ICDcodes.org
FY2027

D71.8Other functional disorders of polymorphonuclear neutrophils

Billable

Is D71.8 billable?

Yes — D71.8 is billable for FY2027. D71.8 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D71.8 may be submitted for encounters from October 1, 2026 through September 30, 2027.

D71.8 at a glance

CodeD71.8
DescriptionOther functional disorders of polymorphonuclear neutrophils
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does D71.8 group to?

D71.8 sits in MDC 16 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.

  • 808Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCCmedical
  • 809Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CCmedical
  • 810Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCCmedical

How is D71.8 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to D71.8. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Dysphagocytosis, congenital
  • Job's syndrome (chronic granulomatous disease)
  • Lipochrome histiocytosis (familial)
  • Defect, defectivecell membrane receptor complex
  • Disease, diseasedchildhood granulomatous
  • Disease, diseasedgranulomatous
  • Granulomatosisprogressive septic
  • SyndromeJob's
  • Disorderfunctional polymorphonuclear neutrophilsspecified NEC (of)
  • Disorderneutrophil, polymorphonuclearspecified NEC (of)
  • Disorderpolymorphonuclear neutrophilsspecified NEC (of)

Inclusion terms

Alternative wording in documentation that is classified to D71.8.

  • Cell membrane receptor complex [CR3] defect
  • Chronic (childhood) granulomatous disease
  • Congenital dysphagocytosis
  • Progressive septic granulomatosis

Excludes2 — not included here — inherited from Chapter 3

The conditions below are not part of D71.8, but a patient may have both at the same time. When documentation supports it, D71.8 and the excluded code may both be reported.

  • autoimmune disease (systemic) NOS (M35.9)
  • certain conditions originating in the perinatal period (P00-P96)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • human immunodeficiency virus [HIV] disease (B20)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

How long has D71.8 existed?

D71.8 first appears in FY2026.

Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.

Which conditions are coded to D71.8?

What other codes are in the D71 family? (2)