| ICD10 (CM) Code | Description |
| D65
|
Disseminated intravascular coagulation |
| D66
|
Hereditary factor VIII deficiency |
| D67
|
Hereditary factor IX deficiency |
| 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 |
| D68.318
|
Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib |
| D68.32
|
Hemorrhagic disord d/t extrinsic circulating anticoagulants |
| D68.4
|
Acquired coagulation factor deficiency |
| 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 |
| D75.821
|
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 |
| D75.84
|
Other platelet-activating anti-PF4 disorders |
| R23.3
|
Spontaneous ecchymoses |
