Glomerular disease associated with congenital nephrotic syndrome; Finnish type (Q108401)

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Congenital nephrotic syndrome of the Finnish type is a genetic nephrotic syndrome characterised by protein loss beginning during fetal life.
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    Glomerular disease associated with congenital nephrotic syndrome; Finnish type
    Congenital nephrotic syndrome of the Finnish type is a genetic nephrotic syndrome characterised by protein loss beginning during fetal life.

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