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References OMIM Gene GeneReviews HGMD HGNC
last update : 05-01-2010
Symbol FSGS3
Location 6p12.3
Name focal segmental glomerulosclerosis 3
Corresponding gene CD2AP
Main clinical features
  • histopathologic finding in several renal disorders characterized by proteinuria and progressive decline in renal function
  • nephrotic syndrome with elevated urine microalbumin excretion without another cause (microalbumin more than 20 mg/g creatinine)
  • Genetic determination autosomal recessive
    Related entries including hereditary/congenital nephrotic syndromes
    Function/system disorder kidney and urinary tract
    Type disease