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This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.1.0: STU 2) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: Elixhauser Hypothyroidism Value Set - TTL Representation

Active as of 2023-03-21

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:ValueSet ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "elixhauser-hypothyroidism-vs"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/5.0.0/CodeSystem-icd10CM.html\"><code>http://hl7.org/fhir/sid/icd-10-cm</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>E00.0</td><td>Congenital iodine-deficiency syndrome, neurological type</td></tr><tr><td>E00.1</td><td>Congenital iodine-deficiency syndrome, myxedematous type</td></tr><tr><td>E00.2</td><td>Congenital iodine-deficiency syndrome, mixed type</td></tr><tr><td>E00.9</td><td>Congenital iodine-deficiency syndrome, unspecified</td></tr><tr><td>E01.0</td><td>Iodine-deficiency related diffuse (endemic) goiter</td></tr><tr><td>E01.1</td><td>Iodine-deficiency related multinodular (endemic) goiter</td></tr><tr><td>E01.2</td><td>Iodine-deficiency related (endemic) goiter, unspecified</td></tr><tr><td>E01.8</td><td>Oth iodine-deficiency related thyroid disord and allied cond</td></tr><tr><td>E02</td><td>Subclinical iodine-deficiency hypothyroidism</td></tr><tr><td>E03.0</td><td>Congenital hypothyroidism with diffuse goiter</td></tr><tr><td>E03.1</td><td>Congenital hypothyroidism without goiter</td></tr><tr><td>E03.2</td><td>Hypothyroidism due to medicaments and other exogenous substances</td></tr><tr><td>E03.3</td><td>Postinfectious hypothyroidism</td></tr><tr><td>E03.4</td><td>Atrophy of thyroid (acquired)</td></tr><tr><td>E03.5</td><td>Myxedema coma</td></tr><tr><td>E03.8</td><td>Other specified hypothyroidism</td></tr><tr><td>E03.9</td><td>Hypothyroidism, unspecified</td></tr><tr><td>E89.0</td><td>Postprocedural hypothyroidism</td></tr></table></li></ul></div>"
  ] ; # 
  fhir:url [ fhir:v "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-hypothyroidism-vs"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "2.1.0"] ; # 
  fhir:name [ fhir:v "ElixhauserHypothyroidismVS"] ; # 
  fhir:title [ fhir:v "Elixhauser Hypothyroidism Value Set"] ; # 
  fhir:status [ fhir:v "active"] ; # 
  fhir:experimental [ fhir:v "false"^^xsd:boolean] ; # 
  fhir:date [ fhir:v "2023-03-21T04:54:56+11:00"^^xsd:dateTime] ; # 
  fhir:publisher [ fhir:v "HL7 International Clinical Interoperability Council"] ; # 
  fhir:contact ( [
fhir:name [ fhir:v "HL7 International Clinical Interoperability Council" ] ;
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://www.hl7.org/Special/committees/cic" ]     ] [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "ciclist@lists.HL7.org" ]     ] )
  ] ) ; # 
  fhir:description [ fhir:v "Elixhauser Comorbid Condition Value Set for Hypothyroidism. ICD-10 codes are drawn from https://www.hcup-us.ahrq.gov/toolssoftware/comorbidityicd10/comorbidity_icd10.jsp, version 2021.1"] ; # 
  fhir:jurisdiction ( [
    ( fhir:coding [
fhir:system [ fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ] ;
fhir:code [ fhir:v "US" ] ;
fhir:display [ fhir:v "United States of America" ]     ] )
  ] ) ; # 
  fhir:compose [
    ( fhir:include [
fhir:system [ fhir:v "http://hl7.org/fhir/sid/icd-10-cm"^^xsd:anyURI ] ;
      ( fhir:concept [
fhir:code [ fhir:v "E00.0" ] ;
fhir:display [ fhir:v "Congenital iodine-deficiency syndrome, neurological type" ]       ] [
fhir:code [ fhir:v "E00.1" ] ;
fhir:display [ fhir:v "Congenital iodine-deficiency syndrome, myxedematous type" ]       ] [
fhir:code [ fhir:v "E00.2" ] ;
fhir:display [ fhir:v "Congenital iodine-deficiency syndrome, mixed type" ]       ] [
fhir:code [ fhir:v "E00.9" ] ;
fhir:display [ fhir:v "Congenital iodine-deficiency syndrome, unspecified" ]       ] [
fhir:code [ fhir:v "E01.0" ] ;
fhir:display [ fhir:v "Iodine-deficiency related diffuse (endemic) goiter" ]       ] [
fhir:code [ fhir:v "E01.1" ] ;
fhir:display [ fhir:v "Iodine-deficiency related multinodular (endemic) goiter" ]       ] [
fhir:code [ fhir:v "E01.2" ] ;
fhir:display [ fhir:v "Iodine-deficiency related (endemic) goiter, unspecified" ]       ] [
fhir:code [ fhir:v "E01.8" ] ;
fhir:display [ fhir:v "Oth iodine-deficiency related thyroid disord and allied cond" ]       ] [
fhir:code [ fhir:v "E02" ] ;
fhir:display [ fhir:v "Subclinical iodine-deficiency hypothyroidism" ]       ] [
fhir:code [ fhir:v "E03.0" ] ;
fhir:display [ fhir:v "Congenital hypothyroidism with diffuse goiter" ]       ] [
fhir:code [ fhir:v "E03.1" ] ;
fhir:display [ fhir:v "Congenital hypothyroidism without goiter" ]       ] [
fhir:code [ fhir:v "E03.2" ] ;
fhir:display [ fhir:v "Hypothyroidism due to medicaments and other exogenous substances" ]       ] [
fhir:code [ fhir:v "E03.3" ] ;
fhir:display [ fhir:v "Postinfectious hypothyroidism" ]       ] [
fhir:code [ fhir:v "E03.4" ] ;
fhir:display [ fhir:v "Atrophy of thyroid (acquired)" ]       ] [
fhir:code [ fhir:v "E03.5" ] ;
fhir:display [ fhir:v "Myxedema coma" ]       ] [
fhir:code [ fhir:v "E03.8" ] ;
fhir:display [ fhir:v "Other specified hypothyroidism" ]       ] [
fhir:code [ fhir:v "E03.9" ] ;
fhir:display [ fhir:v "Hypothyroidism, unspecified" ]       ] [
fhir:code [ fhir:v "E89.0" ] ;
fhir:display [ fhir:v "Postprocedural hypothyroidism" ]       ] )     ] )
  ] . #