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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 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 D57.431
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 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 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 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 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 D59.11
Warm autoimmune hemolytic anemia. This condition involves the body destroying red blood cells more rapidly than it produces them.
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 D57.811
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 D57.41
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 D57.452
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 D57.3
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 D57.433
Sickle-cell thalassemia beta zero with cerebral vascular involvement.
2025 ICD-10-CM code D57.418
Sickle-cell thalassemia, unspecified, with crisis with other specified complication.
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 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 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 D57.02
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 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 D57.451
Sickle-cell thalassemia beta plus with acute chest syndrome.
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 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 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 D59.32
Hereditary hemolytic-uremic syndrome. Atypical hemolytic uremic syndrome with an identified genetic cause.
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 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 D57.453
Sickle-cell thalassemia beta plus with cerebral vascular involvement.
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.
This code designates other sickle-cell disorders not otherwise specified, including Hb-SD disease and Hb-SE disease.
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