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.
Also Known As:
Atypical Hemolytic-Uremic Syndrome; Hemolytic Uremic Syndrome, Atypical; Non-Shiga-Like Toxin-Associated HUS; Non-Stx-Hus; Nonenteropathic HUS; Atypical Hemolytic-Uremic Syndromes; HUS, Non-Shiga-Like Toxin-Associated; HUS, Nonenteropathic; HUSs, Non-Shiga-Like Toxin-Associated; HUSs, Nonenteropathic; Hemolytic-Uremic Syndrome, Atypical; Hemolytic-Uremic Syndromes, Atypical; Non Shiga Like Toxin Associated HUS; Non Stx Hus; Non-Shiga-Like Toxin-Associated HUSs; Nonenteropathic HUSs; Syndrome, Atypical Hemolytic-Uremic; Syndromes, Atypical Hemolytic-Uremic; Toxin-Associated HUS, Non-Shiga-Like; Toxin-Associated HUSs, Non-Shiga-Like