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.