D80.0 Hereditary hypogammaglobulinemia
The ICD-10-CM code for Hereditary hypogammaglobulinemia is D80.0 (FY2026). It is a billable, claim-ready diagnosis code.
Classification
- Section
- D80-D89: Certain disorders involving the immune mechanism (D80-D89)
- Category D80
- 11 codes (10 billable)
- FY2026 Status
- Stable since FY2024
Also Known As
ICD-10-CM Alphabetic Index entries that lead to D80.0:
- Bruton's X-linked agammaglobulinemia
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › hereditary
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › Bruton's X-linked
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › congenital sex-linked
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › Swiss type (autosomal recessive)
- Hypogammaglobulinemia › hereditary
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › autosomal recessive (Swiss type)
- Agammaglobulinemia (acquired (secondary)) (nonfamilial) › X-linked (with growth hormone deficiency) (Bruton)
Inclusion Terms
- Autosomal recessive agammaglobulinemia (Swiss type)
- X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
U.S. Hospital Utilization
- An estimated 420 U.S. inpatient stays in 2023 included D80.0 among the documented diagnoses.
Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.
Official Coding Guidelines
Chapter 3 TOC entry3. Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) ............................................................................................. 39
Reserved for future guideline expansionReserved for future guideline expansion ...................................................................................... 39
Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026