D71.8 Other functional disorders of polymorphonuclear neutrophils

Billable ICD-10-CM code, FY2026.

Applicable to

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

Risk adjustment (HCC)

• CMS-HCC V28: HCC 115 — Specified Immunodeficiencies and White Blood Cell Disorders
• CMS-HCC V22: HCC 47 — Disorders of Immunity
• ESRD V24: HCC 47

MS-DRG index

Defines the logic of DRG(s) 808-810 in MDC 16.

Diagnosis Index entries for D71.8

• Defect, defective › cell membrane receptor complex (CR3)
• Disease, diseased › childhood granulomatous
• Disease, diseased › granulomatous (childhood) (chronic)
• Disorder (of) › functional polymorphonuclear neutrophils › specified NEC
• Disorder (of) › neutrophil, polymorphonuclear › specified NEC
• Disorder (of) › polymorphonuclear neutrophils › specified NEC
• Dysphagocytosis, congenital
• Granulomatosis › progressive septic
• Job's syndrome (chronic granulomatous disease)
• Lipochrome histiocytosis (familial)
• Syndrome › Job's

Nearby codes

• D71 Functional disorders of polymorphonuclear neutrophils
• D71.1 Leukocyte adhesion deficiency
• D71.8 Other functional disorders of polymorphonuclear neutrophils (this code)
• D71.9 Functional disorders of polymorphonuclear neutrophils, unspecified