D57.819
BillableOther sickle-cell disorders with crisis, unspecified
Other sickle-cell disorders with crisis, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Other sickle-cell disorders with crisis NOS
- Other sickle-cell disorders with (vaso-occlusive) pain 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
- •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)
D57.811Other sickle-cell disorders with acute chest syndrome
D57.812Other sickle-cell disorders with splenic sequestration
D57.813Other sickle-cell disorders with cerebral vascular invl
D57.814Other sickle-cell disorders with dactylitis
D57.818Other sickle-cell disorders with crisis with oth comp
Also Known As / Clinical Terms(74)
SNOMED CT
- Double heterozygous for Hb S + Hb D Punjab25472008
- Haemoglobin S-D disease25472008
- Haemoglobin S/D Punjab disease25472008
- HbS-HbD disease25472008
- Hemoglobin S-D disease25472008
- Hemoglobin S/D Punjab disease25472008
- Sickle cell anaemia with haemoglobin D disease25472008
- Sickle cell anemia with hemoglobin D disease25472008
- Sickle cell haemoglobin D25472008
- Sickle cell hemoglobin D25472008
- Sickle cell-haemoglobin D disease25472008
- Sickle cell-hemoglobin D disease25472008
- Mixed haemoglobin disorder38589006
- Mixed haemoglobinopathy38589006
- Mixed hemoglobin disorder38589006
- Mixed hemoglobinopathy38589006
- Double heterozygous for Hb S + Hb E47024008
- Haemoglobin S-E disease47024008
- Haemoglobin S/E disease47024008
- HbS-HbE disease47024008
- Hemoglobin S-E disease47024008
- Hemoglobin S/E disease47024008
- Sickle cell anaemia with haemoglobin E disease47024008
- Sickle cell anemia with hemoglobin E disease47024008
- Sickle cell-haemoglobin E disease47024008
- Sickle cell-hemoglobin E disease47024008
- Sickle cell-haemoglobin E disease with crisis416484003
- Sickle cell-hemoglobin E disease with crisis416484003
- Haemoglobin S sickling disorder with crisis417279003
- Hemoglobin S sickling disorder with crisis417279003
- Sickle cell anaemia crisis417279003
- Sickle cell anemia crisis417279003
- Sickle cell-haemoglobin D disease with crisis417748003
- Sickle cell-hemoglobin D disease with crisis417748003
UMLS
Clinical Terms
- Hemoglobin S-E disease
- Sickle cell anemia with hemoglobin E disease
- Haemoglobin S-E disease
- Sickle cell anaemia with haemoglobin D disease
- Sickle cell-hemoglobin D disease
- Sickle cell-hemoglobin D disease with crisis
- Sickle cell-hemoglobin E disease with crisis
- Double heterozygous for Hb S + Hb D Punjab
- Sickle cell anaemia crisis
- Sickle cell anemia with hemoglobin D disease
- Hemoglobin S-D disease
- Haemoglobin S sickling disorder with crisis
- Sickle cell hemoglobin D
- Hemoglobin S sickling disorder with crisis
- Mixed haemoglobin disorder
- Hemoglobin S/E disease
- Mixed haemoglobinopathy
- Other sickle-cell disorders with (vaso-occlusive) pain NOS
- Sickle cell haemoglobin D
- Double heterozygous for Hb S + Hb E
- Sickle cell anemia crisis
- Sickle cell anaemia with haemoglobin E disease
- Sickle cell-haemoglobin E disease with crisis
- Haemoglobin S/E disease
- Sickle cell-hemoglobin E disease
- HbS-HbD disease
- Other sickle-cell disorders with crisis NOS
- Sickle cell-haemoglobin D disease
- Haemoglobin S-D disease
- Mixed hemoglobin disorder
- HbS-HbE disease
- Sickle cell-haemoglobin D disease with crisis
- Haemoglobin S/D Punjab disease
- Hemoglobin S/D Punjab disease
- Sickle cell-haemoglobin E disease
- Mixed hemoglobinopathy
Frequently Asked Questions
What is the ICD-10 code for other sickle-cell disorders with crisis, unspecified?
The ICD-10-CM code for other sickle-cell disorders with crisis, unspecified is D57.819. The full clinical description is "Other sickle-cell disorders with crisis, unspecified". D57.819 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D57.819 mean?
ICD-10-CM code D57.819 represents “Other sickle-cell disorders with crisis, unspecified”. 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 D57.819 a billable code?
Yes, D57.819 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.819 in?
D57.819 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.819?
D57.819 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.819?
Yes, when using D57.819, also report: any associated fever (R50.81).
What SNOMED CT codes does D57.819 map to?
D57.819 maps to 6 SNOMED CT concepts: 25472008, 47024008, 417279003, 38589006, 417748003, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.819?
D57.819 is linked to 2 UMLS Concept Unique Identifiers: C5385207, C2873773. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D57.819 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other sickle-cell disorders with crisis, unspecified 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 D57.819?
There is no direct ICD-11 mapping available for D57.819 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.