E72.538 - Other specified primary hyperoxaluria
ICD-10-CM Chapter 4: Endocrine, nutritional and metabolic diseases · E70-E88 Metabolic disorders (E70-E88) · Subcategory of E72.53 · FY2027
Inclusion terms listed under E72.538 in the ICD-10-CM tabular list.
- Primary hyperoxaluria, type 2
- Primary hyperoxaluria, type 3
Includes, Excludes and Coding Notes
Mutually exclusive: these conditions are never reported together with this code.
- secondary hyperoxaluria (E72.54-)
Mutually exclusive: these conditions are never reported together with this code.
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
Mutually exclusive: these conditions are never reported together with this code.
- 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)
Not part of this code; report both codes when the patient has both conditions.
- Ehlers-Danlos syndromes (Q79.6-)
Mutually exclusive: these conditions are never reported together with this code.
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Instructional notes from the ICD-10-CM tabular list.
- All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Related condition guides
Documentation requirements, coding pitfalls and FAQs for conditions coded with E72.538.
Codes at the same level as E72.538