ICD-10-CM Codes
D50-D89
D55-D59
D57-
2023 ICD-10-CM Diagnosis Code D57.8

2023 ICD-10-CM Diagnosis Code D57.8

Other sickle-cell disorders

2016

2017

2018

2019

2020

2021

2022

2023

Non-Billable/Non-Specific Code

D57.8 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
The 2023 edition of ICD-10-CM D57.8 became effective on October 1, 2022.
This is the American ICD-10-CM version of D57.8 - other international versions of ICD-10 D57.8 may differ.

Applicable To

Hb-SD disease
Hb-SE disease

The following code(s) above D57.8 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

Applicable To annotations, or
Code Also annotations, or
Code First annotations, or
Excludes1 annotations, or
Excludes2 annotations, or
Includes annotations, or
Note annotations, or
Use Additional annotations

that may be applicable to D57.8:

D50-D89
2023 ICD-10-CM Range D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Type 2 Excludes
- 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)
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
D57
ICD-10-CM Diagnosis Code D57
Sickle-cell disorders
Type 1 Excludes
- other hemoglobinopathies (D58.-)
Use Additional
- code for any associated fever (R50.81)
Sickle-cell disorders

Code History

2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
2017 (effective 10/1/2016): No change
2018 (effective 10/1/2017): No change
2019 (effective 10/1/2018): No change
2020 (effective 10/1/2019): No change
2021 (effective 10/1/2020): No change
2022 (effective 10/1/2021): No change
2023 (effective 10/1/2022): No change

Code annotations containing back-references to D57.8:

Code First: N08

ICD-10-CM Diagnosis Code N08
Glomerular disorders in diseases classified elsewhere
Applicable To
- Glomerulonephritis
- Nephritis
- Nephropathy
Code First
- underlying disease, such as:
- amyloidosis (E85.-)
- congenital syphilis (A50.5)
- cryoglobulinemia (D89.1)
- disseminated intravascular coagulation (D65)
- gout (M1A.-, M10.-)
- microscopic polyangiitis (M31.7)
- multiple myeloma (C90.0-)
- sepsis (A40.0-A41.9)
- sickle-cell disease (D57.0-D57.8)
Type 1 Excludes
- glomerulonephritis, nephritis and nephropathy (in):
- antiglomerular basement membrane disease (M31.0)
- diabetes (E08-E13 with .21)
- gonococcal (A54.21)
- Goodpasture's syndrome (M31.0)
- hemolytic-uremic syndrome (D59.3-)
- lupus (M32.14)
- mumps (B26.83)
- syphilis (A52.75)
- systemic lupus erythematosus (M32.14)
- Wegener's granulomatosis (M31.31)
- pyelonephritis in diseases classified elsewhere (N16)
- renal tubulo-interstitial disorders classified elsewhere (N16)

Diagnosis Index entries containing back-references to D57.8:

Disease, diseased - see also Syndrome
- hemoglobin or Hb
  - SD D57.8-
  - SE D57.8-
- sickle-cell D57.1
  ICD-10-CM Diagnosis Code D57.1
  Sickle-cell disease without crisis
  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  Applicable To
  Hb-SS disease without crisis
  Sickle-cell anemia NOS
  Sickle-cell disease NOS
  Sickle-cell disorder NOS
  - elliptocytosis D57.8-
Disorder (of) - see also Disease
- sickle-cell (sickling) (homozygous) - see Disease, sickle-cell
  - specified type NEC D57.8-
Elliptocytosis (congenital) (hereditary) D58.1
ICD-10-CM Diagnosis Code D58.1
Hereditary elliptocytosis
Applicable To
Elliptocytosis (congenital)
Ovalocytosis (congenital) (hereditary)
- sickle-cell (disease) D57.8-
Spherocytosis (congenital) (familial) (hereditary) D58.0
ICD-10-CM Diagnosis Code D58.0
Hereditary spherocytosis
Applicable To
Acholuric (familial) jaundice
Congenital (spherocytic) hemolytic icterus
Minkowski-Chauffard syndrome
- sickle-cell D57.8- (disease)

ICD-10-CM Codes Adjacent To D57.8

D57.433 Sickle-cell thalassemia beta zero with cerebral vascular involvement

D57.438 …… with other specified complication

D57.439 …… unspecified

D57.44 …… beta plus without crisis

D57.45 Sickle-cell thalassemia beta plus with crisis

D57.451 Sickle-cell thalassemia beta plus with acute chest syndrome

D57.452 Sickle-cell thalassemia beta plus with splenic sequestration

D57.453 Sickle-cell thalassemia beta plus with cerebral vascular involvement

D57.458 …… with other specified complication

D57.459 …… unspecified

D57.8 Other sickle-cell disorders

D57.80 …… without crisis

D57.81 Other sickle-cell disorders with crisis

D57.811 Other sickle-cell disorders with acute chest syndrome

D57.812 Other sickle-cell disorders with splenic sequestration

D57.813 Other sickle-cell disorders with cerebral vascular involvement

D57.818 …… with other specified complication

D57.819 …… unspecified

D58 Other hereditary hemolytic anemias

D58.0 Hereditary spherocytosis

D58.1 Hereditary elliptocytosis

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

2023 ICD-10-CM Diagnosis Code D57.8

Other sickle-cell disorders

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Sickle-cell disorders

Glomerular disorders in diseases classified elsewhere

Sickle-cell disease without crisis

Hereditary elliptocytosis

Hereditary spherocytosis