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ALL MEDICAL CODES IN CATEGORY Hemolytic anemias (D55-D59)

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 D55.0

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

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 D58.0

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

2025 ICD-10-CM code D57.0

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

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 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 D57.80

A genetic blood disorder causing sickle-shaped red blood cells, leading to anemia, but without a crisis.

2025 ICD-10-CM code D56.9

Thalassemia, unspecified.

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 D57.20

Sickle-cell/Hb-C disease without crisis. This is a genetic blood disorder where red blood cells become hard, sticky, and C-shaped, leading to anemia but no vaso-occlusive crisis.

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 D57.411

Sickle-cell thalassemia with acute chest syndrome.

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 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 D57.212

Sickle-cell/Hb-C disease with splenic sequestration. This is a complication of sickle-cell/Hb-C disease characterized by the rapid accumulation of sickle-shaped red blood cells in the spleen.

2025 ICD-10-CM code D59

Acquired hemolytic anemia is a condition characterized by the premature destruction of red blood cells.

2025 ICD-10-CM code D58

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

2025 ICD-10-CM code D56.8

This code represents other specified types of thalassemia, a group of inherited blood disorders characterized by reduced hemoglobin production.

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 D57.219

Sickle-cell/Hb-C disease with crisis, unspecified. This condition involves painful vaso-occlusive crises due to the sickling of red blood cells in individuals with Hb-SC disease.

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 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 D55

Anemia due to enzyme disorders.

2025 ICD-10-CM code D59.9

Acquired hemolytic anemia, unspecified. This condition involves the premature destruction of red blood cells due to an unknown cause.

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 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 D57.03

Hb-SS disease with cerebral vascular involvement. Code also, if applicable, cerebral infarction (I63.-).

2025 ICD-10-CM code D59.6

Hemoglobinuria due to hemolysis from other external causes. This condition involves the destruction of red blood cells due to external factors, resulting in the release of hemoglobin and its excretion in urine.

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 D57.1

Sickle-cell disease without crisis. This is a genetic blood disorder characterized by sickle-shaped red blood cells and anemia, but without a vaso-occlusive crisis.

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 D55.1

A decrease in red blood cells due to disturbances in glutathione metabolism, resulting in a lack of oxygen.

2025 ICD-10-CM code D57.4

Sickle-cell thalassemia. This is a genetic blood disorder where red blood cells become hard, sticky, and C-shaped, leading to anemia.

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 D56.4

Hereditary persistence of fetal hemoglobin (HPFH).

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.

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