D72.89
BillableOther specified disorders of white blood cells
Other specified disorders of white blood cells
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abnormality of white blood cells NEC
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Also Known As / Clinical Terms(249)
SNOMED CT
- Decreased lymphocyte life span2902006
- Leucocyte maturation arrest6346007
- Leukocyte maturation arrest6346007
- Disorder of gamma-glutamyl cycle9128006
- Disorder of the gamma-glutamyl cycle9128006
- Reactive mastocytosis10294000
- Granulocyte abnormality due to immune defect15012007
- Pelger-Huet cell15111002
- Pelger-Huët cell15111002
- Neutrophil cytomatrix disorder21043008
- Abnormal monocyte maturation29663003
- Abnormal monocyte production29663003
- Increased lymphocyte production30684005
- Abnormal granulocyte production33121004
- Neutrophil motility disorder34916006
- Actin dysfunction syndrome40145002
- Congenital neutrophil actin dysfunction40145002
- Decreased granulocyte life span41350008
- Extramedullary haematopoiesis42952007
- Extramedullary hematopoiesis42952007
- Increased granulocyte destruction44393007
- Increased lymphocyte destruction49026002
- Right shift50551008
- Right shift of WBC50551008
- Right shifted white blood cells50551008
- Sensitised cell52976009
- Sensitized cell52976009
- Abnormal eosinophil maturation57180008
- Abnormal eosinophil production57180008
- Sensitised leucocyte64668006
- Sensitized leukocyte64668006
- Pseudoneutrophilia70349007
- Non malignant mast cell disease72272002
- Left shift87361006
- Left shift of WBC87361006
- Left shifted white blood cells87361006
- Decreased lymphocyte destruction87669002
- Abnormal basophil maturation88369005
- Abnormal basophil production88369005
- Increased megakaryocyte production103212007
- Megakaryocytosis103212007
- Quantitative disorder of neutrophils105601003
- Basophilic hyperplasia111037009
- Extramedullary megakaryocytopoiesis124960000
- Myeloperoxidase deficiency syndrome129644003
- Adult G6PD deficiency of leucocytes syndrome129645002
- Adult G6PD deficiency of leukocytes syndrome129645002
- Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome129645002
- White blood cell abnormality134199001
- Abnormal monocytes165540007
- Immature white blood cells165543009
- Lymphocytoid disorder234428005
- Chemotactic disorder234429002
- SGD - Specific granule deficiency234431006
- Specific granule deficiency234431006
- MPO - Myeloperoxidase deficiency234433009
- Myeloperoxidase deficiency234433009
- Phagocytic cell defect234573000
- Disorder of phagocytic cell number234574006
- Defective phagocytic cell opsonisation234578009
- Defective phagocytic cell opsonization234578009
- Defective phagocytic cell chemotaxis234580003
- Defective phagocytic cell adhesion234581004
- Defective phagocytic cell killing234585008
- Leucocyte glucose-6-phosphate dehydrogenase deficiency234586009
- Leukocyte glucose-6-phosphate dehydrogenase deficiency234586009
- Neutrophil secondary granule deficiency234588005
- Glutathione synthetase deficiency234589002
- Pyroglutamic aciduria234589002
- Pyroglutamicaciduria234589002
- Gluthathione peroxidase deficiency234590006
- Neutrophil abnormality250274006
- Pseudo-Pelger-Huet form250276008
- Doughnut cell250277004
- Ring-form250277004
- Ring-form neutrophil250277004
- Alius-Grignaschi anomaly250280003
- Cytoplasmic vacuolation250281004
- Drumstick nuclear appendage250282006
- Lymphocyte abnormality250284007
- Plasmacytoid lymphocytes250286009
- Giant granulation250294002
- White blood cell chromosome abnormality250306005
- Toxic granulation259714005
- Amato body259715006
- Dohle body259715006
- Döhle body259715006
- Granulation anomaly288327009
- Granulocyte granule deficiency289317009
- Phagocytic cell dysfunction302874002
- Finding of white blood cell age365627007
- White blood cell age365627007
- White blood cell age - finding365627007
- Finding of white blood cell granularity365629005
- White blood cell granularity - finding365629005
- Platycytes398938001
- Heritable disorder of neutrophil production402793008
- Heritable disorder of neutrophil function402794002
- Jung syndrome403838000
- Siccardi syndrome403839008
- Alder-Reilly anomaly405274002
- Alder-Reilly body405274002
- Granulocyte destruction finding414366001
- Lymphocyte finding414627001
- Monocyte finding414774002
- Disorder of basophils417389002
- Leucocyte morulae440577009
- Leukocyte morulae440577009
- Morulae in leucocyte440577009
- Morulae in leukocyte440577009
- Cytoplasmic vacuolation of lymphocyte445920003
- Eosinophil peroxidase deficiency711160007
- Peroxidase and phospholipid deficiency in eosinophils711160007
- Presentey anomaly711160007
- Acquired disorder of neutrophil function735436001
- Disorder of neutrophil adhesion735437005
- Disorder of neutrophil chemotaxis735438000
- Recurrent infection due to specific granule deficiency1144934003
- Periodontitis due to leukocyte adhesion deficiency1186967001
- Leucocyte adherence deficiency1187233008
- Leucocyte adhesion deficiency1187233008
- Leukocyte adherence deficiency1187233008
- Leukocyte adhesion deficiency1187233008
UMLS
Clinical Terms
- Pelger-Huet cell
- Acquired disorder of neutrophil function
- Jung syndrome
- Right shift of WBC
- Siccardi syndrome
- Platycytes
- White blood cell abnormality
- Actin dysfunction syndrome
- Right shifted white blood cells
- Increased megakaryocyte production
- Presentey anomaly
- Leukocyte maturation arrest
- Abnormal granulocyte production
- Granulocyte abnormality due to immune defect
- Increased lymphocyte destruction
- Abnormal eosinophil maturation
- Disorder of gamma-glutamyl cycle
- Leukocyte morulae
- Disorder of basophils
- Gluthathione peroxidase deficiency
- Alder-Reilly body
- Ring-form neutrophil
- Decreased lymphocyte destruction
- Defective phagocytic cell killing
- Lymphocytoid disorder
- Pseudo-Pelger-Huet form
- Disorder of neutrophil chemotaxis
- Leucocyte glucose-6-phosphate dehydrogenase deficiency
- Myeloperoxidase deficiency
- Plasmacytoid lymphocytes
- Defective phagocytic cell opsonisation
- Lymphocyte abnormality
- Toxic granulation
- Pelger-Huët cell
- SGD - Specific granule deficiency
- White blood cell chromosome abnormality
- Sensitized cell
- Reactive mastocytosis
- Left shift of WBC
- Decreased lymphocyte life span
- Alius-Grignaschi anomaly
- Periodontitis due to leukocyte adhesion deficiency
- Cytoplasmic vacuolation of lymphocyte
- Glutathione synthetase deficiency
- Döhle body
- Extramedullary hematopoiesis
- Pyroglutamicaciduria
- Myeloperoxidase deficiency syndrome
- Left shift
- Granulocyte granule deficiency
- Non malignant mast cell disease
- Abnormal monocyte maturation
- Monocyte finding
- Finding of white blood cell granularity
- Dohle body
- Specific granule deficiency
- MPO - Myeloperoxidase deficiency
- Drumstick nuclear appendage
- Finding of white blood cell age
- Abnormal monocyte production
- Abnormal basophil maturation
- Neutrophil cytomatrix disorder
- Adult G6PD deficiency of leucocytes syndrome
- Alder-Reilly anomaly
- Abnormality of white blood cells NEC
- Left shifted white blood cells
- Granulation anomaly
- Leucocyte maturation arrest
- Leucocyte morulae
- Defective phagocytic cell opsonization
- Morulae in leukocyte
- Right shift
- Sensitised leucocyte
- White blood cell granularity - finding
- Pseudoneutrophilia
- Phagocytic cell dysfunction
- Congenital neutrophil actin dysfunction
- Quantitative disorder of neutrophils
- Chemotactic disorder
- Defective phagocytic cell chemotaxis
- Extramedullary haematopoiesis
- Increased granulocyte destruction
- Neutrophil secondary granule deficiency
- Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome
- Giant granulation
- Eosinophil peroxidase deficiency
- White blood cell age
- Lymphocyte finding
- Heritable disorder of neutrophil function
- Sensitized leukocyte
- Cytoplasmic vacuolation
- Leucocyte adherence deficiency
- Amato body
- Leukocyte adherence deficiency
- Leukocyte glucose-6-phosphate dehydrogenase deficiency
- Leukocyte adhesion deficiency
- Decreased granulocyte life span
- Extramedullary megakaryocytopoiesis
- Leucocyte adhesion deficiency
- Phagocytic cell defect
- Peroxidase and phospholipid deficiency in eosinophils
- Megakaryocytosis
- Adult G6PD deficiency of leukocytes syndrome
- Disorder of neutrophil adhesion
- Abnormal basophil production
- Disorder of the gamma-glutamyl cycle
- Ring-form
- Abnormal monocytes
- Doughnut cell
- Increased lymphocyte production
- Immature white blood cells
- Sensitised cell
- Neutrophil abnormality
- Basophilic hyperplasia
- Abnormal eosinophil production
- Defective phagocytic cell adhesion
- Granulocyte destruction finding
- Heritable disorder of neutrophil production
- Recurrent infection due to specific granule deficiency
- White blood cell age - finding
- Disorder of phagocytic cell number
- Neutrophil motility disorder
- Morulae in leucocyte
- Pyroglutamic aciduria
Frequently Asked Questions
What is the ICD-10 code for other specified disorders of white blood cells?
The ICD-10-CM code for other specified disorders of white blood cells is D72.89. The full clinical description is "Other specified disorders of white blood cells". D72.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D72.89 mean?
ICD-10-CM code D72.89 represents “Other specified disorders of white blood cells”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D72.89 a billable code?
Yes, D72.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D72.89 in?
D72.89 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D72.89?
D72.89 has Excludes1 notes indicating codes that cannot be used together with it, including: basophilia (D72.824); immunity disorders (D80-D89); neutropenia (D70); and 2 more.
What SNOMED CT codes does D72.89 map to?
D72.89 maps to 84 SNOMED CT concepts: 88369005, 57180008, 33121004, 29663003, 165540007, and 79 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D72.89?
D72.89 is linked to 2 UMLS Concept Unique Identifiers: C2873818, C0477318. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D72.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified disorders of white blood cells affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D72.89?
There is no direct ICD-11 mapping available for D72.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.