D89.44 Hereditary alpha tryptasemia

The ICD-10-CM code for Hereditary alpha tryptasemia is D89.44 (FY2026). It is a billable, claim-ready diagnosis code.

Classification

Chapter

3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

Section

D80-D89: Certain disorders involving the immune mechanism (D80-D89)

Category D89

29 codes (24 billable)

FY2026 Status

Stable since FY2024

Also Known As

ICD-10-CM Alphabetic Index entries that lead to D89.44:

• Tryptasemia, hereditary alpha
• Hereditary alpha tryptasemia (syndrome)
• Syndrome › hereditary alpha tryptasemia

U.S. Hospital Utilization

• An estimated 75 U.S. inpatient stays in 2023 included D89.44 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 entry

3. Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) ............................................................................................. 39

Reserved for future guideline expansion

Reserved for future guideline expansion ...................................................................................... 39

Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026

References

• CMS — ICD-10-CM Official Code Set and Guidelines, FY2026
• CDC/NCHS — ICD-10-CM Files and Browser Tool
• AHRQ — HCUP National Inpatient Sample, Frequencies by Diagnosis Code (2016–2023)

Cite This Page

Reference D89.44 with the canonical source and edition:

D89.44 — Hereditary alpha tryptasemia. ICD-10 Coding Pro (ICD-10-CM FY2026). https://icd10codingpro.com/codes/D89.44

Canonical URL: https://icd10codingpro.com/codes/D89.44