D72.0

ICD-10Billable

Genetic anomalies of leukocytes

Official ICD-10-CM descriptor (FY2026)

Genetic anomalies of leukocytes

D72.0 is valid for submission on a claim — CMS flags it as a billable, specific code.

Inclusion terms

  • 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

Excludes1

Not coded here. An Excludes1 code should never be reported at the same time as the code above it.

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

Related codes in D72

Where this code sits

Parent code
D72

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Source

ICD-10-CM FY2026. Centers for Medicare & Medicaid Services (CMS) / National Center for Health Statistics (NCHS), “2026 ICD-10-CM Code Descriptions in Tabular Order” (icd10cm_order_2026.txt). Download the original file from cms.gov. Public domain (US Government work). Descriptors, billable flags and instructional notes on this page are reproduced from that file without modification. Krasyn adds no clinical guidance.

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