2025 ICD-10 CM DIAGNOSIS INDEX TERMS STARTING WITH D
- Lymphocytosis (symptomatic) - D72.820
- Monocytosis (symptomatic) - D72.821
- Plasmacytosis - D72.822
- Leukemoid reaction - D72.823
- Basophilia - D72.824
- Bandemia - D72.825
- Other elevated white blood cell count - D72.828
- Elevated white blood cell count, unspecified - D72.829
- Other specified disorders of white blood cells - D72.89
- Disorder of white blood cells, unspecified - D72.9
- Hyposplenism - D73.0
- Hypersplenism - D73.1
- Chronic congestive splenomegaly - D73.2
- Abscess of spleen - D73.3
- Cyst of spleen - D73.4
- Infarction of spleen - D73.5
- Other diseases of spleen - D73.8
- Neutropenic splenomegaly - D73.81
- Other diseases of spleen - D73.89
- Disease of spleen, unspecified - D73.9
- Congenital methemoglobinemia - D74.0
- Other methemoglobinemias - D74.8
- Methemoglobinemia, unspecified - D74.9
- Familial erythrocytosis - D75.0
- Secondary polycythemia - D75.1
- Other specified diseases of blood and blood-forming organs - D75.8
- Myelofibrosis - D75.81
- Heparin induced thrombocytopenia (HIT) - D75.82
- Non-immune heparin-induced thrombocytopenia - D75.821
- Immune-mediated heparin-induced thrombocytopenia - D75.822
- Other heparin-induced thrombocytopenia syndrome - D75.828
- Heparin-induced thrombocytopenia, unspecified - D75.829
- Thrombocytosis - D75.83
- Other thrombocytosis - D75.838
- Thrombocytosis, unspecified - D75.839
- Other platelet-activating anti-PF4 disorders - D75.84
- Other specified diseases of blood and blood-forming organs - D75.89
- Disease of blood and blood-forming organs, unspecified - D75.9
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia - D75.A
- Hemophagocytic lymphohistiocytosis - D76.1
- Hemophagocytic syndrome, infection-associated - D76.2
- Other histiocytosis syndromes - D76.3
- Intraoperative hemorrhage and hematoma of the spleen complicating a procedure - D78.0
- Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen - D78.01
- Intraoperative hemorrhage and hematoma of the spleen complicating other procedure - D78.02
- Accidental puncture and laceration of the spleen during a procedure - D78.1
- Accidental puncture and laceration of the spleen during a procedure on the spleen - D78.11
- Accidental puncture and laceration of the spleen during other procedure - D78.12
- Postprocedural hemorrhage of the spleen following a procedure - D78.2
- Postprocedural hemorrhage of the spleen following a procedure on the spleen - D78.21
- Postprocedural hemorrhage of the spleen following other procedure - D78.22
- Postprocedural hematoma and seroma of the spleen following a procedure - D78.3
- Postprocedural hematoma of the spleen following a procedure on the spleen - D78.31
- Postprocedural hematoma of the spleen following other procedure - D78.32
- Postprocedural seroma of the spleen following a procedure on the spleen - D78.33
- Postprocedural seroma of the spleen following other procedure - D78.34
- Other intraoperative and postprocedural complications of the spleen - D78.8
- Other intraoperative complications of the spleen - D78.81
- Other postprocedural complications of the spleen - D78.89
- Hereditary hypogammaglobulinemia - D80.0
- Nonfamilial hypogammaglobulinemia - D80.1
- Selective deficiency of immunoglobulin A [IgA] - D80.2
- Selective deficiency of immunoglobulin G [IgG] subclasses - D80.3
- Selective deficiency of immunoglobulin M [IgM] - D80.4
- Immunodeficiency with increased immunoglobulin M [IgM] - D80.5
- Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia - D80.6
- Transient hypogammaglobulinemia of infancy - D80.7
- Other immunodeficiencies with predominantly antibody defects - D80.8
- Immunodeficiency with predominantly antibody defects, unspecified - D80.9
- Severe combined immunodeficiency [SCID] with reticular dysgenesis - D81.0
- Severe combined immunodeficiency [SCID] with low T- and B-cell numbers - D81.1
- Severe combined immunodeficiency [SCID] with low or normal B-cell numbers - D81.2
- Adenosine deaminase [ADA] deficiency - D81.3
- Adenosine deaminase deficiency, unspecified - D81.30
- Severe combined immunodeficiency due to adenosine deaminase deficiency - D81.31
- Adenosine deaminase 2 deficiency - D81.32
- Other adenosine deaminase deficiency - D81.39
- Nezelof's syndrome - D81.4
- Purine nucleoside phosphorylase [PNP] deficiency - D81.5
- Major histocompatibility complex class I deficiency - D81.6
- Major histocompatibility complex class II deficiency - D81.7
- Other combined immunodeficiencies - D81.8
- Biotin-dependent carboxylase deficiency - D81.81
- Biotinidase deficiency - D81.810
- Other biotin-dependent carboxylase deficiency - D81.818
- Biotin-dependent carboxylase deficiency, unspecified - D81.819
- Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] - D81.82
- Other combined immunodeficiencies - D81.89
- Combined immunodeficiency, unspecified - D81.9
- Wiskott-Aldrich syndrome - D82.0
- Di George's syndrome - D82.1
- Immunodeficiency with short-limbed stature - D82.2
- Immunodeficiency following hereditary defective response to Epstein-Barr virus - D82.3
- Hyperimmunoglobulin E [IgE] syndrome - D82.4
- Immunodeficiency associated with other specified major defects - D82.8
- Immunodeficiency associated with major defect, unspecified - D82.9
- Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function - D83.0
- Common variable immunodeficiency with predominant immunoregulatory T-cell disorders - D83.1
- Common variable immunodeficiency with autoantibodies to B- or T-cells - D83.2
- Other common variable immunodeficiencies - D83.8