Is E83.822 a billable code?
Yes. E83.822 is a billable ICD-10-CM code and can be used on claims and superbills for dates of service from October 1, 2026 to September 30, 2027.
ICD-10-CM FY2027 diagnosis code
E83.822: ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Billable codeValid for dates of service October 1, 2026 to September 30, 2027
E83.822 is a billable ICD-10-CM diagnosis code for enpp1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. It is specific enough to use on an insurance claim, a superbill or a Good Faith Estimate.
Superbill GeneratorStart a superbill with E83.822 already added.Good Faith EstimateStart a cost estimate with E83.822 already added.CMS-1500 Claim FormFill a claim form with E83.822 in box 21.
Other codes in E83.82 Disorders of pyrophosphate metabolism
- E83.820Generalized arterial calcification of infancy with unspecified genetic causality
- E83.821ENPP1 deficiency causing generalized arterial calcification of infancy
- E83.823ABCC6 deficiency causing generalized arterial calcification of infancy
- E83.824ABCC6 deficiency causing pseudoxanthoma elasticum
- E83.825CD73 deficiency causing arterial calcification
E83.822 questions
What does E83.822 mean?
E83.822 is the ICD-10-CM code for ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. It is in chapter 4, Endocrine, nutritional and metabolic diseases (E00-E89).
Code titles come from the official ICD-10-CM files published by the CDC National Center for Health Statistics. Always check payer rules and the clinical record before billing.