E83.32
Billable codeHereditary vitamin D-dependent rickets (type 1) (type 2)
The ICD-10 code for hereditary vitamin d-dependent rickets (type 1) (type 2) is E83.32.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
- Pseudovitamin D deficiency
- Vitamin D receptor defect
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- E83.30Disorder of phosphorus metabolism, unspecified
- E83.31Familial hypophosphatemia
- E83.39Other disorders of phosphorus metabolism
- E83.32Hereditary vitamin D-dependent rickets (type 1) (type 2)
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 2753Approximate match
Associated MS-DRGs
E83.32 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.