D72.0
BillableGenetic anomalies of leukocytes
D72.0 is the ICD-10-CM code for Genetic anomalies of leukocytes. It is a billable, specific code valid for reimbursement.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Includes
- •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
- •Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Frequently asked questions
- What is ICD-10 code D72.0?
- D72.0 is the ICD-10-CM code for "Genetic anomalies of leukocytes". It falls under D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Is D72.0 a billable code?
- Yes — D72.0 is a billable, specific ICD-10-CM code valid for reimbursement.
- What is excluded from D72.0?
- Excludes1 (not coded here): Chédiak (-Steinbrinck)-Higashi syndrome (E70.330).
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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