Other functional disorders of polymorphonuclear neutrophils
Billable / specificHCC V28 115
D71.8 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Cell membrane receptor complex [CR3] defect
- Chronic (childhood) granulomatous disease
- Congenital dysphagocytosis
- Progressive septic granulomatosis
Excludes2
Not included here — may be reported together when both conditions exist.
- autoimmune disease (systemic) NOS (M35.9) (from D71)
- certain conditions originating in the perinatal period (P00-P96) (from D71)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D71)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D71)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D71)
- human immunodeficiency virus [HIV] disease (B20) (from D71)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D71)
- neoplasms (C00-D49) (from D71)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D71)
Also known as
- Cell membrane receptor complex [CR3] defect
- Chronic (childhood) granulomatous disease
- Congenital dysphagocytosis
- Progressive septic granulomatosis
- Defect, defective, cell membrane receptor complex
- Disease, diseased, childhood granulomatous
- Disease, diseased, granulomatous
- Disorder, functional polymorphonuclear neutrophils, specified NEC
- Disorder, neutrophil, polymorphonuclear, specified NEC
- Disorder, polymorphonuclear neutrophils, specified NEC
- Dysphagocytosis, congenital
- Granulomatosis, progressive septic
- Job's syndrome
- Lipochrome histiocytosis
- Syndrome, Job's
Parent code
- D71Functional disorders of polymorphonuclear neutrophilsHeader