{
  "resourceType": "ValueSet",
  "id": "elixhauser-coagulation-deficiency-vs",
  "text": {
    "status": "generated",
    "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/3.0.0/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>"
  },
  "url": "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-coagulation-deficiency-vs",
  "version": "2.0.0",
  "name": "ElixhauserCoagulationDeficiencyVS",
  "title": "Elixhauser Coagulation Deficiency Value Set",
  "status": "active",
  "date": "2022-01-18T03:17:40+00:00",
  "publisher": "HL7 International Clinical Interoperability Council",
  "contact": [
    {
      "name": "HL7 International Clinical Interoperability Council",
      "telecom": [
        {
          "system": "url",
          "value": "http://www.hl7.org/Special/committees/cic"
        },
        {
          "system": "email",
          "value": "ciclist@lists.HL7.org"
        }
      ]
    }
  ],
  "description": "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": "urn:iso:std:iso:3166",
          "code": "US",
          "display": "United States of America"
        }
      ]
    }
  ],
  "compose": {
    "include": [
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "concept": [
          {
            "code": "D61.09",
            "display": "Other constitutional aplastic anemia"
          },
          {
            "code": "D61.1",
            "display": "Drug-induced aplastic anemia"
          },
          {
            "code": "D61.2",
            "display": "Aplastic anemia due to other external agents"
          },
          {
            "code": "D61.3",
            "display": "Idiopathic aplastic anemia"
          },
          {
            "code": "D61.810",
            "display": "Antineoplastic chemotherapy induced pancytopenia"
          },
          {
            "code": "D61.811",
            "display": "Other drug-induced pancytopenia"
          },
          {
            "code": "D61.818",
            "display": "Other pancytopenia"
          },
          {
            "code": "D61.82",
            "display": "Myelophthisis"
          },
          {
            "code": "D61.89",
            "display": "Oth aplastic anemias and other bone marrow failure syndromes"
          },
          {
            "code": "D61.9",
            "display": "Aplastic anemia, unspecified"
          },
          {
            "code": "D65",
            "display": "Disseminated intravascular coagulation"
          },
          {
            "code": "D66",
            "display": "Hereditary factor VIII deficiency"
          },
          {
            "code": "D67",
            "display": "Hereditary factor IX deficiency"
          },
          {
            "code": "D68.0",
            "display": "Von Willebrand's disease"
          },
          {
            "code": "D68.1",
            "display": "Hereditary factor XI deficiency"
          },
          {
            "code": "D68.2",
            "display": "Hereditary deficiency of other clotting factors"
          },
          {
            "code": "D68.311",
            "display": "Acquired hemophilia"
          },
          {
            "code": "D68.312",
            "display": "Antiphospholipid antibody with hemorrhagic disorder"
          },
          {
            "code": "D68.318",
            "display": "Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib"
          },
          {
            "code": "D68.32",
            "display": "Hemorrhagic disord d/t extrinsic circulating anticoagulants"
          },
          {
            "code": "D68.4",
            "display": "Acquired coagulation factor deficiency"
          },
          {
            "code": "D68.8",
            "display": "Other specified coagulation defects"
          },
          {
            "code": "D68.9",
            "display": "Coagulation defect, unspecified"
          },
          {
            "code": "D69.1",
            "display": "Qualitative platelet defects"
          },
          {
            "code": "D69.3",
            "display": "Immune thrombocytopenic purpura"
          },
          {
            "code": "D69.41",
            "display": "Evans syndrome"
          },
          {
            "code": "D69.42",
            "display": "Congenital and hereditary thrombocytopenia purpura"
          },
          {
            "code": "D69.49",
            "display": "Other primary thrombocytopenia"
          },
          {
            "code": "D69.51",
            "display": "Posttransfusion purpura"
          },
          {
            "code": "D69.59",
            "display": "Other secondary thrombocytopenia"
          },
          {
            "code": "D69.6",
            "display": "Thrombocytopenia, unspecified"
          },
          {
            "code": "D69.8",
            "display": "Other specified hemorrhagic conditions"
          },
          {
            "code": "D69.9",
            "display": "Hemorrhagic condition, unspecified"
          },
          {
            "code": "D75.82",
            "display": "Heparin induced thrombocytopenia (HIT)"
          },
          {
            "code": "O99.111",
            "display": "Oth dis of bld/bld-form org/immun mechnsm comp preg, 1st tri"
          },
          {
            "code": "O99.112",
            "display": "Oth dis of bld/bld-form org/immun mechnsm comp preg, 2nd tri"
          },
          {
            "code": "O99.113",
            "display": "Oth dis of bld/bld-form org/immun mechnsm comp preg, 3rd tri"
          },
          {
            "code": "O99.119",
            "display": "Oth dis of bld/bld-form org/immun mechnsm comp preg,unsp tri"
          },
          {
            "code": "O99.12",
            "display": "Oth dis of the bld/bld-form org/immun mechnsm comp chldbrth"
          },
          {
            "code": "O99.13",
            "display": "Oth dis of the bld/bld-form org/immun mechnsm comp the puerp"
          }
        ]
      }
    ]
  }
}