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ICD-10-CM Codes
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D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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D55-D59
Hemolytic anemias
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D57-
Sickle-cell disorders
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2019 ICD-10-CM Diagnosis Code D57.3
Sickle-cell trait
2016 2017 2018 2019 Billable/Specific Code
- D57.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2019 edition of ICD-10-CM D57.3 became effective on October 1, 2018.
- This is the American ICD-10-CM version of D57.3 - other international versions of ICD-10 D57.3 may differ.
Applicable To- Hb-S trait
- Heterozygous hemoglobin S
The following code(s) above
D57.3 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
D57.3:
- Maternal ickle cell trait in pregnancy
- Maternal sickle cell trait in pregnancy
- Postpartum (after childbirth) sickle cell trait
- Postpartum sickle cell trait
- Sickle cell trait
- Sickle cell trait in childbirth
Clinical Information
- The condition of being heterozygous for hemoglobin s.
ICD-10-CM D57.3 is grouped within Diagnostic Related Group(s) (MS-DRG v36.0):
- 811 Red blood cell disorders with mcc
- 812 Red blood cell disorders without mcc
Convert D57.3 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
Code annotations containing back-references to D57.3:
- Disease, diseased - see also Syndrome
- Disorder (of) - see also Disease
- Elliptocytosis (congenital) (hereditary) D58.1
ICD-10-CM Diagnosis Code D58.1
Hereditary elliptocytosis
2016 2017 2018 2019 Billable/Specific Code
Applicable To- Elliptocytosis (congenital)
- Ovalocytosis (congenital) (hereditary)
- sickle-cell (disease) D57.8-
ICD-10-CM Diagnosis Code D57.8-
Other sickle-cell disorders
2016 2017 2018 2019 Non-Billable/Non-Specific Code
Applicable To- Hb-SD disease
- Hb-SE disease
- Hemoglobin - see also condition
- AS genotype D57.3
- S D57.3 (Hb S)
- Sickle-cell
- Sicklemia - see also Disease, sickle-cell
- Trait(s)
ICD-10-CM Codes Adjacent To D57.3
D57.01 Hb-SS disease with acute chest syndrome
D57.02 Hb-SS disease with splenic sequestration
D57.1 Sickle-cell disease without crisis
D57.2 Sickle-cell/Hb-C disease
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
D57.3
Sickle-cell trait
D57.4 Sickle-cell thalassemia
D57.41 Sickle-cell thalassemia with crisis
D57.411 Sickle-cell thalassemia with acute chest syndrome
D57.412 Sickle-cell thalassemia with splenic sequestration
D57.8 Other sickle-cell disorders
D57.81 Other sickle-cell disorders with crisis
D57.811 Other sickle-cell disorders with acute chest syndrome
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
