Preferred Label : Atypical Hemolytic Uremic Syndrome;
MeSH definition : 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.;
MeSH synonym : 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; Non-Stx-Hus; Non Stx Hus; Atypical Hemolytic-Uremic Syndrome; Atypical Hemolytic-Uremic Syndromes; Hemolytic-Uremic Syndrome, Atypical; Hemolytic-Uremic Syndromes, Atypical; Syndrome, Atypical Hemolytic-Uremic; Syndromes, Atypical Hemolytic-Uremic; Hemolytic Uremic Syndrome, Atypical;
Wikipedia link : https://en.wikipedia.org/wiki/Atypical hemolytic uremic syndrome;
Origin ID : D065766;
UMLS CUI : C2931788;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
Record concept(s)
Semantic type(s)
UMLS correspondences (same concept)
Validated automatic mappings to NTBT
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.
https://www.cochrane.org/fr/CD012862/RENAL_quel-est-le-traitement-le-plus-efficace-du-syndrome-hemolytique-et-uremique-atypique
2021
false
false
false
France
United Kingdom
review of literature
french abstract
hemolytic uremic syndrome, nos
Atypical Hemolytic Uremic Syndrome
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