Collagen-vascular disease, NOS: Difference between revisions
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{{ICD10 category|Musculoskeletal/soft tissue}} | {{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category|{{ICD10 category| | ||
== Additional Info == | == Additional Info == |
Revision as of 12:52, 2017 November 7
ICD10 Diagnosis | |
Dx: | Collagen-vascular disease, NOS |
ICD10 code: | M35.9 |
Pre-ICD10 counterpart: | Other CollVasc Diseases |
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.
{{ICD10 category|{{ICD10 category|Additional Info
Collagen vascular disease is sometimes also called connective tissue disease. Collagen vascular diseases can be heritable (inherited from one’s parents) or autoimmune (resulting from activity of the body’s immune system against itself).
Alternate ICD10s to consider coding instead or in addition
- Polyarteritis nodosa (PAN)
- Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis)
- Kawasaki disease (mucocutaneous lymph node syndrome)
- Goodpasture syndrome (hypersensitivity angiitis)
- Thrombotic thrombocytopenic purpura (TTP)
- Wegener's Granulomatosis / Granulomatosis with polyangiitis
- Takayasu's arteritis (aortic arch syndrome)
- Giant cell arteritis/temporal arteritis
- Systemic lupus erythematosis (SLE, lupus)
- Dermatomyositis/polymyositis
- Scleroderma or CREST syndrome (systemic sclerosis)
- Collagen-vascular overlap syndrome
- Behcet's disease}
- Polymyalgia rheumatica
Candidate Combined ICD10 codes
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