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ICD-10-CM 2027 diagnosis code

D71.8Other functional disorders of polymorphonuclear neutrophils

✓ Billable / specific

D71.8 is a valid, billable ICD-10-CM code for other functional disorders of polymorphonuclear neutrophils. It can be reported on claims for dates of service from October 1, 2026 – September 30, 2027.

Looking up by condition? See ICD-10 code for Job's syndrome, ICD-10 code for Dysphagocytosis, ICD-10 code for Lipochrome histiocytosis.

Code last changed in FY2026 (effective October 1, 2025). Source: official FY2027 ICD-10-CM release from CDC/NCHS and CMS. Page updated September 29, 2026. About our data

About D71.8

D71.8 is the ICD-10-CM diagnosis code for other functional disorders of polymorphonuclear neutrophils. It belongs to category D71 (functional disorders of polymorphonuclear neutrophils), block D70-D77 (other disorders of blood and blood-forming organs) and chapter 3 (diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.

Within D71, choose D71.8 (Other functional disorders of polymorphonuclear neutrophils) only when documentation doesn't support a more specific option: Leukocyte adhesion deficiency (D71.1) and unspecified (D71.9).

It is not a CC or MCC, so as a secondary diagnosis it doesn't change the MS-DRG severity level.

In MS-DRG v44.0, it is part of the grouping logic for DRG 808 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCC, relative weight 2.1705), DRG 809 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC, relative weight 1.2262) and DRG 810 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCC, relative weight 1.075), in MDC 16 (Diseases and Disorders of the Blood and Blood Forming Organs and Immunological Disorders), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.

It was added in FY2026, effective October 1, 2025.

Coding notes

Applicable toConditions and synonyms classified to this code
  • Cell membrane receptor complex [CR3] defect
  • Chronic (childhood) granulomatous disease
  • Congenital dysphagocytosis
  • Progressive septic granulomatosis

Notes that apply from higher levels

Instructions written at a parent level also apply to D71.8.

Alphabetic index entries

11 entries

Terms in the official ICD-10-CM index that lead to D71.8.

MS-DRG v44.0 grouping

All DRGs →

Inpatient MS-DRGs this diagnosis can group to, as the principal or a secondary diagnosis, depending on the rest of the claim.

Code history

  1. 2016
  2. 2017
  3. 2018
  4. 2019
  5. 2020
  6. 2021
  7. 2022
  8. 2023
  9. 2024
  10. 2025
  11. 2026
  12. 2027
  • FY2026 (effective 10/1/2025): Added
  • No changes since FY2026.

Common questions about D71.8

Is D71.8 billable?

Yes. D71.8 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).

Can D71.8 be used as a principal diagnosis?

Yes. The Medicare Code Editor doesn't restrict D71.8 as a principal diagnosis.

Is D71.8 a CC or MCC?

No. D71.8 is neither a CC nor an MCC under MS-DRG v44.0.

What DRG does D71.8 group to?

D71.8 is used in the MS-DRG v44.0 logic for MS-DRG 808 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCC), MS-DRG 809 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC) and MS-DRG 810 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCC). Which one applies depends on whether it is the principal diagnosis and on the rest of the claim.