2021 ICD-10-CM Diagnosis Code D71

Functional disorders of polymorphonuclear neutrophils

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
  • D71 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2021 edition of ICD-10-CM D71 became effective on October 1, 2020.
  • This is the American ICD-10-CM version of D71 - other international versions of ICD-10 D71 may differ.
Applicable To
  • Cell membrane receptor complex [CR3] defect
  • Chronic (childhood) granulomatous disease
  • Congenital dysphagocytosis
  • Progressive septic granulomatosis
The following code(s) above D71 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to D71:
  • D50-D89
    2021 ICD-10-CM Range D50-D89

    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

    Type 2 Excludes
    • 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)
    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Approximate Synonyms
  • Chronic granulomatous disease
  • Congenital dysphagocytosis
  • Dysphagocytosis, congenital
  • Granulomatous disease
  • Granulomatous disorder
Clinical Information
  • A recessive x-linked defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation.
  • Recessive x-linked defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation.
ICD-10-CM D71 is grouped within Diagnostic Related Group(s) (MS-DRG v38.0):
  • 808 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with mcc
  • 809 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with cc
  • 810 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders without cc/mcc

Convert D71 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
  • 2021 (effective 10/1/2020): No change

Diagnosis Index entries containing back-references to D71:
  • Defect, defective Q89.9
    ICD-10-CM Diagnosis Code Q89.9

    Congenital malformation, unspecified

      2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital anomaly NOS
    • Congenital deformity NOS
    • cell membrane receptor complex D71 (CR3)
  • Disease, diseased - see also Syndrome
    • childhood granulomatous D71
    • granulomatous D71 (childhood) (chronic)
  • Disorder (of) - see also Disease
    • functional polymorphonuclear neutrophils D71
    • neutrophil, polymorphonuclear D71
    • polymorphonuclear neutrophils D71
  • Dysphagocytosis, congenital D71
  • Granulomatosis L92.9
    ICD-10-CM Diagnosis Code L92.9

    Granulomatous disorder of the skin and subcutaneous tissue, unspecified

      2016 2017 2018 2019 2020 2021 Billable/Specific Code
    Type 2 Excludes
    • progressive septic D71
  • Job's syndrome D71 (chronic granulomatous disease)
  • Lipochrome histiocytosis D71 (familial)
  • Syndrome - see also Disease
    • Job's D71

ICD-10-CM Codes Adjacent To D71
D69.8 Other specified hemorrhagic conditions
D69.9 Hemorrhagic condition, unspecified
D70 Neutropenia
D70.0 Congenital agranulocytosis
D70.1 Agranulocytosis secondary to cancer chemotherapy
D70.2 Other drug-induced agranulocytosis
D70.3 Neutropenia due to infection
D70.4 Cyclic neutropenia
D70.8 Other neutropenia
D70.9 Neutropenia, unspecified
D71 Functional disorders of polymorphonuclear neutrophils
D72 Other disorders of white blood cells
D72.0 Genetic anomalies of leukocytes
D72.1 Eosinophilia
D72.10 …… unspecified
D72.11 Hypereosinophilic syndrome [HES]
D72.110 Idiopathic hypereosinophilic syndrome [IHES]
D72.111 Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
D72.118 Other hypereosinophilic syndrome
D72.119 …… unspecified
D72.12 Drug rash with eosinophilia and systemic symptoms syndrome

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.