E83.32

Billable

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

Status

Billable / Specific

Chapter

4: Endocrine, Nutritional and Metabolic Diseases

Block

E70-E88

Parent Code

E83.3

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

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

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

•Ehlers-Danlos syndromesQ79.6

Related Codes(3)

E83.30

Disorder of phosphorus metabolism, unspecified

Billable E83.31

Familial hypophosphatemia

Billable E83.39

Other disorders of phosphorus metabolism

Billable

Also Known As / Clinical Terms(117)

SNOMED CT

UMLS

Clinical Terms

Vitamin D-dependent rickets type II with alopecia
Lesion of bone
Autosomal recessive hypophosphataemic rickets
Pseudovitamin D deficiency rickets
X-linked vitamin D-resistant rickets
25-Hydroxycholecalciferol-1-hydroxylase deficiency
Autosomal recessive hypophosphatemic bone disease
VDDR - vitamin D-dependent rickets
VDDR IIb - Vitamin D-dependent rickets IIb
Dysplasia with defective mineralization
Vitamin D receptor defect
Familial hypophosphatemic bone disease
Autosomal recessive hypophosphatemic rickets
HPDR I - Hypophosphataemic vitamin D-resistant rickets
Autosomal recessive hypophosphataemic bone disease
Pseudodeficiency rickets
Type 2 vitamin D-dependent rickets
Hereditary hypophosphataemia
Familial hypophosphataemic osteomalacia
Hereditary hypophosphatemia
Familial vitamin D-resistant rickets
Familial hypophosphataemic bone disease
Familial x-linked hypophosphataemic vitamin D refractory rickets
Vitamin D-dependent rickets
Autosomal recessive hypophosphataemic vitamin D refractory rickets
1-alpha-hydroxylase deficiency
Familial hypophosphataemia
Autosomal recessive hypophosphatemic vitamin D refractory rickets
PDDR - Pseudovitamin D deficiency rickets
Dysplasia with defective mineralisation
HPDR I - Hypophosphatemic vitamin D-resistant rickets
Calcitriol receptor defect
Vitamin D-dependent rickets, type 2
Familial hypophosphatemic rickets
Vitamin D-dependent rickets type IIa
Vitamin D-dependent rickets, type 1
Vitamin D-dependent rickets type II
Calcidiol 1-monooxygenase defect
VDDR I - Vitamin D-dependent rickets type I
Familial hypophosphatemic osteomalacia
Pseudo-vitamin-D-deficient rickets
Familial x-linked hypophosphatemic vitamin D refractory rickets
25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
Vitamin D-resistant rickets
Familial hypophosphatemia
Vitamin D-dependent rickets type II without alopecia
Pseudovitamin D-resistant rickets
End organ unresponsiveness to 1,25-dihydroxycholecalciferol
VDDR IIa - Vitamin D-dependent rickets IIa
X-linked hypophosphataemic osteomalacia
X-linked hypophosphatemic osteomalacia
Familial hypophosphataemic rickets
Pseudovitamin D deficiency
Vitamin D-resistant osteomalacia
X-linked hypophosphataemic rickets
Rickets - alopecia syndrome
X-linked hypophosphatemic rickets
Vitamin D-dependent rickets type I

Frequently Asked Questions

What is the ICD-10 code for hereditary vitamin d-dependent rickets (type 1) (type 2)?

The ICD-10-CM code for hereditary vitamin d-dependent rickets (type 1) (type 2) is E83.32. The full clinical description is "Hereditary vitamin D-dependent rickets (type 1) (type 2)". E83.32 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E83.32 mean?

ICD-10-CM code E83.32 represents “Hereditary vitamin D-dependent rickets (type 1) (type 2)”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E83.32 a billable code?

Yes, E83.32 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E83.32 in?

E83.32 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E83.32?

E83.32 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 8 more.

What SNOMED CT codes does E83.32 map to?

E83.32 maps to 10 SNOMED CT concepts: 67049004, 237891005, 90505000, 72831007, 254117007, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E83.32?

E83.32 is linked to 4 UMLS Concept Unique Identifiers: C2874302, C2874305, C2874303, C2874304. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E83.32 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary vitamin d-dependent rickets (type 1) (type 2) affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E83.32?

There is no direct ICD-11 mapping available for E83.32 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.