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Atypical Hemolytic Uremic Syndrome MeSH Descriptor Data 2021


MeSH Heading
Atypical Hemolytic Uremic Syndrome
Tree Number(s)
C12.777.419.936.463.500
C13.351.968.419.936.463.500
C15.378.071.141.610.500
C15.378.140.855.925.500.500
Unique ID
D065766
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D065766
Scope Note
An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome.
Entry Term(s)
Atypical Hemolytic-Uremic Syndrome
Hemolytic Uremic Syndrome, Atypical
Non-Shiga-Like Toxin-Associated HUS
Non-Stx-Hus
Nonenteropathic HUS
Public MeSH Note
2015; see HEMOLYTIC-UREMIC SYNDROME 2010-2014;
History Note
2015; use Hemolytic-Uremic Syndrome 2010-2014
Date Established
2015/01/01
Date of Entry
2014/06/26
Revision Date
2015/11/23
Atypical Hemolytic Uremic Syndrome Preferred
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