D55-D59
Medium Complexity

Hemolytic anemias

Primary Specialty: Hematology
Last Updated: 2025-09-09

ICD-10 Codes (87)

87 billable
0 category headers
D56
Billable
Thalassemia
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D56.0
Billable
Alpha thalassemia
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D56.1
Billable
Beta thalassemia
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D56.2
Billable
Delta-beta thalassemia
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D56.3
Billable
Thalassemia minor
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D56.4
Billable
Hereditary persistence of fetal hemoglobin [HPFH]
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D56.5
Billable
Hemoglobin E-beta thalassemia
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D56.8
Billable
Other thalassemias
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D56.9
Billable
Thalassemia, unspecified
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D57
Billable
Sickle-cell disorders
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D57.0
Billable
Hb-SS disease with crisis
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D57.00
Billable
Hb-SS disease with crisis, unspecified
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D57.01
Billable
Hb-SS disease with acute chest syndrome
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D57.02
Billable
Hb-SS disease with splenic sequestration
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D57.03
Billable
Hb-SS disease with cerebral vascular involvement
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D57.04
Billable
Hb-SS disease with dactylitis
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D57.09
Billable
Hb-SS disease with crisis with other specified complication
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D57.1
Billable
Sickle-cell disease without crisis
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D57.2
Billable
Sickle-cell/Hb-C disease
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D57.20
Billable
Sickle-cell/Hb-C disease without crisis
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D57.21
Billable
Sickle-cell/Hb-C disease with crisis
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D57.211
Billable
Sickle-cell/Hb-C disease with acute chest syndrome
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D57.212
Billable
Sickle-cell/Hb-C disease with splenic sequestration
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D57.213
Billable
Sickle-cell/Hb-C disease with cerebral vascular involvement
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D57.214
Billable
Sickle-cell/Hb-C disease with dactylitis
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D57.218
Billable
Sickle-cell/Hb-C disease with crisis with other specified complication
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D57.219
Billable
Sickle-cell/Hb-C disease with crisis, unspecified
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D57.3
Billable
Sickle-cell trait
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D57.4
Billable
Sickle-cell thalassemia
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D57.40
Billable
Sickle-cell thalassemia without crisis
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D57.41
Billable
Sickle-cell thalassemia, unspecified, with crisis
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D57.411
Billable
Sickle-cell thalassemia, unspecified, with acute chest syndrome
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D57.412
Billable
Sickle-cell thalassemia, unspecified, with splenic sequestration
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D57.413
Billable
Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
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D57.414
Billable
Sickle-cell thalassemia, unspecified, with dactylitis
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D57.418
Billable
Sickle-cell thalassemia, unspecified, with crisis with other specified complication
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D57.419
Billable
Sickle-cell thalassemia, unspecified, with crisis
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D57.42
Billable
Sickle-cell thalassemia beta zero without crisis
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D57.43
Billable
Sickle-cell thalassemia beta zero with crisis
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D57.431
Billable
Sickle-cell thalassemia beta zero with acute chest syndrome
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D57.432
Billable
Sickle-cell thalassemia beta zero with splenic sequestration
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D57.433
Billable
Sickle-cell thalassemia beta zero with cerebral vascular involvement
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D57.434
Billable
Sickle-cell thalassemia beta zero with dactylitis
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D57.438
Billable
Sickle-cell thalassemia beta zero with crisis with other specified complication
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D57.439
Billable
Sickle-cell thalassemia beta zero with crisis, unspecified
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D57.44
Billable
Sickle-cell thalassemia beta plus without crisis
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D57.45
Billable
Sickle-cell thalassemia beta plus with crisis
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D57.451
Billable
Sickle-cell thalassemia beta plus with acute chest syndrome
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D57.452
Billable
Sickle-cell thalassemia beta plus with splenic sequestration
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D57.453
Billable
Sickle-cell thalassemia beta plus with cerebral vascular involvement
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D57.454
Billable
Sickle-cell thalassemia beta plus with dactylitis
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D57.458
Billable
Sickle-cell thalassemia beta plus with crisis with other specified complication
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D57.459
Billable
Sickle-cell thalassemia beta plus with crisis, unspecified
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D57.8
Billable
Other sickle-cell disorders
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D57.80
Billable
Other sickle-cell disorders without crisis
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D57.81
Billable
Other sickle-cell disorders with crisis
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D57.811
Billable
Other sickle-cell disorders with acute chest syndrome
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D57.812
Billable
Other sickle-cell disorders with splenic sequestration
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D57.813
Billable
Other sickle-cell disorders with cerebral vascular involvement
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D57.814
Billable
Other sickle-cell disorders with dactylitis
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D57.818
Billable
Other sickle-cell disorders with crisis with other specified complication
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D57.819
Billable
Other sickle-cell disorders with crisis, unspecified
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D58
Billable
Other hereditary hemolytic anemias
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D58.0
Billable
Hereditary spherocytosis
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D58.1
Billable
Hereditary elliptocytosis
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D58.2
Billable
Other hemoglobinopathies
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D58.8
Billable
Other specified hereditary hemolytic anemias
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D58.9
Billable
Hereditary hemolytic anemia, unspecified
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D59
Billable
Acquired hemolytic anemia
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D59.0
Billable
Drug-induced autoimmune hemolytic anemia
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D59.1
Billable
Other autoimmune hemolytic anemias
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D59.10
Billable
Autoimmune hemolytic anemia, unspecified
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D59.11
Billable
Warm autoimmune hemolytic anemia
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D59.12
Billable
Cold autoimmune hemolytic anemia
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D59.13
Billable
Mixed type autoimmune hemolytic anemia
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D59.19
Billable
Other autoimmune hemolytic anemia
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D59.2
Billable
Drug-induced nonautoimmune hemolytic anemia
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D59.3
Billable
Hemolytic-uremic syndrome
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D59.30
Billable
Hemolytic-uremic syndrome, unspecified
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D59.31
Billable
Infection-associated hemolytic-uremic syndrome
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D59.32
Billable
Hereditary hemolytic-uremic syndrome
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D59.39
Billable
Other hemolytic-uremic syndrome
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D59.4
Billable
Other nonautoimmune hemolytic anemias
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D59.5
Billable
Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
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D59.6
Billable
Hemoglobinuria due to hemolysis from other external causes
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D59.8
Billable
Other acquired hemolytic anemias
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D59.9
Billable
Acquired hemolytic anemia, unspecified
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Updates & Changes

FY 2026 Updates

Current Year

Deleted Codes

No codes deleted in this range for FY 2026

No significant changes for FY 2026

This range maintains stability with current coding practices

Historical Changes

  • FY 2025: Routine maintenance updates with minor terminology clarifications
  • FY 2024: Enhanced specificity requirements for certain code ranges
  • FY 2023: Updated documentation guidelines for improved clarity

Upcoming Changes

  • Proposed updates pending review by Coordination and Maintenance Committee
  • Under consideration: Enhanced digital health integration codes

Implementation Guidance

  • Review all FY 2026 updates for D55-D59 codes before implementation
  • Always verify the most current codes in the ICD-10-CM manual
  • Ensure clinical documentation supports the selected diagnosis codes
  • +3 more guidance items...

Range Overview

high priority

The ICD-10 code range D55-D59 represents Hemolytic anemias, a group of disorders characterized by premature destruction of red blood cells. These codes are used to document various types of hemolytic anemias, including hereditary spherocytosis, sickle-cell disorders, thalassemia, and glucose-6-phosphate dehydrogenase (G6PD) deficiency. The codes also account for autoimmune hemolytic anemias and other acquired hemolytic anemias.

Key Usage Points:

  • Always code to the highest level of specificity.
  • Use additional codes to identify any associated conditions.
  • For drug-induced hemolytic anemia, use additional code for adverse effect, if applicable.
  • When coding sickle-cell disorders, use additional code to identify any crisis.
  • For hereditary hemolytic anemias, the hereditary condition should be sequenced first.

Coding Guidelines

When to Use:

  • When a patient is diagnosed with any type of hemolytic anemia.
  • When a patient with sickle-cell disease experiences a crisis.
  • When a patient has a hereditary hemolytic anemia.
  • When a patient has drug-induced hemolytic anemia.

When NOT to Use:

  • When a patient has anemia not specified as hemolytic.
  • When a patient has anemia due to chemotherapy.
  • When a patient has iron deficiency anemia.
  • When a patient has anemia of chronic disease.

Code Exclusions

Always verify exclusions in the ICD-10-CM manual before assigning a code.

Documentation Requirements

Proper documentation for hemolytic anemias should include the specific type of anemia, the cause if known, and any associated conditions. It should also include the severity of the anemia and any complications.

Clinical Information:

  • Specific type of hemolytic anemia
  • Cause of the anemia, if known
  • Severity of the anemia
  • Any associated conditions
  • Any complications

Supporting Evidence:

  • Laboratory test results
  • Clinical notes
  • Radiology reports
  • Pathology reports
Good Documentation Example:

Patient diagnosed with severe autoimmune hemolytic anemia due to lupus. Hemoglobin level is 7.2 g/dL.

Poor Documentation Example:

Patient has anemia.

Common Documentation Errors:

  • Not specifying the type of hemolytic anemia
  • Not documenting the cause of the anemia
  • Not documenting the severity of the anemia
  • Not documenting any associated conditions

Range Statistics

5
Total Codes
87
Billable
Complexity:
Medium
Primary Use:Clinical Documentation
Chapter:3

Coding Complexity

Medium
Complexity Rating

The complexity of coding hemolytic anemias lies in the need to accurately identify the specific type of anemia, the cause if known, and any associated conditions or complications. This requires a thorough understanding of the condition and careful review of the medical documentation.

Key Factors:
  • Determining the specific type of hemolytic anemia
  • Identifying the cause of the anemia
  • Coding any associated conditions
  • Coding any complications

Specialty Focus

Hemolytic anemias are most commonly encountered in hematology, but can also be relevant in pediatrics, internal medicine, and family practice.

Primary Specialties:
Hematology
60%
Pediatrics
20%
Clinical Scenarios:
  • A patient with sickle-cell disease presenting with vaso-occlusive crisis.
  • A patient with hereditary spherocytosis experiencing hemolytic crisis.
  • A patient with G6PD deficiency after exposure to fava beans.
  • A patient with autoimmune hemolytic anemia secondary to lupus.

Resources & References

Resources for coding hemolytic anemias include the ICD-10-CM manual, official coding guidelines, and clinical references.

Official Guidelines:

  • ICD-10-CM Official Guidelines for Coding and Reporting
  • American Health Information Management Association (AHIMA) Coding Guidelines
  • Centers for Medicare & Medicaid Services (CMS) Coding Guidelines

Clinical References:

  • American Society of Hematology
  • National Heart, Lung, and Blood Institute

Educational Materials:

  • AHIMA ICD-10-CM Coding Workbook
  • AAPC ICD-10-CM Training Manual

Frequently Asked Questions

How do I code for a patient with sickle-cell disease and vaso-occlusive crisis?

You would use a code from the D57.0-D57.2 range for the sickle-cell disease, and an additional code from the D57.40-D57.42 range for the vaso-occlusive crisis.