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GTR Home > Conditions/Phenotypes > Focal segmental glomerulosclerosis 6

Focal segmental glomerulosclerosis 6

Summary

Focal segmental glomerulosclerosis-6 is an autosomal recessive childhood-onset kidney disorder manifest clinically by the nephrotic syndrome, which is characterized by proteinuria, hematuria, hypoalbuminemia, and progressive renal failure. It is a disease of the glomerular podocyte (summary by Mele et al., 2011). For a general phenotypic description and a discussion of genetic heterogeneity of focal segmental glomerulosclerosis and nephrotic syndrome, see FSGS1 (603278). [from OMIM]

Available tests

31 tests are in the database for this condition.

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Clinical tests (31 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: FSGS6, HuncM-IC, MYO1C, MYO1E
    Summary: myosin IE

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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