D59.32
BillableHereditary hemolytic-uremic syndrome
Hereditary hemolytic-uremic syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Atypical hemolytic uremic syndrome with an identified genetic cause
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, any associated:
- •acute kidney failureN17
- •chronic kidney diseaseN18
- , if applicable:
- •defects in the complement systemD84.1
- •methylmalonic acidemiaE71.120
Related Codes(3)
Also Known As / Clinical Terms(15)
SNOMED CT
- Congenital haemolytic uraemic syndrome444976001
- Congenital hemolytic uremic syndrome444976001
- Haemolytic uraemic syndrome with DGKE deficiency1269225005
- Haemolytic uraemic syndrome with diacylglycerol kinase epsilon deficiency1269225005
- Hemolytic uremic syndrome with DGKE deficiency1269225005
- Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency1269225005
UMLS
Clinical Terms
- Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency
- Congenital haemolytic uraemic syndrome
- Atypical hemolytic uremic syndrome with an identified genetic cause
- Congenital hemolytic uremic syndrome
- Haemolytic uraemic syndrome with DGKE deficiency
- Haemolytic uraemic syndrome with diacylglycerol kinase epsilon deficiency
- Hemolytic uremic syndrome with DGKE deficiency
Frequently Asked Questions
What is the ICD-10 code for hereditary hemolytic-uremic syndrome?
The ICD-10-CM code for hereditary hemolytic-uremic syndrome is D59.32. The full clinical description is "Hereditary hemolytic-uremic syndrome". D59.32 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D59.32 mean?
ICD-10-CM code D59.32 represents “Hereditary hemolytic-uremic syndrome”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D59.32 a billable code?
Yes, D59.32 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D59.32 in?
D59.32 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What SNOMED CT codes does D59.32 map to?
D59.32 maps to 2 SNOMED CT concepts: 444976001, 1269225005. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D59.32?
D59.32 is linked to 2 UMLS Concept Unique Identifiers: C5676588, C5674883. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D59.32 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary hemolytic-uremic syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D59.32?
There is no direct ICD-11 mapping available for D59.32 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.