Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency)

Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists E79.89 for the term on its own. It has 1 subterm and 2 code entries. First-level subterms include anemia. Confirm any code you find here in the Tabular List before you report it.