D57
Clinical Information
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A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia.
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A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin s.
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An inherited disease in which the red blood cells have an abnormal crescent shape, block small blood vessels, and do not last as long as normal red blood cells. Sickle cell anemia is caused by a mutation change) in one of the genes for hemoglobin the substance inside red blood cells that binds to oxygen and carries it from the lungs to the tissues). It is most common in people of west and central african descent.
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Disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs; the clinical expression of homozygosity for hemoglobin s.
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Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. The cells are shaped like a crescent or sickle. They don’t last as long as normal, round red blood cells, which leads to anemia. The sickle cells also get stuck in blood vessels, blocking blood flow. This can cause pain and organ damage. A genetic problem causes sickle cell anemia. People with the disease are born with two sickle cell genes, one from each parent. If you only have one sickle cell gene, it’s called sickle cell trait. About 1 in 12 african americans has sickle cell trait. A blood test can show if you have the trait or anemia. Most states test newborn babies as part of their newborn screening programs.
Details
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underlying condition when associated fever is present, such as with:
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leukemia (C91-C95)
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neutropenia (D70.-)
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sickle-cell disease (D57.-)
- D57.0
Hb-SS disease with crisis
- D57.00
Hb-SS disease with crisis unspecified
- D57.01
Hb-SS disease with acute chest syndrome
- D57.02
Hb-SS disease with splenic sequestration
- D57.03
Hb-SS disease with cerebral vascular involvement
- D57.09
Hb-SS disease with crisis with other specified complication
- D57.1
Sickle-cell disease without crisis
- D57.2
Sickle-cell/Hb-C disease
- D57.20
Sickle-cell/Hb-C disease without crisis
- D57.21
Sickle-cell/Hb-C disease with crisis
- D57.211
Sickle-cell/Hb-C disease with acute chest syndrome
- D57.212
Sickle-cell/Hb-C disease with splenic sequestration
- D57.213
Sickle-cell/Hb-C disease with cerebral vascular involvement
- D57.218
Sickle-cell/Hb-C disease with crisis with other specified complication
- D57.219
Sickle-cell/Hb-C disease with crisis unspecified
- D57.3
Sickle-cell trait
- D57.4
Sickle-cell thalassemia
- D57.40
Sickle-cell thalassemia without crisis
- D57.41
Sickle-cell thalassemia, unspecified, with crisis
- D57.411
Sickle-cell thalassemia, unspecified, with acute chest syndrome
- D57.412
Sickle-cell thalassemia, unspecified, with splenic sequestration
- D57.413
Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
- D57.418
Sickle-cell thalassemia, unspecified, with crisis with other specified complication
- D57.419
Sickle-cell thalassemia, unspecified, with crisis
- D57.42
Sickle-cell thalassemia beta zero without crisis
- D57.43
Sickle-cell thalassemia beta zero with crisis
- D57.431
Sickle-cell thalassemia beta zero with acute chest syndrome
- D57.432
Sickle-cell thalassemia beta zero with splenic sequestration
- D57.433
Sickle-cell thalassemia beta zero with cerebral vascular involvement
- D57.438
Sickle-cell thalassemia beta zero with crisis with other specified complication
- D57.439
Sickle-cell thalassemia beta zero with crisis unspecified
- D57.44
Sickle-cell thalassemia beta plus without crisis
- D57.45
Sickle-cell thalassemia beta plus with crisis
- D57.451
Sickle-cell thalassemia beta plus with acute chest syndrome
- D57.452
Sickle-cell thalassemia beta plus with splenic sequestration
- D57.453
Sickle-cell thalassemia beta plus with cerebral vascular involvement
- D57.458
Sickle-cell thalassemia beta plus with crisis with other specified complication
- D57.459
Sickle-cell thalassemia beta plus with crisis unspecified
- D57.8
Other sickle-cell disorders
- D57.80
Other sickle-cell disorders without crisis
- D57.81
Other sickle-cell disorders with crisis
- D57.811
Other sickle-cell disorders with acute chest syndrome
- D57.812
Other sickle-cell disorders with splenic sequestration
- D57.813
Other sickle-cell disorders with cerebral vascular involvement
- D57.818
Other sickle-cell disorders with crisis with other specified complication
- D57.819
Other sickle-cell disorders with crisis unspecified