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ALL MEDICAL CODES IN CATEGORY Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

2025 ICD-10-CM code D59.31

Infection-associated hemolytic-uremic syndrome. This condition is characterized by the destruction of red blood cells, low platelet count, and kidney failure, typically associated with an infection.

2025 ICD-10-CM code D59.3

Hemolytic-uremic syndrome (HUS)

2025 ICD-10-CM code D68.0

Von Willebrand disease. This is a bleeding disorder characterized by a deficiency or dysfunction of von Willebrand factor (VWF), a protein crucial for blood clotting.

2025 ICD-10-CM code D75.84

Other platelet-activating anti-PF4 disorders.

2025 ICD-10-CM code D55.0

Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency.

2025 ICD-10-CM code D72.829

Elevated white blood cell count, unspecified.This condition signifies an increase in white blood cells without specifying the type of white blood cell affected.

2025 ICD-10-CM code D81.31

Severe combined immunodeficiency due to adenosine deaminase deficiency.

2025 ICD-10-CM code D61.01

Constitutional (pure) red blood cell aplasia, also known as Blackfan-Diamond anemia.

2025 ICD-10-CM code D72.118

Other hypereosinophilic syndrome. This includes episodic angioedema with eosinophilia (Gleich's syndrome).

2025 ICD-10-CM code D70.8

Other neutropenia. This code represents neutropenia not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code D58.0

Hereditary spherocytosis, a genetic blood disorder causing abnormal, sphere-shaped red blood cells and hemolytic anemia.

2025 ICD-10-CM code D69

Purpura and other hemorrhagic conditions.This code excludes conditions such as benign hypergammaglobulinemic purpura (D89.0), cryoglobulinemic purpura (D89.1), essential (hemorrhagic) thrombocythemia (D47.3), purpura fulminans (D65), thrombotic thrombocytopenic purpura (M31.19), and Waldenström hypergammaglobulinemic purpura (D89.0).

2025 ICD-10-CM code D86.0

Sarcoidosis of lung.

2025 ICD-10-CM code D89.81

Graft-versus-host disease. Code first the underlying cause, such as complications of transplanted organs and tissues (T86.-) or complications of blood transfusion (T80.89).

2025 ICD-10-CM code D57.44

Sickle-cell thalassemia beta plus without crisis.This condition combines sickle cell trait with beta-plus thalassemia, resulting in mild to moderate anemia but without a painful crisis.

2025 ICD-10-CM code D72.119

Hypereosinophilic syndrome [HES], unspecified.

2025 ICD-10-CM code D86.89

Sarcoidosis of other sites.This includes hepatic granuloma and uveoparotid fever [Heerfordt].

2025 ICD-10-CM code D57.413

Sickle-cell thalassemia, unspecified, with cerebral vascular involvement.

2025 ICD-10-CM code D70.2

Drug-induced agranulocytosis not otherwise specified.

2025 ICD-10-CM code D61.3

Idiopathic aplastic anemia. This is a rare blood disorder where the bone marrow doesn't produce enough blood cells.

2025 ICD-10-CM code D57.0

Hb-SS disease with crisis; Sickle cell disease with crisis.

2025 ICD-10-CM code D64.2

Secondary sideroblastic anemia due to drugs and toxins.

2025 ICD-10-CM code D73

Diseases of the spleen.

2025 ICD-10-CM code D64.8

Anemia characterized by a decrease in red blood cell count, leading to reduced oxygen supply to body tissues, not classified elsewhere.

2025 ICD-10-CM code D89.4

Mast cell activation syndrome and related disorders. This condition involves the inappropriate and excessive release of chemical mediators by mast cells, leading to a range of chronic symptoms.

2025 ICD-10-CM code D57.431

Sickle-cell thalassemia beta zero with acute chest syndrome.

2025 ICD-10-CM code D80.4

Selective deficiency of immunoglobulin M (IgM).

2025 ICD-10-CM code D76

Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue.

2025 ICD-10-CM code D55.29

Anemia due to other disorders of glycolytic enzymes. This includes hexokinase deficiency anemia and triose-phosphate isomerase deficiency anemia.

2025 ICD-10-CM code D57.819

A genetic blood disorder characterized by sickle-shaped red blood cells, leading to anemia and painful crises.This specific code indicates the presence of a crisis not otherwise specified (e.g., acute chest syndrome or splenic sequestration).

2025 ICD-10-CM code D51.9

Vitamin B12 deficiency anemia, unspecified.

2025 ICD-10-CM code D89.1

Cryoglobulinemia is a condition characterized by the presence of cryoglobulins in the blood.

2025 ICD-10-CM code D53.0

Protein deficiency anemia resulting from inadequate hemoglobin formation due to lack of dietary protein.

2025 ICD-10-CM code D53.8

A nutritional anemia not otherwise specified. Examples include anemia associated with copper, molybdenum, or zinc deficiency.

2025 ICD-10-CM code D75.821

Non-immune heparin-induced thrombocytopenia (Type 1).

2025 ICD-10-CM code D68.01

Von Willebrand disease, type 1. Partial quantitative deficiency of von Willebrand factor. Type 1C von Willebrand disease.

2025 ICD-10-CM code D68.1

Hereditary factor XI deficiency, also known as hemophilia C or Rosenthal's disease.It is a genetic bleeding disorder caused by a deficiency of factor XI, a protein that helps blood clot.

2025 ICD-10-CM code D57.41

Sickle-cell thalassemia with crisis. This is a type of sickle cell disease where a person inherits a sickle cell gene and a beta thalassemia gene, leading to abnormal red blood cells that can cause painful vaso-occlusive crises.

2025 ICD-10-CM code D81.810

Biotinidase deficiency is an inherited disorder that affects the body's ability to recycle biotin.

2025 ICD-10-CM code D68.51

Activated protein C resistance due to Factor V Leiden mutation.

2025 ICD-10-CM code D72.820

Symptomatic lymphocytosis is an elevated lymphocyte count in the bloodstream that presents with symptoms.

2025 ICD-10-CM code D78.2

Postprocedural hemorrhage of the spleen following a procedure.

2025 ICD-10-CM code D81.5

Purine nucleoside phosphorylase (PNP) deficiency is a rare inherited disorder affecting the immune system.

2025 ICD-10-CM code D74

Methemoglobinemia is a blood disorder characterized by an elevated level of methemoglobin, a form of hemoglobin that cannot effectively carry oxygen.

2025 ICD-10-CM code D52

Folate deficiency anemia

2025 ICD-10-CM code D74.8

Other methemoglobinemias

2025 ICD-10-CM code D56.2

Delta-beta thalassemia, also known as homozygous delta-beta thalassemia, is a rare blood disorder characterized by reduced or absent production of delta and beta globin chains.

2025 ICD-10-CM code D70

Neutropenia. A condition characterized by abnormally low levels of neutrophils in the blood.

2025 ICD-10-CM code D60

Acquired pure red cell aplasia (PRCA), also known as erythroblastopenia, is a rare form of anemia characterized by a significant decrease or absence of red blood cell production in the bone marrow, while white blood cell and platelet counts remain normal.

2025 ICD-10-CM code D57.418

Sickle-cell thalassemia, unspecified, with crisis with other specified complication.