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Concept information

Preferred term

Atypical Hemolytic Uremic Syndrome  

Type

  • Topical Descriptor

Entry terms

  • Atypical Hemolytic-Uremic Syndrome
  • Atypical Hemolytic-Uremic Syndromes
  • Hemolytic Uremic Syndrome, Atypical
  • Hemolytic-Uremic Syndrome, Atypical
  • Hemolytic-Uremic Syndromes, Atypical
  • HUS, Nonenteropathic
  • HUS, Non-Shiga-Like Toxin-Associated
  • HUSs, Nonenteropathic
  • HUSs, Non-Shiga-Like Toxin-Associated
  • Nonenteropathic HUS
  • Nonenteropathic HUSs
  • Non Shiga Like Toxin Associated HUS
  • Non-Shiga-Like Toxin-Associated HUS
  • Non-Shiga-Like Toxin-Associated HUSs
  • Non Stx Hus
  • Non-Stx-Hus
  • Syndrome, Atypical Hemolytic-Uremic
  • Syndromes, Atypical Hemolytic-Uremic
  • Toxin-Associated HUS, Non-Shiga-Like
  • Toxin-Associated HUSs, Non-Shiga-Like

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.

History note

  • 2015; use Hemolytic-Uremic Syndrome 2010-2014

In other languages

URI

http://www.yso.fi/onto/mesh/D065766

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