E83.32 - Hereditary vitamin D-dependent rickets (type 1) (type 2)
- Applicable to Hereditary vitamin D-dependent rickets (type 1) (type 2)
- The 2025 edition of ICD10-CM E83.32 became effective on October 1, 2024.
- This is the American ICD10-CM version of E83.32 - other international versions of ICD10 E83.32 may differ.
- E83.32 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
- Pseudovitamin D deficiency
- Vitamin D receptor defect
Billable/Specific Code
The following codes above E83.32 contain annotation back-references that may be applicable to E83.32:
- Chapter: E00-E89 - Endocrine, nutritional and metabolic diseases
- Section: E70-E88 - Metabolic disorders
- Category: E83 - Disorders of mineral metabolism
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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