E72.4 Disorders of ornithine metabolism

Type 1 Excludes:
  • Hereditary Choroidal Dystrophy (H31.2-)
  • Applicable To:
    • Hyperammonemia-Hyperornithinemia-Homocitrullinemia Syndrome
    • Ornithinemia (types I, II)
    • Ornithine Transcarbamylase Deficiency

    The following code(s) above E72.4 may contain annotation back-references that may be applicable to E72.4:

    Diagnosis Index