Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis): Difference between revisions
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{{ICD10 category|Heme/immunology}}, {{ICD10 category|Allergy}}, {{ICD10 category|Allergy}} | {{ICD10 category|Heme/immunology}}, {{ICD10 category|Allergy}}, {{ICD10 category|Allergy}} | ||
{{ICD10 category|Vasculitis}} | {{ICD10 category|Vasculitis}}{{ICD10 category|ANCA-associated Vasculitis (AAV)}} | ||
== Additional Info == | == Additional Info == | ||
*Churg-Strauss syndrome, now also referred to by its medically more accurate term eosinophilic granulomatosis with polyangiitis (EGPA), is a rare systemic vasculitis (inflammation in the wall of blood vessels of the body), predominantly affecting small-sized vessels. This is considered to be an ANCA-associated | *Churg-Strauss syndrome, now also referred to by its medically more accurate term eosinophilic granulomatosis with polyangiitis (EGPA), is a rare systemic vasculitis (inflammation in the wall of blood vessels of the body), predominantly affecting small-sized vessels. This is considered to be an ANCA-associated Vasculitis (AAV) | ||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
more specifically: | |||
{{ListICD10Category | categoryName = ANCA-associated Vasculitis (AAV)}} | |||
more generally: | |||
{{ListICD10Category | categoryName = Vasculitis}} | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == |
Revision as of 09:15, 2023 August 24
ICD10 Diagnosis | |
Dx: | Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis) |
ICD10 code: | M30.1 |
Pre-ICD10 counterpart: | Churg-Strauss Syndrome |
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
- Churg-Strauss syndrome, now also referred to by its medically more accurate term eosinophilic granulomatosis with polyangiitis (EGPA), is a rare systemic vasculitis (inflammation in the wall of blood vessels of the body), predominantly affecting small-sized vessels. This is considered to be an ANCA-associated Vasculitis (AAV)
Alternate ICD10s to consider coding instead or in addition
more specifically:
ANCA-associated Vasculitis (AAV) codes: |
more generally:
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
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