Takayasu's arteritis (aortic arch syndrome): Difference between revisions
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Ttenbergen (talk | contribs) m →Candidate [[Combined ICD10 codes]]: cleaning up the ICD10 formatting that went bad on import |
Ttenbergen (talk | contribs) m Text replacement - "== Related Articles == {{Related Articles}} " to "== Related CCI Codes == == Related Articles == {{Related Articles}} " |
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Revision as of 19:35, 21 November 2017
ICD10 Diagnosis | |
Dx: | Takayasu's arteritis (aortic arch syndrome) |
ICD10 code: | M31.4 |
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.
Additional Info
Takayasu's arteritis] is a rare, systemic, inflammatory large-vessel vasculitis of unknown etiology that most commonly affects women of childbearing age. It is defined as "granulomatous inflammation of the aorta and its major branches" by the Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitis
Alternate ICD10s to consider coding instead or in addition
Candidate Combined ICD10 codes
Related CCI Codes
Related Articles
Show all ICD10 Subcategories