D57.412
BillableSickle-cell thalassemia, unsp, with splenic sequestration
Sickle-cell thalassemia, unspecified, with splenic sequestration
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(5)
D57.411Sickle-cell thalassemia, unsp, with acute chest syndrome
D57.413Sickle-cell thalassemia, unsp, with cerebral vascular invl
D57.414Sickle-cell thalassemia, unspecified, with dactylitis
D57.418Sickle-cell thalassemia, unsp, with crisis with oth comp
D57.419Sickle-cell thalassemia, unspecified, with crisis
Also Known As / Clinical Terms(66)
SNOMED CT
- RBC sequestration in spleen95846001
- RBC trapping in spleen95846001
- Red blood cell sequestration in spleen95846001
- Red blood cell trapping in spleen95846001
- Drepanocythaemia127040003
- Drepanocythemia127040003
- Haemoglobin S disease127040003
- Haemoglobin S-S disease127040003
- Hb S disease127040003
- Hb SS disease127040003
- Hemoglobin S disease127040003
- Hemoglobin S-S disease127040003
- Hereditary haemoglobinopathy disorder homozygous for haemoglobin S127040003
- Hereditary hemoglobinopathy disorder homozygous for hemoglobin S127040003
- Sickle cell anaemia127040003
- Sickle cell anemia127040003
- Sickle cell-haemoglobin SS disease127040003
- Sickle cell-hemoglobin SS disease127040003
- Haemoglobin S sickling disorder with crisis417279003
- Hemoglobin S sickling disorder with crisis417279003
- Sickle cell anaemia crisis417279003
- Sickle cell anemia crisis417279003
- Haemoglobin SS disease with crisis417425009
- Hemoglobin SS disease with crisis417425009
- Sickle cell anaemia with crisis417425009
- Sickle cell anemia with crisis417425009
- Sickle cell crisis417425009
- Acute sickle cell splenic sequestration crisis444108000
- Acute sequestration of spleen due to sickle cell thalassaemia with crisis1153413001
- Acute sequestration of spleen due to sickle cell thalassemia with crisis1153413001
- Acute splenic sequestration of spleen due to sickle cell thalassaemia with crisis1153413001
- Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis1153413001
UMLS
Clinical Terms
- Sickle cell-haemoglobin SS disease
- Hemoglobin SS disease with crisis
- Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
- Sickle cell anaemia crisis
- Haemoglobin S sickling disorder with crisis
- Haemoglobin SS disease with crisis
- Acute sequestration of spleen due to sickle cell thalassaemia with crisis
- Hemoglobin S sickling disorder with crisis
- Hemoglobin S-S disease
- Haemoglobin S-S disease
- Sickle cell anemia crisis
- Hb SS disease
- Red blood cell sequestration in spleen
- Drepanocythaemia
- Hemoglobin S disease
- Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
- Acute splenic sequestration of spleen due to sickle cell thalassaemia with crisis
- Sickle cell anaemia
- Hereditary haemoglobinopathy disorder homozygous for haemoglobin S
- RBC sequestration in spleen
- Sickle cell-hemoglobin SS disease
- Drepanocythemia
- Red blood cell trapping in spleen
- Acute sickle cell splenic sequestration crisis
- Sickle cell anemia
- Sickle cell anaemia with crisis
- Hb S disease
- RBC trapping in spleen
- Sickle cell anemia with crisis
- Haemoglobin S disease
- Acute sequestration of spleen due to sickle cell thalassemia with crisis
- Sickle cell crisis
Frequently Asked Questions
What is the ICD-10 code for sickle-cell thalassemia, unsp, with splenic sequestration?
The ICD-10-CM code for sickle-cell thalassemia, unsp, with splenic sequestration is D57.412. The full clinical description is "Sickle-cell thalassemia, unspecified, with splenic sequestration". D57.412 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D57.412 mean?
ICD-10-CM code D57.412 represents “Sickle-cell thalassemia, unspecified, with splenic sequestration”. 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 D57.412 a billable code?
Yes, D57.412 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.412 in?
D57.412 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.412?
D57.412 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.412?
Yes, when using D57.412, also report: any associated fever (R50.81).
What SNOMED CT codes does D57.412 map to?
D57.412 maps to 6 SNOMED CT concepts: 1153413001, 444108000, 127040003, 417279003, 417425009, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.412?
D57.412 is linked to 1 UMLS Concept Unique Identifier: C5384625. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D57.412 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sickle-cell thalassemia, unsp, with splenic sequestration 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 D57.412?
There is no direct ICD-11 mapping available for D57.412 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.