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RHYNS syndrome

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Description

RHYNS syndrome is characterized by gaze palsy, retinitis pigmentosa, sensorineural hearing loss, hypopituitarism, nephronophthisis, and mild skeletal dysplasia (Di Rocco et al., 1997).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

10

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Genes

External Links

  • OMIM

    602152

  • Orphanet

    140976

  • HPO
  • Medgen

    C1865794

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