Billable / specific codes

Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

• D50.0Iron deficiency anemia secondary to blood loss (chronic)
• D50.1Sideropenic dysphagia
• D50.8Other iron deficiency anemias
• D50.9Iron deficiency anemia, unspecified
• D51.0Vitamin B12 deficiency anemia due to intrinsic factor deficiency
• D51.1Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
• D51.2Transcobalamin II deficiency
• D51.3Other dietary vitamin B12 deficiency anemia
• D51.8Other vitamin B12 deficiency anemias
• D51.9Vitamin B12 deficiency anemia, unspecified
• D52.0Dietary folate deficiency anemia
• D52.1Drug-induced folate deficiency anemia
• D52.8Other folate deficiency anemias
• D52.9Folate deficiency anemia, unspecified
• D53.0Protein deficiency anemia
• D53.1Other megaloblastic anemias, not elsewhere classified
• D53.2Scorbutic anemia
• D53.8Other specified nutritional anemias
• D53.9Nutritional anemia, unspecified
• D55.0Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
• D55.1Anemia due to other disorders of glutathione metabolism
• D55.21Anemia due to pyruvate kinase deficiency
• D55.29Anemia due to other disorders of glycolytic enzymes
• D55.3Anemia due to disorders of nucleotide metabolism
• D55.8Other anemias due to enzyme disorders
• D55.9Anemia due to enzyme disorder, unspecified
• D56.0Alpha thalassemia
• D56.1Beta thalassemia
• D56.2Delta-beta thalassemia
• D56.3Thalassemia minor
• D56.4Hereditary persistence of fetal hemoglobin [HPFH]
• D56.5Hemoglobin E-beta thalassemia
• D56.8Other thalassemias
• D56.9Thalassemia, unspecified
• D57.00Hb-SS disease with crisis, unspecified
• D57.01Hb-SS disease with acute chest syndrome
• D57.02Hb-SS disease with splenic sequestration
• D57.03Hb-SS disease with cerebral vascular involvement
• D57.04Hb-SS disease with dactylitis
• D57.09Hb-SS disease with crisis with other specified complication
• D57.1Sickle-cell disease without crisis
• D57.20Sickle-cell/Hb-C disease without crisis
• D57.211Sickle-cell/Hb-C disease with acute chest syndrome
• D57.212Sickle-cell/Hb-C disease with splenic sequestration
• D57.213Sickle-cell/Hb-C disease with cerebral vascular involvement
• D57.214Sickle-cell/Hb-C disease with dactylitis
• D57.218Sickle-cell/Hb-C disease with crisis with other specified complication
• D57.219Sickle-cell/Hb-C disease with crisis, unspecified
• D57.3Sickle-cell trait
• D57.40Sickle-cell thalassemia without crisis
• D57.411Sickle-cell thalassemia, unspecified, with acute chest syndrome
• D57.412Sickle-cell thalassemia, unspecified, with splenic sequestration
• D57.413Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
• D57.414Sickle-cell thalassemia, unspecified, with dactylitis
• D57.418Sickle-cell thalassemia, unspecified, with crisis with other specified complication
• D57.419Sickle-cell thalassemia, unspecified, with crisis
• D57.42Sickle-cell thalassemia beta zero without crisis
• D57.431Sickle-cell thalassemia beta zero with acute chest syndrome
• D57.432Sickle-cell thalassemia beta zero with splenic sequestration
• D57.433Sickle-cell thalassemia beta zero with cerebral vascular involvement
• D57.434Sickle-cell thalassemia beta zero with dactylitis
• D57.438Sickle-cell thalassemia beta zero with crisis with other specified complication
• D57.439Sickle-cell thalassemia beta zero with crisis, unspecified
• D57.44Sickle-cell thalassemia beta plus without crisis
• D57.451Sickle-cell thalassemia beta plus with acute chest syndrome
• D57.452Sickle-cell thalassemia beta plus with splenic sequestration
• D57.453Sickle-cell thalassemia beta plus with cerebral vascular involvement
• D57.454Sickle-cell thalassemia beta plus with dactylitis
• D57.458Sickle-cell thalassemia beta plus with crisis with other specified complication
• D57.459Sickle-cell thalassemia beta plus with crisis, unspecified
• D57.80Other sickle-cell disorders without crisis
• D57.811Other sickle-cell disorders with acute chest syndrome
• D57.812Other sickle-cell disorders with splenic sequestration
• D57.813Other sickle-cell disorders with cerebral vascular involvement
• D57.814Other sickle-cell disorders with dactylitis
• D57.818Other sickle-cell disorders with crisis with other specified complication
• D57.819Other sickle-cell disorders with crisis, unspecified
• D58.0Hereditary spherocytosis
• D58.1Hereditary elliptocytosis
• D58.2Other hemoglobinopathies
• D58.8Other specified hereditary hemolytic anemias
• D58.9Hereditary hemolytic anemia, unspecified
• D59.0Drug-induced autoimmune hemolytic anemia
• D59.10Autoimmune hemolytic anemia, unspecified
• D59.11Warm autoimmune hemolytic anemia
• D59.12Cold autoimmune hemolytic anemia
• D59.13Mixed type autoimmune hemolytic anemia
• D59.19Other autoimmune hemolytic anemia
• D59.2Drug-induced nonautoimmune hemolytic anemia
• D59.30Hemolytic-uremic syndrome, unspecified
• D59.31Infection-associated hemolytic-uremic syndrome
• D59.32Hereditary hemolytic-uremic syndrome
• D59.39Other hemolytic-uremic syndrome
• D59.4Other nonautoimmune hemolytic anemias
• D59.5Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
• D59.6Hemoglobinuria due to hemolysis from other external causes
• D59.8Other acquired hemolytic anemias
• D59.9Acquired hemolytic anemia, unspecified
• D60.0Chronic acquired pure red cell aplasia
• D60.1Transient acquired pure red cell aplasia
• D60.8Other acquired pure red cell aplasias
• D60.9Acquired pure red cell aplasia, unspecified
• D61.01Constitutional (pure) red blood cell aplasia
• D61.02Shwachman-Diamond syndrome
• D61.03Fanconi anemia
• D61.09Other constitutional aplastic anemia
• D61.1Drug-induced aplastic anemia
• D61.2Aplastic anemia due to other external agents
• D61.3Idiopathic aplastic anemia
• D61.810Antineoplastic chemotherapy induced pancytopenia
• D61.811Other drug-induced pancytopenia
• D61.818Other pancytopenia
• D61.82Myelophthisis
• D61.89Other specified aplastic anemias and other bone marrow failure syndromes
• D61.9Aplastic anemia, unspecified
• D62Acute posthemorrhagic anemia
• D63.0Anemia in neoplastic disease
• D63.1Anemia in chronic kidney disease
• D63.8Anemia in other chronic diseases classified elsewhere
• D64.0Hereditary sideroblastic anemia
• D64.1Secondary sideroblastic anemia due to disease
• D64.2Secondary sideroblastic anemia due to drugs and toxins
• D64.3Other sideroblastic anemias
• D64.4Congenital dyserythropoietic anemia
• D64.81Anemia due to antineoplastic chemotherapy
• D64.89Other specified anemias
• D64.9Anemia, unspecified
• D65Disseminated intravascular coagulation [defibrination syndrome]
• D66Hereditary factor VIII deficiency
• D67Hereditary factor IX deficiency
• D68.00Von Willebrand disease, unspecified
• D68.01Von Willebrand disease, type 1
• D68.020Von Willebrand disease, type 2A
• D68.021Von Willebrand disease, type 2B
• D68.022Von Willebrand disease, type 2M
• D68.023Von Willebrand disease, type 2N
• D68.029Von Willebrand disease, type 2, unspecified
• D68.03Von Willebrand disease, type 3
• D68.04Acquired von Willebrand disease
• D68.09Other von Willebrand disease
• D68.1Hereditary factor XI deficiency
• D68.2Hereditary deficiency of other clotting factors
• D68.311Acquired hemophilia
• D68.312Antiphospholipid antibody with hemorrhagic disorder
• D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
• D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulants
• D68.4Acquired coagulation factor deficiency
• D68.51Activated protein C resistance
• D68.52Prothrombin gene mutation
• D68.59Other primary thrombophilia
• D68.61Antiphospholipid syndrome
• D68.62Lupus anticoagulant syndrome
• D68.69Other thrombophilia
• D68.8Other specified coagulation defects
• D68.9Coagulation defect, unspecified
• D69.0Allergic purpura
• D69.11Glanzmann thrombasthenia
• D69.19Other qualitative platelet defects
• D69.2Other nonthrombocytopenic purpura
• D69.3Immune thrombocytopenic purpura
• D69.41Evans syndrome
• D69.42Congenital and hereditary thrombocytopenia purpura
• D69.49Other primary thrombocytopenia
• D69.51Posttransfusion purpura
• D69.59Other secondary thrombocytopenia
• D69.6Thrombocytopenia, unspecified
• D69.8Other specified hemorrhagic conditions
• D69.9Hemorrhagic condition, unspecified
• D70.0Congenital agranulocytosis
• D70.1Agranulocytosis secondary to cancer chemotherapy
• D70.2Other drug-induced agranulocytosis
• D70.3Neutropenia due to infection
• D70.4Cyclic neutropenia
• D70.8Other neutropenia
• D70.9Neutropenia, unspecified
• D71.1Leukocyte adhesion deficiency
• D71.8Other functional disorders of polymorphonuclear neutrophils
• D71.9Functional disorders of polymorphonuclear neutrophils, unspecified
• D72.0Genetic anomalies of leukocytes
• D72.10Eosinophilia, unspecified
• D72.110Idiopathic hypereosinophilic syndrome [IHES]
• D72.111Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
• D72.118Other hypereosinophilic syndrome
• D72.119Hypereosinophilic syndrome [HES], unspecified
• D72.12Drug rash with eosinophilia and systemic symptoms syndrome
• D72.18Eosinophilia in diseases classified elsewhere
• D72.19Other eosinophilia
• D72.810Lymphocytopenia
• D72.818Other decreased white blood cell count
• D72.819Decreased white blood cell count, unspecified
• D72.820Lymphocytosis (symptomatic)
• D72.821Monocytosis (symptomatic)
• D72.822Plasmacytosis
• D72.823Leukemoid reaction
• D72.824Basophilia
• D72.825Bandemia
• D72.828Other elevated white blood cell count
• D72.829Elevated white blood cell count, unspecified
• D72.89Other specified disorders of white blood cells
• D72.9Disorder of white blood cells, unspecified
• D73.0Hyposplenism
• D73.1Hypersplenism
• D73.2Chronic congestive splenomegaly
• D73.3Abscess of spleen
• D73.4Cyst of spleen
• D73.5Infarction of spleen
• D73.81Neutropenic splenomegaly
• D73.89Other diseases of spleen
• D73.9Disease of spleen, unspecified
• D74.0Congenital methemoglobinemia
• D74.8Other methemoglobinemias
• D74.9Methemoglobinemia, unspecified
• D75.0Familial erythrocytosis
• D75.1Secondary polycythemia
• D75.81Myelofibrosis
• D75.821Non-immune heparin-induced thrombocytopenia
• D75.822Immune-mediated heparin-induced thrombocytopenia
• D75.828Other heparin-induced thrombocytopenia syndrome
• D75.829Heparin-induced thrombocytopenia, unspecified
• D75.838Other thrombocytosis
• D75.839Thrombocytosis, unspecified
• D75.84Other platelet-activating anti-PF4 disorders
• D75.89Other specified diseases of blood and blood-forming organs
• D75.9Disease of blood and blood-forming organs, unspecified
• D75.AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
• D76.1Hemophagocytic lymphohistiocytosis
• D76.2Hemophagocytic syndrome, infection-associated
• D76.3Other histiocytosis syndromes
• D77Other disorders of blood and blood-forming organs in diseases classified elsewhere
• D78.01Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
• D78.02Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
• D78.11Accidental puncture and laceration of the spleen during a procedure on the spleen
• D78.12Accidental puncture and laceration of the spleen during other procedure
• D78.21Postprocedural hemorrhage of the spleen following a procedure on the spleen
• D78.22Postprocedural hemorrhage of the spleen following other procedure
• D78.31Postprocedural hematoma of the spleen following a procedure on the spleen
• D78.32Postprocedural hematoma of the spleen following other procedure
• D78.33Postprocedural seroma of the spleen following a procedure on the spleen
• D78.34Postprocedural seroma of the spleen following other procedure
• D78.81Other intraoperative complications of the spleen
• D78.89Other postprocedural complications of the spleen
• D80.0Hereditary hypogammaglobulinemia
• D80.1Nonfamilial hypogammaglobulinemia
• D80.2Selective deficiency of immunoglobulin A [IgA]
• D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
• D80.4Selective deficiency of immunoglobulin M [IgM]
• D80.5Immunodeficiency with increased immunoglobulin M [IgM]
• D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
• D80.7Transient hypogammaglobulinemia of infancy
• D80.8Other immunodeficiencies with predominantly antibody defects
• D80.9Immunodeficiency with predominantly antibody defects, unspecified
• D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
• D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
• D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
• D81.30Adenosine deaminase deficiency, unspecified
• D81.31Severe combined immunodeficiency due to adenosine deaminase deficiency
• D81.32Adenosine deaminase 2 deficiency
• D81.39Other adenosine deaminase deficiency
• D81.4Nezelof's syndrome
• D81.5Purine nucleoside phosphorylase [PNP] deficiency
• D81.6Major histocompatibility complex class I deficiency
• D81.7Major histocompatibility complex class II deficiency
• D81.810Biotinidase deficiency
• D81.818Other biotin-dependent carboxylase deficiency
• D81.819Biotin-dependent carboxylase deficiency, unspecified
• D81.82Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
• D81.89Other combined immunodeficiencies
• D81.9Combined immunodeficiency, unspecified
• D82.0Wiskott-Aldrich syndrome
• D82.1Di George's syndrome
• D82.2Immunodeficiency with short-limbed stature
• D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
• D82.4Hyperimmunoglobulin E [IgE] syndrome
• D82.8Immunodeficiency associated with other specified major defects
• D82.9Immunodeficiency associated with major defect, unspecified
• D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
• D83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
• D83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
• D83.8Other common variable immunodeficiencies
• D83.9Common variable immunodeficiency, unspecified
• D84.0Lymphocyte function antigen-1 [LFA-1] defect
• D84.1Defects in the complement system
• D84.81Immunodeficiency due to conditions classified elsewhere
• D84.821Immunodeficiency due to drugs
• D84.822Immunodeficiency due to external causes
• D84.89Other immunodeficiencies
• D84.9Immunodeficiency, unspecified
• D86.0Sarcoidosis of lung
• D86.1Sarcoidosis of lymph nodes
• D86.2Sarcoidosis of lung with sarcoidosis of lymph nodes
• D86.3Sarcoidosis of skin
• D86.81Sarcoid meningitis
• D86.82Multiple cranial nerve palsies in sarcoidosis
• D86.83Sarcoid iridocyclitis
• D86.84Sarcoid pyelonephritis
• D86.85Sarcoid myocarditis
• D86.86Sarcoid arthropathy
• D86.87Sarcoid myositis
• D86.89Sarcoidosis of other sites
• D86.9Sarcoidosis, unspecified
• D89.0Polyclonal hypergammaglobulinemia
• D89.1Cryoglobulinemia
• D89.2Hypergammaglobulinemia, unspecified
• D89.3Immune reconstitution syndrome
• D89.40Mast cell activation, unspecified
• D89.41Monoclonal mast cell activation syndrome
• D89.42Idiopathic mast cell activation syndrome
• D89.43Secondary mast cell activation
• D89.44Hereditary alpha tryptasemia
• D89.49Other mast cell activation disorder
• D89.810Acute graft-versus-host disease
• D89.811Chronic graft-versus-host disease
• D89.812Acute on chronic graft-versus-host disease
• D89.813Graft-versus-host disease, unspecified
• D89.82Autoimmune lymphoproliferative syndrome [ALPS]
• D89.831Cytokine release syndrome, grade 1
• D89.832Cytokine release syndrome, grade 2
• D89.833Cytokine release syndrome, grade 3
• D89.834Cytokine release syndrome, grade 4
• D89.835Cytokine release syndrome, grade 5
• D89.839Cytokine release syndrome, grade unspecified
• D89.84IgG4-related disease
• D89.89Other specified disorders involving the immune mechanism, not elsewhere classified
• D89.9Disorder involving the immune mechanism, unspecified