E83.822 - ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2

Applicable to ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
The 2026 edition of ICD10-CM E83.822 became effective on October 1, 2025.
This is the American ICD10-CM version of E83.822 - other international versions of ICD10 E83.822 may differ.
E83.822 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

The following codes above E83.822 contain annotation back-references that may be applicable to E83.822:

Billable/Specific Code