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  4. Term: "ICD-10-CM Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) References"

ICD-10-CM Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) References

"Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency)" Annotation Back-References in the 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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