D71.8
Other functional disorders of polymorphonuclear neutrophils
HCC risk adjustment mapping
CMS-HCC V28
Specified Immunodeficiencies and White Blood Cell Disorders
CMS-HCC ESRD V24
Disorders of Immunity
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Cell membrane receptor complex [CR3] defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis
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)
Official Guidelines for D71.8
FY 2026 ›Find D71.8 in the alphabetic index
11 index paths lead to this code
- Dysphagocytosis, congenital
- Job's syndrome
- Lipochrome histiocytosis
- Defect, defective › cell membrane receptor complex
- Disease, diseased › childhood granulomatous
- Disease, diseased › granulomatous
- Granulomatosis › progressive septic
- Syndrome › Job's
- Disorder › functional polymorphonuclear neutrophils › specified NEC
- Disorder › neutrophil, polymorphonuclear › specified NEC
- Disorder › polymorphonuclear neutrophils › specified NEC