D57.80
BillableOther sickle-cell disorders without crisis
Other sickle-cell disorders without crisis
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(1)
Also Known As / Clinical Terms(101)
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
- 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
- Sickle cell-Haemoglobin O Arab disease127048005
- Sickle cell-Hemoglobin O Arab disease127048005
- Sickle cell anaemia with high haemoglobin F234391009
- Sickle cell anemia with high hemoglobin F234391009
- Sickle cell-haemoglobin D disease without crisis416214006
- Sickle cell-hemoglobin D disease without crisis416214006
- Haemoglobin S sickling disorder without crisis416290001
- Hemoglobin S sickling disorder without crisis416290001
- Sickle cell-haemoglobin E disease without crisis416638004
- Sickle cell-hemoglobin E disease without crisis416638004
Clinical Terms
- Hemoglobin S-E disease
- Sickle cell anemia with hemoglobin E disease
- Sickle cell-haemoglobin SS disease
- Haemoglobin S-E disease
- Sickle cell anaemia with haemoglobin D disease
- Sickle cell-hemoglobin D disease
- Double heterozygous for Hb S + Hb D Punjab
- Sickle cell anemia with hemoglobin D disease
- Hemoglobin S-D disease
- Sickle cell hemoglobin D
- Haemoglobin S sickling disorder without crisis
- Hemoglobin S-S disease
- Hemoglobin S/E disease
- Sickle cell-haemoglobin D disease without crisis
- Hemoglobin S sickling disorder without crisis
- Mixed haemoglobinopathy
- Haemoglobin S-S disease
- Sickle cell haemoglobin D
- Double heterozygous for Hb S + Hb E
- Hb SS disease
- Sickle cell-hemoglobin E disease without crisis
- Sickle cell anaemia with haemoglobin E disease
- Sickle cell-Haemoglobin O Arab disease
- Drepanocythaemia
- Haemoglobin S/E disease
- Hemoglobin S disease
- Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
- Sickle cell-hemoglobin E disease
- HbS-HbD disease
- Sickle cell anaemia
- Hereditary haemoglobinopathy disorder homozygous for haemoglobin S
- Sickle cell-haemoglobin D disease
- Haemoglobin S-D disease
- Mixed hemoglobin disorder
- Sickle cell anaemia with high haemoglobin F
- HbS-HbE disease
- Sickle cell-hemoglobin SS disease
- Drepanocythemia
- Sickle cell anemia with high hemoglobin F
- Haemoglobin S/D Punjab disease
- Hemoglobin S/D Punjab disease
- Hb S disease
- Mixed hemoglobinopathy
- Sickle cell anemia
- Sickle cell-haemoglobin E disease
- Haemoglobin S disease
- Sickle cell-haemoglobin E disease without crisis
- Mixed haemoglobin disorder
- Sickle cell-hemoglobin D disease without crisis
- Sickle cell-Hemoglobin O Arab disease
Frequently Asked Questions
What is the ICD-10 code for other sickle-cell disorders without crisis?
The ICD-10-CM code for other sickle-cell disorders without crisis is D57.80. The full clinical description is "Other sickle-cell disorders without crisis". D57.80 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D57.80 mean?
ICD-10-CM code D57.80 represents “Other sickle-cell disorders 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 D57.80 a billable code?
Yes, D57.80 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D57.80 in?
D57.80 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D57.80?
D57.80 has Excludes1 notes indicating codes that cannot be used together with it, including: other hemoglobinopathies (D58.-).
Are additional codes required with D57.80?
Yes, when using D57.80, also report: any associated fever (R50.81).
What SNOMED CT codes does D57.80 map to?
D57.80 maps to 9 SNOMED CT concepts: 25472008, 47024008, 127040003, 416290001, 38589006, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D57.80?
D57.80 is linked to 1 UMLS Concept Unique Identifier: C2873770. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D57.80 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other sickle-cell disorders 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 D57.80?
There is no direct ICD-11 mapping available for D57.80 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.