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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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2018/2019 ICD-10-CM Diagnosis Code D57.2
Sickle-cell/Hb-C disease
2016 2017 2018 2019 Non-Billable/Non-Specific Code
- D57.2 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2018/2019 edition of ICD-10-CM D57.2 became effective on October 1, 2018.
- This is the American ICD-10-CM version of D57.2 - other international versions of ICD-10 D57.2 may differ.
Applicable To- Hb-SC disease
- Hb-S/Hb-C disease
The following code(s) above
D57.2 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
D57.2:
- One of the sickle cell disorders characterized by the presence of both hemoglobin s and hemoglobin c. It is similar to, but less severe than sickle cell anemia.
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
- Disease, diseased - see also Syndrome
- hemoglobin or Hb
- C (Hb-C) D58.2
ICD-10-CM Diagnosis Code D58.2
Other hemoglobinopathies
2016 2017 2018 2019 Billable/Specific Code
Applicable To- Abnormal hemoglobin NOS
- Congenital Heinz body anemia
- Hb-C disease
- Hb-D disease
- Hb-E disease
- Hemoglobinopathy NOS
- Unstable hemoglobin hemolytic disease
Type 1 Excludes- familial polycythemia (D75.0)
- Hb-M disease (D74.0)
- hemoglobin E-beta thalassemia (D56.5)
- hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
- high-altitude polycythemia (D75.1)
- methemoglobinemia (D74.-)
- other hemoglobinopathies with thalassemia (D56.8)
- Hb-S D57.2-
- sickle-cell D57.2-
- SC D57.2-
ICD-10-CM Codes Adjacent To D57.2
D56.4 Hereditary persistence of fetal hemoglobin [HPFH]
D56.5 Hemoglobin E-beta thalassemia
D56.9 Thalassemia, unspecified
D57 Sickle-cell disorders
D57.0 Hb-SS disease with crisis
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
D57.4 Sickle-cell thalassemia
D57.41 Sickle-cell thalassemia with crisis
D57.411 Sickle-cell thalassemia 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.
