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Packageus.nlm.vsac
Resource TypeValueSet
IdValueSet-2.16.840.1.113762.1.4.1248.23.json
FHIR VersionR4
Sourcehttps://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1248.23/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1248.23
Version20250205
Statusactive
Date2025-02-05T01:09:18-05:00
NameCoagulationDisorders
TitleCoagulation Disorders
Realmus
Authorityhl7
DescriptionICD-10-CM codes for coagulation disorders, based on AHRQ's PSI- 09 'Coagulation Disorders' code list.
Purpose(Clinical Focus: The purpose of this value set is to represent concepts for coagulation disorders.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts for coagulation disorders.),(Exclusion Criteria: None)

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
icd-10-cmInternational Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)

Narrative

No narrative content found in resource


Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1248.23",
  "meta": {
    "versionId": "19",
    "lastUpdated": "2025-02-05T01:09:18.000-05:00",
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  "extension": [
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      "valueDate": "2025-02-05"
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  "version": "20250205",
  "name": "CoagulationDisorders",
  "title": "Coagulation Disorders",
  "status": "active",
  "date": "2025-02-05T01:09:18-05:00",
  "publisher": "Mathematica PSI Steward",
  "description": "ICD-10-CM codes for coagulation disorders, based on AHRQ's PSI- 09 'Coagulation Disorders' code list.",
  "jurisdiction": [
    {
      "coding": [
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          "system": "urn:iso:std:iso:3166",
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  "purpose": "(Clinical Focus: The purpose of this value set is to represent concepts for coagulation disorders.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts for coagulation disorders.),(Exclusion Criteria: None)",
  "compose": {
    "include": [
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "concept": [
          {
            "code": "D47.3",
            "display": "Essential (hemorrhagic) thrombocythemia"
          },
          {
            "code": "D61.02",
            "display": "Shwachman-Diamond syndrome"
          },
          {
            "code": "D61.03",
            "display": "Fanconi anemia"
          },
          {
            "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": "Other specified aplastic anemias and other bone marrow failure syndromes"
          },
          {
            "code": "D61.9",
            "display": "Aplastic anemia, unspecified"
          },
          {
            "code": "D65",
            "display": "Disseminated intravascular coagulation [defibrination syndrome]"
          },
          {
            "code": "D66",
            "display": "Hereditary factor VIII deficiency"
          },
          {
            "code": "D67",
            "display": "Hereditary factor IX deficiency"
          },
          {
            "code": "D68.00",
            "display": "Von Willebrand disease, unspecified"
          },
          {
            "code": "D68.01",
            "display": "Von Willebrand disease, type 1"
          },
          {
            "code": "D68.020",
            "display": "Von Willebrand disease, type 2A"
          },
          {
            "code": "D68.021",
            "display": "Von Willebrand disease, type 2B"
          },
          {
            "code": "D68.022",
            "display": "Von Willebrand disease, type 2M"
          },
          {
            "code": "D68.023",
            "display": "Von Willebrand disease, type 2N"
          },
          {
            "code": "D68.029",
            "display": "Von Willebrand disease, type 2, unspecified"
          },
          {
            "code": "D68.03",
            "display": "Von Willebrand disease, type 3"
          },
          {
            "code": "D68.04",
            "display": "Acquired von Willebrand disease"
          },
          {
            "code": "D68.09",
            "display": "Other von Willebrand 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": "Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors"
          },
          {
            "code": "D68.32",
            "display": "Hemorrhagic disorder due to 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"
          }
        ]
      }
    ]
  },
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    "timestamp": "2025-05-23T20:55:39-04:00",
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      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D47.3",
        "display": "Essential (hemorrhagic) thrombocythemia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
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        "display": "Shwachman-Diamond syndrome"
      },
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        "version": "2025",
        "code": "D61.03",
        "display": "Fanconi anemia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.09",
        "display": "Other constitutional aplastic anemia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.1",
        "display": "Drug-induced aplastic anemia"
      },
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        "system": "http://hl7.org/fhir/sid/icd-10-cm",
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        "version": "2025",
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        "display": "Idiopathic aplastic anemia"
      },
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        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.810",
        "display": "Antineoplastic chemotherapy induced pancytopenia"
      },
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        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.811",
        "display": "Other drug-induced pancytopenia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.818",
        "display": "Other pancytopenia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.82",
        "display": "Myelophthisis"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.89",
        "display": "Other specified aplastic anemias and other bone marrow failure syndromes"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D61.9",
        "display": "Aplastic anemia, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D65",
        "display": "Disseminated intravascular coagulation [defibrination syndrome]"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D66",
        "display": "Hereditary factor VIII deficiency"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D67",
        "display": "Hereditary factor IX deficiency"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.00",
        "display": "Von Willebrand disease, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.01",
        "display": "Von Willebrand disease, type 1"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.020",
        "display": "Von Willebrand disease, type 2A"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.021",
        "display": "Von Willebrand disease, type 2B"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.022",
        "display": "Von Willebrand disease, type 2M"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.023",
        "display": "Von Willebrand disease, type 2N"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.029",
        "display": "Von Willebrand disease, type 2, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.03",
        "display": "Von Willebrand disease, type 3"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.04",
        "display": "Acquired von Willebrand disease"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.09",
        "display": "Other von Willebrand disease"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.1",
        "display": "Hereditary factor XI deficiency"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.2",
        "display": "Hereditary deficiency of other clotting factors"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.311",
        "display": "Acquired hemophilia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.312",
        "display": "Antiphospholipid antibody with hemorrhagic disorder"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.318",
        "display": "Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.32",
        "display": "Hemorrhagic disorder due to extrinsic circulating anticoagulants"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.4",
        "display": "Acquired coagulation factor deficiency"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.8",
        "display": "Other specified coagulation defects"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D68.9",
        "display": "Coagulation defect, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.1",
        "display": "Qualitative platelet defects"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.3",
        "display": "Immune thrombocytopenic purpura"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.41",
        "display": "Evans syndrome"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.42",
        "display": "Congenital and hereditary thrombocytopenia purpura"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.49",
        "display": "Other primary thrombocytopenia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.51",
        "display": "Posttransfusion purpura"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.59",
        "display": "Other secondary thrombocytopenia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.6",
        "display": "Thrombocytopenia, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.8",
        "display": "Other specified hemorrhagic conditions"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "D69.9",
        "display": "Hemorrhagic condition, unspecified"
      }
    ]
  }
}