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

From determinar.ia.br - Determine suas informações
Congenital nephrotic syndrome of the Finnish type is a genetic nephrotic syndrome characterised by protein loss beginning during fetal life.
Language Label Description Also known as
default for all languages
ID_1024559544
    English
    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.

      Statements

      CID11:ID_1024559544
      0 references
      dki-india-ID_1024559544
      0 references
      Concluído
      0 references
      16 August 2026
      0 references