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Atypical hemolytic-uremic syndrome

MONDO:0016244

A rare, genetic thrombotic microangiopathy due to dysregulation of the alternative complement pathway and characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal dysfunction.

Also known as: Atypical Hemolytic Uremic Syndrome, D-HUS, aHUS, atypical HUS, atypical hemolytic uremic syndrome, hemolytic-uremic syndrome without diarrhea, hemolytic-uremic syndrome without diarrhoea, non-diarrhea-associated hemolytic uremic syndrome

65 clinical trials for this condition and its sub-types, 19 tagged with Atypical hemolytic-uremic syndrome itself.

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