MeSH 搜索器

Neurofibromatoses

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)
推出的年份: 2000(1993)
副标题
树号: C04.557.580.600.580.590, C04.700.631, C10.562.600, C10.574.500.549, C16.320.400.560, C16.320.700.633
MeSH 单一 ID: D017253
进入的组:
  • Neurofibromatosis
  • Neurofibromatosis Syndrome
  • Neurofibromatosis Syndromes
  • Syndrome, Neurofibromatosis
  • Syndromes, Neurofibromatosis
  • Multiple Neurofibromas
  • Multiple Neurofibroma
  • Neurofibroma, Multiple
  • Neurofibromas, Multiple
  • Neurofibromatosis 3
  • Neurofibromatosis 3s
  • Neurofibromatosis Type 3
  • Neurofibromatosis Type 3s
  • Type 3, Neurofibromatosis

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