Specific code icon 2017 ICD-10-CM Diagnosis Code D57.1

Sickle-cell disease without crisis

    2016 2017 Billable/Specific Code

  • 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.

Clinical Information
  • 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.
Applicable To
  • Hb-SS disease without crisis
  • Sickle-cell anemia NOS
  • Sickle-cell disease NOS
  • Sickle-cell disorder NOS
Approximate Synonyms
  • 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):
  • 811 Red blood cell disorders with mcc
  • 812 Red blood cell disorders without mcc

Convert ICD-10-CM D57.1 to ICD-9-CM

The following ICD-10-CM Index entries contain back-references to ICD-10-CM D57.1: