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

  1. ICD-10-CM Index to Diseases and Injuries
  2. Terms starting with: "O"
  3. Term: "Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) - ICD-10-CM Index to Diseases and Injuries"

"Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency)" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency)"

  • Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) - E79.8 Other 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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