Von Willebrand's disease (hereditary deficiency of F8 von Willebrand factor): Difference between revisions

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Hereditary bleeding disorder due to low level protein ([http://en.wikipedia.org/wiki/Von_Willebrand_factor Von Willebrand factor]) or protein not functioning properly.
Hereditary bleeding disorder due to low level protein ([http://en.wikipedia.org/wiki/Von_Willebrand_factor Von Willebrand factor]) or protein not functioning properly.


{{DA | Can this code be used for instances of acquired von Willebrand's disease as well? }}
{{DA | 1
* Can this code be used for instances of acquired von Willebrand's disease as well? }}


See [http://en.wikipedia.org/wiki/Von_Willebrand_disease Von Willebrand Disease] on wikipedia
See [http://en.wikipedia.org/wiki/Von_Willebrand_disease Von Willebrand Disease] on wikipedia

Revision as of 11:04, 2021 January 7

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.

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    • 2019-01-01
    • 2999-12-31
    • D68.0
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Additional Info

Hereditary bleeding disorder due to low level protein (Von Willebrand factor) or protein not functioning properly.


1

  • Can this code be used for instances of acquired von Willebrand's disease as well?
  • SMW


  • Cargo


  • Categories

See Von Willebrand Disease on wikipedia

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

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