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GTR Home > Conditions/Phenotypes > Galloway-Mowat syndrome 5


Galloway-Mowat syndrome is a renal-neurologic disease characterized by early-onset nephrotic syndrome associated with microcephaly, gyral abnormalities, and delayed psychomotor development. Most patients have dysmorphic facial features, often including hypertelorism and ear abnormalities. Other features, such as arachnodactyly and visual or hearing impairment, are more variable. Most patients die in the first years of life (summary by Braun et al., 2017). For a general phenotypic description and a discussion of genetic heterogeneity of GAMOS, see GAMOS1 (251300). [from OMIM]

Available tests

11 tests are in the database for this condition.

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Genes See tests for all associated and related genes

  • Also known as: CGI-121, CGI121, GAMOS5, TPRKB
    Summary: TP53RK binding protein

Clinical features


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