D72.0 is the ICD-10 code for Genetic anomalies of leukocytes. It is a four-character subcategory of D72 (Other disorders of white blood cells), the most specific level in the WHO edition. It belongs to the block D70–D77 (Other diseases of blood and blood-forming organs) in Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Code type
- Subcategory (4 characters)
- Chapter
- III · D50–D89
- Classification
- WHO ICD-10, 2019 version
What D72.0 includes
Conditions and terms that are coded here.
- Anomaly (granulation)(granulocyte) or syndrome:
- Alder
- May-Hegglin
- Pelger-Huët
- Hereditary:
- leukocytic: hypersegmentation
- leukocytic: hyposegmentation
- leukomelanopathy
What D72.0 excludes
Conditions that look similar but belong under another code.
- Chediak(-Steinbrinck)-Higashi syndrome E70.3
D72.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D72.0Genetisk anomali i leukocytter
DD720Genetisk betinget leukocytanomali
- DD720AAlder's anomali
- DD720BHereditær leukocytær hypersegmentation
- DD720CHereditær leukocytær hyposegmentation
- DD720DHereditær leukomelanopati
- DD720EMay-Hegglins anomali
- DD720FPelger-Huëts anomali
D72.0Perinnölliset valkosolujen poikkeavuudet
D72.0Genetisch bedingte Leukozytenanomalien
D72.0Anomalies génétiques des leucocytes
D72.0genetische anomalieën van leukocyten
D72.0Genetic anomalies of leukocytes
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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