Variants
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X-linked cone-rod dystrophy 3

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Description

Cone-rod dystrophy is a retinal disorder with predominantly cone involvement. Rod impairment may occur at the same time as the cone impairment or appear later. Patients with CORD usually have reduced visual acuity, photophobia, and color vision defects (summary by Huang et al., 2013). For a discussion of genetic heterogeneity of X-linked cone-rod dystrophy, see 304020.

OMIM

  • Mode of Inheritance

  • X-linked recessive inheritance

VARIANTS

7

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Genes

External Links

  • OMIM

    300476

  • Orphanet
  • HPO
  • Medgen

    C1845407

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