Home > 2016/17 ICD-10-CM Diagnosis Codes > Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism D50-D89 > Hemolytic anemias D55-D59 > Sickle-cell disorders D57-
2016/17 ICD-10-CM Diagnosis Code D57.1
Sickle-cell disease without crisis
D57.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
This is the American ICD-10-CM version of D57.1. Other international versions of ICD-10 D57.1 may differ.
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia.
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.
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.
Disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs; the clinical expression of homozygosity for hemoglobin s.
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.
Hb-SS disease without crisis
Sickle-cell anemia NOS
Sickle-cell disease NOS
Sickle-cell disorder NOS
Hb SS disease
Hemoglobin S sickling disorder without crisis
Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
Maternal sickle cell anemia in pregnancy
Microhematuria due to sickle cell disease
Postpartum (after childbirth) sickle cell anemia
Postpartum sickle cell anemia
Priapism due to sickle cell disease
Proliferative retinopathy due to sickle cell disease
Sickle cell anemia
Sickle cell anemia in childbirth
Sickle cell anemia in pregnancy
Sickle cell anemia wo crisis
Sickle cell anemia, without crisis
Sickle cell proliferative retinopathy
Sickle cell retinopathy
Sickle cell w microhematuria
Sickle cell w/ microhematuria
ICD-10-CM D57.1 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0):