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Concept information

Eye Diseases > Uveal Diseases > Choroid Diseases > Choroideremia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Choroideremia
Eye Diseases > Eye Diseases, Hereditary > Choroideremia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Choroideremia

Término preferido

Choroideremia  

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Tipo

  • mesh:Descriptor

Definición

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

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Progressive Tapetochoroidal Dystrophy
  • Tapetochoroidal Dystrophy, Progressive

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-KQG0FKCK-3

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RDF/XML TURTLE JSON-LD Creado 25/5/89, última modificación 8/7/13