ICD-10-CM › E00-E89 › E70-E88 › E83.82 Disorders of pyrophosphate metabolism › E83.825
E83.825
CD73 deficiency causing arterial calcification
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2026 to now.
- FY2026 Added to the code set CD73 deficiency causing arterial calcification
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from E83 Disorders of mineral metabolism
Excludes1 - never coded here
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
Inherited from the E70-E88 section Metabolic disorders (E70-E88)
Excludes1 - never coded here
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
Excludes2 - not included here
- Ehlers-Danlos syndromes (Q79.6-)
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Deficit
- Avitaminosis
- Hypovitaminosis
- Vitamin deficiency
- Leukoencephalopathy
- Deprivation > vitamins
- Deficiency, deficient > factor
- Defect, defective > coagulation
- Deficiency, deficient > clotting
- Disturbance > absorption > vitamin
- Encephalopathy > in > lack of vitamin
- Deficiency, deficient > clotting factor NEC
- Deficiency, deficient > coagulation NOS > clotting factor NEC
- Deficiency, deficient > CD73 deficiency causing arterial calcification
Codes in the same group
| Code | Description | Status |
|---|---|---|
| E83.820 | Generalized arterial calcification of infancy with unspecified genetic causality | Valid |
| E83.821 | ENPP1 deficiency causing generalized arterial calcification of infancy | Valid |
| E83.822 | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | Valid |
| E83.823 | ABCC6 deficiency causing generalized arterial calcification of infancy | Valid |
| E83.824 | ABCC6 deficiency causing pseudoxanthoma elasticum | Valid |