Variants
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Focal segmental glomerulosclerosis 5

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Description

Focal segmental glomerulosclerosis (FSGS) is a pathologic entity associated clinically with proteinuria, the nephrotic syndrome (NPHS), and progressive loss of renal function. It is a common cause of end-stage renal disease (ESRD) (Meyrier, 2005). Dominant intermediate Charcot-Marie-Tooth disease E and focal segmental glomerulonephritis (CMTDIE; 614455) is also caused by heterozygous mutation in the INF2 gene. For a general phenotypic description and a discussion of genetic heterogeneity of focal segmental glomerulosclerosis and nephrotic syndrome, see FSGS1 (603278).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

490

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Genes

External Links

  • OMIM

    613237

  • Orphanet
  • HPO
  • Medgen

    C2750475

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