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... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Hemolytic-Uremic Syndrome > Atypical Hemolytic Uremic Syndrome
... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Uremia > Hemolytic-Uremic Syndrome > Atypical Hemolytic Uremic Syndrome
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Uremia > Hemolytic-Uremic Syndrome > Atypical Hemolytic Uremic Syndrome
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Platelet Disorders > Thrombocytopenia > Thrombotic Microangiopathies > Hemolytic-Uremic Syndrome > Atypical Hemolytic Uremic Syndrome

Término preferido

Atypical Hemolytic Uremic Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Etiquetas alternativas

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

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-PK9WWKNF-C

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RDF/XML TURTLE JSON-LD Creado 26/6/14, última modificación 30/6/21