Hereditary hemolytic-uremic syndrome
Billable / specificHCC V28 109
D59.32 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Atypical hemolytic uremic syndrome with an identified genetic cause
Excludes2
Not included here — may be reported together when both conditions exist.
- autoimmune disease (systemic) NOS (M35.9) (from D59)
- certain conditions originating in the perinatal period (P00-P96) (from D59)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D59)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D59)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D59)
- human immunodeficiency virus [HIV] disease (B20) (from D59)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D59)
- neoplasms (C00-D49) (from D59)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D59)
Code also
An additional code may be needed.
Also known as
- Atypical hemolytic uremic syndrome with an identified genetic cause
- Syndrome, hemolytic-uremic, atypical, genetic
- Syndrome, hemolytic-uremic, atypical, hereditary
- Syndrome, hemolytic-uremic, due to genetic disorder
- Syndrome, hemolytic-uremic, familial
- Syndrome, hemolytic-uremic, hereditary
Parent code
- D59.3Hemolytic-uremic syndromeHeader