Other specified disorders of purine and pyrimidine metabolism
- E79.89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Short description: Oth disrd of purine and pyrimidine metabolism
- ICD-10-CM E79.89 is a new 2024 ICD-10-CM code that became effective on October 1, 2023.
- This is the American ICD-10-CM version of E79.89 – other international versions of ICD-10 E79.89 may differ.
The following code(s) above E79.89 contain annotation back-references
that may be applicable to E79.89:
- E00-E89 Endocrine, nutritional and metabolic diseases
- E70-E88 Metabolic disorders
- E79 Disorders of purine and pyrimidine metabolism
ICD-10-CM E79.89 is grouped within Diagnostic Related Group(s) (MS-DRG v41.0):
- 642 Inborn and other disorders of metabolism
Code History
- 2024 (effective 10/1/2023): New code
Diagnosis Index entries containing back-references to E79.89:
- Aciduria
- orotic (congenital) (hereditary) (pyrimidine deficiency) E79.89
- Disorder (of) – see also Disease
- metabolism NOSE88.9
- purineE79.9
- specified NEC E79.89
- pyrimidineE79.9
- specified NEC E79.89
- purineE79.9
- metabolism NOSE88.9
- Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) E79.89