- D59.32 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM D59.32 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.
ICD-10-CM D59.32 is grouped within Diagnostic Related Group(s):
- 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
Applicable To
- Atypical hemolytic uremic syndrome with an identified genetic cause
Code History
- 2024 (effective 10/1/2022): New code
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to D59.32:
- genetic > atypical D59.39
- hereditary > atypical D59.39
- due to genetic disorder > hemolytic-uremic D59.30
- familial > hemolytic-uremic D59.30
- hereditary > hemolytic-uremic D59.30