D57.40
BillableSickle-cell thalassemia without crisis
Sickle-cell thalassemia without crisis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Microdrepanocytosis
- Sickle-cell thalassemia NOS
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
- 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
- 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^0^-thalassaemia127043001
- Sickle cell-beta^0^-thalassemia127043001
- Sickle cell trait with coexistent alpha-thalassaemia127046009
- Sickle cell trait with coexistent alpha-thalassemia127046009
- Sickle cell-Hb Lepore disease127047000
- Sickle cell-haemoglobin Lepore disease127047000
- Sickle cell-hemoglobin Lepore disease127047000
- Sickle cell-thalassaemia disease without crisis417048006
- Sickle cell-thalassemia disease without crisis417048006
UMLS
- Haemoglobin S-F diseaseC2242796
- Hemoglobin S-F diseaseC2242796
- Microdrepanocytic diseaseC2242796
- MicrodrepanocytosisC2242796
- Sickle Cell-ThalassemiaC2242796
- Sickle cell thalassaemiaC2242796
- Sickle cell thalassaemia diseaseC2242796
- Sickle cell thalassemiaC2242796
- Sickle cell thalassemia diseaseC2242796
- Sickle cell-thalassaemia diseaseC2242796
- Sickle cell-thalassemia diseaseC2242796
- Sickle cell-thalassemia disease (disorder)C2242796
- Sickle-cell thalassemiaC2242796
- Sickle-cell thalassemia NOSC2242796
- Thalassaemia sickle cellC2242796
- Thalassaemia-haemoglobin S diseaseC2242796
- Thalassemia sickle cellC2242796
- Thalassemia-hemoglobin S diseaseC2242796
- hemoglobin s thalassemiaC2242796
- sickle cell thalassaemiaC2242796
- sickle cell thalassemiaC2242796
- Sickle-cell thalassemia without crisisC1260393
Frequently Asked Questions
What is the ICD-10 code for sickle-cell thalassemia without crisis?
The ICD-10-CM code for sickle-cell thalassemia without crisis is D57.40. The full clinical description is "Sickle-cell thalassemia without crisis". D57.40 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D57.40 mean?
ICD-10-CM code D57.40 represents "Sickle-cell thalassemia 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 D57.40 a billable code?
Yes, D57.40 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.40 in?
D57.40 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.40?
D57.40 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.40?
Yes, when using D57.40 you should also code: code for any associated fever (R50.81).
What SNOMED CT codes does D57.40 map to?
D57.40 maps to 9 SNOMED CT concepts: 16402000, 86715000, 127041004, 36472007, 123773003, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.40?
D57.40 is linked to 2 UMLS Concept Unique Identifiers: C2242796, C1260393. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.