minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.0.0 - STU 2
minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.0.0 - STU 2
This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.0.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions 
{
"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"
}
]
}
]
}
}
IG © 2019+ HL7 International Clinical Interoperability Council. Package hl7.fhir.us.mcode#2.0.0 based on FHIR 4.0.1. Generated 2022-01-18
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