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Fraser syndrome 2

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Description

Fraser syndrome is an autosomal recessive malformation disorder characterized by cryptophthalmos, syndactyly, and abnormalities of the respiratory and urogenital tract (summary by van Haelst et al., 2008). For a general phenotypic description and a discussion of genetic heterogeneity of Fraser syndrome, see 219000.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

347

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Genes

External Links

  • OMIM

    617666

  • Orphanet
  • HPO
  • Medgen

    C4540036

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