Wegener's granulomatosis: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Wegener's Granulomatosis | | OldDxArticle = Wegener's Granulomatosis / Granulomatosis with polyangiitis | ||
| CurrentStatus = reconciled | |||
| InitialEditorAssigned = Marla Penner | | InitialEditorAssigned = Marla Penner | ||
| MinimumCombinedCodes = | | MinimumCombinedCodes = | ||
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{{ICD10 category|Heme/immunology}} | |||
== Additional Info == | == Additional Info == | ||
Wegener's granulomatosis is also known as Granulomatosis with polyangiitis (GPA) or Wegener's Granulomatosis -P ANCA+. It is a rare autoimmune disorder that interrupts blood flow to essential organs by causing vasculitis, or inflammation of the blood vessels | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == |
Revision as of 00:01, 2017 November 6
ICD10 Diagnosis | |
Dx: | Wegener's granulomatosis |
ICD10 code: | M31.3 |
Pre-ICD10 counterpart: | Wegener's Granulomatosis / Granulomatosis with polyangiitis |
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
Wegener's granulomatosis is also known as Granulomatosis with polyangiitis (GPA) or Wegener's Granulomatosis -P ANCA+. It is a rare autoimmune disorder that interrupts blood flow to essential organs by causing vasculitis, or inflammation of the blood vessels
Alternate ICD10s to consider coding instead or in addition
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
Candidate Combined ICD10 codes
(put links to likely candidates coded with this one, eg. a cause for a trauma.)
Related Articles
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