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Start free with EleplanAtypical hemolytic uremic syndrome with anti-factor H antibodies
ORPHA:93581Etiological subtype
Also called Atypical HUS with anti-factor H antibodies · aHUS with anti-factor H antibodies · aHUS with neutralizing autoantibodies against factor H
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Classified as
- Etiological subtype
Recorded for the broader condition
- Prevalence
- 1-9 / 100 000 (Europe)Atypical hemolytic uremic syndrome
- Age of onset
- All agesAtypical hemolytic uremic syndrome
- Inheritance
- Autosomal dominant, Autosomal recessive, Not applicableAtypical hemolytic uremic syndrome
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
ICD-10 codes
ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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