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GTR Home > Conditions/Phenotypes > Focal segmental glomerulosclerosis 2

Focal segmental glomerulosclerosis 2

Summary

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) (review by Meyrier, 2005). For a general phenotypic description and a discussion of genetic heterogeneity of focal segmental glomerulosclerosis and nephrotic syndrome (NPHS), see FSGS1 (603278). [from OMIM]

Available tests

40 tests are in the database for this condition.

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Clinical tests (39 available)

Molecular Genetics Tests

Research tests

Genes See tests for all associated and related genes

  • Also known as: FSGS2, TRP6, TRPC6
    Summary: transient receptor potential cation channel subfamily C member 6

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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