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Neurofibromatosis 2  

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Tipo

  • mesh:Descriptor

Definición

  • An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.

Etiquetas alternativas

  • Bilateral Acoustic Neurofibromatosis
  • Central Neurofibromatosis
  • Neurofibromatosis, Acoustic, Bilateral
  • Neurofibromatosis, Central, NF 2
  • Neurofibromatosis, Central NF2
  • Neurofibromatosis, Central, NF2
  • Neurofibromatosis, central type
  • Neurofibromatosis II
  • Neurofibromatosis Type 2
  • Neurofibromatosis, Type 2
  • Neurofibromatosis Type II
  • Neurofibromatosis, Type II
  • NF2 (Neurofibromatosis 2)

En otras lenguas

  • francés

  • Neurofibromatose acoustique bilatérale
  • Neurofibromatose centrale NF2
  • Neurofibromatose de type II
  • NF-2 (NeuroFibromatose de type 2)
  • NF2 (NeuroFibromatose de type 2)
  • NF2 acoustique

URI

http://data.loterre.fr/ark:/67375/JVR-LTTBC8CQ-Z

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