2027 ICD-10-CM Diagnosis Code D57Sickle-cell disorders
D57 is a non-billable ICD-10-CM category code for sickle-cell disorders, so it cannot be submitted on claims. Use a more specific code from this category instead, such as D57.00, D57.01, D57.02, and D57.03.
Code Identity
Code Classification
Specific Coding for Sickle-cell disordersOverview
Non-specific codes like D57 require more characters. Use one of these billable codes instead:
D57.0 for Hb-SS disease with crisis
Use D57.00 for Hb-SS disease with crisis, unspecified
Use D57.01 for Hb-SS disease with acute chest syndrome
Use D57.02 for Hb-SS disease with splenic sequestration
Use D57.03 for Hb-SS disease with cerebral vascular involvement
Use D57.04 for Hb-SS disease with dactylitis
Use D57.09 for Hb-SS disease with crisis with other specified complication
Use D57.1 for Sickle-cell disease without crisis
D57.2 for Sickle-cell/Hb-C disease
Use D57.20 for Sickle-cell/Hb-C disease without crisis
D57.21 for Sickle-cell/Hb-C disease with crisis
Use D57.3 for Sickle-cell trait
D57.4 for Sickle-cell thalassemia
Use D57.40 for Sickle-cell thalassemia without crisis
D57.41 for Sickle-cell thalassemia, unspecified, with crisis
Use D57.42 for Sickle-cell thalassemia beta zero without crisis
D57.43 for Sickle-cell thalassemia beta zero with crisis
Use D57.44 for Sickle-cell thalassemia beta plus without crisis
D57.45 for Sickle-cell thalassemia beta plus with crisis
D57.8 for Other sickle-cell disorders
Use D57.80 for Other sickle-cell disorders without crisis
D57.81 for Other sickle-cell disorders with crisis
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to D57: its own notes plus those printed at Chapter 3. A note printed at a category, block or chapter applies to every code under it.
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
- other hemoglobinopathies (D58.-)
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Use Additional Code
Add a second code, after this one, to fully describe the condition.
- code for any associated fever (R50.81)
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name D57, its category, or a range that includes it.
Excludes1 2
These codes carry an Excludes1 note naming D57: they are not reported together with it, unless the two conditions are unrelated.
- D56.8 Other thalassemiassickle-cell anemia (D57.-)
- Block P50-P61 Hemorrhagic and hematological disorders of newborn
Code First 3
These codes say to code first a condition named in the note, and D57 is one of the conditions named.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Arthropathy See Also: Arthritis; M12.9
gouty See Also: Gout;
Disorder (of) See Also: Disease;
Glomerulonephritis See Also: Nephritis; N05.9
Nephropathy See Also: Nephritis; N28.9
sickle-cell D57
Clinical InformationClinical
Anemia, Sickle Cell
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.
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.
Code HistoryHistory
Questions About D57Overview
What is the ICD-10 code for sickle-cell disorders?
D57 is the ICD-10-CM category for sickle-cell disorders, but it is a non-billable header: claims need a more specific code from this category, listed on this page.
Is D57 (Sickle-cell disorders) a billable code?
No. This is a category header that groups the codes for sickle-cell disorders, and headers cannot be submitted on claims. Claims for sickle-cell disorders need a more specific code from this category, such as D57.00, D57.01, and D57.02.
Can D57 be reported with a code from D58?
Not as a rule. The Excludes1 note on D57 lists "other hemoglobinopathies (D58.-)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).
Does D57 need an additional code?
When the condition applies, yes. The Use Additional Code note reads: code for any associated fever (R50.81). The additional code is reported after D57.