E83.822
✓ Billable
ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
ICD-10-CM · FY2026 · Endocrine, Nutritional and Metabolic Diseases
Code
E83.822
System
ICD-10-CM
Billable
Yes — valid for submission
Effective
FY2026
Chapter
Endocrine, Nutritional and Metabolic Diseases
Source
CMS / CDC NCHS
⚠ Verify before billing. Confirm against the current CMS/NCHS ICD-10-CM files and your payer's rules before claims submission.
Frequently asked questions
What is ICD-10 code E83.822?
ICD-10-CM code E83.822 represents ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2. It is a billable diagnosis code in the Endocrine, Nutritional and Metabolic Diseases chapter, effective October 1, 2025 – September 30, 2026.
Is E83.822 billable?
Yes. E83.822 is a valid billable ICD-10-CM code for insurance claims and clinical documentation.
What chapter is E83.822 in?
E83.822 belongs to the Endocrine, Nutritional and Metabolic Diseases chapter (E00–E89) of ICD-10-CM.
Related codes in the E83 category
E83
Disorders of mineral metabolism
Non-billable
E83.0
Disorders of copper metabolism
Non-billable
E83.1
Disorders of iron metabolism
Non-billable
E83.2
Disorders of zinc metabolism
Billable
E83.3
Disorders of phosphorus metabolism and phosphatases
Non-billable
E83.4
Disorders of magnesium metabolism
Non-billable
E83.5
Disorders of calcium metabolism
Non-billable
E83.8
Other disorders of mineral metabolism
Non-billable
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