D59.32 Hereditary hemolytic-uremic syndrome

Instructional Notes:

D59.32
Description: Hereditary hemolytic-uremic syndrome
Inclusion Term:
- Atypical hemolytic uremic syndrome with an identified genetic cause
Code Also: [', if applicable:', 'defects in the complement system (D84.1)', 'methylmalonic acidemia (E71.120)']
↓
D59.3
Description: Hemolytic-uremic syndrome
Code Also: [', if applicable, any associated:', 'acute kidney failure (N17.-)', 'chronic kidney disease (N18.-)']
↓
D59
Description: Acquired hemolytic anemia
↓
D55-D59
Description: Hemolytic anemias (D55-D59)
↓
D50-D89
Description: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Exclude2:
- 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)