D72.0 Genetic anomalies of leukocytes
The ICD-10-CM code for Genetic anomalies of leukocytes is D72.0 (FY2026). It is a billable, claim-ready diagnosis code.
Classification
- Section
- D70-D77: Other disorders of blood and blood-forming organs (D70-D77)
- Category D72
- 28 codes (22 billable)
- FY2026 Status
- Stable since FY2024
Also Known As
ICD-10-CM Alphabetic Index entries that lead to D72.0:
- Leukomelanopathy, hereditary
- Alder (-Reilly) anomaly or syndrome (leukocyte granulation)
- May (-Hegglin) anomaly or syndrome
- Jordan's anomaly or syndrome
- Dohle body panmyelopathic syndrome
- Hypersegmentation, leukocytic, hereditary
- Hegglin's anomaly or syndrome
- Hyposegmentation, leukocytic, hereditary
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
U.S. Hospital Utilization
- An estimated 2,065 U.S. inpatient stays in 2023 included D72.0 among the documented diagnoses.
Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.
Official Coding Guidelines
Chapter 3 TOC entry3. Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) ............................................................................................. 39
Reserved for future guideline expansionReserved for future guideline expansion ...................................................................................... 39
Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026