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References OMIM Gene GeneReviews HGMD HGNC
last update : 6/09/2006
Symbol FILWP
Location Xp11.2
Name familial idiopathic low molecular weight proteinuria
Corresponding gene CLCN5
Main clinical features
  • proximal tubulopathy with relatively conserved renal function in young patients, without rickets with hypercalciuria and nephrocalcinosis
  • Genetic determination sex linked
    Function/system disorder kidney and urinary tract
    Type disease
    Gene product
    Name chloride voltage-gated channel 5 (CLCN5)