2024 ICD-10-CM Diagnosis Code D72.89

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• Abnormal basophil production
• Abnormal eosinophil production
• Abnormal granulocyte production
• Abnormal granulocyte production
• Abnormal monocyte production
• Abnormal monocytes
• Acquired disorder of neutrophil function
• Adult G6PD deficiency of leukocytes syndrome
• Alder-Reilly body
• Alius-Grignaschi anomaly
• Basophilic hyperplasia
• Chemotactic disorder
• Congenital neutrophil actin dysfunction
• Cytoplasmic vacuolation
• Cytoplasmic vacuolation of lymphocyte
• Decreased granulocyte life span
• Decreased lymphocyte destruction
• Decreased lymphocyte life span
• Defective phagocytic cell adhesion
• Defective phagocytic cell chemotaxis
• Defective phagocytic cell killing
• Defective phagocytic cell opsonization
• Disorder of basophils
• Disorder of neutrophil adhesion
• Disorder of neutrophil chemotaxis
• Disorder of phagocytic cell number
• Disorder of the gamma-glutamyl cycle
• Döhle body
• Drumstick nuclear appendage
• Eosinophil peroxidase deficiency
• Extramedullary hematopoiesis
• Extramedullary megakaryocytopoiesis
• Giant granulation
• Glutathione synthetase deficiency
• Gluthathione peroxidase deficiency
• Granulation anomaly
• Granulocyte abnormality due to immune defect
• Granulocyte destruction finding
• Granulocyte granule deficiency
• Heritable disorder of neutrophil function
• Heritable disorder of neutrophil function
• Heritable disorder of neutrophil production
• Immature white blood cells
• Increased granulocyte destruction
• Increased lymphocyte destruction
• Increased lymphocyte production
• Increased megakaryocyte production
• Jung syndrome
• Left shifted white blood cells
• Leukocyte adhesion deficiency
• Leukocyte glucose-6-phosphate dehydrogenase deficiency
• Leukocyte maturation arrest
• Lymphocyte abnormality
• Lymphocyte finding
• Lymphocyte finding
• Lymphocyte finding
• Lymphocyte finding
• Lymphocytoid disorder
• Monocyte finding
• Morulae in leukocyte
• Myeloperoxidase deficiency
• Myeloperoxidase deficiency syndrome
• Neutrophil abnormality
• Neutrophil cytomatrix disorder
• Neutrophil motility disorder
• Neutrophil secondary granule deficiency
• Non malignant mast cell disease
• Pelger-Huët cell
• Periodontitis due to leukocyte adhesion deficiency
• Phagocytic cell defect
• Phagocytic cell dysfunction
• Plasmacytoid lymphocytes
• Platycytes
• Pseudoneutrophilia
• Pseudo-Pelger-Huet form
• Quantitative disorder of neutrophils
• Reactive mastocytosis
• Recurrent infection due to specific granule deficiency
• Right shifted white blood cells
• Ring-form neutrophil
• Sensitized cell
• Sensitized leukocyte
• Siccardi syndrome
• Specific granule deficiency
• Toxic granulation
• White blood cell abnormality
• White blood cell age - finding
• White blood cell age - finding
• White blood cell chromosome abnormality
• White blood cell granularity - finding
• White blood cell granularity - finding

Clinical Information

• Leukocyte Adhesion Deficiency

  a rare autosomal recessive immunodeficiency disorder caused by deficiency of cd18 expression. it is characterized by defects in neutrophil adhesion and bacterial infections.

• Leukocyte Adhesion Deficiency Type 1|LAD-1|LAD-1 Deficiency|LAD-Type I|LAD1|LFA-I Deficiency|LFA1 Immunodeficiency

  a rare immunodeficiency with an autosomal recessive pattern of inheritance. it is caused by mutation in the itgb2 gene on chromosome 21 which codes for the beta subunit of beta-2 integrin (cd18). the mutation results in significantly reduced or absent expression of cd18 on the surface of leukocytes which impairs their ability to migrate and interact with antigens. initial clinical signs include omphalitis and delayed separation of the umbilical cord. the clinical course is marked by recurrent bacterial and fungal infection without pus formation. in instances where there is < 1% expression of cd18, prognosis is dismal with a high likelihood for life-threatening infection within the first year of life.

• Leukocyte Adhesion Deficiency Type 2|CDGIIc|Congenital Disorder of Glycosylation Type IIc|LAD-Type II|Sialyl-Lewis X Defect

  leukocyte adhesion deficiency, type ii. an inherited disease affecting the metabolism of fucose, which affects the expression of the sialyl lewis x antigen, the fucose-containing ligand for e- and p-selectins, resulting in a deficiency in neutrophil adhesion. syn sialyl-lewis x defect.

• Leukocyte Adhesion Deficiency Type 3|LAD-3|LAD-III

  an autosomal recessive condition caused by mutation(s) in the fermt3 gene, encoding fermitin family homolog 3. it is characterized by a defect in activation of all beta integrins. it manifests clinically as severe infections with marked leukocytosis, accompanied by life-threatening bleeding episodes.

D72.89 is grouped with Diagnostic Related Groups - MS-DRG Mapping

Diagnostic Related Groups (DRGs) are a classification system used to group together diagnosis codes for the purpose of reimbursement and healthcare management. DRGs are used to standardize the way hospitals and other providers are paid for inpatient services. In this system patients are grouped together based on their principal diagnosis in areas referred to as Major Diagnostic Categories (MDC). Once a patient is assigned a particular diagnostic category, providers receive a predetermined payment rate for the services rendered. This reimbursement rate is often fixed and is meant to cover the cost of care for that patient. Reimbursement is also affected by the relative weight of a diagnostic related group based on the severity of a patient's illness and the associated cost of care during hospitalization.

Diagnostic related groups encourage healthcare providers to focus on quality and efficiency in patient care while managing costs effectively. The diagnosis code is present in the following groups for version MS-DRG V41.0 applicable from 10/01/2023 through 09/30/2024.

The relative weight of a diagnostic related group determines the reimbursement rate based on the severity of a patient's illness and the associated cost of care during hospitalization.

Convert D72.89 to ICD-9-CM

• ICD-9-CM Code: 288.8 - Wbc disease NEC

Patient Education

Blood Disorders

Your blood is living tissue made up of liquid and solids. The liquid part, called plasma, is made of water, salts and protein. Over half of your blood is plasma. The solid part of your blood contains red blood cells, white blood cells and platelets.

Blood disorders affect one or more parts of the blood and prevent your blood from doing its job. They can be acute or chronic. Many blood disorders are inherited. Other causes include other diseases, side effects of medicines, and a lack of certain nutrients in your diet.

Types of blood disorders include:

• Platelet disorders, excessive clotting, and bleeding problems, which affect how your blood clots
• Anemia, which happens when your blood does not carry enough oxygen to the rest of your body
• Cancers of the blood, such as leukemia and myeloma
• Eosinophilic disorders, which are problems with one type of white blood cell.

Code History

• FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
• FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
• FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
• FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
• FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
• FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
• FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
• FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
• FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.