Icd 10 Code For Vitamin D 25 Hydroxy
- ICD-10-CM Codes ›
- E00-E89 Endocrine, nutritional and metabolic diseases ›
- E70-E88 Metabolic disorders ›
- E83- Disorders of mineral metabolism ›
- 2022 ICD-10-CM Diagnosis Code E83.32
2022 ICD-10-CM Diagnosis Code E83.32
Hereditary vitamin D-dependent rickets (type 1) (type 2)
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- E83.32 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2022 edition of ICD-10-CM E83.32 became effective on October 1, 2021.
- This is the American ICD-10-CM version of E83.32 - other international versions of ICD-10 E83.32 may differ.
Applicable To
- 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency
- Pseudovitamin D deficiency
- Vitamin D receptor defect
The following code(s) above E83.32 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to E83.32:
- E00-E89
2022 ICD-10-CM Range E00-E89
Endocrine, nutritional and metabolic diseasesEndocrine, nutritional and metabolic diseases
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.
Type 1 Excludes
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- E70-E88
2022 ICD-10-CM Range E70-E88
Metabolic disordersMetabolic disorders
Type 1 Excludes
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan's syndrome (Q87.4)
- 5-alpha-reductase deficiency (E29.1)
Type 2 Excludes
- Ehlers-Danlos syndromes (Q79.6-)
- E83
ICD-10-CM Diagnosis Code E83
Disorders of mineral metabolismDisorders of mineral metabolism
- 2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code
Type 1 Excludes
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
- E83.3
ICD-10-CM Diagnosis Code E83.3
Disorders of phosphorus metabolism and phosphatasesDisorders of phosphorus metabolism and phosphatases
- 2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code
Type 1 Excludes
- adult osteomalacia (M83.-)
- osteoporosis (M80.-)
Approximate Synonyms
- Hereditary vitamin d dependent rickets type 2
- Vitamin d-dependent rickets, type 2
ICD-10-CM E83.32 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0):
- 642 Inborn and other disorders of metabolism
Convert E83.32 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
Code annotations containing back-references to E83.32:
- Type 1 Excludes: E55.0
ICD-10-CM Diagnosis Code E55.0
Rickets, active
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
- Infantile osteomalacia
- Juvenile osteomalacia
Type 1 Excludes
- celiac rickets (K90.0)
- Crohn's rickets (K50.-)
- hereditary vitamin D-dependent rickets (E83.32)
- inactive rickets (E64.3)
- renal rickets (N25.0)
- sequelae of rickets (E64.3)
- vitamin D-resistant rickets (E83.31)
Diagnosis Index entries containing back-references to E83.32:
- Deficiency, deficient
- vitamin (multiple) E56.9
ICD-10-CM Diagnosis Code E56.9
Vitamin deficiency, unspecified
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- D E55.9
ICD-10-CM Diagnosis Code E55.9
Vitamin D deficiency, unspecified
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
- Avitaminosis D
- 25-hydroxylase E83.32
- D E55.9
- vitamin (multiple) E56.9
- Disorder (of) - see also Disease
- metabolism NOS E88.9
ICD-10-CM Diagnosis Code E88.9
Metabolic disorder, unspecified
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- phosphorus E83.30
ICD-10-CM Diagnosis Code E83.30
Disorder of phosphorus metabolism, unspecified
- 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- pseudovitamin D deficiency E83.32
- phosphorus E83.30
- metabolism NOS E88.9
ICD-10-CM Codes Adjacent To E83.32
E83.110 Hereditary hemochromatosis
E83.111 …… due to repeated red blood cell transfusions
E83.118 Other hemochromatosis
E83.19 Other disorders of iron metabolism
E83.2 Disorders of zinc metabolism
E83.3 Disorders of phosphorus metabolism and phosphatases
E83.30 Disorder of phosphorus metabolism, unspecified
E83.31 Familial hypophosphatemia
E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2)
E83.39 Other disorders of phosphorus metabolism
E83.4 Disorders of magnesium metabolism
E83.49 Other disorders of magnesium metabolism
E83.5 Disorders of calcium metabolism
E83.50 Unspecified disorder of calcium metabolism
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
Icd 10 Code For Vitamin D 25 Hydroxy
Source: https://www.icd10data.com/ICD10CM/Codes/E00-E89/E70-E88/E83-/E83.32#:~:text=32-,Hereditary%20vitamin%20D%2Ddependent%20rickets,type%201)%20(type%202)&text=Billable%2FSpecific%20Code-,E83.,a%20diagnosis%20for%20reimbursement%20purposes.
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