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GTR Home > Conditions/Phenotypes > Nephrotic syndrome, type 11

Nephrotic syndrome, type 11

Summary

Nephrotic syndrome type 11 (NPHS11) is an autosomal recessive disorder of the kidney with onset in the first decade of life. The disorder is progressive and usually results in end-stage renal disease necessitating renal transplantation, although some patients may have a slightly milder phenotype (Miyake et al., 2015). For a general phenotypic description and a discussion of genetic heterogeneity of nephrotic syndrome, see NPHS1 (256300). [from OMIM]

Available tests

21 tests are in the database for this condition.

Clinical tests (21 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: NPHS11, NUP84, ODG6, ODG6; GAMOS7, NUP107
    Summary: nucleoporin 107

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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