Diseases of white blood cells
CCSR category BLD007 · 38 ICD-10-CM codes
Code Families in This Category
ICD-10-CM Codes in This Category (38)
- D70.0 — Congenital agranulocytosis
- D70.1 — Agranulocytosis secondary to cancer chemotherapy
- D70.2 — Other drug-induced agranulocytosis
- D70.3 — Neutropenia due to infection
- D70.4 — Cyclic neutropenia
- D70.8 — Other neutropenia
- D70.9 — Neutropenia, unspecified
- D71 — Functional disorders of polymorphonuclear neutrophils
- D71.1 — Leukocyte adhesion deficiency
- D71.8 — Other functional disorders of polymorphonuclear neutrophils
- D71.9 — Functional disorders of polymorphonuclear neutrophils, unspecified
- D72.0 — Genetic anomalies of leukocytes
- D72.1 — Eosinophilia
- D72.10 — Eosinophilia, unspecified
- D72.110 — Idiopathic hypereosinophilic syndrome [IHES]
- D72.111 — Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
- D72.118 — Other hypereosinophilic syndrome
- D72.119 — Hypereosinophilic syndrome [HES], unspecified
- D72.12 — Drug rash with eosinophilia and systemic symptoms syndrome
- D72.18 — Eosinophilia in diseases classified elsewhere
- D72.19 — Other eosinophilia
- D72.810 — Lymphocytopenia
- D72.818 — Other decreased white blood cell count
- D72.819 — Decreased white blood cell count, unspecified
- D72.820 — Lymphocytosis (symptomatic)
- D72.821 — Monocytosis (symptomatic)
- D72.822 — Plasmacytosis
- D72.823 — Leukemoid reaction
- D72.824 — Basophilia
- D72.825 — Bandemia
- D72.828 — Other elevated white blood cell count
- D72.829 — Elevated white blood cell count, unspecified
- D72.89 — Other specified disorders of white blood cells
- D72.9 — Disorder of white blood cells, unspecified
- D73.81 — Neutropenic splenomegaly
- D76.1 — Hemophagocytic lymphohistiocytosis
- D76.2 — Hemophagocytic syndrome, infection-associated
- D76.3 — Other histiocytosis syndromes
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, Rockville, MD. All data sources.