Start New EnglishEspañol中文РусскийالعربيةTiếng ViệtFrançaisDeutsch한국어Tagalog Library Performance
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 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 D75.84

Other platelet-activating anti-PF4 disorders.

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 D55.0

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

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 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 D81.31

Severe combined immunodeficiency due to adenosine deaminase deficiency.

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 D61.01

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

2025 ICD-10-CM code D89.811

Chronic graft-versus-host disease. This condition is an immune disorder characterized by a recipient’s abnormal response to a donor organ, bone marrow, or stem cells that persists over time or occurs post-acute GVHD.

2025 ICD-10-CM code D72.118

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

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 D89.833

Cytokine release syndrome, grade 3. This is an acute systemic inflammatory syndrome characterized by fever and multiple organ dysfunction.

2025 ICD-10-CM code D86.89

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

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 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 D57.413

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

2025 ICD-10-CM code D57.0

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

2025 ICD-10-CM code D59.4

Other nonautoimmune hemolytic anemias encompass various types of anemia where red blood cell destruction exceeds production, caused by mechanical, microangiopathic, or toxic factors.

2025 ICD-10-CM code D56.0

Alpha thalassemia encompasses various forms, including alpha thalassemia major, hemoglobin H disease, and hemoglobin H Constant Spring.It's characterized by a reduction in alpha-globin chains, leading to anemia.

2025 ICD-10-CM code D89.43

Secondary mast cell activation.This condition involves the improper activation of mast cells, leading to an excessive allergic response due to an underlying disease.

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 D89.3

Immune reconstitution syndrome.A condition where the immune system, after being suppressed (e.g., by HIV), rebounds excessively when treatment begins, causing an inflammatory response against infections or the body's own tissues.

2025 ICD-10-CM code D82.0

Wiskott-Aldrich syndrome, a rare X-linked recessive genetic disorder characterized by immunodeficiency, eczema, and thrombocytopenia (low platelet count).

2025 ICD-10-CM code D81.818

Other biotin-dependent carboxylase deficiency. This includes holocarboxylase synthetase deficiency and other multiple carboxylase deficiencies.

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 D57.431

Sickle-cell thalassemia beta zero with acute chest syndrome.

2025 ICD-10-CM code D57.81

Other sickle-cell disorders with crisis.

2025 ICD-10-CM code D78.11

Accidental puncture and laceration of the spleen during a procedure on the spleen.

2025 ICD-10-CM code D64.81

Anemia due to antineoplastic chemotherapy.

2025 ICD-10-CM code D68.4

Acquired coagulation factor deficiency. This condition involves a deficiency in proteins necessary for blood clot formation, often developing later in life.

2025 ICD-10-CM code D59.8

A type of anemia caused by the destruction of red blood cells faster than they are produced in the bone marrow.

2025 ICD-10-CM code D81.30

Adenosine deaminase deficiency, unspecified. This condition involves a deficiency in the enzyme adenosine deaminase.

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 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 D83.2

Common variable immunodeficiency (CVID) with autoantibodies to B- or T-cells.

2025 ICD-10-CM code D84.822

Immunodeficiency due to external causes.

2025 ICD-10-CM code D68.3

Hemorrhagic disorder due to circulating anticoagulants. This is a bleeding disorder caused by an abnormal production of anticoagulants in the blood.

2025 ICD-10-CM code D57.211

Sickle-cell/Hb-C disease with acute chest syndrome. This is a genetic blood disorder where red blood cells become hard, sticky, and C-shaped, leading to anemia and acute chest syndrome.

2025 ICD-10-CM code D64.89

Other specified anemias. This code is used for anemias not otherwise specified in the ICD-10-CM.