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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

Término preferido

Optic Atrophies, Hereditary  

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Tipo

  • mesh:Descriptor

Definición

  • 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).

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • Hereditary Optic Atrophy
  • Optic Atrophy, Hereditary

En otras lenguas

URI

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

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