Mesh term Atypical Hemolytic Uremic Syndrome
Browse to parent terms:Hemolytic-Uremic Syndrome
Description
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.Search for this term in our Faculty Database
View this term at the NCBI website
