D59.32 - Hereditary hemolytic-uremic syndrome
- Applicable to Hereditary hemolytic-uremic syndrome
- The 2025 edition of ICD10-CM D59.32 became effective on October 1, 2024.
- This is the American ICD10-CM version of D59.32 - other international versions of ICD10 D59.32 may differ.
- D59.32 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Atypical hemolytic uremic syndrome with an identified genetic cause
codeAlso
- , if applicable:
- defects in the complement system (D84.1)
- methylmalonic acidemia (E71.120)
Billable/Specific Code
The following codes above D59.32 contain annotation back-references that may be applicable to D59.32:
- Chapter: D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- Section: D55-D59 - Hemolytic anemias
- Category: D59 - Acquired hemolytic anemia
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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