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