FY2027Upcoming
Effective from
- Inherited rules changed
Combined immunodeficiencies
Category — select a more specific code
CDC/NCHS · FY2027autosomal recessive agammaglobulinemia (Swiss type) (D80.0)
For US diagnosis claims covered by HIPAA, ICD-10-CM is required from October 1, 2015.
Use the service date for outpatient/professional claims and the discharge date for hospital inpatient claims. Earlier encounters use ICD-9-CM; each individual code must also be valid for the applicable date.
Official coding guidelines → · CMS ↗First observed · 2015-10-01
Latest recorded change · FY2027
Effective from
Combined immunodeficiencies
Category — select a more specific code
CDC/NCHS · FY2027| All editions | Effective from | Code history |
|---|---|---|
| FY2016 | 2015-10-01 | First observed |
| FY2017 | 2016-10-01 | No tabular change |
| FY2018 | 2017-10-01 | No tabular change |
| FY2019 | 2018-10-01 | No tabular change |
| FY2020 | 2019-10-01 | No tabular change |
| FY2020 · April | 2020-04-01 | No tabular change |
| FY2021 | 2020-10-01 | No tabular change |
| FY2021 · 01-01 | 2021-01-01 | No tabular change |
| FY2022 | 2021-10-01 | No tabular change |
| FY2022 · 04-01 | 2022-04-01 | No tabular change |
| FY2023 | 2022-10-01 | No tabular change |
| FY2023 · 04-01 | 2023-04-01 | No tabular change |
| FY2024 | 2023-10-01 | No tabular change |
| FY2024 · 04-01 | 2024-04-01 | No tabular change |
| FY2025 | 2024-10-01 | No tabular change |
| FY2025 · 04-01 | 2025-04-01 | No tabular change |
| FY2026 | 2025-10-01 | Inherited rules changed |
| FY2026 · April | 2026-04-01 | No tabular change |
| FY2027 | 2026-10-01 | Inherited rules changed |
autosomal recessive agammaglobulinemia (Swiss type) (D80.0)
D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesisBillable / specificD81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbersBillable / specificD81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbersBillable / specificD81.3Adenosine deaminase [ADA] deficiencyCategory · further specificity requiredD81.4Nezelof's syndromeBillable / specificD81.5Purine nucleoside phosphorylase [PNP] deficiencyBillable / specificD81.6Major histocompatibility complex class I deficiencyBillable / specificD81.7Major histocompatibility complex class II deficiencyBillable / specificD81.8Other combined immunodeficienciesCategory · further specificity requiredD81.9Combined immunodeficiency, unspecifiedBillable / specificOfficial titles and instructions are preserved in their source language. Official sources ↗