Scleroderma or CREST syndrome (systemic sclerosis): Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Scleroderma| CurrentStatus = | | OldDxArticle =Scleroderma| CurrentStatus = reconciled | ||
| InitialEditorAssigned = Marla Penner | | InitialEditorAssigned = Marla Penner | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=M34 | | ICD10 Code=M34 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Skin}}{{ICD10 category|Cardiovascular}}{{ICD10 category| Gastrointestinal}}{{ICD10 category|Vasculitis}} | |||
== 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 | ||
*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. | *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 == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Disorder of skin pigmentation]] | |||
== Candidate [[Combined ICD10 codes]] == | |||
== | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
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