D72.0 - Genetic anomalies of leukocytes

Code

D72.0 - Genetic anomalies of leukocytes
[Billable]

Includes

  • Alder (granulation) (granulocyte) anomaly
  • Alder syndrome
  • Hereditary leukocytic hypersegmentation
  • Hereditary leukocytic hyposegmentation
  • Hereditary leukomelanopathy
  • May-Hegglin (granulation) (granulocyte) anomaly
  • May-Hegglin syndrome
  • Pelger-Huët (granulation) (granulocyte) anomaly
  • Pelger-Huët syndrome

Not Coded Here

  • Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)

Code Tree

D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
  • D70-D77 - Other disorders of blood and blood-forming organs
    • D72 - Other disorders of white blood cells
      • D72.0 - Genetic anomalies of leukocytes
      • D72.1 - Eosinophilia
      • D72.8 - Other specified disorders of white blood cells
      • D72.9 - Disorder of white blood cells, unspecified

Map to ⑨

D72.0 converts to ICD-9-CM:
  • 288.2 - Genetic anomalies of leukocytes
D72.0 - Genetic anomalies of leukocytes is a sample topic from the ICD-10-CM.

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