Other disorders of white blood cells (D72)
ICD-10 Index
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
Other disorders of blood and blood-forming organs (D70-D77)
- D72 - Other disorders of white blood cells NON-BILLABLE CODE
- D72.0 - Genetic anomalies of leukocytes BILLABLE CODE
- D72.1 - Eosinophilia NON-BILLABLE CODE
- D72.10 - Eosinophilia, unspecified BILLABLE CODE
- D72.11 - Hypereosinophilic syndrome [HES] NON-BILLABLE CODE
- D72.110 - Idiopathic hypereosinophilic syndrome [IHES] BILLABLE CODE
- D72.111 - Lymphocytic Variant Hypereosinophilic Syndrome [LHES] BILLABLE CODE
- D72.118 - Other hypereosinophilic syndrome BILLABLE CODE
- D72.119 - Hypereosinophilic syndrome [HES], unspecified BILLABLE CODE
- D72.12 - Drug rash with eosinophilia and systemic symptoms syndrome BILLABLE CODE
- D72.18 - Eosinophilia in diseases classified elsewhere BILLABLE CODE
- D72.19 - Other eosinophilia BILLABLE CODE
- D72.8 - Other specified disorders of white blood cells NON-BILLABLE CODE
- D72.81 - Decreased white blood cell count NON-BILLABLE CODE
- D72.810 - Lymphocytopenia BILLABLE CODE
- D72.818 - Other decreased white blood cell count BILLABLE CODE
- D72.819 - Decreased white blood cell count, unspecified BILLABLE CODE
- D72.82 - Elevated white blood cell count NON-BILLABLE CODE
- D72.820 - Lymphocytosis (symptomatic) BILLABLE CODE
- D72.821 - Monocytosis (symptomatic) BILLABLE CODE
- D72.822 - Plasmacytosis BILLABLE CODE
- D72.823 - Leukemoid reaction BILLABLE CODE
- D72.824 - Basophilia BILLABLE CODE
- D72.825 - Bandemia BILLABLE CODE
- D72.828 - Other elevated white blood cell count BILLABLE CODE
- D72.829 - Elevated white blood cell count, unspecified BILLABLE CODE
- D72.89 - Other specified disorders of white blood cells BILLABLE CODE
- D72.9 - Disorder of white blood cells, unspecified BILLABLE CODE
Other disorders of white blood cells (D72)
Clinical Information for Other disorders of white blood cells (D72)
Hypereosinophilic Syndrome - A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs.
Leukemia, Large Granular Lymphocytic - A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease.
Lymphocytosis - Excess of normal lymphocytes in the blood or in any effusion.
Lymphohistiocytosis, Hemophagocytic - A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive.
Pertussis Toxin - One of the virulence factors produced by BORDETELLA PERTUSSIS. It is a multimeric protein composed of five subunits S1 - S5. S1 contains mono ADPribose transferase activity.
Virulence Factors, Bordetella - A set of BACTERIAL ADHESINS and TOXINS, BIOLOGICAL produced by BORDETELLA organisms that determine the pathogenesis of BORDETELLA INFECTIONS, such as WHOOPING COUGH. They include filamentous hemagglutinin; FIMBRIAE PROTEINS; pertactin; PERTUSSIS TOXIN; ADENYLATE CYCLASE TOXIN; dermonecrotic toxin; tracheal cytotoxin; Bordetella LIPOPOLYSACCHARIDES; and tracheal colonization factor.
Eosinophilia - Abnormal increase of EOSINOPHILS in the blood, tissues or organs.
Eosinophilia-Myalgia Syndrome - A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
Pulmonary Eosinophilia - A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents.
Leukemoid Reaction - A peripheral blood picture resembling that of leukemia or indistinguishable from it on the basis of morphologic appearance alone. (Dorland, 27th ed)
Eosinophilia - Abnormal increase of EOSINOPHILS in the blood, tissues or organs.
Eosinophilia-Myalgia Syndrome - A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
Pulmonary Eosinophilia - A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents.
Pulmonary Eosinophilia - A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents.
Eosinophilia - Abnormal increase of EOSINOPHILS in the blood, tissues or organs.
Eosinophilia-Myalgia Syndrome - A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
Hypereosinophilic Syndrome - A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs.
Hypereosinophilic Syndrome - A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs.
Leukopenia - A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000).
Hypereosinophilic Syndrome - A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs.
Hodgkin Disease - A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen.
Lymphocyte Depletion - Immunosuppression by reduction of circulating lymphocytes or by T-cell depletion of bone marrow. The former may be accomplished in vivo by thoracic duct drainage or administration of antilymphocyte serum. The latter is performed ex vivo on bone marrow before its transplantation.
Leukocytosis - A transient increase in the number of leukocytes in a body fluid.
Virulence Factors, Bordetella - A set of BACTERIAL ADHESINS and TOXINS, BIOLOGICAL produced by BORDETELLA organisms that determine the pathogenesis of BORDETELLA INFECTIONS, such as WHOOPING COUGH. They include filamentous hemagglutinin; FIMBRIAE PROTEINS; pertactin; PERTUSSIS TOXIN; ADENYLATE CYCLASE TOXIN; dermonecrotic toxin; tracheal cytotoxin; Bordetella LIPOPOLYSACCHARIDES; and tracheal colonization factor.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Bordetella pertussis - A species of gram-negative, aerobic bacteria that is the causative agent of WHOOPING COUGH. Its cells are minute coccobacilli that are surrounded by a slime sheath.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Reed-Sternberg Cells - Large cells, usually multinucleate, whose presence is a common histologic characteristic of classical HODGKIN DISEASE.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Eosinophils - Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.