E83.822
BillableENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
E83.822 is the ICD-10-CM code for ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. It is a billable, specific code valid for reimbursement.
E00-E89 Endocrine, nutritional and metabolic diseases
What this means — in plain language
MedlinePlus · NIHRickets causes soft, weak bones in children. It usually occurs when they do not get enough vitamin D , which helps growing bones absorb the minerals calcium and phosphorous. It can also happen when calcium or phosphorus levels are too low. Your child might not get enough vitamin D if he or she: Has dark skin Spends too little time outside Has on sunscreen all the time when out of doors Doesn't eat foods containing…
Read more about Rickets at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Frequently asked questions
- What is ICD-10 code E83.822?
- E83.822 is the ICD-10-CM code for "ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2". It falls under E00-E89 Endocrine, nutritional and metabolic diseases.
- Is E83.822 a billable code?
- Yes — E83.822 is a billable, specific ICD-10-CM code valid for reimbursement.
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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