minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.1.0 - STU 2.1
minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.1.0 - STU 2.1
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 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 
| Official URL: http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-coagulation-deficiency-vs | Version: 2.1.0 | |||
| Active as of 2023-03-21 | Computable Name: ElixhauserCoagulationDeficiencyVS | |||
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
References
http://hl7.org/fhir/sid/icd-10-cm| Code | Display |
| D61.09 | Other constitutional aplastic anemia |
| D61.1 | Drug-induced aplastic anemia |
| D61.2 | Aplastic anemia due to other external agents |
| D61.3 | Idiopathic aplastic anemia |
| D61.810 | Antineoplastic chemotherapy induced pancytopenia |
| D61.811 | Other drug-induced pancytopenia |
| D61.818 | Other pancytopenia |
| D61.82 | Myelophthisis |
| D61.89 | Oth aplastic anemias and other bone marrow failure syndromes |
| D61.9 | Aplastic anemia, unspecified |
| D65 | Disseminated intravascular coagulation |
| D66 | Hereditary factor VIII deficiency |
| D67 | Hereditary factor IX deficiency |
| D68.0 | Von Willebrand's disease |
| D68.1 | Hereditary factor XI deficiency |
| D68.2 | Hereditary deficiency of other clotting factors |
| D68.311 | Acquired hemophilia |
| D68.312 | Antiphospholipid antibody with hemorrhagic disorder |
| D68.318 | Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib |
| D68.32 | Hemorrhagic disord d/t extrinsic circulating anticoagulants |
| D68.4 | Acquired coagulation factor deficiency |
| D68.8 | Other specified coagulation defects |
| D68.9 | Coagulation defect, unspecified |
| D69.1 | Qualitative platelet defects |
| D69.3 | Immune thrombocytopenic purpura |
| D69.41 | Evans syndrome |
| D69.42 | Congenital and hereditary thrombocytopenia purpura |
| D69.49 | Other primary thrombocytopenia |
| D69.51 | Posttransfusion purpura |
| D69.59 | Other secondary thrombocytopenia |
| D69.6 | Thrombocytopenia, unspecified |
| D69.8 | Other specified hemorrhagic conditions |
| D69.9 | Hemorrhagic condition, unspecified |
| D75.82 | Heparin induced thrombocytopenia (HIT) |
| O99.111 | Oth dis of bld/bld-form org/immun mechnsm comp preg, 1st tri |
| O99.112 | Oth dis of bld/bld-form org/immun mechnsm comp preg, 2nd tri |
| O99.113 | Oth dis of bld/bld-form org/immun mechnsm comp preg, 3rd tri |
| O99.119 | Oth dis of bld/bld-form org/immun mechnsm comp preg,unsp tri |
| O99.12 | Oth dis of the bld/bld-form org/immun mechnsm comp chldbrth |
| O99.13 | Oth dis of the bld/bld-form org/immun mechnsm comp the puerp |
This value set contains 40 concepts
Expansion based on http://hl7.org/fhir/sid/icd-10-cm version 2021
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |
IG © 2022+ HL7 International Clinical Interoperability Council. Package hl7.fhir.us.mcode#2.1.0 based on FHIR 4.0.1. Generated 2023-03-21
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