D72.0Genetic anomalies of leukocytes
Code usage status
Primary diagnosis
May be used as the primary diagnosis
Apply only when it matches the confirmed diagnosis and the documented clinical record.
Specificity
Complete code in the classification
Use when the diagnosis matches and no exclusion applies.
- Chapter III
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- Group D70-D77
- Other diseases of blood and blood- forming organs
- Official Vietnamese name
- Bất thường di truyền của bạch cầu
- Additional WHO coding guidance
- Anomaly (granulation)(granulocy te) or syndrome: Alder May-Hegglin Pelger-Huët Hereditary: leukocytic: hypersegmentation hyposegmentation leukomelanopathy Excl.: Chediak(- Steinbrinck)-Higashi syndrome (E70.3)
Related D72 codes
Clinical record checklist
View coding guide →- Confirm that the code matches the final documented diagnosis.
- Use one primary-diagnosis code and record only relevant additional conditions.
- Review Ministry indicators, inclusions, exclusions and notes.
- Do not infer a diagnosis beyond the clinical record.
2026 regulatory basis
Indicators are taken from columns 24–29 of the classification accompanying Circular 06/2026/TT-BYT, cross-referenced with Decision 1849/QĐ-BYT and Official Dispatch 4059/BYT-BH.
