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An X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness.

Year introduced: 1990

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Tree Number(s): C11.270.142, C11.941.160.300, C16.320.290.142, C16.320.322.092

MeSH Unique ID: D015794

Entry Terms:

  • Choroideremias
  • Progressive Tapetochoroidal Dystrophy
  • Tapetochoroidal Dystrophy, Progressive
  • Dystrophies, Progressive Tapetochoroidal
  • Dystrophy, Progressive Tapetochoroidal
  • Progressive Tapetochoroidal Dystrophies
  • Tapetochoroidal Dystrophies, Progressive

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