Hereditary vitamin D-dependent rickets (type 1) (type 2)
Billable / specific
E83.32 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
- Pseudovitamin D deficiency
- Vitamin D receptor defect
Includes (from E83)
- 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.
Excludes1
Not coded here — never report together with this code.
- adult osteomalacia (M83.-) (from E83.3)
- osteoporosis (M80.-) (from E83.3)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E83)
- androgen insensitivity syndrome (E34.5-) (from E83)
- congenital adrenal hyperplasia (E25.0) (from E83)
- hemolytic anemias attributable to enzyme disorders (D55.-) (from E83)
- Marfan syndrome (Q87.4-) (from E83)
- 5-alpha-reductase deficiency (E29.1) (from E83)
- dietary mineral deficiency (E58-E61) (from E83)
- parathyroid disorders (E20-E21) (from E83)
- vitamin D deficiency (E55.-) (from E83)
Excludes2
Not included here — may be reported together when both conditions exist.
Also known as
- 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
- Pseudovitamin D deficiency
- Vitamin D receptor defect
- Deficiency, deficient, vitaminNOS, D, 25-hydroxylase
- Disorder, metabolism NOS, phosphorus, pseudovitamin D deficiency
Parent code
- E83.3Disorders of phosphorus metabolism and phosphatasesHeader