t(16;16)(p13.1q22) CBFB-/MYH11"
          },
          {
            "code" : "M98663",
            "display" : "t(15;17)(q22;q21) PML-RARA"
          },
          {
            "code" : "M98973",
            "display" : "t(9;11)(p22;q23) MLLT3-MLL"
          },
          {
            "code" : "M98653",
            "display" : "t(6;9)(p22;q34) DEK-NUP214"
          },
          {
            "code" : "M98693",
            "display" : "inv(3)(q21q26.2) eller t(3;3)(q21q26.2) RPN1-EV1"
          },
          {
            "code" : "M99113",
            "display" : "t(1;22)(p13;q13) RBM15-MKL1"
          },
          {
            "code" : "M98063",
            "display" : "t(9;22)(q34;q11.2) BCR-ABL1"
          },
          {
            "code" : "M98073",
            "display" : "t(v;11q23) MLL rearrangeret"
          },
          {
            "code" : "M98143",
            "display" : "t(12;21)(p13;q22) d"
          },
          {
            "code" : "M98173",
            "display" : "t(5;14)(q31;q32) IL3-IGH@"
          },
          {
            "code" : "M98153",
            "display" : "B-lymfoblast leukæmi med hyperdiploidi"
          }
        ]
      },
      {
        "system" : "https://kip.rkkp.dk/fhir/CodeSystem/GenericValues",
        "concept" : [
          {
            "code" : "none",
            "display" : "Ingen"
          }
        ]
      }
    ]
  }
}

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