ICD-10-CM Codes
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
D80-D89 Certain disorders involving the immune mechanism
D83- Common variable immunodeficiency
2022 ICD-10-CM Diagnosis Code D83

2022 ICD-10-CM Diagnosis Code D83

Common variable immunodeficiency

2016

2017

2018

2019

2020

2021

2022

Non-Billable/Non-Specific Code

D83 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
The 2022 edition of ICD-10-CM D83 became effective on October 1, 2021.
This is the American ICD-10-CM version of D83 - other international versions of ICD-10 D83 may differ.

The following code(s) above D83 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

that may be applicable to D83:

Clinical Information

A primary immunodeficiency characterized by low levels or absence of all the immunoglobulin classes and lack of b-lymphocytes or plasma cells. It results in recurrent bacterial infections. Complications include autoimmune phenomena and cancer development.
Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable b-cell defects, and the presence of recurrent bacterial infections.

Code History

2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
2017 (effective 10/1/2016): No change
2018 (effective 10/1/2017): No change
2019 (effective 10/1/2018): No change
2020 (effective 10/1/2019): No change
2021 (effective 10/1/2020): No change
2022 (effective 10/1/2021): No change

ICD-10-CM Codes Adjacent To D83

D81.89 Other combined immunodeficiencies

D81.9 Combined immunodeficiency, unspecified

D82 Immunodeficiency associated with other major defects

D82.0 Wiskott-Aldrich syndrome

D82.1 Di George's syndrome

D82.2 Immunodeficiency with short-limbed stature

D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus

D82.4 Hyperimmunoglobulin E [IgE] syndrome

D82.8 Immunodeficiency associated with other specified major defects

D82.9 Immunodeficiency associated with major defect, unspecified

D83 Common variable immunodeficiency

D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders

D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells

D83.8 Other common variable immunodeficiencies

D83.9 Common variable immunodeficiency, unspecified

D84 Other immunodeficiencies

D84.0 Lymphocyte function antigen-1 [LFA-1] defect

D84.1 Defects in the complement system

D84.8 Other specified immunodeficiencies

D84.81 Immunodeficiency due to conditions classified elsewhere

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.