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GTR Home > Conditions/Phenotypes > Galloway-Mowat syndrome 7

Galloway-Mowat syndrome 7

Summary

Galloway-Mowat syndrome-7 (GAMOS7) is an autosomal recessive disorder characterized by developmental delay, microcephaly, and early-onset nephrotic syndrome (summary by Rosti et al., 2017). For a general phenotypic description and a discussion of genetic heterogeneity of GAMOS, see GAMOS1 (251300). [from OMIM]

Available tests

9 tests are in the database for this condition.

Clinical tests (9 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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