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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 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 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 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 D84.822
Immunodeficiency due to external causes.
2025 ICD-10-CM code D68.021
Von Willebrand disease, type 2B. This type involves qualitative defects of von Willebrand factor with high-molecular-weight von Willebrand factor loss, hyper-adhesive forms, and increased affinity for platelet glycoprotein l.
2025 ICD-10-CM code D68.2
Hereditary deficiency of other clotting factors. This includes deficiencies of factors I, II, V, VII, X, XI, XII, and XIII.
2025 ICD-10-CM code D53.2
Scorbutic anemia. This condition is characterized by the inadequate formation of hemoglobin due to severe vitamin C deficiency, which impairs iron absorption and reduces the production of healthy red blood cells.
2025 ICD-10-CM code D81.2
Severe combined immunodeficiency (SCID) with low or normal B-cell numbers is a type of SCID where T cells are absent, and B and/or NK cell counts can be low, none, high, or normal.B cells, even if present, are non-functional due to the absence of T cells.
2025 ICD-10-CM code D72.11
Hypereosinophilic syndrome [HES].
2025 ICD-10-CM code D78.32
Postprocedural hematoma of the spleen following a procedure other than on the spleen.
2025 ICD-10-CM code D75.838
Other thrombocytosis. This includes reactive and secondary thrombocytosis.
2025 ICD-10-CM code D68.9
Unspecified coagulation defect. This code is used when the specific type of coagulation defect is not documented.
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 D57.43
Sickle-cell thalassemia beta zero with crisis.
2025 ICD-10-CM code D81.32
Adenosine deaminase 2 deficiency.
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.
2025 ICD-10-CM code D72.9
Disorder of white blood cells, unspecified. Abnormal leukocyte differential NOS.
2025 ICD-10-CM code D57.812
A genetic blood disorder causing hard, sticky, C-shaped red blood cells, leading to anemia and rapid-onset complications in the spleen.Deformed red blood cells accumulate in the spleen, causing enlargement.
2025 ICD-10-CM code D78
Intraoperative and postprocedural complications of the spleen.
2025 ICD-10-CM code D52.1
Drug-induced folate deficiency anemia. Use additional code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5).
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