Collagen-vascular disease, NOS: Difference between revisions
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{{ICD10 dx | {{ICD10 dx | ||
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| ICD10 Code=M35.9 | | ICD10 Code=M35.9 | ||
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{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Hereditary/congenital}} | {{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Hereditary/congenital}}{{ICD10 category|Rheumatic disease}}{{ICD10 category|Vasculitis}} | ||
== 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). | 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). | ||
'''Includes''' | |||
*Ehlers Danlos syndrome, combine with [[Malformation/disorder NOS, congenital]] | |||
* connective tissue disease | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
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* [[Scleroderma or CREST syndrome (systemic sclerosis)]] | * [[Scleroderma or CREST syndrome (systemic sclerosis)]] | ||
* [[Collagen-vascular overlap syndrome]] | * [[Collagen-vascular overlap syndrome]] | ||
* [[Behcet's disease]] | * [[Behcet's disease]] | ||
* [[Polymyalgia rheumatica]] | * [[Polymyalgia rheumatica]] | ||
* [[:Category:Rheumatic disease]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} |
Latest revision as of 08:19, 20 June 2023
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).
Includes
- Ehlers Danlos syndrome, combine with Malformation/disorder NOS, congenital
- connective tissue disease
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
- Category:Rheumatic disease
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
Show all ICD10 Subcategories