Primary hypercoagulability (thrombophilia): Difference between revisions

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{{ICD10 transition status
{{ICD10 transition status
| OldDxArticle =| CurrentStatus = reconciled
| OldDxArticle =
| CurrentStatus = reconciled
| InitialEditorAssigned = Elaine Nagy
| InitialEditorAssigned = Elaine Nagy
| MinimumCombinedCodes =
}}
}}
{{ICD10 dx
{{ICD10 dx
| MinimumCombinedCodes =
| ICD10 Code=D68.5
| ICD10 Code=D68.5
| BugRequired=  
| BugRequired=  
}}
}}
{{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}}


{{ICD10 category|Heme/immunology}}{{ICD10 category|Heredary/congenital}}
== Additional Info ==
== Additional Info ==
incl factor V (Leiden) mutatation, deficiency of Protein S, Protein C or antithrombin, prothrombin gene mutation
'''Includes'''
*Factor V (Factor 5, Leiden) mutation or deficiency, combine with [[Malformation/disorder NOS, congenital]]
*deficiency of Protein S, Protein C  
*antithrombin, prothrombin gene mutation or deficiency
* Hypercoagulable state NOS


== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
*[[Hypercoagulability due to Lupus anticoagulant, anticardiolipin syndrome, antiphospholipid syndrome]]
*[[Hypercoagulability due to Lupus anticoagulant, anticardiolipin syndrome, antiphospholipid syndrome]]


(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
== Candidate [[Combined ICD10 codes]] ==


== Related CCI Codes ==


== Candidate [[Combined ICD10 codes]] ==
{{Data Integrity Check List}}
(put links to likely candidates coded with this one, eg. a cause for a trauma.)


== Related Articles ==
== Related Articles ==
{{Related Articles}}
{{Related Articles}}


{{ICD10 footer}}
{{ICD10 footer}}
{{EndPlaceHolder}}
{{EndPlaceHolder}}

Latest revision as of 12:14, 12 September 2023

ICD10 Diagnosis
Dx: Primary hypercoagulability (thrombophilia)
ICD10 code: D68.5
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
Data Dependencies(Reports/Indicators/Data Elements): No results
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • D68.5
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories

Additional Info

Includes

  • Factor V (Factor 5, Leiden) mutation or deficiency, combine with Malformation/disorder NOS, congenital
  • deficiency of Protein S, Protein C
  • antithrombin, prothrombin gene mutation or deficiency
  • Hypercoagulable state NOS

Alternate ICD10s to consider coding instead or in addition

Data Integrity Checks (automatic list)

none found

Related articles:


Show all ICD10 Subcategories

ICD10 Categories: