Bleeding Disorder

active

URL

http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.287

Version

20220127

PublisherJoint CommissionDate2022-01-27T01:02:42-05:00Purpose

(Clinical Focus: The purpose of this value set is to group diagnoses of a bleeding disorders.),(Data Element Scope: This value set may use a model element related to diagnosis.),(Inclusion Criteria: Includes concepts that identify a diagnosis of a bleeding disorder.),(Exclusion Criteria: No exclusions.)

Expansion

Code	Display	System
D66	Hereditary factor VIII deficiency	http://hl7.org/fhir/sid/icd-10-cm
D67	Hereditary factor IX deficiency	http://hl7.org/fhir/sid/icd-10-cm
D68.00	Von Willebrand disease, unspecified	http://hl7.org/fhir/sid/icd-10-cm
D68.01	Von Willebrand disease, type 1	http://hl7.org/fhir/sid/icd-10-cm
D68.020	Von Willebrand disease, type 2A	http://hl7.org/fhir/sid/icd-10-cm
D68.021	Von Willebrand disease, type 2B	http://hl7.org/fhir/sid/icd-10-cm
D68.022	Von Willebrand disease, type 2M	http://hl7.org/fhir/sid/icd-10-cm
D68.023	Von Willebrand disease, type 2N	http://hl7.org/fhir/sid/icd-10-cm
D68.029	Von Willebrand disease, type 2, unspecified	http://hl7.org/fhir/sid/icd-10-cm
D68.03	Von Willebrand disease, type 3	http://hl7.org/fhir/sid/icd-10-cm
D68.04	Acquired von Willebrand disease	http://hl7.org/fhir/sid/icd-10-cm
D68.09	Other von Willebrand disease	http://hl7.org/fhir/sid/icd-10-cm
D68.1	Hereditary factor XI deficiency	http://hl7.org/fhir/sid/icd-10-cm
D68.2	Hereditary deficiency of other clotting factors	http://hl7.org/fhir/sid/icd-10-cm
D68.311	Acquired hemophilia	http://hl7.org/fhir/sid/icd-10-cm
D68.312	Antiphospholipid antibody with hemorrhagic disorder	http://hl7.org/fhir/sid/icd-10-cm
D68.318	Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors	http://hl7.org/fhir/sid/icd-10-cm
D68.32	Hemorrhagic disorder due to extrinsic circulating anticoagulants	http://hl7.org/fhir/sid/icd-10-cm
D68.4	Acquired coagulation factor deficiency	http://hl7.org/fhir/sid/icd-10-cm
D68.51	Activated protein C resistance	http://hl7.org/fhir/sid/icd-10-cm

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      "version" : "2024"
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      "code" : "D68.029",
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      "version" : "2024"
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      "code" : "D68.03",
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      "code" : "D68.2",
      "display" : "Hereditary deficiency of other clotting factors",
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    }, {
      "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" : "D68.51",
      "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" : "D68.61",
      "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" : "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" : "D69.41",
      "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" : "D69.51",
      "display" : "Posttransfusion purpura",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.59",
      "display" : "Other secondary thrombocytopenia",
      "version" : "2024"
    }, {
      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.6",
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      "code" : "D69.8",
      "display" : "Other specified hemorrhagic conditions",
      "version" : "2024"
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      "system" : "http://hl7.org/fhir/sid/icd-10-cm",
      "code" : "D69.9",
      "display" : "Hemorrhagic condition, unspecified",
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