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Coagulation and hemorrhagic disorders

CCSR category BLD006 · 52 ICD-10-CM codes

Code Families in This Category

  • D68 Other coagulation defects · 26
  • D69 Purpura and other hemorrhagic conditions · 12
  • D75 Other and unspecified diseases of blood and blood-forming organs · 8
  • D47 Other neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue · 1
  • D65 Disseminated intravascular coagulation [defibrination syndrome] · 1
  • D66 Hereditary factor VIII deficiency · 1
  • D67 Hereditary factor IX deficiency · 1
  • M36 Systemic disorders of connective tissue in diseases classified elsewhere · 1
  • O72 Postpartum hemorrhage · 1

ICD-10-CM Codes in This Category (52)

  • D47.3 — Essential (hemorrhagic) thrombocythemia
  • D65 — Disseminated intravascular coagulation [defibrination syndrome]
  • D66 — Hereditary factor VIII deficiency
  • D67 — Hereditary factor IX deficiency
  • D68.0 — Von Willebrand disease
  • D68.00 — Von Willebrand disease, unspecified
  • D68.01 — Von Willebrand disease, type 1
  • D68.020 — Von Willebrand disease, type 2A
  • D68.021 — Von Willebrand disease, type 2B
  • D68.022 — Von Willebrand disease, type 2M
  • D68.023 — Von Willebrand disease, type 2N
  • D68.029 — Von Willebrand disease, type 2, unspecified
  • D68.03 — Von Willebrand disease, type 3
  • D68.04 — Acquired von Willebrand disease
  • D68.09 — Other von Willebrand 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 — Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
  • D68.32 — Hemorrhagic disorder due to extrinsic circulating anticoagulants
  • D68.4 — Acquired coagulation factor deficiency
  • D68.51 — Activated protein C resistance
  • D68.52 — Prothrombin gene mutation
  • D68.59 — Other primary thrombophilia
  • D68.61 — Antiphospholipid syndrome
  • D68.62 — Lupus anticoagulant syndrome
  • D68.69 — Other thrombophilia
  • D68.8 — Other specified coagulation defects
  • D68.9 — Coagulation defect, unspecified
  • D69.0 — Allergic purpura
  • D69.1 — Qualitative platelet defects
  • D69.2 — Other nonthrombocytopenic purpura
  • 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)
  • D75.821 — Non-immune heparin-induced thrombocytopenia
  • D75.822 — Immune-mediated heparin-induced thrombocytopenia
  • D75.828 — Other heparin-induced thrombocytopenia syndrome
  • D75.829 — Heparin-induced thrombocytopenia, unspecified
  • D75.838 — Other thrombocytosis
  • D75.839 — Thrombocytosis, unspecified
  • D75.84 — Other platelet-activating anti-PF4 disorders
  • M36.2 — Hemophilic arthropathy
  • O72.3 — Postpartum coagulation defects

Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, Rockville, MD. All data sources.