ICD-10-CM · Chapter 3 · D50–D89
D72.0
Genetic anomalies of leukocytes
Diseases of the blood and immune mechanism
Quick facts
- Code
- D72.0
- Type
- Billable code
- ICD-10-CM chapter
- Chapter 3 — Diseases of the blood and immune mechanism
- Category
- D72 — Other disorders of white blood cells
- Specificity
- 4 characters
How coders use this code
ICD-10-CM D72.0 is a billable, fully specified code, so it can be reported directly on a claim to document a diagnosis of genetic anomalies of leukocytes. Coders assign it when the chart documentation supports this level of detail, always matching to the most specific code available and verifying against the chapter-specific guidelines published annually by NCHS/CMS.
Related codes in D72
- D72Other disorders of white blood cells
- D72.1Eosinophilia
- D72.10Eosinophilia, unspecified
- D72.11Hypereosinophilic syndrome [HES]
- D72.110Idiopathic hypereosinophilic syndrome [IHES]
- D72.111Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
- D72.118Other hypereosinophilic syndrome
- D72.119Hypereosinophilic syndrome [HES], unspecified
- D72.12Drug rash with eosinophilia and systemic symptoms syndrome
- D72.18Eosinophilia in diseases classified elsewhere
- D72.19Other eosinophilia
- D72.8Other specified disorders of white blood cells
- D72.81Decreased white blood cell count
- D72.810Lymphocytopenia
- D72.818Other decreased white blood cell count
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