Collagen-vascular disease, NOS: Difference between revisions
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== Additional Info == | == 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 == | == Alternate ICD10s to consider coding instead or in addition == |
Revision as of 12:51, 7 November 2017
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: | |
Data Dependencies(Reports/Indicators/Data Elements): | No results |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
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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