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Concept information

Preferred term

Neurofibromatosis 2  

Type

  • mesh:Descriptor

Definition

  • 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.

Entry terms

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

In other languages

  • French

  • 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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