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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 D56

Thalassemia is a genetic blood disorder characterized by a reduced amount of hemoglobin and red blood cells, leading to anemia.

2025 ICD-10-CM code D59.10

Autoimmune hemolytic anemia, unspecified.

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

Other hereditary hemolytic anemias. This code excludes hemolytic anemia of the newborn (P55.-).

2025 ICD-10-CM code D57.40

Sickle-cell thalassemia without crisis. This is a genetic blood disorder characterized by the formation of abnormal, C-shaped red blood cells and a reduced red blood cell count, leading to mild anemia but no vaso-occlusive crisis.

2025 ICD-10-CM code D59.13

Mixed type autoimmune hemolytic anemia is characterized by the presence of both warm and cold autoantibodies affecting red blood cells at both normal and lower body temperatures.

2025 ICD-10-CM code D58.2

Other hemoglobinopathies.These are genetic blood disorders characterized by abnormal hemoglobin production due to genetic mutations, often leading to anemia.

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 D59.0

Drug-induced autoimmune hemolytic anemia. Use additional code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)

2025 ICD-10-CM code D55.9

A decrease in red blood cells due to missing or malfunctioning enzymes, leading to reduced oxygen levels. The specific type of enzyme disorder is not specified.

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 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).