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D83.0

Billable

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

Last updated: FY2026 ICD-10-CM (Oct 1, 2025 – Sep 30, 2026) | CMS-HCC V28 (100% phase-in, PY2026)

Is D83.0 an HCC code?

Yes. D83.0 maps to Severe Combined Immunodeficiency and Other Immune Disorders under the CMS-HCC V28 risk adjustment model (and Disorders of Immunity under V24).

HCC Category Mapping

V28HCC 114Severe Combined Immunodeficiency and Other Immune Disorders
0.000
V24HCC 47Disorders of Immunity
0.472
ESRDHCC 47Disorders of Immunity
0.000
RxHCCHCC 99Immunodeficiencies
0.000

RAF weights shown are the community, non-dual, aged base weights from the CMS risk adjustment model file. Actual per-patient RAF contribution depends on member segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.

MEAT Criteria for D83.0

For D83.0 to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically — it has to be re-documented and supported each calendar year.

  • MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
  • EEvaluate: test results, medication response, or physical findings reviewed by the provider
  • AAssess: explicit mention in the assessment or plan with acknowledgment of status
  • TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis

Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed D83.0 during that encounter — not just copy-forwarded from a problem list.

What This Code Means

D83.0 is the ICD-10-CM diagnosis code for common variable immunodeficiency with predominant abnormalities of b-cell numbers and function. A common immune disorder where the body doesn't produce enough antibodies or the B cells that make them don't function properly. D83.0 sits in the ICD-10-CM chapter for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (d50-d89), within the section covering certain disorders involving the immune mechanism (d80-d89).

Under the CMS-HCC V28 risk adjustment model, D83.0 maps to Severe Combined Immunodeficiency and Other Immune Disorders (HCC 114) with a community, non-dual, aged base RAF weight of 0.000. Under the older CMS-HCC V24 model, D83.0 maps to Disorders of Immunity (HCC 47) with a community, non-dual, aged base RAF weight of 0.472. V28 is the CMS-HCC risk adjustment model that reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition.

Document specific B-cell count abnormalities and functional deficits from immunological testing. Because D83.0 maps to a payment HCC, the provider's documentation must satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's Medicare Advantage risk adjustment score. When documentation is ambiguous, coders should issue a provider query rather than assume the highest-specificity variant.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for D83.0 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Document specific B-cell count abnormalities and functional deficits from immunological testing
  • Distinguish from D83.1 and D83.2 by confirming the primary problem is B-cell related, not T-cell or autoimmune

Clinical Significance

Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function is the most common symptomatic primary immunodeficiency in adults, characterized by significantly reduced B-cell numbers or function leading to hypogammaglobulinemia. Patients present with recurrent sinopulmonary infections, gastrointestinal disease, granulomatous inflammation, and increased risk of autoimmune cytopenias and lymphoid malignancy.

Documentation Requirements

  • Documentation must include quantitative immunoglobulin levels (Immunoglobulin G, Immunoglobulin A, and often Immunoglobulin M significantly reduced), B-cell enumeration by flow cytometry, poor response to vaccination challenge testing, clinical manifestations including infection history, and treatment with immunoglobulin replacement therapy.
  • Specify that B-cell abnormalities are the predominant finding to justify D83.0 over D83.1 or D83.2.

Commonly Confused Codes

  • D83.1 (common variable immunodeficiency with predominant T-cell disorders), D83.2 (common variable immunodeficiency with autoantibodies to B
  • or T-cells), D83.9 (common variable immunodeficiency, unspecified, used when the predominant abnormality is not specified), D80.0 (hereditary hypogammaglobulinemia which typically presents earlier in life).

Code Hierarchy

D83Common variable immunodeficiencyD83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

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