2026 ICD-10-CM Diagnosis Code D57.80Other sickle-cell disorders without crisis
ICD-10-CM Codes›D50–D89›D55-D59›D57
- Billable — Valid for Submission
- Chronic Condition
D57.80 is a billable ICD-10-CM diagnosis code for other sickle-cell disorders without crisis. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 811 through 812. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Sickle cell trait/anemia.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Hemoglobin S sickling disorder without crisis
- Mixed hemoglobin disorder
- Sickle cell anemia with high hemoglobin F
- Sickle cell-hemoglobin D disease
- Sickle cell-hemoglobin D disease without crisis
- Sickle cell-hemoglobin E disease
- Sickle cell-hemoglobin E disease without crisis
- Sickle cell-Hemoglobin O Arab disease
- Sickle cell-hemoglobin SS disease
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Disease, diseased - See Also: Syndrome;
- sickle-cell - D57.1
- Hb-SD - D57.80
- without crisis - D57.80
- Hb-SE - D57.80
- without crisis - D57.80
- specified NEC - D57.80
- without crisis - D57.80
- spherocytosis - D57.80
- without crisis - D57.80
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Disease, diseased
- sickle-cell
- Hb-SD
- Disease, diseased
- sickle-cell
- Hb-SD
- without crisis
- Disease, diseased
- sickle-cell
- Hb-SE
- Disease, diseased
- sickle-cell
- Hb-SE
- without crisis
- Disease, diseased
- sickle-cell
- specified NEC
- Disease, diseased
- sickle-cell
- specified NEC
- without crisis
- Disease, diseased
- sickle-cell
- spherocytosis
- Disease, diseased
- sickle-cell
- spherocytosis
- without crisis
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Sickle Cell Disease
Sickle cell disease (SCD) is a group of inherited red blood cell disorders. If you have SCD, there is a problem with your hemoglobin. Hemoglobin is a protein in red blood cells that carries oxygen throughout the body. With SCD, the hemoglobin forms into stiff rods within the red blood cells. This changes the shape of the red blood cells.
The full article covers:
- What is sickle cell disease (SCD)?
- What causes sickle cell disease (SCD)?
- Who is more likely to have sickle cell disease (SCD)?
- What are the symptoms of sickle cell disease (SCD)?
- How is sickle cell disease (SCD) diagnosed?
- What are the treatments for sickle cell disease (SCD)?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert D57.80 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About D57.80Overview
Is D57.80 (Other sickle-cell disorders) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other sickle-cell disorders without crisis on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does D57.80 group to?
When other sickle-cell disorders without crisis is the principal diagnosis on an inpatient stay, it groups to MS-DRG 811, 812, with relative weights from 0.9182 to 1.4043 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of D57.80?
Under the General Equivalence Mappings, other sickle-cell disorders without crisis converts to ICD-9-CM 282.68 (Hb-S dis w/o crisis NEC). The mapping is a direct match.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
