AutoICD API

D57.40

Billable

Sickle-cell thalassemia without crisis

Sickle-cell thalassemia without crisis

Status

Billable / Specific

Block

D55-D59

Parent Code

D57.4

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)

Excludes 2

Conditions not included here, but the patient may have both

Use Additional Code

Additional codes that should follow this code

Related Codes(5)
D57.41

Sickle-cell thalassemia, unspecified, with crisis

D57.42

Sickle-cell thalassemia beta zero without crisis

BillableD57.43

Sickle-cell thalassemia beta zero with crisis

D57.44

Sickle-cell thalassemia beta plus without crisis

BillableD57.45

Sickle-cell thalassemia beta plus with crisis

Also Known As / Clinical Terms(131)

SNOMED CT

UMLS

Clinical Terms

  • Haemoglobin S-F disease
  • Hemoglobin S-F disease
  • sickle cell thalassemia
  • Haemoglobin S trait
  • Sickle cell-haemoglobin Lepore disease
  • Thalassaemia-haemoglobin S disease
  • Sickle cell-beta^0^-thalassaemia
  • Sickle cell-thalassaemia disease without crisis
  • Double heterozygous for Hb S and beta thalassemia
  • beta zero thalassemia
  • Microdrepanocytosis
  • Sickle-cell thalassemia
  • sickle cell thalassaemia
  • AS - Sickle cell trait
  • Sickle-cell thalassemia NOS
  • Hemoglobin A-S genotype
  • Microdrepanocytic disease
  • Thalassaemia with haemoglobin S disease
  • Sickle cell-thalassemia disease
  • Thalassemia sickle cell
  • Haemoglobin S/beta thalassaemia
  • Beta 0 thalassemia
  • Sickle cell thalassaemia disease
  • Sickle cell trait
  • Sickle cell thalassemia disease
  • Sickle cell-thalassaemia disease
  • Trait haemoglobinopathy
  • beta zero thalassaemia
  • Sickle cell trait with coexistent alpha-thalassemia
  • Heterozygous haemoglobin S
  • Sickle cell-hemoglobin Lepore disease
  • Trait hemoglobinopathy
  • Sickle Cell-Thalassemia
  • Hemoglobin S/beta thalassemia
  • Hemoglobin S trait
  • Haemoglobin S-A disorder
  • Heterozygous haemoglobinopathy
  • Heterozygous hemoglobin S
  • hemoglobin s thalassemia
  • Sickle cell trait with coexistent alpha-thalassaemia
  • Sickle cells present
  • Heterozygous hemoglobinopathy
  • Sickle cell-beta-thalassemia
  • Sickle cell-thalassemia disease without crisis
  • Drepanocytosis
  • Hemoglobin S-A disorder
  • Sickle cell-Hb Lepore disease
  • Sickle cell-beta-thalassaemia
  • Beta 0 thalassaemia
  • Sickle cell-thalassemia disease (disorder)
  • RBC's - sickle cells present
  • Thalassemia with hemoglobin S disease
  • Double heterozygous for Hb S and beta thalassaemia
  • Heterozygous for Hb S
  • Sickle cell-beta^0^-thalassemia
  • Thalassemia-hemoglobin S disease
  • Thalassaemia sickle cell
  • Haemoglobin A-S genotype
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, also report: 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.

How does D57.40 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sickle-cell thalassemia 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 D57.40?

There is no direct ICD-11 mapping available for D57.40 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.