Orphanet: Full schwannomatosis
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Full schwannomatosis

Disease definition

A rare form of neurofibromatosis characterized by the development of multiple schwannomas (nerve sheath tumors), without involvement of the vestibular nerves, and often associated with chronic pain. Dysesthesia and paresthesia may also be present. Common localizations include the spine, peripheral nerves, and the cranium.

ORPHA:93921

Classification level: Disorder
  • Synonym(s):
    • Full NF3
    • Full SWN
    • Full neurofibromatosis type 3
    • Neurilemmomatosis
    • Nonmosaic schwannomatosis
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult, Elderly
  • ICD-10: Q85.0
  • OMIM: 162091  162260  615670
  • UMLS: C1335929
  • MeSH: C536641
  • GARD: 4768
  • MedDRA: -

  A summary on this disease is available in Español (2016) Italiano (2016) Nederlands (2016) Polski (2014, pdf) Polski ()

Detailed information

General public

Disease review articles

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.