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2. ICD-10 Codes
3. Chapter - D50-D89
4. Section - D70-D77
5. Category - D72
6. D72.0

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.

• 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

Browse other similar CM codes:

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