E83.822 ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
Billable / valid for submission ICD10CM Release FY2026
Short description: ENPP1 def cause autosom recess hypophosphate rickets type 2
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | yes |
Related codes in E83
- E83 Disorders of mineral metabolism
- E83.0 Disorders of copper metabolism
- E83.00 Disorder of copper metabolism, unspecified
- E83.01 Wilson's disease
- E83.09 Other disorders of copper metabolism
- E83.1 Disorders of iron metabolism
- E83.10 Disorder of iron metabolism, unspecified
- E83.11 Hemochromatosis
- E83.110 Hereditary hemochromatosis
- E83.111 Hemochromatosis due to repeated red blood cell transfusions
- E83.118 Other hemochromatosis
- E83.119 Hemochromatosis, unspecified
- E83.19 Other disorders of iron metabolism
- E83.2 Disorders of zinc metabolism
- E83.3 Disorders of phosphorus metabolism and phosphatases
- E83.30 Disorder of phosphorus metabolism, unspecified
- E83.31 Familial hypophosphatemia
- E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2)
- E83.39 Other disorders of phosphorus metabolism
- E83.4 Disorders of magnesium metabolism