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References OMIM Gene GeneReviews HGMD HGNC
last update : 25/04/2007
Symbol HUS2
Location 6p21.3
Name hemolytic-uremic syndrome, atypical 2
Corresponding gene CFB
Main clinical features
  • characterized by the simultaneous occurence of microangiopathic hemolytic anemia and acute renal insufficency that was not preceded by either a diarrheal prodrome or an enteric infection . thrombocytopenia, Coomb's test-negative microangiopathic hemolytic anemia and acute renal failure
  • Genetic determination not applicable
    Function/system disorder hematology
    kidney and urinary tract
    Type disease
    Gene mutationChromosome rearrangementEffectComments
    unknown   abnormal protein/gain of function