E83.32
BillableHereditary vitamin D-dependent rickets (type 1) (type 2)
Hereditary vitamin D-dependent rickets (type 1) (type 2)
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)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- 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)
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
- adult osteomalacia (M83.-)
- osteoporosis (M80.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- 1-alpha-hydroxylase deficiency67049004
- 25-Hydroxycholecalciferol-1-hydroxylase deficiency67049004
- Calcidiol 1-monooxygenase defect67049004
- PDDR - Pseudovitamin D deficiency rickets67049004
- Pseudo-vitamin-D-deficient rickets67049004
- Pseudodeficiency rickets67049004
- Pseudovitamin D deficiency rickets67049004
- Pseudovitamin D-resistant rickets67049004
- VDDR I - Vitamin D-dependent rickets type I67049004
- Vitamin D-dependent rickets type I67049004
- Vitamin D-dependent rickets, type 167049004
- VDDR - vitamin D-dependent rickets68295002
- Vitamin D-dependent rickets68295002
- Calcitriol receptor defect72831007
- End organ unresponsiveness to 1,25-dihydroxycholecalciferol72831007
- Type 2 vitamin D-dependent rickets72831007
- Vitamin D-dependent rickets type II72831007
- Vitamin D-dependent rickets, type 272831007
- Familial hypophosphataemia82236004
- Familial hypophosphataemic bone disease82236004
- Familial hypophosphataemic osteomalacia82236004
- Familial hypophosphataemic rickets82236004
- Familial hypophosphatemia82236004
- Familial hypophosphatemic bone disease82236004
- Familial hypophosphatemic osteomalacia82236004
- Familial hypophosphatemic rickets82236004
- Familial vitamin D-resistant rickets82236004
- Familial x-linked hypophosphataemic vitamin D refractory rickets82236004
- Familial x-linked hypophosphatemic vitamin D refractory rickets82236004
- HPDR I - Hypophosphataemic vitamin D-resistant rickets82236004
- HPDR I - Hypophosphatemic vitamin D-resistant rickets82236004
- Hereditary hypophosphataemia82236004
- Hereditary hypophosphatemia82236004
- Vitamin D-resistant osteomalacia82236004
- Vitamin D-resistant rickets82236004
- X-linked hypophosphataemic osteomalacia82236004
- X-linked hypophosphataemic rickets82236004
- X-linked hypophosphatemic osteomalacia82236004
- X-linked hypophosphatemic rickets82236004
- X-linked vitamin D-resistant rickets82236004
- Autosomal recessive hypophosphataemic rickets90505000
- Autosomal recessive hypophosphataemic vitamin D refractory rickets90505000
- Autosomal recessive hypophosphatemic rickets90505000
- Autosomal recessive hypophosphatemic vitamin D refractory rickets90505000
- Autosomal recessive hypophosphataemic bone disease237891005
- Autosomal recessive hypophosphatemic bone disease237891005
- Rickets - alopecia syndrome237894002
- VDDR IIa - Vitamin D-dependent rickets IIa237894002
- Vitamin D-dependent rickets type II with alopecia237894002
- Vitamin D-dependent rickets type IIa237894002
- VDDR IIb - Vitamin D-dependent rickets IIb237895001
- Vitamin D-dependent rickets type II without alopecia237895001
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Lesion of bone879976004
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.
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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.