Billable/Specific ICD-10-CM Codes - Page 30

There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.

  • D69.51 - Posttransfusion purpura
  • D69.59 - Other secondary thrombocytopenia
  • D69.6 - Thrombocytopenia, unspecified
  • D69.8 - Other specified hemorrhagic conditions
  • D69.9 - Hemorrhagic condition, unspecified
  • D70.0 - Congenital agranulocytosis
  • D70.1 - Agranulocytosis secondary to cancer chemotherapy
  • D70.2 - Other drug-induced agranulocytosis
  • D70.3 - Neutropenia due to infection
  • D70.4 - Cyclic neutropenia
  • D70.8 - Other neutropenia
  • D70.9 - Neutropenia, unspecified
  • D72.0 - Genetic anomalies of leukocytes
  • D72.10 - Eosinophilia, unspecified
  • D72.110 - Idiopathic hypereosinophilic syndrome [IHES]
  • D72.111 - Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
  • D72.118 - Other hypereosinophilic syndrome
  • D72.119 - Hypereosinophilic syndrome [HES], unspecified
  • D72.12 - Drug rash with eosinophilia and systemic symptoms syndrome
  • D72.18 - Eosinophilia in diseases classified elsewhere
  • D72.19 - Other eosinophilia
  • D72.810 - Lymphocytopenia
  • D72.818 - Other decreased white blood cell count
  • D72.819 - Decreased white blood cell count, unspecified
  • D72.820 - Lymphocytosis (symptomatic)
  • D72.821 - Monocytosis (symptomatic)
  • D72.822 - Plasmacytosis
  • D72.823 - Leukemoid reaction
  • D72.824 - Basophilia
  • D72.825 - Bandemia
  • D72.828 - Other elevated white blood cell count
  • D72.829 - Elevated white blood cell count, unspecified
  • D72.89 - Other specified disorders of white blood cells
  • D72.9 - Disorder of white blood cells, unspecified
  • D73.0 - Hyposplenism
  • D73.1 - Hypersplenism
  • D73.2 - Chronic congestive splenomegaly
  • D73.3 - Abscess of spleen
  • D73.4 - Cyst of spleen
  • D73.5 - Infarction of spleen
  • D73.81 - Neutropenic splenomegaly
  • D73.89 - Other diseases of spleen
  • D73.9 - Disease of spleen, unspecified
  • D74.0 - Congenital methemoglobinemia
  • D74.8 - Other methemoglobinemias
  • D74.9 - Methemoglobinemia, unspecified
  • D75.0 - Familial erythrocytosis
  • D75.1 - Secondary polycythemia
  • D75.81 - Myelofibrosis
  • D75.821 - Non-immune heparin-induced thrombocytopenia
  • D75.822 - Immune-mediated heparin-induced thrombocytopenia
  • D75.828 - Other heparin-induced thrombocytopenia syndrome
  • D75.829 - Heparin-induced thrombocytopenia, unspecified
  • D75.838 - Other thrombocytosis
  • D75.839 - Thrombocytosis, unspecified
  • D75.84 - Other platelet-activating anti-PF4 disorders
  • D75.89 - Other specified diseases of blood and blood-forming organs
  • D75.9 - Disease of blood and blood-forming organs, unspecified
  • D75.A - Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
  • D76.1 - Hemophagocytic lymphohistiocytosis
  • D76.2 - Hemophagocytic syndrome, infection-associated
  • D76.3 - Other histiocytosis syndromes
  • D78.01 - Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
  • D78.02 - Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
  • D78.11 - Accidental puncture and laceration of the spleen during a procedure on the spleen
  • D78.12 - Accidental puncture and laceration of the spleen during other procedure
  • D78.21 - Postprocedural hemorrhage of the spleen following a procedure on the spleen
  • D78.22 - Postprocedural hemorrhage of the spleen following other procedure
  • D78.31 - Postprocedural hematoma of the spleen following a procedure on the spleen
  • D78.32 - Postprocedural hematoma of the spleen following other procedure
  • D78.33 - Postprocedural seroma of the spleen following a procedure on the spleen
  • D78.34 - Postprocedural seroma of the spleen following other procedure
  • D78.81 - Other intraoperative complications of the spleen
  • D78.89 - Other postprocedural complications of the spleen
  • D80.0 - Hereditary hypogammaglobulinemia
  • D80.1 - Nonfamilial hypogammaglobulinemia
  • D80.2 - Selective deficiency of immunoglobulin A [IgA]
  • D80.3 - Selective deficiency of immunoglobulin G [IgG] subclasses
  • D80.4 - Selective deficiency of immunoglobulin M [IgM]
  • D80.5 - Immunodeficiency with increased immunoglobulin M [IgM]
  • D80.6 - Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
  • D80.7 - Transient hypogammaglobulinemia of infancy
  • D80.8 - Other immunodeficiencies with predominantly antibody defects
  • D80.9 - Immunodeficiency with predominantly antibody defects, unspecified
  • D81.0 - Severe combined immunodeficiency [SCID] with reticular dysgenesis
  • D81.1 - Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
  • D81.2 - Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
  • D81.30 - Adenosine deaminase deficiency, unspecified
  • D81.31 - Severe combined immunodeficiency due to adenosine deaminase deficiency
  • D81.32 - Adenosine deaminase 2 deficiency
  • D81.39 - Other adenosine deaminase deficiency
  • D81.4 - Nezelof's syndrome
  • D81.5 - Purine nucleoside phosphorylase [PNP] deficiency
  • D81.6 - Major histocompatibility complex class I deficiency
  • D81.7 - Major histocompatibility complex class II deficiency
  • D81.810 - Biotinidase deficiency
  • D81.818 - Other biotin-dependent carboxylase deficiency
  • D81.819 - Biotin-dependent carboxylase deficiency, unspecified
  • D81.82 - Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
  • D81.89 - Other combined immunodeficiencies