Primary hypercoagulability (thrombophilia): Difference between revisions
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Ttenbergen (talk | contribs) |
Ttenbergen (talk | contribs) m Text replacement - "Heredary/congenital" to "Hereditary/congenital" |
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{{ICD10 category|Heme/immunology}}{{ICD10 category| | {{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}} | ||
== Additional Info == | == Additional Info == | ||
incl factor V (Leiden) mutatation, deficiency of Protein S, Protein C or antithrombin, prothrombin gene mutation | incl factor V (Leiden) mutatation, deficiency of Protein S, Protein C or antithrombin, prothrombin gene mutation |
Revision as of 22:29, 6 November 2017
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: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
incl factor V (Leiden) mutatation, deficiency of Protein S, Protein C or antithrombin, prothrombin gene mutation
Alternate ICD10s to consider coding instead or in addition
Candidate Combined ICD10 codes
(put links to likely candidates coded with this one, eg. a cause for a trauma.)
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