D57.1
BillableSickle-cell disease without crisis
Sickle-cell disease without crisis
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)
- other hemoglobinopathies (D58.-)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Use Additional Code
Additional codes that should follow this code
- code for any associated fever (R50.81)
Also Known As / Clinical Terms
SNOMED CT
- Mentulagra6273006
- Pathologic erection6273006
- Priapism6273006
- Sickle cell retinopathy11603001
- Sickle cell nephropathy13886001
- Double heterozygous sickling disorder23269001
- Haemoglobin S-F disease36472007
- Hemoglobin S-F disease36472007
- Microdrepanocytic disease36472007
- Microdrepanocytosis36472007
- Sickle cell thalassaemia disease36472007
- Sickle cell thalassemia disease36472007
- Sickle cell-thalassaemia disease36472007
- Sickle cell-thalassemia disease36472007
- Thalassaemia-haemoglobin S disease36472007
- Thalassemia-hemoglobin S disease36472007
- Nondiabetic proliferative retinopathy46674002
- Necrotising papillitis90241004
- Necrotising renal papillitis90241004
- Necrotizing papillitis90241004
- Necrotizing renal papillitis90241004
- Papillary necrosis90241004
- Renal papillary necrosis90241004
- 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 anaemia with coexistent alpha-thalassaemia127045008
- Sickle cell anemia with coexistent alpha-thalassemia127045008
- HPFH - Hereditary persistence of fetal haemoglobin191201002
- HPFH - Hereditary persistence of fetal hemoglobin191201002
- HPFH - Hereditary persistence of foetal haemoglobin191201002
- Hb F disease191201002
- Hereditary persistence of fetal haemoglobin191201002
- Hereditary persistence of fetal hemoglobin191201002
- Hereditary persistence of foetal haemoglobin191201002
- Proliferative retinopathy due to sickle cell disease193370005
- FSGS - Focal segmental glomerulosclerosis236403004
- Focal segmental glomerulosclerosis236403004
- Arthropathy secondary to haemoglobinopathy275325009
- Arthropathy secondary to hemoglobinopathy275325009
- Haemoglobin SS disease without crisis416180004
- Hemoglobin SS disease without crisis416180004
- Sickle cell disease without crisis416180004
- Haemoglobin S sickling disorder without crisis416290001
- Hemoglobin S sickling disorder without crisis416290001
- Sickle cell disease417357006
- Sickle cell syndrome417357006
- Sickling disorder due to haemoglobin S417357006
- Sickling disorder due to hemoglobin S417357006
- Disorder of heart muscle due to sickle cell haemoglobinopathy471863000
- Disorder of heart muscle due to sickle cell hemoglobinopathy471863000
- Disorder of myocardium due to sickle cell haemoglobinopathy471863000
- Disorder of myocardium due to sickle cell hemoglobinopathy471863000
- Arthropathy due to sickle cell disease709142003
- Sickle cell arthropathy709142003
- Renal papillary necrosis due to sickle cell disease722085003
- Focal segmental glomerulosclerosis due to sickle cell disease722147003
- Disorder of liver due to sickle cell disease763096004
- Sickle cell disease of liver763096004
- Sickle cell disorder of liver763096004
- Sickle cell hepatic disease763096004
- Sickle cell hepatic dysfunction763096004
- Sickle cell hepatopathy763096004
- Sickle cell liver disease763096004
- Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome783254003
- Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome783254003
- Disorder of glomerulus due to haematological disease1148873009
- Disorder of glomerulus due to hematological disease1148873009
- Glomerular disease due to haematological disease1148873009
- Glomerular disease due to hematological disease1148873009
- Gouty arthropathy due to double heterozygous sickling disorder1148911004
- Disorder of glomerulus due to double heterozygous sickling disorder1148919002
- Glomerular disease due to double heterozygous sickling disorder1148919002
- Nonproliferative retinopathy due to sickle cell disease1285514002
- Nonproliferative sickle cell retinopathy1285514002
- Bilateral nonproliferative retinopathy due to sickle cell disease777474191000119103
- Nonproliferative retinopathy of bilateral eyes due to sickle cell disease777474191000119103
- Nonproliferative retinopathy of both eyes due to sickle cell disease777474191000119103
- Bilateral proliferative retinopathy due to sickle cell disease680047951000119104
- Proliferative retinopathy of bilateral eyes due to sickle cell disease680047951000119104
- Proliferative retinopathy of both eyes due to sickle cell disease680047951000119104
- Non-diabetic proliferative retinopathy of bilateral eyes677741000119109
- Nonproliferative retinopathy of left eye due to sickle cell disease327768421000119103
- Nonproliferative retinopathy of right eye due to sickle cell disease838183371000119103
- Priapism due to sickle cell disease367061000119107
- Proliferative retinopathy of bilateral eyes15735041000119108
- Proliferative retinopathy of both eyes15735041000119108
- Proliferative retinopathy of left eye due to sickle cell disease685574841000119108
- Proliferative retinopathy of right eye due to sickle cell disease961739241000119108
- Sickle cell anaemia in childbirth10759351000119103
- Sickle cell anaemia in mother complicating childbirth10759351000119103
- Sickle cell anemia in childbirth10759351000119103
- Sickle cell anemia in mother complicating childbirth10759351000119103
UMLS
- Anaemia sickle cellC0002895
- Anemia sickle cellC0002895
- Anemia, Sickle CellC0002895
- Anemias, Sickle CellC0002895
- Cell Disease, SickleC0002895
- Cell Diseases, SickleC0002895
- Cell Disorder, SickleC0002895
- Cell Disorders, SickleC0002895
- Disease, Hemoglobin SC0002895
- DrepanocythaemiaC0002895
- DrepanocythemiaC0002895
- HEMOGLOBIN S DISC0002895
- Haemoglobin S diseaseC0002895
- Haemoglobin S-S diseaseC0002895
- Hb S diseaseC0002895
- Hb SS diseaseC0002895
- HbS DiseaseC0002895
- HbS diseaseC0002895
- Hemoglobin S DiseaseC0002895
- Hemoglobin S DiseasesC0002895
- Hemoglobin S diseaseC0002895
- Hemoglobin S-S diseaseC0002895
- Hemoglobin SS DiseaseC0002895
- Hemoglobin SS diseaseC0002895
- Hereditary haemoglobinopathy disorder homozygous for haemoglobin SC0002895
- Hereditary hemoglobinopathy disorder homozygous for hemoglobin SC0002895
- SCDC0002895
- SICKLE CELL ANEMIAC0002895
- SICKLE CELL DISEASEC0002895
- Sickle Cell AnemiaC0002895
- Sickle Cell AnemiasC0002895
- Sickle Cell DiseaseC0002895
- Sickle Cell DiseasesC0002895
- Sickle Cell DisorderC0002895
- Sickle Cell DisordersC0002895
- Sickle cell anaemiaC0002895
- Sickle cell anemiaC0002895
- Sickle cell diseaseC0002895
- Sickle cell disease NOSC0002895
- Sickle cell disordersC0002895
- Sickle cell syndromeC0002895
- Sickle cell-haemoglobin SS diseaseC0002895
- Sickle cell-hemoglobin SS diseaseC0002895
- Sickle cell-hemoglobin SS disease (disorder)C0002895
- Sickle-cell anaemiaC0002895
- Sickle-cell anaemia, unspecifiedC0002895
- Sickle-cell anemiaC0002895
- Sickle-cell anemia NOSC0002895
- Sickle-cell anemia, unspecifiedC0002895
- Sickle-cell disease NOSC0002895
- Sickle-cell disorder NOSC0002895
- Sickle-cell disordersC0002895
- Sickling Disorder Due to Hemoglobin SC0002895
- Sickling disorder due to haemoglobin SC0002895
- Sickling disorder due to hemoglobin SC0002895
- Sickling disorder due to hemoglobin S (disorder)C0002895
- anaemia cell sickleC0002895
- anemia cell disorder sickleC0002895
- anemia cell disorders sickleC0002895
- anemia cells sickleC0002895
- anemia cells sicklesC0002895
- anemia sickle cellC0002895
- anemia sickle celledC0002895
- anemia sickle-cellC0002895
- cell diseases sickleC0002895
- cell disorder sickleC0002895
- cell sickle syndromeC0002895
- cell sickle syndromesC0002895
- cells disease sickleC0002895
- disease hb sC0002895
- disease sickle cellC0002895
- disease sickle-cellC0002895
- hb s diseaseC0002895
- scdsC0002895
- sickle cell anaemiaC0002895
- sickle cell anemiaC0002895
- sickle cell anemiasC0002895
- sickle cell diseaseC0002895
- sickle cell disorderC0002895
- sickle cell syndromeC0002895
- sickle-cell anaemiaC0002895
- sickle-cell anemiaC0002895
- sickle-cell diseaseC0002895
- sicklemiaC0002895
- syndrome sickle cellC0002895
- Haemoglobin SS disease without crisisC0272078
- Hb-SS disease without crisisC0272078
- Hemoglobin SS disease without crisisC0272078
- Hemoglobin SS disease without crisis (disorder)C0272078
- Sickle cell disease without crisisC0272078
- Sickle-cell disease without crisisC0272078
Frequently Asked Questions
What is ICD-10 code D57.1?
ICD-10-CM code D57.1 represents "Sickle-cell disease without crisis". It 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 you should also code: code for 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.
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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.