Discover free eBooks, guides and med spa templates on our new resources page

ICD-11

ICD-11 Codes
for 4A00 - Primary immunodeficiencies due to disorders of innate immunity
Tanja Lepcheska January 1, 1970
Fact checked by: Teodor Jurukovski
Use Code

Understanding Primary Immunodeficiencies of Innate Immunity

Primary immunodeficiencies due to disorders of innate immunity are congenital conditions classified under ICD-11 code 4A00. These disorders affect the innate immune system, which is the body’s first and fastest line of defense against pathogens.

The innate immune system responds immediately and non-specifically to bacteria, viruses, fungi, and parasites. It relies on physical barriers, immune cells, and soluble proteins to control infection before the adaptive immune system is activated. When these mechanisms are impaired from birth, affected individuals experience increased susceptibility to infection and immune dysregulation.

Recognizing the Signs of Innate Immune Deficiency

Clinical manifestations often appear early in life, although milder forms may present later. Infections tend to be recurrent, unusually severe, or caused by uncommon organisms. Ongoing immune activation may also result in chronic inflammation.

Common signs and symptoms
? Recurrent bacterial infections such as pneumonia, sinusitis, or skin and soft tissue infections
? Persistent or difficult to treat viral or fungal infections
? Chronic inflammation or autoimmune-like manifestations
? Failure to thrive or delayed growth in infants and children

Genetic Basis of Innate Immune Disorders

Primary immunodeficiencies of innate immunity are caused by inherited genetic mutations. These mutations disrupt the development, signaling, or function of innate immune components that are essential for early pathogen recognition and clearance.

Although present from birth, the timing and severity of symptoms depend on the specific gene affected and the degree of immune dysfunction.

Innate immune components commonly affected
? Neutrophils with impaired microbial killing or migration
? Macrophages and dendritic cells with defective pathogen recognition
? Natural killer cells with reduced cytotoxic activity
? Complement system proteins required for opsonization and cell lysis

Diagnosing Primary Innate Immunodeficiencies

Diagnosis requires careful clinical evaluation combined with targeted laboratory testing. Early identification is important to prevent severe infections and long term complications.

Testing focuses on both immune cell quantity and functional capacity, as normal cell counts may still be associated with impaired immune responses.

Diagnostic evaluation may include
? Detailed infection history and family history of immune disorders
? Complete blood count with differential to assess immune cell levels
? Flow cytometry to characterize innate immune cell populations
? Functional assays and genetic testing to identify pathway defects

Managing Innate Immune Deficiencies

Management focuses on reducing infection risk, treating infections promptly, and preventing immune mediated complications. The approach is individualized based on disease severity and genetic diagnosis.

Long term follow up by immunology specialists is essential to monitor disease progression and treatment effectiveness.

Management strategies may include
? Prophylactic antibiotics to prevent recurrent bacterial infections
? Early and aggressive treatment of acute infections
? Immune modulating therapies to control inflammation
? Hematopoietic stem cell transplantation or gene therapy in selected severe cases

Are Primary Immunodeficiencies of Innate Immunity ICD codes billable

ICD-11 code 4A00 is a billable diagnosis code when used with appropriate clinical documentation. The code represents confirmed congenital disorders of innate immunity and supports reimbursement for diagnostic evaluation, treatment, and long term management.

Use of the most specific available subcode improves billing accuracy and reduces the risk of claim denial.

ICD-11 Coding for Innate Immune Disorders

Accurate coding is essential for clinical documentation, health system reporting, and research. ICD-11 allows further classification of innate immune disorders based on the underlying defect.

Common ICD-11 subcodes under 4A00
? 4A00.0 Functional neutrophil defects
? 4A00.1 Complement system deficiencies
? 4A00.2 Genetic susceptibility to specific pathogens

Frequently asked questions

What is the ICD-11 classification for Primary immunodeficiencies due to disorders of innate immunity?
ICD-11 code 4A00 is classified under Chapter 04, Diseases of the immune system, and represents primary immunodeficiencies that result from disorders of the innate immune system.
What are the specific categories included within ICD-11 code 4A00?
ICD-11 code 4A00 includes categories such as Functional neutrophil defects (4A00.0), Defects in the complement system (4A00.1), Genetic susceptibility to particular pathogens (4A00.2), and Immunodeficiency with natural-killer cell deficiency (4A00.3).
How does ICD-11 handle unspecified or other specified primary immunodeficiencies due to disorders of innate immunity?
ICD-11 provides codes for 'Other specified primary immunodeficiencies due to disorders of innate immunity' (4A00.Y) and 'Primary immunodeficiencies due to disorders of innate immunity, unspecified' (4A00.Z) to accommodate cases where a more specific category cannot be identified.
What is the primary distinction of ICD-11 code 4A00?
ICD-11 code 4A00 specifically addresses primary immunodeficiencies that stem from impairments in the innate immune system, differentiating them from those related to the adaptive immune system.
×