2026 ICD-10-CM Diagnosis Code D89.44Hereditary alpha tryptasemia
ICD-10-CM Codes›D50–D89›D80-D89›D89
- Billable — Valid for Submission
- Chronic Condition
D89.44 is a billable ICD-10-CM diagnosis code for hereditary alpha tryptasemia. 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.
D89.44 no longer risk-adjusts for Medicare Advantage: it mapped to HCC 47 under the retired CMS-HCC V24 model through payment year 2025 but maps to no category in the live V28 model. It still risk-adjusts in the PACE (CMS-HCC V22) category 47, ESRD (V21) category 47, ESRD (V24) category 47, and RxHCC Part D (V08) category 99 for payment year 2026.
Code Identity
Code Classification
Medicare Risk Adjustment (HCC)Billing
D89.44 no longer risk-adjusts for Medicare Advantage: it maps to no payment category in the live CMS-HCC V28 model, although it still risk-adjusts in the other CMS models shown below.
Source: CMS Payment Year 2026 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Use Additional Code
- code, if applicable, for:
- allergy status, other than to drugs and biological substances Z91.0
- personal history of anaphylaxis Z87.892
The “use additional code” indicates that a secondary code could be used to further specify the patient’s condition. This note is not mandatory and is only used if enough information is available to assign an additional code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Syndrome See Also: Disease;
hereditary alpha tryptasemia D89.44
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Code History & ChangesHistory
Replacement D89.44 replaces the following previously assigned code(s):
- D89.49 - Other mast cell activation disorder
Questions About D89.44Overview
What is the ICD-10 code for hereditary alpha tryptasemia?
The ICD-10-CM code for hereditary alpha tryptasemia is D89.44 (sometimes written as D8944). It is billable on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
Is D89.44 (Mast cell activation syndrome and related disorders) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report hereditary alpha tryptasemia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does D89.44 group to?
When hereditary alpha tryptasemia 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.
Does D89.44 risk-adjust for Medicare Advantage payment?
Not for Medicare Advantage. D89.44 mapped to HCC 47 in the retired CMS-HCC V24 model, which last determined payment in 2025, but it maps to no category in the live V28 model; see all codes that no longer risk-adjust. It still risk-adjusts in the PACE (CMS-HCC V22) category 47 (Disorders of Immunity), ESRD (V21) category 47 (Disorders of Immunity), ESRD (V24) category 47 (Disorders of Immunity), and RxHCC Part D (V08) category 99 (Immune Disorders).