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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Optic Atrophies, Hereditary
Eye Diseases > Eye Diseases, Hereditary > Optic Atrophies, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Optic Atrophies, Hereditary
Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System > Optic Atrophies, Hereditary
Nervous System Diseases > Cranial Nerve Diseases > Optic Nerve Diseases > Optic Atrophy > Optic Atrophies, Hereditary
Eye Diseases > Optic Nerve Diseases > Optic Atrophy > Optic Atrophies, Hereditary

Terme préférentiel

Optic Atrophies, Hereditary  

Type

  • mesh:Descriptor

Définition

  • Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).

Concept générique

Concepts spécifiques

Synonyme(s)

  • Hereditary Optic Atrophy
  • Optic Atrophy, Hereditary

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-RBXH1300-0

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RDF/XML TURTLE JSON-LD Date de création 07/06/1988, dernière modification le 25/07/2001