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Vitelliform Macular Dystrophy

Autosomal dominant hereditary maculopathy with childhood-onset accumulation of LIPOFUSION in RETINAL PIGMENT EPITHELIUM. Affected individuals develop progressive central acuity loss, and distorted vision (METAMORPHOPSIA). It is associated with mutations in bestrophin, a chloride channel.

Year introduced: 2011

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Tree Number(s): C11.768.585.439.433, C16.320.290.763

MeSH Unique ID: D057826

Entry Terms:

  • Dystrophies, Vitelliform Macular
  • Dystrophy, Vitelliform Macular
  • Macular Dystrophies, Vitelliform
  • Vitelliform Macular Dystrophies
  • Best Macular Dystrophy
  • Dystrophy, Best Macular
  • Macular Dystrophy, Best
  • Best Vitelliform Macular Dystrophy
  • Macular Degeneration, Polymorphic Vitelline
  • Macular Dystrophy, Vitelliform
  • Vitelliform Dystrophy
  • Best Disease
  • Disease, Best
  • Best's Disease
  • Disease, Best's
  • Adult-Onset Vitelliform Macular Dystrophy
  • Adult Onset Vitelliform Macular Dystrophy
  • Vitelliform Macular Dystrophy, Adult-Onset
  • Vitelliform Macular Dystrophy, Adult Onset
  • Macular Dystrophy, Vitelliform, Adult-Onset
  • Foveomacular Dystrophy, Adult-Onset
  • Adult-Onset Foveomacular Dystrophies
  • Adult-Onset Foveomacular Dystrophy
  • Dystrophies, Adult-Onset Foveomacular
  • Dystrophy, Adult-Onset Foveomacular
  • Foveomacular Dystrophies, Adult-Onset
  • Foveomacular Dystrophy, Adult Onset
  • Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization
  • Juvenile-Onset Vitelliform Macular Dystrophy
  • Juvenile Onset Vitelliform Macular Dystrophy
  • Vitelliform Macular Dystrophy, Early-Onset
  • Vitelliform Macular Dystrophy, Early Onset
  • Vitelliform Macular Dystrophy, Juvenile-Onset
  • Vitelliform Macular Dystrophy, Juvenile Onset
  • Vitelliform Macular Dystrophy Type 2

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