Scleroderma or CREST syndrome (systemic sclerosis): Difference between revisions
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{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|{{ICD10 category|{{ICD10 category| | {{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Skin}}{{ICD10 category|{{ICD10 category| | ||
== Additional Info == | == Additional Info == | ||
*Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs | *Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs |
Revision as of 13:04, 2017 November 7
ICD10 Diagnosis | |
Dx: | Scleroderma or CREST syndrome (systemic sclerosis) |
ICD10 code: | M34 |
Pre-ICD10 counterpart: | Scleroderma |
Charlson/ALERT Scale: | Rheumatic disease |
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
- Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs
- CREST syndrome, also known as the limited cutaneous form of systemic sclerosis (lcSSc) is a multisystem connective tissue disorder. The acronym "CREST" refers to the five main features: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia.
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
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