| D68.00 |
Von Willebrand disease, unspecified |
Notes ↗
|
| D68.01 |
Von Willebrand disease, type 1 |
Notes ↗
|
| D68.020 |
Von Willebrand disease, type 2A |
Notes ↗
|
| D68.021 |
Von Willebrand disease, type 2B |
Notes ↗
|
| D68.022 |
Von Willebrand disease, type 2M |
Notes ↗
|
| D68.023 |
Von Willebrand disease, type 2N |
Notes ↗
|
| D68.029 |
Von Willebrand disease, type 2, unspecified |
Notes ↗
|
| D68.03 |
Von Willebrand disease, type 3 |
Notes ↗
|
| D68.04 |
Acquired von Willebrand disease |
Notes ↗
|
| D68.09 |
Other von Willebrand disease |
Notes ↗
|
| D68.1 |
Hereditary factor XI deficiency |
Notes ↗
|
| D68.2 |
Hereditary deficiency of other clotting factors |
Notes ↗
|
| D68.311 |
Acquired hemophilia |
Notes ↗
|
| D69.1 |
Qualitative platelet defects |
Notes ↗
|
| D69.3 |
Immune thrombocytopenic purpura |
Notes ↗
|
| D69.41 |
Evans syndrome |
Notes ↗
|
| D69.42 |
Congenital and hereditary thrombocytopenia purpura |
Notes ↗
|
| D69.49 |
Other primary thrombocytopenia |
Notes ↗
|
| D75.84 |
Other platelet-activating anti-PF4 disorders |
Notes ↗
|
| M31.10 |
Thrombotic microangiopathy, unspecified |
Notes ↗
|
| M31.19 |
Other thrombotic microangiopathy |
Notes ↗
|