Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

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)