Variants
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Usher syndrome type 3A

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Description

Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

26

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Genes

External Links

  • OMIM
  • Orphanet
  • HPO
  • Medgen

    C3510450

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