Variants
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Congenital stationary night blindness autosomal dominant 2

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Description

Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

125

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Genes

External Links

  • OMIM

    163500

  • Orphanet
  • HPO
  • Medgen

    C1876182

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