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ALL MEDICAL CODES IN CATEGORY Hemolytic anemias

2025 ICD-10-CM code D59.3

Hemolytic-uremic syndrome (HUS)

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 D57.413

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

2025 ICD-10-CM code D57

Sickle cell disorders.Use additional code for any associated fever.

2025 ICD-10-CM code D57.0

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

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 D55.3

Anemia due to disorders of nucleotide metabolism. This condition involves a decrease in red blood cells due to disrupted nucleotide metabolism, often caused by a genetic enzyme deficiency.

2025 ICD-10-CM code D57.3

Sickle-cell trait (SCT) is a condition where a person inherits one sickle cell gene and one normal gene, leading to the formation of some hard, sticky, sickle-shaped red blood cells.

2025 ICD-10-CM code D57.09

Hb-SS disease with crisis with other specified complication. Use additional code to identify complications.

2025 ICD-10-CM code D57.42

Sickle-cell thalassemia beta zero without crisis.

2025 ICD-10-CM code D55.2

Anemia due to disorders of glycolytic enzymes. This condition involves a decrease in red blood cells due to dysfunctional glycolytic enzymes.

2025 ICD-10-CM code D57.459

Sickle-cell thalassemia beta plus with crisis, unspecified.

2025 ICD-10-CM code D57.439

Sickle-cell thalassemia beta zero with crisis, unspecified.

2025 ICD-10-CM code D56.1

Beta thalassemia major, also known as Cooley's anemia, is a severe form of beta thalassemia characterized by a significant reduction in beta-globin production, leading to severe anemia and other complications.

2025 ICD-10-CM code D57.453

Sickle-cell thalassemia beta plus with cerebral vascular involvement.

2025 ICD-10-CM code D59.12

Chronic cold hemagglutinin disease characterized by the premature destruction of red blood cells due to cold-reacting autoantibodies.

2025 ICD-10-CM code D58.1

Hereditary elliptocytosis is a genetic blood disorder characterized by oval or elliptical-shaped red blood cells (RBCs).It is a type of hereditary hemolytic anemia caused by genetic mutations in the RBC membrane.

2025 ICD-10-CM code D57.432

Sickle-cell thalassemia beta zero with splenic sequestration.

2025 ICD-10-CM code D57.213

Sickle-cell/Hb-C disease with cerebral vascular involvement. Code also, if applicable, cerebral infarction (I63.-).

2025 ICD-10-CM code D59.30

Hemolytic-uremic syndrome, unspecified.

2025 ICD-10-CM code D57.2

Sickle-cell/Hb-C disease. This is a type of sickle cell disease (SCD) where a patient inherits hemoglobin C, an abnormal gene leading to the formation of sickle-shaped red blood cells and anemia.

2025 ICD-10-CM code D57.412

Sickle-cell thalassemia with splenic sequestration.

2025 ICD-10-CM code D57.21

Sickle-cell/Hb-C disease with crisis. This is a type of sickle cell disease where a patient inherits one copy of the gene for hemoglobin S and one copy of the gene for hemoglobin C.A crisis occurs when the abnormally shaped red blood cells block blood flow, causing pain and other complications.

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 D57.811

A genetic blood disorder causing hard, sticky, C-shaped red blood cells, leading to anemia and acute chest complications.

2025 ICD-10-CM code D58.9

A hereditary condition causing premature destruction of red blood cells.

2025 ICD-10-CM code D57.818

Other sickle-cell disorders with crisis with other specified complication.

2025 ICD-10-CM code D57.452

Sickle-cell thalassemia beta plus with splenic sequestration.

2025 ICD-10-CM code D59.39

Other hemolytic-uremic syndrome.This includes atypical (non-genetic) and secondary hemolytic-uremic syndrome.

2025 ICD-10-CM code D57.43

Sickle-cell thalassemia beta zero with crisis.

2025 ICD-10-CM code D57.418

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

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 D57.02

Hb-SS disease with splenic sequestration. This is a complication of sickle cell disease where deformed red blood cells accumulate in the spleen, causing it to enlarge rapidly.

2025 ICD-10-CM code D59.1

A type of anemia caused by the immune system attacking and destroying red blood cells faster than they are produced.

2025 ICD-10-CM code D56.3

Thalassemia minor is a genetic blood disorder characterized by a reduced amount of hemoglobin and red blood cells, leading to mild anemia. It's inherited from one parent.

2025 ICD-10-CM code D57.813

Other sickle-cell disorders with cerebral vascular involvement.Code also , if applicable: cerebral infarction (I63.-)

2025 ICD-10-CM code D57.218

Sickle-cell/Hb-C disease with crisis with other specified complication. Use additional code to identify complications.

2025 ICD-10-CM code D55

Anemia due to enzyme disorders.

2025 ICD-10-CM code D59.2

Drug-induced nonautoimmune hemolytic anemia. This occurs when certain drug reactions damage red blood cells, usually destroying cell membranes.

2025 ICD-10-CM code D59.5

Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]

2025 ICD-10-CM code D57.8

This code designates other sickle-cell disorders not otherwise specified, including Hb-SD disease and Hb-SE disease.

2025 ICD-10-CM code D58.8

A genetic blood disorder causing premature destruction of red blood cells, leading to a reduced red blood cell count and oxygen deficiency.This code specifies hereditary hemolytic anemias not otherwise classified.

2025 ICD-10-CM code D57.01

Hb-SS disease with acute chest syndrome. This condition involves rapid-onset chest complications in individuals with Hb-SS disease, a severe form of sickle cell disease.

2025 ICD-10-CM code D57.458

Sickle-cell thalassemia beta plus with crisis with other specified complication. Use additional code to identify complications, such as cholelithiasis (K80.-) or priapism (N48.32).

2025 ICD-10-CM code D57.419

Sickle-cell thalassemia with crisis, unspecified.

2025 ICD-10-CM code D57.45

Sickle-cell thalassemia beta plus with crisis. This condition involves a combination of sickle cell trait and beta thalassemia, resulting in a crisis.

2025 ICD-10-CM code D56.5

Hemoglobin E-beta thalassemia. This is a condition where there is a reduced amount of hemoglobin and red blood cells due to a combination of Hemoglobin E and beta thalassemia mutations.

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.

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