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ICD-11

ICD-11 Codes
for 4A00.00 - Neutrophil immunodeficiency syndrome
Teodor Jurukovski January 1, 1970
Fact checked by: Teodor Jurukovski
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Understanding neutrophil immunodeficiency syndrome

Neutrophil immunodeficiency syndrome is a rare primary immunodeficiency disorder classified under ICD-11 code 4A00.00. It is characterised by an elevated white blood cell count, specifically neutrophilia, combined with profound functional impairment of neutrophils.

Despite increased neutrophil numbers, these cells are unable to perform essential immune functions effectively. As a result, affected individuals are highly susceptible to bacterial infections and demonstrate impaired wound healing. A distinguishing clinical feature is the relative absence of pus formation at sites of infection, reflecting defective neutrophil migration and activity.

Alternative names for neutrophil immunodeficiency syndrome

Several alternative terms are used in specialist literature and diagnostic settings. Recognition of these synonyms supports accurate clinical documentation and interpretation of historical records.

Alternative names
? Infantile leukocyte adhesion deficiency due to Rac family small GTPase 2 deficiency
? Infantile LAD-like disease due to RAC2 deficiency

Recognising the symptoms

Clinical manifestations typically begin in infancy or early childhood and are dominated by recurrent, severe infections. These infections may be bacterial or fungal and often involve multiple organ systems.

Common symptoms and clinical features
? Recurrent severe bacterial and fungal infections
? Skin and soft tissue infections including abscesses and cellulitis
? Oral infections such as gingivitis and mouth ulcers
? Respiratory and gastrointestinal infections including pneumonia and colitis
? Peri-anal abscesses and poor wound healing
? Delayed growth, anaemia, and a tendency to bruise or bleed easily

Rare associations with haematological malignancies, including certain forms of leukaemia, have been reported and warrant long term monitoring.

Genetic basis and pathophysiology

Neutrophil immunodeficiency syndrome is primarily caused by a dominant negative mutation in the RAC2 gene. This gene encodes Rac2, a small GTPase that plays a critical role in neutrophil signalling pathways.

Reduced Rac2 protein expression disrupts cytoskeletal organisation, impairing neutrophil shape change and motility. It also interferes with assembly and activation of the NADPH oxidase complex, which is essential for generating reactive oxygen species required to kill ingested microorganisms.

These combined defects result in neutrophils that circulate in high numbers but are functionally ineffective.

Diagnosis of neutrophil immunodeficiency syndrome

Diagnosis is based on a combination of clinical features, laboratory findings, and genetic confirmation. Early identification is important to reduce infection related morbidity.

Diagnostic investigations
? Full blood count demonstrating neutrophilia
? Microbiological cultures to identify recurrent or unusual pathogens
? Autoimmune and autoantibody testing when clinically indicated
? Genetic testing to confirm RAC2 mutation
? Bone marrow biopsy in selected cases to exclude alternative diagnoses

Management and treatment strategies

Management focuses on reducing infection risk, treating active infections promptly, and correcting immune dysfunction where possible. Care is typically coordinated by specialist immunology and haematology teams.

Treatment approaches
? Prompt and aggressive antibiotic or antifungal therapy for infections
? Prophylactic antimicrobial medications to prevent recurrent infections
? Granulocyte colony-stimulating factor therapy for selected patients
? Hematopoietic stem cell transplantation for severe, treatment resistant disease

Good skin and dental hygiene are essential supportive measures. Gene therapy is an area of ongoing research and may provide future therapeutic options for selected genetic neutrophil disorders.

Are neutrophil immunodeficiency syndrome ICD codes billable

Yes. ICD-11 code 4A00.00 is a billable diagnosis code when supported by appropriate clinical documentation and diagnostic evidence. Accurate recording of laboratory findings, genetic confirmation, and infection history is essential for correct coding, reporting, and reimbursement.

Frequently asked questions

What is the ICD-11 code for Neutrophil immunodeficiency syndrome?
The ICD-11 code for Neutrophil immunodeficiency syndrome is 4A00.00.
How is Neutrophil immunodeficiency syndrome classified in ICD-11?
Neutrophil immunodeficiency syndrome is classified under Chapter 04, Diseases of the immune system, specifically within the category of Primary immunodeficiencies due to disorders of innate immunity. The code 4A00.00 falls under Functional neutrophil defects.
What does the ICD-11 code 4A00.00 represent?
The ICD-11 code 4A00.00 represents Neutrophil immunodeficiency syndrome, which is a specific type of functional neutrophil defect.
How does ICD-11 handle unspecified functional neutrophil defects?
For unspecified functional neutrophil defects, ICD-11 provides the code 4A00.0Z.
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