E83.822
Billable

ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2

Billable / Specific Code

What is ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2?

ICD-10-CM E83.822 is the diagnosis code for ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. This code falls under the section "Metabolic disorders" within Chapter 4 — Endocrine, nutritional and metabolic diseases (E00-E89). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.

Coding Guidelines for E83.822

Always refer to the official ICD-10-CM Tabular List for complete coding guidelines. Ensure documentation supports the specificity of the code selected. When in doubt, consult a certified medical coder or the latest CMS guidelines.

ICD-10-CM Code Hierarchy

Understanding where E83.822 sits in the ICD-10-CM classification helps ensure proper coding:

Current CodeE83.822 — ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Related Codes

Frequently Asked Questions

Is E83.822 a billable ICD-10-CM code?

Yes, E83.822 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What does E83.822 mean?

E83.822 is the ICD-10-CM diagnosis code for "ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.

What is the parent code of E83.822?

The parent code of E83.822 is E83.82 ("Disorders of pyrophosphate metabolism"). E83.822 provides a more specific classification within this category.

What section is E83.822 in?

E83.822 is located in Section E70-E88 — "Metabolic disorders" within Chapter 4 of the ICD-10-CM Tabular List.

When should I use E83.822?

Use E83.822 when the patients documented diagnosis matches "ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.

People Also Ask

What is the ICD-10 code for ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2?

The ICD-10-CM code for ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 is E83.822.

Can E83.822 be used for primary diagnosis?

Yes, E83.822 can be used as a primary diagnosis code since it is billable and specific.

What chapter is E83.822 in?

E83.822 is in Chapter 4 of the ICD-10-CM Tabular List.

Is E83.822 valid for 2026?

Yes, E83.822 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.

See Also

← PreviousE83.821ENPP1 deficiency causing generalized arterial calcification of infancyNext →E83.823ABCC6 deficiency causing generalized arterial calcification of infancy
Code Details
E83.822
ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Billable / Specific Code
4 — Endocrine, nutritional and metabolic diseases (E00-E89)
E70-E88 — Metabolic disorders
2026 ICD-10-CM