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D57.1

Billable

Sickle-cell disease without crisis

Sickle-cell disease without crisis

Status

Billable / Specific

Block

D55-D59

Parent Code

D57

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Hb-SS disease without crisis
  • Sickle-cell anemia NOS
  • Sickle-cell disease NOS
  • Sickle-cell disorder 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)
D57.0

Hb-SS disease with crisis

D57.2

Sickle-cell/Hb-C disease

D57.3

Sickle-cell trait

BillableD57.4

Sickle-cell thalassemia

D57.8

Other sickle-cell disorders

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

3A51.1Sickle cell disease without crisisequivalentPrimary
Also Known As / Clinical Terms(348)

SNOMED CT

UMLS

Clinical Terms

  • sickle-cell disease
  • Hemoglobin S-F disease
  • Nonproliferative retinopathy of left eye due to sickle cell disease
  • Nondiabetic proliferative retinopathy
  • sickle cell anaemia
  • Sickle-cell anemia, unspecified
  • cells disease sickle
  • Haemoglobin SS disease without crisis
  • Sickle Cell Disease
  • Focal segmental glomerulosclerosis
  • Sickle cell hepatic disease
  • HEMOGLOBIN S DIS
  • Sickle Cell Anemia
  • Hereditary persistence of foetal haemoglobin
  • Hemoglobin S-S disease
  • Mentulagra
  • Hemoglobin S sickling disorder without crisis
  • Haemoglobin S-S disease
  • Disorder of glomerulus due to double heterozygous sickling disorder
  • Hb SS disease
  • HPFH - Hereditary persistence of fetal haemoglobin
  • anemia cells sickle
  • Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
  • Sickle cell nephropathy
  • Sickle cell anaemia in mother complicating childbirth
  • disease sickle cell
  • Necrotising papillitis
  • HPFH - Hereditary persistence of foetal haemoglobin
  • Sickle-cell anaemia
  • Drepanocythemia
  • Sickling Disorder Due to Hemoglobin S
  • Hb S disease
  • Nonproliferative retinopathy due to sickle cell disease
  • Papillary necrosis
  • Microdrepanocytosis
  • Sickle cell hepatopathy
  • Disorder of heart muscle due to sickle cell hemoglobinopathy
  • Haemoglobin S-F disease
  • Sickle cell anemia with coexistent alpha-thalassemia
  • cell disorder sickle
  • Proliferative retinopathy of bilateral eyes due to sickle cell disease
  • Sickle-cell anemia NOS
  • scds
  • Focal segmental glomerulosclerosis due to sickle cell disease
  • Hereditary persistence of fetal hemoglobin
  • Anemias, Sickle Cell
  • Disorder of myocardium due to sickle cell hemoglobinopathy
  • Pathologic erection
  • Hemoglobin S Disease
  • Nonproliferative sickle cell retinopathy
  • Sickle cell anaemia in childbirth
  • Disorder of glomerulus due to haematological disease
  • Proliferative retinopathy of both eyes due to sickle cell disease
  • Sickle cell-thalassemia disease
  • cell diseases sickle
  • HbS disease
  • Nonproliferative retinopathy of right eye due to sickle cell disease
  • Sickle cell-thalassaemia disease
  • Anemia, Sickle Cell
  • Necrotizing papillitis
  • anemia sickle-cell
  • Sickle Cell Disorder
  • Non-diabetic proliferative retinopathy of bilateral eyes
  • Disorder of myocardium due to sickle cell haemoglobinopathy
  • Sickle Cell Diseases
  • Drepanocythaemia
  • Sickle cell arthropathy
  • Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
  • Proliferative retinopathy of both eyes
  • Sickle-cell anaemia, unspecified
  • anemia sickle celled
  • Hereditary haemoglobinopathy disorder homozygous for haemoglobin S
  • Sickle cell hepatic dysfunction
  • sickle cell anemias
  • syndrome sickle cell
  • Sickle cell syndrome
  • Sickle cell disease of liver
  • Double heterozygous sickling disorder
  • Sickling disorder due to hemoglobin S (disorder)
  • Sickle cell-haemoglobin SS disease
  • Glomerular disease due to haematological disease
  • Cell Disorder, Sickle
  • Sickle cell-hemoglobin SS disease (disorder)
  • SCD
  • anemia cells sickles
  • Priapism
  • Arthropathy secondary to hemoglobinopathy
  • Microdrepanocytic disease
  • Haemoglobin S sickling disorder without crisis
  • Disease, Hemoglobin S
  • Arthropathy secondary to haemoglobinopathy
  • Proliferative retinopathy of right eye due to sickle cell disease
  • anemia sickle cell
  • Sickling disorder due to haemoglobin S
  • cell sickle syndrome
  • disease hb s
  • Sickle cell anaemia with coexistent alpha-thalassaemia
  • FSGS - Focal segmental glomerulosclerosis
  • Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome
  • Sickle cell retinopathy
  • Necrotising renal papillitis
  • anaemia cell sickle
  • Nonproliferative retinopathy of bilateral eyes due to sickle cell disease
  • Disorder of glomerulus due to hematological disease
  • Sickle cell disorders
  • Hemoglobin SS disease without crisis (disorder)
  • Hemoglobin SS disease without crisis
  • Renal papillary necrosis due to sickle cell disease
  • Gouty arthropathy due to double heterozygous sickling disorder
  • Haemoglobin S disease
  • Nonproliferative retinopathy of both eyes due to sickle cell disease
  • Priapism due to sickle cell disease
  • Thalassemia-hemoglobin S disease
  • Hemoglobin S Diseases
  • disease sickle-cell
  • Hereditary persistence of fetal haemoglobin
  • Bilateral nonproliferative retinopathy due to sickle cell disease
  • Sickle cell liver disease
  • Thalassaemia-haemoglobin S disease
  • anemia cell disorders sickle
  • Anaemia sickle cell
  • Sickle-cell disorder NOS
  • Proliferative retinopathy of bilateral eyes
  • Arthropathy due to sickle cell disease
  • Necrotizing renal papillitis
  • Sickle cell disorder of liver
  • Disorder of heart muscle due to sickle cell haemoglobinopathy
  • Sickle cell thalassaemia disease
  • Sickle cell thalassemia disease
  • Sickle-cell anemia
  • Disorder of liver due to sickle cell disease
  • Sickle-cell disease NOS
  • anemia cell disorder sickle
  • Cell Diseases, Sickle
  • Bilateral proliferative retinopathy due to sickle cell disease
  • Hemoglobin SS disease
  • Cell Disorders, Sickle
  • Glomerular disease due to hematological disease
  • Proliferative retinopathy due to sickle cell disease
  • cell sickle syndromes
  • Glomerular disease due to double heterozygous sickling disorder
  • Renal papillary necrosis
  • Sickle cell-hemoglobin SS disease
  • Cell Disease, Sickle
  • sicklemia
  • Sickle cell disease NOS
  • Sickle cell anemia in childbirth
  • Proliferative retinopathy of left eye due to sickle cell disease
  • Sickle cell anemia in mother complicating childbirth
  • HPFH - Hereditary persistence of fetal hemoglobin
  • Hb-SS disease without crisis
  • Sickle cell disease without crisis
  • Hb F disease
Frequently Asked Questions
What is the ICD-10 code for sickle-cell disease without crisis?

The ICD-10-CM code for sickle-cell disease without crisis is D57.1. The full clinical description is "Sickle-cell disease without crisis". D57.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D57.1 mean?

ICD-10-CM code D57.1 represents “Sickle-cell 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 D57.1 a billable code?

Yes, D57.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D57.1 in?

D57.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D57.1?

D57.1 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).

Are additional codes required with D57.1?

Yes, when using D57.1, also report: any associated fever (R50.81).

What SNOMED CT codes does D57.1 map to?

D57.1 maps to 36 SNOMED CT concepts: 709142003, 275325009, 777474191000119103, 680047951000119104, 1148919002, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D57.1?

D57.1 is linked to 2 UMLS Concept Unique Identifiers: C0002895, C0272078. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D57.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sickle-cell 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 D57.1?

D57.1 maps to the ICD-11 code: 3A51.1 (Sickle cell disease without crisis).

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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.