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  5. Term: "Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) - in the ICD-10-CM Index"

Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) - in the ICD-10-CM Index

Annotation Back-References in the 2025 ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency)"

  • Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) - E79.89 Other specified disorders of purine and pyrimidine metabolism

    • anemia - D53.0 Protein deficiency anemia

Applicable Clinical Terms Definitions

Anemia: A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN.

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