2023 ICD-10-CM Diagnosis Code D59.32

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Hereditary hemolytic-uremic syndrome

    2023 - New Code Billable/Specific Code
  • D59.32 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • ICD-10-CM D59.32 is a new 2023 ICD-10-CM code that became effective on October 1, 2022.
  • This is the American ICD-10-CM version of D59.32 - other international versions of ICD-10 D59.32 may differ.
Applicable To
  • Atypical hemolytic uremic syndrome with an identified genetic cause
Code Also
Code Also Help
A code also note instructs that 2 codes may be required to fully describe a condition but the sequencing of the two codes is discretionary, depending on the severity of the conditions and the reason for the encounter.
  • , if applicable:
  • defects in the complement system (
    ICD-10-CM Diagnosis Code D84.1

    Defects in the complement system

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    Applicable To
    • C1 esterase inhibitor [C1-INH] deficiency
    D84.1
    )
  • methylmalonic acidemia (
    ICD-10-CM Diagnosis Code E71.120

    Methylmalonic acidemia

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    E71.120
    )
The following code(s) above D59.32 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 D59.32:
  • 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
  • D59.3
    ICD-10-CM Diagnosis Code D59.3

    Hemolytic-uremic syndrome

      2016 2017 2018 2019 2020 2021 2022 2023 - Converted to Parent Code Non-Billable/Non-Specific Code
    Code Also
    • , if applicable, any associated:
    • acute kidney failure (N17.-)
    • chronic kidney disease (N18.-)
    Hemolytic-uremic syndrome
ICD-10-CM D59.32 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
  • 791 Prematurity with major problems
  • 793 Full term neonate with major problems
  • 811 Red blood cell disorders with mcc
  • 812 Red blood cell disorders without mcc
Code History
  • 2023 (effective 10/1/2022): New code

Diagnosis Index entries containing back-references to D59.32:
  • Syndrome - see also Disease
    • hemolytic-uremic D59.30
      ICD-10-CM Diagnosis Code D59.30

      Hemolytic-uremic syndrome, unspecified

        2023 - New Code Billable/Specific Code
      Applicable To
      • Hemolytic-uremic syndrome NOS
      • atypical D59.39
        ICD-10-CM Diagnosis Code D59.39

        Other hemolytic-uremic syndrome

          2023 - New Code Billable/Specific Code
        Applicable To
        • Atypical (nongenetic) hemolytic uremic syndrome
        • Secondary hemolytic-uremic syndrome
        Code First
        • , if applicable, any associated:
        • COVID-19 (U07.1)
        • complications of kidney transplant (T86.1-)
        • complications of heart transplant (T86.2-)
        • complications of liver transplant (T86.4-)
        Code Also
        • , if applicable, any associated condition, such as:
        • hypertensive emergency (I16.1)
        • malignant neoplasm (C00-C96)
        • systemic lupus erythematosus (M32.-)
        Use Additional
        • code, if applicable, for adverse effect to identify drug (T36-T50 with fifth or sixth character 5)
        • genetic D59.32
        • hereditary D59.32
      • due to genetic disorder D59.32
      • familial D59.32
      • hereditary D59.32

ICD-10-CM Codes Adjacent To D59.32
D59.1 Other autoimmune hemolytic anemias
D59.10 Autoimmune hemolytic anemia, unspecified
D59.11 Warm autoimmune hemolytic anemia
D59.12 Cold autoimmune hemolytic anemia
D59.13 Mixed type autoimmune hemolytic anemia
D59.19 Other autoimmune hemolytic anemia
D59.2 Drug-induced nonautoimmune hemolytic anemia
D59.3 Hemolytic-uremic syndrome
D59.30 …… unspecified
D59.31 Infection-associated hemolytic-uremic syndrome
D59.32 Hereditary hemolytic-uremic syndrome
D59.39 Other hemolytic-uremic syndrome
D59.4 Other nonautoimmune hemolytic anemias
D59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D59.6 Hemoglobinuria due to hemolysis from other external causes
D59.8 Other acquired hemolytic anemias
D59.9 Acquired hemolytic anemia, unspecified
D60 Acquired pure red cell aplasia [erythroblastopenia]
D60.0 Chronic acquired pure red cell aplasia
D60.1 Transient acquired pure red cell aplasia
D60.8 Other acquired pure red cell aplasias

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