ICD-10-CM Diagnosis Code (2025)
Official Description for D72.0
Genetic anomalies of leukocytes
Coding Notes & Guidelines for D72.0
Excludes1: Not Coded Here
Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
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
Parent Code (Less Specific):
About ICD-10-CM Code D72.0 (Genetic anomalies of leukocytes)
ICD-10-CM code D72.0 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM D72.0 became effective on October 1, 2024.
This page provides detailed information about D72.0 - Genetic anomalies of leukocytes. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Genetic anomalies of leukocytes.