What is the code for Hypogammaglobulinemia?

Hereditary hypogammaglobulinemia D80. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D80. 0 became effective on October 1, 2021.

What does Hypogammaglobulinemia mean?

Hypogammaglobulinemia refers to a laboratory finding (low immunoglobulin G, or IgG) that may be asymptomatic if mild or may be associated with a number of clinical entities with varied causes and manifestations if more extreme.

What is the ICD-10 code for IgG deficiency?

ICD-10 code: D80. 3 Selective deficiency of immunoglobulin G [IgG] subclasses.

What is the ICD-10 code for CVID?

ICD-10 | Common variable immunodeficiency, unspecified (D83. 9)

What is the ICD-10 code for Hypergammaglobulinemia?

Hypergammaglobulinemia, unspecified D89. 2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D89. 2 became effective on October 1, 2021.

What is an immunoglobulin deficiency?

What are IgG deficiencies? An IgG deficiency is a health problem in which your body doesn’t make enough Immunoglobulin G (IgG). People with IgG deficiency are more likely to get infections. When your body feels it is under attack, it makes special proteins called immunoglobulins or antibodies.

Is hypogammaglobulinemia an immunodeficiency?

Among the conditions associated with hypogammaglobulinemia, common variable immunodeficiency (CVI) is the most common disorder associated with antibody deficiency and has a notably high prevalence, affecting one in every 10,000–50,000 live births.

What is the difference between hypogammaglobulinemia and CVID?

Hypogammaglobulinemia is a nonspecific diagnosis. Basically, it describes a laboratory value that shows antibody levels are low, but gives no other information on the condition. CVID, on the other hand, has specific criteria: low IgG plus low IgA and/or IgM levels.

What causes Hypogammaglobulinemia?

The most common cause is common variable immunodeficiency (CVID). Causes of secondary hypogammaglobulinemia include gastrointestinal losses (e.g., malabsorption/protein-losing enteropathy), nephrotic syndrome, hematologic malignancy, and medication (e.g., immunosuppressives, such as corticosteroids and chemotherapy).

What is IgG deficiency?

An IgG deficiency is a health problem in which your body doesn’t make enough Immunoglobulin G (IgG). People with IgG deficiency are more likely to get infections. When your body feels it is under attack, it makes special proteins called immunoglobulins or antibodies. These antibodies are made by the plasma cells.

What is primary immunodeficiency disorder?

Primary immune deficiency diseases (PIDDs) are rare, genetic disorders that impair the immune system. Without a functional immune response, people with PIDDs may be subject to chronic, debilitating infections, such as Epstein-Barr virus (EBV), which can increase the risk of developing cancer. Some PIDDs can be fatal.

What are immunodeficiency disorders?

Immunodeficiency disorders impair the immune system’s ability to defend the body against foreign or abnormal cells that invade or attack it (such as bacteria, viruses, fungi, and cancer cells). As a result, unusual bacterial, viral, or fungal infections or lymphomas.