D72.0 - Genetic anomalies of leukocytes

  • Applicable to Genetic anomalies of leukocytes
  • The 2025 edition of ICD10-CM D72.0 became effective on October 1, 2024.
  • This is the American ICD10-CM version of D72.0 - other international versions of ICD10 D72.0 may differ.
  • D72.0 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

 Inclusion Term

  • 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

Type 1 Excludes

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

The following codes above D72.0 contain annotation back-references that may be applicable to D72.0:

Chapter: D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Section: D70-D77 Other disorders of blood and blood-forming organs

Category: D72 Other disorders of white blood cells

   
Billable/Specific Code

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