Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor)
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|Dx:||Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor)|
|Pre-ICD10 counterpart:||Von Willebrand Disease|
|APACHE Como Component:||none|
|APACHE Acute Component:||none|
|External ICD10 Documentation|
This diagnosis is a part of ICD10 collection.
- Hereditary bleeding disorder due to low level protein (Von Willebrand factor) or protein not functioning properly.
- The entity called "Acquired von Willebrand's syndrome" is DIFFERENT from the hereditary disorder. For that entity instead use the code Acquired deficiency of clotting factors
See Von Willebrand Disease on wikipedia
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