Billable / Specific Code
ICD-10-CM E83.32 is the diagnosis code for Hereditary vitamin D-dependent rickets (type 1) (type 2). This code falls under the section "Metabolic disorders" within Chapter 4 — Endocrine, nutritional and metabolic diseases (E00-E89). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where E83.32 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, E83.32 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
E83.32 is the ICD-10-CM diagnosis code for "Hereditary vitamin D-dependent rickets (type 1) (type 2)". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
The parent code of E83.32 is E83.3 ("Disorders of phosphorus metabolism and phosphatases"). E83.32 provides a more specific classification within this category.
E83.32 is located in Section E70-E88 — "Metabolic disorders" within Chapter 4 of the ICD-10-CM Tabular List.
Use E83.32 when the patients documented diagnosis matches "Hereditary vitamin D-dependent rickets (type 1) (type 2)" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for Hereditary vitamin D-dependent rickets (type 1) (type 2) is E83.32.
Yes, E83.32 can be used as a primary diagnosis code since it is billable and specific.
E83.32 is in Chapter 4 of the ICD-10-CM Tabular List.
Yes, E83.32 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.