Takayasu's arteritis (aortic arch syndrome): Difference between revisions
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| ICD10 Code=M31.4 | | ICD10 Code=M31.4 | ||
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== Additional Info == | == Additional Info == | ||
[https://en.wikipedia.org/wiki/Takayasu%27s_arteritis 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 | |||
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Latest revision as of 01:57, 18 November 2018
| 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: | |
| 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
Data Integrity Checks (automatic list)
none found
Related Articles
| Related articles: |
Show all ICD10 Subcategories