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Concept information

disease > tumor > benign neoplasm > neurofibromatosis > neurofibromatosis II
disease > nervous system diseases > neurofibromatosis > neurofibromatosis II
disease > congenital disease > phacomatosis > neurofibromatosis > neurofibromatosis II

Terme préférentiel

neurofibromatosis II  

Définition

  • Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition which may be inherited or may arise spontaneously. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-XVHTVV5Q-2

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