D57.3
BillableSickle-cell trait
Sickle-cell trait
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hb-S trait
- Heterozygous hemoglobin S
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- other hemoglobinopathies (D58.-)
Excludes 2
Conditions not included here, but the patient may have both
- 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)
Use Additional Code
Additional codes that should follow this code
- code for any associated fever (R50.81)
Also Known As / Clinical Terms
SNOMED CT
- Sickle cell retinopathy11603001
- Delta beta thalassaemia16360009
- Delta beta thalassemia16360009
- Delta-beta thalassaemia16360009
- Delta-beta thalassemia16360009
- F thalassaemia16360009
- F thalassemia16360009
- AS - Sickle cell trait16402000
- Drepanocytosis16402000
- Haemoglobin A-S genotype16402000
- Haemoglobin S trait16402000
- Haemoglobin S-A disorder16402000
- Hemoglobin A-S genotype16402000
- Hemoglobin S trait16402000
- Hemoglobin S-A disorder16402000
- Heterozygous for Hb S16402000
- Heterozygous haemoglobin S16402000
- Heterozygous hemoglobin S16402000
- RBC's - sickle cells present16402000
- Sickle cell trait16402000
- Sickle cells present16402000
- Haemoglobin S-F disease36472007
- Hemoglobin S-F disease36472007
- Microdrepanocytic disease36472007
- Microdrepanocytosis36472007
- Sickle cell thalassaemia disease36472007
- Sickle cell thalassemia disease36472007
- Sickle cell-thalassaemia disease36472007
- Sickle cell-thalassemia disease36472007
- Thalassaemia-haemoglobin S disease36472007
- Thalassemia-hemoglobin S disease36472007
- Delta beta zero thalassaemia76336008
- Delta beta zero thalassemia76336008
- Beta plus thalassaemia79592006
- Beta plus thalassemia79592006
- beta plus thalassaemia79592006
- beta plus thalassemia79592006
- Beta 0 thalassaemia86715000
- Beta 0 thalassemia86715000
- Beta zero thalassaemia86715000
- Beta zero thalassemia86715000
- beta zero thalassaemia86715000
- beta zero thalassemia86715000
- Heterozygous haemoglobinopathy123773003
- Heterozygous hemoglobinopathy123773003
- Trait haemoglobinopathy123773003
- Trait hemoglobinopathy123773003
- Double heterozygous for Hb S and beta thalassaemia127041004
- Double heterozygous for Hb S and beta thalassemia127041004
- Haemoglobin S/beta thalassaemia127041004
- Hemoglobin S/beta thalassemia127041004
- Sickle cell-beta-thalassaemia127041004
- Sickle cell-beta-thalassemia127041004
- Thalassaemia with haemoglobin S disease127041004
- Thalassemia with hemoglobin S disease127041004
- Sickle cell beta plus thalassaemia127042006
- Sickle cell beta plus thalassemia127042006
- Sickle cell-delta beta^0^-thalassaemia127044007
- Sickle cell-delta beta^0^-thalassemia127044007
- Hereditary haemoglobin S416417002
- Hereditary hemoglobin S416417002
- Disorder of glomerulus due to haematological disease1148873009
- Disorder of glomerulus due to hematological disease1148873009
- Glomerular disease due to haematological disease1148873009
- Glomerular disease due to hematological disease1148873009
- Gouty arthropathy due to sickle-cell trait1148918005
- Disorder of glomerulus due to sickle cell trait1148921007
- Glomerular disorder due to sickle cell trait1148921007
- Disorder of retina due to sickle cell trait1231702003
- Retinopathy due to sickle cell trait1231702003
- Maternal sickle cell trait in pregnancy72321000119107
- Sickle cell trait in mother complicating pregnancy72321000119107
- Sickle cell trait in childbirth10759401000119105
- Sickle cell trait in mother complicating childbirth10759401000119105
UMLS
- AS - Sickle cell traitC0037054
- Cell Trait, SickleC0037054
- Cell Traits, SickleC0037054
- DrepanocytosisC0037054
- Haemoglobin A-S genotypeC0037054
- Haemoglobin S traitC0037054
- Haemoglobin S-A disorderC0037054
- Hb-S traitC0037054
- Hemoglobin A-S genotypeC0037054
- Hemoglobin S traitC0037054
- Hemoglobin S-A disorderC0037054
- Heterozygous for Hb SC0037054
- Heterozygous haemoglobin SC0037054
- Heterozygous hemoglobin SC0037054
- RBC's - sickle cells presentC0037054
- Sickle Cell TraitC0037054
- Sickle Cell TraitsC0037054
- Sickle cell traitC0037054
- Sickle cell trait (disorder)C0037054
- Sickle cells presentC0037054
- Sickle-cell traitC0037054
- Trait, Sickle CellC0037054
- Traits, Sickle CellC0037054
- cell sickle traitC0037054
- cells sickle traitC0037054
- drepanocytosisC0037054
- sickle and cell traitC0037054
- sickle cell traitC0037054
- sickle cell traitsC0037054
- sickle-cell traitC0037054
- trait sickle cellC0037054
Frequently Asked Questions
What is ICD-10 code D57.3?
ICD-10-CM code D57.3 represents "Sickle-cell trait". It is a billable/specific code that can be used on a claim.
Is D57.3 a billable code?
Yes, D57.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.3 in?
D57.3 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.3?
D57.3 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.3?
Yes, when using D57.3 you should also code: code for any associated fever (R50.81).
What SNOMED CT codes does D57.3 map to?
D57.3 maps to 18 SNOMED CT concepts: 16402000, 86715000, 79592006, 16360009, 76336008, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.3?
D57.3 is linked to 1 UMLS Concept Unique Identifier: C0037054. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.