Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor)
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ICD10 Diagnosis | |
Dx: | Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor) |
ICD10 code: | D68.0 |
Pre-ICD10 counterpart: | Von Willebrand Disease |
Charlson/ALERT Scale: | none |
APACHE Como Component: | none |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
- 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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