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Isolated microphthalmia 2

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Description

Any isolated microphthalmia in which the cause of the disease is a mutation in the VSX2 gene.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

110

SEE THE VARIANTS →

Genes

  • VSX2

External Links

  • OMIM

    610093

  • Orphanet
  • HPO
  • Medgen

    C1864720

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