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: Elixhauser Coagulation Deficiency Value Set - XML Representation

Active as of 2023-03-21

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<ValueSet xmlns="http://hl7.org/fhir">
  <id value="elixhauser-coagulation-deficiency-vs"/>
  <text>
    <status value="generated"/>
    <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>D61.09</td><td>Other constitutional aplastic anemia</td></tr><tr><td>D61.1</td><td>Drug-induced aplastic anemia</td></tr><tr><td>D61.2</td><td>Aplastic anemia due to other external agents</td></tr><tr><td>D61.3</td><td>Idiopathic aplastic anemia</td></tr><tr><td>D61.810</td><td>Antineoplastic chemotherapy induced pancytopenia</td></tr><tr><td>D61.811</td><td>Other drug-induced pancytopenia</td></tr><tr><td>D61.818</td><td>Other pancytopenia</td></tr><tr><td>D61.82</td><td>Myelophthisis</td></tr><tr><td>D61.89</td><td>Oth aplastic anemias and other bone marrow failure syndromes</td></tr><tr><td>D61.9</td><td>Aplastic anemia, unspecified</td></tr><tr><td>D65</td><td>Disseminated intravascular coagulation</td></tr><tr><td>D66</td><td>Hereditary factor VIII deficiency</td></tr><tr><td>D67</td><td>Hereditary factor IX deficiency</td></tr><tr><td>D68.0</td><td>Von Willebrand's disease</td></tr><tr><td>D68.1</td><td>Hereditary factor XI deficiency</td></tr><tr><td>D68.2</td><td>Hereditary deficiency of other clotting factors</td></tr><tr><td>D68.311</td><td>Acquired hemophilia</td></tr><tr><td>D68.312</td><td>Antiphospholipid antibody with hemorrhagic disorder</td></tr><tr><td>D68.318</td><td>Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib</td></tr><tr><td>D68.32</td><td>Hemorrhagic disord d/t extrinsic circulating anticoagulants</td></tr><tr><td>D68.4</td><td>Acquired coagulation factor deficiency</td></tr><tr><td>D68.8</td><td>Other specified coagulation defects</td></tr><tr><td>D68.9</td><td>Coagulation defect, unspecified</td></tr><tr><td>D69.1</td><td>Qualitative platelet defects</td></tr><tr><td>D69.3</td><td>Immune thrombocytopenic purpura</td></tr><tr><td>D69.41</td><td>Evans syndrome</td></tr><tr><td>D69.42</td><td>Congenital and hereditary thrombocytopenia purpura</td></tr><tr><td>D69.49</td><td>Other primary thrombocytopenia</td></tr><tr><td>D69.51</td><td>Posttransfusion purpura</td></tr><tr><td>D69.59</td><td>Other secondary thrombocytopenia</td></tr><tr><td>D69.6</td><td>Thrombocytopenia, unspecified</td></tr><tr><td>D69.8</td><td>Other specified hemorrhagic conditions</td></tr><tr><td>D69.9</td><td>Hemorrhagic condition, unspecified</td></tr><tr><td>D75.82</td><td>Heparin induced thrombocytopenia (HIT)</td></tr><tr><td>O99.111</td><td>Oth dis of bld/bld-form org/immun mechnsm comp preg, 1st tri</td></tr><tr><td>O99.112</td><td>Oth dis of bld/bld-form org/immun mechnsm comp preg, 2nd tri</td></tr><tr><td>O99.113</td><td>Oth dis of bld/bld-form org/immun mechnsm comp preg, 3rd tri</td></tr><tr><td>O99.119</td><td>Oth dis of bld/bld-form org/immun mechnsm comp preg,unsp tri</td></tr><tr><td>O99.12</td><td>Oth dis of the bld/bld-form org/immun mechnsm comp chldbrth</td></tr><tr><td>O99.13</td><td>Oth dis of the bld/bld-form org/immun mechnsm comp the puerp</td></tr></table></li></ul></div>
  </text>
  <url
       value="http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-coagulation-deficiency-vs"/>
  <version value="2.1.0"/>
  <name value="ElixhauserCoagulationDeficiencyVS"/>
  <title value="Elixhauser Coagulation Deficiency Value Set"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2023-03-21T04:50:14+11:00"/>
  <publisher value="HL7 International Clinical Interoperability Council"/>
  <contact>
    <name value="HL7 International Clinical Interoperability Council"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/cic"/>
    </telecom>
    <telecom>
      <system value="email"/>
      <value value="ciclist@lists.HL7.org"/>
    </telecom>
  </contact>
  <description
               value="Elixhauser Comorbid Condition Value Set for Coagulation Deficiency. ICD-10 codes are drawn from https://www.hcup-us.ahrq.gov/toolssoftware/comorbidityicd10/comorbidity_icd10.jsp, version 2021.1"/>
  <jurisdiction>
    <coding>
      <system value="urn:iso:std:iso:3166"/>
      <code value="US"/>
      <display value="United States of America"/>
    </coding>
  </jurisdiction>
  <compose>
    <include>
      <system value="http://hl7.org/fhir/sid/icd-10-cm"/>
      <concept>
        <code value="D61.09"/>
        <display value="Other constitutional aplastic anemia"/>
      </concept>
      <concept>
        <code value="D61.1"/>
        <display value="Drug-induced aplastic anemia"/>
      </concept>
      <concept>
        <code value="D61.2"/>
        <display value="Aplastic anemia due to other external agents"/>
      </concept>
      <concept>
        <code value="D61.3"/>
        <display value="Idiopathic aplastic anemia"/>
      </concept>
      <concept>
        <code value="D61.810"/>
        <display value="Antineoplastic chemotherapy induced pancytopenia"/>
      </concept>
      <concept>
        <code value="D61.811"/>
        <display value="Other drug-induced pancytopenia"/>
      </concept>
      <concept>
        <code value="D61.818"/>
        <display value="Other pancytopenia"/>
      </concept>
      <concept>
        <code value="D61.82"/>
        <display value="Myelophthisis"/>
      </concept>
      <concept>
        <code value="D61.89"/>
        <display
                 value="Oth aplastic anemias and other bone marrow failure syndromes"/>
      </concept>
      <concept>
        <code value="D61.9"/>
        <display value="Aplastic anemia, unspecified"/>
      </concept>
      <concept>
        <code value="D65"/>
        <display value="Disseminated intravascular coagulation"/>
      </concept>
      <concept>
        <code value="D66"/>
        <display value="Hereditary factor VIII deficiency"/>
      </concept>
      <concept>
        <code value="D67"/>
        <display value="Hereditary factor IX deficiency"/>
      </concept>
      <concept>
        <code value="D68.0"/>
        <display value="Von Willebrand's disease"/>
      </concept>
      <concept>
        <code value="D68.1"/>
        <display value="Hereditary factor XI deficiency"/>
      </concept>
      <concept>
        <code value="D68.2"/>
        <display value="Hereditary deficiency of other clotting factors"/>
      </concept>
      <concept>
        <code value="D68.311"/>
        <display value="Acquired hemophilia"/>
      </concept>
      <concept>
        <code value="D68.312"/>
        <display value="Antiphospholipid antibody with hemorrhagic disorder"/>
      </concept>
      <concept>
        <code value="D68.318"/>
        <display
                 value="Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib"/>
      </concept>
      <concept>
        <code value="D68.32"/>
        <display
                 value="Hemorrhagic disord d/t extrinsic circulating anticoagulants"/>
      </concept>
      <concept>
        <code value="D68.4"/>
        <display value="Acquired coagulation factor deficiency"/>
      </concept>
      <concept>
        <code value="D68.8"/>
        <display value="Other specified coagulation defects"/>
      </concept>
      <concept>
        <code value="D68.9"/>
        <display value="Coagulation defect, unspecified"/>
      </concept>
      <concept>
        <code value="D69.1"/>
        <display value="Qualitative platelet defects"/>
      </concept>
      <concept>
        <code value="D69.3"/>
        <display value="Immune thrombocytopenic purpura"/>
      </concept>
      <concept>
        <code value="D69.41"/>
        <display value="Evans syndrome"/>
      </concept>
      <concept>
        <code value="D69.42"/>
        <display value="Congenital and hereditary thrombocytopenia purpura"/>
      </concept>
      <concept>
        <code value="D69.49"/>
        <display value="Other primary thrombocytopenia"/>
      </concept>
      <concept>
        <code value="D69.51"/>
        <display value="Posttransfusion purpura"/>
      </concept>
      <concept>
        <code value="D69.59"/>
        <display value="Other secondary thrombocytopenia"/>
      </concept>
      <concept>
        <code value="D69.6"/>
        <display value="Thrombocytopenia, unspecified"/>
      </concept>
      <concept>
        <code value="D69.8"/>
        <display value="Other specified hemorrhagic conditions"/>
      </concept>
      <concept>
        <code value="D69.9"/>
        <display value="Hemorrhagic condition, unspecified"/>
      </concept>
      <concept>
        <code value="D75.82"/>
        <display value="Heparin induced thrombocytopenia (HIT)"/>
      </concept>
      <concept>
        <code value="O99.111"/>
        <display
                 value="Oth dis of bld/bld-form org/immun mechnsm comp preg, 1st tri"/>
      </concept>
      <concept>
        <code value="O99.112"/>
        <display
                 value="Oth dis of bld/bld-form org/immun mechnsm comp preg, 2nd tri"/>
      </concept>
      <concept>
        <code value="O99.113"/>
        <display
                 value="Oth dis of bld/bld-form org/immun mechnsm comp preg, 3rd tri"/>
      </concept>
      <concept>
        <code value="O99.119"/>
        <display
                 value="Oth dis of bld/bld-form org/immun mechnsm comp preg,unsp tri"/>
      </concept>
      <concept>
        <code value="O99.12"/>
        <display
                 value="Oth dis of the bld/bld-form org/immun mechnsm comp chldbrth"/>
      </concept>
      <concept>
        <code value="O99.13"/>
        <display
                 value="Oth dis of the bld/bld-form org/immun mechnsm comp the puerp"/>
      </concept>
    </include>
  </compose>
</ValueSet>