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MeSH 搜索器

Atypical Hemolytic Uremic Syndrome

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.
推出的年份: 2015
副标题
树号: C12.050.351.968.419.936.463.500, C12.200.777.419.936.463.500, C12.950.419.936.463.500, C15.378.071.141.610.500, C15.378.140.855.925.500.500
MeSH 单一 ID: D065766
进入的组:
  • Hemolytic Uremic Syndrome, Atypical
  • Atypical Hemolytic-Uremic Syndrome
  • Atypical Hemolytic-Uremic Syndromes
  • Hemolytic-Uremic Syndrome, Atypical
  • Hemolytic-Uremic Syndromes, Atypical
  • Syndrome, Atypical Hemolytic-Uremic
  • Syndromes, Atypical Hemolytic-Uremic
  • Non-Stx-Hus
  • Non Stx Hus
  • Nonenteropathic HUS
  • HUS, Nonenteropathic
  • HUSs, Nonenteropathic
  • Nonenteropathic HUSs
  • Non-Shiga-Like Toxin-Associated HUS
  • HUS, Non-Shiga-Like Toxin-Associated
  • HUSs, Non-Shiga-Like Toxin-Associated
  • Non Shiga Like Toxin Associated HUS
  • Non-Shiga-Like Toxin-Associated HUSs
  • Toxin-Associated HUS, Non-Shiga-Like
  • Toxin-Associated HUSs, Non-Shiga-Like

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