COVID19 ICD10CM Value Set for Coagulopathies

retired

URL

http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.3616.200.110.102.3136

Version

20221206

PublisherClinical ArchitectureDate2023-06-21T18:16:37-04:00Purpose

(Clinical Focus: This set of values contains terms related to coagulopathies and is listed as a blood disorder/hemoglobinopathy on the CDC SARS-CoV-2 hospitalization surveillance case report form.),(Data Element Scope: ),(Inclusion Criteria: Includes acquired coagulopathies (e.g., Thrombocytopenia) and inherited coagulopathies (e.g., Von Willebrand's disease).),(Exclusion Criteria: Excludes neonatal, pregnancy related, neoplasm related or anticoagulant overdose induced coagulopathies.)

Expansion

Code	Display	System
D65		http://hl7.org/fhir/sid/icd-10-cm
D66		http://hl7.org/fhir/sid/icd-10-cm
D67		http://hl7.org/fhir/sid/icd-10-cm
D68		http://hl7.org/fhir/sid/icd-10-cm
D68.0		http://hl7.org/fhir/sid/icd-10-cm
D68.00		http://hl7.org/fhir/sid/icd-10-cm
D68.01		http://hl7.org/fhir/sid/icd-10-cm
D68.02		http://hl7.org/fhir/sid/icd-10-cm
D68.020		http://hl7.org/fhir/sid/icd-10-cm
D68.021		http://hl7.org/fhir/sid/icd-10-cm
D68.022		http://hl7.org/fhir/sid/icd-10-cm
D68.023		http://hl7.org/fhir/sid/icd-10-cm
D68.029		http://hl7.org/fhir/sid/icd-10-cm
D68.03		http://hl7.org/fhir/sid/icd-10-cm
D68.04		http://hl7.org/fhir/sid/icd-10-cm
D68.09		http://hl7.org/fhir/sid/icd-10-cm
D68.1		http://hl7.org/fhir/sid/icd-10-cm
D68.2		http://hl7.org/fhir/sid/icd-10-cm
D68.3		http://hl7.org/fhir/sid/icd-10-cm
D68.31		http://hl7.org/fhir/sid/icd-10-cm

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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D65",
      "display" : "Disseminated intravascular coagulation [defibrination syndrome]",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D65-D69",
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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
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      "code" : "D68.00",
      "display" : "Von Willebrand disease, unspecified",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.01",
      "display" : "Von Willebrand disease, type 1",
      "version" : "2024"
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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.02",
      "display" : "Von Willebrand disease, type 2",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.020",
      "display" : "Von Willebrand disease, type 2A",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.021",
      "display" : "Von Willebrand disease, type 2B",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.022",
      "display" : "Von Willebrand disease, type 2M",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.023",
      "display" : "Von Willebrand disease, type 2N",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.029",
      "display" : "Von Willebrand disease, type 2, unspecified",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.03",
      "display" : "Von Willebrand disease, type 3",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.04",
      "display" : "Acquired von Willebrand disease",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.09",
      "display" : "Other von Willebrand disease",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.1",
      "display" : "Hereditary factor XI deficiency",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.2",
      "display" : "Hereditary deficiency of other clotting factors",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.3",
      "display" : "Hemorrhagic disorder due to circulating anticoagulants",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.31",
      "display" : "Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.311",
      "display" : "Acquired hemophilia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.312",
      "display" : "Antiphospholipid antibody with hemorrhagic disorder",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.318",
      "display" : "Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.32",
      "display" : "Hemorrhagic disorder due to extrinsic circulating anticoagulants",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.4",
      "display" : "Acquired coagulation factor deficiency",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.5",
      "display" : "Primary thrombophilia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.51",
      "display" : "Activated protein C resistance",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.52",
      "display" : "Prothrombin gene mutation",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.59",
      "display" : "Other primary thrombophilia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.6",
      "display" : "Other thrombophilia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.61",
      "display" : "Antiphospholipid syndrome",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.62",
      "display" : "Lupus anticoagulant syndrome",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.69",
      "display" : "Other thrombophilia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.8",
      "display" : "Other specified coagulation defects",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D68.9",
      "display" : "Coagulation defect, unspecified",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69",
      "display" : "Purpura and other hemorrhagic conditions",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.0",
      "display" : "Allergic purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.1",
      "display" : "Qualitative platelet defects",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.2",
      "display" : "Other nonthrombocytopenic purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.3",
      "display" : "Immune thrombocytopenic purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.4",
      "display" : "Other primary thrombocytopenia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.41",
      "display" : "Evans syndrome",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.42",
      "display" : "Congenital and hereditary thrombocytopenia purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.49",
      "display" : "Other primary thrombocytopenia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.5",
      "display" : "Secondary thrombocytopenia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.51",
      "display" : "Posttransfusion purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.59",
      "display" : "Other secondary thrombocytopenia",
      "version" : "2024"
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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.6",
      "display" : "Thrombocytopenia, unspecified",
      "version" : "2024"
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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.8",
      "display" : "Other specified hemorrhagic conditions",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.9",
      "display" : "Hemorrhagic condition, unspecified",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "Z14.02",
      "display" : "Symptomatic hemophilia A carrier",
      "version" : "2024"
    } ],
    "total" : 52,
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    "timestamp" : "2024-06-14T16:13:35-04:00"
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