2026 ICD-10-CM Diagnosis Code D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
ICD-10-CM Codes›D50–D89›D80-D89›D82
- Billable — Valid for Submission
- Chronic Condition
D82.3 is a billable ICD-10-CM diagnosis code for immunodeficiency following hereditary defective response to Epstein-Barr virus. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 814 through 816. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Immunity disorders.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Immunodeficiency following hereditary defective response to Epstein-Barr virus
- X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
- X-linked lymphoproliferative disease due to SH2D1A deficiency
- X-linked lymphoproliferative disease due to XIAP deficiency
- X-linked lymphoproliferative syndrome
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- X-linked lymphoproliferative disease
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Disease, diseased - See Also: Syndrome;
- X-linked - D82.3
- Lymphoproliferation, X-linked disease - D82.3
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Disease, diseased
- lymphoproliferative
- X-linked
- Immunodeficiency
- following hereditary defective response to Epstein-Barr virus (EBV)
- Lymphoproliferation, X-linked disease
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Immune System and Disorders
Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other diseases.
The full article covers:
- What is the immune system?
- What are the parts of the immune system?
- How does the immune system work?
- What are the types of immunity?
- What can go wrong with the immune system?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert D82.3 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About D82.3Overview
Is D82.3 (Immunodeficiency associated with other major defects) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report immunodeficiency following hereditary defective response to Epstein-Barr virus on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does D82.3 group to?
When immunodeficiency following hereditary defective response to Epstein-Barr virus is the principal diagnosis on an inpatient stay, it groups to MS-DRG 814, 815, 816, with relative weights from 0.6320 to 2.1267 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of D82.3?
Under the General Equivalence Mappings, immunodeficiency following hereditary defective response to Epstein-Barr virus converts to ICD-9-CM 279.8 (immune mechanism dis NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
