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] |
No resources found
CodeSystem | |
GenericValues ![]() | Generic values |
PatobankSNOMED ![]() | Den Danske SNOMED for Patologi |
Note: links and images are rebased to the (stated) source
Generated Narrative: ValueSet CytogeneticCancerChangesALD
This value set includes codes based on the following rules:
https://kip.rkkp.dk/fhir/CodeSystem/PatobankSNOMED
Code | Display | Definition |
M98963 | t(8;21)(q22;q22) RUNX1-RUNX1T1 | AML m. t(8;21); RUNX1-RUNX1T1 |
M98713 | inv(16)(p13.1q22) or t(16;16)(p13.1q22) CBFB-/MYH11 | AML m. inv(16) el. t(16;16); CBFß-MYH11 |
M98663 | t(15;17)(q22;q21) PML-RARA | akut promyelocyt leukæmi m. t(15;17); PML-RARa |
M98973 | t(9;11)(p22;q23) MLLT3-MLL | AML m. t(9;11); KMT2A-MLLT3 |
M98653 | t(6;9)(p22;q34) DEK-NUP214 | AML m. t(6;9); DEK-NUP214 |
M98693 | inv(3)(q21q26.2) eller t(3;3)(q21q26.2) RPN1-EV1 | AML m inv(3)(q21q26.2)el t(3;3)(q21;q26.2);RPN1-EVI1 |
M99113 | t(1;22)(p13;q13) RBM15-MKL1 | AML(megakaryoblastisk)m t(1;22)(p13;q13);RBM15-MLK1 |
M98063 | t(9;22)(q34;q11.2) BCR-ABL1 | bl. fænotype akut leukæmi m. t(9;22); BCR-ABL1 |
M98073 | t(v;11q23) MLL rearrangeret | bl. fænotype akut leukæmi m. t(v;11q); KMT2A rearr. |
M98143 | t(12;21)(p13;q22) d | B-lymfobl. leukæmi/lymfom m. t(12;21); ETV6-RUNX1 |
M98173 | t(5;14)(q31;q32) IL3-IGH@ | B-lymfobl. leukæmi/lymfom m. t(5;14); IgH/IL3 |
M98153 | B-lymfoblast leukæmi med hyperdiploidi | B-lymfobl. leukæmi/lymfom med hyperdiploidi |
https://kip.rkkp.dk/fhir/CodeSystem/GenericValues
Code | Display | Definition |
none | Ingen | None - used to choose none of the available values |
{
"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"
}
]
}
]
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.