Variants
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Retinitis pigmentosa 11

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Description

Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of retinal dystrophies characterized by a progressive degeneration of photoreceptors, eventually resulting in severe visual impairment. For a discussion of genetic heterogeneity of RP, see 268000.

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

20

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Genes

External Links

  • OMIM

    600138

  • Orphanet
  • HPO
  • Medgen

    C1838601

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