ICD-10-CM
ICD-10 code for Westphal-Strümpell syndrome: E83.01
The ICD-10-CM index points "Westphal-Strümpell syndrome" to E83.01, Wilson's disease. E83.01 is a billable code.
Source: CDC ICD-10-CM FY2027 Alphabetic Index file dated June 16, 2026. Publisher page
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More specific codes in E83
A header groups codes and is not billed. A billable code is one you can report.
- E83Disorders of mineral metabolismHeader
- E83.0Disorders of copper metabolismHeader
- E83.00Disorder of copper metabolism, unspecifiedBillable
- E83.01Wilson's diseaseBillable
- E83.09Other disorders of copper metabolismBillable
- E83.1Disorders of iron metabolismHeader
- E83.10Disorder of iron metabolism, unspecifiedBillable
- E83.11HemochromatosisHeader
- E83.110Hereditary hemochromatosisBillable
- E83.111Hemochromatosis due to repeated red blood cell transfusionsBillable
- E83.118Other hemochromatosisBillable
- E83.119Hemochromatosis, unspecifiedBillable
- E83.19Other disorders of iron metabolismBillable
- E83.2Disorders of zinc metabolismBillable
- E83.3Disorders of phosphorus metabolism and phosphatasesHeader
- E83.30Disorder of phosphorus metabolism, unspecifiedBillable
- E83.31Familial hypophosphatemiaBillable
- E83.32Hereditary vitamin D-dependent rickets (type 1) (type 2)Billable
- E83.39Other disorders of phosphorus metabolismBillable
- E83.4Disorders of magnesium metabolismHeader
- E83.40Disorders of magnesium metabolism, unspecifiedBillable
- E83.41HypermagnesemiaBillable
- E83.42HypomagnesemiaBillable
- E83.49Other disorders of magnesium metabolismBillable
- E83.5Disorders of calcium metabolismHeader
- E83.50Unspecified disorder of calcium metabolismBillable
- E83.51HypocalcemiaBillable
- E83.52HypercalcemiaBillable
- E83.59Other disorders of calcium metabolismBillable
- E83.8Other disorders of mineral metabolismHeader
- E83.81Hungry bone syndromeBillable
- E83.82Disorders of pyrophosphate metabolismHeader
- E83.820Generalized arterial calcification of infancy with unspecified genetic causalityBillable
- E83.821ENPP1 deficiency causing generalized arterial calcification of infancyBillable
- E83.822ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2Billable
- E83.823ABCC6 deficiency causing generalized arterial calcification of infancyBillable
- E83.824ABCC6 deficiency causing pseudoxanthoma elasticumBillable
- E83.825CD73 deficiency causing arterial calcificationBillable
- E83.89Other disorders of mineral metabolismBillable
- E83.9Disorder of mineral metabolism, unspecifiedBillable
Code also
The CDC tabular list says a second code may be needed with this one. The note does not set which is listed first.
Code also associated Kayser Fleischer ring (H18.04-)
Excludes1
Excludes1 means these codes are not reported together.
From E83. A note on a category applies to every code under it.
Related conditions
Related pages
- E83.01 code detailsNotes, nearby codes, CMS-HCC group
- Category E83Every code under it
- Chapter 4Endocrine, nutritional and metabolic diseases
- ICD-10 codes by conditionA to Z
- Check a list of ICD-10 codes
- Denial code CO-11Diagnosis does not support the procedure
- Denial code CO-146Diagnosis invalid for the date of service
- HCPCS Level II code lookup
Questions
What is the ICD-10 code for Westphal-Strümpell syndrome?
The ICD-10-CM index points "Westphal-Strümpell syndrome" to E83.01, Wilson's disease. E83.01 is a billable code.
Is E83.01 billable?
Yes. E83.01 is a billable code in the FY2027 ICD-10-CM file. Use a more specific code when the record documents one.
What documentation notes apply to E83.01?
The CDC tabular list gives 3 Excludes1 notes (not coded together) for E83.01 and the categories above it. They are listed on this page.
What chapter is E83.01 in?
Chapter 4. Endocrine, nutritional and metabolic diseases.
When do ICD-10-CM codes change?
Every October 1, with the new fiscal year file. Some years add April 1 updates. This page uses the FY2027 file, effective October 1, 2026.