View source for Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor)

{{ICD10 transition status
| OldDxArticle = Von Willebrand Disease
| CurrentStatus = reconciled
| InitialEditorAssigned = Elaine Nagy
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{{ICD10 dx
| MinimumCombinedCodes =
| ICD10 Code=D68.0
| BugRequired= 
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{{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}} 

== Additional Info ==
*Hereditary bleeding disorder due to low level protein ([http://en.wikipedia.org/wiki/Von_Willebrand_factor 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 [http://en.wikipedia.org/wiki/Von_Willebrand_disease Von Willebrand Disease] on wikipedia

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