D57.20
BillableSickle-cell/Hb-C disease without crisis
Sickle-cell/Hb-C disease without crisis
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Use Additional Code
Additional codes that should follow this code
Related Codes(1)
Also Known As / Clinical Terms(116)
SNOMED CT
- Sickle cell retinopathy11603001
- Double heterozygous for Hb S and Hb D35434009
- Haemoglobin S-C disease35434009
- Haemoglobin S/C disease35434009
- Hb SC disease35434009
- HbS-HbC disease35434009
- Hemoglobin S-C disease35434009
- Hemoglobin S/C disease35434009
- Sickle cell anaemia with haemoglobin C disease35434009
- Sickle cell anemia with hemoglobin C disease35434009
- Sickle cell haemoglobin C35434009
- Sickle cell hemoglobin C35434009
- Sickle cell-haemoglobin C disease35434009
- Sickle cell-hemoglobin C disease35434009
- Mixed haemoglobin disorder38589006
- Mixed haemoglobinopathy38589006
- Mixed hemoglobin disorder38589006
- Mixed hemoglobinopathy38589006
- Sickle cell-haemoglobin C retinopathy232033003
- Sickle cell-hemoglobin C retinopathy232033003
- Haemoglobin S sickling disorder without crisis416290001
- Hemoglobin S sickling disorder without crisis416290001
- Sickle cell-haemoglobin C disease without crisis417683006
- Sickle cell-hemoglobin C disease without crisis417683006
UMLS
- Disease, Hemoglobin SCC0019034
- Disease, SCC0019034
- Diseases, Hemoglobin SCC0019034
- Diseases, SCC0019034
- Double heterozygous for Hb S and Hb DC0019034
- HEMOGLOBIN SC DISC0019034
- Haemoglobin S-C diseaseC0019034
- Haemoglobin S/C diseaseC0019034
- Haemoglobin SC diseaseC0019034
- Hb SC diseaseC0019034
- Hb-S/Hb-C diseaseC0019034
- Hb-SCC0019034
- Hb-SC diseaseC0019034
- HbS-HbC diseaseC0019034
- HbSCC0019034
- Hemoglobin S-C diseaseC0019034
- Hemoglobin S/C diseaseC0019034
- Hemoglobin SC DiseaseC0019034
- Hemoglobin SC DiseasesC0019034
- Hemoglobin SC diseaseC0019034
- SC DISC0019034
- SC DiseaseC0019034
- SC Disease, HemoglobinC0019034
- SC DiseasesC0019034
- SC Diseases, HemoglobinC0019034
- SICKLE CELL HEMOGLOBIN C DISC0019034
- Sickle Cell Hemoglobin C DiseaseC0019034
- Sickle Cell-Hemoglobin C DiseaseC0019034
- Sickle cell Hb-C diseaseC0019034
- Sickle cell anaemia with haemoglobin C diseaseC0019034
- Sickle cell anemia with hemoglobin C diseaseC0019034
- Sickle cell haemoglobin CC0019034
- Sickle cell hemoglobin CC0019034
- Sickle cell-haemoglobin C diseaseC0019034
- Sickle cell-hemoglobin C diseaseC0019034
- Sickle cell-hemoglobin C disease (disorder)C0019034
- Sickle-cell/Hb-C diseaseC0019034
- Sickle-cell/Hb-C disease without crisisC0019034
- hemoglobin s c diseaseC0019034
- hemoglobin s-c diseaseC0019034
- hemoglobin scC0019034
- hemoglobin sc diseaseC0019034
- sc diseaseC0019034
- sickle cell-hemoglobin c diseaseC0019034
Clinical Terms
- Hemoglobin S-C disease
- Diseases, Hemoglobin SC
- Hemoglobin S/C disease
- SC Disease, Hemoglobin
- SICKLE CELL HEMOGLOBIN C DIS
- Sickle cell-haemoglobin C disease
- Sickle cell-hemoglobin C disease
- hemoglobin sc disease
- Sickle cell-hemoglobin C disease without crisis
- Disease, Hemoglobin SC
- Hb-S/Hb-C disease
- Sickle cell-haemoglobin C retinopathy
- HEMOGLOBIN SC DIS
- Diseases, SC
- Double heterozygous for Hb S and Hb D
- Haemoglobin S sickling disorder without crisis
- Mixed haemoglobin disorder
- Hemoglobin S sickling disorder without crisis
- Mixed haemoglobinopathy
- Sickle cell-hemoglobin C retinopathy
- HbSC
- hemoglobin s c disease
- Haemoglobin SC disease
- sc disease
- Hb SC disease
- Sickle cell Hb-C disease
- Sickle Cell Hemoglobin C Disease
- Hb-SC disease
- Sickle cell hemoglobin C
- Sickle cell anaemia with haemoglobin C disease
- Sickle cell-haemoglobin C disease without crisis
- Hb-SC
- SC DIS
- hemoglobin sc
- Hemoglobin SC Diseases
- SC Diseases
- Mixed hemoglobin disorder
- Haemoglobin S/C disease
- Sickle cell retinopathy
- Sickle cell-hemoglobin C disease (disorder)
- Sickle cell haemoglobin C
- Sickle-cell/Hb-C disease
- SC Diseases, Hemoglobin
- Sickle cell anemia with hemoglobin C disease
- HbS-HbC disease
- Disease, SC
- Mixed hemoglobinopathy
- Haemoglobin S-C disease
Frequently Asked Questions
What is the ICD-10 code for sickle-cell/hb-c disease without crisis?
The ICD-10-CM code for sickle-cell/hb-c disease without crisis is D57.20. The full clinical description is "Sickle-cell/Hb-C disease without crisis". D57.20 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D57.20 mean?
ICD-10-CM code D57.20 represents “Sickle-cell/Hb-C disease without crisis”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D57.20 a billable code?
Yes, D57.20 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.20 in?
D57.20 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.20?
D57.20 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.20?
Yes, when using D57.20, also report: any associated fever (R50.81).
What SNOMED CT codes does D57.20 map to?
D57.20 maps to 6 SNOMED CT concepts: 35434009, 416290001, 38589006, 11603001, 417683006, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.20?
D57.20 is linked to 1 UMLS Concept Unique Identifier: C0019034. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D57.20 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sickle-cell/hb-c disease without crisis affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D57.20?
There is no direct ICD-11 mapping available for D57.20 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.