E83.32

Hereditary vitamin D-dependent rickets (type 1) (type 2)

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

RxHCC V08

RXHCC43

Pituitary, Adrenal Gland, and Other Endocrine and Metabolic Disorders

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · E83.32

Synonyms

25-hydroxyvitamin D 1-alpha-hydroxylase deficiency Pseudovitamin D deficiency Vitamin D receptor defect

Inherited from E83.3Disorders of phosphorus metabolism and phosphatases

Excludes 1

adult osteomalacia (M83.-) osteoporosis (M80.-)

Excludes 2

disorders of pyrophosphate metabolism (E83.82-)

Inherited from E83Disorders of mineral metabolism

Excludes 1

dietary mineral deficiency (E58-E61) parathyroid disorders (E20-E21) vitamin D deficiency (E55.-)

Inherited from E70-E88Metabolic disorders

Excludes 1

androgen insensitivity syndrome (E34.5-) congenital adrenal hyperplasia (E25.0) hemolytic anemias attributable to enzyme disorders (D55.-) Marfan syndrome (Q87.4-) 5-alpha-reductase deficiency (E29.1)

Excludes 2

Ehlers-Danlos syndromes (Q79.6-)

Inherited from chapter 4Endocrine, nutritional and metabolic diseases

Excludes 1

transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Note

All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.

Official Guidelines for E83.32

FY 2026 ›

I.C.4Chapter-specific guidanceChapter 4: Endocrine, Nutritional, and Metabolic Diseases (E00-E89)

Subsections

Find E83.32 in the alphabetic index

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