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:
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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Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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