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ICD-10-CM Codes
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D50-D89
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D55-D59
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D57-
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2023 ICD-10-CM Diagnosis Code D57.8
2023 ICD-10-CM Diagnosis Code D57.8
Other sickle-cell disorders
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
- D57.8 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2023 edition of ICD-10-CM D57.8 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D57.8 - other international versions of ICD-10 D57.8 may differ.
Applicable To- Hb-SD disease
- Hb-SE disease
The following code(s) above
D57.8 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
D57.8:
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
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to D57.8:
- Disease, diseased - see also Syndrome
- hemoglobin or Hb
- sickle-cell D57.1
ICD-10-CM Diagnosis Code D57.1
Sickle-cell disease without crisis
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Hb-SS disease without crisis
- Sickle-cell anemia NOS
- Sickle-cell disease NOS
- Sickle-cell disorder NOS
- Disorder (of) - see also Disease
- Elliptocytosis (congenital) (hereditary) D58.1
ICD-10-CM Diagnosis Code D58.1
Hereditary elliptocytosis
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Elliptocytosis (congenital)
- Ovalocytosis (congenital) (hereditary)
- Spherocytosis (congenital) (familial) (hereditary) D58.0
ICD-10-CM Diagnosis Code D58.0
Hereditary spherocytosis
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Acholuric (familial) jaundice
- Congenital (spherocytic) hemolytic icterus
- Minkowski-Chauffard syndrome
- sickle-cell D57.8- (disease)
ICD-10-CM Codes Adjacent To D57.8
D57.433 Sickle-cell thalassemia beta zero with cerebral vascular involvement
D57.438 …… with other specified complication
D57.44 …… beta plus without crisis
D57.45 Sickle-cell thalassemia beta plus with crisis
D57.451 Sickle-cell thalassemia beta plus with acute chest syndrome
D57.452 Sickle-cell thalassemia beta plus with splenic sequestration
D57.453 Sickle-cell thalassemia beta plus with cerebral vascular involvement
D57.458 …… with other specified complication
D57.8
Other sickle-cell disorders
D57.81 Other sickle-cell disorders with crisis
D57.811 Other sickle-cell disorders with acute chest syndrome
D57.812 Other sickle-cell disorders with splenic sequestration
D57.813 Other sickle-cell disorders with cerebral vascular involvement
D57.818 …… with other specified complication
D58 Other hereditary hemolytic anemias
D58.0 Hereditary spherocytosis
D58.1 Hereditary elliptocytosis
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.