E83.822
E83.822: ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Billable / specific codeICD-10-CM
E83.822 is a billable, specific ICD-10-CM code for enpp1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. It is valid for submission on a claim.
Check E83.822 with the rest of the claim: free scrubberOther codes that can never be billed with E83.822
Their own Excludes1 notes name this code, so the conflict is not listed above.
Risk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Medicare coverage
E83.822 is named in 1 Medicare coverage policy: 1 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A57122Billing and Coding: Parathormone (Parathyroid Hormone)
Alphabetic index entries that lead here
- Deficiency, deficient›ENPP1›causing›autosomal recessive hypophosphatemic rickets type 2
Code history
- addedFY2024-FY2027
ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Other codes under E83.82
- 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