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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 ICD-10-CM Diagnosis Code D57.20
Sickle-cell/Hb-C disease without crisis
2016 2017 2018 Billable/Specific Code
- D57.20 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2018 edition of ICD-10-CM D57.20 became effective on October 1, 2017.
- This is the American ICD-10-CM version of D57.20 - other international versions of ICD-10 D57.20 may differ.
The following code(s) above
D57.20 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
D57.20:
- D50-D89
2018 ICD-10-CM Range D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanismType 2 Excludes- 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)
- D57
ICD-10-CM Diagnosis Code D57
Sickle-cell disorders
2016 2017 2018 Non-Billable/Non-Specific Code
Type 1 Excludes- other hemoglobinopathies (D58.-)
Use Additional- code for any associated fever (R50.81)
- D57.2
ICD-10-CM Diagnosis Code D57.2
Sickle-cell/Hb-C disease
2016 2017 2018 Non-Billable/Non-Specific Code
Applicable To- Hb-SC disease
- Hb-S/Hb-C disease
- Sickle cell, hemoglobin c
- Sickle cell-hemoglobin c disease
Clinical Information
- 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.
ICD-10-CM D57.20 is grouped within Diagnostic Related Group(s) (MS-DRG v35.0):
- 811 Red blood cell disorders with mcc
- 812 Red blood cell disorders without mcc
Convert D57.20 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
- Disease, diseased - see also Syndrome
- sickle-cell D57.1
ICD-10-CM Diagnosis Code D57.1
Sickle-cell disease without crisis
2016 2017 2018 Billable/Specific Code
Applicable To- Hb-SS disease without crisis
- Sickle-cell anemia NOS
- Sickle-cell disease NOS
- Sickle-cell disorder NOS
ICD-10-CM Codes Adjacent To D57.20
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
D57.20
…… without crisis
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
D57.412 Sickle-cell thalassemia with splenic sequestration
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
