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Concept information

Preferred term

Neurofibromatoses  

Type

  • mesh:Descriptor

Definition

  • A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)

Entry terms

  • Multiple Neurofibromas
  • Neurofibromatosis
  • Neurofibromatosis Syndrome

In other languages

URI

http://data.loterre.fr/ark:/67375/JVR-F3PSCGTG-4

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