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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Autosomal dominant optic atrophy plus syndrome


Other Names for this Disease
  • Congenital fibrinogen deficiency
  • DOA+
  • DOMINANT OPTIC ATROPHY PLUS SYNDROME
  • Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy
  • Optic atrophy - deafness- polyneuropathy - myopathy
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Other Names for this Disease
  • Congenital fibrinogen deficiency
  • DOA+
  • DOMINANT OPTIC ATROPHY PLUS SYNDROME
  • Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy
  • Optic atrophy - deafness- polyneuropathy - myopathy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.