2025
ICD-10-CM
Diagnosis
Code

D72.0 Genetic anomalies of leukocytes

  • Billable
  • 2016–2025

D72.0 is a billable/specific diagnosis code from the 2025 ICD-10-CM used to classify the following condition: Genetic anomalies of leukocytes.

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-Huu00ebt (granulation) (granulocyte) anomaly

  • Pelger-Huu00ebt syndrome

Type 1 excludes

  • Chu00e9diak (-Steinbrinck)-Higashi syndrome (E70.330)

Versions

  1. 2025

    Code changed

    • Type 1 excludes

        • Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
        • Chu00e9diak (-Steinbrinck)-Higashi syndrome (E70.330)

    • 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
        • Alder (granulation) (granulocyte) anomaly
        • Alder syndrome
        • Hereditary leukocytic hypersegmentation
        • Hereditary leukocytic hyposegmentation
        • Hereditary leukomelanopathy
        • May-Hegglin (granulation) (granulocyte) anomaly
        • May-Hegglin syndrome
        • Pelger-Huu00ebt (granulation) (granulocyte) anomaly
        • Pelger-Huu00ebt syndrome

  2. 2024

    No changes

  3. 2023

    No changes

  4. 2022

    No changes

  5. 2021

    No changes

  6. 2020

    No changes

  7. 2019

    No changes

  8. 2018

    No changes

  9. 2017

    No changes

  10. 2016

    New code